| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74889927-74890076 | Rare:56; Clinvar (pathogenic):1 | ||||
| chr15:74995404-74995626 | Common:6; Rare:94 | ||||
| chr15:75347531-75347887 | Common:2; Rare:89 | ||||
| chr15:75368189-75368444 | Common:1; Rare:83 | ||||
| chr15:75451548-75452022 | Common:1; Rare:131 | ||||
| chr15:75625606-75625848 | Common:2; Rare:59 | ||||
| chr15:75647664-75647950 | Common:2; Rare:64 | ||||
| chr15:75712688-75712853 | Rare:58 | ||||
| chr15:76905313-76905485 | Common:1; Rare:61 | ||||
| chr15:77420084-77420467 | Common:2; Rare:113 | ||||
| chr15:78149176-78149406 | Common:1; Rare:75 | ||||
| chr15:78299576-78299751 | Common:1; Rare:66 | ||||
| chr15:78540675-78540824 | Common:2; Rare:46 | ||||
| chr15:79923638-79923928 | Common:7; Rare:119 | ||||
| chr15:80989691-80990025 | Common:5; Rare:146 |