Variant report

Variant	rs35099594
Chromosome Location	chr19:21734064-21734065
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10420016	0.81[EUR][1000 genomes]
rs10854050	0.83[ASN][1000 genomes]
rs10854051	0.83[ASN][1000 genomes]
rs11085462	0.83[ASN][1000 genomes]
rs11085465	0.83[ASN][1000 genomes]
rs11668606	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11671579	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1879234	0.81[EUR][1000 genomes]
rs2562398	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2562408	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2562417	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2562428	0.90[AFR][1000 genomes]
rs2562466	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2562468	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2562471	0.81[AMR][1000 genomes]
rs2562487	0.90[AFR][1000 genomes]
rs2562507	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2562508	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2650793	0.81[EUR][1000 genomes]
rs2650804	0.81[EUR][1000 genomes]
rs2650805	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2650825	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2681370	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2681377	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2681388	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2681389	0.81[EUR][1000 genomes]
rs2681392	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2681395	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2946790	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35008138	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55771551	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs58001930	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62110163	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6511253	0.81[EUR][1000 genomes]
rs6511254	0.81[EUR][1000 genomes]
rs6511256	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7259708	0.84[ASN][1000 genomes]
rs9304986	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9304987	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	esv3363678	chr19:21483148-21756908	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv578952	chr19:21535707-21868584	Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv833782	chr19:21663537-21845722	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv2762028	chr19:21685778-21755476	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1059328	chr19:21691123-21775948	Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv543942	chr19:21711611-21767567	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv543943	chr19:21713945-21759080	Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv543944	chr19:21713945-21767567	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv543945	chr19:21717518-21767567	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	esv3428682	chr19:21733091-21735458	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs35099594	RP11-678G14.3	cis	Adipose Subcutaneous	GTEx
rs35099594	RP11-678G14.2	cis	Adipose Subcutaneous	GTEx
rs35099594	ZNF708	cis	Muscle Skeletal	GTEx
rs35099594	ZNF708	cis	Skin Sun Exposed Lower leg	GTEx
rs35099594	CTD-2561J22.5	cis	Thyroid	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21720400-21740800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr19:21726200-21737400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr19:21726200-21737800	Weak transcription	Right Ventricle	heart
4	chr19:21726200-21737800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr19:21726400-21740800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:21726600-21740800	Weak transcription	Placenta Amnion	Placenta Amnion

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