| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16324619-16324862 | Common:1; Rare:65 | ||||
| chr19:16471343-16471473 | Rare:20 | ||||
| chr19:16471798-16472226 | Common:5; Rare:132 | ||||
| chr19:16496042-16496456 | Common:2; Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:16542204-16542705 | Common:2; Rare:165 | ||||
| chr19:16542803-16542921 | Rare:29 | ||||
| chr19:16571231-16571539 | Common:2; Rare:56 | ||||
| chr19:16571975-16572055 | Rare:15 | ||||
| chr19:16572243-16572735 | Common:5; Rare:169 | ||||
| chr19:16628119-16628669 | Common:1; Rare:211 | ||||
| chr19:16628772-16628948 | Rare:43 | ||||
| chr19:16629249-16629392 | Common:1; Rare:23 | ||||
| chr19:16659652-16660000 | Common:3; Rare:130 | ||||
| chr19:16660045-16660406 | Common:3; Rare:144 | ||||
| chr19:16660543-16660685 | Common:1; Rare:23 |