| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91244642-91244822 | Common:2; Rare:34 | ||||
| chr14:91283461-91283615 | Rare:37 | ||||
| chr14:91510151-91510631 | Common:1; Rare:161 | ||||
| chr14:91836377-91836667 | Common:13; Rare:50 | ||||
| chr14:91946976-91947136 | Common:1; Rare:23 | ||||
| chr14:92039549-92039593 | Common:2; Rare:14; Clinvar (benign):2 | ||||
| chr14:92039623-92039692 | Rare:18 | ||||
| chr14:92039756-92040193 | Common:3; Rare:109; Clinvar:7; Clinvar (benign):2 | ||||
| chr14:92121656-92122005 | Common:5; Rare:120 | ||||
| chr14:92793998-92794446 | Rare:141 | ||||
| chr14:92922507-92922733 | Common:3; Rare:39 | ||||
| chr14:92923101-92923405 | Rare:79 | ||||
| chr14:92926379-92926703 | Common:1; Rare:72 | ||||
| chr14:92931151-92931183 | Common:1; Rare:7 | ||||
| chr14:92932039-92932279 | Common:2; Rare:51 |