Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201071623-201072034 | Rare:87 | ||||
chr2:201116130-201116458 | Rare:60 | ||||
chr2:201780896-201781207 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202911915-202912250 | Common:2; Rare:87 | ||||
chr2:206159343-206159896 | Common:4; Rare:149; Clinvar (benign):1 | ||||
chr2:206444056-206444073 | Rare:6 | ||||
chr2:206765299-206765657 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165905-207166115 | Rare:41 | ||||
chr2:208255024-208255213 | Common:2; Rare:49 | ||||
chr2:215311937-215312164 | Common:7; Rare:98 | ||||
chr2:216498740-216498877 | Common:5; Rare:54 | ||||
chr2:218217227-218217390 | Common:1; Rare:43 | ||||
chr2:218270095-218270532 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
chr2:218659342-218659756 | Common:4; Rare:101 | ||||
chr2:218671936-218672339 | Common:2; Rare:115 |