| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170972-43171274 | Common:1; Rare:102 | ||||
| chr17:43211793-43211903 | Rare:21 | ||||
| chr17:43530436-43530505 | Rare:11 | ||||
| chr17:43778872-43779094 | Common:1; Rare:58 | ||||
| chr17:43833101-43833273 | Rare:49 | ||||
| chr17:44070612-44070911 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44111229-44111394 | Rare:48 | ||||
| chr17:44123599-44123844 | Common:3; Rare:70 | ||||
| chr17:44170634-44170747 | Rare:26 | ||||
| chr17:44186643-44187022 | Common:1; Rare:137 | ||||
| chr17:44187178-44187274 | Rare:26 | ||||
| chr17:44220825-44221052 | Rare:73 | ||||
| chr17:44221200-44221453 | Rare:68 | ||||
| chr17:44268096-44268367 | Rare:55; Clinvar:3 | ||||
| chr17:44324774-44325025 | Common:2; Rare:87 |