Variant report

Variant	rs73680357
Chromosome Location	chr7:14898876-14898877
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10085625	1.00[EUR][1000 genomes]
rs10238323	1.00[EUR][1000 genomes]
rs10251472	1.00[EUR][1000 genomes]
rs1404622	1.00[EUR][1000 genomes]
rs1614700	1.00[EUR][1000 genomes]
rs1723242	1.00[EUR][1000 genomes]
rs55954033	1.00[EUR][1000 genomes]
rs56905045	1.00[EUR][1000 genomes]
rs60540005	1.00[EUR][1000 genomes]
rs61058262	1.00[EUR][1000 genomes]
rs61147906	1.00[EUR][1000 genomes]
rs61272991	1.00[EUR][1000 genomes]
rs6966072	1.00[EUR][1000 genomes]
rs73276014	1.00[EUR][1000 genomes]
rs73280239	1.00[EUR][1000 genomes]
rs73680193	1.00[EUR][1000 genomes]
rs73680202	1.00[EUR][1000 genomes]
rs73680304	1.00[EUR][1000 genomes]
rs73680340	1.00[EUR][1000 genomes]
rs73680371	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73680372	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73680375	1.00[EUR][1000 genomes]
rs73680376	1.00[EUR][1000 genomes]
rs73680379	1.00[EUR][1000 genomes]
rs73680382	1.00[EUR][1000 genomes]
rs73682503	1.00[EUR][1000 genomes]
rs73682511	1.00[EUR][1000 genomes]
rs73682513	1.00[EUR][1000 genomes]
rs73682548	1.00[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	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv887713	chr7:14888418-14939924	Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
4	nsv887714	chr7:14888418-14941576	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv2758104	chr7:14896877-15299786	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2759512	chr7:14896877-15299786	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv887715	chr7:14898282-14939924	Active TSS Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14898200-14899000	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr7:14898600-14899000	Enhancers	Osteobl	bone

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