Variant report

Variant	rs159705
Chromosome Location	chr12:29750547-29750548
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10400534	0.89[CHB][hapmap]
rs10400541	0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs10771545	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs10771546	0.90[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10771547	0.85[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10771549	0.83[ASN][1000 genomes]
rs10843443	0.82[ASN][1000 genomes]
rs10843446	0.90[ASN][1000 genomes]
rs11050270	0.90[CHB][hapmap];0.96[JPT][hapmap]
rs11050271	0.91[CHB][hapmap];0.96[JPT][hapmap]
rs11050273	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs11050278	0.91[CHB][hapmap];0.96[JPT][hapmap];0.87[ASN][1000 genomes]
rs11050280	0.90[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs11050281	0.81[CHB][hapmap];0.87[ASN][1000 genomes]
rs11050288	0.89[ASN][1000 genomes]
rs11050291	0.89[ASN][1000 genomes]
rs11050292	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs11050293	0.95[CHB][hapmap];0.96[JPT][hapmap];0.89[ASN][1000 genomes]
rs11050295	0.89[ASN][1000 genomes]
rs11050296	0.89[ASN][1000 genomes]
rs11050297	0.94[CHB][hapmap];0.90[JPT][hapmap];0.88[ASN][1000 genomes]
rs11050298	0.86[ASN][1000 genomes]
rs11050299	0.95[CHB][hapmap];0.96[JPT][hapmap];0.90[ASN][1000 genomes]
rs11050300	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs11050301	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs11050302	0.95[CHB][hapmap];0.96[JPT][hapmap];0.90[ASN][1000 genomes]
rs11050319	0.95[CEU][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11611194	0.91[CHB][hapmap];0.96[JPT][hapmap];0.85[ASN][1000 genomes]
rs12368037	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12371221	0.91[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs12579805	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12581671	0.85[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12810291	0.89[ASN][1000 genomes]
rs12819780	1.00[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12820673	0.82[ASN][1000 genomes]
rs1326758	0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs1409616	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1409617	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs159696	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs159701	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs159703	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs159704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs159707	1.00[CEU][hapmap];0.95[CHB][hapmap];0.96[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs159708	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159709	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs159714	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs159715	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1988548	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs2060569	0.83[ASN][1000 genomes]
rs2113879	0.83[JPT][hapmap]
rs2113880	0.83[JPT][hapmap]
rs2182547	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2288131	0.90[CHB][hapmap]
rs2288132	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs2288133	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs2350532	0.83[JPT][hapmap]
rs2478469	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2478470	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2553077	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2766605	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2766606	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs299444	0.85[CHB][hapmap]
rs299445	0.85[CHB][hapmap]
rs299455	0.90[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs299456	0.90[CHB][hapmap]
rs299459	0.90[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs299462	0.80[JPT][hapmap]
rs299463	0.81[JPT][hapmap]
rs299465	0.83[JPT][hapmap]
rs299466	0.80[JPT][hapmap]
rs299472	0.83[JPT][hapmap]
rs299475	0.81[JPT][hapmap]
rs34020170	0.87[ASN][1000 genomes]
rs34187264	0.87[ASN][1000 genomes]
rs34555972	0.87[ASN][1000 genomes]
rs35111056	0.82[ASN][1000 genomes]
rs35536095	0.90[ASN][1000 genomes]
rs35741143	0.80[ASN][1000 genomes]
rs375109	0.83[ASN][1000 genomes]
rs4931201	0.91[CHB][hapmap];0.96[JPT][hapmap];0.82[ASN][1000 genomes]
rs60500145	0.90[ASN][1000 genomes]
rs7294502	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs7295284	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7301491	0.91[CHB][hapmap];0.96[JPT][hapmap];0.83[ASN][1000 genomes]
rs7306397	0.83[ASN][1000 genomes]
rs7310555	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs7310895	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs7314549	0.84[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs7971202	0.83[ASN][1000 genomes]
rs9300191	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs9738399	0.92[ASN][1000 genomes]
rs994172	1.00[CEU][hapmap];0.91[CHB][hapmap];0.96[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv469190	chr12:29612425-29811471	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv557917	chr12:29612425-29811471	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv1053629	chr12:29680163-29826626	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv529328	chr12:29692414-30246209	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1051913	chr12:29741676-29770807	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29709800-29756200	Weak transcription	HMEC	breast
2	chr12:29716200-29764800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:29726000-29751400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:29731800-29769600	Weak transcription	Hela-S3	cervix
5	chr12:29736000-29752200	Weak transcription	HSMM	muscle
6	chr12:29736800-29762800	Weak transcription	Fetal Stomach	stomach
7	chr12:29737200-29761800	Weak transcription	Right Ventricle	heart
8	chr12:29737200-29762400	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:29737200-29762800	Weak transcription	Psoas Muscle	Psoas
10	chr12:29742800-29752200	Weak transcription	HSMMtube	muscle
11	chr12:29743200-29751800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr12:29743200-29769800	Weak transcription	NHLF	lung
13	chr12:29744400-29790800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr12:29744600-29752600	Weak transcription	Left Ventricle	heart
15	chr12:29744600-29754200	Weak transcription	Brain Anterior Caudate	brain
16	chr12:29744600-29765400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr12:29744600-29791000	Weak transcription	Fetal Muscle Leg	muscle
18	chr12:29744800-29764600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr12:29744800-29778200	Weak transcription	Ovary	ovary
20	chr12:29745200-29751000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:29745200-29751600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:29745200-29755000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr12:29745200-29762000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:29745400-29752000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:29746000-29751000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr12:29746200-29752200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr12:29746200-29757200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:29746200-29762200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr12:29746400-29750800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr12:29746400-29751000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr12:29747000-29757800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr12:29747400-29756400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr12:29748600-29751800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr12:29748600-29751800	Weak transcription	Adipose Nuclei	Adipose
35	chr12:29748600-29762600	Weak transcription	Spleen	Spleen
36	chr12:29749000-29751800	Weak transcription	Liver	Liver
37	chr12:29749200-29753600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr12:29749400-29752000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:29749800-29751800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:29750000-29751600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr12:29750000-29762200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr12:29750200-29752000	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr12:29750400-29750600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:29750400-29757000	Weak transcription	Aorta	Aorta
45	chr12:29750400-29762600	Weak transcription	Stomach Smooth Muscle	stomach

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