Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:101001967-101002324 | Rare:103 | ||||
chr2:101252592-101252907 | Common:5; Rare:105 | ||||
chr2:102736825-102736932 | Common:1; Rare:53 | ||||
chr2:105037886-105038117 | Common:3; Rare:83 | ||||
chr2:105337443-105337653 | Common:2; Rare:89 | ||||
chr2:108534177-108534534 | Common:8; Rare:141 | ||||
chr2:108719372-108719586 | Common:3; Rare:90; Clinvar (benign):2 | ||||
chr2:109613846-109614065 | Common:2; Rare:80 | ||||
chr2:110115677-110115808 | Common:1; Rare:36 | ||||
chr2:110115810-110115932 | Common:2; Rare:29 | ||||
chr2:110204971-110205056 | Rare:39 | ||||
chr2:110677998-110678202 | Rare:66 | ||||
chr2:111884117-111884255 | Rare:40 | ||||
chr2:111898305-111898656 | Common:2; Rare:77 | ||||
chr2:112275330-112275594 | Common:1; Rare:94 |