| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38374407-38374817 | Rare:154 | ||||
| chr19:38618849-38619276 | Common:4; Rare:126 | ||||
| chr19:38647378-38647733 | Common:3; Rare:128 | ||||
| chr19:38831753-38832061 | Common:4; Rare:93; Clinvar (benign):1 | ||||
| chr19:38899504-38900033 | Rare:160 | ||||
| chr19:38930726-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390862-39390917 | Rare:27 | ||||
| chr19:39390990-39391460 | Common:1; Rare:181 | ||||
| chr19:39406710-39406893 | Rare:78 | ||||
| chr19:39413647-39413816 | Rare:33 | ||||
| chr19:39435885-39436188 | Common:6; Rare:122 | ||||
| chr19:39480752-39480931 | Common:3; Rare:96; Clinvar (pathogenic):1 | ||||
| chr19:39846312-39846473 | Common:1; Rare:75 | ||||
| chr19:39970957-39971200 | Common:3; Rare:64 | ||||
| chr19:39996956-39997113 | Common:4; Rare:55 |