Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206159436-206159681 | Rare:82 | ||||
chr2:206765297-206765609 | Common:1; Rare:75; Clinvar:3 | ||||
chr2:208255051-208255214 | Common:2; Rare:42 | ||||
chr2:216498721-216498886 | Common:6; Rare:67 | ||||
chr2:218270103-218270447 | Common:5; Rare:101; Clinvar (benign):1 | ||||
chr2:218671977-218672003 | Rare:12 | ||||
chr2:232550555-232550713 | Rare:58 | ||||
chr2:241102280-241102370 | Common:2; Rare:32 | ||||
chr2:241315156-241315387 | Common:4; Rare:76 | ||||
chr2:241315656-241315969 | Common:5; Rare:123 | ||||
chr2:241508575-241508864 | Common:1; Rare:88 | ||||
chr20:2664193-2664235 | Rare:22 | ||||
chr20:5950531-5950689 | Common:8; Rare:47 | ||||
chr20:13784894-13785043 | Common:2; Rare:59 | ||||
chr20:21303235-21303364 | Rare:47 |