| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:183634188-183634307 | Common:2; Rare:21 | ||||
| chr1:183635010-183635311 | Common:2; Rare:91 | ||||
| chr1:183635533-183636094 | Common:8; Rare:370 | ||||
| chr1:183804730-183805256 | Common:2; Rare:153 | ||||
| chr1:184051560-184051859 | Common:10; Rare:239 | ||||
| chr1:184051949-184052148 | Common:1; Rare:50 | ||||
| chr1:184386644-184387375 | Common:8; Rare:429 | ||||
| chr1:184754711-184755260 | Common:3; Rare:327 | ||||
| chr1:184974369-184974591 | Rare:60 | ||||
| chr1:185045195-185045640 | Common:4; Rare:283 | ||||
| chr1:185156696-185157315 | Common:6; Rare:387 | ||||
| chr1:185157345-185157549 | Common:2; Rare:90 | ||||
| chr1:185316930-185317769 | Common:7; Rare:415 | ||||
| chr1:185734232-185734709 | Common:7; Rare:159; Clinvar:3 | ||||
| chr1:186152690-186153390 | Common:4; Rare:149; Clinvar:2; Clinvar (benign):2 |