| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39413373-39413539 | Common:1; Rare:49 | ||||
| chr19:39435893-39436132 | Common:4; Rare:91 | ||||
| chr19:39445470-39445829 | Common:2; Rare:99 | ||||
| chr19:39480619-39480919 | Common:3; Rare:151; Clinvar (pathogenic):1 | ||||
| chr19:39846308-39846539 | Common:1; Rare:112 | ||||
| chr19:39970957-39971205 | Common:3; Rare:66 | ||||
| chr19:39996925-39997132 | Common:5; Rare:64 | ||||
| chr19:40056130-40056330 | Rare:29 | ||||
| chr19:40090858-40091011 | Common:1; Rare:44 | ||||
| chr19:40284888-40285170 | Common:1; Rare:93 | ||||
| chr19:40285216-40285623 | Common:3; Rare:137 | ||||
| chr19:40348388-40348746 | Common:4; Rare:119 | ||||
| chr19:40425984-40426147 | Common:1; Rare:46 | ||||
| chr19:40444233-40444517 | Common:3; Rare:91 | ||||
| chr19:40465697-40466098 | Common:3; Rare:125 |