Variant report

Variant	rs62355923
Chromosome Location	chr5:107119641-107119642
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs62355930	1.00[EUR][1000 genomes]

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	nsv830440	chr5:107074116-107278905	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107114600-107119800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr5:107116800-107124400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:107117800-107120000	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr5:107117800-107120000	Enhancers	Fetal Lung	lung
5	chr5:107119200-107119800	Enhancers	A549	lung
6	chr5:107119600-107121600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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

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