Variant report

Variant	rs57845501
Chromosome Location	chr2:234234192-234234193
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10170001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13389943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13390054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13395852	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13403445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13406449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13422131	1.00[AMR][1000 genomes]
rs13426533	1.00[AMR][1000 genomes]
rs58172277	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58592401	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59148909	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59937078	1.00[AMR][1000 genomes]
rs73110079	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73110095	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv584699	chr2:234182240-234255547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv584700	chr2:234199401-234364426	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1002075	chr2:234225979-234277508	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234223600-234245400	Weak transcription	Pancreas	Pancrea
2	chr2:234228400-234240000	Weak transcription	Fetal Intestine Small	intestine
3	chr2:234229800-234235000	Enhancers	Primary B cells from cord blood	blood
4	chr2:234229800-234235600	Enhancers	Primary B cells from peripheral blood	blood
5	chr2:234232800-234237800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:234233400-234237600	Weak transcription	Lung	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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