| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41353584-41353810 | Rare:56 | ||||
| chr19:41363824-41364007 | Common:1; Rare:112; Clinvar:2 | ||||
| chr19:41364050-41364340 | Common:1; Rare:143; Clinvar:4 | ||||
| chr19:41397317-41397840 | Common:18; Rare:254; Clinvar (benign):8 | ||||
| chr19:41439360-41439710 | Common:4; Rare:162 | ||||
| chr19:41859540-41859920 | Common:2; Rare:195 | ||||
| chr19:41860078-41860449 | Common:6; Rare:236; Clinvar:7; Clinvar (benign):3 | ||||
| chr19:41883067-41883264 | Common:2; Rare:70 | ||||
| chr19:41884100-41884452 | Rare:151 | ||||
| chr19:41959269-41959612 | Common:2; Rare:143 | ||||
| chr19:42075794-42076209 | Common:4; Rare:231 | ||||
| chr19:42217644-42217931 | Common:1; Rare:199 | ||||
| chr19:42220075-42220396 | Common:4; Rare:161 | ||||
| chr19:42242518-42242739 | Rare:117 | ||||
| chr19:42243102-42243347 | Common:4; Rare:186 |