| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22541031-22541668 | Common:1; Rare:179 | ||||
| chr14:22545862-22546397 | Common:10; Rare:146 | ||||
| chr14:22550015-22550390 | Common:15; Rare:178 | ||||
| chr14:22550410-22550790 | Common:7; Rare:231; Clinvar (pathogenic):3 | ||||
| chr14:22550820-22551358 | Common:19; Rare:209 | ||||
| chr14:22554525-22555172 | Common:13; Rare:167 | ||||
| chr14:22555306-22555738 | Common:2; Rare:116 | ||||
| chr14:22556170-22556751 | Common:25; Rare:335 | ||||
| chr14:22556960-22557616 | Common:21; Rare:279 | ||||
| chr14:22558070-22558651 | Common:10; Rare:266 | ||||
| chr14:22558680-22558970 | Common:2; Rare:70 | ||||
| chr14:22561033-22561624 | Common:17; Rare:111 | ||||
| chr14:22561634-22562180 | Common:12; Rare:234 | ||||
| chr14:22562145-22562545 | Common:11; Rare:116 | ||||
| chr14:22562543-22562745 | Common:2; Rare:36 |