ID: 130065741 | ATAC-STARR-seq lymphoblastoid active region 17771 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34955954..34956133) | | |
ID: 130065740 | ATAC-STARR-seq lymphoblastoid active region 17770 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34955614..34955713) | | |
ID: 130065739 | ATAC-STARR-seq lymphoblastoid silent region 12851 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34876471..34876900) | | |
ID: 130065738 | ATAC-STARR-seq lymphoblastoid silent region 12850 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34876251..34876390) | | |
ID: 130065737 | ATAC-STARR-seq lymphoblastoid active region 17769 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34875931..34875980) | | |
ID: 130065736 | ATAC-STARR-seq lymphoblastoid active region 17768 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34875831..34875910) | | |
ID: 130065735 | ATAC-STARR-seq lymphoblastoid silent region 12849 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34872738..34873027) | | |
ID: 129664604 | ReSE screen-validated silencer GRCh37_chr20:33554901-33555058 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34967098..34967255) | | |
ID: 127893143 | H3K4me1 hESC enhancer GRCh37_chr20:33574067-33574618 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34986264..34986815) | | |
ID: 127893142 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:33573515-33574066 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34985712..34986263) | | |
ID: 127893141 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:33571861-33572412 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34984058..34984609) | | |
ID: 127893140 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:33568001-33568552 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34980198..34980749) | | |
ID: 127893139 | H3K4me1 hESC enhancer GRCh37_chr20:33450836-33451387 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34863033..34863584) | | |
ID: 126863018 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr20:33508643-33509842 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34920840..34922039) | | |
ID: 100616134 | microRNA 499b [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34990400..34990472, complement) | MIR499A, hsa-mir-499b | |
ID: 574501 | microRNA 499a [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34990376..34990497) | MIR499, MIRN499, hsa-mir-499a, mir-499a | 613614 |
ID: 128872 | high mobility group box 3 pseudogene 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34833575..34834462, complement) | HMG4L, HMGB3L1, dJ18C9.3 | |
ID: 57644 | myosin heavy chain 7B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34955868..35002437) | MHC14, MYH14, lncMYH7b | 609928 |
ID: 55902 | acyl-CoA synthetase short chain family member 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34874989..34927959) | ACAS2, ACECS, ACS, ACSA, AceCS1, dJ1161H23.1 | 605832 |
ID: 2937 | glutathione synthetase [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34928432..34956027, complement) | CNSHA6, GSHS, HEL-S-64p, HEL-S-88n | 601002 |