| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49210591-49210718 | Rare:20 | ||||
| chr17:49414833-49415147 | Common:2; Rare:80 | ||||
| chr17:49708148-49708343 | Common:1; Rare:59 | ||||
| chr17:49788462-49788718 | Common:1; Rare:81 | ||||
| chr17:50373160-50373255 | Common:3; Rare:42 | ||||
| chr17:50719504-50719654 | Rare:59 | ||||
| chr17:50866355-50866655 | Common:3; Rare:88 | ||||
| chr17:51260389-51260581 | Common:3; Rare:94 | ||||
| chr17:54968611-54968792 | Common:3; Rare:88 | ||||
| chr17:56914016-56914177 | Rare:42 | ||||
| chr17:57084971-57085335 | Rare:124 | ||||
| chr17:57849981-57850281 | Common:1; Rare:100 | ||||
| chr17:57988164-57988536 | Common:5; Rare:109 | ||||
| chr17:58007199-58007384 | Common:1; Rare:81 | ||||
| chr17:58692530-58692678 | Common:1; Rare:81; Clinvar:15; Clinvar (benign):20 |