Variant report

Variant	rs7422204
Chromosome Location	chr2:77192765-77192766
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10177731	0.89[CHB][hapmap]
rs10187466	0.85[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10191141	0.94[CHB][hapmap]
rs10192262	1.00[ASW][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];0.98[GIH][hapmap];0.87[JPT][hapmap];0.92[LWK][hapmap];0.85[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10198799	0.85[YRI][hapmap]
rs10201530	0.85[LWK][hapmap];0.81[TSI][hapmap];0.85[YRI][hapmap]
rs10520176	0.88[CHB][hapmap]
rs11126575	0.84[CEU][hapmap];0.85[YRI][hapmap]
rs11126576	0.84[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11896560	0.84[CEU][hapmap];0.88[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11896587	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12621674	0.94[CHB][hapmap];0.82[CHD][hapmap];0.81[JPT][hapmap]
rs12987907	0.81[TSI][hapmap]
rs13385651	0.81[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]
rs13385727	0.81[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]
rs13385839	0.94[CHB][hapmap]
rs13393238	0.94[CHB][hapmap]
rs13416719	0.81[CHB][hapmap]
rs13422716	0.81[CEU][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];0.98[GIH][hapmap];0.87[JPT][hapmap];0.85[MEX][hapmap];0.93[TSI][hapmap]
rs1446710	0.80[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.87[JPT][hapmap];0.81[TSI][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1446712	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1446724	0.86[GIH][hapmap];0.81[TSI][hapmap]
rs1446725	0.86[GIH][hapmap];0.81[TSI][hapmap]
rs1470503	0.88[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap]
rs1470504	0.86[GIH][hapmap];0.81[TSI][hapmap]
rs1470506	0.80[CEU][hapmap]
rs17013340	0.94[CHB][hapmap]
rs17013341	0.89[CHB][hapmap]
rs17013455	0.94[CHB][hapmap];0.87[CHD][hapmap]
rs1929452	0.94[CHB][hapmap]
rs1997468	0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]
rs2028913	0.81[TSI][hapmap]
rs2065375	0.94[CHB][hapmap];0.81[CHD][hapmap]
rs2178574	0.94[CHB][hapmap]
rs2860872	0.88[CHB][hapmap];0.89[GIH][hapmap]
rs2860934	0.83[CHB][hapmap]
rs4143794	0.94[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4143796	0.80[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.87[JPT][hapmap];0.81[TSI][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4853283	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6547104	0.88[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6719689	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6751097	0.94[CHB][hapmap]
rs727000	0.82[GIH][hapmap];0.83[MKK][hapmap];0.81[TSI][hapmap]
rs7563917	0.89[CHB][hapmap];0.86[CHD][hapmap];0.91[GIH][hapmap];0.81[JPT][hapmap];0.94[MKK][hapmap];0.81[TSI][hapmap]
rs7586363	0.82[CHB][hapmap];1.00[YRI][hapmap]
rs7592470	0.94[CHB][hapmap];0.84[CHD][hapmap]
rs7592608	0.94[CHB][hapmap]
rs7597923	0.83[MKK][hapmap];0.81[TSI][hapmap]
rs7601256	0.88[CEU][hapmap];0.85[EUR][1000 genomes]
rs9309508	0.84[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9309509	0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs953854	0.94[CHB][hapmap]
rs992313	0.85[CEU][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];0.89[GIH][hapmap];0.88[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv874328	chr2:77096124-77196122	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv874329	chr2:77096124-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv874330	chr2:77103719-77209750	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	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
9	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
10	nsv818054	chr2:77172693-77192765	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1008307	chr2:77174354-77197565	Weak transcription Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv2756931	chr2:77185856-77209051	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv2759066	chr2:77185856-77209051	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7422204	MRPL19	cis	cerebellum	SCAN

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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