Variant report

Variant	rs4933666
Chromosome Location	chr10:93327377-93327378
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:93325037..93327659-chr10:93375294..93378275,2	K562	blood:
2	chr10:93325816..93328522-chr10:93329853..93331382,2	MCF-7	breast:
3	chr10:93327358..93329492-chr10:93329757..93331419,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10881918	0.81[ASN][1000 genomes]
rs10881919	0.81[ASN][1000 genomes]
rs10881923	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11186608	0.87[GIH][hapmap]
rs11186610	0.81[ASN][1000 genomes]
rs11186613	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12241797	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12246543	1.00[CHB][hapmap];0.87[CHD][hapmap];0.81[ASN][1000 genomes]
rs12253464	0.84[CEU][hapmap]
rs12255223	0.81[ASN][1000 genomes]
rs12256369	0.81[ASN][1000 genomes]
rs12256726	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260905	0.89[CEU][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263117	0.89[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12268133	0.90[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.87[GIH][hapmap];0.94[MEX][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1411120	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1411121	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106760	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2094710	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933659	1.00[CHB][hapmap];0.87[CHD][hapmap];0.81[ASN][1000 genomes]
rs4933660	0.81[ASN][1000 genomes]
rs4933661	0.81[ASN][1000 genomes]
rs4933662	0.81[ASN][1000 genomes]
rs4933663	0.81[ASN][1000 genomes]
rs4933665	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933667	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933668	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933669	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56198147	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59997744	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7068979	1.00[CHB][hapmap];0.87[CHD][hapmap];0.87[GIH][hapmap];0.81[ASN][1000 genomes]
rs7074115	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs716361	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.95[GIH][hapmap];0.93[TSI][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72819249	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72819252	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7477129	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7895083	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7908831	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7910891	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs7911125	0.91[ASN][1000 genomes]
rs928118	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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	esv19622	chr10:93305214-93361590	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93315200-93335600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr10:93322800-93328000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr10:93323200-93338000	Weak transcription	HSMMtube	muscle
4	chr10:93323400-93334600	Weak transcription	Pancreas	Pancrea
5	chr10:93323800-93331000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr10:93324400-93341800	Weak transcription	Aorta	Aorta
7	chr10:93325400-93329000	Weak transcription	K562	blood
8	chr10:93325600-93330200	Weak transcription	Psoas Muscle	Psoas
9	chr10:93325800-93328600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr10:93325800-93334800	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr10:93326200-93328600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr10:93326200-93330000	Weak transcription	Fetal Heart	heart
13	chr10:93326200-93334200	Weak transcription	Left Ventricle	heart
14	chr10:93326400-93330000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr10:93326600-93329000	Weak transcription	HepG2	liver
16	chr10:93327000-93327600	Weak transcription	Esophagus	oesophagus
17	chr10:93327200-93327800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr10:93327200-93327800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:93327200-93329600	Enhancers	NHEK	skin

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