Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:43370824-43371101 | Common:3; Rare:61 | ||||
chr15:43493091-43493421 | Common:1; Rare:87 | ||||
chr15:43746180-43746459 | Common:2; Rare:101 | ||||
chr15:43776961-43777094 | Rare:37 | ||||
chr15:43777116-43777409 | Rare:65 | ||||
chr15:43824651-43824814 | Common:2; Rare:41 | ||||
chr15:43826884-43827021 | Rare:54 | ||||
chr15:44288436-44288943 | Common:32; Rare:235 | ||||
chr15:44427472-44427642 | Rare:44 | ||||
chr15:44536863-44537221 | Common:3; Rare:131 | ||||
chr15:44710785-44710869 | Common:1; Rare:11 | ||||
chr15:44711287-44711640 | Rare:105; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr15:44711852-44712018 | Rare:33 | ||||
chr15:44712571-44712721 | Rare:40 | ||||
chr15:44712856-44712926 | Rare:14 |