Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:103298744-103298876 | Common:1; Rare:31 | ||||
chr8:103371401-103371636 | Common:1; Rare:73 | ||||
chr8:103415090-103415444 | Common:6; Rare:182 | ||||
chr8:108443487-108443669 | Common:2; Rare:84 | ||||
chr8:109334065-109334452 | Common:1; Rare:106 | ||||
chr8:116874613-116874929 | Common:6; Rare:134; Clinvar (benign):1 | ||||
chr8:116938418-116938472 | Common:1; Rare:17 | ||||
chr8:118951875-118952146 | Common:1; Rare:69; Clinvar:7; Clinvar (benign):1 | ||||
chr8:119832826-119832900 | Common:1; Rare:27 | ||||
chr8:120445102-120445451 | Common:1; Rare:85 | ||||
chr8:123396408-123396504 | Rare:40 | ||||
chr8:124539044-124539282 | Common:2; Rare:115; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr8:125091755-125091915 | Common:1; Rare:51 | ||||
chr8:127735890-127736076 | Rare:41 | ||||
chr8:133571863-133572166 | Rare:75 |