ID: 127826140 | H3K4me1 hESC enhancer GRCh37_chr13:40341964-40342464 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39767827..39768327) | | |
ID: 127826139 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:40145878-40146444 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39571741..39572307) | | |
ID: 127826138 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:40145310-40145877 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39571173..39571740) | | |
ID: 127826137 | H3K27ac hESC enhancer GRCh37_chr13:40138121-40138621 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39563984..39564484) | | |
ID: 127826136 | H3K27ac hESC enhancer GRCh37_chr13:40137620-40138120 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39563483..39563983) | | |
ID: 127826135 | NANOG hESC enhancer GRCh37_chr13:40089286-40089967 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39515149..39515830) | | |
ID: 127826134 | H3K4me1 hESC enhancer GRCh37_chr13:40086605-40087104 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39512468..39512967) | | |
ID: 127826133 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:40073025-40073669 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39498888..39499532) | | |
ID: 127826132 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:40072380-40073024 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39498243..39498887) | | |
ID: 127826131 | H3K27ac hESC enhancer GRCh37_chr13:39991180-39992122 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39417043..39417985) | | |
ID: 127826130 | OCT4-NANOG hESC enhancer GRCh37_chr13:39903548-39904177 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39329411..39330040) | | |
ID: 127826129 | OCT4-NANOG hESC enhancer GRCh37_chr13:39902917-39903547 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39328780..39329410) | | |
ID: 126861745 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:40139174-40140373 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39565037..39566236) | | |
ID: 124903266 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39447115..39447216, complement) | | |
ID: 112268119 | protein SPT2 homolog [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39601324..39608996) | | |
ID: 107984580 | uncharacterized LOC107984580 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39307786..39337719, complement) | | |
ID: 105370170 | uncharacterized LOC105370170 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39505306..39516575) | | |
ID: 100422940 | microRNA 4305 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39664034..39664135, complement) | | |
ID: 57511 | component of oligomeric golgi complex 6 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39655627..39791666) | CDG2L, COD2, SHNS | 606977 |
ID: 10186 | LHFPL tetraspan subfamily member 6 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (39342892..39603193, complement) | LHFP | 606710 |