| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:54716085-54716115 | Rare:10 | ||||
| chr1:54763764-54764050 | Common:1; Rare:55 | ||||
| chr1:54764390-54764845 | Common:7; Rare:135; Clinvar (benign):1 | ||||
| chr1:54801279-54801384 | Rare:21 | ||||
| chr1:54886707-54887015 | Common:1; Rare:104; Clinvar:1 | ||||
| chr1:54887122-54887523 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:55214674-55214978 | Common:2; Rare:86 | ||||
| chr1:55215274-55215703 | Common:2; Rare:148 | ||||
| chr1:56517004-56517126 | Common:1; Rare:18 | ||||
| chr1:56579357-56579411 | Rare:14 | ||||
| chr1:58546238-58546409 | Common:4; Rare:46 | ||||
| chr1:58546635-58546968 | Common:4; Rare:114 | ||||
| chr1:58699972-58700247 | Common:4; Rare:122 | ||||
| chr1:58783880-58784425 | Common:2; Rare:143 | ||||
| chr1:58784578-58784748 | Common:1; Rare:47 |