| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37594753-37594917 | Rare:46 | ||||
| chr19:37655781-37655874 | Common:2; Rare:26 | ||||
| chr19:37692206-37692396 | Common:2; Rare:36 | ||||
| chr19:37779579-37779662 | Rare:18 | ||||
| chr19:37817268-37817421 | Common:1; Rare:31 | ||||
| chr19:38252892-38253442 | Common:3; Rare:136 | ||||
| chr19:38647370-38647795 | Common:3; Rare:140 | ||||
| chr19:38724153-38724565 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38815617-38815995 | Common:2; Rare:128; Clinvar (benign):1 | ||||
| chr19:38899532-38900033 | Rare:153 | ||||
| chr19:38930726-38930996 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975676-38975884 | Common:1; Rare:52 | ||||
| chr19:39389154-39389433 | Common:1; Rare:68 | ||||
| chr19:39390861-39390923 | Rare:28 | ||||
| chr19:39390981-39391425 | Common:1; Rare:170 |