Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:135531172-135531502 | Common:1; Rare:66 | ||||
chr2:135984948-135985155 | Common:1; Rare:48 | ||||
chr2:135985404-135985666 | Common:4; Rare:118; Clinvar (benign):1 | ||||
chr2:138501645-138501907 | Common:3; Rare:109 | ||||
chr2:144517535-144517756 | Common:5; Rare:60 | ||||
chr2:148020657-148021099 | Common:2; Rare:101; Clinvar (benign):2 | ||||
chr2:148021498-148021678 | Rare:38; Clinvar (benign):1 | ||||
chr2:149587310-149587372 | Rare:11 | ||||
chr2:152717875-152718029 | Rare:58 | ||||
chr2:152718509-152718650 | Rare:54 | ||||
chr2:159712416-159712534 | Common:2; Rare:51 | ||||
chr2:161308390-161308750 | Common:2; Rare:76 | ||||
chr2:162073389-162073581 | Common:2; Rare:62 | ||||
chr2:162318650-162318794 | Rare:29 | ||||
chr2:169584729-169584864 | Rare:37 |