Variant report

Variant	rs7791672
Chromosome Location	chr7:3781676-3781677
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1004142	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10226577	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10233941	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10248562	0.83[AFR][1000 genomes]
rs10264350	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10266535	0.97[AFR][1000 genomes]
rs10275231	0.94[AFR][1000 genomes]
rs10275232	0.91[AFR][1000 genomes]
rs10277000	1.00[AMR][1000 genomes]
rs10279770	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10279868	1.00[AMR][1000 genomes]
rs11978042	1.00[EUR][1000 genomes]
rs17133790	1.00[EUR][1000 genomes]
rs17133792	1.00[EUR][1000 genomes]
rs17133795	1.00[EUR][1000 genomes]
rs17133803	1.00[EUR][1000 genomes]
rs17133812	1.00[EUR][1000 genomes]
rs28379281	1.00[AMR][1000 genomes]
rs28394711	0.91[AFR][1000 genomes]
rs28650199	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28689669	1.00[AMR][1000 genomes]
rs41881	1.00[EUR][1000 genomes]
rs41884	1.00[EUR][1000 genomes]
rs41885	1.00[AMR][1000 genomes]
rs41886	1.00[EUR][1000 genomes]
rs41889	1.00[EUR][1000 genomes]
rs41891	1.00[EUR][1000 genomes]
rs41892	1.00[EUR][1000 genomes]
rs41894	1.00[EUR][1000 genomes]
rs41896	1.00[AMR][1000 genomes]
rs41898	1.00[EUR][1000 genomes]
rs42233	1.00[AMR][1000 genomes]
rs55806931	1.00[AMR][1000 genomes]
rs6462287	1.00[AMR][1000 genomes]
rs6946134	0.97[AFR][1000 genomes]
rs6951452	1.00[AMR][1000 genomes]
rs6963031	0.96[AFR][1000 genomes]
rs6964615	0.97[AFR][1000 genomes]
rs6967027	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6970269	0.87[AMR][1000 genomes]
rs6971516	1.00[AMR][1000 genomes]
rs6980395	0.82[AFR][1000 genomes]
rs73304253	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73304284	1.00[AMR][1000 genomes]
rs73306103	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73306106	1.00[EUR][1000 genomes]
rs73306109	1.00[EUR][1000 genomes]
rs73306117	1.00[EUR][1000 genomes]
rs73306119	1.00[EUR][1000 genomes]
rs73306123	1.00[EUR][1000 genomes]
rs73306126	1.00[EUR][1000 genomes]
rs73306128	1.00[EUR][1000 genomes]
rs7805255	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1017868	chr7:3698885-3820159	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1021443	chr7:3705273-3889334	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv605935	chr7:3713194-3799580	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1019582	chr7:3718061-3814514	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv538682	chr7:3718061-3814514	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1022650	chr7:3723035-3847680	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1024704	chr7:3736254-3831859	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1031610	chr7:3744536-3838844	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3773000-3820000	Weak transcription	Pancreas	Pancrea
2	chr7:3780200-3795400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3780800-3782400	Enhancers	Primary B cells from peripheral blood	blood
4	chr7:3781400-3782000	Weak transcription	Primary B cells from cord blood	blood

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