Variant report

Variant	rs10733599
Chromosome Location	chr9:115634234-115634235
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:115628888..115632126-chr9:115633392..115636528,4	K562	blood:
2	chr9:115629889..115631673-chr9:115633392..115635288,2	K562	blood:
3	chr9:115632762..115634297-chr9:115636411..115638284,2	K562	blood:

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10115576	1.00[CEU][hapmap]
rs10115711	0.82[CEU][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124260	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs10124939	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs10124979	0.82[CEU][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10733594	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs10733598	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs10739370	0.82[CEU][hapmap];1.00[ASN][1000 genomes]
rs10739373	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs10739374	1.00[ASN][1000 genomes]
rs10739376	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs10739378	1.00[CEU][hapmap]
rs10739380	0.83[EUR][1000 genomes]
rs10759590	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs10759603	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs10759604	1.00[ASN][1000 genomes]
rs1158331	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1324931	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs1361720	0.85[CEU][hapmap]
rs1418409	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1475293	1.00[CEU][hapmap]
rs1539338	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1570754	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1693411	1.00[ASN][1000 genomes]
rs1711746	1.00[ASN][1000 genomes]
rs1711747	1.00[ASN][1000 genomes]
rs1832890	1.00[ASN][1000 genomes]
rs1891402	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1891403	0.85[CEU][hapmap]
rs2025544	1.00[CEU][hapmap];0.82[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2051018	1.00[ASN][1000 genomes]
rs2147643	1.00[ASN][1000 genomes]
rs2147646	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2153837	1.00[ASN][1000 genomes]
rs2182048	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2185769	1.00[ASN][1000 genomes]
rs2645985	1.00[ASN][1000 genomes]
rs2645993	0.85[CEU][hapmap]
rs2645994	1.00[ASN][1000 genomes]
rs2796025	1.00[ASN][1000 genomes]
rs2796028	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs2796031	1.00[ASN][1000 genomes]
rs2796035	1.00[ASN][1000 genomes]
rs4246892	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs4304397	0.85[CEU][hapmap]
rs4360356	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4549852	1.00[ASN][1000 genomes]
rs4978507	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs4978510	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4978511	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs4979153	0.85[CEU][hapmap]
rs4979154	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs4979155	1.00[ASN][1000 genomes]
rs4979157	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs4979165	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs4979170	1.00[CEU][hapmap]
rs4979171	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4979183	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4979184	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4979186	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6477959	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs700122	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs7026450	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7030795	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs7038684	1.00[ASN][1000 genomes]
rs7040954	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7041965	1.00[ASN][1000 genomes]
rs7047914	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7859175	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs7868830	0.85[CEU][hapmap]
rs7869100	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs786961	1.00[ASN][1000 genomes]
rs786965	1.00[ASN][1000 genomes]
rs786966	1.00[ASN][1000 genomes]
rs786967	1.00[ASN][1000 genomes]
rs786968	1.00[ASN][1000 genomes]
rs786969	1.00[ASN][1000 genomes]
rs786972	1.00[ASN][1000 genomes]
rs786973	1.00[ASN][1000 genomes]
rs786977	1.00[ASN][1000 genomes]
rs7872628	1.00[ASN][1000 genomes]
rs787271	0.85[CEU][hapmap]
rs787276	0.85[CEU][hapmap]
rs787278	1.00[ASN][1000 genomes]
rs787280	0.85[CEU][hapmap]
rs787281	1.00[ASN][1000 genomes]
rs787284	0.85[CEU][hapmap]
rs787285	1.00[ASN][1000 genomes]
rs787286	1.00[ASN][1000 genomes]
rs787287	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs787291	1.00[ASN][1000 genomes]
rs787294	0.85[CEU][hapmap]
rs787295	0.85[CEU][hapmap]
rs787296	1.00[ASN][1000 genomes]
rs787297	0.85[CEU][hapmap]
rs787298	0.85[CEU][hapmap]
rs787299	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs787301	0.85[CEU][hapmap]
rs787302	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs787303	1.00[ASN][1000 genomes]
rs7873289	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs813101	0.85[CEU][hapmap]
rs885387	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs912662	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9409123	0.85[CEU][hapmap]
rs947609	1.00[ASN][1000 genomes]
rs980345	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758198	chr9:115240454-116002951	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759710	chr9:115240454-116002951	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv893733	chr9:115397206-115712068	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	esv2422302	chr9:115550339-115656433	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv1047000	chr9:115610445-115884038	ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115594200-115634400	Weak transcription	NH-A	brain
2	chr9:115601200-115641200	Weak transcription	Fetal Brain Male	brain
3	chr9:115607400-115643400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr9:115611400-115634600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:115612000-115634600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:115613600-115642600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr9:115615600-115639200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:115615600-115646400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:115621200-115639400	Weak transcription	Stomach Mucosa	stomach
10	chr9:115624200-115652600	Weak transcription	Fetal Heart	heart
11	chr9:115624800-115635200	Strong transcription	Primary T cells from cord blood	blood
12	chr9:115625800-115645200	Weak transcription	Thymus	Thymus
13	chr9:115626000-115636200	Weak transcription	NHLF	lung
14	chr9:115626400-115635000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr9:115626400-115635200	Strong transcription	Fetal Stomach	stomach
16	chr9:115626400-115650800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr9:115627000-115647000	Weak transcription	Colonic Mucosa	Colon
18	chr9:115627200-115637200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:115627600-115642000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr9:115627600-115646800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:115627800-115640600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr9:115628600-115640800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr9:115630600-115634800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr9:115630600-115636400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr9:115630600-115642000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:115630600-115643400	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr9:115630600-115646400	Weak transcription	Fetal Lung	lung
28	chr9:115630600-115647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr9:115630800-115634800	Strong transcription	Brain Hippocampus Middle	brain
30	chr9:115630800-115634800	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr9:115630800-115636000	Weak transcription	NHDF-Ad	bronchial
32	chr9:115630800-115643400	Weak transcription	NHEK	skin
33	chr9:115630800-115643600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:115630800-115643600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:115630800-115646400	Weak transcription	Placenta	Placenta
36	chr9:115631000-115639200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr9:115631200-115634400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr9:115631200-115634600	Strong transcription	Lung	lung
39	chr9:115631200-115634800	Strong transcription	Fetal Intestine Large	intestine
40	chr9:115631200-115634800	Strong transcription	Spleen	Spleen
41	chr9:115631200-115639600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr9:115631200-115643600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr9:115631200-115646400	Weak transcription	Fetal Kidney	kidney
44	chr9:115631400-115643800	Weak transcription	Colon Smooth Muscle	Colon
45	chr9:115631600-115642800	Weak transcription	Ovary	ovary
46	chr9:115631800-115635000	Strong transcription	Fetal Intestine Small	intestine
47	chr9:115631800-115642800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr9:115631800-115642800	Weak transcription	HSMM	muscle
49	chr9:115631800-115646400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr9:115631800-115652200	Weak transcription	Gastric	stomach

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