Variant report

Variant	rs890548
Chromosome Location	chr9:92854205-92854206
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10992036	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1329045	0.82[ASN][1000 genomes]
rs2379208	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482303	chr9:92752928-92890226	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv614852	chr9:92786722-93100550	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv893563	chr9:92816727-92967125	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92839200-92855200	Weak transcription	Pancreas	Pancrea
2	chr9:92848400-92858000	Weak transcription	Right Atrium	heart
3	chr9:92848800-92855000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:92848800-92857800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:92848800-92862200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:92849000-92856000	Weak transcription	Fetal Brain Female	brain
7	chr9:92851400-92854400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:92851800-92855000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr9:92854200-92854800	Enhancers	Primary T cells from cord blood	blood
10	chr9:92854200-92856200	Enhancers	Fetal Thymus	thymus

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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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