| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99312585-99312818 | Rare:32 | ||||
| chr13:100088890-100089127 | Rare:85; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674774-100675060 | Common:3; Rare:117 | ||||
| chr13:102596794-102597045 | Common:1; Rare:119; Clinvar (benign):1 | ||||
| chr13:102773740-102773822 | Rare:40 | ||||
| chr13:102798962-102799180 | Rare:44 | ||||
| chr13:102845605-102846190 | Common:9; Rare:149; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567709-106568280 | Rare:154 | ||||
| chr13:108215495-108215666 | Common:1; Rare:50 | ||||
| chr13:108218256-108218608 | Common:2; Rare:126 | ||||
| chr13:110305501-110305750 | Common:1; Rare:37 | ||||
| chr13:110306975-110307526 | Common:7; Rare:171; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110307615-110307893 | Common:3; Rare:79 | ||||
| chr13:110561615-110561967 | Common:6; Rare:114 | ||||
| chr13:110615478-110615671 | Rare:70 |