| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79679236-79679566 | Common:3; Rare:160 | ||||
| chr18:79988416-79988667 | Common:4; Rare:95; Clinvar (pathogenic):2 | ||||
| chr19:344788-344933 | Common:3; Rare:47 | ||||
| chr19:507417-507506 | Common:2; Rare:29 | ||||
| chr19:572252-572694 | Common:4; Rare:216 | ||||
| chr19:633520-633745 | Common:8; Rare:99 | ||||
| chr19:663138-663379 | Common:2; Rare:92 | ||||
| chr19:804683-805174 | Common:1; Rare:183 | ||||
| chr19:893155-893478 | Common:3; Rare:134 | ||||
| chr19:913144-913296 | Rare:49 | ||||
| chr19:984277-984348 | Rare:22 | ||||
| chr19:1103785-1104104 | Common:4; Rare:136 | ||||
| chr19:1105485-1105777 | Common:3; Rare:136 | ||||
| chr19:1438255-1438435 | Rare:66 | ||||
| chr19:1490335-1490451 | Common:3; Rare:38 |