Variant report

Variant	rs12535033
Chromosome Location	chr7:104335852-104335853
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10244859	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs10249869	0.90[CHD][hapmap];0.85[JPT][hapmap]
rs10273020	0.90[CHD][hapmap];0.90[JPT][hapmap]
rs10464615	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[YRI][hapmap]
rs11768712	0.90[JPT][hapmap]
rs11982043	0.90[CHD][hapmap];0.90[JPT][hapmap]
rs12531723	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap]
rs12534285	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12536801	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs12705261	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap]
rs12705263	1.00[CEU][hapmap];0.89[CHB][hapmap]
rs12705264	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs13241253	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs13242612	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs17269890	0.90[CHD][hapmap];0.90[JPT][hapmap]
rs4255068	0.94[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4311596	0.89[JPT][hapmap]
rs4419737	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs4496900	0.80[ASN][1000 genomes]
rs4512324	0.81[CHB][hapmap]
rs4566971	0.85[CHB][hapmap]
rs4624947	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs4730035	0.96[ASN][1000 genomes]
rs4730037	0.85[CHB][hapmap];0.85[GIH][hapmap];0.97[ASN][1000 genomes]
rs4730038	0.96[CEU][hapmap];0.80[TSI][hapmap]
rs6466014	0.90[JPT][hapmap]
rs6945225	0.81[CHB][hapmap]
rs6952413	0.96[CEU][hapmap];0.80[TSI][hapmap]
rs6962309	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs6966224	0.92[CEU][hapmap]
rs7782285	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7801294	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9885990	0.83[JPT][hapmap]
rs9886292	0.81[CHB][hapmap]

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	nsv429790	chr7:104314049-104488049	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12535033	ATXN7L1	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104333200-104340400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:104334600-104338400	Enhancers	Colon Smooth Muscle	Colon

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