Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:98444760-98444912 | Rare:68 | ||||
chr2:98608403-98608649 | Common:1; Rare:109; Clinvar (benign):1 | ||||
chr2:98731067-98731231 | Common:1; Rare:59 | ||||
chr2:99141119-99141787 | Common:3; Rare:239 | ||||
chr2:99154835-99155094 | Common:3; Rare:106; Clinvar (benign):3 | ||||
chr2:99180830-99181265 | Common:2; Rare:137 | ||||
chr2:99181302-99181480 | Rare:43 | ||||
chr2:99337303-99337584 | Rare:104 | ||||
chr2:99406135-99406344 | Common:2; Rare:51 | ||||
chr2:100417331-100417696 | Rare:106 | ||||
chr2:100562912-100563047 | Rare:42 | ||||
chr2:101002102-101002324 | Rare:82 | ||||
chr2:101151349-101151667 | Common:6; Rare:102 | ||||
chr2:101252647-101252982 | Common:5; Rare:113 | ||||
chr2:101253356-101253450 | Rare:38 |