Variant report

Variant	rs17303769
Chromosome Location	chr6:100967531-100967532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10457808	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10457809	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10782302	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs108422	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11155496	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11155498	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12190903	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12191199	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12192249	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12200565	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12206182	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12206564	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12206945	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12374612	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12660725	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151573	0.80[EUR][1000 genomes]
rs1875400	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1875401	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2001102	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2062634	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2062635	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs239237	0.80[EUR][1000 genomes]
rs239238	0.80[EUR][1000 genomes]
rs239239	0.80[EUR][1000 genomes]
rs239242	0.80[EUR][1000 genomes]
rs239245	0.80[EUR][1000 genomes]
rs239246	0.80[EUR][1000 genomes]
rs239247	0.80[EUR][1000 genomes]
rs239249	0.80[EUR][1000 genomes]
rs2398132	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs240115	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs240143	0.80[EUR][1000 genomes]
rs240145	0.80[EUR][1000 genomes]
rs240146	0.80[EUR][1000 genomes]
rs240154	0.80[EUR][1000 genomes]
rs240164	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs240764	0.88[EUR][1000 genomes]
rs395521	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4461738	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62422675	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[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	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1023710	chr6:100810738-101001115	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv538388	chr6:100810738-101001115	Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv886444	chr6:100961198-101084946	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:100951600-100969800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:100952600-100967600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:100952800-100997400	Weak transcription	A549	lung
4	chr6:100953000-100968400	Weak transcription	Fetal Kidney	kidney
5	chr6:100954600-100986200	Weak transcription	Spleen	Spleen
6	chr6:100955200-100972800	Weak transcription	Right Ventricle	heart
7	chr6:100955800-100991200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:100957400-100992400	Weak transcription	Small Intestine	intestine
9	chr6:100958200-100976600	Weak transcription	NHDF-Ad	bronchial
10	chr6:100958600-100974000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:100960200-100978000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:100960600-100973800	Weak transcription	HUVEC	blood vessel
13	chr6:100960600-100990200	Weak transcription	Brain Substantia Nigra	brain
14	chr6:100960800-100969400	Weak transcription	Esophagus	oesophagus
15	chr6:100960800-100970800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:100960800-100971200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr6:100960800-100971200	Weak transcription	Thymus	Thymus
18	chr6:100960800-100974000	Weak transcription	NH-A	brain
19	chr6:100960800-100977600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:100960800-100981000	Weak transcription	Gastric	stomach
21	chr6:100960800-100986000	Weak transcription	GM12878-XiMat	blood
22	chr6:100960800-100986200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:100960800-100986600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:100960800-100989600	Weak transcription	K562	blood
25	chr6:100960800-100989800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr6:100960800-101035000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:100961000-100986600	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr6:100961000-100987200	Weak transcription	Osteobl	bone
29	chr6:100961000-100988800	Weak transcription	NHEK	skin
30	chr6:100961000-100991200	Weak transcription	HSMMtube	muscle
31	chr6:100961000-100992000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr6:100961000-100997200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr6:100961200-100989000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr6:100961400-100986000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr6:100963000-100986800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:100964000-100990800	Weak transcription	Primary hematopoietic stem cells	blood
37	chr6:100964200-100968800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr6:100964200-100986200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr6:100964200-101020000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:100964800-100998400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:100965200-100972800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr6:100965200-100984000	Weak transcription	HepG2	liver
43	chr6:100965200-100986600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr6:100965200-100989600	Weak transcription	Aorta	Aorta
45	chr6:100965200-100990200	Weak transcription	Left Ventricle	heart
46	chr6:100965200-101000800	Weak transcription	Fetal Intestine Small	intestine
47	chr6:100965200-101011400	Weak transcription	Pancreas	Pancrea
48	chr6:100965400-100968000	Weak transcription	Primary T cells from cord blood	blood
49	chr6:100965400-100969200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:100965400-100976600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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