| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:165698504-165698744 | Common:5; Rare:94 | ||||
| chr1:165768732-165768925 | Common:1; Rare:74 | ||||
| chr1:165895461-165895657 | Rare:28 | ||||
| chr1:166839322-166839530 | Rare:62 | ||||
| chr1:167220565-167220923 | Common:1; Rare:102 | ||||
| chr1:167721777-167722064 | Common:4; Rare:79 | ||||
| chr1:167722127-167722237 | Rare:21 | ||||
| chr1:167935750-167936280 | Common:2; Rare:158 | ||||
| chr1:167936507-167936709 | Common:1; Rare:74 | ||||
| chr1:167936841-167937010 | Rare:68 | ||||
| chr1:167937012-167937139 | Rare:48 | ||||
| chr1:168225704-168226126 | Common:4; Rare:138 | ||||
| chr1:169367714-169368340 | Common:4; Rare:131 | ||||
| chr1:169485519-169485791 | Common:4; Rare:106; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:169485803-169486198 | Common:1; Rare:96; Clinvar:4 |