Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:215311778-215312122 | Common:7; Rare:116 | ||||
chr2:216081777-216081904 | Common:1; Rare:41 | ||||
chr2:216412667-216412791 | Rare:15 | ||||
chr2:216498689-216498886 | Common:6; Rare:80 | ||||
chr2:218217058-218217249 | Common:1; Rare:69 | ||||
chr2:218270062-218270538 | Common:5; Rare:149; Clinvar:3; Clinvar (benign):1 | ||||
chr2:218292475-218292646 | Common:1; Rare:50 | ||||
chr2:218568290-218568598 | Common:2; Rare:84 | ||||
chr2:218568691-218568913 | Common:1; Rare:53 | ||||
chr2:218659312-218659738 | Common:4; Rare:99 | ||||
chr2:218671973-218672329 | Common:2; Rare:88 | ||||
chr2:219176897-219177109 | Common:4; Rare:64 | ||||
chr2:219206688-219206827 | Rare:57 | ||||
chr2:219229330-219229422 | Rare:29 | ||||
chr2:219229577-219229920 | Common:2; Rare:102 |