Variant report

Variant	rs7645188
Chromosome Location	chr3:113224011-113224012
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:113223951..113225818-chr3:113242726..113245430,2	MCF-7	breast:
2	chr3:113213186..113216151-chr3:113223551..113226748,3	MCF-7	breast:
3	chr3:113218601..113224275-chr3:113232367..113235656,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000163611	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs13326562	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13327031	1.00[EUR][1000 genomes]
rs13353449	1.00[EUR][1000 genomes]
rs2399487	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28539944	0.81[EUR][1000 genomes]
rs28614095	0.81[EUR][1000 genomes]
rs4419353	1.00[CEU][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6438154	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6763234	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6779241	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6780720	1.00[CEU][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6781507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6797630	0.81[EUR][1000 genomes]
rs6808103	1.00[CEU][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72950895	0.81[EUR][1000 genomes]
rs7612448	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7618195	0.86[EUR][1000 genomes]
rs7625829	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7629636	1.00[CEU][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9810059	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9810754	0.81[EUR][1000 genomes]
rs9811168	0.90[EUR][1000 genomes]
rs9827490	0.81[EUR][1000 genomes]
rs9827772	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs9836199	0.90[EUR][1000 genomes]
rs9846529	0.81[EUR][1000 genomes]
rs9851183	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9851407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9852068	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9860473	0.95[EUR][1000 genomes]
rs9863114	0.90[EUR][1000 genomes]
rs9878186	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv1004000	chr3:113116778-113513899	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv877349	chr3:113208224-113323787	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv877350	chr3:113208224-113332235	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113160800-113224800	Weak transcription	Placenta	Placenta
2	chr3:113160800-113232600	Weak transcription	Right Ventricle	heart
3	chr3:113172800-113232800	Weak transcription	HSMMtube	muscle
4	chr3:113176400-113233200	Weak transcription	Gastric	stomach
5	chr3:113177400-113225800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr3:113177600-113224400	Weak transcription	Spleen	Spleen
7	chr3:113179600-113232400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr3:113179600-113232800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr3:113184000-113233200	Weak transcription	Pancreas	Pancrea
10	chr3:113187200-113224400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:113201400-113232600	Weak transcription	Brain Hippocampus Middle	brain
12	chr3:113202400-113232800	Weak transcription	Fetal Brain Female	brain
13	chr3:113203400-113229200	Weak transcription	Lung	lung
14	chr3:113204400-113224600	Weak transcription	Aorta	Aorta
15	chr3:113204400-113230600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:113204600-113232800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr3:113204600-113233200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:113204600-113233200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:113204600-113233200	Weak transcription	Esophagus	oesophagus
20	chr3:113204800-113232400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr3:113204800-113232600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr3:113204800-113232800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr3:113204800-113233200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:113205000-113224200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:113205000-113224400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:113207600-113232600	Weak transcription	NHEK	skin
27	chr3:113207600-113233000	Weak transcription	Psoas Muscle	Psoas
28	chr3:113207800-113233000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr3:113209000-113232600	Weak transcription	Fetal Kidney	kidney
30	chr3:113209200-113232800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr3:113209400-113232800	Weak transcription	Stomach Mucosa	stomach
32	chr3:113209800-113228800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr3:113209800-113232800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr3:113210000-113224400	Weak transcription	Thymus	Thymus
35	chr3:113210000-113233000	Weak transcription	HSMM	muscle
36	chr3:113210200-113233200	Weak transcription	Colonic Mucosa	Colon
37	chr3:113210400-113231600	Weak transcription	Fetal Intestine Small	intestine
38	chr3:113210400-113232600	Weak transcription	NHLF	lung
39	chr3:113212200-113232800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr3:113212400-113232600	Weak transcription	Brain Angular Gyrus	brain
41	chr3:113212400-113232600	Weak transcription	NHDF-Ad	bronchial
42	chr3:113213000-113224200	Weak transcription	Colon Smooth Muscle	Colon
43	chr3:113216000-113232600	Weak transcription	HMEC	breast
44	chr3:113217400-113232400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr3:113217600-113224200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr3:113217600-113232800	Weak transcription	Brain Anterior Caudate	brain
47	chr3:113217800-113224200	Weak transcription	Brain Substantia Nigra	brain
48	chr3:113217800-113224400	Weak transcription	Left Ventricle	heart
49	chr3:113217800-113224400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:113217800-113224600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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