Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206086281-206086328 | Rare:10 | ||||
chr2:206159345-206160058 | Common:4; Rare:214; Clinvar (benign):1 | ||||
chr2:206765276-206765661 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207529817-207530116 | Common:1; Rare:82 | ||||
chr2:208255024-208255238 | Common:2; Rare:57 | ||||
chr2:208266032-208266302 | Common:9; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210314911-210315272 | Common:7; Rare:103 | ||||
chr2:215311879-215312139 | Common:8; Rare:100 | ||||
chr2:215436013-215436253 | Common:2; Rare:74 | ||||
chr2:216081792-216081882 | Rare:22 | ||||
chr2:216498754-216499051 | Common:10; Rare:115 | ||||
chr2:217905385-217905604 | Rare:40 | ||||
chr2:218217049-218217246 | Common:1; Rare:70 | ||||
chr2:218270061-218270587 | Common:5; Rare:167; Clinvar:5; Clinvar (benign):2 | ||||
chr2:218382066-218382308 | Rare:48 |