Variant report

Variant	rs2705526
Chromosome Location	chr3:112226170-112226171
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10511317	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11919639	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11921669	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13059364	0.92[EUR][1000 genomes]
rs13063173	0.92[EUR][1000 genomes]
rs13064534	0.86[EUR][1000 genomes]
rs13065703	0.92[EUR][1000 genomes]
rs13070342	0.92[EUR][1000 genomes]
rs13071492	0.92[EUR][1000 genomes]
rs13080547	0.85[EUR][1000 genomes]
rs13080749	0.92[EUR][1000 genomes]
rs13081201	0.85[EUR][1000 genomes]
rs13081265	0.96[EUR][1000 genomes]
rs13081632	0.96[EUR][1000 genomes]
rs13088339	0.85[EUR][1000 genomes]
rs13088349	0.85[EUR][1000 genomes]
rs13088467	0.85[EUR][1000 genomes]
rs13092057	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13094161	0.85[EUR][1000 genomes]
rs13094649	0.92[EUR][1000 genomes]
rs13095000	0.85[EUR][1000 genomes]
rs13096943	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16845067	0.85[EUR][1000 genomes]
rs16859661	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16859674	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16859727	0.92[EUR][1000 genomes]
rs16859758	0.92[EUR][1000 genomes]
rs16859779	0.85[EUR][1000 genomes]
rs16859787	0.85[EUR][1000 genomes]
rs16859793	0.85[EUR][1000 genomes]
rs1817694	0.91[AFR][1000 genomes]
rs1906519	0.96[AFR][1000 genomes]
rs2220656	0.85[EUR][1000 genomes]
rs28365853	0.85[EUR][1000 genomes]
rs34080815	0.92[EUR][1000 genomes]
rs34139211	0.92[EUR][1000 genomes]
rs34248586	0.92[EUR][1000 genomes]
rs34284082	0.82[EUR][1000 genomes]
rs34541731	0.85[EUR][1000 genomes]
rs34596334	0.85[EUR][1000 genomes]
rs34597203	0.92[EUR][1000 genomes]
rs34645913	0.92[EUR][1000 genomes]
rs34829517	0.85[EUR][1000 genomes]
rs34889961	0.92[EUR][1000 genomes]
rs34949685	0.85[EUR][1000 genomes]
rs34962178	0.85[EUR][1000 genomes]
rs35107041	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35240469	0.92[EUR][1000 genomes]
rs35255669	0.85[EUR][1000 genomes]
rs35349986	0.85[EUR][1000 genomes]
rs35512450	0.92[EUR][1000 genomes]
rs35526995	0.92[EUR][1000 genomes]
rs35529363	0.85[EUR][1000 genomes]
rs35692417	0.85[EUR][1000 genomes]
rs35709173	0.85[EUR][1000 genomes]
rs35725070	0.92[EUR][1000 genomes]
rs35748518	0.92[EUR][1000 genomes]
rs35803911	0.85[EUR][1000 genomes]
rs35840933	0.85[EUR][1000 genomes]
rs35931975	0.85[EUR][1000 genomes]
rs36025914	0.85[EUR][1000 genomes]
rs36031379	0.83[EUR][1000 genomes]
rs36045008	0.85[EUR][1000 genomes]
rs36061184	0.85[EUR][1000 genomes]
rs36146261	0.85[EUR][1000 genomes]
rs36153507	0.85[EUR][1000 genomes]
rs3736269	0.92[EUR][1000 genomes]
rs3736270	0.92[EUR][1000 genomes]
rs3736271	0.92[EUR][1000 genomes]
rs3773698	0.85[EUR][1000 genomes]
rs3773701	0.85[EUR][1000 genomes]
rs3773704	0.85[EUR][1000 genomes]
rs3773706	0.85[EUR][1000 genomes]
rs3773710	0.85[EUR][1000 genomes]
rs3821684	0.85[EUR][1000 genomes]
rs55742760	0.85[EUR][1000 genomes]
rs56662636	0.92[EUR][1000 genomes]
rs56856838	0.92[EUR][1000 genomes]
rs56970524	0.85[EUR][1000 genomes]
rs57346109	0.92[EUR][1000 genomes]
rs58891772	0.92[EUR][1000 genomes]
rs59279185	0.92[EUR][1000 genomes]
rs59858117	0.92[EUR][1000 genomes]
rs60321074	0.85[EUR][1000 genomes]
rs60646325	0.85[EUR][1000 genomes]
rs66486470	0.92[EUR][1000 genomes]
rs66698345	0.82[EUR][1000 genomes]
rs66791711	0.85[EUR][1000 genomes]
rs66910014	0.92[EUR][1000 genomes]
rs67021100	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67204151	0.85[EUR][1000 genomes]
rs67513863	0.89[EUR][1000 genomes]
rs67940544	0.85[EUR][1000 genomes]
rs67944354	0.92[EUR][1000 genomes]
rs71317505	0.92[EUR][1000 genomes]
rs71317506	0.96[EUR][1000 genomes]
rs71317507	0.92[EUR][1000 genomes]
rs71317508	0.92[EUR][1000 genomes]
rs71317510	0.85[EUR][1000 genomes]
rs724125	0.85[EUR][1000 genomes]
rs73229350	0.92[EUR][1000 genomes]
rs73229353	0.92[EUR][1000 genomes]
rs73229398	0.85[EUR][1000 genomes]
rs958935	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010208	chr3:112098542-112227212	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1003936	chr3:112125931-112274613	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv998309	chr3:112130290-112278804	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv591300	chr3:112144026-112270857	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv1006065	chr3:112147080-112276983	Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1005323	chr3:112171990-112274613	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv877342	chr3:112185025-112332629	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2705526	SLC35A5	cis	Nerve Tibial	GTEx

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112214600-112228600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:112218800-112241600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr3:112219800-112227200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr3:112221200-112227000	Weak transcription	Primary T cells from cord blood	blood
5	chr3:112223200-112226200	Enhancers	Primary B cells from cord blood	blood
6	chr3:112223200-112228400	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:112225200-112228000	Enhancers	GM12878-XiMat	blood
8	chr3:112225400-112227600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr3:112225600-112227200	Weak transcription	Fetal Stomach	stomach

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