| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38899513-38900018 | Rare:153 | ||||
| chr19:38930723-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975691-38975844 | Common:1; Rare:35 | ||||
| chr19:39390862-39391461 | Common:1; Rare:227 | ||||
| chr19:39406706-39406928 | Rare:91 | ||||
| chr19:39413705-39413820 | Rare:21 | ||||
| chr19:39480731-39480909 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
| chr19:39846335-39846473 | Common:1; Rare:62 | ||||
| chr19:39970918-39971237 | Common:4; Rare:89 | ||||
| chr19:39996937-39997113 | Common:5; Rare:58 | ||||
| chr19:40056163-40056262 | Rare:15 | ||||
| chr19:40348393-40348739 | Common:4; Rare:112 | ||||
| chr19:40377783-40378063 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr19:40444287-40444517 | Common:3; Rare:71 | ||||
| chr19:40465608-40466096 | Common:3; Rare:168 |