Variant report

Variant	rs4297485
Chromosome Location	chr11:87148324-87148325
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11235141	0.96[ASN][1000 genomes]
rs11827772	1.00[ASN][1000 genomes]
rs12272384	0.89[ASN][1000 genomes]
rs12274398	0.96[ASN][1000 genomes]
rs12277664	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12281027	0.96[ASN][1000 genomes]
rs12282338	1.00[ASN][1000 genomes]
rs12287179	0.96[ASN][1000 genomes]
rs12291004	0.89[ASN][1000 genomes]
rs12291930	1.00[ASN][1000 genomes]
rs12294204	0.93[ASN][1000 genomes]
rs12295921	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17759922	0.93[ASN][1000 genomes]
rs73537969	0.89[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	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv1046288	chr11:86757573-87158571	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv555714	chr11:87058981-87399218	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1039172	chr11:87068731-87385458	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:87142800-87150800	Weak transcription	Right Atrium	heart
2	chr11:87143800-87155800	Weak transcription	Adipose Nuclei	Adipose
3	chr11:87144000-87148400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:87144000-87148400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr11:87144000-87148400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:87144000-87148600	Weak transcription	HSMM	muscle
7	chr11:87144400-87148400	Weak transcription	NHDF-Ad	bronchial
8	chr11:87144400-87149600	Weak transcription	HSMMtube	muscle
9	chr11:87144800-87150800	Weak transcription	Colon Smooth Muscle	Colon
10	chr11:87145800-87148400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:87145800-87148400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:87147400-87152200	Enhancers	NHLF	lung
13	chr11:87147800-87149000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:87147800-87149800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:87148000-87150200	Enhancers	Osteobl	bone
16	chr11:87148200-87149000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:87148200-87149000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:87148200-87149600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:87148200-87149800	Enhancers	NH-A	brain

Quick Search:

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

what's new

Quick links