| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43125284-43125710 | Rare:318; Clinvar:15; Clinvar (benign):12 | ||||
| chr17:43169757-43170157 | Common:8; Rare:111 | ||||
| chr17:43170191-43170712 | Common:7; Rare:209 | ||||
| chr17:43170969-43171305 | Common:3; Rare:293 | ||||
| chr17:43211650-43212040 | Common:3; Rare:118 | ||||
| chr17:43483605-43484102 | Rare:261 | ||||
| chr17:43484208-43484327 | Common:3; Rare:30 | ||||
| chr17:43545890-43546168 | Common:4; Rare:78 | ||||
| chr17:43778170-43778600 | Rare:144 | ||||
| chr17:43778863-43779130 | Common:1; Rare:171 | ||||
| chr17:43832395-43832840 | Common:1; Rare:128 | ||||
| chr17:43833077-43833325 | Common:2; Rare:69 | ||||
| chr17:43900578-43900795 | Rare:122 | ||||
| chr17:44014157-44014722 | Common:3; Rare:313 | ||||
| chr17:44014801-44015401 | Common:9; Rare:227 |