| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38565535-38565685 | Common:1; Rare:73; Clinvar:10; Clinvar (benign):6 | ||||
| chr19:38569382-38569622 | Common:5; Rare:35 | ||||
| chr19:38667164-38667220 | Rare:7 | ||||
| chr19:38667882-38668031 | Rare:33 | ||||
| chr19:38676516-38676681 | Common:1; Rare:32 | ||||
| chr19:38686300-38686448 | Rare:18 | ||||
| chr19:38686644-38686862 | Common:1; Rare:41 | ||||
| chr19:38693920-38694082 | Common:1; Rare:33 | ||||
| chr19:38734347-38734536 | Common:3; Rare:67 | ||||
| chr19:38976485-38976643 | Common:1; Rare:21 | ||||
| chr19:39237848-39238060 | Common:3; Rare:58 | ||||
| chr19:39397870-39398018 | Common:1; Rare:26 | ||||
| chr19:39401213-39401354 | Common:1; Rare:28 | ||||
| chr19:39401538-39401902 | Common:1; Rare:83 | ||||
| chr19:39402514-39402896 | Rare:89 |