Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100346939-100347389 | Common:1; Rare:102 | ||||
chr10:100912759-100913074 | Common:1; Rare:92 | ||||
chr10:100913328-100913461 | Rare:33 | ||||
chr10:100987268-100987599 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996990-100997138 | Rare:42 | ||||
chr10:101031098-101031517 | Common:1; Rare:96 | ||||
chr10:101061842-101062012 | Rare:29 | ||||
chr10:101131030-101131104 | Common:1; Rare:15 | ||||
chr10:101131113-101131477 | Common:1; Rare:87 | ||||
chr10:101588140-101588329 | Rare:78 | ||||
chr10:101695093-101695362 | Common:1; Rare:65 | ||||
chr10:101817567-101817642 | Rare:21 | ||||
chr10:101817879-101817912 | Common:1; Rare:14 | ||||
chr10:101818095-101818778 | Common:1; Rare:198 | ||||
chr10:102056089-102056382 | Common:1; Rare:72 |