Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:106657568-106657901 | Common:4; Rare:91 | ||||
chr8:108248614-108248873 | Rare:98 | ||||
chr8:108443463-108443654 | Common:3; Rare:80 | ||||
chr8:109334055-109334412 | Common:1; Rare:92 | ||||
chr8:109539635-109539882 | Rare:66 | ||||
chr8:117520540-117520778 | Common:5; Rare:60 | ||||
chr8:119416181-119416451 | Common:1; Rare:49 | ||||
chr8:119832821-119832916 | Common:1; Rare:34 | ||||
chr8:120125293-120125312 | Rare:4 | ||||
chr8:120445100-120445467 | Common:1; Rare:96 | ||||
chr8:121641391-121641450 | Rare:12 | ||||
chr8:122781582-122781655 | Rare:9 | ||||
chr8:123416425-123416769 | Rare:90 | ||||
chr8:124474949-124475099 | Rare:47 | ||||
chr8:124539040-124539204 | Common:2; Rare:90; Clinvar (benign):5; Clinvar (pathogenic):1 |