| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77761109-77761193 | Rare:38 | ||||
| chr14:81220612-81221079 | Common:4; Rare:159 | ||||
| chr14:85530030-85530267 | Common:1; Rare:50 | ||||
| chr14:87993142-87993432 | Common:1; Rare:113; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr14:88562907-88563154 | Rare:113 | ||||
| chr14:88824305-88824728 | Common:2; Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89417005-89417326 | Rare:87 | ||||
| chr14:89954492-89954947 | Common:3; Rare:153 | ||||
| chr14:89955628-89955996 | Common:10; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:91114303-91114395 | Rare:15 | ||||
| chr14:91510225-91510652 | Common:1; Rare:141 | ||||
| chr14:92039624-92039672 | Rare:11 | ||||
| chr14:92040013-92040148 | Common:3; Rare:43; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92106535-92106825 | Common:3; Rare:87 | ||||
| chr14:92121654-92122119 | Common:5; Rare:156 |