| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89918691-89918879 | Common:4; Rare:59; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:89972470-89972645 | Common:1; Rare:63 | ||||
| chr17:714782-714885 | Common:2; Rare:36 | ||||
| chr17:752253-752347 | Rare:28 | ||||
| chr17:1400048-1400273 | Common:2; Rare:86 | ||||
| chr17:1491612-1491764 | Common:1; Rare:45 | ||||
| chr17:1516572-1516949 | Common:1; Rare:133 | ||||
| chr17:1648851-1649206 | Common:3; Rare:124 | ||||
| chr17:1684794-1685030 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716197-1716523 | Common:3; Rare:97 | ||||
| chr17:1829769-1830117 | Common:9; Rare:143 | ||||
| chr17:2303770-2303996 | Common:2; Rare:82 | ||||
| chr17:2336329-2336546 | Rare:98 | ||||
| chr17:2711747-2712016 | Common:1; Rare:79 | ||||
| chr17:3636231-3636479 | Common:4; Rare:71; Clinvar (benign):1 |