| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6444104-6444460 | Common:2; Rare:101 | ||||
| chr17:6556366-6556444 | Rare:21; Clinvar (benign):2 | ||||
| chr17:6556445-6556704 | Common:2; Rare:61; Clinvar:1 | ||||
| chr17:6639688-6639817 | Rare:23 | ||||
| chr17:6640068-6640391 | Common:1; Rare:79 | ||||
| chr17:6640395-6640519 | Common:1; Rare:28 | ||||
| chr17:6640610-6641129 | Common:7; Rare:164 | ||||
| chr17:6641338-6641525 | Rare:33 | ||||
| chr17:6651447-6651863 | Common:1; Rare:137 | ||||
| chr17:6786764-6786934 | Common:2; Rare:58 | ||||
| chr17:6831668-6831924 | Common:2; Rare:42 | ||||
| chr17:6832011-6832021 | Rare:2 | ||||
| chr17:7011925-7011956 | Rare:7 | ||||
| chr17:7012260-7012691 | Rare:142 | ||||
| chr17:7012735-7013044 | Rare:83 |