Variant report

Variant	rs1623926
Chromosome Location	chr9:8206145-8206146
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:8)

rs_ID	r²[population]
rs10976827	0.82[EUR][1000 genomes]
rs10976828	0.82[EUR][1000 genomes]
rs12003225	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4130580	0.81[EUR][1000 genomes]
rs7026216	0.87[AMR][1000 genomes]
rs7048886	0.81[EUR][1000 genomes]
rs7860307	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7867627	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1022320	chr9:8163549-8216832	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
3	nsv613284	chr9:8165192-8279622	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	inside rSNPs	diseases
4	nsv892222	chr9:8172046-8253019	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8205200-8206600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr9:8205200-8208200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:8205200-8210400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr9:8205600-8206400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr9:8205800-8206200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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