| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42676966-42677148 | Common:1; Rare:58 | ||||
| chr17:42682301-42682597 | Rare:59 | ||||
| chr17:42745023-42745123 | Common:2; Rare:33 | ||||
| chr17:42761060-42761264 | Rare:55 | ||||
| chr17:42798685-42798760 | Rare:21 | ||||
| chr17:42833338-42833461 | Rare:45 | ||||
| chr17:42964408-42964528 | Rare:59 | ||||
| chr17:43125345-43125580 | Rare:46; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170375 | Rare:16 | ||||
| chr17:43170972-43171245 | Rare:88 | ||||
| chr17:43778908-43779078 | Rare:40 | ||||
| chr17:44070620-44070942 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44093459-44093659 | Common:1; Rare:67 | ||||
| chr17:44186669-44187002 | Common:1; Rare:119 | ||||
| chr17:44187173-44187274 | Rare:29 |