Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154974287-154974733 | Rare:113 | ||||
chr1:154974853-154975154 | Common:3; Rare:103 | ||||
chr1:154975507-154975579 | Rare:16 | ||||
chr1:154975584-154975927 | Common:1; Rare:74 | ||||
chr1:154983056-154983447 | Common:2; Rare:81; Clinvar (benign):2 | ||||
chr1:155002086-155002263 | Common:1; Rare:53 | ||||
chr1:155002951-155003220 | Common:2; Rare:50 | ||||
chr1:155050556-155050651 | Rare:25 | ||||
chr1:155051092-155051370 | Common:2; Rare:94 | ||||
chr1:155063601-155063829 | Rare:70 | ||||
chr1:155063951-155064005 | Rare:19 | ||||
chr1:155084929-155085034 | Common:2; Rare:31 | ||||
chr1:155085328-155085551 | Common:2; Rare:48 | ||||
chr1:155135623-155136030 | Common:4; Rare:161 | ||||
chr1:155136078-155136491 | Common:3; Rare:109 |