Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:91659918-91660045 | Rare:22 | ||||
chr2:95526711-95526984 | Common:1; Rare:87 | ||||
chr2:96297470-96297708 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
chr2:100321002-100321022 | Rare:3 | ||||
chr2:113584012-113584120 | Rare:29 | ||||
chr2:124987005-124987275 | Common:1; Rare:63 | ||||
chr2:130992117-130992276 | Common:3; Rare:43 | ||||
chr2:131682380-131682533 | Common:3; Rare:43 | ||||
chr2:159747736-159747835 | Rare:25 | ||||
chr2:159764938-159765234 | Common:3; Rare:48 | ||||
chr2:160270306-160270623 | Common:2; Rare:76 | ||||
chr2:168656752-168656955 | Common:4; Rare:48 | ||||
chr2:170770789-170771104 | Common:2; Rare:53 | ||||
chr2:176120959-176121251 | Common:1; Rare:76 | ||||
chr2:176135907-176136052 | Common:1; Rare:26 |