| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161153732-161154003 | Common:1; Rare:71 | ||||
| chr1:161166279-161166504 | Common:2; Rare:53; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161199051-161199304 | Rare:41 | ||||
| chr1:161314265-161314408 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:161766133-161766376 | Common:3; Rare:72 | ||||
| chr1:162497761-162497859 | Common:1; Rare:33 | ||||
| chr1:162790545-162790789 | Common:4; Rare:70 | ||||
| chr1:163321727-163322086 | Common:1; Rare:95 | ||||
| chr1:165768781-165769039 | Common:2; Rare:108 | ||||
| chr1:167935988-167936266 | Common:1; Rare:86 | ||||
| chr1:167936549-167936961 | Common:1; Rare:146 | ||||
| chr1:168178729-168179097 | Common:4; Rare:114 | ||||
| chr1:168225891-168226056 | Common:1; Rare:58 | ||||
| chr1:169367728-169368254 | Common:3; Rare:113 | ||||
| chr1:169485773-169486142 | Rare:96; Clinvar:4; Clinvar (benign):3 |