| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7931869-7932245 | Common:5; Rare:99 | ||||
| chr17:8151174-8151491 | Common:3; Rare:80 | ||||
| chr17:8152378-8152611 | Common:2; Rare:55 | ||||
| chr17:8162900-8163119 | Common:1; Rare:80 | ||||
| chr17:8176331-8176441 | Rare:37 | ||||
| chr17:8248042-8248182 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249207-8249317 | Common:1; Rare:31 | ||||
| chr17:8435715-8436034 | Common:4; Rare:121 | ||||
| chr17:8630613-8630790 | Rare:55 | ||||
| chr17:8965675-8965783 | Common:1; Rare:34 | ||||
| chr17:9576591-9576638 | Rare:15 | ||||
| chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:11997454-11997618 | Common:3; Rare:56 | ||||
| chr17:12665960-12666084 | Common:1; Rare:28 | ||||
| chr17:14069341-14069593 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):3 |