| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15999572-16000028 | Common:3; Rare:193; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16215530-16215657 | Common:1; Rare:52 | ||||
| chr17:17591580-17591926 | Common:2; Rare:98 | ||||
| chr17:18314953-18315326 | Rare:107 | ||||
| chr17:18682218-18682465 | Common:8; Rare:25 | ||||
| chr17:18781076-18781305 | Common:5; Rare:63 | ||||
| chr17:19378162-19378530 | Common:2; Rare:90 | ||||
| chr17:19648627-19648800 | Common:2; Rare:57 | ||||
| chr17:19977804-19978130 | Common:2; Rare:90 | ||||
| chr17:21214144-21214322 | Common:2; Rare:74 | ||||
| chr17:27293958-27294132 | Common:1; Rare:73 | ||||
| chr17:28335429-28335834 | Common:1; Rare:91 | ||||
| chr17:28357451-28357667 | Common:5; Rare:108 | ||||
| chr17:28571497-28571702 | Rare:48 | ||||
| chr17:28576876-28577009 | Common:1; Rare:37 |