Variant report

Variant	rs2256164
Chromosome Location	chr8:104151381-104151382
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104149297..104151496-chr8:104160491..104162824,2	MCF-7	breast:
2	chr8:104149065..104151675-chr8:104155454..104157651,2	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10088491	0.81[ASN][1000 genomes]
rs10955310	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12056711	0.83[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs13259545	0.82[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs13264626	0.82[CHB][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap]
rs1494276	0.80[YRI][hapmap]
rs1497449	0.92[ASN][1000 genomes]
rs1497450	0.91[JPT][hapmap]
rs1497451	0.82[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs1497452	0.87[ASN][1000 genomes]
rs1845430	0.81[ASN][1000 genomes]
rs1846063	0.87[JPT][hapmap]
rs1846064	0.87[ASN][1000 genomes]
rs1976326	0.81[ASN][1000 genomes]
rs2132867	0.81[ASN][1000 genomes]
rs2249240	0.83[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs2249255	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs2249256	0.83[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs2454000	0.82[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs2454001	0.81[ASN][1000 genomes]
rs2454002	0.81[ASN][1000 genomes]
rs2454003	0.83[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs2454004	0.81[ASN][1000 genomes]
rs2454006	0.83[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs2454012	0.85[YRI][hapmap];0.83[AFR][1000 genomes]
rs2454013	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2454014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2454032	0.91[JPT][hapmap]
rs2454033	0.91[JPT][hapmap]
rs2454036	0.91[JPT][hapmap]
rs2454037	0.91[JPT][hapmap]
rs2454038	0.91[JPT][hapmap]
rs2515175	0.91[JPT][hapmap]
rs2515181	0.82[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs2515184	0.87[ASN][1000 genomes]
rs2515185	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs2515186	0.82[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs2515190	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2935579	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3019158	0.91[JPT][hapmap]
rs3019159	0.91[JPT][hapmap]
rs4734071	0.96[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4734687	0.91[JPT][hapmap]
rs4734689	0.92[ASN][1000 genomes]
rs4734690	0.92[ASN][1000 genomes]
rs7001897	0.92[ASN][1000 genomes]
rs7014418	0.91[ASN][1000 genomes]
rs953253	0.80[ASN][1000 genomes]
rs991312	0.96[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][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	nsv831413	chr8:104085141-104269789	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104146800-104152000	Weak transcription	Fetal Brain Male	brain
2	chr8:104146800-104152600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:104148400-104152200	Enhancers	Brain Hippocampus Middle	brain
4	chr8:104149000-104151400	Enhancers	Brain Cingulate Gyrus	brain
5	chr8:104149000-104153200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:104149200-104151800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:104149200-104151800	Enhancers	Brain Substantia Nigra	brain
8	chr8:104149600-104152200	Enhancers	Brain Angular Gyrus	brain
9	chr8:104150000-104152600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:104150200-104152200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:104150200-104152400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:104150200-104152600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:104150400-104151400	Enhancers	Spleen	Spleen
14	chr8:104150400-104151600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:104150400-104152200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr8:104150600-104151600	Enhancers	Lung	lung
17	chr8:104150600-104152800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr8:104150600-104152800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:104150800-104151400	Weak transcription	Right Atrium	heart
20	chr8:104150800-104152200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr8:104150800-104152200	Weak transcription	Pancreas	Pancrea
22	chr8:104150800-104152200	Weak transcription	Right Ventricle	heart
23	chr8:104150800-104153000	Enhancers	Primary B cells from peripheral blood	blood
24	chr8:104151000-104151400	Flanking Active TSS	GM12878-XiMat	blood
25	chr8:104151000-104151600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
26	chr8:104151000-104152200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr8:104151000-104152600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:104151000-104152600	Weak transcription	Ovary	ovary
29	chr8:104151200-104151400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr8:104151200-104151400	Enhancers	Fetal Thymus	thymus
31	chr8:104151200-104151600	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr8:104151200-104151600	Bivalent Enhancer	Thymus	Thymus
33	chr8:104151200-104151800	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr8:104151200-104152000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr8:104151200-104152200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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