Variant report

Variant	rs370133
Chromosome Location	chr7:107838045-107838046
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	chr7:107834413..107838118-chr7:108096452..108098366,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000091129	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1155	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs1269621	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1269622	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1269623	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1269625	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1269628	0.82[CEU][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1269629	0.82[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1269634	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs1269640	0.85[CHB][hapmap];0.83[JPT][hapmap]
rs1269642	0.92[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1269643	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs1269650	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1269651	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1269655	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1269656	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1269658	0.83[CEU][hapmap]
rs1269659	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs36065373	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3819747	0.84[JPT][hapmap]
rs403622	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs405945	1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs422011	0.92[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6970096	0.84[JPT][hapmap]
rs888189	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs926146	0.84[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033979	chr7:107003734-107877761	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv949344	chr7:107396502-107987085	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv831089	chr7:107687618-107877240	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
5	nsv831090	chr7:107786650-108011196	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv888941	chr7:107796150-107863395	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv1030222	chr7:107809927-107844916	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107786800-107857800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr7:107787800-107844200	Weak transcription	Brain Germinal Matrix	brain
3	chr7:107818200-107851800	Weak transcription	HSMMtube	muscle
4	chr7:107818600-107848400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:107820600-107867400	Weak transcription	Brain Angular Gyrus	brain
6	chr7:107820800-107840800	Weak transcription	Placenta	Placenta
7	chr7:107820800-107846800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr7:107820800-107850600	Weak transcription	Fetal Intestine Large	intestine
9	chr7:107820800-107851200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:107821000-107852200	Weak transcription	Fetal Muscle Leg	muscle
11	chr7:107821600-107850400	Weak transcription	Fetal Brain Male	brain
12	chr7:107828000-107852000	Weak transcription	Pancreas	Pancrea
13	chr7:107828600-107838200	Strong transcription	A549	lung
14	chr7:107828800-107846600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:107828800-107851400	Weak transcription	Fetal Intestine Small	intestine
16	chr7:107829600-107848600	Weak transcription	Brain Anterior Caudate	brain
17	chr7:107830400-107839800	Weak transcription	Brain Substantia Nigra	brain
18	chr7:107830400-107857200	Weak transcription	Fetal Brain Female	brain
19	chr7:107830400-107886400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:107834800-107841800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:107835000-107838400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:107835000-107840600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:107835000-107851400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:107835400-107841600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr7:107835400-107845400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:107835600-107844200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:107836000-107844800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:107836200-107838600	Enhancers	HUVEC	blood vessel
29	chr7:107836400-107840800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:107836600-107843200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:107836800-107839000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:107836800-107839400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:107836800-107839800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:107836800-107851200	Weak transcription	HMEC	breast
35	chr7:107836800-107852000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:107837400-107839800	Enhancers	NHEK	skin
37	chr7:107837600-107838400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr7:107838000-107838200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:107838000-107839600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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