Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:68277450-68277804 | Common:6; Rare:125 | ||||
chr15:68278021-68278365 | Common:2; Rare:101 | ||||
chr15:68817536-68817712 | Common:1; Rare:63 | ||||
chr15:68820741-68821090 | Rare:105 | ||||
chr15:69452770-69453020 | Common:5; Rare:109 | ||||
chr15:70702239-70702324 | Rare:19 | ||||
chr15:70854101-70854289 | Rare:62 | ||||
chr15:70892371-70892488 | Rare:30 | ||||
chr15:72118019-72118423 | Common:3; Rare:136 | ||||
chr15:72206856-72207136 | Common:2; Rare:61 | ||||
chr15:72231094-72231288 | Rare:71 | ||||
chr15:72375957-72376105 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72474228-72474555 | Rare:112 | ||||
chr15:73633178-73633312 | Rare:56 | ||||
chr15:73994600-73994756 | Rare:31 |