Variant report

Variant	rs3750751
Chromosome Location	chr10:50665928-50665929
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50664489..50667007-chr10:50746262..50748316,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000258838	Chromatin interaction
ENSG00000225830	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10857499	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11101159	0.83[EUR][1000 genomes]
rs12220638	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12242851	0.95[EUR][1000 genomes]
rs12412526	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12412748	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12570332	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs12572848	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1917801	1.00[EUR][1000 genomes]
rs1917802	0.98[EUR][1000 genomes]
rs1949883	1.00[CEU][hapmap];0.83[GIH][hapmap];0.88[TSI][hapmap]
rs3750746	0.92[GIH][hapmap]
rs4240510	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4253023	1.00[EUR][1000 genomes]
rs4253079	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4253231	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4453140	0.88[CEU][hapmap]
rs4838522	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4838527	1.00[EUR][1000 genomes]
rs4838529	1.00[CEU][hapmap];0.83[EUR][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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv895377	chr10:50588990-50678212	ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv831867	chr10:50607857-50788751	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
6	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50656600-50672600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:50660000-50666800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr10:50660400-50672400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:50662000-50669800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:50662200-50669600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr10:50662200-50669600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr10:50662200-50669600	Strong transcription	Left Ventricle	heart
8	chr10:50662200-50669800	Strong transcription	Muscle Satellite Cultured Cells	--
9	chr10:50662200-50677800	Weak transcription	Fetal Heart	heart
10	chr10:50662200-50691600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:50662400-50666000	Strong transcription	Hela-S3	cervix
12	chr10:50662400-50667000	Weak transcription	Psoas Muscle	Psoas
13	chr10:50662400-50690000	Weak transcription	Stomach Mucosa	stomach
14	chr10:50662400-50693200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:50662600-50666000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr10:50662600-50666600	Weak transcription	Brain Germinal Matrix	brain
17	chr10:50662600-50667000	Weak transcription	Brain Hippocampus Middle	brain
18	chr10:50662600-50669600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr10:50662600-50669600	Strong transcription	Duodenum Mucosa	Duodenum
20	chr10:50662600-50670200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:50662600-50670400	Strong transcription	Osteobl	bone
22	chr10:50662600-50674800	Weak transcription	Colonic Mucosa	Colon
23	chr10:50662600-50676600	Weak transcription	Small Intestine	intestine
24	chr10:50662600-50677600	Weak transcription	NHDF-Ad	bronchial
25	chr10:50662600-50691400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:50662800-50666800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr10:50662800-50666800	Weak transcription	GM12878-XiMat	blood
28	chr10:50662800-50667000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr10:50662800-50667000	Weak transcription	Brain Angular Gyrus	brain
30	chr10:50662800-50667800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr10:50663000-50666400	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr10:50663000-50666600	Weak transcription	Primary B cells from cord blood	blood
33	chr10:50663000-50669400	Strong transcription	Stomach Smooth Muscle	stomach
34	chr10:50663000-50669600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:50663000-50675800	Weak transcription	Colon Smooth Muscle	Colon
36	chr10:50663200-50669600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr10:50663200-50672600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr10:50663200-50693800	Weak transcription	HepG2	liver
39	chr10:50663400-50669600	Strong transcription	Brain Anterior Caudate	brain
40	chr10:50663400-50669600	Strong transcription	Fetal Muscle Leg	muscle
41	chr10:50663400-50669800	Strong transcription	HUVEC	blood vessel
42	chr10:50663400-50671200	Strong transcription	HMEC	breast
43	chr10:50663600-50669600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr10:50663600-50669600	Strong transcription	Liver	Liver
45	chr10:50663600-50669600	Strong transcription	Brain Inferior Temporal Lobe	brain
46	chr10:50663600-50671000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr10:50663600-50671000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr10:50663800-50666400	Strong transcription	Brain Cingulate Gyrus	brain
49	chr10:50663800-50667000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr10:50663800-50669600	Strong transcription	Primary B cells from peripheral blood	blood

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