Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:2993285-2993482 | Common:1; Rare:33 | ||||
chr2:3100405-3100737 | Common:3; Rare:75 | ||||
chr2:3101466-3101819 | Common:1; Rare:66 | ||||
chr2:3127296-3127562 | Common:1; Rare:44 | ||||
chr2:3127722-3127830 | Rare:20 | ||||
chr2:3303685-3303792 | Common:2; Rare:30 | ||||
chr2:3483208-3483610 | Common:5; Rare:106 | ||||
chr2:3603478-3603659 | Common:2; Rare:45 | ||||
chr2:3604118-3604506 | Common:2; Rare:127; Clinvar (benign):1 | ||||
chr2:3651718-3651945 | Rare:52 | ||||
chr2:3652159-3652328 | Common:6; Rare:42 | ||||
chr2:5539975-5540197 | Common:2; Rare:42 | ||||
chr2:5691254-5691591 | Rare:101 | ||||
chr2:5694054-5694200 | Common:1; Rare:41 | ||||
chr2:5694296-5694880 | Common:6; Rare:77 |