Variant report

Variant	rs2468067
Chromosome Location	chr15:45031347-45031348
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:45003364..45004905-chr15:45029799..45032305,2	MCF-7	breast:
2	chr15:44954304..44956887-chr15:45029224..45032187,2	K562	blood:

Variant related genes	Relation type
ENSG00000229474	Chromatin interaction
ENSG00000104133	Chromatin interaction
ENSG00000166710	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10163110	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10444818	0.89[ASN][1000 genomes]
rs1137516	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11634059	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11634063	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11639157	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12912870	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1630168	0.94[EUR][1000 genomes]
rs1669833	0.94[EUR][1000 genomes]
rs1690313	0.81[EUR][1000 genomes]
rs16974543	0.94[EUR][1000 genomes]
rs1720723	0.94[EUR][1000 genomes]
rs1720724	0.94[EUR][1000 genomes]
rs1869125	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1901530	0.81[EUR][1000 genomes]
rs1901538	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1993152	0.94[ASN][1000 genomes]
rs1993153	0.94[ASN][1000 genomes]
rs2084835	0.96[ASN][1000 genomes]
rs2167595	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2470908	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2470913	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2960206	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3100140	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3100141	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3110677	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3759878	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3759881	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4923990	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4923991	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4923993	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62024991	0.81[EUR][1000 genomes]
rs62025968	1.00[EUR][1000 genomes]
rs62025969	0.97[EUR][1000 genomes]
rs6416439	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6416440	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6493110	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6493111	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6493112	0.94[ASN][1000 genomes]
rs6493114	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6493116	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6493118	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6493119	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6493124	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6493125	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6493126	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6493127	0.94[EUR][1000 genomes]
rs6493128	1.00[EUR][1000 genomes]
rs7151	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7165535	0.93[ASN][1000 genomes]
rs7168090	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7172357	1.00[EUR][1000 genomes]
rs7172376	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7496437	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7496559	0.94[EUR][1000 genomes]
rs7497862	0.84[ASN][1000 genomes]
rs8035787	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8036223	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8038532	0.97[EUR][1000 genomes]
rs935885	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs935888	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs935889	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3386433	chr15:44654644-45037538	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	135 gene(s)	inside rSNPs	diseases
2	esv2758380	chr15:44968868-45422842	Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
3	esv2760029	chr15:44968868-45422842	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
4	nsv832990	chr15:44990765-45162714	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45024200-45032200	Weak transcription	Right Atrium	heart
2	chr15:45028800-45031400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr15:45028800-45031600	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr15:45029000-45031400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr15:45029000-45031400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr15:45029000-45031600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr15:45029000-45032600	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr15:45030800-45031400	Enhancers	Primary T cells from cord blood	blood
9	chr15:45031000-45031400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr15:45031000-45031400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:45031200-45031400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:45031200-45031400	Enhancers	HMEC	breast
13	chr15:45031200-45032400	Weak transcription	Primary T helper cells PMA-I stimulated	--

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