| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20460410-20460669 | Rare:62 | ||||
| chr14:20461739-20462052 | Common:2; Rare:76 | ||||
| chr14:20469247-20469533 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:20469564-20469707 | Rare:45 | ||||
| chr14:20470042-20470128 | Common:1; Rare:16 | ||||
| chr14:20609408-20609711 | Common:5; Rare:80 | ||||
| chr14:20609874-20610130 | Common:3; Rare:69 | ||||
| chr14:20683368-20683687 | Common:2; Rare:83 | ||||
| chr14:20683693-20684014 | Common:8; Rare:77 | ||||
| chr14:20684021-20684247 | Common:11; Rare:113; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20684423-20684465 | Common:1; Rare:7; Clinvar (benign):1 | ||||
| chr14:20780993-20781170 | Common:1; Rare:30 | ||||
| chr14:20989653-20990078 | Common:7; Rare:110 | ||||
| chr14:20990343-20990506 | Common:2; Rare:60 | ||||
| chr14:21070827-21071073 | Rare:52 |