| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5420054-5420217 | Rare:66 | ||||
| chr17:5438820-5439042 | Rare:70 | ||||
| chr17:5439064-5439223 | Common:2; Rare:61 | ||||
| chr17:5468218-5468361 | Rare:39 | ||||
| chr17:5468798-5469135 | Common:3; Rare:123 | ||||
| chr17:5486069-5486652 | Common:6; Rare:198 | ||||
| chr17:5486767-5486933 | Common:4; Rare:54 | ||||
| chr17:6640395-6641226 | Common:10; Rare:252 | ||||
| chr17:6651448-6651767 | Common:1; Rare:113 | ||||
| chr17:7012312-7012726 | Rare:135 | ||||
| chr17:7035826-7036221 | Common:1; Rare:97 | ||||
| chr17:7219821-7219974 | Common:3; Rare:72; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7223289-7223328 | Rare:15 | ||||
| chr17:7223557-7223885 | Rare:94; Clinvar:12; Clinvar (benign):3; Clinvar (pathogenic):7 | ||||
| chr17:7224009-7224388 | Rare:129; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):7 |