Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:200510027-200510116 | Rare:30 | ||||
chr2:200888986-200889439 | Common:3; Rare:143 | ||||
chr2:200963601-200963873 | Common:1; Rare:71 | ||||
chr2:201071615-201072002 | Rare:80 | ||||
chr2:201116142-201116396 | Rare:43 | ||||
chr2:201451375-201451767 | Common:1; Rare:94 | ||||
chr2:201642620-201642741 | Common:1; Rare:54; Clinvar (benign):1 | ||||
chr2:201780876-201781213 | Common:2; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202911886-202912288 | Common:2; Rare:109 | ||||
chr2:203328063-203328395 | Common:2; Rare:121 | ||||
chr2:203328417-203328564 | Rare:38 | ||||
chr2:203535185-203535504 | Common:3; Rare:116 | ||||
chr2:206159345-206159925 | Common:4; Rare:157; Clinvar (benign):1 | ||||
chr2:206765297-206765668 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165766-207166097 | Rare:64 |