Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2213150-2213352 | Common:2; Rare:70 | ||||
chr1:2229181-2229313 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):5 | ||||
chr1:2391482-2391933 | Common:2; Rare:159 | ||||
chr1:2392343-2392401 | Rare:18 | ||||
chr1:2412330-2412336 | Rare:3 | ||||
chr1:2412341-2412376 | Rare:8 | ||||
chr1:2412395-2412858 | Common:2; Rare:181; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:2412973-2413101 | Rare:28 | ||||
chr1:2413292-2413338 | Rare:13 | ||||
chr1:2413424-2413537 | Common:1; Rare:21 | ||||
chr1:2526163-2526390 | Common:1; Rare:59 | ||||
chr1:2526543-2526753 | Common:4; Rare:84 | ||||
chr1:2526921-2527059 | Rare:32 | ||||
chr1:2556350-2556436 | Rare:34 | ||||
chr1:2586307-2586897 | Common:4; Rare:163 |