Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:68774732-68774970 | Common:1; Rare:48 | ||||
chr2:69012941-69013502 | Common:11; Rare:149 | ||||
chr2:69387096-69387398 | Common:1; Rare:84; Clinvar:3 | ||||
chr2:69437395-69437523 | Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
chr2:69437564-69437675 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):1 | ||||
chr2:69643508-69643859 | Rare:108 | ||||
chr2:69643923-69644241 | Common:7; Rare:53 | ||||
chr2:69674382-69674420 | Rare:6 | ||||
chr2:69741884-69742169 | Common:1; Rare:63 | ||||
chr2:69829517-69829741 | Common:1; Rare:89 | ||||
chr2:69893924-69894016 | Rare:29 | ||||
chr2:69914644-69915161 | Common:2; Rare:127 | ||||
chr2:70086931-70087116 | Common:1; Rare:93 | ||||
chr2:70190888-70191119 | Common:1; Rare:55 | ||||
chr2:70248499-70248820 | Common:5; Rare:128 |