| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79069132-79069523 | Common:4; Rare:149 | ||||
| chr18:79679060-79679640 | Common:8; Rare:441 | ||||
| chr18:79679717-79679868 | Common:3; Rare:70 | ||||
| chr18:79951576-79951860 | Common:6; Rare:209 | ||||
| chr18:79964427-79964709 | Common:2; Rare:121 | ||||
| chr18:79988344-79988703 | Common:8; Rare:212; Clinvar:1; Clinvar (pathogenic):4 | ||||
| chr18:80033892-80034534 | Common:17; Rare:272 | ||||
| chr19:344769-344890 | Common:3; Rare:50 | ||||
| chr19:460130-460600 | Common:13; Rare:124 | ||||
| chr19:488987-489225 | Common:15; Rare:141 | ||||
| chr19:507790-507996 | Common:4; Rare:117 | ||||
| chr19:530960-531290 | Common:4; Rare:138 | ||||
| chr19:531483-531808 | Common:22; Rare:247 | ||||
| chr19:531825-532077 | Common:1; Rare:144 | ||||
| chr19:571085-571375 | Common:2; Rare:62 |