Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13302087-13302213 | Common:1; Rare:20 | ||||
chr10:13348026-13348316 | Rare:96 | ||||
chr10:14838040-14838355 | Common:2; Rare:81 | ||||
chr10:14878637-14878897 | Common:2; Rare:78 | ||||
chr10:14954014-14954194 | Rare:64 | ||||
chr10:15097138-15097399 | Common:3; Rare:121 | ||||
chr10:17228458-17228610 | Rare:37 | ||||
chr10:17233582-17233930 | Common:3; Rare:111; Clinvar (benign):1 | ||||
chr10:17454050-17454196 | Common:1; Rare:44 | ||||
chr10:17454314-17454739 | Common:1; Rare:107 | ||||
chr10:17617287-17617593 | Common:4; Rare:108 | ||||
chr10:17643871-17644317 | Common:2; Rare:139 | ||||
chr10:18140438-18140736 | Common:4; Rare:86; Clinvar (benign):5 | ||||
chr10:18659236-18659491 | Common:2; Rare:91 | ||||
chr10:18659725-18659769 | Rare:12 |