Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102086987-102087460 | Common:5; Rare:202 | ||||
chr14:102139678-102139919 | Rare:82 | ||||
chr14:102362862-102363089 | Rare:101 | ||||
chr14:103333969-103334252 | Common:1; Rare:117 | ||||
chr14:103385260-103385423 | Rare:57 | ||||
chr14:103529070-103529233 | Common:1; Rare:50 | ||||
chr14:103562623-103563053 | Common:8; Rare:170; Clinvar (benign):5 | ||||
chr15:23039546-23039703 | Common:1; Rare:60 | ||||
chr15:23565566-23565680 | Rare:32 | ||||
chr15:24954879-24954999 | Rare:51 | ||||
chr15:32615397-32615566 | Common:3; Rare:43 | ||||
chr15:34101846-34102112 | Common:1; Rare:52 | ||||
chr15:34582854-34582926 | Rare:26 | ||||
chr15:34583574-34583948 | Common:7; Rare:114 | ||||
chr15:34988236-34988409 | Common:1; Rare:70 |