| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:6393659-6393948 | Common:5; Rare:234 | ||||
| chr1:6419873-6420115 | Common:2; Rare:115 | ||||
| chr1:6424632-6424799 | Common:2; Rare:95 | ||||
| chr1:6424755-6424898 | Common:2; Rare:39 | ||||
| chr1:6440370-6440880 | Common:22; Rare:226; Clinvar (benign):4 | ||||
| chr1:6471491-6471781 | Common:4; Rare:227; Clinvar:2; Clinvar (benign):10 | ||||
| chr1:6490464-6490715 | Common:1; Rare:131 | ||||
| chr1:6490840-6491110 | Rare:51 | ||||
| chr1:6497260-6497720 | Common:7; Rare:286 | ||||
| chr1:6554439-6554716 | Common:20; Rare:234 | ||||
| chr1:6579803-6580098 | Common:8; Rare:188 | ||||
| chr1:6602758-6603159 | Common:12; Rare:367 | ||||
| chr1:6603445-6603630 | Common:1; Rare:37 | ||||
| chr1:6613322-6613906 | Common:6; Rare:543 | ||||
| chr1:6614470-6614910 | Common:3; Rare:195 |