Variant report

Variant	rs73366863
Chromosome Location	chr6:11371302-11371303
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10484453	0.92[ASN][1000 genomes]
rs10484454	0.92[ASN][1000 genomes]
rs12524463	0.85[ASN][1000 genomes]
rs12525329	0.88[ASN][1000 genomes]
rs12525704	0.88[ASN][1000 genomes]
rs12525719	0.88[ASN][1000 genomes]
rs12526759	0.96[ASN][1000 genomes]
rs12527813	0.85[ASN][1000 genomes]
rs16871291	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16871294	0.96[ASN][1000 genomes]
rs16871306	0.92[ASN][1000 genomes]
rs4607428	0.92[ASN][1000 genomes]
rs6903648	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7742703	0.85[ASN][1000 genomes]
rs7752886	0.85[ASN][1000 genomes]
rs7760294	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs926314	0.85[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	nsv1021078	chr6:10819083-11558560	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv538135	chr6:10819083-11558560	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11364600-11381200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:11365600-11374400	Weak transcription	Stomach Mucosa	stomach
3	chr6:11365600-11374800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:11367600-11372000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:11368400-11371400	Weak transcription	Fetal Intestine Small	intestine
6	chr6:11368400-11371800	Enhancers	HepG2	liver
7	chr6:11368400-11373800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:11368400-11374400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr6:11368400-11374400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr6:11368400-11374600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:11368800-11376800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:11369000-11371600	Strong transcription	Primary T cells from cord blood	blood
13	chr6:11369000-11380200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr6:11369200-11371600	Genic enhancers	Primary B cells from peripheral blood	blood
15	chr6:11369200-11374400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr6:11369200-11374600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:11369400-11373600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:11370000-11372000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
19	chr6:11370200-11371400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr6:11370200-11371800	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr6:11370200-11374000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:11370200-11374400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:11370400-11371400	Enhancers	Pancreas	Pancrea
24	chr6:11370600-11371400	Genic enhancers	Primary T cells fromperipheralblood	blood
25	chr6:11370600-11371400	Genic enhancers	Spleen	Spleen
26	chr6:11370600-11371800	Strong transcription	Primary B cells from cord blood	blood
27	chr6:11370800-11371400	Enhancers	Placenta	Placenta
28	chr6:11370800-11371600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
29	chr6:11370800-11371600	Enhancers	Esophagus	oesophagus
30	chr6:11370800-11372000	ZNF genes & repeats	GM12878-XiMat	blood
31	chr6:11371000-11371400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr6:11371200-11371400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr6:11371200-11372800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr6:11371200-11373600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr6:11371200-11374000	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:11371200-11374400	Weak transcription	Colonic Mucosa	Colon
37	chr6:11371200-11374400	Weak transcription	Left Ventricle	heart
38	chr6:11371200-11374400	Weak transcription	Thymus	Thymus
39	chr6:11371200-11374600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:11371200-11374600	Weak transcription	Gastric	stomach
41	chr6:11371200-11375800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:11371200-11376600	Weak transcription	Adipose Nuclei	Adipose
43	chr6:11371200-11377000	Weak transcription	Lung	lung
44	chr6:11371200-11378400	Weak transcription	Fetal Thymus	thymus
45	chr6:11371200-11380200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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