| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41528275-41528542 | Common:1; Rare:64; Clinvar:1 | ||||
| chr17:41688637-41688889 | Common:1; Rare:80 | ||||
| chr17:41689251-41689569 | Common:4; Rare:121 | ||||
| chr17:41734641-41734910 | Common:5; Rare:55 | ||||
| chr17:41786680-41786822 | Common:1; Rare:39 | ||||
| chr17:41812604-41812739 | Common:3; Rare:24; Clinvar:1 | ||||
| chr17:41812841-41813029 | Rare:50; Clinvar:2 | ||||
| chr17:41818198-41818442 | Common:1; Rare:90; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:41819160-41819277 | Common:1; Rare:24; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:41836189-41836322 | Rare:39 | ||||
| chr17:41918878-41919195 | Common:1; Rare:128; Clinvar:1 | ||||
| chr17:41966631-41966831 | Common:1; Rare:73 | ||||
| chr17:42017120-42017494 | Rare:117 | ||||
| chr17:42019963-42020124 | Common:1; Rare:46 | ||||
| chr17:42154915-42155279 | Common:4; Rare:100 |