Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96868484-96868789 | Rare:73 | ||||
chr2:96869929-96870200 | Common:2; Rare:61 | ||||
chr2:97663993-97664271 | Rare:79 | ||||
chr2:98608416-98608690 | Common:1; Rare:112; Clinvar (benign):1 | ||||
chr2:99154863-99155051 | Common:2; Rare:80; Clinvar (benign):2 | ||||
chr2:99180985-99181243 | Common:2; Rare:74 | ||||
chr2:99337226-99337559 | Rare:118 | ||||
chr2:101252672-101252955 | Common:5; Rare:93 | ||||
chr2:102736832-102736935 | Common:1; Rare:46 | ||||
chr2:105337419-105337578 | Common:3; Rare:75 | ||||
chr2:108534204-108534477 | Common:7; Rare:113 | ||||
chr2:110678027-110678248 | Rare:68 | ||||
chr2:112542111-112542493 | Common:1; Rare:117 | ||||
chr2:112645656-112645947 | Common:2; Rare:101 | ||||
chr2:113627078-113627303 | Common:3; Rare:64 |