| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9716606-9717006 | Common:3; Rare:96; Clinvar (benign):1 | ||||
| chr1:9823890-9824405 | Common:5; Rare:349 | ||||
| chr1:9910164-9911024 | Common:26; Rare:1019 | ||||
| chr1:9942621-9943061 | Common:13; Rare:355 | ||||
| chr1:9943016-9943670 | Common:27; Rare:635 | ||||
| chr1:9943700-9944100 | Common:2; Rare:66 | ||||
| chr1:10032503-10033786 | Common:37; Rare:1247 | ||||
| chr1:10210231-10210649 | Common:28; Rare:475 | ||||
| chr1:10211771-10212171 | Common:2; Rare:110 | ||||
| chr1:10212112-10212356 | Common:1; Rare:39 | ||||
| chr1:10398727-10399160 | Common:14; Rare:760 | ||||
| chr1:10399196-10399882 | Common:13; Rare:266 | ||||
| chr1:10412940-10413420 | Common:2; Rare:122 | ||||
| chr1:10415061-10415461 | Common:2; Rare:84 | ||||
| chr1:10415367-10415704 | Common:2; Rare:133 |