| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74597371-74597484 | Common:1; Rare:27 | ||||
| chr18:74597584-74597920 | Common:2; Rare:90 | ||||
| chr18:77087441-77087533 | Common:4; Rare:26 | ||||
| chr18:79400236-79400330 | Common:1; Rare:37 | ||||
| chr18:79679193-79679560 | Common:3; Rare:169 | ||||
| chr18:79681888-79682066 | Common:2; Rare:41 | ||||
| chr18:79988331-79988680 | Common:4; Rare:122; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:507431-507512 | Common:2; Rare:25 | ||||
| chr19:572322-572649 | Rare:174 | ||||
| chr19:633520-633759 | Common:8; Rare:106 | ||||
| chr19:663147-663475 | Common:2; Rare:132 | ||||
| chr19:797197-797500 | Rare:138 | ||||
| chr19:804912-805152 | Common:1; Rare:106 | ||||
| chr19:893158-893484 | Common:3; Rare:139 | ||||
| chr19:913153-913275 | Rare:39 |