| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:75208854-75209451 | Common:5; Rare:199 | ||||
| chr18:76822226-76822638 | Common:11; Rare:116 | ||||
| chr19:507887-507987 | Rare:34 | ||||
| chr19:572322-572612 | Rare:146 | ||||
| chr19:582509-582830 | Common:6; Rare:116 | ||||
| chr19:633497-633780 | Common:8; Rare:129 | ||||
| chr19:663140-663482 | Common:2; Rare:138 | ||||
| chr19:680448-680783 | Common:2; Rare:121 | ||||
| chr19:913159-913278 | Rare:38 | ||||
| chr19:1026350-1026698 | Common:1; Rare:119 | ||||
| chr19:1103753-1104121 | Common:7; Rare:156 | ||||
| chr19:1105185-1105507 | Common:1; Rare:143; Clinvar (pathogenic):1 | ||||
| chr19:1177748-1177921 | Rare:37 | ||||
| chr19:1241586-1241820 | Rare:73 | ||||
| chr19:1269032-1269395 | Common:3; Rare:137 |