Variant report

Variant	rs7805064
Chromosome Location	chr7:110597720-110597721
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10229697	1.00[EUR][1000 genomes]
rs10235732	1.00[EUR][1000 genomes]
rs10235831	1.00[EUR][1000 genomes]
rs10240065	1.00[EUR][1000 genomes]
rs10241294	1.00[EUR][1000 genomes]
rs10245552	1.00[EUR][1000 genomes]
rs10248851	1.00[EUR][1000 genomes]
rs10256612	1.00[EUR][1000 genomes]
rs10259851	1.00[EUR][1000 genomes]
rs10261307	1.00[EUR][1000 genomes]
rs10266782	1.00[EUR][1000 genomes]
rs10280198	1.00[EUR][1000 genomes]
rs10282715	1.00[EUR][1000 genomes]
rs10487295	1.00[EUR][1000 genomes]
rs11505728	1.00[EUR][1000 genomes]
rs11505729	1.00[EUR][1000 genomes]
rs11505730	1.00[EUR][1000 genomes]
rs11505731	1.00[EUR][1000 genomes]
rs11505732	1.00[EUR][1000 genomes]
rs11505733	1.00[EUR][1000 genomes]
rs11505901	1.00[EUR][1000 genomes]
rs16873234	1.00[EUR][1000 genomes]
rs17158038	1.00[EUR][1000 genomes]
rs17158040	1.00[EUR][1000 genomes]
rs17158074	1.00[EUR][1000 genomes]
rs17158107	1.00[EUR][1000 genomes]
rs17158283	1.00[EUR][1000 genomes]
rs1860807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2214972	1.00[EUR][1000 genomes]
rs28435168	1.00[EUR][1000 genomes]
rs28441083	1.00[EUR][1000 genomes]
rs28545077	1.00[EUR][1000 genomes]
rs28607108	1.00[EUR][1000 genomes]
rs28687586	1.00[EUR][1000 genomes]
rs28709655	1.00[EUR][1000 genomes]
rs57796825	1.00[EUR][1000 genomes]
rs6466364	1.00[EUR][1000 genomes]
rs6975872	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73419241	1.00[EUR][1000 genomes]
rs73419250	1.00[EUR][1000 genomes]
rs73423031	1.00[EUR][1000 genomes]
rs73423032	1.00[EUR][1000 genomes]
rs73423072	1.00[EUR][1000 genomes]
rs73423074	1.00[EUR][1000 genomes]
rs73425039	1.00[EUR][1000 genomes]
rs73425043	1.00[EUR][1000 genomes]
rs73425066	1.00[EUR][1000 genomes]
rs73435151	1.00[EUR][1000 genomes]
rs7776859	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7779848	1.00[EUR][1000 genomes]
rs7780566	1.00[EUR][1000 genomes]
rs7795999	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7801502	1.00[EUR][1000 genomes]
rs7809830	1.00[EUR][1000 genomes]
rs7810646	1.00[EUR][1000 genomes]
rs7810802	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023596	chr7:109984459-110708071	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv539061	chr7:109984459-110708071	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv608147	chr7:110292046-110617845	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv531434	chr7:110310931-110839892	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv888972	chr7:110470629-110635497	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3506497	chr7:110484691-111091738	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	esv3506498	chr7:110484750-111091689	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv888973	chr7:110509579-110699652	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv888974	chr7:110516659-110660055	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	esv2758129	chr7:110523298-110787849	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	esv2759554	chr7:110523298-110787849	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1031546	chr7:110549137-110978256	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv817555	chr7:110564801-110990927	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv1033286	chr7:110588021-110990928	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv539063	chr7:110588021-110990928	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110567600-110614400	Weak transcription	Psoas Muscle	Psoas
2	chr7:110589000-110604600	Weak transcription	Pancreas	Pancrea
3	chr7:110589200-110598800	Weak transcription	Aorta	Aorta
4	chr7:110593600-110603000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:110597200-110597800	Enhancers	Muscle Satellite Cultured Cells	--

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