Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102773740-102773847 | Rare:52 | ||||
chr13:102798950-102799207 | Common:1; Rare:54 | ||||
chr13:102845639-102845926 | Common:6; Rare:81; Clinvar (benign):3 | ||||
chr13:106567587-106567699 | Rare:45 | ||||
chr13:106567703-106568258 | Rare:149 | ||||
chr13:108218278-108218532 | Common:1; Rare:92 | ||||
chr13:110307015-110307526 | Common:6; Rare:158; Clinvar:3; Clinvar (benign):9 | ||||
chr13:110477891-110478164 | Rare:67; Clinvar:4; Clinvar (benign):1 | ||||
chr13:110561647-110561889 | Common:5; Rare:83 | ||||
chr13:110712442-110712587 | Rare:62 | ||||
chr13:110712995-110713266 | Common:2; Rare:120 | ||||
chr13:110713487-110713626 | Common:2; Rare:57 | ||||
chr13:110914559-110914796 | Common:2; Rare:86 | ||||
chr13:111153614-111153720 | Common:2; Rare:46 | ||||
chr13:113208625-113208775 | Rare:86 |