Variant report

Variant	rs11932992
Chromosome Location	chr4:119798044-119798045
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10004721	1.00[AMR][1000 genomes]
rs11932966	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28718468	1.00[AMR][1000 genomes]
rs55907729	0.82[AFR][1000 genomes]
rs73844621	1.00[AMR][1000 genomes]
rs73844626	1.00[AMR][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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119791400-119803000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:119791400-119809800	Weak transcription	Left Ventricle	heart
3	chr4:119792200-119802600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr4:119797400-119798200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:119797800-119799200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:119798000-119798200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr4:119798000-119802600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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