Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102930786-102930928 | Common:1; Rare:46 | ||||
chr14:103663636-103663656 | Rare:1 | ||||
chr14:103694186-103694494 | Common:2; Rare:59 | ||||
chr14:103897038-103897258 | Common:3; Rare:42 | ||||
chr14:104681152-104681445 | Common:1; Rare:64 | ||||
chr14:104688243-104688330 | Rare:28 | ||||
chr14:104703144-104703480 | Rare:112; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
chr14:104868410-104868432 | Rare:2 | ||||
chr14:105092516-105092811 | Common:2; Rare:54 | ||||
chr14:105093890-105093966 | Rare:15 | ||||
chr14:105093974-105094156 | Common:1; Rare:40 | ||||
chr14:105587271-105587594 | Common:4; Rare:85 | ||||
chr14:105587763-105587881 | Common:1; Rare:53 | ||||
chr14:105587950-105588086 | Rare:40 | ||||
chr14:105588109-105588150 | Common:1; Rare:12 |