ID: 130006797 | ATAC-STARR-seq lymphoblastoid silent region 3924 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116787726..116787975) | | |
ID: 130006796 | ATAC-STARR-seq lymphoblastoid active region 5555 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116774899..116775068) | | |
ID: 130006795 | ATAC-STARR-seq lymphoblastoid active region 5554 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116773446..116773535) | | |
ID: 130006794 | ATAC-STARR-seq lymphoblastoid silent region 3923 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116773126..116773325) | | |
ID: 130006793 | ATAC-STARR-seq lymphoblastoid silent region 3922 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116742967..116743066) | | |
ID: 130006792 | ATAC-STARR-seq lymphoblastoid silent region 3921 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116732934..116732983) | | |
ID: 129663045 | ReSE screen-validated silencer GRCh37_chr11:116658726-116658949 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116788010..116788325) | | |
ID: 127822611 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr11:116580386-116581272 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116709670..116710556) | | |
ID: 127822610 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:116558904-116559465 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116688188..116688749) | | |
ID: 127822609 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:116558341-116558903 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116687625..116688187) | | |
ID: 127822608 | H3K4me1 hESC enhancer GRCh37_chr11:116512271-116513100 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116641554..116642383) | | |
ID: 127822607 | H3K4me1 hESC enhancer GRCh37_chr11:116511441-116512270 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116640724..116641553) | | |
ID: 124902762 | lncRNA regulator of hepatic lineages 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116812909..116814182, complement) | lnc-RHL | |
ID: 122455333 | BUD13 divergent transcript [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116773471..116774205) | | |
ID: 110121415 | VISTA enhancer hs1632 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116651165..116651910) | | |
ID: 108491825 | enhancer-blocking element 11-1-2 overlapping APOA5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116791046..116792831) | | |
ID: 108449897 | PATRR11 recombination region [Homo sapiens (human)] | | | |
ID: 101929011 | long intergenic non-protein coding RNA 2702 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116639422..116658252) | LASER | |
ID: 116519 | apolipoprotein A5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116789367..116792420, complement) | APOAV, RAP3 | 606368 |
ID: 84811 | BUD13 homolog [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116748173..116772987, complement) | Cwc26, fSAP71 | 620691 |