| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47149970-47150350 | Common:7; Rare:245 | ||||
| chr18:47150396-47150646 | Common:11; Rare:228 | ||||
| chr18:47176243-47176394 | Common:1; Rare:83; Clinvar (benign):2 | ||||
| chr18:47930278-47930849 | Common:2; Rare:453 | ||||
| chr18:47930784-47931384 | Common:2; Rare:520 | ||||
| chr18:47931480-47932038 | Common:4; Rare:180 | ||||
| chr18:48409301-48409526 | Rare:129 | ||||
| chr18:48410220-48410570 | Common:12; Rare:161 | ||||
| chr18:48538872-48539298 | Common:2; Rare:151 | ||||
| chr18:48539460-48539924 | Common:2; Rare:160 | ||||
| chr18:48540427-48540910 | Common:3; Rare:209 | ||||
| chr18:48948400-48948760 | Common:1; Rare:236 | ||||
| chr18:48949276-48949579 | Common:5; Rare:143 | ||||
| chr18:48949872-48950127 | Rare:152 | ||||
| chr18:48950120-48950446 | Common:2; Rare:163 |