Variant report

Variant	rs10977873
Chromosome Location	chr9:9608981-9608982
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10491608	0.81[CHD][hapmap];0.88[GIH][hapmap];0.88[JPT][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs10759082	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10816148	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10977862	1.00[YRI][hapmap]
rs10977863	1.00[YRI][hapmap]
rs10977874	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.87[TSI][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10977875	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10977876	0.92[ASN][1000 genomes]
rs10977879	0.88[JPT][hapmap]
rs10977896	0.83[CHD][hapmap]
rs10977903	1.00[YRI][hapmap]
rs10977905	0.84[MKK][hapmap]
rs1409618	1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs16929917	1.00[CHB][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs16929919	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs17181634	1.00[YRI][hapmap]
rs17772815	1.00[YRI][hapmap]
rs17785914	1.00[YRI][hapmap]
rs1831032	0.90[ASN][1000 genomes]
rs1831033	1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs1926665	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs56272077	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs60214844	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs647190	1.00[YRI][hapmap]
rs656074	1.00[YRI][hapmap]
rs664921	1.00[YRI][hapmap]
rs680032	1.00[YRI][hapmap]
rs7029761	0.81[CHD][hapmap]
rs7044621	0.88[JPT][hapmap]
rs73641337	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs943298	0.81[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025791	chr9:9294304-9626331	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv613308	chr9:9409606-9750139	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1033808	chr9:9431799-9777960	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv892264	chr9:9440838-9796577	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv892265	chr9:9476425-9796116	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1023524	chr9:9496356-9666553	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv892266	chr9:9506817-9704501	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv466133	chr9:9516348-9609283	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv613315	chr9:9516348-9609283	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv892270	chr9:9591059-9860735	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10977873	FAM53C	trans	cerebellum	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9607000-9612200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:9607400-9612200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:9608200-9612400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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