Variant report

Variant	rs3750656
Chromosome Location	chr10:5926034-5926035
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:5852595..5861125-chr10:5921136..5936216,31	MCF-7	breast:
2	chr10:5915609..5918597-chr10:5924591..5926431,2	K562	blood:
3	chr10:5912111..5919800-chr10:5923492..5927477,10	MCF-7	breast:
4	chr10:5914288..5916815-chr10:5925333..5927218,2	MCF-7	breast:
5	chr10:5925580..5929335-chr10:5933926..5939138,5	K562	blood:

Variant related genes	Relation type
ENSG00000134452	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000272764	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11592964	1.00[AFR][1000 genomes]
rs11594153	1.00[AFR][1000 genomes]
rs11594794	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11595457	1.00[AFR][1000 genomes]
rs11598581	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11598865	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11813102	1.00[CEU][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs12357094	0.86[ASN][1000 genomes]
rs1512694	0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs17146333	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17146580	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17146587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17146629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1886057	0.86[ASN][1000 genomes]
rs2031230	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2137422	1.00[AFR][1000 genomes]
rs2274026	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2274027	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2274028	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2274031	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2274033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2296136	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2296137	0.87[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2296138	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34249852	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34455477	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3750659	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs41290311	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs41306916	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4330991	0.82[JPT][hapmap]
rs4749325	1.00[AFR][1000 genomes]
rs4749407	1.00[AFR][1000 genomes]
rs55718140	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56103646	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56213022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56296494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56333805	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56354230	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61834499	0.92[ASN][1000 genomes]
rs6602312	0.83[CHD][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs6602322	0.83[CHD][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs7072283	0.85[ASN][1000 genomes]
rs7893821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7899635	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7899847	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7902223	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7904512	1.00[CEU][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7904712	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7907053	0.83[CHD][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs7912210	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7913876	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7918162	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs7919410	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7919785	0.83[CHD][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs7923781	0.82[JPT][hapmap];0.97[EUR][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	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats 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 target site	34 gene(s)	inside rSNPs	diseases
5	nsv5654	chr10:5868365-5930634	Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv825229	chr10:5886905-5967697	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv466723	chr10:5920836-5930579	Strong transcription Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
8	nsv549905	chr10:5920836-5930579	Flanking Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
9	nsv466724	chr10:5920836-5938544	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
10	nsv549906	chr10:5920836-5938544	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5911600-5926800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr10:5913000-5929800	Weak transcription	Fetal Heart	heart
3	chr10:5913000-5929800	Weak transcription	Psoas Muscle	Psoas
4	chr10:5914000-5929600	Weak transcription	NHLF	lung
5	chr10:5915600-5930000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr10:5915600-5930000	Weak transcription	HUVEC	blood vessel
7	chr10:5915800-5930000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr10:5915800-5930200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr10:5916200-5926400	Strong transcription	Skeletal Muscle Male	skeletal muscle
10	chr10:5916200-5927600	Strong transcription	Fetal Intestine Small	intestine
11	chr10:5916200-5928200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr10:5916200-5929000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:5916200-5929400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr10:5916200-5929800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:5916200-5929800	Strong transcription	Fetal Intestine Large	intestine
16	chr10:5916400-5928200	Strong transcription	Fetal Brain Female	brain
17	chr10:5916400-5929200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr10:5916400-5929800	Strong transcription	Fetal Muscle Trunk	muscle
19	chr10:5916600-5928400	Weak transcription	Small Intestine	intestine
20	chr10:5916600-5929400	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr10:5916600-5930600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr10:5916800-5930200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr10:5917800-5927800	Strong transcription	Thymus	Thymus
24	chr10:5917800-5928600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:5918000-5929800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr10:5918000-5930000	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:5918200-5926200	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr10:5918200-5927800	Strong transcription	Primary B cells from peripheral blood	blood
29	chr10:5918200-5928400	Strong transcription	Fetal Thymus	thymus
30	chr10:5918200-5929200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:5918200-5929600	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr10:5918200-5930200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr10:5918600-5927600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr10:5918800-5929000	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr10:5919200-5930000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr10:5919400-5929000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr10:5919600-5926400	Strong transcription	Osteobl	bone
38	chr10:5919600-5928200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr10:5919600-5929800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:5920200-5929800	Weak transcription	Right Ventricle	heart
41	chr10:5920200-5930600	Weak transcription	Aorta	Aorta
42	chr10:5920400-5929800	Weak transcription	Colonic Mucosa	Colon
43	chr10:5920400-5930000	Weak transcription	Hela-S3	cervix
44	chr10:5923600-5928000	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr10:5923600-5929200	Strong transcription	Fetal Stomach	stomach
46	chr10:5923800-5927000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr10:5923800-5928000	Strong transcription	Adipose Nuclei	Adipose
48	chr10:5923800-5928200	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr10:5923800-5928400	Strong transcription	Stomach Smooth Muscle	stomach
50	chr10:5923800-5929000	Strong transcription	HUES6 Cell Line	embryonic stem cell

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