Variant report

Variant	rs1201149
Chromosome Location	chr2:189739769-189739770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1201147	1.00[AMR][1000 genomes]
rs1201148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1201156	0.81[AFR][1000 genomes]
rs1211717	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1518007	0.96[AFR][1000 genomes]
rs1607318	0.90[AFR][1000 genomes]
rs1882678	1.00[AFR][1000 genomes]
rs2675403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2708211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2708212	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2708213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6759257	0.96[AFR][1000 genomes]
rs781235	0.96[AFR][1000 genomes]
rs781274	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003974	chr2:189331760-189827814	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1008847	chr2:189603961-189769705	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv997454	chr2:189615728-189770133	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1002175	chr2:189615728-189776301	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv834490	chr2:189703550-189840963	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv4236	chr2:189730546-189740139	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv821858	chr2:189733808-189740029	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189735200-189740000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:189737200-189743200	Weak transcription	Fetal Lung	lung
3	chr2:189739000-189755600	Weak transcription	Aorta	Aorta

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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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