Variant report

Variant	rs11638294
Chromosome Location	chr15:92817858-92817859
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11630700	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11631126	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11632217	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11632525	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11633492	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11633660	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634765	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634816	0.83[ASN][1000 genomes]
rs11634854	0.83[ASN][1000 genomes]
rs11634942	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11635853	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11638245	0.83[ASN][1000 genomes]
rs11638327	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16946658	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16946659	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16946674	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55791132	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56280645	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs899522	0.95[EUR][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	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1049561	chr15:92758434-93097965	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 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	chr15:92813200-92822800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:92817200-92821200	Weak transcription	Fetal Muscle Leg	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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