Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 | ||||
chr2:19990079-19990180 | Rare:22 | ||||
chr2:20446851-20447074 | Common:3; Rare:89 | ||||
chr2:20823043-20823206 | Common:1; Rare:57 | ||||
chr2:23940388-23940518 | Common:3; Rare:49 | ||||
chr2:24049634-24049757 | Rare:32 | ||||
chr2:24076231-24076597 | Rare:101 | ||||
chr2:24123272-24123510 | Common:1; Rare:63 | ||||
chr2:26033792-26034159 | Common:3; Rare:131 | ||||
chr2:26244573-26244965 | Common:2; Rare:144; Clinvar:6; Clinvar (benign):9 | ||||
chr2:26345812-26346171 | Common:1; Rare:108 | ||||
chr2:26764183-26764325 | Common:1; Rare:56 | ||||
chr2:27032867-27033004 | Rare:51 | ||||
chr2:27071505-27071882 | Common:1; Rare:112 | ||||
chr2:27211920-27212049 | Common:3; Rare:52 |