Variant report

Variant	rs3805352
Chromosome Location	chr14:36787516-36787517
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TCF7L2	chr14:36786926-36787538	HEK293	kidney:	n/a	chr14:36786992-36787001 chr14:36787085-36787101 chr14:36787162-36787169 chr14:36787085-36787099 chr14:36787085-36787101 chr14:36787162-36787172 chr14:36787086-36787100 chr14:36787161-36787170
2	FOS	chr14:36786587-36787607	MCF10A-Er-Src	breast:	n/a	chr14:36786990-36787002 chr14:36786991-36787001 chr14:36786992-36787001 chr14:36786992-36787000 chr14:36786990-36787001 chr14:36787047-36787056 chr14:36786993-36787000

No.	Distal block	Cell Line	Cell type
1	chr14:36780477..36782487-chr14:36786743..36788959,2	MCF-7	breast:
2	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
3	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
4	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:

Variant related genes	Relation type
MBIP	TF binding region
ENSG00000151332	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10133125	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10139030	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11156909	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11558802	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11844502	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12884915	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12890888	0.95[EUR][1000 genomes]
rs12897795	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1535722	0.85[EUR][1000 genomes]
rs17104430	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2415332	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[EUR][1000 genomes]
rs2415334	0.86[ASN][1000 genomes]
rs2415335	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2415339	0.83[EUR][1000 genomes]
rs2553575	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2899849	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3168891	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3742592	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs3762904	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3805353	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805354	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805355	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3842844	1.00[EUR][1000 genomes]
rs3844012	0.81[EUR][1000 genomes]
rs3844013	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3850257	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3850258	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3850259	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3850260	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3850267	0.95[EUR][1000 genomes]
rs3850268	0.95[EUR][1000 genomes]
rs3861477	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3861481	0.95[EUR][1000 genomes]
rs3909608	0.95[EUR][1000 genomes]
rs3909615	0.91[EUR][1000 genomes]
rs4083518	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4127807	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4378535	0.88[EUR][1000 genomes]
rs4898561	0.91[EUR][1000 genomes]
rs4898563	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4898597	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4898598	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4900716	0.91[EUR][1000 genomes]
rs4900717	0.91[EUR][1000 genomes]
rs4900732	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4900733	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4900790	0.91[EUR][1000 genomes]
rs4900833	0.82[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4900924	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4901456	1.00[EUR][1000 genomes]
rs4901597	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes]
rs6571742	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7140630	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7141354	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7142835	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7142956	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7146921	0.81[EUR][1000 genomes]
rs7154340	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7155498	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157811	1.00[EUR][1000 genomes]
rs7159366	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8013261	0.86[EUR][1000 genomes]
rs9788479	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040256	chr14:36501452-37172046	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv542040	chr14:36501452-37172046	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv1047290	chr14:36564568-37445157	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
4	nsv1037952	chr14:36670484-37294692	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
5	nsv542042	chr14:36670484-37294692	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	esv3429093	chr14:36674701-36827119	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	esv3367425	chr14:36674721-36827089	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1042408	chr14:36693910-36810554	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv542043	chr14:36693910-36810554	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv534143	chr14:36747497-36787893	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	esv2752577	chr14:36768276-36805529	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1040487	chr14:36770813-36805621	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv832771	chr14:36771007-36964041	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv1054427	chr14:36780743-36819931	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv518747	chr14:36787226-36809926	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36765400-36788800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:36766600-36788000	Weak transcription	Fetal Heart	heart
3	chr14:36767400-36789200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:36767400-36789200	Weak transcription	Spleen	Spleen
5	chr14:36772600-36788800	Weak transcription	Stomach Mucosa	stomach
6	chr14:36773400-36789200	Weak transcription	Esophagus	oesophagus
7	chr14:36779200-36788600	Weak transcription	Fetal Intestine Small	intestine
8	chr14:36779400-36789000	Weak transcription	Colonic Mucosa	Colon
9	chr14:36780400-36788800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr14:36780400-36789200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:36780400-36789200	Weak transcription	Small Intestine	intestine
12	chr14:36780600-36788400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:36780600-36788400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr14:36780600-36788400	Weak transcription	Fetal Stomach	stomach
15	chr14:36780600-36788600	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr14:36780600-36788600	Weak transcription	Colon Smooth Muscle	Colon
17	chr14:36780600-36789200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:36780800-36788000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr14:36780800-36788000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr14:36780800-36788400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr14:36780800-36788400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr14:36780800-36788600	Weak transcription	Thymus	Thymus
23	chr14:36781000-36787800	Weak transcription	NHDF-Ad	bronchial
24	chr14:36781000-36787800	Weak transcription	NHLF	lung
25	chr14:36781000-36788000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr14:36781000-36788000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr14:36781000-36788000	Weak transcription	Fetal Brain Male	brain
28	chr14:36781000-36788400	Weak transcription	Fetal Kidney	kidney
29	chr14:36781000-36788400	Weak transcription	Fetal Muscle Leg	muscle
30	chr14:36781000-36788400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr14:36781000-36788600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr14:36781000-36788600	Weak transcription	Aorta	Aorta
33	chr14:36781000-36788600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr14:36781000-36788600	Weak transcription	Ovary	ovary
35	chr14:36781000-36788600	Weak transcription	Psoas Muscle	Psoas
36	chr14:36781000-36788600	Weak transcription	Rectal Smooth Muscle	rectum
37	chr14:36781000-36788600	Weak transcription	HSMMtube	muscle
38	chr14:36781000-36788800	Weak transcription	Right Ventricle	heart
39	chr14:36781000-36789000	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr14:36781000-36789200	Weak transcription	Gastric	stomach
41	chr14:36781000-36789200	Weak transcription	Left Ventricle	heart
42	chr14:36781000-36789200	Weak transcription	Lung	lung
43	chr14:36781000-36789200	Weak transcription	Pancreas	Pancrea
44	chr14:36781200-36788400	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr14:36781200-36788600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr14:36781200-36788600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr14:36783000-36788200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:36783000-36788600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:36783200-36787800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:36783200-36788200	Weak transcription	Monocytes-CD14+_RO01746	blood

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