Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43171046-43171239 | Rare:58 | ||||
chr17:44070624-44070940 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123631-44123840 | Common:3; Rare:55 | ||||
chr17:44186696-44187038 | Rare:109 | ||||
chr17:44324774-44324980 | Common:2; Rare:75 | ||||
chr17:44899375-44899460 | Rare:37 | ||||
chr17:45060936-45061420 | Common:3; Rare:142 | ||||
chr17:45148173-45148486 | Common:1; Rare:98 | ||||
chr17:46193411-46193600 | Common:3; Rare:52 | ||||
chr17:47189193-47189581 | Common:1; Rare:103 | ||||
chr17:47649414-47650050 | Common:2; Rare:221 | ||||
chr17:47831464-47831701 | Rare:77 | ||||
chr17:48048048-48048369 | Rare:86 | ||||
chr17:48048577-48048813 | Common:4; Rare:44 | ||||
chr17:48544451-48544522 | Common:1; Rare:24 |