| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:81221275-81221468 | Common:1; Rare:47 | ||||
| chr14:85530030-85530178 | Common:1; Rare:32 | ||||
| chr14:88824337-88824710 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89954713-89954950 | Rare:63 | ||||
| chr14:90331906-90332179 | Common:1; Rare:80 | ||||
| chr14:90396870-90397107 | Common:2; Rare:123 | ||||
| chr14:91114004-91114106 | Rare:30 | ||||
| chr14:91510277-91510595 | Common:1; Rare:96 | ||||
| chr14:91836473-91836780 | Common:12; Rare:62 | ||||
| chr14:92040019-92040195 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121667-92121990 | Common:4; Rare:105 | ||||
| chr14:93184834-93185004 | Rare:56 | ||||
| chr14:93207024-93207281 | Common:2; Rare:126 | ||||
| chr14:94081144-94081328 | Common:4; Rare:61 | ||||
| chr14:94293208-94293446 | Common:1; Rare:48 |