ID: 127816488 | H3K27ac hESC enhancer GRCh37_chr9:136203003-136203973 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133336166..133337136) | | |
ID: 127816487 | H3K27ac hESC enhancer GRCh37_chr9:136202031-136203002 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133335195..133336165) | | |
ID: 127816486 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:136179717-136180405 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133304236..133304924) | | |
ID: 127816485 | H3K4me1 hESC enhancer GRCh37_chr9:136133484-136134469 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133258094..133259078) | | |
ID: 127816484 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:136130804-136131336 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133255417..133255949) | | |
ID: 127816483 | H3K4me1 hESC enhancer GRCh37_chr9:136115033-136115642 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133239646..133240255) | | |
ID: 127816482 | H3K4me1 hESC enhancer GRCh37_chr9:136114423-136115032 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133239036..133239645) | | |
ID: 127816481 | H3K4me1 hESC enhancer GRCh37_chr9:136102720-136103675 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133227333..133228288) | | |
ID: 124902294 | uncharacterized LOC124902294 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133233276..133238303, complement) | | |
ID: 112679202 | ABO promoter region [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133275187..133276053) | | |
ID: 112679198 | ABO +5.8 intron 1 enhancer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133267998..133270594) | | |
ID: 112639999 | ABO 3' regulatory region [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133251819..133254521) | | |
ID: 112637025 | ABO +36.0 downstream enhancer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133238319..133239388) | | |
ID: 112637023 | ABO upstream enhancer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133278438..133279007) | | |
ID: 653163 | lipocalin 1 pseudogene 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133317738..133318480) | LCN1L2, bA244N20.11 | |
ID: 286310 | lipocalin 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133224905..133228647, complement) | LCN1L1, bA430N14.2 | |
ID: 6838 | surfeit 6 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133328776..133336188, complement) | RRP14 | 185642 |
ID: 3933 | lipocalin 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135521440..135526540) | PMFA, TLC, TP, VEGP | 151675 |
ID: 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133250401..133275201, complement) | A3GALNT, A3GALT1, GTB, NAGAT | 110300 |