| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:62186956-62187329 | Common:5; Rare:103 | ||||
| chr18:63367012-63367305 | Common:1; Rare:101 | ||||
| chr18:63422370-63422801 | Common:2; Rare:125 | ||||
| chr18:68714977-68715255 | Common:5; Rare:124 | ||||
| chr18:70205659-70205725 | Common:2; Rare:34; Clinvar (benign):2 | ||||
| chr18:74148358-74148552 | Common:1; Rare:60 | ||||
| chr18:74291906-74292165 | Common:1; Rare:72 | ||||
| chr18:74496033-74496434 | Common:4; Rare:127 | ||||
| chr18:74597804-74597914 | Common:1; Rare:29 | ||||
| chr18:79988241-79988653 | Common:3; Rare:129; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344784-344945 | Common:3; Rare:56 | ||||
| chr19:572337-572661 | Rare:174 | ||||
| chr19:633508-633715 | Common:8; Rare:100 | ||||
| chr19:799094-799428 | Common:6; Rare:146 | ||||
| chr19:815266-815505 | Common:2; Rare:82 |