Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:72231114-72231523 | Common:3; Rare:131 | ||||
chr15:72272487-72272842 | Common:1; Rare:103 | ||||
chr15:72375957-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72474160-72474351 | Rare:71 | ||||
chr15:72686108-72686225 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73752200-73752334 | Rare:35 | ||||
chr15:73994587-73994801 | Rare:46 | ||||
chr15:74174239-74174599 | Common:3; Rare:70 | ||||
chr15:74208986-74209153 | Common:1; Rare:29 | ||||
chr15:74367578-74367890 | Rare:55; Clinvar:1 | ||||
chr15:74461107-74461315 | Rare:64 | ||||
chr15:74540966-74541268 | Common:3; Rare:107 | ||||
chr15:74615648-74615924 | Common:4; Rare:90 | ||||
chr15:74843106-74843305 | Common:1; Rare:62 | ||||
chr15:74873299-74873444 | Common:5; Rare:51 |