| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:90022527-90022711 | Rare:71 | ||||
| chr17:714799-714956 | Common:2; Rare:53 | ||||
| chr17:752152-752309 | Common:2; Rare:66 | ||||
| chr17:1400140-1400452 | Common:3; Rare:128 | ||||
| chr17:1516607-1516960 | Common:1; Rare:125 | ||||
| chr17:1684794-1685067 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1829786-1830071 | Common:8; Rare:119 | ||||
| chr17:2303734-2304015 | Common:2; Rare:103 | ||||
| chr17:2336430-2336512 | Rare:29 | ||||
| chr17:2511806-2512021 | Common:2; Rare:68 | ||||
| chr17:2593861-2593984 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:3636241-3636459 | Common:4; Rare:61; Clinvar (benign):1 | ||||
| chr17:3668575-3668830 | Common:1; Rare:97 | ||||
| chr17:3723752-3723932 | Common:1; Rare:102 | ||||
| chr17:4142992-4143245 | Rare:86 |