| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:131889296-131889311 | Rare:3 | ||||
| chr12:21255-21350 | Common:2; Rare:7 | ||||
| chr12:21389-21476 | Common:3; Rare:5 | ||||
| chr12:291312-291616 | Rare:63 | ||||
| chr12:1262925-1263040 | Common:2; Rare:27 | ||||
| chr12:1589285-1589514 | Common:1; Rare:31 | ||||
| chr12:1699541-1699836 | Rare:65 | ||||
| chr12:1780953-1781219 | Common:1; Rare:54 | ||||
| chr12:1939805-1939958 | Rare:33 | ||||
| chr12:2931094-2931480 | Rare:108 | ||||
| chr12:3045303-3045528 | Rare:44 | ||||
| chr12:3045657-3045814 | Common:9; Rare:41 | ||||
| chr12:3211628-3211725 | Rare:13 | ||||
| chr12:4682279-4682481 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr12:5430287-5430382 | Rare:17 |