| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38899531-38900108 | Rare:334 | ||||
| chr19:38930420-38930660 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38930722-38931076 | Common:7; Rare:179; Clinvar:4; Clinvar (benign):6 | ||||
| chr19:38975625-38976075 | Common:2; Rare:161 | ||||
| chr19:39341849-39342750 | Common:14; Rare:658 | ||||
| chr19:39390977-39391449 | Common:2; Rare:343 | ||||
| chr19:39406688-39406867 | Rare:121 | ||||
| chr19:39435848-39436203 | Common:13; Rare:235 | ||||
| chr19:39445280-39445730 | Common:10; Rare:252 | ||||
| chr19:39480691-39480880 | Common:3; Rare:100; Clinvar (pathogenic):1 | ||||
| chr19:39839940-39840540 | Common:5; Rare:247 | ||||
| chr19:39840560-39840980 | Common:2; Rare:215 | ||||
| chr19:39846303-39846524 | Common:2; Rare:191 | ||||
| chr19:39970831-39971228 | Common:5; Rare:114 | ||||
| chr19:39996898-39997144 | Common:10; Rare:132 |