Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24971578-24971830 | Common:2; Rare:86 | ||||
chr2:24971902-24972159 | Common:1; Rare:82 | ||||
chr2:25041925-25042295 | Common:4; Rare:97 | ||||
chr2:25342443-25342655 | Common:1; Rare:47 | ||||
chr2:25878263-25878398 | Rare:30 | ||||
chr2:26033702-26033953 | Common:3; Rare:95 | ||||
chr2:26034017-26034732 | Common:4; Rare:197 | ||||
chr2:26244227-26244418 | Rare:39 | ||||
chr2:26244536-26245016 | Common:2; Rare:170; Clinvar:7; Clinvar (benign):9 | ||||
chr2:26345789-26346208 | Common:1; Rare:125 | ||||
chr2:26764183-26764421 | Common:3; Rare:80 | ||||
chr2:27032862-27033011 | Rare:58 | ||||
chr2:27051546-27051734 | Rare:59 | ||||
chr2:27071348-27071882 | Common:2; Rare:170 | ||||
chr2:27086537-27086788 | Common:2; Rare:74 |