Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:202911886-202912038 | Rare:32 | ||||
chr2:202912127-202912568 | Common:4; Rare:132 | ||||
chr2:203238789-203239054 | Common:1; Rare:99 | ||||
chr2:203239220-203239358 | Rare:49 | ||||
chr2:203328045-203328484 | Common:2; Rare:154 | ||||
chr2:205682356-205682583 | Rare:40 | ||||
chr2:206085771-206085960 | Common:1; Rare:54 | ||||
chr2:206159362-206160057 | Common:4; Rare:210; Clinvar (benign):1 | ||||
chr2:206274918-206275041 | Rare:45 | ||||
chr2:206765273-206765654 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165906-207166088 | Rare:36 | ||||
chr2:207529779-207530108 | Common:3; Rare:92 | ||||
chr2:207625204-207625506 | Common:1; Rare:86 | ||||
chr2:208025480-208025618 | Common:1; Rare:37 | ||||
chr2:208254983-208255228 | Common:2; Rare:62 |