Variant report

Variant	rs7244936
Chromosome Location	chr18:29546206-29546207
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1030403	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12455103	0.98[ASN][1000 genomes]
rs4239371	0.94[ASN][1000 genomes]
rs4254394	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4799610	0.97[ASN][1000 genomes]
rs4799611	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4799612	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4799614	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67236500	0.98[ASN][1000 genomes]
rs7245194	0.95[ASN][1000 genomes]
rs8083160	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8086309	0.86[ASN][1000 genomes]
rs8095233	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8096737	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8097869	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8098106	0.97[ASN][1000 genomes]
rs9676072	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs972357	0.81[EUR][1000 genomes];0.98[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	nsv1067252	chr18:29475073-29583744	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1065285	chr18:29527884-29614986	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29544200-29552000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:29544800-29547000	Enhancers	Fetal Intestine Large	intestine
3	chr18:29545200-29547200	Enhancers	Duodenum Mucosa	Duodenum
4	chr18:29545200-29547400	Enhancers	Fetal Intestine Small	intestine
5	chr18:29545800-29551000	Weak transcription	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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