Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:75671099-75671145 | Rare:4 | ||||
chr2:85674523-85674804 | Common:3; Rare:42 | ||||
chr2:85734013-85734292 | Common:3; Rare:37 | ||||
chr2:88016540-88016802 | Common:9; Rare:111 | ||||
chr2:99399161-99399426 | Rare:62 | ||||
chr2:100832814-100832939 | Common:1; Rare:22 | ||||
chr2:101021681-101021798 | Rare:32 | ||||
chr2:101111441-101111692 | Common:4; Rare:55 | ||||
chr2:109760367-109760635 | Common:1; Rare:59 | ||||
chr2:110610820-110611146 | Common:1; Rare:59 | ||||
chr2:113584024-113584110 | Rare:20 | ||||
chr2:127060594-127060865 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr2:127068924-127069318 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:127076838-127077180 | Common:5; Rare:55 | ||||
chr2:127081032-127081402 | Common:3; Rare:69 |