Variant report

Variant	rs55943578
Chromosome Location	chr11:18226943-18226944
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12577038	0.92[ASN][1000 genomes]
rs2445174	0.86[ASN][1000 genomes]
rs2445225	0.82[ASN][1000 genomes]
rs2445226	0.82[ASN][1000 genomes]
rs2445228	0.86[ASN][1000 genomes]
rs2460827	0.85[ASN][1000 genomes]
rs2468789	0.91[ASN][1000 genomes]
rs2468790	0.82[ASN][1000 genomes]
rs2956633	0.86[ASN][1000 genomes]
rs2956634	0.86[ASN][1000 genomes]
rs3100768	0.89[ASN][1000 genomes]
rs56149966	0.86[ASN][1000 genomes]
rs7927495	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv428569	chr11:18194030-18350869	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv521662	chr11:18225742-18227151	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 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	chr11:18226000-18230800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:18226800-18227000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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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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