ID: 127824151 | H3K27ac hESC enhancer GRCh37_chr12:51155479-51156347 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50761696..50762564) | | |
ID: 127824150 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:51142690-51143323 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50748907..50749540) | | |
ID: 127824149 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:51142055-51142689 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50748272..50748906) | | |
ID: 127824148 | H3K27ac hESC enhancer GRCh37_chr12:51005781-51006280 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50611998..50612497) | | |
ID: 127824147 | H3K27ac hESC enhancer GRCh37_chr12:51005279-51005780 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50611496..50611997) | | |
ID: 127824146 | H3K4me1 hESC enhancer GRCh37_chr12:50924015-50924515 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50530232..50530732) | | |
ID: 127824145 | H3K4me1 hESC enhancer GRCh37_chr12:50923514-50924014 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50529731..50530231) | | |
ID: 124903127 | uncharacterized LOC124903127 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50488484..50488566, complement) | | |
ID: 124902932 | uncharacterized LOC124902932 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50743576..50757650, complement) | | |
ID: 124629356 | Sharpr-MPRA regulatory region 12282 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50550526..50550820) | | |
ID: 109286554 | fragile site, folic acid type, rare, fra(12)(q13.1) [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50505002..50505053) | | |
ID: 106633800 | small nucleolar RNA, C/D box 133 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50456571..50456786) | ZL142, ZL42, ggn68 | |
ID: 106481253 | RNA, U6 small nuclear 238, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50656973..50657072) | | |
ID: 106479906 | RNA, U6 small nuclear 769, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50633273..50633376) | | |
ID: 113251 | La ribonucleoprotein 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50400885..50480004) | PP13296 | 618657 |
ID: 57609 | disco interacting protein 2 homolog B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50504985..50748657) | | 611379 |