Variant report

Variant	rs3819416
Chromosome Location	chr7:39484132-39484133
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12111665	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12112344	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12533673	0.84[ASN][1000 genomes]
rs17171576	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17171578	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17713095	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17713107	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17713143	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17769981	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17769987	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2052017	0.84[ASN][1000 genomes]
rs2052018	0.84[ASN][1000 genomes]
rs2052019	0.84[ASN][1000 genomes]
rs2073539	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2073545	0.89[ASN][1000 genomes]
rs2237384	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2237386	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2237387	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2237388	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2237392	0.89[ASN][1000 genomes]
rs2237394	0.89[ASN][1000 genomes]
rs2237397	0.89[ASN][1000 genomes]
rs2237398	0.89[ASN][1000 genomes]
rs2237399	0.89[ASN][1000 genomes]
rs2282915	0.84[ASN][1000 genomes]
rs2299134	0.89[ASN][1000 genomes]
rs3800850	0.87[ASN][1000 genomes]
rs73388309	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73388311	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs980392	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv966782	chr7:39454992-39581886	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1018430	chr7:39455497-39643569	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39473000-39498000	Weak transcription	Pancreas	Pancrea
2	chr7:39480400-39485600	Weak transcription	H9 Cell Line	embryonic stem cell

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