Variant report

Variant	rs7755324
Chromosome Location	chr6:79243615-79243616
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11753268	1.00[ASN][1000 genomes]
rs11753781	1.00[ASN][1000 genomes]
rs11755496	1.00[ASN][1000 genomes]
rs12525083	1.00[ASN][1000 genomes]
rs1588044	1.00[ASN][1000 genomes]
rs1588045	1.00[ASN][1000 genomes]
rs17225876	1.00[ASN][1000 genomes]
rs17226851	1.00[ASN][1000 genomes]
rs17822220	1.00[ASN][1000 genomes]
rs17822917	1.00[ASN][1000 genomes]
rs17825291	1.00[ASN][1000 genomes]
rs2021251	1.00[ASN][1000 genomes]
rs2321449	1.00[ASN][1000 genomes]
rs35919105	1.00[ASN][1000 genomes]
rs62425666	1.00[ASN][1000 genomes]
rs62425667	1.00[ASN][1000 genomes]
rs62425668	1.00[ASN][1000 genomes]
rs62425669	1.00[ASN][1000 genomes]
rs62425696	1.00[ASN][1000 genomes]
rs62425700	1.00[ASN][1000 genomes]
rs62425701	1.00[ASN][1000 genomes]
rs62425702	1.00[ASN][1000 genomes]
rs62425703	1.00[ASN][1000 genomes]
rs6909051	1.00[ASN][1000 genomes]
rs6909644	1.00[ASN][1000 genomes]
rs6910018	1.00[ASN][1000 genomes]
rs72893289	1.00[ASN][1000 genomes]
rs73763418	1.00[ASN][1000 genomes]
rs959139	1.00[ASN][1000 genomes]
rs997649	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886235	chr6:78861808-79369972	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv604011	chr6:79042990-79455282	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv886300	chr6:79129963-79341891	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv522646	chr6:79185106-79333988	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1028767	chr6:79200713-79341224	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79243000-79244000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr6:79243000-79244800	Enhancers	HUVEC	blood vessel
3	chr6:79243400-79247600	Weak transcription	NH-A	brain
4	chr6:79243400-79247600	Weak transcription	Osteobl	bone
5	chr6:79243600-79244200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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