Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:129980400-129980516 | Common:1; Rare:33 | ||||
chr2:130183872-130184146 | Common:1; Rare:102 | ||||
chr2:130428499-130428855 | Common:2; Rare:96 | ||||
chr2:131682421-131682557 | Common:3; Rare:45 | ||||
chr2:132347186-132347541 | Common:3; Rare:82 | ||||
chr2:134028531-134028654 | Rare:25 | ||||
chr2:134031212-134031465 | Common:1; Rare:41 | ||||
chr2:136131562-136131790 | Common:3; Rare:34 | ||||
chr2:142108891-142109059 | Common:3; Rare:34 | ||||
chr2:144519112-144519433 | Common:1; Rare:52 | ||||
chr2:151460993-151461242 | Common:2; Rare:70 | ||||
chr2:151490370-151490661 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr2:151538209-151538429 | Rare:41; Clinvar:1 | ||||
chr2:152390065-152390324 | Rare:51 | ||||
chr2:152639827-152640047 | Rare:48 |