| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74149075-74149094 | Rare:7 | ||||
| chr18:74291886-74292213 | Common:2; Rare:90 | ||||
| chr18:74496025-74496305 | Common:3; Rare:78 | ||||
| chr18:74496342-74496442 | Common:1; Rare:35 | ||||
| chr18:74597380-74597425 | Common:1; Rare:7 | ||||
| chr18:74597606-74597925 | Common:2; Rare:84 | ||||
| chr18:75208404-75208562 | Common:1; Rare:35 | ||||
| chr18:75208927-75209227 | Common:3; Rare:118 | ||||
| chr18:75210762-75211054 | Common:8; Rare:79; Clinvar:9; Clinvar (benign):2 | ||||
| chr18:75211412-75211470 | Rare:18 | ||||
| chr18:76822226-76822645 | Common:11; Rare:119 | ||||
| chr18:79679714-79679877 | Common:2; Rare:53 | ||||
| chr18:79988365-79988671 | Common:4; Rare:114; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:488866-489194 | Common:9; Rare:113 | ||||
| chr19:572322-572612 | Rare:146 |