Variant report

Variant	rs10128549
Chromosome Location	chr11:86610317-86610318
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11601476	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11602556	1.00[ASN][1000 genomes]
rs11602664	1.00[ASN][1000 genomes]
rs11604559	1.00[ASN][1000 genomes]
rs11604650	1.00[ASN][1000 genomes]
rs11608188	1.00[ASN][1000 genomes]
rs17758573	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56119716	1.00[ASN][1000 genomes]
rs56156145	1.00[ASN][1000 genomes]
rs72957504	1.00[ASN][1000 genomes]
rs72957509	1.00[ASN][1000 genomes]
rs72957525	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72957535	1.00[ASN][1000 genomes]
rs72959670	1.00[ASN][1000 genomes]
rs72959672	1.00[ASN][1000 genomes]
rs72959695	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	esv2756074	chr11:86456552-86729552	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv1037042	chr11:86586876-86978492	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv541119	chr11:86586876-86978492	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86578200-86627400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:86597200-86617400	Weak transcription	Aorta	Aorta
3	chr11:86597600-86620800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:86597600-86627400	Weak transcription	Ovary	ovary
5	chr11:86599600-86627600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr11:86600600-86627600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:86602400-86627600	Weak transcription	Left Ventricle	heart
8	chr11:86606800-86623000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:86607600-86614400	Weak transcription	HSMMtube	muscle
10	chr11:86608200-86613000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:86608200-86623200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:86608400-86613200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:86608400-86626000	Weak transcription	Fetal Lung	lung
14	chr11:86608400-86627400	Weak transcription	NHLF	lung
15	chr11:86608600-86613200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:86608600-86616600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:86608800-86625800	Weak transcription	Fetal Stomach	stomach
18	chr11:86609600-86610600	Enhancers	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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