| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31658546-31658946 | Common:4; Rare:60 | ||||
| chr12:31658970-31659811 | Common:10; Rare:514 | ||||
| chr12:31659890-31660290 | Common:2; Rare:47 | ||||
| chr12:31715080-31715800 | Common:12; Rare:323 | ||||
| chr12:31728264-31729785 | Common:23; Rare:1120 | ||||
| chr12:31958850-31959248 | Common:7; Rare:214 | ||||
| chr12:31959180-31959660 | Common:19; Rare:714 | ||||
| chr12:31959695-31960095 | Common:5; Rare:243 | ||||
| chr12:31960064-31960221 | Rare:52 | ||||
| chr12:32106514-32107203 | Common:25; Rare:577 | ||||
| chr12:32107691-32108344 | Common:7; Rare:185 | ||||
| chr12:32399080-32399560 | Common:9; Rare:223 | ||||
| chr12:32399550-32399970 | Common:7; Rare:208 | ||||
| chr12:32678987-32679409 | Common:7; Rare:508; Clinvar:3; Clinvar (benign):13 | ||||
| chr12:32679530-32679973 | Common:10; Rare:254 |