Variant report

Variant	rs10857397
Chromosome Location	chr4:143579753-143579754
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	chr4:143577881..143580712-chr4:143582795..143584320,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1017527	0.82[CHD][hapmap]
rs1031104	0.88[CHD][hapmap];0.89[MEX][hapmap];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11100754	0.82[ASN][1000 genomes]
rs1116690	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11723809	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11942731	0.84[YRI][hapmap]
rs11943397	0.87[ASW][hapmap];0.84[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.92[LWK][hapmap];0.94[MEX][hapmap];0.84[MKK][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11944455	0.91[CHB][hapmap];0.88[YRI][hapmap];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12500698	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12508480	0.81[ASN][1000 genomes]
rs12644329	0.82[ASN][1000 genomes]
rs13102191	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13109603	0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13109664	0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13114452	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13119090	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13125362	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13125853	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13133181	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13149611	0.83[CHD][hapmap]
rs1364921	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1364922	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1364923	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1364925	0.93[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];0.93[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1373032	0.81[ASN][1000 genomes]
rs1373041	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1443185	0.83[ASN][1000 genomes]
rs1443186	0.83[ASN][1000 genomes]
rs1443187	0.81[ASN][1000 genomes]
rs1443190	0.83[CHD][hapmap]
rs1443191	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1473222	0.92[CHB][hapmap]
rs1899565	0.83[CEU][hapmap];0.83[CHB][hapmap];0.80[YRI][hapmap];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2017146	0.81[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2083781	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2120158	0.87[ASW][hapmap];0.84[CEU][hapmap];0.83[CHB][hapmap];0.94[CHD][hapmap];0.92[LWK][hapmap];0.94[MEX][hapmap];0.83[MKK][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2165820	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2197216	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2217017	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2874870	0.87[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.89[GIH][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2874871	0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4690699	0.81[ASN][1000 genomes]
rs4975311	0.92[CHB][hapmap];0.81[AMR][1000 genomes]
rs61371792	0.84[ASN][1000 genomes]
rs6537123	0.92[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6830053	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6830886	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6831966	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6839894	0.90[CHB][hapmap];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7434705	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7437824	0.81[ASN][1000 genomes]
rs7441478	0.92[ASN][1000 genomes]
rs7675305	0.83[CHD][hapmap]
rs7680076	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7680631	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7682731	0.83[CHD][hapmap]
rs7688435	0.82[CHD][hapmap]
rs7695514	0.82[CHB][hapmap];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7698691	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs978361	0.88[CHD][hapmap]
rs979194	0.92[YRI][hapmap];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs979195	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs979196	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830101	chr4:143518810-143684392	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143574400-143583800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:143575400-143583800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:143575600-143582400	ZNF genes & repeats	Dnd41	blood
4	chr4:143575800-143579800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:143576200-143579800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
6	chr4:143577200-143580000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
7	chr4:143578600-143579800	Weak transcription	Left Ventricle	heart
8	chr4:143578600-143600600	Weak transcription	Fetal Heart	heart
9	chr4:143579200-143582400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
10	chr4:143579600-143580000	ZNF genes & repeats	Stomach Smooth Muscle	stomach

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