| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35400091-35400351 | Common:1; Rare:55 | ||||
| chr14:35401369-35401769 | Common:2; Rare:160; Clinvar:4; Clinvar (benign):3 | ||||
| chr14:35405336-35405949 | Common:10; Rare:163 | ||||
| chr14:35416100-35416470 | Common:3; Rare:113 | ||||
| chr14:35416908-35417164 | Common:4; Rare:50 | ||||
| chr14:35932520-35933015 | Common:2; Rare:128 | ||||
| chr14:35932949-35933349 | Common:4; Rare:76 | ||||
| chr14:38989903-38990303 | Common:3; Rare:76 | ||||
| chr14:39174005-39174600 | Common:5; Rare:179 | ||||
| chr14:39175859-39176141 | Common:4; Rare:69 | ||||
| chr14:39430245-39430645 | Rare:147 | ||||
| chr14:39430820-39431040 | Common:2; Rare:66 | ||||
| chr14:39447856-39448178 | Common:5; Rare:48 | ||||
| chr14:40119741-40120141 | Common:1; Rare:127 | ||||
| chr14:41606220-41606750 | Common:4; Rare:96 |