Variant report

Variant	rs1914028
Chromosome Location	chr2:189754013-189754014
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1516440	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1516441	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16830872	0.92[EUR][1000 genomes]
rs17241638	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17291017	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17357358	0.84[AMR][1000 genomes]
rs17357387	0.84[AMR][1000 genomes]
rs17357408	0.84[AMR][1000 genomes]
rs1914029	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1914030	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67712818	0.84[AMR][1000 genomes]
rs73033503	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73033510	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73050211	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73050212	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73050213	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73050229	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73052303	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73052342	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv875608	chr2:189753823-189837995	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189739000-189755600	Weak transcription	Aorta	Aorta
2	chr2:189753800-189757200	Weak transcription	Fetal Lung	lung

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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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