Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:152189240-152189352 | Common:1; Rare:39 | ||||
chr1:153783730-153783859 | Common:3; Rare:40 | ||||
chr1:153881019-153881324 | Rare:74 | ||||
chr1:154329730-154329909 | Common:1; Rare:23 | ||||
chr1:155227531-155227732 | Common:1; Rare:55 | ||||
chr1:155976079-155976128 | Rare:7 | ||||
chr1:155976181-155976243 | Common:1; Rare:15 | ||||
chr1:155983382-155983496 | Rare:13 | ||||
chr1:156418561-156418639 | Common:1; Rare:14 | ||||
chr1:156427965-156428110 | Rare:20 | ||||
chr1:156435022-156435134 | Rare:16 | ||||
chr1:156456522-156456774 | Rare:57 | ||||
chr1:159188214-159188621 | Rare:86 | ||||
chr1:160130215-160130489 | Common:3; Rare:72; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr1:160317002-160317307 | Common:2; Rare:55 |