Variant report

Variant	rs534934479
Chromosome Location	chr6:75243817-75243818
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520746	chr6:75211546-75691814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917283	chr6:75234428-75641440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75243600-75244000	Enhancers	A549	lung
2	chr6:75243600-75244600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:75243600-75245800	Enhancers	Hela-S3	cervix
4	chr6:75243600-75246000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:75243600-75246200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:75243800-75244000	Flanking Active TSS	HepG2	liver
7	chr6:75243800-75244400	Enhancers	Stomach Mucosa	stomach
8	chr6:75243800-75244800	Enhancers	Small Intestine	intestine
9	chr6:75243800-75245000	Enhancers	Fetal Intestine Small	intestine
10	chr6:75243800-75245000	Enhancers	Fetal Kidney	kidney
11	chr6:75243800-75245000	Enhancers	NHLF	lung
12	chr6:75243800-75246000	Enhancers	Fetal Intestine Large	intestine

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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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