Variant report

Variant	rs6833560
Chromosome Location	chr4:106103084-106103085
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:106066588..106068608-chr4:106102134..106104288,2	MCF-7	breast:
2	chr4:106094476..106097193-chr4:106102038..106103844,2	K562	blood:
3	chr4:106064646..106070521-chr4:106098298..106104512,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168769	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10003144	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10006632	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10006721	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10008189	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10017522	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10018267	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10022126	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10022891	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10023701	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10026237	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10027791	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10033325	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11932794	0.89[ASN][1000 genomes]
rs11938493	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11941838	0.92[ASN][1000 genomes]
rs11943394	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11944001	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11944085	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11947617	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12505746	0.97[ASN][1000 genomes]
rs2017763	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28394039	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28707121	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3733609	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3796927	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4235413	1.00[ASN][1000 genomes]
rs55793049	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58862751	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59339947	0.86[ASN][1000 genomes]
rs59806714	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60886348	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6826102	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6831247	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6831445	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6835030	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6839609	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6843141	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6857812	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72955167	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72955198	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73836047	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836048	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836052	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836055	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73838074	0.92[ASN][1000 genomes]
rs7662448	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7696287	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7696337	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7698398	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7698522	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[ASN][1000 genomes]
rs7700148	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs871215	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs931653	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9985622	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9993497	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9997323	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9998069	1.00[EUR][1000 genomes];0.92[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	nsv461609	chr4:105869548-106366209	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv470063	chr4:105869548-106366209	Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv595007	chr4:105869548-106366209	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv830025	chr4:105988876-106137946	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106069400-106114200	Weak transcription	Esophagus	oesophagus
2	chr4:106070400-106107800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:106070400-106111600	Weak transcription	Placenta	Placenta
4	chr4:106077000-106112000	Weak transcription	Aorta	Aorta
5	chr4:106078000-106112800	Weak transcription	Fetal Kidney	kidney
6	chr4:106080600-106105800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:106080600-106107800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr4:106083600-106109200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr4:106083800-106104800	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr4:106083800-106111400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr4:106084000-106105000	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:106084800-106127400	Weak transcription	Brain Germinal Matrix	brain
13	chr4:106085600-106112800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr4:106086000-106105600	Weak transcription	Fetal Lung	lung
15	chr4:106090400-106105600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr4:106090600-106107000	Weak transcription	NH-A	brain
17	chr4:106092000-106105800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:106092000-106110600	Weak transcription	Primary B cells from peripheral blood	blood
19	chr4:106093800-106111200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr4:106093800-106112400	Weak transcription	Primary B cells from cord blood	blood
21	chr4:106094000-106112600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr4:106096200-106111600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:106096400-106111200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr4:106096600-106107200	Weak transcription	Psoas Muscle	Psoas
25	chr4:106097400-106105800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr4:106097600-106105600	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr4:106098000-106111400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr4:106098200-106103400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:106098200-106113200	Weak transcription	Fetal Stomach	stomach
30	chr4:106099000-106114200	Weak transcription	Gastric	stomach
31	chr4:106100800-106103800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:106100800-106108000	Weak transcription	Osteobl	bone
33	chr4:106101000-106103400	Weak transcription	Stomach Mucosa	stomach
34	chr4:106101000-106103400	Weak transcription	HMEC	breast
35	chr4:106101000-106103600	Enhancers	Fetal Heart	heart
36	chr4:106101000-106103800	Enhancers	Fetal Intestine Large	intestine
37	chr4:106101000-106105800	Weak transcription	Left Ventricle	heart
38	chr4:106101000-106146600	Weak transcription	Spleen	Spleen
39	chr4:106101200-106105200	Weak transcription	Small Intestine	intestine
40	chr4:106101200-106105600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr4:106101200-106112600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr4:106101200-106112800	Weak transcription	NHDF-Ad	bronchial
43	chr4:106101400-106104800	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr4:106101400-106105400	Weak transcription	HepG2	liver
45	chr4:106101400-106105800	Weak transcription	Adipose Nuclei	Adipose
46	chr4:106101400-106112200	Weak transcription	Right Atrium	heart
47	chr4:106101600-106105400	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr4:106101600-106112800	Weak transcription	HSMM	muscle
49	chr4:106101800-106104000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:106101800-106105800	Weak transcription	Duodenum Mucosa	Duodenum

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