ID: 127825026 | NANOG hESC enhancer GRCh37_chr12:110318928-110319429 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109881123..109881624) | | |
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: 124903012 | uncharacterized LOC124903012 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109880898..109881401, complement) | | |
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: 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 | |
ID: 84983 | FAM222A antisense RNA 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109734209..109773487, complement) | | |
ID: 84915 | family with sequence similarity 222 member A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109713825..109770495) | C12orf34 | |
ID: 84260 | trichoplein keratin filament binding [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109880667..109918069) | TpMs | 612654 |
ID: 59341 | transient receptor potential cation channel subfamily V member 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109783087..109833398, complement) | BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA, SSQTL1, TRP12, VRL2, VROAC | 605427 |