| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9943238-9943505 | Common:3; Rare:73 | ||||
| chr1:10032774-10033089 | Common:2; Rare:83 | ||||
| chr1:10398724-10399125 | Common:2; Rare:146 | ||||
| chr1:10472415-10472694 | Rare:70 | ||||
| chr1:10661128-10661419 | Common:5; Rare:65 | ||||
| chr1:10796578-10796728 | Common:2; Rare:49 | ||||
| chr1:11071829-11072007 | Common:2; Rare:33 | ||||
| chr1:11099719-11099921 | Common:2; Rare:81 | ||||
| chr1:11189122-11189361 | Common:1; Rare:49 | ||||
| chr1:11262478-11262817 | Common:2; Rare:106 | ||||
| chr1:11273430-11273534 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:11654342-11654505 | Rare:46 | ||||
| chr1:11654731-11654925 | Common:4; Rare:56 | ||||
| chr1:11663808-11664113 | Common:3; Rare:60 | ||||
| chr1:11805879-11806315 | Common:2; Rare:127; Clinvar:2 |