Variant report

Variant	rs6912139
Chromosome Location	chr6:53565153-53565154
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4295480	0.88[ASN][1000 genomes]
rs6937819	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7773852	0.89[JPT][hapmap]
rs7774024	0.83[CHB][hapmap];0.84[ASN][1000 genomes]
rs9474636	0.81[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034955	chr6:53447607-53931055	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53557400-53565800	Weak transcription	Psoas Muscle	Psoas
2	chr6:53558000-53566200	Weak transcription	Fetal Muscle Leg	muscle
3	chr6:53560200-53575600	Weak transcription	Pancreas	Pancrea
4	chr6:53563400-53566800	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr6:53563600-53566800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr6:53565000-53565200	Enhancers	Fetal Brain Male	brain

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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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