| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:203795468-203795637 | Rare:46 | ||||
| chr1:203861490-203861855 | Common:2; Rare:125 | ||||
| chr1:204072959-204073214 | Common:1; Rare:65 | ||||
| chr1:204151981-204152282 | Common:2; Rare:82 | ||||
| chr1:204214091-204214470 | Rare:79 | ||||
| chr1:204377947-204378362 | Rare:84 | ||||
| chr1:204411806-204412100 | Common:9; Rare:88 | ||||
| chr1:204494648-204494963 | Common:1; Rare:97 | ||||
| chr1:204516176-204516476 | Common:1; Rare:88 | ||||
| chr1:204685800-204685921 | Common:1; Rare:22 | ||||
| chr1:204828542-204828675 | Rare:63 | ||||
| chr1:205061660-205061910 | Common:2; Rare:47 | ||||
| chr1:205121906-205122621 | Common:7; Rare:190 | ||||
| chr1:205211293-205211473 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
| chr1:205211658-205211859 | Rare:35 |