Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100535644-100536050 | Common:19; Rare:382 | ||||
chr10:100536170-100536490 | Common:2; Rare:62 | ||||
chr10:100912003-100912442 | Rare:208 | ||||
chr10:100912577-100913584 | Common:11; Rare:901 | ||||
chr10:100969073-100969544 | Common:14; Rare:350 | ||||
chr10:100987080-100987790 | Common:11; Rare:978; Clinvar:8; Clinvar (benign):11 | ||||
chr10:100996479-100996587 | Rare:21 | ||||
chr10:100996835-100997235 | Common:6; Rare:280 | ||||
chr10:100997400-100998370 | Common:11; Rare:520 | ||||
chr10:100998387-100998980 | Common:6; Rare:150 | ||||
chr10:100999124-100999420 | Common:6; Rare:85 | ||||
chr10:100999570-101000001 | Common:10; Rare:585 | ||||
chr10:101019000-101019330 | Common:6; Rare:142; Clinvar:3; Clinvar (benign):6 | ||||
chr10:101030966-101031366 | Common:6; Rare:274 | ||||
chr10:101061582-101062002 | Rare:134 |