Variant report

Variant	rs11187842
Chromosome Location	chr10:96052511-96052512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:96051798..96054215-chr10:96059614..96061716,2	MCF-7	breast:
2	chr10:95579387..95581432-chr10:96050777..96053319,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10509671	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10509672	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10882435	0.84[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10882436	0.81[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11187826	0.88[AMR][1000 genomes]
rs11187837	1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11187840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187845	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];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11187851	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11187852	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187856	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11187863	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187864	1.00[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187866	1.00[CEU][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187869	0.90[ASN][1000 genomes]
rs11187870	1.00[CEU][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11187877	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187882	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11187883	1.00[CEU][hapmap];0.86[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187890	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187893	0.86[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11187894	0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11187895	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187897	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11187899	0.89[ASN][1000 genomes]
rs11187900	0.89[ASN][1000 genomes]
rs11187906	0.84[AMR][1000 genomes]
rs11558740	0.89[ASN][1000 genomes]
rs12217597	0.86[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12217792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12220091	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12781451	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs17109875	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3740359	0.85[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3740360	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3740365	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];0.99[ASN][1000 genomes]
rs3781264	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3781266	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]
rs6583935	0.82[JPT][hapmap]
rs7096678	0.99[ASN][1000 genomes]
rs7096883	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7100626	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7101207	0.88[AMR][1000 genomes]
rs752140	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs753724	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][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]

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	nsv1036676	chr10:95851376-96103876	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2761616	chr10:95966768-96303701	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96015000-96070200	Weak transcription	Fetal Brain Female	brain
2	chr10:96031800-96121000	Weak transcription	Stomach Mucosa	stomach
3	chr10:96034600-96052600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr10:96035600-96066800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr10:96036000-96081600	Weak transcription	Left Ventricle	heart
6	chr10:96037800-96069000	Weak transcription	Gastric	stomach
7	chr10:96040200-96066200	Weak transcription	Pancreas	Pancrea
8	chr10:96043600-96121000	Weak transcription	Psoas Muscle	Psoas
9	chr10:96045600-96058200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr10:96045800-96061800	Weak transcription	Colonic Mucosa	Colon
11	chr10:96046200-96066200	Weak transcription	Right Atrium	heart
12	chr10:96047400-96060800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:96047800-96068200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr10:96048800-96074800	Weak transcription	Placenta	Placenta
15	chr10:96049000-96058200	Weak transcription	Aorta	Aorta
16	chr10:96049400-96058000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr10:96049400-96081600	Weak transcription	Spleen	Spleen
18	chr10:96049600-96058200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr10:96050200-96056800	Weak transcription	Fetal Intestine Small	intestine
20	chr10:96051000-96052600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr10:96051200-96054400	Weak transcription	Fetal Intestine Large	intestine
22	chr10:96051400-96058200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr10:96051600-96052800	Genic enhancers	Fetal Muscle Leg	muscle
24	chr10:96051600-96053800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr10:96051600-96057200	Weak transcription	Fetal Muscle Trunk	muscle
26	chr10:96051800-96052800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr10:96051800-96053000	Enhancers	Fetal Kidney	kidney
28	chr10:96052000-96052600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
29	chr10:96052000-96052800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr10:96052000-96052800	Enhancers	Ovary	ovary
31	chr10:96052000-96053000	Enhancers	HSMM	muscle
32	chr10:96052000-96053000	Enhancers	HSMMtube	muscle
33	chr10:96052000-96053400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:96052000-96053400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:96052000-96053400	Enhancers	Colon Smooth Muscle	Colon
36	chr10:96052000-96053400	Enhancers	Fetal Lung	lung
37	chr10:96052000-96055400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr10:96052200-96052600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr10:96052200-96052800	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr10:96052200-96052800	Enhancers	Rectal Smooth Muscle	rectum
41	chr10:96052200-96053200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr10:96052200-96053400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr10:96052200-96053400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr10:96052200-96053400	Enhancers	Brain Hippocampus Middle	brain
45	chr10:96052200-96053400	Enhancers	NH-A	brain
46	chr10:96052200-96053400	Enhancers	NHLF	lung
47	chr10:96052200-96053600	Enhancers	Osteobl	bone
48	chr10:96052200-96053800	Enhancers	Adipose Nuclei	Adipose
49	chr10:96052200-96053800	Enhancers	Fetal Stomach	stomach
50	chr10:96052400-96052800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood

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