| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52488067-52488396 | Common:3; Rare:105; Clinvar:1 | ||||
| chr12:76030508-76030598 | Rare:33 | ||||
| chr12:76030930-76031089 | Rare:51 | ||||
| chr12:84911178-84911473 | Common:2; Rare:51 | ||||
| chr12:127230857-127231147 | Common:3; Rare:43 | ||||
| chr13:20360019-20360284 | Common:3; Rare:48 | ||||
| chr14:49633956-49634079 | Common:1; Rare:49; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49862655-49862988 | Common:1; Rare:160 | ||||
| chr14:74616586-74616748 | Common:1; Rare:26 | ||||
| chr14:100825929-100826118 | Rare:27 | ||||
| chr17:10791164-10791314 | Common:1; Rare:33 | ||||
| chr17:64145768-64145984 | Common:2; Rare:55 | ||||
| chr17:64975564-64975748 | Common:2; Rare:72 | ||||
| chr17:76557668-76557815 | Common:1; Rare:52 | ||||
| chr18:5238010-5238125 | Common:1; Rare:48 |