| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236604408-236604691 | Common:13; Rare:206 | ||||
| chr1:236795028-236795555 | Common:20; Rare:546; Clinvar:14; Clinvar (benign):2 | ||||
| chr1:236795750-236795930 | Common:1; Rare:60 | ||||
| chr1:239386360-239386870 | Common:1; Rare:107 | ||||
| chr1:241519650-241520037 | Common:5; Rare:284; Clinvar:26; Clinvar (benign):18; Clinvar (pathogenic):9 | ||||
| chr1:241640193-241640607 | Common:21; Rare:390 | ||||
| chr1:241749148-241749789 | Common:5; Rare:154 | ||||
| chr1:241750032-241750182 | Rare:20 | ||||
| chr1:241847620-241848010 | Common:5; Rare:229 | ||||
| chr1:241848027-241848283 | Common:8; Rare:140 | ||||
| chr1:243254160-243254620 | Common:4; Rare:96 | ||||
| chr1:243254910-243255497 | Common:3; Rare:310 | ||||
| chr1:243255745-243256170 | Common:1; Rare:323; Clinvar:12; Clinvar (benign):1 | ||||
| chr1:243850930-243851290 | Common:3; Rare:123 | ||||
| chr1:244048056-244048754 | Common:1; Rare:209 |