ID: 127267166 | H3K4me1 hESC enhancer GRCh37_chr1:6239139-6239638 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6179079..6179578) | | |
ID: 127267165 | H3K4me1 hESC enhancer GRCh37_chr1:6238637-6239138 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6178577..6179078) | | |
ID: 127267164 | H3K4me1 hESC enhancer GRCh37_chr1:6225727-6226227 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6165667..6166167) | | |
ID: 127267163 | H3K4me1 hESC enhancer GRCh37_chr1:6186229-6187116 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6126169..6127056) | | |
ID: 127267162 | H3K4me1 hESC enhancer GRCh37_chr1:6162691-6163190 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6102631..6103130) | | |
ID: 127267161 | H3K4me1 hESC enhancer GRCh37_chr1:6162189-6162690 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6102129..6102669) | | |
ID: 127267160 | H3K4me1 hESC enhancer GRCh37_chr1:6120127-6120627 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6060067..6060567) | | |
ID: 126805596 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:6133526-6134725 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6073466..6074665) | | |
ID: 124903831 | uncharacterized LOC124903831 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6085255..6086371) | | |
ID: 121967056 | Sharpr-MPRA regulatory region 5942 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6205149..6205443) | | |
ID: 112590813 | Sharpr-MPRA regulatory region 11871 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6127057..6128003) | | |
ID: 102724450 | RNF207 antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6204840..6205780, complement) | | |
ID: 26038 | chromodomain helicase DNA binding protein 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6101787..6180321, complement) | CHD-5, PMNDS | 610771 |
ID: 8514 | potassium voltage-gated channel subfamily A regulatory beta subunit 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (5992676..6101180) | AKR6A5, HKvbeta2, HKvbeta2.1, HKvbeta2.2, KCNA2B, KV-BETA-2 | 601142 |
ID: 6146 | ribosomal protein L22 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6185020..6199595, complement) | EAP, HBP15, HBP15/L22, L22, eL22 | 180474 |