Variant report

Variant	rs73195225
Chromosome Location	chr7:111906237-111906238
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:111900844..111903692-chr7:111905399..111908941,4	MCF-7	breast:
2	chr7:111897692..111901157-chr7:111901324..111906297,5	K562	blood:

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10046468	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10224789	0.93[ASN][1000 genomes]
rs10227494	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10232109	1.00[ASN][1000 genomes]
rs10232110	1.00[ASN][1000 genomes]
rs10237213	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10239663	1.00[ASN][1000 genomes]
rs10243005	1.00[ASN][1000 genomes]
rs10246422	1.00[ASN][1000 genomes]
rs10248314	1.00[ASN][1000 genomes]
rs10251698	1.00[ASN][1000 genomes]
rs10253148	0.86[ASN][1000 genomes]
rs10261860	1.00[ASN][1000 genomes]
rs10266976	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10269057	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10274016	0.93[ASN][1000 genomes]
rs10275406	1.00[ASN][1000 genomes]
rs10276140	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10276369	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10276727	0.93[ASN][1000 genomes]
rs10276853	1.00[ASN][1000 genomes]
rs10278420	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10281805	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10282279	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1047550	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1047551	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12530699	1.00[ASN][1000 genomes]
rs12532522	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12534930	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12537934	1.00[ASN][1000 genomes]
rs17159353	1.00[ASN][1000 genomes]
rs17159566	0.86[ASN][1000 genomes]
rs17159604	1.00[ASN][1000 genomes]
rs17402962	1.00[ASN][1000 genomes]
rs17491423	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2189289	1.00[ASN][1000 genomes]
rs2285732	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28532417	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2894646	1.00[ASN][1000 genomes]
rs3109106	1.00[ASN][1000 genomes]
rs3109108	1.00[ASN][1000 genomes]
rs3109116	1.00[ASN][1000 genomes]
rs3109117	1.00[ASN][1000 genomes]
rs3128395	1.00[ASN][1000 genomes]
rs35134215	1.00[ASN][1000 genomes]
rs41281060	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs56132236	1.00[ASN][1000 genomes]
rs56341778	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57214357	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60127009	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60691495	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61669542	1.00[ASN][1000 genomes]
rs67064485	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67604537	1.00[ASN][1000 genomes]
rs6943448	1.00[ASN][1000 genomes]
rs6944498	1.00[ASN][1000 genomes]
rs6947063	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6949234	1.00[ASN][1000 genomes]
rs6950282	1.00[ASN][1000 genomes]
rs6964483	1.00[ASN][1000 genomes]
rs6965896	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6969176	1.00[ASN][1000 genomes]
rs6971023	1.00[ASN][1000 genomes]
rs73192992	1.00[ASN][1000 genomes]
rs73192993	1.00[ASN][1000 genomes]
rs73193000	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73195204	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73195211	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73195218	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73195220	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73195223	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73195224	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197338	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197343	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73197349	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197363	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197366	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197367	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73197376	1.00[ASN][1000 genomes]
rs7786555	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7790065	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7806811	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810149	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810734	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7812188	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][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	nsv531435	chr7:111333900-111926292	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv491934	chr7:111333900-111975504	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv532335	chr7:111411990-112054905	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111881800-111906400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:111893200-111926000	Weak transcription	Primary T cells from cord blood	blood
3	chr7:111896000-111913000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:111896800-111922200	Weak transcription	Pancreas	Pancrea
5	chr7:111897600-111908000	Weak transcription	HepG2	liver
6	chr7:111903400-111906400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:111903400-111949200	Weak transcription	Fetal Intestine Small	intestine
8	chr7:111903800-111906400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:111903800-111907000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:111903800-111907000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:111903800-111908600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:111903800-111913000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:111903800-111916000	Weak transcription	Small Intestine	intestine
14	chr7:111903800-111917000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr7:111903800-111926000	Weak transcription	Psoas Muscle	Psoas
16	chr7:111904000-111907400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr7:111904000-111907400	Weak transcription	Brain Hippocampus Middle	brain
18	chr7:111904000-111907600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:111904000-111907600	Weak transcription	Brain Angular Gyrus	brain
20	chr7:111904000-111907600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr7:111904000-111907800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:111904200-111906400	Weak transcription	Liver	Liver
23	chr7:111904200-111906800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:111904200-111907600	Weak transcription	Brain Substantia Nigra	brain
25	chr7:111904200-111908200	Weak transcription	Fetal Lung	lung
26	chr7:111905000-111906400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:111905000-111907200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:111905000-111907200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:111905000-111907200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr7:111905000-111907200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:111905000-111908200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr7:111905200-111906400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:111905200-111907600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr7:111905400-111906400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr7:111905400-111907000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:111905400-111907800	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr7:111905400-111908200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:111905400-111926000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr7:111905600-111906800	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr7:111905600-111907800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:111905800-111906800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr7:111905800-111907200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr7:111906000-111906400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr7:111906000-111906400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr7:111906000-111906400	Enhancers	Spleen	Spleen
46	chr7:111906000-111906600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:111906000-111906600	Enhancers	Ovary	ovary
48	chr7:111906000-111906600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr7:111906000-111906800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:111906000-111907800	Enhancers	HMEC	breast

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