| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40444279-40444532 | Common:4; Rare:80 | ||||
| chr19:40465684-40466112 | Common:3; Rare:136 | ||||
| chr19:40601218-40601384 | Rare:53 | ||||
| chr19:40609534-40609768 | Common:1; Rare:75; Clinvar (benign):3 | ||||
| chr19:40623575-40623608 | Rare:9 | ||||
| chr19:40714980-40715176 | Rare:48 | ||||
| chr19:40716853-40716969 | Rare:34 | ||||
| chr19:40717210-40717358 | Common:1; Rare:47 | ||||
| chr19:40750426-40750924 | Common:6; Rare:120 | ||||
| chr19:40751064-40751283 | Common:3; Rare:69 | ||||
| chr19:40751719-40752154 | Common:2; Rare:99 | ||||
| chr19:40771263-40771394 | Common:1; Rare:25 | ||||
| chr19:40777934-40778280 | Common:1; Rare:97 | ||||
| chr19:40798762-40799248 | Common:6; Rare:175 | ||||
| chr19:40799688-40799756 | Common:2; Rare:20 |