Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:68820733-68821090 | Rare:106 | ||||
chr15:69298769-69298975 | Common:3; Rare:42 | ||||
chr15:69414208-69414356 | Rare:40 | ||||
chr15:70097846-70098079 | Common:1; Rare:56 | ||||
chr15:70892381-70892619 | Common:1; Rare:56 | ||||
chr15:71547221-71547287 | Rare:14 | ||||
chr15:72117966-72118443 | Common:5; Rare:166 | ||||
chr15:72231102-72231435 | Common:3; Rare:107 | ||||
chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72686129-72686230 | Common:2; Rare:38; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr15:73926322-73926499 | Rare:50 | ||||
chr15:73994587-73994756 | Rare:34 | ||||
chr15:74461107-74461314 | Rare:64 | ||||
chr15:74695988-74696092 | Rare:32 | ||||
chr15:74872961-74873098 | Rare:31 |