| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97589528-97589611 | Common:2; Rare:25 | ||||
| chr2:97589670-97590039 | Common:7; Rare:100 | ||||
| chr2:97590244-97590644 | Common:1; Rare:77 | ||||
| chr2:97645834-97646164 | Common:3; Rare:98 | ||||
| chr2:97663886-97664255 | Common:1; Rare:117 | ||||
| chr2:97995926-97995979 | Rare:23 | ||||
| chr2:98086999-98087286 | Common:1; Rare:74 | ||||
| chr2:98245314-98245456 | Rare:19 | ||||
| chr2:98608234-98608822 | Common:3; Rare:212; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98869237-98869355 | Common:1; Rare:24 | ||||
| chr2:99141109-99141246 | Common:1; Rare:54 | ||||
| chr2:99141308-99141730 | Common:2; Rare:150 | ||||
| chr2:99154639-99155151 | Common:7; Rare:164; Clinvar (benign):3 | ||||
| chr2:99180979-99181239 | Common:2; Rare:73 | ||||
| chr2:99337138-99337291 | Common:1; Rare:30 |