| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38618970-38619246 | Common:2; Rare:79 | ||||
| chr19:38647372-38647785 | Common:3; Rare:138 | ||||
| chr19:38647804-38647850 | Rare:14 | ||||
| chr19:38788962-38789202 | Common:4; Rare:51 | ||||
| chr19:38899586-38900018 | Rare:127 | ||||
| chr19:38930742-38930988 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39391035-39391418 | Common:1; Rare:155 | ||||
| chr19:39406701-39406931 | Rare:93 | ||||
| chr19:39407513-39407875 | Common:1; Rare:97 | ||||
| chr19:39412497-39412714 | Common:2; Rare:75 | ||||
| chr19:39480744-39480893 | Common:3; Rare:78; Clinvar (pathogenic):1 | ||||
| chr19:39970969-39971199 | Common:2; Rare:60 | ||||
| chr19:40348364-40348724 | Common:4; Rare:116 | ||||
| chr19:40377800-40378070 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr19:40444243-40444513 | Common:3; Rare:85 |