Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:30757659-30757913 | Common:2; Rare:64 | ||||
chr1:31296738-31297139 | Common:5; Rare:121 | ||||
chr1:31576396-31576595 | Common:1; Rare:72 | ||||
chr1:31703917-31704062 | Common:1; Rare:37 | ||||
chr1:31937738-31937975 | Common:1; Rare:61 | ||||
chr1:31938308-31938591 | Rare:87 | ||||
chr1:32013684-32013881 | Rare:88 | ||||
chr1:32014141-32014373 | Rare:67 | ||||
chr1:32072793-32073001 | Rare:59 | ||||
chr1:32200532-32200688 | Rare:34 | ||||
chr1:32222294-32222628 | Rare:135 | ||||
chr1:32291919-32292171 | Common:1; Rare:85 | ||||
chr1:32394418-32394672 | Common:1; Rare:69 | ||||
chr1:32650925-32651318 | Common:2; Rare:149 | ||||
chr1:32817248-32817689 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):2 |