| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99307397-99307537 | Common:1; Rare:17 | ||||
| chr13:99606467-99606727 | Common:6; Rare:87 | ||||
| chr13:100088853-100089167 | Rare:122; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100588759-100588885 | Common:2; Rare:33 | ||||
| chr13:100674778-100675060 | Common:3; Rare:115 | ||||
| chr13:102596773-102597156 | Common:1; Rare:153; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102656706-102657018 | Common:2; Rare:54 | ||||
| chr13:102773630-102773896 | Common:1; Rare:98 | ||||
| chr13:102798991-102799124 | Rare:30 | ||||
| chr13:102845734-102846179 | Common:8; Rare:109; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567583-106567917 | Rare:101 | ||||
| chr13:106567919-106568267 | Rare:94 | ||||
| chr13:107866893-107867055 | Common:1; Rare:44 | ||||
| chr13:108215495-108215613 | Common:1; Rare:33 | ||||
| chr13:108218307-108218532 | Rare:85 |