Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119113929-119114171 | Common:1; Rare:36 | ||||
chr10:119164875-119165115 | Rare:40 | ||||
chr10:119165214-119165320 | Rare:23 | ||||
chr10:119165323-119165513 | Common:2; Rare:44 | ||||
chr10:119165542-119165874 | Common:2; Rare:128; Clinvar:1; Clinvar (benign):5 | ||||
chr10:119165975-119166078 | Rare:18 | ||||
chr10:119178429-119178675 | Common:2; Rare:64 | ||||
chr10:119178721-119179083 | Common:3; Rare:117 | ||||
chr10:119207127-119207203 | Rare:12 | ||||
chr10:119207270-119207619 | Common:2; Rare:117 | ||||
chr10:119542606-119543017 | Common:6; Rare:111 | ||||
chr10:119543026-119543679 | Common:3; Rare:139 | ||||
chr10:119595830-119596178 | Rare:84 | ||||
chr10:119596411-119596496 | Rare:28 | ||||
chr10:119596599-119596801 | Common:1; Rare:51 |