Variant report

Variant	rs936198
Chromosome Location	chr3:142819277-142819278
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:142815403..142818636-chr3:142818743..142822345,3	K562	blood:
2	chr3:142818890..142821632-chr3:142833075..142835373,2	K562	blood:
3	chr3:142814752..142820591-chr3:142836443..142840865,5	K562	blood:

Variant related genes	Relation type
ENSG00000175040	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11914346	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11917259	1.00[CEU][hapmap];0.89[CHB][hapmap]
rs11924590	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11925953	1.00[CEU][hapmap];0.89[CHB][hapmap];0.92[GIH][hapmap];0.81[JPT][hapmap];0.88[TSI][hapmap];0.82[EUR][1000 genomes]
rs11926643	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11928485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13327838	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1531139	0.96[CEU][hapmap];0.85[CHB][hapmap];0.84[CHD][hapmap];0.97[GIH][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16852909	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs17557349	0.91[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[TSI][hapmap]
rs17633378	0.91[ASW][hapmap];1.00[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[TSI][hapmap]
rs1869894	0.80[EUR][1000 genomes]
rs2173599	1.00[CEU][hapmap];0.88[CHB][hapmap]
rs2353403	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2353404	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2353407	0.81[EUR][1000 genomes]
rs41374546	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55644607	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55874224	0.91[EUR][1000 genomes]
rs56022259	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56216546	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56407378	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57654114	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58124018	0.98[ASN][1000 genomes]
rs62276932	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62276933	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73157700	0.82[EUR][1000 genomes]
rs73867496	0.97[ASN][1000 genomes]
rs9834271	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9846508	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877562	chr3:142573789-142846370	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	esv2757893	chr3:142720230-142962932	Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759183	chr3:142720230-142964373	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv591921	chr3:142762487-142841740	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs936198	U2SURP	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142817800-142819600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr3:142818000-142819600	Enhancers	Fetal Muscle Leg	muscle
3	chr3:142818800-142819600	Bivalent Enhancer	NHDF-Ad	bronchial
4	chr3:142819200-142819400	Enhancers	Fetal Brain Male	brain
5	chr3:142819200-142819600	Enhancers	Fetal Brain Female	brain

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