Variant report

Variant	rs10212191
Chromosome Location	chr3:43067138-43067139
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:43059886..43061659-chr3:43065331..43067767,2	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10510736	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13080201	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs13087788	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs1392319	0.84[YRI][hapmap]
rs17390473	0.81[CHB][hapmap];0.86[ASN][1000 genomes]
rs17455509	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs17455760	0.81[CHB][hapmap]
rs17469719	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs2001682	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2062517	0.92[CHB][hapmap]
rs28435122	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28548208	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2948619	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35110063	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3953390	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs531888	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs532792	0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55701670	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62247060	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62247061	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62247062	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6442134	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs644534	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67186096	0.86[ASN][1000 genomes]
rs6764648	0.81[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6783218	0.92[CEU][hapmap];0.87[CHB][hapmap];0.84[JPT][hapmap];0.84[EUR][1000 genomes]
rs6793871	0.92[CEU][hapmap];0.81[CHB][hapmap];0.85[EUR][1000 genomes]
rs6794402	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6806427	0.81[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs704918	0.82[ASN][1000 genomes]
rs7616750	0.81[CHB][hapmap]
rs7619227	0.81[CHB][hapmap]
rs7624799	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs7633590	0.80[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7634125	0.81[CHB][hapmap]
rs7637698	0.81[CHB][hapmap]
rs7643433	1.00[CEU][hapmap];0.87[CHB][hapmap];0.84[JPT][hapmap];0.89[YRI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs834177	0.81[CEU][hapmap];1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs872126	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9311332	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9812262	1.00[CEU][hapmap];0.87[CHB][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9816391	0.88[YRI][hapmap]
rs9821320	0.92[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9828785	0.83[YRI][hapmap]
rs9848904	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9858123	0.87[EUR][1000 genomes]
rs9863179	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9870478	0.88[YRI][hapmap]
rs9872107	0.83[EUR][1000 genomes]
rs9874514	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460522	chr3:42967597-43175207	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv590149	chr3:42967597-43175207	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv432417	chr3:43045796-43098296	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43053600-43073200	Weak transcription	Right Atrium	heart
2	chr3:43059600-43074400	Weak transcription	Lung	lung
3	chr3:43059600-43084600	Weak transcription	Pancreas	Pancrea
4	chr3:43060800-43069600	Weak transcription	Stomach Mucosa	stomach
5	chr3:43061000-43072200	Weak transcription	Liver	Liver
6	chr3:43061000-43080200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:43061800-43073000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr3:43063000-43077400	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:43063400-43072000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr3:43063600-43072600	Weak transcription	Fetal Muscle Leg	muscle
11	chr3:43063600-43084800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr3:43064000-43077800	Weak transcription	Brain Substantia Nigra	brain
13	chr3:43064800-43067400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:43065000-43067200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr3:43065200-43072400	Weak transcription	Placenta	Placenta
16	chr3:43065400-43084400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:43065800-43067400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:43065800-43067800	Enhancers	Primary T cells fromperipheralblood	blood
19	chr3:43065800-43067800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr3:43066000-43067200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr3:43066000-43068000	Enhancers	Fetal Thymus	thymus
22	chr3:43066200-43067800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:43066200-43068000	Enhancers	Thymus	Thymus
24	chr3:43066200-43068200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr3:43066200-43068200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr3:43066400-43067400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:43066400-43067600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:43066400-43067600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr3:43066400-43068200	Enhancers	Primary T cells from cord blood	blood
30	chr3:43066400-43068200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr3:43066400-43068200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr3:43066600-43067400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:43066600-43067600	Enhancers	Dnd41	blood
34	chr3:43066600-43067800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:43066600-43068000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr3:43066800-43067400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:43066800-43067600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr3:43067000-43067200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr3:43067000-43067400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:43067000-43067800	Enhancers	Gastric	stomach
41	chr3:43067000-43068400	Weak transcription	Fetal Intestine Small	intestine

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