Variant report

Variant	rs11015236
Chromosome Location	chr10:26993080-26993081
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	chr10:26985752..26988058-chr10:26992017..26994907,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000148459	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10829053	0.91[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[CHD][hapmap];0.90[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.80[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11015223	0.81[EUR][1000 genomes]
rs11015237	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015238	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015239	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015244	1.00[CEU][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes]
rs11015245	0.90[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs11015249	0.90[CHB][hapmap];0.84[CHD][hapmap]
rs11015250	0.81[CEU][hapmap];0.92[EUR][1000 genomes]
rs12245888	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12252759	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1677728	0.89[ASN][1000 genomes]
rs1677730	0.91[ASN][1000 genomes]
rs1748353	0.91[ASN][1000 genomes]
rs1748354	0.91[ASN][1000 genomes]
rs1748355	0.91[ASN][1000 genomes]
rs1748356	0.90[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs1748357	0.90[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs1780179	0.90[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs1780181	0.91[ASN][1000 genomes]
rs1780182	0.91[ASN][1000 genomes]
rs1780184	0.87[ASN][1000 genomes]
rs1780192	0.91[ASN][1000 genomes]
rs2448107	0.89[ASN][1000 genomes]
rs2477295	0.80[ASN][1000 genomes]
rs2477297	0.91[ASN][1000 genomes]
rs2477298	0.84[ASN][1000 genomes]
rs2477299	0.90[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs2489581	0.90[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs3118155	0.91[ASN][1000 genomes]
rs56290865	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6482571	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090448	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7100835	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.81[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72797950	0.88[AMR][1000 genomes];0.97[EUR][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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv3415799	chr10:26929831-27233591	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats 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	23 gene(s)	inside rSNPs	diseases
3	esv1798973	chr10:26968171-27001814	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv550233	chr10:26968171-27011323	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26987600-26994200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr10:26987600-26994400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:26987600-26994800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr10:26987600-26994800	Weak transcription	Brain Substantia Nigra	brain
5	chr10:26987600-26994800	Weak transcription	Esophagus	oesophagus
6	chr10:26987600-26994800	Weak transcription	Ovary	ovary
7	chr10:26987600-26994800	Weak transcription	HSMMtube	muscle
8	chr10:26987600-26995000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr10:26987600-26995000	Weak transcription	Gastric	stomach
10	chr10:26987600-26995000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr10:26987600-26996200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr10:26987600-26996200	Weak transcription	Pancreas	Pancrea
13	chr10:26987600-26996800	Weak transcription	Aorta	Aorta
14	chr10:26987600-27010400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr10:26987600-27024400	Weak transcription	Fetal Kidney	kidney
16	chr10:26987800-26994800	Weak transcription	Brain Hippocampus Middle	brain
17	chr10:26987800-26994800	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr10:26987800-26995400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr10:26987800-27010800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr10:26987800-27020400	Weak transcription	Primary hematopoietic stem cells	blood
21	chr10:26987800-27031200	Weak transcription	NHDF-Ad	bronchial
22	chr10:26988000-26993800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr10:26988000-26994400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr10:26988000-26994600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr10:26988000-26994600	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr10:26988000-26994600	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr10:26988000-26994600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:26988000-26994600	Weak transcription	Adipose Nuclei	Adipose
29	chr10:26988000-26994800	Weak transcription	Primary B cells from peripheral blood	blood
30	chr10:26988000-26994800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr10:26988000-26994800	Weak transcription	Fetal Brain Female	brain
32	chr10:26988000-26994800	Weak transcription	Fetal Lung	lung
33	chr10:26988000-26994800	Weak transcription	Spleen	Spleen
34	chr10:26988000-26995000	Weak transcription	NHLF	lung
35	chr10:26988000-26995200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr10:26988000-26995400	Weak transcription	Placenta	Placenta
37	chr10:26988000-26995800	Weak transcription	Brain Angular Gyrus	brain
38	chr10:26988000-26996200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr10:26988000-26996400	Weak transcription	HSMM	muscle
40	chr10:26988000-26996400	Weak transcription	Osteobl	bone
41	chr10:26988000-26996600	Weak transcription	HUVEC	blood vessel
42	chr10:26988000-27069600	Weak transcription	Colon Smooth Muscle	Colon
43	chr10:26988200-26993600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr10:26988200-26993800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr10:26988200-26994200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr10:26988200-26994200	Weak transcription	Fetal Stomach	stomach
47	chr10:26988200-26994400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr10:26988200-26994400	Weak transcription	Left Ventricle	heart
49	chr10:26988200-26994600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr10:26988200-26994600	Weak transcription	Fetal Muscle Leg	muscle

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