Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:202912474-202912571 | Common:2; Rare:32 | ||||
chr2:203014412-203014933 | Common:1; Rare:155 | ||||
chr2:203238785-203239050 | Common:1; Rare:97 | ||||
chr2:203239220-203239304 | Rare:28 | ||||
chr2:205682353-205682603 | Rare:44 | ||||
chr2:206085944-206085979 | Rare:5 | ||||
chr2:206086078-206086209 | Rare:17 | ||||
chr2:206086252-206086303 | Rare:4 | ||||
chr2:206159362-206160058 | Common:4; Rare:211; Clinvar (benign):1 | ||||
chr2:206274548-206274844 | Common:1; Rare:91 | ||||
chr2:206274931-206275067 | Common:1; Rare:48 | ||||
chr2:206765260-206765625 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
chr2:207165937-207166094 | Rare:27 | ||||
chr2:207529571-207530126 | Common:3; Rare:143 | ||||
chr2:207625204-207625417 | Common:1; Rare:63 |