ID: 130008719 | ATAC-STARR-seq lymphoblastoid silent region 4844 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109845321..109845600) | | |
ID: 130008718 | ATAC-STARR-seq lymphoblastoid silent region 4843 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109713916..109713965) | | |
ID: 130008717 | ATAC-STARR-seq lymphoblastoid silent region 4842 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109713556..109713885) | | |
ID: 129663233 | ReSE screen-validated silencer GRCh37_chr12:110105927-110106096 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109668122..109668291) | | |
ID: 127825025 | H3K27ac hESC enhancer GRCh37_chr12:110258983-110259483 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109821178..109821678) | | |
ID: 127825024 | H3K4me1 hESC enhancer GRCh37_chr12:110209881-110210380 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109772076..109772575) | | |
ID: 127825023 | H3K4me1 hESC enhancer GRCh37_chr12:110177667-110178166 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109739862..109740361) | | |
ID: 127825022 | H3K4me1 hESC enhancer GRCh37_chr12:110177165-110177666 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109739360..109739861) | | |
ID: 127825021 | H3K4me1 hESC enhancer GRCh37_chr12:110174581-110175080 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109736671..109737275) | | |
ID: 127825020 | H3K4me1 hESC enhancer GRCh37_chr12:110169301-110169801 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109731496..109731996) | | |
ID: 127825019 | H3K4me1 hESC enhancer GRCh37_chr12:110164162-110164872 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109726357..109727067) | | |
ID: 127825018 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:110150092-110150655 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109712287..109712850) | | |
ID: 127825017 | H3K4me1 hESC enhancer GRCh37_chr12:110133637-110134446 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109695832..109696641) | | |
ID: 126861634 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:110108888-110110087 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109671083..109672282) | | |
ID: 124819397 | Sharpr-MPRA regulatory region 11384 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109775304..109775598) | | |
ID: 111429608 | HNF1 motif-containing MPRA enhancer 206 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109737779..109737923) | | |
ID: 106479383 | RNA, 7SL, cytoplasmic 441, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109866214..109866509, complement) | | |
ID: 106479206 | RN7SK pseudogene 250 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109662863..109663183, complement) | | |
ID: 105369975 | uncharacterized LOC105369975 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109840327..109843482, complement) | | |
ID: 100616454 | microRNA 4497 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109833348..109833436) | mir-4497 | |