| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160031828-160032066 | Common:2; Rare:63 | ||||
| chr1:160070104-160070510 | Common:4; Rare:191; Clinvar:4 | ||||
| chr1:160098370-160099151 | Common:8; Rare:279 | ||||
| chr1:160261370-160261960 | Common:2; Rare:161 | ||||
| chr1:160262418-160262635 | Common:1; Rare:128 | ||||
| chr1:160343159-160343462 | Rare:219 | ||||
| chr1:160343460-160343820 | Common:2; Rare:91 | ||||
| chr1:161021095-161021312 | Common:2; Rare:116 | ||||
| chr1:161045875-161046075 | Common:2; Rare:100 | ||||
| chr1:161117969-161118167 | Rare:199 | ||||
| chr1:161118200-161118590 | Common:3; Rare:157 | ||||
| chr1:161133070-161133490 | Common:2; Rare:105 | ||||
| chr1:161153510-161153830 | Rare:81 | ||||
| chr1:161154080-161154380 | Common:4; Rare:148 | ||||
| chr1:161166268-161166523 | Common:4; Rare:123; Clinvar:6; Clinvar (benign):2 |