| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:99850454-99850514 | Rare:10 | ||||
| chr1:99969433-99969511 | Rare:11 | ||||
| chr1:99969859-99970082 | Rare:47 | ||||
| chr1:99970364-99970534 | Rare:41 | ||||
| chr1:100037675-100038326 | Common:3; Rare:194 | ||||
| chr1:100038339-100038481 | Common:1; Rare:41 | ||||
| chr1:100038489-100038992 | Common:5; Rare:154 | ||||
| chr1:100132981-100133259 | Rare:112 | ||||
| chr1:100133335-100133405 | Rare:24 | ||||
| chr1:100249567-100249630 | Common:1; Rare:13 | ||||
| chr1:100249743-100250042 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:100266074-100266438 | Common:4; Rare:129 | ||||
| chr1:100351289-100351520 | Rare:51 | ||||
| chr1:100351530-100351837 | Common:4; Rare:98 | ||||
| chr1:100351948-100352031 | Common:5; Rare:24 |