Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190534707-190534779 | Rare:17 | ||||
chr2:197453273-197453553 | Rare:96 | ||||
chr2:197499829-197500425 | Common:1; Rare:235; Clinvar:1; Clinvar (benign):1 | ||||
chr2:200510049-200510208 | Rare:49 | ||||
chr2:200811483-200811567 | Common:1; Rare:30 | ||||
chr2:200889134-200889444 | Common:3; Rare:102 | ||||
chr2:200963630-200963904 | Common:1; Rare:67 | ||||
chr2:201071620-201072034 | Rare:88 | ||||
chr2:201451445-201451720 | Rare:58 | ||||
chr2:203238939-203239035 | Rare:38 | ||||
chr2:206085824-206085986 | Common:1; Rare:44 | ||||
chr2:206159359-206159711 | Common:3; Rare:105; Clinvar (benign):1 | ||||
chr2:206765284-206765653 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207529722-207530106 | Common:3; Rare:114 | ||||
chr2:208255047-208255238 | Common:2; Rare:51 |