Variant report

Variant	rs17305329
Chromosome Location	chr9:98750707-98750708
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:98681098..98682813-chr9:98750330..98752671,2	K562	blood:
2	chr9:98745793..98747738-chr9:98750041..98751835,2	K562	blood:

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10512243	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10512244	0.85[YRI][hapmap];0.80[AFR][1000 genomes]
rs1410297	1.00[AMR][1000 genomes]
rs1434729	0.81[AMR][1000 genomes]
rs16910291	0.84[CEU][hapmap];0.90[AMR][1000 genomes]
rs16910302	0.83[CEU][hapmap];0.98[AMR][1000 genomes]
rs16910370	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs16910376	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16910382	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16910396	0.85[YRI][hapmap]
rs16910422	0.80[AFR][1000 genomes]
rs16910436	0.94[YRI][hapmap];0.90[AFR][1000 genomes]
rs17303045	0.83[CEU][hapmap];0.88[AMR][1000 genomes]
rs17304942	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17305138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17305917	0.84[EUR][1000 genomes]
rs17393861	0.83[CEU][hapmap]
rs17394582	0.83[CEU][hapmap];0.90[AMR][1000 genomes]
rs17394881	0.98[AMR][1000 genomes]
rs17396240	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17396338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17396553	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17396860	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1972802	0.86[AMR][1000 genomes]
rs2149099	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2149100	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2176026	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs34191478	0.90[AFR][1000 genomes]
rs3802439	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4144585	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs55645821	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs55699149	0.90[AMR][1000 genomes]
rs55746108	0.90[AMR][1000 genomes]
rs55787215	0.96[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs55810950	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55923424	0.90[AMR][1000 genomes]
rs55936120	0.80[AFR][1000 genomes]
rs55962207	0.83[AMR][1000 genomes]
rs55983886	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56016781	0.82[EUR][1000 genomes]
rs56087522	0.80[AFR][1000 genomes]
rs56108623	0.98[AMR][1000 genomes]
rs56162045	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56217203	1.00[AMR][1000 genomes]
rs56225283	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs56379566	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56678652	1.00[AMR][1000 genomes]
rs62559011	0.90[AMR][1000 genomes]
rs62559012	0.90[AMR][1000 genomes]
rs62559013	0.90[AMR][1000 genomes]
rs62559025	0.90[AMR][1000 genomes]
rs62559027	0.90[AMR][1000 genomes]
rs62559029	0.93[AMR][1000 genomes]
rs62559030	0.93[AMR][1000 genomes]
rs62559031	0.93[AMR][1000 genomes]
rs62559053	0.98[AMR][1000 genomes]
rs62559054	1.00[AMR][1000 genomes]
rs62559055	1.00[AMR][1000 genomes]
rs62559057	1.00[AMR][1000 genomes]
rs62559058	0.98[AMR][1000 genomes]
rs62559059	1.00[AMR][1000 genomes]
rs62559760	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62559762	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559763	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559766	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62559769	0.96[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs62559794	0.84[EUR][1000 genomes]
rs62559796	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs62562960	1.00[AMR][1000 genomes]
rs62562961	1.00[AMR][1000 genomes]
rs62562963	1.00[AMR][1000 genomes]
rs62562966	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562967	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562970	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562979	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562980	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562981	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562982	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562985	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562986	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562988	0.90[AFR][1000 genomes]
rs62562989	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62562992	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73532684	0.82[AMR][1000 genomes]
rs7848465	0.84[CEU][hapmap]
rs7864473	0.82[JPT][hapmap]

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	nsv893599	chr9:98542410-98991254	Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
2	nsv893600	chr9:98608989-98775459	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 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	chr9:98706400-98777400	Weak transcription	Psoas Muscle	Psoas
2	chr9:98714000-98782600	Weak transcription	HUVEC	blood vessel
3	chr9:98719000-98751400	Weak transcription	Stomach Mucosa	stomach
4	chr9:98719200-98752800	Weak transcription	Pancreas	Pancrea
5	chr9:98719200-98764200	Weak transcription	Spleen	Spleen
6	chr9:98719200-98767800	Weak transcription	Rectal Smooth Muscle	rectum
7	chr9:98719400-98767200	Weak transcription	Right Ventricle	heart
8	chr9:98719400-98771000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:98719600-98766800	Weak transcription	Colon Smooth Muscle	Colon
10	chr9:98726400-98767800	Weak transcription	Gastric	stomach
11	chr9:98730600-98751200	Weak transcription	Small Intestine	intestine
12	chr9:98732200-98751200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:98734600-98764400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr9:98734600-98767800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr9:98734600-98782400	Weak transcription	NHEK	skin
16	chr9:98735200-98751600	Weak transcription	NHDF-Ad	bronchial
17	chr9:98735400-98778400	Weak transcription	Hela-S3	cervix
18	chr9:98735800-98764200	Weak transcription	Placenta	Placenta
19	chr9:98735800-98766600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr9:98735800-98770600	Weak transcription	K562	blood
21	chr9:98735800-98771200	Weak transcription	HepG2	liver
22	chr9:98736000-98751400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:98736200-98752800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr9:98736400-98751000	Weak transcription	Ovary	ovary
25	chr9:98736600-98778800	Weak transcription	Fetal Brain Male	brain
26	chr9:98737000-98766800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr9:98738800-98756400	Weak transcription	Aorta	Aorta
28	chr9:98741800-98778600	Weak transcription	NH-A	brain
29	chr9:98743200-98755800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr9:98744600-98768000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr9:98744800-98751600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr9:98744800-98752800	Weak transcription	Brain Anterior Caudate	brain
33	chr9:98744800-98753000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr9:98744800-98753000	Weak transcription	Brain Substantia Nigra	brain
35	chr9:98744800-98753200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr9:98744800-98755400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr9:98744800-98766800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr9:98744800-98770800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr9:98744800-98771000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr9:98745000-98755600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr9:98745000-98766800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr9:98745200-98753200	Weak transcription	Fetal Lung	lung
43	chr9:98747200-98750800	Strong transcription	A549	lung
44	chr9:98747200-98753000	Strong transcription	Primary B cells from cord blood	blood
45	chr9:98747200-98753800	Strong transcription	Primary T cells from cord blood	blood
46	chr9:98747400-98751000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr9:98747800-98753000	Weak transcription	Left Ventricle	heart
48	chr9:98747800-98782800	Weak transcription	Fetal Kidney	kidney
49	chr9:98748000-98751000	Weak transcription	Osteobl	bone
50	chr9:98748000-98764200	Weak transcription	Primary T cells fromperipheralblood	blood

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