| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49623284-49623572 | Common:1; Rare:80 | ||||
| chr12:49828359-49828543 | Common:1; Rare:69 | ||||
| chr12:50025366-50025626 | Common:1; Rare:72 | ||||
| chr12:50085055-50085364 | Common:1; Rare:82 | ||||
| chr12:50283420-50283665 | Common:2; Rare:71 | ||||
| chr12:50400749-50401008 | Common:1; Rare:86 | ||||
| chr12:50763926-50764306 | Common:1; Rare:102 | ||||
| chr12:51026308-51026495 | Common:3; Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048079-51048379 | Common:2; Rare:105 | ||||
| chr12:51238658-51238915 | Common:8; Rare:114 | ||||
| chr12:51269810-51269887 | Rare:20 | ||||
| chr12:51270116-51270367 | Common:4; Rare:66 | ||||
| chr12:51270371-51270687 | Common:5; Rare:77 | ||||
| chr12:51391613-51391737 | Common:1; Rare:39 | ||||
| chr12:52051152-52051461 | Common:1; Rare:101 |