| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5420110-5420219 | Rare:46 | ||||
| chr17:5438706-5438881 | Rare:49 | ||||
| chr17:5438930-5439307 | Common:5; Rare:125 | ||||
| chr17:5468535-5468668 | Common:1; Rare:43 | ||||
| chr17:5468724-5469068 | Common:1; Rare:133 | ||||
| chr17:5485847-5485946 | Common:1; Rare:24 | ||||
| chr17:5486105-5486631 | Common:6; Rare:180 | ||||
| chr17:5486726-5486945 | Common:6; Rare:66 | ||||
| chr17:6443776-6443965 | Common:3; Rare:35 | ||||
| chr17:6444107-6444485 | Common:2; Rare:112 | ||||
| chr17:6556261-6556418 | Rare:37; Clinvar (benign):1 | ||||
| chr17:6640640-6640854 | Common:2; Rare:52 | ||||
| chr17:6640877-6641129 | Common:4; Rare:102 | ||||
| chr17:6641581-6641691 | Common:2; Rare:26 | ||||
| chr17:6651451-6651873 | Common:1; Rare:138 |