| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50866351-50866554 | Common:2; Rare:64 | ||||
| chr17:51153326-51153643 | Common:1; Rare:83 | ||||
| chr17:51166702-51166954 | Rare:77 | ||||
| chr17:51260368-51260582 | Common:3; Rare:99 | ||||
| chr17:54968632-54968792 | Common:3; Rare:77 | ||||
| chr17:56593454-56593707 | Rare:46 | ||||
| chr17:56833896-56834152 | Common:2; Rare:76 | ||||
| chr17:56914009-56914176 | Rare:42 | ||||
| chr17:56960828-56961130 | Common:2; Rare:107 | ||||
| chr17:56978036-56978153 | Common:2; Rare:62 | ||||
| chr17:57084985-57085200 | Rare:74 | ||||
| chr17:57850013-57850274 | Common:1; Rare:80 | ||||
| chr17:58007199-58007393 | Common:1; Rare:85 | ||||
| chr17:58279296-58279568 | Rare:97; Clinvar (pathogenic):2 | ||||
| chr17:59106711-59107080 | Common:2; Rare:120; Clinvar:4; Clinvar (benign):2 |