Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:11703123-11703464 | Common:5; Rare:86; Clinvar:2 | ||||
chr8:12522323-12522478 | Common:1; Rare:5 | ||||
chr8:12522519-12522684 | Rare:7 | ||||
chr8:12601407-12601615 | Common:3; Rare:22 | ||||
chr8:12607581-12607796 | Common:8; Rare:13 | ||||
chr8:13107474-13107770 | Common:2; Rare:58 | ||||
chr8:22950637-22950838 | Common:1; Rare:41 | ||||
chr8:24955938-24956100 | Rare:65; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr8:25480567-25480678 | Rare:22 | ||||
chr8:30412198-30412340 | Rare:15 | ||||
chr8:36553693-36553871 | Rare:27 | ||||
chr8:38382982-38383084 | Rare:23 | ||||
chr8:38770350-38770592 | Common:1; Rare:54 | ||||
chr8:42498895-42499128 | Rare:35 | ||||
chr8:42513183-42513361 | Rare:26 |