Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206765294-206765674 | Common:3; Rare:100; Clinvar:5; Clinvar (benign):5 | ||||
chr2:207165912-207166088 | Rare:36 | ||||
chr2:208255032-208255239 | Common:2; Rare:54 | ||||
chr2:208266049-208266291 | Common:8; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477538-210477691 | Rare:46 | ||||
chr2:215435632-215435779 | Common:2; Rare:39 | ||||
chr2:215435841-215435933 | Rare:14 | ||||
chr2:215435940-215436307 | Common:2; Rare:115 | ||||
chr2:216081753-216081925 | Common:1; Rare:62 | ||||
chr2:216498689-216498886 | Common:6; Rare:80 | ||||
chr2:218217044-218217369 | Common:2; Rare:102 | ||||
chr2:218270104-218270385 | Common:5; Rare:87 | ||||
chr2:218659334-218659798 | Common:4; Rare:119 | ||||
chr2:218671935-218672329 | Common:2; Rare:114 | ||||
chr2:218710707-218710999 | Common:2; Rare:69 |