Variant report

Variant	rs10490012
Chromosome Location	chr2:234843494-234843495
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	2:234840450-234842402..2:234842402-234843685	K562	blood:

Variant related genes	Relation type
ENSG00000144481	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1003540	0.95[CEU][hapmap];0.88[TSI][hapmap]
rs10166942	1.00[CEU][hapmap];0.85[TSI][hapmap]
rs10170399	0.95[CEU][hapmap]
rs10189040	1.00[CEU][hapmap];0.87[MEX][hapmap];0.96[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10929319	0.91[MEX][hapmap]
rs11563063	0.95[CEU][hapmap]
rs11563216	0.91[MEX][hapmap]
rs11892538	0.95[CEU][hapmap]
rs13418652	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1965629	0.95[CEU][hapmap]
rs2108809	0.91[MEX][hapmap]
rs2302153	0.89[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2362290	0.95[CEU][hapmap];0.85[TSI][hapmap]
rs2362292	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2362293	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4233636	1.00[CEU][hapmap]
rs4663986	1.00[CEU][hapmap]
rs4663988	0.91[MEX][hapmap]
rs6431648	1.00[CEU][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap]
rs6711120	1.00[CEU][hapmap];0.87[MEX][hapmap];0.96[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6738979	0.95[CEU][hapmap]
rs6740118	0.91[MEX][hapmap]
rs737636	1.00[CEU][hapmap]
rs758275	1.00[CEU][hapmap];0.87[MEX][hapmap];0.96[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs758276	1.00[CEU][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7604471	1.00[CEU][hapmap]
rs9646719	0.86[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9646720	0.95[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap]

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	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv876024	chr2:234842650-234856421	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10490012	COL6A3	cis	cerebellum	SCAN
rs10490012	NMUR1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234841000-234844800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:234841800-234847600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:234843000-234845400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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