| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42924699-42925101 | Common:8; Rare:163 | ||||
| chr1:42925470-42925870 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:42928026-42928426 | Rare:127 | ||||
| chr1:42931751-42932130 | Rare:116 | ||||
| chr1:42932150-42932476 | Common:6; Rare:92 | ||||
| chr1:42932948-42933097 | Common:2; Rare:27 | ||||
| chr1:42935129-42935576 | Rare:215 | ||||
| chr1:42936554-42937464 | Common:9; Rare:194 | ||||
| chr1:42952607-42952817 | Rare:34 | ||||
| chr1:42956874-42957414 | Common:7; Rare:118 | ||||
| chr1:42957970-42958320 | Common:8; Rare:203 | ||||
| chr1:42961344-42961744 | Common:5; Rare:90 | ||||
| chr1:42980504-42980613 | Rare:25 | ||||
| chr1:43058430-43058810 | Common:5; Rare:91 | ||||
| chr1:43199137-43199479 | Common:2; Rare:121 |