Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151008197-151008532 | Common:2; Rare:86 | ||||
chr1:151057826-151057955 | Rare:27 | ||||
chr1:151059217-151059419 | Rare:33 | ||||
chr1:151060085-151060422 | Common:1; Rare:63 | ||||
chr1:151070741-151070814 | Common:1; Rare:22 | ||||
chr1:151165880-151166152 | Common:3; Rare:80 | ||||
chr1:151190122-151190279 | Rare:45 | ||||
chr1:151281895-151282312 | Rare:114 | ||||
chr1:151288333-151288642 | Rare:94 | ||||
chr1:151327400-151327436 | Rare:10 | ||||
chr1:151346590-151346717 | Rare:18 | ||||
chr1:151346843-151347076 | Rare:63 | ||||
chr1:151347164-151347534 | Rare:86 | ||||
chr1:151347820-151347847 | Rare:2 | ||||
chr1:151399427-151399642 | Common:2; Rare:79; Clinvar (pathogenic):2 |