Variant report

Variant	rs9484844
Chromosome Location	chr6:144424116-144424117
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11961603	1.00[EUR][1000 genomes]
rs11963031	1.00[EUR][1000 genomes]
rs2010247	1.00[EUR][1000 genomes]
rs57960633	1.00[EUR][1000 genomes]
rs59407195	1.00[EUR][1000 genomes]
rs6909239	1.00[EUR][1000 genomes]
rs6917779	1.00[EUR][1000 genomes]
rs6925139	1.00[EUR][1000 genomes]
rs73778567	1.00[EUR][1000 genomes]
rs7743408	1.00[EUR][1000 genomes]
rs7768171	1.00[EUR][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	nsv886738	chr6:144387698-144428387	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144417800-144425800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr6:144417800-144432600	Weak transcription	Right Atrium	heart

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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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