Variant report

Variant	rs7301810
Chromosome Location	chr12:117547237-117547238
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10850760	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11068320	1.00[ASN][1000 genomes]
rs12313308	1.00[ASN][1000 genomes]
rs2893705	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3862136	0.83[AMR][1000 genomes]
rs4271458	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7300649	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7967489	0.81[AMR][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	nsv832526	chr12:117530234-117723821	Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 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	chr12:117537600-117556400	Weak transcription	Right Atrium	heart
2	chr12:117538800-117549200	Weak transcription	Pancreas	Pancrea
3	chr12:117540000-117548200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr12:117540400-117548200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:117540800-117549200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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