Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69398595-69398707 | Rare:27 | ||||
chr14:70417031-70417112 | Rare:22 | ||||
chr14:73463601-73463642 | Common:1; Rare:6 | ||||
chr14:74493568-74493771 | Common:3; Rare:76; Clinvar (benign):4 | ||||
chr14:74713100-74713189 | Rare:44 | ||||
chr14:75002616-75002943 | Common:1; Rare:92; Clinvar:2 | ||||
chr14:92040035-92040124 | Common:2; Rare:22; Clinvar (benign):1 | ||||
chr14:94081154-94081345 | Common:3; Rare:63 | ||||
chr14:102139678-102139914 | Rare:80 | ||||
chr14:102305131-102305308 | Common:1; Rare:59 | ||||
chr14:102362862-102363092 | Rare:103 | ||||
chr14:103562629-103563028 | Common:7; Rare:147; Clinvar (benign):3 | ||||
chr15:39933901-39934188 | Common:4; Rare:91 | ||||
chr15:40039112-40039320 | Rare:90 | ||||
chr15:40695094-40695171 | Rare:21 |