Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151198950-151199019 | Rare:27 | ||||
chr1:151232068-151232254 | Common:3; Rare:40 | ||||
chr1:151254650-151254806 | Rare:44 | ||||
chr1:151281925-151282364 | Rare:127 | ||||
chr1:151327377-151327485 | Common:1; Rare:28 | ||||
chr1:151344684-151344762 | Rare:17 | ||||
chr1:151346815-151347086 | Rare:75 | ||||
chr1:151347173-151347503 | Rare:78 | ||||
chr1:151399526-151400042 | Common:4; Rare:162; Clinvar (pathogenic):2 | ||||
chr1:151459128-151459402 | Common:3; Rare:80 | ||||
chr1:151562345-151562627 | Common:2; Rare:60 | ||||
chr1:151566031-151566212 | Common:1; Rare:43 | ||||
chr1:151612441-151612468 | Rare:8 | ||||
chr1:151763477-151763541 | Common:1; Rare:19 | ||||
chr1:151790440-151790856 | Common:2; Rare:97 |