| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48048599-48048813 | Common:4; Rare:31 | ||||
| chr17:48543809-48544019 | Rare:50 | ||||
| chr17:48544441-48544667 | Common:1; Rare:95 | ||||
| chr17:48590236-48590435 | Common:1; Rare:43 | ||||
| chr17:48944758-48944886 | Common:1; Rare:47 | ||||
| chr17:49788576-49788697 | Rare:32 | ||||
| chr17:50195274-50195457 | Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:50201619-50201863 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:50373163-50373220 | Common:2; Rare:25 | ||||
| chr17:50866351-50866646 | Common:3; Rare:87 | ||||
| chr17:51260320-51260561 | Common:3; Rare:91 | ||||
| chr17:54968623-54968772 | Common:3; Rare:74 | ||||
| chr17:56914031-56914176 | Rare:33 | ||||
| chr17:58007223-58007382 | Common:1; Rare:69 | ||||
| chr17:59106843-59106999 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 |