Variant report

Variant	rs35059516
Chromosome Location	chr10:91613208-91613209
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:91611570..91614233-chr10:91624005..91626634,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11593892	1.00[ASN][1000 genomes]
rs11594682	1.00[ASN][1000 genomes]
rs11595126	1.00[ASN][1000 genomes]
rs11597847	1.00[ASN][1000 genomes]
rs11598015	1.00[ASN][1000 genomes]
rs11598257	1.00[ASN][1000 genomes]
rs12413697	1.00[ASN][1000 genomes]
rs12414269	1.00[ASN][1000 genomes]
rs12415422	1.00[ASN][1000 genomes]
rs1326195	1.00[ASN][1000 genomes]
rs17413232	1.00[ASN][1000 genomes]
rs17484219	1.00[ASN][1000 genomes]
rs2026553	1.00[ASN][1000 genomes]
rs34354493	1.00[ASN][1000 genomes]
rs56318555	1.00[ASN][1000 genomes]
rs7071258	1.00[ASN][1000 genomes]
rs72818744	1.00[ASN][1000 genomes]
rs72818750	1.00[ASN][1000 genomes]
rs72818751	1.00[ASN][1000 genomes]
rs72818757	1.00[ASN][1000 genomes]
rs72818758	1.00[ASN][1000 genomes]
rs72818759	1.00[ASN][1000 genomes]
rs72818766	1.00[ASN][1000 genomes]
rs72818768	1.00[ASN][1000 genomes]
rs72818770	1.00[ASN][1000 genomes]
rs72818773	1.00[ASN][1000 genomes]
rs72818774	1.00[ASN][1000 genomes]
rs72818781	1.00[ASN][1000 genomes]
rs72818786	1.00[ASN][1000 genomes]
rs72818790	1.00[ASN][1000 genomes]
rs72818792	1.00[ASN][1000 genomes]
rs728852	1.00[ASN][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	nsv1046241	chr10:91478562-91614437	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv869080	chr10:91498641-91712834	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1036581	chr10:91526705-91691536	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1043571	chr10:91568555-92036154	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS 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
5	nsv551874	chr10:91570211-92036154	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv949678	chr10:91589048-92016474	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv895883	chr10:91610601-92195828	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91607000-91621600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:91610400-91613600	Weak transcription	Right Atrium	heart
3	chr10:91613200-91614000	Enhancers	Fetal Intestine Large	intestine

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