| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16352361-16352768 | Common:4; Rare:172 | ||||
| chr1:16366912-16367311 | Common:1; Rare:123 | ||||
| chr1:16367685-16367924 | Common:3; Rare:61 | ||||
| chr1:16440154-16440368 | Common:1; Rare:50 | ||||
| chr1:16440476-16440793 | Common:3; Rare:95 | ||||
| chr1:16613009-16613147 | Rare:2 | ||||
| chr1:16613245-16613385 | Common:1; Rare:1 | ||||
| chr1:16613431-16613737 | Common:4; Rare:1 | ||||
| chr1:16613856-16613986 | Common:1 | ||||
| chr1:16921823-16921981 | Rare:22 | ||||
| chr1:16980073-16980241 | Common:5; Rare:27 | ||||
| chr1:16980570-16980727 | Common:1; Rare:49 | ||||
| chr1:17011895-17012136 | Common:2; Rare:67; Clinvar:1 | ||||
| chr1:17053942-17054422 | Common:3; Rare:143; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr1:17119441-17119611 | Rare:46 |