| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562615-103563313 | Common:11; Rare:284; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103629117-103629470 | Common:4; Rare:139 | ||||
| chr14:103715442-103715853 | Common:1; Rare:138 | ||||
| chr14:104752921-104753218 | Common:3; Rare:112 | ||||
| chr14:104985651-104985803 | Common:3; Rare:54 | ||||
| chr14:105021044-105021402 | Common:1; Rare:127 | ||||
| chr14:105248421-105248623 | Common:6; Rare:99 | ||||
| chr14:105300989-105301121 | Rare:30 | ||||
| chr14:105301300-105301447 | Rare:37 | ||||
| chr14:105419662-105420054 | Common:1; Rare:111 | ||||
| chr15:22838450-22838750 | Common:3; Rare:115 | ||||
| chr15:23039534-23039758 | Common:1; Rare:90 | ||||
| chr15:23565423-23565693 | Common:1; Rare:76 | ||||
| chr15:23566242-23566368 | Rare:60; Clinvar (pathogenic):1 | ||||
| chr15:23647842-23648222 | Common:2; Rare:91 |