Variant report

Variant	rs4672105
Chromosome Location	chr2:56517169-56517170
allele	A/C
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:17)

rs_ID	r²[population]
rs12463587	0.85[EUR][1000 genomes]
rs13384655	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13384837	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13389344	0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13392111	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1549031	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17047791	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4671278	0.85[EUR][1000 genomes]
rs4672106	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4672107	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6545564	0.86[AFR][1000 genomes]
rs6714529	0.96[AFR][1000 genomes]
rs6732270	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72803024	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72803026	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7355411	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7566597	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530516	chr2:56447922-56633505	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv522006	chr2:56496589-56545845	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv874170	chr2:56496589-56590865	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56514200-56517800	Enhancers	Fetal Intestine Large	intestine
2	chr2:56515000-56517200	Enhancers	Left Ventricle	heart
3	chr2:56515600-56526600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:56516000-56517400	Enhancers	Adipose Nuclei	Adipose
5	chr2:56516400-56517600	Enhancers	HUVEC	blood vessel
6	chr2:56516400-56517800	Enhancers	Fetal Intestine Small	intestine
7	chr2:56516400-56523400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:56516400-56525800	Weak transcription	HSMM	muscle
9	chr2:56516800-56524800	Weak transcription	Psoas Muscle	Psoas
10	chr2:56517000-56517200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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