| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4946671-4946977 | Common:1; Rare:77 | ||||
| chr17:4948932-4949133 | Common:1; Rare:66 | ||||
| chr17:4967725-4967937 | Rare:91 | ||||
| chr17:4987640-4987753 | Rare:47 | ||||
| chr17:5078181-5078518 | Common:4; Rare:82 | ||||
| chr17:5191826-5192109 | Common:2; Rare:89 | ||||
| chr17:5419618-5419882 | Common:3; Rare:89 | ||||
| chr17:5420010-5420233 | Rare:87 | ||||
| chr17:5433370-5433577 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
| chr17:5486157-5486630 | Common:5; Rare:158 | ||||
| chr17:5486822-5486943 | Common:3; Rare:36 | ||||
| chr17:6640645-6641128 | Common:7; Rare:155 | ||||
| chr17:6651553-6651752 | Common:1; Rare:71 | ||||
| chr17:6995886-6996120 | Common:1; Rare:50 | ||||
| chr17:7012297-7012720 | Rare:139 |