| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44123608-44123854 | Common:3; Rare:71 | ||||
| chr17:44141790-44141936 | Common:1; Rare:31 | ||||
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44187171-44187274 | Rare:29 | ||||
| chr17:44221211-44221367 | Rare:46 | ||||
| chr17:44222089-44222256 | Rare:35 | ||||
| chr17:44268095-44268365 | Rare:55; Clinvar:3 | ||||
| chr17:44308432-44308619 | Common:1; Rare:58 | ||||
| chr17:44324760-44324966 | Common:2; Rare:74 | ||||
| chr17:44345030-44345321 | Rare:61; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44385344-44385542 | Common:4; Rare:57; Clinvar:1 | ||||
| chr17:44503377-44503713 | Rare:132 | ||||
| chr17:44899379-44899767 | Common:3; Rare:123; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44913781-44913956 | Rare:47; Clinvar:4 | ||||
| chr17:44914026-44914225 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):3 |