Variant report

Variant	rs2860934
Chromosome Location	chr2:77200916-77200917
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10177731	0.89[CHB][hapmap]
rs10183619	0.82[EUR][1000 genomes]
rs10183642	0.82[EUR][1000 genomes]
rs10186912	0.82[EUR][1000 genomes]
rs10187466	0.89[CHB][hapmap];0.96[ASN][1000 genomes]
rs10191141	0.89[CHB][hapmap]
rs10192262	0.89[CHB][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10196630	0.82[EUR][1000 genomes]
rs10196749	0.81[EUR][1000 genomes]
rs10196758	0.81[EUR][1000 genomes]
rs10196801	0.82[EUR][1000 genomes]
rs10196895	0.82[EUR][1000 genomes]
rs10196939	0.82[EUR][1000 genomes]
rs10520176	0.84[CHB][hapmap]
rs11126576	0.89[CHB][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11896560	0.83[CHB][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11896587	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12621674	0.89[CHB][hapmap];0.83[EUR][1000 genomes]
rs13385651	0.89[CHB][hapmap]
rs13385727	0.89[CHB][hapmap]
rs13385839	0.89[CHB][hapmap]
rs13393238	0.89[CHB][hapmap]
rs13422716	0.89[CHB][hapmap]
rs13427438	0.82[EUR][1000 genomes]
rs13427514	0.82[EUR][1000 genomes]
rs1446710	0.88[CHB][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1446712	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1470503	0.89[CHB][hapmap]
rs1470504	0.82[EUR][1000 genomes]
rs1470505	0.82[EUR][1000 genomes]
rs1470506	0.87[CHB][hapmap];0.82[EUR][1000 genomes]
rs1470507	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1470508	0.82[EUR][1000 genomes]
rs1584235	0.82[EUR][1000 genomes]
rs1584236	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1584237	0.82[EUR][1000 genomes]
rs17013340	0.89[CHB][hapmap]
rs17013341	0.89[CHB][hapmap]
rs17013455	0.89[CHB][hapmap]
rs1838880	0.80[EUR][1000 genomes]
rs1838881	0.80[EUR][1000 genomes]
rs1929452	0.89[CHB][hapmap]
rs1997468	0.89[CHB][hapmap]
rs2065375	0.89[CHB][hapmap]
rs2121410	0.82[EUR][1000 genomes]
rs2121411	0.82[EUR][1000 genomes]
rs2178574	0.89[CHB][hapmap]
rs2860872	0.84[CHB][hapmap]
rs2860937	0.82[EUR][1000 genomes]
rs2901812	0.80[EUR][1000 genomes]
rs34372910	0.81[EUR][1000 genomes]
rs4143794	0.89[CHB][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4143796	0.89[CHB][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4853283	0.89[CHB][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56314043	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6547104	0.83[CHB][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6547110	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6719689	0.89[CHB][hapmap];0.88[ASN][1000 genomes]
rs6751097	0.89[CHB][hapmap]
rs7422204	0.83[CHB][hapmap]
rs7561361	0.81[EUR][1000 genomes]
rs7563917	0.83[CHB][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7586363	0.84[CHB][hapmap]
rs7592470	0.89[CHB][hapmap]
rs7592608	0.89[CHB][hapmap]
rs9309508	0.89[CHB][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9309509	0.89[CHB][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs953854	0.89[CHB][hapmap]
rs992313	0.89[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874322	chr2:77031247-77209750	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv2752990	chr2:77038541-77217310	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv874324	chr2:77048896-77201916	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv874327	chr2:77085752-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv874329	chr2:77096124-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv874330	chr2:77103719-77209750	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv834266	chr2:77120236-77287504	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv949670	chr2:77125218-77712607	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	esv2756931	chr2:77185856-77209051	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv2759066	chr2:77185856-77209051	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv3382201	chr2:77199044-77203242	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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