Variant report

Variant	rs73738797
Chromosome Location	chr6:27375851-27375852
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000271755	TF binding region
ENSG00000233224	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000197153	Chromatin interaction

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

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

rs_ID	r²[population]
rs1102568	1.00[ASN][1000 genomes]
rs11750956	1.00[ASN][1000 genomes]
rs11751859	1.00[ASN][1000 genomes]
rs11753029	1.00[ASN][1000 genomes]
rs11753248	1.00[ASN][1000 genomes]
rs11753483	1.00[ASN][1000 genomes]
rs11753572	1.00[ASN][1000 genomes]
rs11754166	1.00[ASN][1000 genomes]
rs11756458	1.00[ASN][1000 genomes]
rs11757216	1.00[ASN][1000 genomes]
rs11757320	1.00[ASN][1000 genomes]
rs11757748	1.00[ASN][1000 genomes]
rs11961333	1.00[ASN][1000 genomes]
rs11962403	1.00[ASN][1000 genomes]
rs11965377	1.00[ASN][1000 genomes]
rs11965529	1.00[ASN][1000 genomes]
rs11966553	1.00[ASN][1000 genomes]
rs11966985	1.00[ASN][1000 genomes]
rs11967073	1.00[ASN][1000 genomes]
rs11967759	1.00[ASN][1000 genomes]
rs11969536	1.00[ASN][1000 genomes]
rs11970095	1.00[ASN][1000 genomes]
rs11970261	1.00[ASN][1000 genomes]
rs2021277	1.00[ASN][1000 genomes]
rs2893912	1.00[ASN][1000 genomes]
rs34979454	1.00[ASN][1000 genomes]
rs6933702	1.00[ASN][1000 genomes]
rs7744248	1.00[ASN][1000 genomes]
rs858978	1.00[ASN][1000 genomes]
rs858979	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	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases
2	nsv1031803	chr6:27355881-27423655	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv538166	chr6:27355881-27423655	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv5235	chr6:27358498-27404074	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr6:27369000-27376600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:27369200-27382000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:27370600-27379800	Weak transcription	Ovary	ovary
4	chr6:27373800-27376400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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Input of quick search could be:

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

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