Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:119128231-119128414 | Rare:30 | ||||
chr4:119168787-119168923 | Rare:19 | ||||
chr4:119454590-119454861 | Common:13; Rare:91 | ||||
chr4:140756866-140757002 | Rare:39 | ||||
chr4:143350212-143350462 | Common:2; Rare:47 | ||||
chr4:158706057-158706354 | Rare:85; Clinvar:2; Clinvar (pathogenic):4 | ||||
chr4:158841506-158841833 | Common:1; Rare:47 | ||||
chr4:168924941-168925277 | Common:5; Rare:93; Clinvar:3; Clinvar (benign):7 | ||||
chr4:173509545-173509689 | Common:1; Rare:36 | ||||
chr4:173518147-173518274 | Rare:37 | ||||
chr4:173698911-173699172 | Common:2; Rare:49 | ||||
chr4:184815076-184815253 | Common:2; Rare:41 | ||||
chr4:185642945-185643210 | Common:1; Rare:45 | ||||
chr4:185662053-185662291 | Common:1; Rare:89 | ||||
chr4:186015524-186015547 | Rare:10 |