| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:51989277-51989671 | Common:6; Rare:287 | ||||
| chr14:52313900-52314410 | Common:9; Rare:334 | ||||
| chr14:52552369-52552935 | Common:5; Rare:450 | ||||
| chr14:52553881-52554088 | Common:1; Rare:38 | ||||
| chr14:52694900-52695299 | Common:2; Rare:114 | ||||
| chr14:52695475-52695865 | Common:2; Rare:212 | ||||
| chr14:52695866-52696093 | Common:2; Rare:92 | ||||
| chr14:52706793-52707286 | Common:5; Rare:338 | ||||
| chr14:52729804-52730412 | Common:6; Rare:316 | ||||
| chr14:52783072-52783218 | Rare:27 | ||||
| chr14:52791385-52791979 | Common:8; Rare:430 | ||||
| chr14:52950967-52951500 | Common:12; Rare:513 | ||||
| chr14:52951762-52952108 | Common:2; Rare:74 | ||||
| chr14:53152197-53152597 | Rare:311; Clinvar (benign):5 | ||||
| chr14:53153024-53153520 | Common:11; Rare:398; Clinvar:2; Clinvar (benign):2 |