Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132887546-132887810 | Rare:82 | ||||
chr12:132956252-132956421 | Common:1; Rare:37 | ||||
chr12:132986269-132986448 | Rare:45 | ||||
chr12:133130238-133130652 | Common:7; Rare:137 | ||||
chr13:19633449-19633737 | Common:1; Rare:111 | ||||
chr13:19863448-19863984 | Common:6; Rare:191 | ||||
chr13:20192773-20193015 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr13:20231403-20231759 | Common:1; Rare:59 | ||||
chr13:20232161-20232435 | Common:2; Rare:84 | ||||
chr13:21140370-21140651 | Rare:123 | ||||
chr13:21176473-21176728 | Common:2; Rare:114 | ||||
chr13:23579241-23579412 | Common:3; Rare:54 | ||||
chr13:23889268-23889484 | Common:1; Rare:76 | ||||
chr13:24160562-24160775 | Rare:64 | ||||
chr13:24512732-24512864 | Common:3; Rare:39 |