Variant report

Variant	rs6703980
Chromosome Location	chr1:212350975-212350976
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	chr1:212347420..212350421-chr1:212350572..212353527,5	K562	blood:
2	chr1:212350500..212353669-chr1:212356287..212359186,4	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10863948	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10863951	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10863961	1.00[JPT][hapmap]
rs10863963	1.00[JPT][hapmap]
rs11119869	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11119870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11119871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11119872	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11119876	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11119877	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11119878	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11119889	0.84[TSI][hapmap]
rs11119919	1.00[JPT][hapmap]
rs11119920	1.00[JPT][hapmap]
rs11576437	1.00[JPT][hapmap]
rs11580285	1.00[JPT][hapmap]
rs11587555	1.00[JPT][hapmap]
rs11588867	1.00[JPT][hapmap]
rs11589817	1.00[JPT][hapmap]
rs12082507	0.84[TSI][hapmap]
rs12085064	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12086905	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12096035	1.00[JPT][hapmap]
rs12726409	1.00[JPT][hapmap]
rs12727947	1.00[JPT][hapmap]
rs12728266	1.00[JPT][hapmap]
rs12734895	1.00[JPT][hapmap]
rs12736502	1.00[JPT][hapmap]
rs12743785	0.82[JPT][hapmap]
rs12745269	1.00[JPT][hapmap]
rs12756678	1.00[JPT][hapmap]
rs1470390	1.00[JPT][hapmap]
rs1493600	1.00[JPT][hapmap]
rs17721302	1.00[JPT][hapmap]
rs2120770	1.00[JPT][hapmap]
rs2358454	1.00[JPT][hapmap]
rs6661987	1.00[JPT][hapmap]
rs6667199	1.00[JPT][hapmap]
rs6691330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7518399	1.00[JPT][hapmap]
rs7531219	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999738	chr1:212218618-212513690	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1009376	chr1:212292357-212680320	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv549139	chr1:212332294-212876902	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212336800-212359600	Weak transcription	Dnd41	blood
2	chr1:212340800-212351600	Weak transcription	Left Ventricle	heart
3	chr1:212345600-212352600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:212350600-212359600	Weak transcription	K562	blood

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