| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110424793-110424994 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:114065810-114065972 | Rare:40 | ||||
| chr14:20456816-20457097 | Common:2; Rare:108; Clinvar:1 | ||||
| chr14:32203267-32203571 | Common:12; Rare:128 | ||||
| chr14:49862651-49863120 | Common:2; Rare:202 | ||||
| chr14:61570562-61570688 | Common:1; Rare:27 | ||||
| chr14:61618669-61618870 | Common:1; Rare:39 | ||||
| chr14:61721508-61721776 | Common:1; Rare:54 | ||||
| chr14:68795244-68795333 | Common:3; Rare:24 | ||||
| chr14:75259111-75259373 | Rare:57 | ||||
| chr14:77033492-77033554 | Rare:14 | ||||
| chr14:81170391-81170492 | Rare:28 | ||||
| chr14:81219339-81219502 | Rare:36 | ||||
| chr14:95516612-95516771 | Common:2; Rare:36 | ||||
| chr14:100825921-100826129 | Rare:32 |