| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:58417838-58418145 | Common:2; Rare:61 | ||||
| chr18:58445635-58445913 | Common:1; Rare:53 | ||||
| chr18:58446047-58446310 | Rare:57 | ||||
| chr18:58450180-58450286 | Rare:12 | ||||
| chr18:70335162-70335358 | Common:2; Rare:40 | ||||
| chr18:74229857-74230041 | Common:3; Rare:27 | ||||
| chr18:74241032-74241077 | Common:1; Rare:9 | ||||
| chr18:74288710-74288959 | Common:5; Rare:54 | ||||
| chr18:74290031-74290265 | Common:1; Rare:33 | ||||
| chr19:1207888-1208237 | Common:2; Rare:89 | ||||
| chr19:1398976-1399176 | Common:1; Rare:74; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):5 | ||||
| chr19:1633042-1633213 | Common:2; Rare:57 | ||||
| chr19:1839980-1840208 | Common:1; Rare:62 | ||||
| chr19:1876142-1876284 | Common:1; Rare:54 | ||||
| chr19:2543645-2543723 | Common:2; Rare:14 |