| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:149841186-149841424 | |||||
| chr1:149842748-149842980 | Rare:3 | ||||
| chr1:149850826-149851067 | Rare:1 | ||||
| chr1:149852388-149852618 | |||||
| chr1:149861142-149861386 | |||||
| chr1:149886608-149887003 | Common:2; Rare:152 | ||||
| chr1:149887012-149887179 | Common:1; Rare:67 | ||||
| chr1:149887513-149887687 | Rare:74 | ||||
| chr1:149887831-149888481 | Rare:188 | ||||
| chr1:149899496-149899720 | Common:1; Rare:47 | ||||
| chr1:149899799-149900044 | Common:1; Rare:61 | ||||
| chr1:149917810-149918003 | Common:1; Rare:50 | ||||
| chr1:149927693-149927997 | Common:2; Rare:112; Clinvar (benign):6 | ||||
| chr1:149928192-149928426 | Common:2; Rare:47 | ||||
| chr1:149928444-149928491 | Rare:9 |