Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:631617-631827 | Common:2; Rare:36 | ||||
chr1:633776-634040 | Common:5; Rare:99 | ||||
chr1:634056-634125 | Rare:27 | ||||
chr1:778598-778819 | Common:4; Rare:94 | ||||
chr1:827482-827853 | Common:2; Rare:123 | ||||
chr1:846987-847272 | Common:3; Rare:41 | ||||
chr1:2229563-2229648 | Rare:30; Clinvar (benign):3 | ||||
chr1:2240390-2240586 | Common:2; Rare:40 | ||||
chr1:2585486-2585634 | Common:1; Rare:34 | ||||
chr1:3063759-3063776 | Rare:5 | ||||
chr1:5891961-5892094 | Rare:34 | ||||
chr1:8096580-8096900 | Rare:41 | ||||
chr1:8232519-8232575 | Rare:14 | ||||
chr1:8422791-8422830 | Rare:10 | ||||
chr1:8899995-8900178 | Common:3; Rare:41 |