| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35155110-35155165 | Rare:12 | ||||
| chr19:35329032-35329198 | Rare:38 | ||||
| chr19:35545474-35545689 | Common:4; Rare:71 | ||||
| chr19:35612632-35612850 | Common:1; Rare:72 | ||||
| chr19:35628863-35629091 | Common:4; Rare:68 | ||||
| chr19:35648093-35648402 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745406-35745698 | Rare:83 | ||||
| chr19:35757841-35758218 | Common:2; Rare:114 | ||||
| chr19:35900530-35900657 | Rare:30 | ||||
| chr19:35902247-35902572 | Common:4; Rare:58 | ||||
| chr19:36014199-36014553 | Common:2; Rare:95 | ||||
| chr19:36054045-36054179 | Rare:55 | ||||
| chr19:36054396-36054503 | Common:2; Rare:35 | ||||
| chr19:36054705-36054990 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:36114842-36114982 | Common:2; Rare:61 |