| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34961412-34961575 | Common:1; Rare:80 | ||||
| chr17:34981096-34981174 | Rare:12 | ||||
| chr17:34981176-34981190 | |||||
| chr17:35063653-35063836 | Rare:29 | ||||
| chr17:35242901-35243106 | Rare:70 | ||||
| chr17:35373608-35373821 | Common:4; Rare:41 | ||||
| chr17:35432482-35432706 | Common:1; Rare:36 | ||||
| chr17:35578476-35578684 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587222-35587562 | Rare:83 | ||||
| chr17:36211004-36211068 | Rare:8 | ||||
| chr17:36486476-36486721 | Common:3; Rare:86 | ||||
| chr17:36534852-36535033 | Common:2; Rare:85 | ||||
| chr17:36544787-36545096 | Common:6; Rare:87 | ||||
| chr17:36545480-36545677 | Rare:63 | ||||
| chr17:36601488-36601616 | Rare:41 |