| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:43221254-43221412 | Rare:23 | ||||
| chr1:43221513-43221711 | Common:2; Rare:24 | ||||
| chr1:43239550-43240000 | Rare:86 | ||||
| chr1:43295360-43295730 | Common:3; Rare:54 | ||||
| chr1:43330315-43330490 | Common:1; Rare:25 | ||||
| chr1:43349014-43349267 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr1:43349418-43349630 | Rare:48 | ||||
| chr1:43349746-43350166 | Rare:108 | ||||
| chr1:43379700-43380434 | Common:3; Rare:166 | ||||
| chr1:43385768-43386168 | Common:1; Rare:108 | ||||
| chr1:43454556-43454777 | Rare:80 | ||||
| chr1:43565590-43565960 | Common:5; Rare:108 | ||||
| chr1:43569150-43569540 | Common:7; Rare:157 | ||||
| chr1:43578734-43579134 | Common:2; Rare:133 | ||||
| chr1:43664470-43664710 | Rare:35 |