| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109409843-109410285 | Common:4; Rare:167 | ||||
| chr5:109689246-109689448 | Common:4; Rare:97 | ||||
| chr5:109689804-109690187 | Common:3; Rare:123 | ||||
| chr5:110738895-110739270 | Common:3; Rare:145; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:110739331-110739348 | Rare:6 | ||||
| chr5:111092238-111092426 | Common:2; Rare:100; Clinvar (benign):4 | ||||
| chr5:111224148-111224475 | Rare:128 | ||||
| chr5:111512472-111512780 | Common:3; Rare:119 | ||||
| chr5:111757577-111757825 | Common:1; Rare:106 | ||||
| chr5:111757946-111757994 | Rare:12 | ||||
| chr5:112419180-112419293 | Common:1; Rare:52 | ||||
| chr5:112707772-112707799 | Rare:10; Clinvar:4; Clinvar (benign):1 | ||||
| chr5:112861161-112861378 | Common:4; Rare:84 | ||||
| chr5:112922093-112922563 | Common:2; Rare:167 | ||||
| chr5:112976518-112976851 | Common:2; Rare:151 |