| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:166839278-166839532 | Rare:81 | ||||
| chr1:166876219-166876552 | Common:1; Rare:105 | ||||
| chr1:167220533-167220936 | Common:2; Rare:125 | ||||
| chr1:167935858-167936271 | Common:1; Rare:116 | ||||
| chr1:167936531-167936974 | Common:1; Rare:161 | ||||
| chr1:168178724-168179176 | Common:4; Rare:133 | ||||
| chr1:168225712-168226072 | Common:4; Rare:114 | ||||
| chr1:169107832-169107968 | Common:1; Rare:28 | ||||
| chr1:169367739-169367923 | Common:2; Rare:41 | ||||
| chr1:169367936-169368257 | Common:1; Rare:61 | ||||
| chr1:169485713-169485790 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:169485904-169486194 | Rare:76; Clinvar:2 | ||||
| chr1:169794687-169794785 | Rare:16 | ||||
| chr1:169794847-169795115 | Common:3; Rare:71 | ||||
| chr1:169893885-169894007 | Common:1; Rare:32 |