Variant report

Variant	rs1071922
Chromosome Location	chr7:150340795-150340796
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10155859	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10224387	0.81[CHD][hapmap];0.95[JPT][hapmap]
rs10225462	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10227548	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10228706	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10230559	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10235151	0.86[JPT][hapmap];0.84[TSI][hapmap];0.82[ASN][1000 genomes]
rs10238979	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10243208	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10252841	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10253121	0.81[ASN][1000 genomes]
rs10253490	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10255380	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10258838	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10272462	0.82[ASN][1000 genomes]
rs10274439	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10282548	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10952281	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11763094	0.81[ASN][1000 genomes]
rs11763374	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11766040	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11768445	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11770532	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12111764	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1879868	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1879869	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1879870	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2373817	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3088115	0.86[JPT][hapmap];0.85[TSI][hapmap];0.81[ASN][1000 genomes]
rs3735084	0.82[ASN][1000 genomes]
rs3735085	0.86[JPT][hapmap];0.85[TSI][hapmap];0.81[ASN][1000 genomes]
rs4490747	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4993563	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55642497	0.89[ASN][1000 genomes]
rs57269277	0.81[ASN][1000 genomes]
rs6942976	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6947239	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6948827	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6952002	0.95[CEU][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs6969364	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6980253	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7808210	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription 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	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	esv2758617	chr7:150251949-150463804	Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	esv2759573	chr7:150251949-150463804	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	esv3388935	chr7:150301204-150374532	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1030109	chr7:150312916-150701010	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv967475	chr7:150323577-150610034	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv831187	chr7:150325913-150503500	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs1071922	MLL3	cis	parietal	SCAN
rs1071922	TMEM176B	cis	cerebellum	SCAN
rs1071922	GIMAP2	cis	parietal	SCAN
rs1071922	LR8	cis	multi-tissue	Pritchard
rs1071922	HCA112	cis	multi-tissue	Pritchard

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150337000-150341000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr7:150337400-150341800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr7:150338600-150342400	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr7:150339400-150341800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr7:150339400-150342400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:150339600-150341400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr7:150340200-150340800	ZNF genes & repeats	GM12878-XiMat	blood
8	chr7:150340400-150341000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr7:150340400-150341400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr7:150340400-150341800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr7:150340400-150341800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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