Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100987921-100987991 | Rare:17; Clinvar (benign):1 | ||||
chr10:100996953-100997312 | Common:2; Rare:93 | ||||
chr10:100997443-100997949 | Common:3; Rare:100 | ||||
chr10:100998083-100998344 | Common:1; Rare:66 | ||||
chr10:100999167-100999446 | Common:3; Rare:51 | ||||
chr10:100999545-100999882 | Common:1; Rare:96 | ||||
chr10:101031072-101031336 | Common:1; Rare:58 | ||||
chr10:101060964-101061362 | Common:2; Rare:106 | ||||
chr10:101061375-101061496 | Rare:22 | ||||
chr10:101061589-101061771 | Rare:32 | ||||
chr10:101062640-101062766 | Common:1; Rare:45 | ||||
chr10:101066182-101066292 | Rare:25 | ||||
chr10:101066589-101066733 | Common:1; Rare:29 | ||||
chr10:101353735-101354261 | Common:1; Rare:156 | ||||
chr10:101354314-101354434 | Common:1; Rare:25 |