Variant report

Variant	rs74153348
Chromosome Location	chr10:96199094-96199095
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:96169823..96172016-chr10:96197395..96199700,2	MCF-7	breast:
2	chr10:96198485..96200699-chr10:96202037..96204075,2	MCF-7	breast:
3	chr10:96162530..96165019-chr10:96199067..96201077,2	MCF-7	breast:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1575935	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2094295	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55783943	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55852558	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55902049	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56104261	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56188429	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56281613	0.85[AFR][1000 genomes]
rs56309155	1.00[AMR][1000 genomes]
rs56666225	1.00[EUR][1000 genomes]
rs56735703	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56778943	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57096906	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57257088	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57721947	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58262373	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58283794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58430331	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58643119	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58776336	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58984186	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59365366	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59962294	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60234155	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61410136	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61668937	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7084812	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7101234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150807	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150809	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150810	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150811	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150813	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150814	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150816	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150822	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150830	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150837	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150849	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150850	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150854	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74150893	1.00[EUR][1000 genomes]
rs74153321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153341	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153344	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153347	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153350	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74153353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7900670	1.00[EUR][1000 genomes]
rs7902619	1.00[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	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
2	nsv831946	chr10:96055190-96226438	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers 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
3	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv1819509	chr10:96064300-96361776	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96184800-96199200	Weak transcription	Gastric	stomach
2	chr10:96188400-96213600	Weak transcription	Stomach Mucosa	stomach
3	chr10:96190800-96234600	Weak transcription	Osteobl	bone
4	chr10:96192000-96211400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:96198200-96199400	Enhancers	Brain Substantia Nigra	brain
6	chr10:96198200-96199400	Enhancers	Pancreas	Pancrea
7	chr10:96198200-96199600	Enhancers	Left Ventricle	heart
8	chr10:96198400-96202800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr10:96198400-96218200	Weak transcription	Aorta	Aorta
10	chr10:96199000-96199200	Enhancers	Fetal Stomach	stomach
11	chr10:96199000-96199200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr10:96199000-96199400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr10:96199000-96199400	Enhancers	Adipose Nuclei	Adipose
14	chr10:96199000-96199400	Enhancers	Brain Angular Gyrus	brain
15	chr10:96199000-96199400	Enhancers	Brain Cingulate Gyrus	brain
16	chr10:96199000-96199400	Enhancers	Brain Hippocampus Middle	brain
17	chr10:96199000-96199400	Enhancers	Stomach Smooth Muscle	stomach
18	chr10:96199000-96199400	Enhancers	HSMM	muscle
19	chr10:96199000-96199400	Enhancers	HUVEC	blood vessel
20	chr10:96199000-96199600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:96199000-96199600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:96199000-96199800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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