| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99606475-99606694 | Common:6; Rare:62 | ||||
| chr13:100088859-100089134 | Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674754-100675060 | Common:3; Rare:124 | ||||
| chr13:102596782-102597039 | Common:1; Rare:119 | ||||
| chr13:102773766-102773860 | Rare:37 | ||||
| chr13:102798910-102799163 | Common:1; Rare:55 | ||||
| chr13:102845728-102846179 | Common:8; Rare:113; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567923-106568268 | Rare:94 | ||||
| chr13:108215483-108215729 | Common:1; Rare:65 | ||||
| chr13:108218253-108218654 | Common:2; Rare:140 | ||||
| chr13:110307155-110307472 | Common:5; Rare:98; Clinvar (benign):5 | ||||
| chr13:110561615-110561895 | Common:5; Rare:95 | ||||
| chr13:110615385-110615666 | Common:2; Rare:95 | ||||
| chr13:110712442-110712523 | Rare:28 | ||||
| chr13:110713029-110713266 | Common:2; Rare:102 |