Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958204 | Rare:47 | ||||
chr1:145964558-145964742 | Rare:47 | ||||
chr1:145994085-145994459 | Rare:147 | ||||
chr1:145994918-145995505 | Common:1; Rare:244 | ||||
chr1:145995817-145996808 | Common:3; Rare:366 | ||||
chr1:147172420-147172823 | Common:1; Rare:103 | ||||
chr1:147225259-147225733 | Common:3; Rare:88 | ||||
chr1:147242541-147242744 | Common:4; Rare:88 | ||||
chr1:148951859-148952141 | Common:5; Rare:68 | ||||
chr1:148952264-148952603 | Common:5; Rare:101 | ||||
chr1:149812358-149812560 | Rare:62 | ||||
chr1:149886628-149887142 | Common:3; Rare:202 | ||||
chr1:149887895-149888018 | Rare:63 | ||||
chr1:149927757-149927906 | Common:1; Rare:61; Clinvar (benign):5 |