| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39406981-39407106 | Rare:26 | ||||
| chr19:39407143-39407640 | Rare:96 | ||||
| chr19:39435837-39436167 | Common:7; Rare:120 | ||||
| chr19:39445459-39445861 | Common:2; Rare:113 | ||||
| chr19:39480738-39480931 | Common:3; Rare:103; Clinvar (pathogenic):1 | ||||
| chr19:39846296-39846473 | Common:1; Rare:82 | ||||
| chr19:39934964-39935118 | Common:1; Rare:33 | ||||
| chr19:39970900-39971232 | Common:4; Rare:99 | ||||
| chr19:39996925-39997109 | Common:5; Rare:60 | ||||
| chr19:40056154-40056260 | Rare:15 | ||||
| chr19:40285186-40285493 | Common:1; Rare:107 | ||||
| chr19:40348393-40348724 | Common:4; Rare:105 | ||||
| chr19:40425975-40426141 | Common:1; Rare:51 | ||||
| chr19:40444240-40444518 | Common:3; Rare:88 | ||||
| chr19:40465687-40466031 | Common:2; Rare:110 |