Variant report

Variant	rs73368182
Chromosome Location	chr6:13085855-13085856
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11970697	1.00[ASN][1000 genomes]
rs58469352	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58613497	1.00[ASN][1000 genomes]
rs6903869	1.00[ASN][1000 genomes]
rs6910939	1.00[ASN][1000 genomes]
rs73368123	1.00[ASN][1000 genomes]
rs73368142	1.00[ASN][1000 genomes]
rs73368147	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368149	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368163	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368165	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368168	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368172	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368175	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368177	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73368194	1.00[ASN][1000 genomes]
rs73368196	1.00[ASN][1000 genomes]
rs73368197	1.00[ASN][1000 genomes]
rs73369823	1.00[ASN][1000 genomes]
rs9473446	1.00[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	esv3521000	chr6:12561306-13128519	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3521001	chr6:12561306-13128519	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv817350	chr6:12922859-13137655	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv600992	chr6:12961922-13218549	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13078600-13101400	Weak transcription	Lung	lung
2	chr6:13079600-13089400	Weak transcription	Left Ventricle	heart
3	chr6:13080000-13102000	Weak transcription	Fetal Brain Female	brain
4	chr6:13080000-13105200	Weak transcription	Right Atrium	heart
5	chr6:13080800-13086600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:13081800-13095200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:13082200-13097000	Weak transcription	Brain Hippocampus Middle	brain
8	chr6:13082800-13088600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:13082800-13089000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:13082800-13095000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:13085000-13088600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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