| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20413167-20413233 | Common:1; Rare:10 | ||||
| chr14:20413413-20413562 | Common:3; Rare:46 | ||||
| chr14:20454715-20455372 | Common:7; Rare:173 | ||||
| chr14:20456403-20456728 | Common:1; Rare:86; Clinvar:1 | ||||
| chr14:20683890-20684244 | Common:19; Rare:162; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20684381-20684756 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:20780691-20780993 | Common:4; Rare:36 | ||||
| chr14:20802779-20802970 | Common:1; Rare:26 | ||||
| chr14:21024281-21024307 | Rare:4 | ||||
| chr14:21024733-21024793 | Rare:20 | ||||
| chr14:21024904-21025191 | Common:1; Rare:99 | ||||
| chr14:21025675-21026061 | Common:2; Rare:67 | ||||
| chr14:21070845-21071027 | Rare:37 | ||||
| chr14:21098330-21098542 | Common:1; Rare:54 | ||||
| chr14:21383864-21384057 | Common:1; Rare:67 |