| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:778620-778794 | Common:3; Rare:70 | ||||
| chr1:827477-827667 | Common:1; Rare:73 | ||||
| chr1:9687517-9687655 | Common:1; Rare:36 | ||||
| chr1:12619102-12619236 | Rare:30 | ||||
| chr1:15835856-15836134 | Common:5; Rare:130 | ||||
| chr1:16644653-16644799 | Common:1; Rare:3 | ||||
| chr1:16895618-16895759 | Common:2; Rare:25 | ||||
| chr1:16913997-16914112 | Common:4; Rare:21 | ||||
| chr1:28648302-28648600 | Common:4; Rare:85 | ||||
| chr1:31669854-31670003 | Common:1; Rare:32 | ||||
| chr1:39158639-39158909 | Common:1; Rare:59 | ||||
| chr1:58576122-58576161 | Common:1; Rare:8; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:58782962-58783186 | Common:2; Rare:78 | ||||
| chr1:58783547-58783827 | Common:2; Rare:61 | ||||
| chr1:61230720-61230806 | Rare:14 |