Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100376273-100376511 | Common:3; Rare:77 | ||||
chr14:101809640-101809890 | Rare:50 | ||||
chr14:102086990-102087377 | Common:5; Rare:164 | ||||
chr14:102139678-102139921 | Rare:84 | ||||
chr14:102305096-102305325 | Common:1; Rare:71 | ||||
chr14:102362847-102363092 | Rare:112 | ||||
chr14:103333969-103334241 | Common:1; Rare:112 | ||||
chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
chr14:104579662-104579791 | Rare:25 | ||||
chr14:104970477-104970567 | Common:2; Rare:17 | ||||
chr14:105487032-105487245 | Common:1; Rare:64 | ||||
chr15:23647847-23647971 | Rare:34 | ||||
chr15:30903689-30903946 | Common:2; Rare:63 | ||||
chr15:32615163-32615571 | Common:5; Rare:102 | ||||
chr15:33310667-33310984 | Rare:86 |