Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21841582-21841829 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
chr1:21890426-21890678 | Common:1; Rare:72; Clinvar (benign):1 | ||||
chr1:21907973-21908275 | Common:1; Rare:62 | ||||
chr1:22025185-22025571 | Common:8; Rare:99 | ||||
chr1:22086300-22086536 | Rare:35 | ||||
chr1:22502089-22502324 | Rare:55 | ||||
chr1:22502768-22502997 | Common:2; Rare:39 | ||||
chr1:23126737-23127052 | Rare:58 | ||||
chr1:23167863-23168006 | Rare:41 | ||||
chr1:23281545-23281713 | Rare:39 | ||||
chr1:23313347-23313728 | Common:1; Rare:64 | ||||
chr1:23695764-23696163 | Common:1; Rare:86; Clinvar (benign):1 | ||||
chr1:24317140-24317297 | Common:1; Rare:31 | ||||
chr1:24318322-24318445 | Common:1; Rare:12 | ||||
chr1:24373775-24374048 | Common:1; Rare:60 |