| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5123111-5123420 | Rare:103 | ||||
| chr17:5191836-5192112 | Common:2; Rare:88 | ||||
| chr17:5234811-5234973 | Rare:35 | ||||
| chr17:5419618-5419785 | Common:2; Rare:69 | ||||
| chr17:5419794-5419882 | Common:1; Rare:15 | ||||
| chr17:5420126-5420227 | Rare:42 | ||||
| chr17:5439128-5439181 | Rare:15 | ||||
| chr17:5468725-5469035 | Common:1; Rare:125 | ||||
| chr17:5486157-5486608 | Common:5; Rare:152 | ||||
| chr17:5486796-5486917 | Common:4; Rare:36 | ||||
| chr17:6640646-6641085 | Common:7; Rare:134 | ||||
| chr17:6651574-6651771 | Common:1; Rare:63 | ||||
| chr17:7012308-7012738 | Rare:139 | ||||
| chr17:7219817-7219944 | Common:3; Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:7220367-7221031 | Common:1; Rare:264; Clinvar:21; Clinvar (benign):14; Clinvar (pathogenic):7 |