Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:39782749-39782877 | Rare:35 | ||||
chr15:40039091-40039329 | Rare:99 | ||||
chr15:40358074-40358324 | Common:8; Rare:105 | ||||
chr15:40382806-40383027 | Common:1; Rare:111 | ||||
chr15:40405680-40405827 | Common:2; Rare:47; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr15:40569192-40569332 | Common:3; Rare:24 | ||||
chr15:40695066-40695160 | Rare:25 | ||||
chr15:40755220-40755370 | Common:1; Rare:47 | ||||
chr15:40807450-40807652 | Common:2; Rare:59 | ||||
chr15:41416989-41417213 | Common:2; Rare:100 | ||||
chr15:41544253-41544334 | Rare:35 | ||||
chr15:41621478-41621548 | Rare:15 | ||||
chr15:41660302-41660483 | Rare:58 | ||||
chr15:42208252-42208352 | Rare:32 | ||||
chr15:42273416-42273653 | Rare:85 |