| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:27793239-27793477 | Common:4; Rare:54 | ||||
| chr19:27793891-27794052 | Common:1; Rare:33 | ||||
| chr19:36797313-36797542 | Rare:45 | ||||
| chr2:68799721-68800015 | Common:4; Rare:60 | ||||
| chr2:88016544-88016817 | Common:8; Rare:115 | ||||
| chr2:91659921-91660045 | Rare:22 | ||||
| chr2:178413922-178413981 | Rare:21 | ||||
| chr20:47352534-47352638 | Rare:20 | ||||
| chr21:43600809-43601079 | Common:2; Rare:44 | ||||
| chr22:46069869-46070056 | Rare:42 | ||||
| chr3:75435088-75435377 | Common:3; Rare:97 | ||||
| chr3:101576982-101577088 | Rare:31 | ||||
| chr3:107240581-107240695 | Rare:51 | ||||
| chr3:150408849-150408988 | Rare:41 | ||||
| chr3:169765044-169765117 | Rare:32; Clinvar:2; Clinvar (pathogenic):1 |