Variant report

Variant	rs4755356
Chromosome Location	chr11:34017460-34017461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10836141	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11032474	0.81[AMR][1000 genomes]
rs11032475	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12282240	0.91[ASN][1000 genomes]
rs12290109	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12418479	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12421153	0.91[ASN][1000 genomes]
rs12421249	0.83[ASN][1000 genomes]
rs12787303	0.88[ASN][1000 genomes]
rs12795523	0.92[ASN][1000 genomes]
rs12797090	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35836121	0.91[ASN][1000 genomes]
rs4316483	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4756093	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7112270	0.93[ASN][1000 genomes]
rs7120707	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[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	esv10363	chr11:34015216-34018311	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34006400-34018200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:34013400-34018400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr11:34013400-34018800	Weak transcription	Dnd41	blood
4	chr11:34013600-34018400	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr11:34016400-34018800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:34016400-34020400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:34016800-34018400	Weak transcription	K562	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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