| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103529057-103529243 | Common:1; Rare:55 | ||||
| chr14:103562282-103562394 | Rare:40 | ||||
| chr14:103562620-103563066 | Common:8; Rare:178; Clinvar (benign):5 | ||||
| chr14:103715466-103715853 | Common:1; Rare:126 | ||||
| chr14:103921473-103921716 | Common:3; Rare:78 | ||||
| chr14:104752874-104753212 | Common:3; Rare:117 | ||||
| chr14:104985628-104985810 | Common:3; Rare:71 | ||||
| chr14:105021018-105021440 | Common:1; Rare:155 | ||||
| chr14:105419723-105420044 | Rare:102 | ||||
| chr15:22786492-22786809 | Rare:112; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:22838356-22838744 | Common:3; Rare:137 | ||||
| chr15:23039529-23039716 | Common:1; Rare:80 | ||||
| chr15:23647847-23647995 | Common:1; Rare:39 | ||||
| chr15:24954881-24955051 | Rare:83 | ||||
| chr15:25438982-25439219 | Common:2; Rare:91 |