Variant report

Variant	rs4941575
Chromosome Location	chr13:47475294-47475295
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]
rs1928040	0.88[CEU][hapmap]
rs2149434	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs4941570	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs4941573	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4941574	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4942584	0.91[EUR][1000 genomes]
rs6311	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6313	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6561336	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs731245	0.85[CEU][hapmap]
rs732821	0.85[CEU][hapmap]
rs9316236	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9526246	0.96[CEU][hapmap];0.93[YRI][hapmap];0.88[EUR][1000 genomes]
rs9534504	0.88[EUR][1000 genomes]
rs9534513	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs9534515	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[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	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:47471600-47477600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr13:47471600-47477600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr13:47472400-47477600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr13:47474400-47477400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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