Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:160062482-160062763 | Common:5; Rare:69 | ||||
chr2:161308329-161308508 | Common:2; Rare:46 | ||||
chr2:164840542-164840752 | Common:1; Rare:39 | ||||
chr2:164841192-164841510 | Rare:92 | ||||
chr2:165794128-165794314 | Common:2; Rare:53; Clinvar:6; Clinvar (benign):1 | ||||
chr2:169584564-169584622 | Rare:11 | ||||
chr2:169584727-169584809 | Rare:20 | ||||
chr2:169694360-169694497 | Common:2; Rare:45 | ||||
chr2:170928929-170929331 | Common:4; Rare:122 | ||||
chr2:171160343-171160593 | Rare:87 | ||||
chr2:171433945-171434244 | Common:2; Rare:75 | ||||
chr2:171687720-171687869 | Rare:52 | ||||
chr2:171999837-171999961 | Common:1; Rare:54 | ||||
chr2:172427373-172427682 | Common:9; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr2:173075742-173075956 | Rare:56 |