| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6077847-6078010 | Common:1; Rare:38 | ||||
| chr17:6640641-6641121 | Common:7; Rare:154 | ||||
| chr17:6641468-6641581 | Common:1; Rare:13 | ||||
| chr17:6651553-6651648 | Common:1; Rare:37 | ||||
| chr17:6652055-6652253 | Common:5; Rare:70 | ||||
| chr17:6776098-6776240 | Common:2; Rare:19 | ||||
| chr17:6831528-6831808 | Common:1; Rare:36 | ||||
| chr17:7012307-7012766 | Rare:148 | ||||
| chr17:7035817-7036086 | Rare:64 | ||||
| chr17:7214363-7214608 | Rare:49 | ||||
| chr17:7219784-7219944 | Common:3; Rare:71; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:7221385-7221589 | Common:8; Rare:65; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:7223306-7223365 | Rare:18 | ||||
| chr17:7234226-7234660 | Common:2; Rare:198 | ||||
| chr17:7239384-7239883 | Common:4; Rare:153 |