| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2336265-2336672 | Rare:524 | ||||
| chr17:2337252-2337718 | Common:7; Rare:632 | ||||
| chr17:2337686-2338180 | Common:4; Rare:182 | ||||
| chr17:2392228-2393409 | Common:57; Rare:1606 | ||||
| chr17:2393760-2394078 | Common:9; Rare:332 | ||||
| chr17:2396750-2397140 | Common:8; Rare:330 | ||||
| chr17:2399490-2400686 | Common:10; Rare:544 | ||||
| chr17:2401004-2401910 | Common:7; Rare:1181 | ||||
| chr17:2511420-2511730 | Rare:83 | ||||
| chr17:2511728-2512148 | Common:14; Rare:493 | ||||
| chr17:2593360-2594320 | Common:24; Rare:947; Clinvar:22; Clinvar (benign):20 | ||||
| chr17:2710742-2711142 | Common:3; Rare:172 | ||||
| chr17:2711625-2712160 | Common:10; Rare:616 | ||||
| chr17:2712169-2712569 | Common:2; Rare:76 | ||||
| chr17:3513675-3514151 | Common:8; Rare:294; Clinvar:10; Clinvar (benign):27 |