| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104688218-104688315 | Rare:27 | ||||
| chr14:104709184-104709377 | Rare:62; Clinvar:6; Clinvar (benign):5 | ||||
| chr14:104717980-104718319 | Common:2; Rare:69 | ||||
| chr14:105092578-105092767 | Common:2; Rare:27 | ||||
| chr14:105587271-105587881 | Common:6; Rare:207 | ||||
| chr14:105587984-105588408 | Common:3; Rare:147 | ||||
| chr14:105624539-105624692 | Common:6; Rare:71 | ||||
| chr14:105707232-105707565 | Common:2; Rare:138 | ||||
| chr14:105707783-105708148 | Common:4; Rare:144 | ||||
| chr14:105708254-105708322 | Common:1; Rare:17 | ||||
| chr14:105708357-105708678 | Common:4; Rare:129 | ||||
| chr14:105741654-105741921 | Common:5; Rare:116 | ||||
| chr14:105742331-105742571 | Common:2; Rare:97 | ||||
| chr14:105742778-105743105 | Common:7; Rare:116 | ||||
| chr14:105771395-105771514 | Common:2; Rare:32 |