Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102798970-102799124 | Rare:33 | ||||
chr13:102845731-102846154 | Common:8; Rare:108; Clinvar:4; Clinvar (benign):4 | ||||
chr13:106567583-106567917 | Rare:101 | ||||
chr13:106567919-106568278 | Rare:97 | ||||
chr13:108218313-108218525 | Rare:80 | ||||
chr13:110306996-110307526 | Common:7; Rare:162; Clinvar:3; Clinvar (benign):10 | ||||
chr13:110561647-110561920 | Common:5; Rare:93 | ||||
chr13:110713008-110713266 | Common:2; Rare:114 | ||||
chr13:110715812-110715889 | Rare:57 | ||||
chr13:110914416-110914629 | Common:3; Rare:85 | ||||
chr13:111153599-111153726 | Common:2; Rare:59 | ||||
chr13:112689777-112690001 | Common:5; Rare:73 | ||||
chr13:112968287-112968494 | Rare:54 | ||||
chr13:112969076-112969370 | Common:2; Rare:77 | ||||
chr13:112985135-112985446 | Common:5; Rare:78 |