| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156212872-156213042 | Common:2; Rare:81 | ||||
| chr1:156213181-156213402 | Common:4; Rare:106 | ||||
| chr1:156282360-156282720 | Common:2; Rare:147 | ||||
| chr1:156282654-156283064 | Common:6; Rare:167 | ||||
| chr1:156295597-156295927 | Common:1; Rare:78 | ||||
| chr1:156338160-156338592 | Common:6; Rare:309 | ||||
| chr1:156500710-156501102 | Common:2; Rare:270 | ||||
| chr1:156572500-156572640 | Common:1; Rare:97 | ||||
| chr1:156591614-156592657 | Common:13; Rare:585; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr1:156601406-156601529 | Common:2; Rare:100 | ||||
| chr1:156677280-156677550 | Rare:77 | ||||
| chr1:156728374-156728673 | Common:4; Rare:156 | ||||
| chr1:156728644-156728994 | Rare:176 | ||||
| chr1:156741041-156741395 | Common:1; Rare:99 | ||||
| chr1:156750113-156750560 | Rare:147 |