| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:95676930-95677238 | Common:4; Rare:110 | ||||
| chr13:96053327-96053602 | Common:2; Rare:120 | ||||
| chr13:98142453-98142662 | Common:1; Rare:64 | ||||
| chr13:98977809-98978179 | Common:3; Rare:91 | ||||
| chr13:99200662-99200918 | Common:6; Rare:118 | ||||
| chr13:99307364-99307497 | Rare:16 | ||||
| chr13:99307502-99307592 | Common:2; Rare:14 | ||||
| chr13:99312582-99312854 | Rare:42 | ||||
| chr13:100088909-100089134 | Rare:85; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674774-100675060 | Common:3; Rare:117 | ||||
| chr13:102596760-102597047 | Common:1; Rare:130; Clinvar (benign):1 | ||||
| chr13:102773736-102773820 | Rare:39 | ||||
| chr13:102798998-102799130 | Rare:30 | ||||
| chr13:102845743-102846167 | Common:8; Rare:104; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:108218339-108218520 | Rare:71 |