Variant report

Variant	rs10189015
Chromosome Location	chr2:111918472-111918473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111914389..111917112-chr2:111917290..111919823,3	MCF-7	breast:
2	chr2:111911560..111915041-chr2:111915359..111919056,5	K562	blood:
3	chr2:111877263..111880700-chr2:111917474..111920602,4	K562	blood:
4	chr2:111916941..111919260-chr2:111925363..111927012,2	K562	blood:
5	chr2:111893690..111895905-chr2:111918348..111921261,2	MCF-7	breast:
6	chr2:111877147..111880651-chr2:111918313..111921088,4	MCF-7	breast:
7	chr2:111915696..111917657-chr2:111917984..111921314,3	K562	blood:
8	chr2:111910661..111912271-chr2:111916800..111918815,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000153094	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10166773	0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs10169613	0.85[ASN][1000 genomes]
rs10211562	0.94[ASN][1000 genomes]
rs10439381	0.81[ASN][1000 genomes]
rs10439396	0.85[ASN][1000 genomes]
rs1054873	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11674517	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11899831	0.86[ASN][1000 genomes]
rs13398360	0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs1439287	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1821968	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1837366	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1837367	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1837368	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1837369	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2165107	0.87[ASN][1000 genomes]
rs2241841	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2241842	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2241844	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28723045	0.85[ASN][1000 genomes]
rs3789061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789064	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3789065	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4302219	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4627572	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4848406	0.86[ASN][1000 genomes]
rs4849402	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4849403	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55878194	0.85[ASN][1000 genomes]
rs56952027	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60286362	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60982612	0.85[ASN][1000 genomes]
rs6542350	0.84[ASN][1000 genomes]
rs6708784	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6726007	0.86[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs6732491	0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs6734942	0.99[ASN][1000 genomes]
rs6760053	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs7565473	0.84[ASN][1000 genomes]
rs7567184	0.80[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7569300	0.83[ASN][1000 genomes]
rs7572367	0.84[ASN][1000 genomes]
rs7577824	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7581735	0.85[ASN][1000 genomes]
rs7585054	0.83[ASN][1000 genomes]
rs7588534	0.83[ASN][1000 genomes]
rs7593638	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7596789	0.86[ASN][1000 genomes]
rs7602904	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9308731	0.83[CHB][hapmap]
rs9308742	0.84[ASN][1000 genomes]
rs9808225	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv834331	chr2:111812139-112004678	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS 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	esv1803356	chr2:111899783-112662597	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv428402	chr2:111899783-112662597	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv1801950	chr2:111899783-112746937	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	esv2757825	chr2:111899783-112746937	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	esv2759083	chr2:111899783-112746937	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111881800-111919800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr2:111884800-111925400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr2:111893600-111918600	Weak transcription	Colon Smooth Muscle	Colon
4	chr2:111898800-111920600	Weak transcription	Fetal Kidney	kidney
5	chr2:111904400-111920800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:111906400-111919600	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr2:111906600-111927000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr2:111907400-111920000	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr2:111907400-111920200	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr2:111907600-111919200	Strong transcription	Fetal Intestine Small	intestine
11	chr2:111907600-111919200	Strong transcription	Fetal Stomach	stomach
12	chr2:111907600-111919800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr2:111908000-111920000	Strong transcription	Fetal Intestine Large	intestine
14	chr2:111909200-111919200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:111909600-111918600	Weak transcription	Fetal Brain Male	brain
16	chr2:111909600-111922600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr2:111910000-111925200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr2:111910200-111922800	Weak transcription	Aorta	Aorta
19	chr2:111910400-111919600	Weak transcription	Small Intestine	intestine
20	chr2:111910400-111922400	Weak transcription	Ovary	ovary
21	chr2:111911400-111919000	Weak transcription	K562	blood
22	chr2:111911600-111918600	Weak transcription	Colonic Mucosa	Colon
23	chr2:111912400-111919800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr2:111912800-111919600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr2:111913600-111919000	Weak transcription	Stomach Mucosa	stomach
26	chr2:111913800-111918600	Weak transcription	Brain Angular Gyrus	brain
27	chr2:111914200-111918600	Weak transcription	Brain Substantia Nigra	brain
28	chr2:111914200-111918600	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr2:111914200-111918800	Weak transcription	Brain Hippocampus Middle	brain
30	chr2:111914200-111919000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:111914400-111920600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:111914600-111919600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:111914600-111921400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr2:111914600-111921400	Genic enhancers	Liver	Liver
35	chr2:111915200-111925600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr2:111915400-111920000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:111915400-111920000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr2:111915600-111918600	Weak transcription	Brain Anterior Caudate	brain
39	chr2:111915600-111919000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:111915600-111919400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:111915600-111919400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:111915600-111920200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr2:111915600-111925400	Strong transcription	Dnd41	blood
44	chr2:111915800-111918600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr2:111915800-111919000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr2:111915800-111919200	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr2:111915800-111919400	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr2:111915800-111920000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr2:111915800-111920200	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:111915800-111920200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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