Variant report

Variant	rs7671759
Chromosome Location	chr4:120248094-120248095
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10003567	0.82[AMR][1000 genomes]
rs10005237	0.82[AMR][1000 genomes]
rs10024933	0.82[AMR][1000 genomes]
rs10212714	0.83[AMR][1000 genomes]
rs10212719	0.82[AMR][1000 genomes]
rs10212775	0.82[AMR][1000 genomes]
rs10213158	0.82[AMR][1000 genomes]
rs10213267	0.82[AMR][1000 genomes]
rs10518300	0.82[AMR][1000 genomes]
rs11098501	0.82[AMR][1000 genomes]
rs11098502	0.82[AMR][1000 genomes]
rs11724409	0.82[AMR][1000 genomes]
rs11732087	0.82[AMR][1000 genomes]
rs11732686	0.82[AMR][1000 genomes]
rs12498994	0.81[AMR][1000 genomes]
rs12506610	0.82[AMR][1000 genomes]
rs12507565	0.82[AMR][1000 genomes]
rs12509621	0.81[AMR][1000 genomes]
rs12510269	0.82[AMR][1000 genomes]
rs12511640	0.82[AMR][1000 genomes]
rs12513083	0.81[AMR][1000 genomes]
rs12711071	0.82[AMR][1000 genomes]
rs1511025	0.82[AMR][1000 genomes]
rs1546506	0.81[AMR][1000 genomes]
rs17049949	0.82[AMR][1000 genomes]
rs17595608	0.81[AMR][1000 genomes]
rs1980024	0.82[AMR][1000 genomes]
rs1980025	0.82[AMR][1000 genomes]
rs1980026	0.82[AMR][1000 genomes]
rs1980027	0.82[AMR][1000 genomes]
rs2002049	0.82[AMR][1000 genomes]
rs2036856	0.82[AMR][1000 genomes]
rs2036857	0.82[AMR][1000 genomes]
rs2036860	0.82[AMR][1000 genomes]
rs28363929	0.82[AMR][1000 genomes]
rs28373117	0.81[AMR][1000 genomes]
rs28643450	0.81[AMR][1000 genomes]
rs28652763	0.82[AMR][1000 genomes]
rs28713555	0.82[AMR][1000 genomes]
rs2964	0.82[AMR][1000 genomes]
rs34425882	0.82[AMR][1000 genomes]
rs34685788	0.83[AMR][1000 genomes]
rs4107728	0.82[AMR][1000 genomes]
rs4443261	0.82[AMR][1000 genomes]
rs4472123	0.80[AMR][1000 genomes]
rs66900435	0.82[AMR][1000 genomes]
rs714899	0.82[AMR][1000 genomes]
rs72676046	0.82[AMR][1000 genomes]
rs7671978	0.83[AMR][1000 genomes]
rs7672129	0.85[AMR][1000 genomes]
rs7672594	0.82[AMR][1000 genomes]
rs7672778	0.82[AMR][1000 genomes]
rs7689729	0.82[AMR][1000 genomes]
rs878372	0.82[AMR][1000 genomes]
rs878376	0.82[AMR][1000 genomes]
rs907204	0.82[AMR][1000 genomes]
rs907205	0.82[AMR][1000 genomes]
rs938056	0.82[AMR][1000 genomes]
rs9991166	0.82[AMR][1000 genomes]
rs9991959	0.82[AMR][1000 genomes]
rs9993347	0.82[AMR][1000 genomes]
rs9999724	0.82[AMR][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	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv879840	chr4:120227419-120257417	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv879841	chr4:120244085-120388406	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv879842	chr4:120244085-120424087	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7671759	RP11-384K6.6	cis	Whole Blood	GTEx
rs7671759	LOC645513	Cis_1M	lymphoblastoid	RTeQTL
rs7671759	FLJ14186///LOC284701///LOC441124///LOC728624	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120222000-120251000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:120235600-120251000	Weak transcription	Left Ventricle	heart
3	chr4:120244400-120249800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr4:120245200-120249600	Weak transcription	Fetal Intestine Large	intestine
5	chr4:120245400-120249600	Weak transcription	Fetal Intestine Small	intestine

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