| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27893152-27893375 | Common:2; Rare:75 | ||||
| chr17:28041124-28041954 | Common:7; Rare:260 | ||||
| chr17:28042004-28042178 | Rare:60 | ||||
| chr17:28042390-28042920 | Common:1; Rare:136 | ||||
| chr17:28318840-28319259 | Common:9; Rare:381 | ||||
| chr17:28335348-28335855 | Common:3; Rare:331 | ||||
| chr17:28336110-28336627 | Common:3; Rare:154 | ||||
| chr17:28357390-28357811 | Common:17; Rare:479; Clinvar (pathogenic):5 | ||||
| chr17:28384462-28384912 | Rare:271 | ||||
| chr17:28384960-28385430 | Common:1; Rare:205 | ||||
| chr17:28405727-28405885 | Rare:40 | ||||
| chr17:28406134-28406317 | Rare:66; Clinvar:2 | ||||
| chr17:28570889-28571086 | Rare:68 | ||||
| chr17:28571450-28571776 | Rare:199 | ||||
| chr17:28576840-28577142 | Common:3; Rare:115 |