Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156060964-156061232 | Common:1; Rare:67 | ||||
chr1:156134801-156135312 | Common:3; Rare:122; Clinvar:22; Clinvar (benign):17; Clinvar (pathogenic):12 | ||||
chr1:156149678-156149685 | Rare:1 | ||||
chr1:156193817-156194126 | Common:3; Rare:77 | ||||
chr1:156212893-156213063 | Common:1; Rare:50 | ||||
chr1:156282790-156283027 | Common:2; Rare:56 | ||||
chr1:156338151-156338570 | Common:2; Rare:152 | ||||
chr1:156500564-156501134 | Common:3; Rare:194 | ||||
chr1:156591589-156591849 | Common:5; Rare:114 | ||||
chr1:156601410-156601516 | Common:1; Rare:42 | ||||
chr1:156728396-156728489 | Common:1; Rare:20 | ||||
chr1:156728746-156728881 | Rare:32 | ||||
chr1:156751837-156751963 | Rare:34 | ||||
chr1:156752376-156752452 | Rare:21 | ||||
chr1:156766880-156766911 | Rare:6 |