| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54214907-54215196 | Common:1; Rare:62 | ||||
| chr19:54238334-54238568 | Common:2; Rare:27 | ||||
| chr19:54239932-54240194 | Common:9; Rare:32 | ||||
| chr19:54276414-54276653 | Common:2; Rare:71 | ||||
| chr19:54636514-54636818 | Common:14; Rare:118 | ||||
| chr19:55116136-55116437 | Common:3; Rare:64 | ||||
| chr19:55241006-55241251 | Common:1; Rare:82 | ||||
| chr19:57786208-57786495 | Common:3; Rare:59 | ||||
| chr19:57794066-57794259 | Common:1; Rare:28 | ||||
| chr19:57803756-57803792 | Rare:4 | ||||
| chr19:57865714-57865947 | Common:7; Rare:69 | ||||
| chr19:58255886-58256102 | Common:1; Rare:44 | ||||
| chr19:58550606-58550848 | Rare:71 | ||||
| chr2:1493646-1493941 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:1504385-1504642 | Common:1; Rare:63 |