Variant report

Variant	rs793853
Chromosome Location	chr6:24196925-24196926
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1087294	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12153942	0.84[ASN][1000 genomes]
rs2799373	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs793845	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs793847	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs793862	0.84[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:8 , 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	chr6:24194800-24197000	Enhancers	Fetal Intestine Large	intestine
4	chr6:24194800-24199400	Genic enhancers	HepG2	liver
5	chr6:24195800-24197000	Enhancers	Stomach Mucosa	stomach
6	chr6:24196000-24197400	Strong transcription	Fetal Kidney	kidney
7	chr6:24196400-24205400	Weak transcription	Fetal Intestine Small	intestine
8	chr6:24196800-24198400	Weak transcription	Pancreas	Pancrea

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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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