| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20454793-20455320 | Common:7; Rare:138 | ||||
| chr14:20684048-20684318 | Common:12; Rare:107; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:20684420-20684750 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:21024997-21025228 | Rare:84 | ||||
| chr14:21100985-21101164 | Rare:23 | ||||
| chr14:21476565-21476750 | Rare:80 | ||||
| chr14:21476857-21477261 | Common:2; Rare:130 | ||||
| chr14:21511273-21511556 | Rare:72 | ||||
| chr14:22766578-22766723 | Common:1; Rare:81 | ||||
| chr14:22775832-22776076 | Common:2; Rare:64; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:22829741-22829915 | Rare:52 | ||||
| chr14:22836218-22836761 | Common:6; Rare:124 | ||||
| chr14:22871651-22872271 | Common:2; Rare:155 | ||||
| chr14:22929363-22929643 | Common:1; Rare:76 | ||||
| chr14:22982614-22982916 | Common:2; Rare:100 |