Variant report

Variant	rs229965
Chromosome Location	chr5:57014300-57014301
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	chr5:57012903..57015556-chr5:57025615..57027382,2	MCF-7	breast:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10057570	0.93[AFR][1000 genomes]
rs10057880	1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs10072292	1.00[YRI][hapmap]
rs10077005	1.00[AFR][1000 genomes]
rs10487613	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10487614	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12520986	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13185580	1.00[AFR][1000 genomes]
rs1347071	1.00[YRI][hapmap]
rs170740	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs170741	0.93[AFR][1000 genomes]
rs1821210	1.00[YRI][hapmap]
rs183477	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1861052	0.81[AFR][1000 genomes]
rs1861059	1.00[YRI][hapmap]
rs2017201	1.00[AFR][1000 genomes]
rs2041678	1.00[AFR][1000 genomes]
rs2161500	0.81[AFR][1000 genomes]
rs2191445	1.00[AFR][1000 genomes]
rs2191446	1.00[AFR][1000 genomes]
rs2191448	1.00[AFR][1000 genomes]
rs2215420	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs229960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs229961	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs229963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs230846	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs230853	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs230860	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs230861	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2408849	1.00[AFR][1000 genomes]
rs2408850	0.86[AFR][1000 genomes]
rs2408854	1.00[YRI][hapmap]
rs2568537	1.00[YRI][hapmap]
rs2898028	1.00[AFR][1000 genomes]
rs4235474	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4403130	1.00[YRI][hapmap]
rs4458541	1.00[YRI][hapmap]
rs4508990	0.86[AFR][1000 genomes]
rs4699910	1.00[AFR][1000 genomes]
rs4699913	1.00[YRI][hapmap]
rs4700214	1.00[AFR][1000 genomes]
rs4700233	1.00[YRI][hapmap]
rs6450430	0.82[EUR][1000 genomes]
rs6450431	1.00[AFR][1000 genomes]
rs6866242	0.86[AFR][1000 genomes]
rs6886241	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7726732	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7732108	1.00[AFR][1000 genomes]
rs7737409	0.86[AFR][1000 genomes]
rs854036	1.00[YRI][hapmap]
rs917655	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs986101	1.00[AFR][1000 genomes]
rs991727	1.00[AFR][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	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2756302	chr5:56978143-57180143	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830310	chr5:56989346-57176006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2763454	chr5:57006531-57161140	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57009800-57016400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:57009800-57016400	Weak transcription	Aorta	Aorta
3	chr5:57012400-57017800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:57012800-57020000	Weak transcription	NHEK	skin
5	chr5:57013200-57015400	Enhancers	HepG2	liver
6	chr5:57013400-57014400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:57013400-57014800	Enhancers	Liver	Liver
8	chr5:57013400-57014800	Enhancers	NHLF	lung
9	chr5:57013400-57015400	Enhancers	NHDF-Ad	bronchial
10	chr5:57013600-57014800	Enhancers	Hela-S3	cervix
11	chr5:57013600-57015200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:57013600-57015200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:57013600-57015400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:57013800-57014600	Weak transcription	HSMM	muscle
15	chr5:57013800-57015000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:57014000-57014400	Enhancers	Osteobl	bone
17	chr5:57014000-57015000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr5:57014200-57016200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr5:57014200-57016400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr5:57014200-57016600	Enhancers	A549	lung

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