| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35046139-35046657 | Common:1; Rare:179 | ||||
| chr14:35121908-35122311 | Common:2; Rare:116 | ||||
| chr14:35122429-35122800 | Common:2; Rare:109 | ||||
| chr14:35292233-35292484 | Common:4; Rare:92; Clinvar:1 | ||||
| chr14:35402765-35403120 | Common:4; Rare:98; Clinvar (benign):3 | ||||
| chr14:35404422-35404803 | Common:3; Rare:130; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:35809032-35809084 | Rare:8 | ||||
| chr14:35809267-35809435 | Common:1; Rare:45 | ||||
| chr14:35826717-35826936 | Common:1; Rare:60 | ||||
| chr14:36311664-36311981 | Common:1; Rare:68 | ||||
| chr14:36320338-36320841 | Common:5; Rare:163 | ||||
| chr14:36513100-36514069 | Common:1; Rare:228 | ||||
| chr14:36519717-36519906 | Common:1; Rare:38 | ||||
| chr14:36520071-36520594 | Common:7; Rare:138; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:36520660-36520933 | Common:2; Rare:65 |