Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:74176825-74177225 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr10:74177126-74177360 | Common:2; Rare:73 | ||||
chr10:74825151-74826108 | Rare:359 | ||||
chr10:74826018-74826494 | Common:12; Rare:546 | ||||
chr10:74826513-74826695 | Rare:89; Clinvar (benign):2 | ||||
chr10:74826680-74827180 | Common:2; Rare:154; Clinvar:1 | ||||
chr10:75108259-75109048 | Common:1; Rare:288 | ||||
chr10:75109017-75109410 | Common:6; Rare:414 | ||||
chr10:75109568-75109968 | Common:1; Rare:50 | ||||
chr10:75111090-75111810 | Common:9; Rare:854 | ||||
chr10:75111858-75112258 | Rare:84 | ||||
chr10:75112172-75112572 | Common:1; Rare:110 | ||||
chr10:75209543-75210218 | Common:7; Rare:289 | ||||
chr10:75210162-75210886 | Common:11; Rare:964 | ||||
chr10:75210914-75211882 | Common:11; Rare:575 |