| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74433861-74434067 | Common:7; Rare:113 | ||||
| chr15:74461021-74461454 | Common:1; Rare:197 | ||||
| chr15:74540915-74541296 | Common:10; Rare:260 | ||||
| chr15:74598280-74598511 | Common:2; Rare:176 | ||||
| chr15:74615671-74615930 | Common:8; Rare:162 | ||||
| chr15:74695941-74696101 | Rare:94 | ||||
| chr15:74725509-74725713 | Rare:42 | ||||
| chr15:74725710-74726230 | Common:6; Rare:199 | ||||
| chr15:74781945-74782156 | Common:3; Rare:67 | ||||
| chr15:74782310-74782660 | Common:2; Rare:131 | ||||
| chr15:74843091-74843296 | Common:3; Rare:121 | ||||
| chr15:74889907-74890076 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr15:74906787-74906909 | Rare:96 | ||||
| chr15:74937917-74938272 | Common:5; Rare:205 | ||||
| chr15:74956763-74956887 | Common:1; Rare:50 |