| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22982472-22982980 | Common:6; Rare:257 | ||||
| chr14:23006400-23006920 | Common:8; Rare:164 | ||||
| chr14:23007080-23007345 | Common:5; Rare:154 | ||||
| chr14:23010119-23010245 | Rare:73 | ||||
| chr14:23034350-23034610 | Rare:106 | ||||
| chr14:23034794-23035250 | Common:5; Rare:200 | ||||
| chr14:23057510-23057732 | Common:10; Rare:121 | ||||
| chr14:23094554-23094765 | Common:2; Rare:151 | ||||
| chr14:23095047-23095630 | Common:6; Rare:436 | ||||
| chr14:23286001-23286412 | Common:4; Rare:209 | ||||
| chr14:23301090-23301460 | Common:6; Rare:140 | ||||
| chr14:23302729-23303201 | Common:2; Rare:130 | ||||
| chr14:23306613-23307052 | Common:2; Rare:156 | ||||
| chr14:23320850-23321160 | Common:4; Rare:103 | ||||
| chr14:23321197-23321686 | Common:4; Rare:295; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 |