Variant report

Variant	rs11670158
Chromosome Location	chr19:44296294-44296295
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10404672	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10404692	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs10405457	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10421887	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10422990	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11665924	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11669175	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11671215	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12460161	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12463370	0.82[AMR][1000 genomes]
rs12974061	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3760982	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3760983	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3760984	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4802199	0.84[EUR][1000 genomes]
rs4802200	0.84[EUR][1000 genomes]
rs4803658	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs60184524	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61138927	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[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	nsv532821	chr19:43842383-44357315	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11670158	AC115522.3	cis	Skin Sun Exposed Lower leg	GTEx
rs11670158	KCNN4	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44289400-44302600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr19:44289800-44300800	Weak transcription	Placenta	Placenta
3	chr19:44290000-44302400	Weak transcription	NHEK	skin
4	chr19:44290200-44302200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr19:44295000-44297400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr19:44295000-44297400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:44295200-44297600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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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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