| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47895620-47896236 | Common:6; Rare:234 | ||||
| chr17:47896160-47896319 | Common:2; Rare:101 | ||||
| chr17:47896374-47896694 | Common:5; Rare:150 | ||||
| chr17:47941262-47941940 | Rare:423; Clinvar:23; Clinvar (benign):19; Clinvar (pathogenic):6 | ||||
| chr17:47957617-47958084 | Common:10; Rare:187 | ||||
| chr17:47958084-47958484 | Common:1; Rare:150 | ||||
| chr17:47970707-47971239 | Common:13; Rare:332 | ||||
| chr17:48047620-48047950 | Common:6; Rare:170 | ||||
| chr17:48047972-48048455 | Common:3; Rare:374 | ||||
| chr17:48048505-48048920 | Common:13; Rare:174 | ||||
| chr17:48048860-48049383 | Common:15; Rare:292 | ||||
| chr17:48054200-48054808 | Rare:152 | ||||
| chr17:48055622-48056090 | Rare:111 | ||||
| chr17:48100497-48100961 | Common:2; Rare:157 | ||||
| chr17:48100915-48101186 | Rare:99 |