| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235328119-235328443 | Common:2; Rare:91 | ||||
| chr1:235328474-235328636 | Common:2; Rare:61 | ||||
| chr1:235328757-235329048 | Common:1; Rare:98 | ||||
| chr1:235367242-235367525 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:235504244-235504829 | Common:5; Rare:186; Clinvar (benign):2 | ||||
| chr1:235504931-235505196 | Rare:62 | ||||
| chr1:235866907-235867186 | Common:2; Rare:82 | ||||
| chr1:236281904-236282295 | Common:7; Rare:116 | ||||
| chr1:236523769-236524053 | Common:4; Rare:71 | ||||
| chr1:236524497-236524634 | Common:1; Rare:37 | ||||
| chr1:236604478-236604951 | Common:5; Rare:119 | ||||
| chr1:236794963-236795360 | Common:5; Rare:138; Clinvar:2 | ||||
| chr1:241519678-241520035 | Common:2; Rare:104; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr1:241640320-241640575 | Common:7; Rare:88 | ||||
| chr1:241847829-241848019 | Common:1; Rare:47 |