| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7352054-7352202 | Rare:47 | ||||
| chr17:7479496-7479709 | Common:1; Rare:36 | ||||
| chr17:7484215-7484370 | Common:1; Rare:61 | ||||
| chr17:7583550-7583852 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7687478-7687558 | Rare:19 | ||||
| chr17:7857074-7857285 | Common:2; Rare:99 | ||||
| chr17:7857459-7857714 | Common:2; Rare:81 | ||||
| chr17:7885187-7885346 | Rare:44 | ||||
| chr17:7931858-7932248 | Common:5; Rare:105 | ||||
| chr17:8151221-8151491 | Common:3; Rare:63 | ||||
| chr17:8248042-8248110 | Common:2; Rare:37; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8435710-8436014 | Common:4; Rare:119 | ||||
| chr17:8965688-8965802 | Common:1; Rare:35 | ||||
| chr17:10697505-10697653 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:12665812-12666135 | Common:2; Rare:64 |