| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20609764-20609887 | Rare:28 | ||||
| chr14:20684418-20684690 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20802795-20802965 | Common:1; Rare:23 | ||||
| chr14:20989147-20989310 | Rare:19 | ||||
| chr14:20989955-20990040 | Common:2; Rare:40 | ||||
| chr14:21024965-21025200 | Rare:86 | ||||
| chr14:21025698-21025915 | Common:2; Rare:38 | ||||
| chr14:21030118-21030294 | Common:4; Rare:32 | ||||
| chr14:21070852-21070888 | Rare:8 | ||||
| chr14:21103737-21104086 | Common:3; Rare:83 | ||||
| chr14:21231364-21231473 | Rare:20 | ||||
| chr14:21269488-21269796 | Common:2; Rare:95 | ||||
| chr14:21317488-21317795 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:21383864-21384103 | Common:6; Rare:82 | ||||
| chr14:21384214-21384484 | Rare:89 |