ID: 130060555 | ATAC-STARR-seq lymphoblastoid silent region 8343 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28552351..28552800) | | |
ID: 130060554 | ATAC-STARR-seq lymphoblastoid silent region 8342 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28552241..28552290) | | |
ID: 130060553 | ATAC-STARR-seq lymphoblastoid silent region 8341 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28550141..28550190) | | |
ID: 130060552 | ATAC-STARR-seq lymphoblastoid active region 11928 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28493149..28493218) | | |
ID: 130060551 | ATAC-STARR-seq lymphoblastoid active region 11927 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28484952..28485001) | | |
ID: 129664001 | ReSE screen-validated silencer GRCh37_chr17:26828166-26828362 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28501148..28501344) | | |
ID: 127886339 | H3K4me1 hESC enhancer GRCh37_chr17:26874790-26875626 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28547772..28548608) | | |
ID: 127886338 | H3K4me1 hESC enhancer GRCh37_chr17:26873952-26874789 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28546934..28547788) | | |
ID: 127886337 | H3K4me1 hESC enhancer GRCh37_chr17:26834617-26835569 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28507599..28508551) | | |
ID: 127886336 | H3K4me1 hESC enhancer GRCh37_chr17:26810033-26810546 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28483015..28483528) | | |
ID: 127886335 | NANOG-H3K27ac hESC enhancer GRCh37_chr17:26782409-26783036 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28455391..28456018) | | |
ID: 101060112 | RAP1A, member of RAS oncogene family pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28443357..28445924, complement) | | |
ID: 388363 | ribosomal protein S7 pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28467778..28468443) | RPS7_4_1531 | |
ID: 9094 | unc-119 lipid binding chaperone [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28546707..28552628, complement) | CORD24, HRG4, IMD13, POC7, POC7A | 604011 |
ID: 9058 | solute carrier family 13 member 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28473644..28497781) | NADC1, NaCT, NaDC-1, SDCT1 | 604148 |
ID: 8456 | forkhead box N1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28506348..28538900) | FKHL20, RONU, TIDAND, TLIND, WHN | 600838 |