| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77457997-77458208 | Rare:55 | ||||
| chr14:77707970-77708207 | Common:2; Rare:121 | ||||
| chr14:77761129-77761380 | Common:2; Rare:78 | ||||
| chr14:81220828-81221069 | Common:1; Rare:116 | ||||
| chr14:85530024-85530239 | Common:1; Rare:44 | ||||
| chr14:88562674-88563085 | Rare:145 | ||||
| chr14:89619097-89619260 | Common:1; Rare:58 | ||||
| chr14:89954690-89954937 | Rare:68 | ||||
| chr14:89955801-89955964 | Common:9; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90396991-90397232 | Common:5; Rare:119; Clinvar (benign):2 | ||||
| chr14:91114279-91114402 | Rare:22 | ||||
| chr14:91114583-91114699 | Common:1; Rare:12 | ||||
| chr14:91244664-91244763 | Common:2; Rare:18 | ||||
| chr14:91510242-91510606 | Common:1; Rare:115 | ||||
| chr14:92040019-92040165 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 |