Variant report

Variant	rs9755504
Chromosome Location	chr3:143344794-143344795
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11922426	1.00[AMR][1000 genomes]
rs34029020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59016370	1.00[AMR][1000 genomes]
rs72999725	1.00[AMR][1000 genomes]
rs72999726	1.00[AMR][1000 genomes]
rs72999743	1.00[AMR][1000 genomes]
rs72999747	1.00[AMR][1000 genomes]
rs7614358	0.81[AFR][1000 genomes]
rs7626666	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9755486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv829745	chr3:143278512-143405626	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:143324400-143353800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:143328200-143376200	Weak transcription	Ovary	ovary
3	chr3:143328400-143346000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:143337400-143354200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr3:143338400-143346000	Weak transcription	Primary T cells from cord blood	blood
6	chr3:143339200-143355200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr3:143339400-143346200	Weak transcription	H1 Derived Mesenchymal Stem 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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