| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73192766-73193076 | Common:15; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232096-73232753 | Common:7; Rare:435 | ||||
| chr17:73262250-73262950 | Common:5; Rare:241 | ||||
| chr17:73310883-73311280 | Common:4; Rare:184 | ||||
| chr17:73311963-73312233 | Rare:121 | ||||
| chr17:74213280-74213580 | Common:4; Rare:63 | ||||
| chr17:74430697-74431028 | Common:8; Rare:153 | ||||
| chr17:74431248-74431785 | Common:2; Rare:173 | ||||
| chr17:74431715-74431859 | Rare:25 | ||||
| chr17:74431980-74432204 | Common:2; Rare:195 | ||||
| chr17:74736360-74736810 | Common:2; Rare:151 | ||||
| chr17:74737003-74737403 | Rare:222 | ||||
| chr17:74748417-74748705 | Common:8; Rare:192 | ||||
| chr17:74749129-74749305 | Common:2; Rare:57; Clinvar:1 | ||||
| chr17:74761820-74762333 | Common:3; Rare:310; Clinvar:2 |