| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4518437-4518607 | Common:2; Rare:56 | ||||
| chr19:4539966-4540330 | Common:1; Rare:88 | ||||
| chr19:4831648-4832044 | Common:5; Rare:84 | ||||
| chr19:4867626-4867859 | Common:3; Rare:69 | ||||
| chr19:5293222-5293394 | Common:1; Rare:77 | ||||
| chr19:5622695-5623208 | Common:5; Rare:207 | ||||
| chr19:5978078-5978393 | Common:3; Rare:117 | ||||
| chr19:6361709-6361839 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6415193-6415438 | Common:1; Rare:85 | ||||
| chr19:6416846-6417019 | Common:1; Rare:61 | ||||
| chr19:6684773-6685155 | Rare:100; Clinvar (benign):1 | ||||
| chr19:6693379-6693574 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr19:6710637-6711197 | Common:3; Rare:173; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:6714164-6714448 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6720491-6720756 | Common:2; Rare:63; Clinvar (benign):2 |