| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:165768748-165769019 | Common:2; Rare:106 | ||||
| chr1:166839209-166839530 | Rare:95 | ||||
| chr1:166876237-166876552 | Common:1; Rare:96 | ||||
| chr1:167935988-167936261 | Common:1; Rare:85 | ||||
| chr1:167936531-167936683 | Rare:57 | ||||
| chr1:167936793-167936951 | Rare:65 | ||||
| chr1:168178729-168179098 | Common:4; Rare:114 | ||||
| chr1:168225712-168226086 | Common:4; Rare:125 | ||||
| chr1:169367754-169368254 | Common:3; Rare:98 | ||||
| chr1:169427410-169427534 | Rare:27 | ||||
| chr1:169485729-169486192 | Common:1; Rare:131; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:169486237-169486387 | Rare:28 | ||||
| chr1:169794691-169795094 | Common:3; Rare:85 | ||||
| chr1:170074639-170074798 | Common:2; Rare:44 | ||||
| chr1:170532010-170532203 | Common:1; Rare:80; Clinvar:1 |