| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46194175-46194308 | Rare:15 | ||||
| chr17:46225235-46225543 | Common:4; Rare:72 | ||||
| chr17:46922810-46923240 | Common:5; Rare:137; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:47188591-47188606 | Rare:1 | ||||
| chr17:47188980-47189058 | Rare:20 | ||||
| chr17:47189090-47189134 | Rare:12 | ||||
| chr17:47189187-47189626 | Common:1; Rare:119 | ||||
| chr17:47323850-47324012 | Common:2; Rare:61 | ||||
| chr17:47530978-47531216 | Rare:55 | ||||
| chr17:47649186-47650087 | Common:2; Rare:303 | ||||
| chr17:47650262-47650409 | Rare:63 | ||||
| chr17:47650441-47650788 | Common:3; Rare:140 | ||||
| chr17:47693960-47694072 | Rare:20 | ||||
| chr17:47694604-47694658 | Rare:11 | ||||
| chr17:47694988-47695348 | Common:1; Rare:73 |