Variant report

Variant	rs72485022
Chromosome Location	chr10:26976456-26976457
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:26973781..26976716-chr10:26986143..26988490,2	K562	blood:
2	chr10:26972585..26978071-chr10:26984536..26988033,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000148459	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10128125	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10128192	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10829048	1.00[ASN][1000 genomes]
rs11015220	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015226	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015230	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11015233	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11015234	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11816510	0.83[ASN][1000 genomes]
rs11818450	0.83[ASN][1000 genomes]
rs12242239	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12242414	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12245051	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12246285	1.00[ASN][1000 genomes]
rs12247299	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12247597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12252298	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12252358	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12252368	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12255583	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12255942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260035	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260298	1.00[ASN][1000 genomes]
rs12260466	0.96[ASN][1000 genomes]
rs12262082	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12262401	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263262	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263578	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12264509	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12265505	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12265633	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12265746	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12267744	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12268883	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12269520	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17754039	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17754051	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1980754	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2005120	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2477276	0.81[ASN][1000 genomes]
rs2489564	0.81[ASN][1000 genomes]
rs34314417	0.96[ASN][1000 genomes]
rs34901510	1.00[ASN][1000 genomes]
rs35534478	1.00[ASN][1000 genomes]
rs35687107	1.00[ASN][1000 genomes]
rs35827769	1.00[ASN][1000 genomes]
rs4309054	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7097696	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72481186	1.00[AMR][1000 genomes]
rs72485013	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72485015	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485017	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485018	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485023	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72485026	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs753705	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7899631	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7900674	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7906473	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7920279	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv3333006	chr10:26908323-26985227	Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3415799	chr10:26929831-27233591	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	esv1798973	chr10:26968171-27001814	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv550233	chr10:26968171-27011323	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv947779	chr10:26974259-26977316	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26973000-26978000	Weak transcription	Dnd41	blood
2	chr10:26974200-26978600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr10:26974400-26978200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr10:26974400-26978200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr10:26975200-26977200	Enhancers	Fetal Thymus	thymus
6	chr10:26975200-26977600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr10:26975400-26977800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr10:26975400-26978200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr10:26975600-26977800	Weak transcription	Thymus	Thymus

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