Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151156459-151156685 | Rare:41 | ||||
chr1:151165851-151166167 | Common:3; Rare:91 | ||||
chr1:151190125-151190243 | Rare:37 | ||||
chr1:151198422-151198592 | Common:1; Rare:57 | ||||
chr1:151281941-151282318 | Rare:112 | ||||
chr1:151327371-151327443 | Common:1; Rare:21 | ||||
chr1:151327687-151327820 | Common:2; Rare:31 | ||||
chr1:151346839-151347037 | Rare:55 | ||||
chr1:151347188-151347553 | Rare:84 | ||||
chr1:151399426-151399587 | Common:1; Rare:50; Clinvar (pathogenic):1 | ||||
chr1:151511162-151511397 | Common:3; Rare:54 | ||||
chr1:151763462-151763574 | Common:1; Rare:39 | ||||
chr1:151790461-151790859 | Common:3; Rare:90 | ||||
chr1:151909403-151909716 | Common:4; Rare:113 | ||||
chr1:153658597-153658746 | Common:1; Rare:39 |