| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77457542-77457885 | Common:2; Rare:100 | ||||
| chr14:77457977-77458263 | Rare:70 | ||||
| chr14:77616767-77617120 | Common:1; Rare:83 | ||||
| chr14:77707979-77708211 | Common:2; Rare:119 | ||||
| chr14:77800026-77800153 | Rare:22 | ||||
| chr14:79279134-79279411 | Common:3; Rare:63 | ||||
| chr14:80941682-80941940 | Common:3; Rare:58 | ||||
| chr14:81220726-81221170 | Common:3; Rare:180 | ||||
| chr14:81221238-81221488 | Common:1; Rare:64 | ||||
| chr14:81533747-81534196 | Common:1; Rare:127 | ||||
| chr14:85530024-85530190 | Common:1; Rare:36 | ||||
| chr14:87988585-87988671 | Common:2; Rare:19 | ||||
| chr14:87988682-87988796 | Common:1; Rare:25 | ||||
| chr14:87989930-87990161 | Common:3; Rare:37 | ||||
| chr14:87992746-87993491 | Common:8; Rare:292; Clinvar:19; Clinvar (benign):10; Clinvar (pathogenic):9 |