| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36187083-36187711 | Common:11; Rare:275 | ||||
| chr18:36187760-36188010 | Common:1; Rare:106 | ||||
| chr18:36828721-36829294 | Common:6; Rare:371 | ||||
| chr18:41955072-41955280 | Common:1; Rare:79 | ||||
| chr18:44679844-44680170 | Common:1; Rare:38 | ||||
| chr18:45967219-45967516 | Rare:216; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr18:46098216-46098394 | Common:22; Rare:135; Clinvar (benign):11 | ||||
| chr18:46104198-46104442 | Common:6; Rare:120 | ||||
| chr18:46173898-46174152 | Common:2; Rare:113 | ||||
| chr18:46333576-46334260 | Common:3; Rare:234 | ||||
| chr18:46917336-46917664 | Common:3; Rare:232 | ||||
| chr18:47149980-47150350 | Common:5; Rare:191 | ||||
| chr18:47150406-47150604 | Common:7; Rare:122 | ||||
| chr18:47896280-47896650 | Rare:94 | ||||
| chr18:47930286-47930762 | Common:4; Rare:382 |