| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103715387-103715853 | Common:1; Rare:160 | ||||
| chr14:104689479-104689674 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr14:104752973-104753256 | Common:2; Rare:111 | ||||
| chr14:104970477-104970798 | Common:4; Rare:61 | ||||
| chr14:104985628-104985800 | Common:3; Rare:65 | ||||
| chr14:105021003-105021532 | Common:3; Rare:191 | ||||
| chr14:105398222-105398568 | Common:5; Rare:112 | ||||
| chr14:105419733-105420038 | Rare:97 | ||||
| chr14:105487038-105487251 | Common:1; Rare:68 | ||||
| chr14:105490098-105490212 | Common:2; Rare:43 | ||||
| chr15:22786484-22786752 | Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:22838356-22838926 | Common:4; Rare:185 | ||||
| chr15:23039524-23039746 | Common:1; Rare:95 | ||||
| chr15:24955289-24955419 | Rare:36 | ||||
| chr15:25438982-25439244 | Common:2; Rare:102 |