Variant report

Variant	rs73781365
Chromosome Location	chr6:144389809-144389810
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12211801	1.00[ASN][1000 genomes]
rs12215407	1.00[ASN][1000 genomes]
rs2328535	1.00[ASN][1000 genomes]
rs4896691	1.00[ASN][1000 genomes]
rs71564466	1.00[ASN][1000 genomes]
rs73000545	1.00[ASN][1000 genomes]
rs73004490	1.00[ASN][1000 genomes]
rs73004494	1.00[ASN][1000 genomes]
rs73781334	1.00[ASN][1000 genomes]
rs9484830	1.00[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	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144386400-144408800	Weak transcription	Right Ventricle	heart
2	chr6:144388400-144396600	Weak transcription	K562	blood
3	chr6:144388600-144390200	Enhancers	GM12878-XiMat	blood
4	chr6:144389800-144390000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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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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