Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:3652304-3652574 | Rare:69 | ||||
chr1:3900174-3900361 | Common:11; Rare:99 | ||||
chr1:6199487-6199689 | Common:1; Rare:84 | ||||
chr1:6199753-6199837 | Common:1; Rare:18 | ||||
chr1:6579781-6580038 | Common:4; Rare:82 | ||||
chr1:6602867-6603048 | Common:2; Rare:68 | ||||
chr1:6701769-6701998 | Rare:68 | ||||
chr1:7771172-7771363 | Common:3; Rare:86 | ||||
chr1:7961377-7961823 | Common:4; Rare:155; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8026300-8026503 | Common:2; Rare:89 | ||||
chr1:8318037-8318123 | Rare:29 | ||||
chr1:8878578-8878847 | Rare:138 | ||||
chr1:9943251-9943488 | Common:3; Rare:61 | ||||
chr1:10398888-10399120 | Common:2; Rare:95 | ||||
chr1:10430270-10430502 | Common:6; Rare:68 |