Variant report

Variant	rs11189364
Chromosome Location	chr10:99524513-99524514
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:99520953..99523231-chr10:99523311..99525677,2	K562	blood:
2	chr10:99524037..99526896-chr10:99538605..99541496,2	MCF-7	breast:
3	chr10:99519656..99522050-chr10:99523613..99525578,2	K562	blood:
4	chr10:99523562..99525192-chr10:99527348..99530320,2	MCF-7	breast:
5	chr10:99522811..99525043-chr10:99528774..99531185,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11189365	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11189370	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11189371	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12249138	0.85[ASN][1000 genomes]
rs12264638	0.85[ASN][1000 genomes]
rs12266257	0.85[ASN][1000 genomes]
rs12269197	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13377035	1.00[ASN][1000 genomes]
rs1544178	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17108378	0.86[CHB][hapmap];0.92[ASN][1000 genomes]
rs1934562	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2185365	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28549815	0.85[ASN][1000 genomes]
rs3750613	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4378321	0.81[ASN][1000 genomes]
rs58554424	0.92[ASN][1000 genomes]
rs6584151	0.81[ASN][1000 genomes]
rs6584152	0.85[ASN][1000 genomes]
rs7095551	0.85[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs7097247	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73324634	0.81[ASN][1000 genomes]
rs73324671	0.88[ASN][1000 genomes]
rs73324700	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73326541	0.92[ASN][1000 genomes]
rs946783	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1817777	chr10:99196035-99558169	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv467441	chr10:99472710-99541104	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv552026	chr10:99472710-99541104	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99498600-99524800	Weak transcription	Fetal Brain Male	brain
2	chr10:99514800-99526600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:99515400-99526200	Weak transcription	NH-A	brain
4	chr10:99517200-99525000	Weak transcription	NHDF-Ad	bronchial
5	chr10:99520000-99525200	Weak transcription	Fetal Lung	lung
6	chr10:99520000-99525400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr10:99520000-99526000	Weak transcription	K562	blood
8	chr10:99520000-99527800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr10:99520200-99528400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:99520400-99529200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr10:99520400-99530400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr10:99520600-99526600	Weak transcription	Osteobl	bone
13	chr10:99520600-99528400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr10:99520800-99525000	Weak transcription	HUVEC	blood vessel
15	chr10:99520800-99525200	Weak transcription	Small Intestine	intestine
16	chr10:99521600-99525000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:99521600-99528200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr10:99521800-99526000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:99522000-99524600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr10:99522000-99524600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:99522000-99525200	Weak transcription	Stomach Smooth Muscle	stomach
22	chr10:99522000-99526600	Weak transcription	Ovary	ovary
23	chr10:99522200-99524600	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr10:99522200-99524600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr10:99522200-99526600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr10:99522200-99528000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr10:99522200-99530800	Weak transcription	Right Ventricle	heart
28	chr10:99522400-99524800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr10:99522400-99525200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr10:99522400-99526800	Weak transcription	NHLF	lung
31	chr10:99522400-99527000	Weak transcription	NHEK	skin
32	chr10:99522400-99527400	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr10:99522400-99527600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr10:99522400-99528200	Weak transcription	Aorta	Aorta
35	chr10:99522400-99528400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:99522400-99529000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr10:99522400-99530200	Weak transcription	A549	lung
38	chr10:99522600-99525600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:99522600-99527000	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr10:99522600-99527000	Weak transcription	Esophagus	oesophagus
41	chr10:99522600-99527000	Weak transcription	Gastric	stomach
42	chr10:99522600-99527600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr10:99522600-99528400	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr10:99522600-99530000	Weak transcription	Fetal Intestine Large	intestine
45	chr10:99522600-99530400	Weak transcription	Primary T cells from cord blood	blood
46	chr10:99522800-99524600	Enhancers	Fetal Muscle Trunk	muscle
47	chr10:99522800-99524800	Weak transcription	Right Atrium	heart
48	chr10:99522800-99526000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr10:99522800-99526400	Weak transcription	Liver	Liver
50	chr10:99522800-99528200	Weak transcription	Colonic Mucosa	Colon

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