| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:75210765-75210887 | Rare:24; Clinvar:1 | ||||
| chr18:76822241-76822615 | Common:11; Rare:105 | ||||
| chr18:77127900-77128066 | Common:2; Rare:36 | ||||
| chr18:77128377-77128586 | Common:5; Rare:44 | ||||
| chr18:77131345-77131506 | Common:2; Rare:38 | ||||
| chr18:77133691-77133918 | Common:1; Rare:48 | ||||
| chr18:79679224-79679460 | Common:2; Rare:116 | ||||
| chr18:79988241-79988661 | Common:4; Rare:133; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344781-344957 | Common:3; Rare:64 | ||||
| chr19:572322-572629 | Rare:158 | ||||
| chr19:633508-633745 | Common:8; Rare:109 | ||||
| chr19:663147-663430 | Common:2; Rare:113 | ||||
| chr19:680478-680774 | Common:2; Rare:107 | ||||
| chr19:797061-797469 | Common:1; Rare:165 | ||||
| chr19:893158-893484 | Common:3; Rare:139 |