Variant report

Variant	rs10768123
Chromosome Location	chr11:35293162-35293163
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35283179..35288324-chr11:35290664..35293185,4	MCF-7	breast:
2	chr11:35291446..35293589-chr11:35293877..35296307,2	MCF-7	breast:
3	chr11:35289687..35293483-chr11:35296744..35298908,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000110436	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1043101	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10742339	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10742340	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10742341	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10768118	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10768120	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10768121	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10768122	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10768126	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10836360	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10836361	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836362	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836363	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836364	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10836367	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10836369	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11033045	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11033046	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11033048	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11524863	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12361171	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12796856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1570214	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1570215	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17378105	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3088168	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35629461	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3763888	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3794086	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3794089	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3794090	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3794091	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3794098	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3794099	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3794100	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3794101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3794102	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3794103	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3847604	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4755394	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4755395	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4756203	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756204	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756205	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756206	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57339940	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6484778	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7105505	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7105690	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121587	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs736374	0.83[EUR][1000 genomes]
rs7946149	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs932633	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs932635	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs957350	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9633870	0.87[AMR][1000 genomes];0.94[EUR][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	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv541004	chr11:35122694-35297414	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv832120	chr11:35277410-35490304	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35265800-35305800	Weak transcription	HepG2	liver
2	chr11:35270400-35296400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:35270400-35307000	Weak transcription	Fetal Brain Male	brain
4	chr11:35282200-35297000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:35282200-35297000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:35282400-35296600	Weak transcription	Aorta	Aorta
7	chr11:35282600-35296800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr11:35283000-35302000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr11:35284600-35296600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:35284600-35300800	Weak transcription	Brain Angular Gyrus	brain
11	chr11:35284800-35296600	Weak transcription	Brain Hippocampus Middle	brain
12	chr11:35285800-35308800	Weak transcription	Gastric	stomach
13	chr11:35286400-35293800	Weak transcription	Brain Anterior Caudate	brain
14	chr11:35287600-35296200	Weak transcription	Liver	Liver
15	chr11:35288200-35295600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:35288400-35293600	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr11:35288600-35293600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr11:35288800-35293600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr11:35288800-35297000	Weak transcription	Brain Germinal Matrix	brain
20	chr11:35289600-35293200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr11:35289600-35293200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:35289600-35296600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:35289800-35296600	Weak transcription	NHDF-Ad	bronchial
24	chr11:35290000-35296800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:35290400-35296000	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr11:35290600-35296800	Weak transcription	NHLF	lung
27	chr11:35290800-35294200	Weak transcription	Pancreas	Pancrea
28	chr11:35291000-35293800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr11:35291800-35296800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:35292600-35293800	Enhancers	GM12878-XiMat	blood
31	chr11:35292600-35295400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:35293000-35294800	Enhancers	Primary B cells from peripheral blood	blood
33	chr11:35293000-35295600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:35293000-35296800	Strong transcription	Fetal Brain Female	brain

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