Variant report

Variant	rs10080913
Chromosome Location	chr6:36882658-36882659
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36645356..36648241-chr6:36882559..36884793,2	MCF-7	breast:
2	chr6:36882380..36882909-chr6:36985650..36986552,2	K562	blood:
3	chr6:36880047..36886049-chr6:36952384..36956049,12	MCF-7	breast:
4	chr6:36882284..36884713-chr6:36895663..36897480,2	MCF-7	breast:
5	chr6:36841055..36843830-chr6:36880674..36884413,4	MCF-7	breast:
6	chr6:36853163..36854000-chr6:36881697..36882692,4	MCF-7	breast:
7	chr6:36882074..36882765-chr6:36946753..36947291,2	MCF-7	breast:
8	chr6:36872618..36878206-chr6:36882033..36886554,6	K562	blood:
9	chr6:36856213..36857757-chr6:36880453..36883073,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000137409	Chromatin interaction
ENSG00000137168	Chromatin interaction
ENSG00000124762	Chromatin interaction
ENSG00000198663	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1405068	1.00[EUR][1000 genomes]
rs57023725	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57275916	1.00[EUR][1000 genomes]
rs57680472	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58376164	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59341304	1.00[EUR][1000 genomes]
rs61140519	1.00[EUR][1000 genomes]
rs6900666	1.00[EUR][1000 genomes]
rs6927474	1.00[EUR][1000 genomes]
rs6931297	1.00[EUR][1000 genomes]
rs6931465	1.00[EUR][1000 genomes]
rs6932579	1.00[EUR][1000 genomes]
rs6932789	1.00[EUR][1000 genomes]
rs73420361	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73420362	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73420393	1.00[EUR][1000 genomes]
rs73732090	1.00[EUR][1000 genomes]
rs73732102	1.00[EUR][1000 genomes]
rs7752720	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9296202	1.00[EUR][1000 genomes]
rs9462242	1.00[EUR][1000 genomes]
rs9462243	1.00[EUR][1000 genomes]
rs9462244	1.00[EUR][1000 genomes]
rs9462245	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9462246	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9462247	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9470433	1.00[EUR][1000 genomes]
rs9470435	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9470436	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9470437	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9470438	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9470446	1.00[EUR][1000 genomes]
rs9688391	1.00[EUR][1000 genomes]
rs9688402	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv916833	chr6:36826524-37029833	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36854200-36887400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:36854400-36893000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:36854800-36884600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr6:36866200-36896400	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr6:36867000-36897000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:36870800-36889400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:36871000-36888400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:36876000-36885000	Strong transcription	Fetal Stomach	stomach
9	chr6:36876200-36885800	Weak transcription	Psoas Muscle	Psoas
10	chr6:36876800-36884200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:36876800-36885000	Weak transcription	Ovary	ovary
12	chr6:36876800-36885200	Weak transcription	Fetal Heart	heart
13	chr6:36877000-36884400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr6:36877800-36896000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr6:36879400-36882800	Enhancers	NHEK	skin
16	chr6:36879400-36883000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:36879400-36883200	Strong transcription	Fetal Muscle Leg	muscle
18	chr6:36879400-36883400	Strong transcription	Fetal Lung	lung
19	chr6:36879400-36884400	Strong transcription	Stomach Smooth Muscle	stomach
20	chr6:36879400-36894000	Strong transcription	Fetal Brain Female	brain
21	chr6:36879600-36883200	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr6:36879600-36894000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:36879600-36895400	Strong transcription	Brain Germinal Matrix	brain
24	chr6:36879800-36883200	Strong transcription	Colon Smooth Muscle	Colon
25	chr6:36879800-36884400	Strong transcription	Placenta	Placenta
26	chr6:36879800-36885000	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:36879800-36885000	Strong transcription	Left Ventricle	heart
28	chr6:36879800-36885200	Strong transcription	Right Ventricle	heart
29	chr6:36879800-36885400	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr6:36880000-36892000	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr6:36880200-36883400	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr6:36880200-36884800	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr6:36880200-36887800	Strong transcription	Adipose Nuclei	Adipose
34	chr6:36880200-36893800	Strong transcription	K562	blood
35	chr6:36880400-36883600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr6:36880400-36884600	Strong transcription	Aorta	Aorta
37	chr6:36880400-36885400	Strong transcription	Lung	lung
38	chr6:36880400-36888000	Strong transcription	Brain Angular Gyrus	brain
39	chr6:36880600-36883200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:36880600-36884600	Strong transcription	Rectal Smooth Muscle	rectum
41	chr6:36880600-36893600	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr6:36880600-36900000	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr6:36880800-36883000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr6:36880800-36889800	Strong transcription	Primary B cells from peripheral blood	blood
45	chr6:36881000-36883000	Enhancers	Stomach Mucosa	stomach
46	chr6:36881000-36883800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:36881000-36892000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:36881000-36894800	Weak transcription	Fetal Brain Male	brain
49	chr6:36881200-36882800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr6:36881200-36883800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood

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