Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40979583-40979739 | Common:2; Rare:58 | ||||
chr1:42335134-42335405 | Common:6; Rare:131 | ||||
chr1:42456010-42456108 | Rare:32 | ||||
chr1:42456248-42456583 | Common:1; Rare:101 | ||||
chr1:42658087-42658391 | Common:3; Rare:68 | ||||
chr1:42658396-42658501 | Rare:36 | ||||
chr1:42682170-42682470 | Common:2; Rare:79 | ||||
chr1:42683066-42683243 | Rare:94 | ||||
chr1:42683325-42683465 | Common:2; Rare:53 | ||||
chr1:42766976-42767312 | Common:4; Rare:115; Clinvar (benign):1 | ||||
chr1:42816986-42817141 | Common:1; Rare:42 | ||||
chr1:42817198-42817539 | Rare:114 | ||||
chr1:42846391-42846644 | Common:1; Rare:72 | ||||
chr1:42958823-42959078 | Common:4; Rare:71; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43358818-43359006 | Rare:46 |