Variant report

Variant	rs12436381
Chromosome Location	chr14:66021569-66021570
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:66002294..66004964-chr14:66020886..66023654,2	MCF-7	breast:
2	chr14:66020277..66021956-chr14:66022391..66024795,2	MCF-7	breast:

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs10130526	0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10131727	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10138701	1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10143920	0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10149311	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10483777	0.88[CHB][hapmap];0.86[JPT][hapmap];0.98[ASN][1000 genomes]
rs10483783	0.82[EUR][1000 genomes]
rs11844089	1.00[CEU][hapmap]
rs11844728	1.00[CEU][hapmap]
rs11846196	0.82[EUR][1000 genomes]
rs11846827	1.00[CEU][hapmap]
rs11846860	1.00[CEU][hapmap]
rs11847101	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11848647	0.92[EUR][1000 genomes]
rs11849249	0.81[ASN][1000 genomes]
rs11849408	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11849792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11851934	0.82[EUR][1000 genomes]
rs11852179	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12323434	0.96[ASN][1000 genomes]
rs12431562	0.88[CHB][hapmap];0.86[JPT][hapmap];0.98[ASN][1000 genomes]
rs12431772	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs12432032	0.88[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12432422	0.81[ASN][1000 genomes]
rs12432426	0.88[CHB][hapmap];0.86[JPT][hapmap];0.98[ASN][1000 genomes]
rs12433051	0.93[ASN][1000 genomes]
rs12433273	0.88[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12433688	0.88[CHB][hapmap];0.86[JPT][hapmap];0.98[ASN][1000 genomes]
rs12434375	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12434513	0.98[ASN][1000 genomes]
rs12434626	0.93[ASN][1000 genomes]
rs12435809	0.89[ASN][1000 genomes]
rs12435971	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12436349	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12436402	0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12436434	0.98[ASN][1000 genomes]
rs12436482	0.82[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12436677	0.89[ASN][1000 genomes]
rs12436771	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs12437088	0.88[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12437132	0.88[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs17102688	0.88[CHB][hapmap];0.93[ASN][1000 genomes]
rs17102708	0.88[CHB][hapmap];0.86[JPT][hapmap];0.98[ASN][1000 genomes]
rs17102714	1.00[CEU][hapmap]
rs17102760	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs17102783	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs17102807	0.82[EUR][1000 genomes]
rs17102839	0.88[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs17102894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17102898	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs17102910	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17246385	0.89[ASN][1000 genomes]
rs1952605	0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2268965	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs2300863	0.85[ASN][1000 genomes]
rs2300866	0.85[ASN][1000 genomes]
rs2300870	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2898701	0.81[ASN][1000 genomes]
rs4343192	1.00[CEU][hapmap]
rs55648350	0.82[EUR][1000 genomes]
rs55793205	0.92[EUR][1000 genomes]
rs56191137	0.87[EUR][1000 genomes]
rs56192128	0.85[EUR][1000 genomes]
rs56682283	0.82[EUR][1000 genomes]
rs56821971	0.98[ASN][1000 genomes]
rs58087042	0.93[ASN][1000 genomes]
rs58160832	0.93[ASN][1000 genomes]
rs59036531	0.81[ASN][1000 genomes]
rs61417186	0.93[ASN][1000 genomes]
rs61987778	0.81[ASN][1000 genomes]
rs61987981	0.92[EUR][1000 genomes]
rs61987985	0.87[EUR][1000 genomes]
rs61987988	0.82[EUR][1000 genomes]
rs61987989	0.82[EUR][1000 genomes]
rs61987991	0.82[EUR][1000 genomes]
rs61987995	0.82[EUR][1000 genomes]
rs61987996	0.82[EUR][1000 genomes]
rs61988015	0.82[EUR][1000 genomes]
rs61988016	0.82[EUR][1000 genomes]
rs61990026	0.82[EUR][1000 genomes]
rs61990027	0.82[EUR][1000 genomes]
rs6573620	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs7143112	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs7144234	1.00[CEU][hapmap]
rs7153718	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs7155055	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs7160754	1.00[CEU][hapmap]
rs730127	1.00[CEU][hapmap]
rs7342545	1.00[CEU][hapmap]
rs74056775	0.93[ASN][1000 genomes]
rs74056782	0.98[ASN][1000 genomes]
rs74056787	0.98[ASN][1000 genomes]
rs74056794	0.98[ASN][1000 genomes]
rs74056800	0.98[ASN][1000 genomes]
rs74058505	0.98[ASN][1000 genomes]
rs74058525	0.93[ASN][1000 genomes]
rs74058541	0.93[ASN][1000 genomes]
rs8003093	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs8004564	0.81[ASN][1000 genomes]
rs8005892	1.00[CEU][hapmap]
rs8008705	0.82[EUR][1000 genomes]
rs8013098	0.82[EUR][1000 genomes]
rs8018695	0.82[EUR][1000 genomes]
rs8019214	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs956582	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs997794	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
4	nsv1039168	chr14:65811750-66308343	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
5	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
6	nsv456327	chr14:65955517-66052901	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv564951	chr14:65955517-66052901	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv832819	chr14:65957949-66106019	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking 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	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65985000-66025200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr14:65995200-66028000	Weak transcription	Dnd41	blood
3	chr14:65995400-66061000	Weak transcription	Gastric	stomach
4	chr14:66002400-66028000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr14:66003000-66028000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr14:66003400-66028200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:66003800-66041200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr14:66005400-66028400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr14:66008600-66025800	Weak transcription	Primary T cells from cord blood	blood
10	chr14:66008600-66028000	Weak transcription	Primary B cells from cord blood	blood
11	chr14:66013200-66028200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:66014800-66022000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr14:66015200-66033600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr14:66016000-66032800	Weak transcription	Small Intestine	intestine
15	chr14:66016000-66041400	Weak transcription	Ovary	ovary
16	chr14:66016600-66028000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:66016600-66033800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr14:66018200-66031600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr14:66018400-66022800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr14:66018600-66027800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr14:66019200-66021800	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr14:66019200-66023000	Weak transcription	Left Ventricle	heart
23	chr14:66019400-66022200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr14:66019400-66028200	Weak transcription	GM12878-XiMat	blood
25	chr14:66019800-66023000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:66021200-66023200	Enhancers	Brain Hippocampus Middle	brain
27	chr14:66021200-66023400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr14:66021400-66022200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr14:66021400-66022400	Enhancers	Primary B cells from peripheral blood	blood
30	chr14:66021400-66022400	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr14:66021400-66023600	Enhancers	Brain Cingulate Gyrus	brain
32	chr14:66021400-66046400	Weak transcription	Thymus	Thymus

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