Variant report

Variant	rs2371279
Chromosome Location	chr2:212553703-212553704
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10179476	0.90[ASN][1000 genomes]
rs10183757	0.85[ASN][1000 genomes]
rs10190554	0.90[ASN][1000 genomes]
rs10207288	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10932392	0.93[ASN][1000 genomes]
rs12470629	0.90[ASN][1000 genomes]
rs13001867	0.85[ASN][1000 genomes]
rs13003212	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13019022	0.90[ASN][1000 genomes]
rs16846710	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1829615	0.90[ASN][1000 genomes]
rs1851191	0.90[ASN][1000 genomes]
rs2371278	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34579531	0.81[ASN][1000 genomes]
rs34678713	0.90[ASN][1000 genomes]
rs34807898	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35043628	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35882647	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3817429	0.90[ASN][1000 genomes]
rs4315465	0.92[ASN][1000 genomes]
rs4423543	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58225230	0.85[ASN][1000 genomes]
rs59853762	0.92[ASN][1000 genomes]
rs60655490	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6435654	0.83[ASN][1000 genomes]
rs6705698	0.85[ASN][1000 genomes]
rs6705988	0.85[ASN][1000 genomes]
rs6710649	0.88[ASN][1000 genomes]
rs6714941	0.90[ASN][1000 genomes]
rs6722300	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6725181	0.83[ASN][1000 genomes]
rs6759039	0.85[ASN][1000 genomes]
rs6759054	0.85[ASN][1000 genomes]
rs7425341	0.90[ASN][1000 genomes]
rs7588697	0.90[ASN][1000 genomes]
rs9798120	0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875783	chr2:212530466-212564895	Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212547200-212568600	Weak transcription	Fetal Kidney	kidney
2	chr2:212550400-212569000	Weak transcription	Fetal Heart	heart
3	chr2:212552400-212558400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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