Variant report

Variant	rs28434733
Chromosome Location	chr6:70404911-70404912
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10498869	0.92[EUR][1000 genomes]
rs13437057	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1457498	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16868113	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868129	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17503698	1.00[EUR][1000 genomes]
rs3799109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4707324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4707375	0.90[ASN][1000 genomes]
rs6936974	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9294846	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9294847	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9294849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446157	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446159	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9446161	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9454865	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9454868	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9454873	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9454876	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9454880	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9454881	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9454887	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9454889	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9454890	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9454892	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9454893	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][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	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv830682	chr6:70397851-70592883	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70378800-70407400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:70378800-70409600	Weak transcription	Brain Substantia Nigra	brain
3	chr6:70378800-70416800	Weak transcription	Fetal Kidney	kidney
4	chr6:70378800-70430800	Weak transcription	Fetal Stomach	stomach
5	chr6:70378800-70430800	Weak transcription	Spleen	Spleen
6	chr6:70378800-70435200	Weak transcription	Psoas Muscle	Psoas
7	chr6:70379000-70428400	Weak transcription	Ovary	ovary
8	chr6:70379000-70435400	Weak transcription	Fetal Brain Male	brain
9	chr6:70379600-70431000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr6:70380200-70407600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr6:70380400-70430600	Weak transcription	Fetal Intestine Small	intestine
12	chr6:70380600-70455600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr6:70380800-70467800	Weak transcription	K562	blood
14	chr6:70382000-70406400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr6:70382200-70435400	Weak transcription	Brain Angular Gyrus	brain
16	chr6:70382400-70430200	Weak transcription	Small Intestine	intestine
17	chr6:70383800-70407800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:70383800-70431000	Weak transcription	Lung	lung
19	chr6:70384000-70415800	Weak transcription	Fetal Lung	lung
20	chr6:70384200-70428400	Weak transcription	Aorta	Aorta
21	chr6:70384200-70431000	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:70384400-70405200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr6:70384400-70405600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr6:70384400-70407200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:70384600-70406400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:70384600-70407800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:70384600-70407800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr6:70384600-70409800	Weak transcription	Brain Hippocampus Middle	brain
29	chr6:70384600-70417400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:70384800-70406400	Weak transcription	GM12878-XiMat	blood
31	chr6:70385000-70406400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr6:70385000-70407600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:70385000-70421600	Weak transcription	Fetal Intestine Large	intestine
34	chr6:70385200-70406200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr6:70386400-70408000	Weak transcription	Placenta	Placenta
36	chr6:70387000-70406400	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr6:70387000-70407800	Weak transcription	Dnd41	blood
38	chr6:70387200-70406400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr6:70387200-70407400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr6:70387200-70407800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:70387400-70406000	Weak transcription	Adipose Nuclei	Adipose
42	chr6:70387400-70406400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr6:70387400-70406400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:70387400-70407400	Weak transcription	Fetal Thymus	thymus
45	chr6:70387600-70406000	Weak transcription	Liver	Liver
46	chr6:70387600-70407800	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr6:70387600-70415600	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr6:70388000-70423400	Weak transcription	Left Ventricle	heart
49	chr6:70395400-70407200	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr6:70395800-70405000	Weak transcription	Primary T helper cells PMA-I stimulated	--

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