Variant report

Variant	rs546771400
Chromosome Location	chr8:91517003-91517004
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2621133	chr8:91515761-91517085	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91516400-91517400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr8:91516400-91517800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:91516400-91517800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:91516400-91518000	Enhancers	NHEK	skin
5	chr8:91516400-91518600	Enhancers	NHDF-Ad	bronchial
6	chr8:91516600-91517600	Enhancers	HMEC	breast
7	chr8:91516600-91517800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:91516600-91517800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:91516800-91517600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:91516800-91517600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr8:91517000-91522400	Weak transcription	Placenta Amnion	Placenta Amnion

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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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