Variant report

Variant	rs73711568
Chromosome Location	chr8:130520491-130520492
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130519200-130522400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:130519400-130522200	Enhancers	NHEK	skin
3	chr8:130519400-130524000	Strong transcription	K562	blood
4	chr8:130519600-130520600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:130519600-130521400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr8:130519600-130521400	Enhancers	HSMM	muscle
7	chr8:130519600-130522200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:130519600-130523000	Enhancers	HMEC	breast
9	chr8:130519600-130524400	Weak transcription	Dnd41	blood
10	chr8:130519800-130521000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:130519800-130521400	Enhancers	Osteobl	bone
12	chr8:130520000-130521200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:130520200-130521400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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