Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231370663-231370770 | Rare:30 | ||||
chr1:231387936-231388251 | Common:4; Rare:62 | ||||
chr1:231395484-231395732 | Common:4; Rare:41 | ||||
chr1:231396152-231396240 | Common:1; Rare:19 | ||||
chr1:231420980-231421298 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
chr1:231421301-231421368 | Rare:28; Clinvar:2 | ||||
chr1:231421371-231421566 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):4 | ||||
chr1:231422123-231422444 | Common:5; Rare:136; Clinvar:4; Clinvar (benign):5 | ||||
chr1:231422651-231422765 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
chr1:232630098-232630261 | Rare:62 | ||||
chr1:232963484-232963636 | Rare:31 | ||||
chr1:234429273-234429436 | Common:2; Rare:56 | ||||
chr1:234602584-234602756 | Common:3; Rare:36 | ||||
chr1:234602801-234602980 | Common:1; Rare:37 | ||||
chr1:234604125-234604202 | Rare:19 |