| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:54968595-54968814 | Common:3; Rare:100 | ||||
| chr17:55421757-55422225 | Common:3; Rare:153 | ||||
| chr17:55751104-55751168 | Common:2; Rare:23 | ||||
| chr17:55751301-55751433 | Common:3; Rare:49 | ||||
| chr17:56914021-56914177 | Rare:40 | ||||
| chr17:56960708-56960819 | Rare:49 | ||||
| chr17:56960870-56961117 | Common:1; Rare:88 | ||||
| chr17:57084971-57085377 | Rare:130 | ||||
| chr17:57850002-57850295 | Common:1; Rare:96 | ||||
| chr17:57988107-57988541 | Common:6; Rare:125 | ||||
| chr17:58006604-58006694 | Rare:31 | ||||
| chr17:58007144-58007404 | Common:1; Rare:126 | ||||
| chr17:58007609-58007766 | Rare:40 | ||||
| chr17:58219216-58219381 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58328746-58328968 | Common:1; Rare:60 |