Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:122781589-122781926 | Common:3; Rare:65 | ||||
chr8:123396365-123396555 | Common:2; Rare:86 | ||||
chr8:123416422-123416791 | Rare:99 | ||||
chr8:124474969-124475099 | Rare:44 | ||||
chr8:124538975-124539287 | Common:2; Rare:161; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr8:124998191-124998873 | Common:8; Rare:245 | ||||
chr8:125091626-125091934 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
chr8:126557641-126557914 | Rare:62 | ||||
chr8:126558248-126558628 | Common:2; Rare:127 | ||||
chr8:127735895-127736463 | Common:3; Rare:138 | ||||
chr8:133297150-133297544 | Common:3; Rare:153; Clinvar:4; Clinvar (benign):1 | ||||
chr8:133571810-133572185 | Rare:92 | ||||
chr8:134713020-134713149 | Common:1; Rare:44 | ||||
chr8:140511145-140511533 | Common:3; Rare:143 | ||||
chr8:141001136-141001475 | Common:3; Rare:118 |