| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156282716-156283059 | Common:3; Rare:89 | ||||
| chr1:156291433-156291603 | Rare:78 | ||||
| chr1:156295620-156295808 | Common:1; Rare:56 | ||||
| chr1:156337887-156337908 | Rare:6 | ||||
| chr1:156337914-156337976 | Rare:9 | ||||
| chr1:156338143-156338630 | Common:3; Rare:168 | ||||
| chr1:156338712-156338914 | Rare:56 | ||||
| chr1:156421709-156421972 | Common:1; Rare:79 | ||||
| chr1:156500700-156501153 | Common:3; Rare:166 | ||||
| chr1:156501158-156501246 | Rare:23 | ||||
| chr1:156591568-156591878 | Common:6; Rare:126 | ||||
| chr1:156592013-156592166 | Rare:50; Clinvar (pathogenic):1 | ||||
| chr1:156600968-156601243 | Common:2; Rare:45 | ||||
| chr1:156601258-156601624 | Common:2; Rare:104 | ||||
| chr1:156601656-156601768 | Common:1; Rare:24 |