| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47941729-47941836 | Rare:24; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:47970813-47971204 | Common:1; Rare:99 | ||||
| chr17:47971232-47971404 | Rare:56 | ||||
| chr17:47971600-47971841 | Common:2; Rare:45 | ||||
| chr17:48037735-48037861 | Common:2; Rare:34 | ||||
| chr17:48047570-48048455 | Common:5; Rare:247 | ||||
| chr17:48048513-48048712 | Common:2; Rare:45 | ||||
| chr17:48048722-48048974 | Common:3; Rare:57 | ||||
| chr17:48048994-48049070 | Common:1; Rare:18 | ||||
| chr17:48049076-48049149 | Common:2; Rare:13 | ||||
| chr17:48049199-48049295 | Rare:29 | ||||
| chr17:48054247-48054353 | Rare:22 | ||||
| chr17:48055707-48056069 | Rare:51 | ||||
| chr17:48100289-48100436 | Rare:22 | ||||
| chr17:48100550-48100895 | Common:1; Rare:88 |