| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:204074155-204074772 | Common:1; Rare:141 | ||||
| chr1:204151940-204152360 | Common:2; Rare:177 | ||||
| chr1:204213916-204214254 | Rare:204 | ||||
| chr1:204377450-204377935 | Common:3; Rare:187 | ||||
| chr1:204377940-204378364 | Rare:196 | ||||
| chr1:204411218-204411465 | Common:3; Rare:277; Clinvar:3 | ||||
| chr1:204411470-204411700 | Rare:47 | ||||
| chr1:204411692-204412186 | Common:35; Rare:420 | ||||
| chr1:204493893-204494281 | Rare:148 | ||||
| chr1:204494381-204495011 | Common:3; Rare:408 | ||||
| chr1:204516175-204516816 | Common:5; Rare:374 | ||||
| chr1:204685630-204686060 | Common:3; Rare:91 | ||||
| chr1:205120778-205121773 | Common:9; Rare:250 | ||||
| chr1:205121859-205122451 | Common:14; Rare:410 | ||||
| chr1:205211279-205211599 | Common:4; Rare:314; Clinvar:3; Clinvar (pathogenic):3 |