Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:119454554-119454871 | Common:14; Rare:105 | ||||
chr4:131976173-131976262 | Common:3; Rare:34 | ||||
chr4:139177890-139178155 | Rare:83 | ||||
chr4:139763051-139763081 | Rare:1 | ||||
chr4:140256452-140256608 | Common:1; Rare:22 | ||||
chr4:141332590-141332755 | Rare:47 | ||||
chr4:147733837-147733907 | Rare:11 | ||||
chr4:153684164-153684338 | Rare:54 | ||||
chr4:158172085-158172191 | Common:1; Rare:23 | ||||
chr4:158174134-158174159 | Rare:4 | ||||
chr4:158811788-158812082 | Rare:43 | ||||
chr4:168923997-168924418 | Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
chr4:173416187-173416357 | Common:2; Rare:31 | ||||
chr4:173509545-173509671 | Rare:34 | ||||
chr4:180058677-180058941 | Common:1; Rare:89 |