| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:106567841-106568265 | Rare:117 | ||||
| chr13:108218324-108218520 | Rare:77 | ||||
| chr13:110307155-110307526 | Common:5; Rare:107; Clinvar (benign):6 | ||||
| chr13:110561615-110561893 | Common:5; Rare:95 | ||||
| chr13:110615500-110615689 | Rare:68 | ||||
| chr13:110713018-110713266 | Common:2; Rare:108 | ||||
| chr13:110715576-110715889 | Common:1; Rare:167 | ||||
| chr13:113208630-113208723 | Rare:54 | ||||
| chr13:113490683-113491021 | Common:1; Rare:122 | ||||
| chr13:113759121-113759288 | Common:1; Rare:50 | ||||
| chr13:114281535-114281650 | Common:1; Rare:63 | ||||
| chr14:20343177-20343661 | Common:12; Rare:285 | ||||
| chr14:20455015-20455287 | Common:2; Rare:77 | ||||
| chr14:20456490-20456697 | Common:1; Rare:56; Clinvar:1 | ||||
| chr14:20684438-20684750 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):3 |