Variant report

Variant	rs7246695
Chromosome Location	chr19:21200835-21200836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10406359	1.00[AMR][1000 genomes]
rs10418266	1.00[AMR][1000 genomes]
rs17447963	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2098682	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57505697	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57601660	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57981503	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58002329	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58148410	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59609198	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60170851	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60293432	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61179921	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7247066	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7247670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7248199	1.00[AMR][1000 genomes]
rs7259985	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73531819	0.87[AFR][1000 genomes]
rs73531882	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73531886	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73531897	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73531902	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73533603	1.00[AMR][1000 genomes]
rs73533607	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73533690	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73540426	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73540428	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73540432	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73542615	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73542629	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73542640	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73542656	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73544576	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73546304	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73546306	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8104371	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8108394	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062776	chr19:20818886-21273361	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv932110	chr19:20818886-21278952	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	esv2763043	chr19:20818886-21290543	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv817536	chr19:21041855-21348237	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	esv1850387	chr19:21109758-21294264	Active TSS ZNF genes & repeats Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv911411	chr19:21184533-21263518	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv578949	chr19:21190572-21244049	ZNF genes & repeats Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
9	nsv960811	chr19:21200306-21371757	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21192200-21203000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr19:21192400-21203000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr19:21192400-21203400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:21192600-21203000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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