| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16347482-16347813 | Common:5; Rare:66 | ||||
| chr12:16350792-16350840 | Common:1; Rare:9 | ||||
| chr12:16608055-16608413 | Rare:81 | ||||
| chr12:19129527-19129802 | Common:1; Rare:133 | ||||
| chr12:20369558-20369915 | Common:3; Rare:160 | ||||
| chr12:21501530-21501900 | Common:5; Rare:100 | ||||
| chr12:21638620-21638703 | Common:1; Rare:17 | ||||
| chr12:21657751-21658126 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774670-21774978 | Rare:58 | ||||
| chr12:21941183-21941347 | Rare:34 | ||||
| chr12:21941350-21941389 | Rare:11 | ||||
| chr12:21941394-21941445 | Rare:14 | ||||
| chr12:21941459-21941481 | Rare:4 | ||||
| chr12:22544142-22544292 | Common:1; Rare:73 | ||||
| chr12:22544444-22544677 | Common:2; Rare:57 |