Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140647585-140647889 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691309-140691633 | Common:1; Rare:113; Clinvar:8; Clinvar (benign):1 | ||||
chr5:141320742-141320912 | Common:1; Rare:58 | ||||
chr5:141636808-141637004 | Common:2; Rare:86 | ||||
chr5:142325019-142325215 | Rare:61 | ||||
chr5:144170557-144170832 | Common:2; Rare:91 | ||||
chr5:146182506-146182866 | Common:4; Rare:104 | ||||
chr5:148383854-148384018 | Rare:49 | ||||
chr5:149345339-149345540 | Common:1; Rare:68 | ||||
chr5:149551364-149551625 | Rare:61 | ||||
chr5:149944758-149944884 | Common:1; Rare:20; Clinvar:1 | ||||
chr5:149960575-149960929 | Rare:118; Clinvar:7 | ||||
chr5:150904781-150904819 | Rare:6 | ||||
chr5:151080935-151081210 | Common:2; Rare:94 | ||||
chr5:151157715-151157877 | Common:1; Rare:40 |