Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151047689-151047778 | Common:1; Rare:24 | ||||
chr1:151060210-151060515 | Common:1; Rare:55 | ||||
chr1:151070314-151070598 | Common:3; Rare:82 | ||||
chr1:151165813-151166166 | Common:3; Rare:102 | ||||
chr1:151198422-151198622 | Common:2; Rare:75 | ||||
chr1:151254627-151254803 | Rare:46 | ||||
chr1:151281970-151282318 | Rare:96 | ||||
chr1:151327655-151327788 | Rare:27 | ||||
chr1:151346843-151347037 | Rare:55 | ||||
chr1:151372695-151372894 | Common:2; Rare:35 | ||||
chr1:151399480-151399585 | Common:1; Rare:33; Clinvar (pathogenic):1 | ||||
chr1:151511125-151511436 | Common:4; Rare:68 | ||||
chr1:151716784-151717127 | Common:1; Rare:96 | ||||
chr1:151721227-151721534 | Common:2; Rare:75 | ||||
chr1:151763462-151763528 | Common:1; Rare:21 |