Variant report

Variant	rs793850
Chromosome Location	chr6:24195935-24195936
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1087291	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1087292	0.89[AFR][1000 genomes]
rs1087293	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10946689	1.00[YRI][hapmap]
rs11965772	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1277190	0.89[AFR][1000 genomes]
rs1277191	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13191535	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13207282	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2799372	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712805	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv601146	chr6:24166233-24215665	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24153800-24200800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:24177800-24198400	Weak transcription	A549	lung
3	chr6:24186600-24196000	Weak transcription	Fetal Kidney	kidney
4	chr6:24194800-24197000	Enhancers	Fetal Intestine Large	intestine
5	chr6:24194800-24199400	Genic enhancers	HepG2	liver
6	chr6:24195000-24196200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:24195000-24196200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:24195200-24196000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:24195200-24196000	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr6:24195400-24196000	Enhancers	Pancreas	Pancrea
11	chr6:24195600-24196400	Enhancers	Fetal Intestine Small	intestine
12	chr6:24195800-24197000	Enhancers	Stomach Mucosa	stomach

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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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