Variant report

Variant	rs38902
Chromosome Location	chr7:116889718-116889719
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:116696376..116698519-chr7:116888439..116890411,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10226248	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10226864	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10235236	0.92[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10245615	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10254103	0.85[ASN][1000 genomes]
rs10255896	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10256129	0.92[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10271623	0.95[ASN][1000 genomes]
rs10280067	0.92[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10953839	0.95[ASN][1000 genomes]
rs11981089	1.00[ASW][hapmap];0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12706145	1.00[CEU][hapmap];0.90[CHD][hapmap];0.85[GIH][hapmap];0.84[JPT][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13224335	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13227482	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13246951	0.84[ASN][1000 genomes]
rs1468655	0.95[ASN][1000 genomes]
rs1860698	0.95[ASN][1000 genomes]
rs2402176	0.88[ASN][1000 genomes]
rs34911130	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs38904	0.87[TSI][hapmap]
rs38905	0.87[TSI][hapmap]
rs38909	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs38911	0.87[TSI][hapmap]
rs38916	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4727845	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4730773	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4730775	0.96[CEU][hapmap];0.82[CHD][hapmap];0.82[MEX][hapmap];0.84[TSI][hapmap];0.84[EUR][1000 genomes]
rs6466605	0.92[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6466606	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6466607	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6942558	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6944152	0.84[ASN][1000 genomes]
rs6947786	0.95[ASN][1000 genomes]
rs6950776	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6951125	0.96[CEU][hapmap];0.87[CHD][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6958283	0.92[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6965467	0.83[CHD][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs6968768	0.95[ASN][1000 genomes]
rs6974937	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6975501	0.95[ASN][1000 genomes]
rs718738	0.95[ASN][1000 genomes]
rs739693	0.85[ASN][1000 genomes]
rs7457422	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs7776963	0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7795841	0.84[ASN][1000 genomes]
rs7802930	0.92[ASN][1000 genomes]
rs887573	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9691008	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9692365	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831108	chr7:116749534-116952011	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv516761	chr7:116888161-116892846	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116888000-116890200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:116888000-116892400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:116888600-116889800	Enhancers	NHLF	lung
4	chr7:116888800-116890200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:116888800-116891200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:116888800-116892600	Enhancers	NHDF-Ad	bronchial
7	chr7:116888800-116892600	Enhancers	Osteobl	bone
8	chr7:116889200-116890800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:116889400-116890600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:116889400-116892600	Enhancers	GM12878-XiMat	blood
11	chr7:116889600-116890600	Weak transcription	Placenta	Placenta

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