| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63476631-63477141 | Common:9; Rare:104 | ||||
| chr18:63490279-63490417 | Common:2; Rare:35 | ||||
| chr18:68714987-68715255 | Common:5; Rare:121 | ||||
| chr18:70205635-70205763 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr18:74148352-74148557 | Common:1; Rare:68 | ||||
| chr18:74291855-74292214 | Common:2; Rare:101; Clinvar:1 | ||||
| chr18:74496029-74496423 | Common:4; Rare:127 | ||||
| chr18:74597590-74597929 | Common:2; Rare:95 | ||||
| chr18:76822224-76822591 | Common:11; Rare:102 | ||||
| chr18:79964348-79964738 | Common:3; Rare:110 | ||||
| chr18:79988294-79988645 | Common:3; Rare:118; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr18:80034187-80034532 | Common:5; Rare:140 | ||||
| chr19:374110-374385 | Common:3; Rare:99 | ||||
| chr19:531579-531954 | Common:6; Rare:158 | ||||
| chr19:572237-572691 | Common:4; Rare:220 |