Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:19990083-19990211 | Rare:33 | ||||
chr2:20051605-20051824 | Common:1; Rare:58 | ||||
chr2:20651059-20651255 | Rare:63 | ||||
chr2:20823064-20823159 | Rare:36 | ||||
chr2:23927067-23927339 | Common:3; Rare:96 | ||||
chr2:23940385-23940509 | Common:3; Rare:45 | ||||
chr2:24971938-24972153 | Common:1; Rare:62 | ||||
chr2:26033774-26034141 | Common:4; Rare:130 | ||||
chr2:26244601-26244943 | Common:2; Rare:123; Clinvar:5; Clinvar (benign):6 | ||||
chr2:27032867-27032995 | Rare:46 | ||||
chr2:27212271-27212384 | Common:2; Rare:55 | ||||
chr2:27323043-27323154 | Rare:27; Clinvar (benign):1 | ||||
chr2:27356750-27356854 | Rare:26 | ||||
chr2:27370317-27370641 | Common:1; Rare:128 | ||||
chr2:27582865-27583083 | Rare:76 |