Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:18956624-18956979 | Common:3; Rare:96 | ||||
chr1:19110225-19110625 | Common:1; Rare:120 | ||||
chr1:19210246-19210562 | Common:1; Rare:99 | ||||
chr1:19251460-19251842 | Common:6; Rare:131 | ||||
chr1:19312055-19312362 | Common:8; Rare:145 | ||||
chr1:19484419-19484851 | Rare:187 | ||||
chr1:19485500-19485833 | Rare:128 | ||||
chr1:19596858-19597079 | Common:2; Rare:102 | ||||
chr1:19882173-19882451 | Common:3; Rare:77 | ||||
chr1:20485062-20485892 | Rare:205 | ||||
chr1:20486670-20486880 | Common:1; Rare:56 | ||||
chr1:20508092-20508298 | Common:5; Rare:63 | ||||
chr1:20633323-20633506 | Rare:48 | ||||
chr1:20661355-20661740 | Common:3; Rare:139; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20717670-20718140 | Common:2; Rare:167 |