Variant report

Variant	rs10505548
Chromosome Location	chr8:131270454-131270455
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	chr8:131263978..131265844-chr8:131269482..131272106,2	MCF-7	breast:

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10091130	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10109236	0.90[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes]
rs10505549	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10956513	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10956515	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10956517	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11779014	0.89[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs11781752	1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs11786705	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes]
rs12541083	0.89[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes]
rs12545910	0.84[ASN][1000 genomes]
rs12546088	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs12546603	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs12547397	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12547540	0.83[ASN][1000 genomes]
rs12675390	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12676836	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12679283	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs12681954	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12681955	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1417007	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1469286	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1549455	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16893271	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs16904197	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16904199	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs16904204	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16904208	0.85[ASN][1000 genomes]
rs16904212	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs16904219	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs16904223	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16904231	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs16904239	0.89[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs16904241	0.89[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16904242	0.82[AMR][1000 genomes]
rs16904249	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1960661	0.86[ASN][1000 genomes]
rs1974313	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2027377	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2305511	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.80[ASN][1000 genomes]
rs2395989	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs36004574	0.86[ASN][1000 genomes]
rs3812476	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4733569	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4733573	0.89[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4733772	0.84[ASN][1000 genomes]
rs4733782	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4733783	0.89[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs4733788	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs57198371	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62524643	0.84[ASN][1000 genomes]
rs62524644	0.83[ASN][1000 genomes]
rs62524647	0.84[ASN][1000 genomes]
rs62524649	0.83[ASN][1000 genomes]
rs62525884	0.87[ASN][1000 genomes]
rs62525885	0.86[ASN][1000 genomes]
rs62525888	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62525889	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62525921	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62525922	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62525927	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62525928	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6415511	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6415517	0.85[CEU][hapmap];0.95[CHB][hapmap];0.80[JPT][hapmap]
rs6470813	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6470814	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes]
rs6991714	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6996106	0.87[CHB][hapmap];0.87[JPT][hapmap]
rs6996469	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6999216	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7006336	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs716077	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs72722366	0.86[ASN][1000 genomes]
rs72724420	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs72724433	0.83[AMR][1000 genomes]
rs7462286	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs754021	0.90[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9297806	0.89[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869334	chr8:131025093-131651487	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv915580	chr8:131025093-131667578	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv465810	chr8:131039109-131331012	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv612234	chr8:131039109-131331012	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv533085	chr8:131042781-131755007	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv831461	chr8:131159819-131302900	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv870148	chr8:131206342-131373989	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131225800-131274800	Weak transcription	Hela-S3	cervix
2	chr8:131250800-131270600	Weak transcription	NH-A	brain
3	chr8:131250800-131289200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr8:131257400-131281600	Weak transcription	Gastric	stomach
5	chr8:131258000-131275400	Weak transcription	Stomach Mucosa	stomach
6	chr8:131260000-131275200	Weak transcription	Fetal Intestine Small	intestine
7	chr8:131260600-131271600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr8:131260800-131272800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:131261200-131274400	Weak transcription	Fetal Muscle Leg	muscle
10	chr8:131261400-131271000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr8:131261400-131275800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr8:131261600-131275400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:131261800-131276000	Weak transcription	K562	blood
14	chr8:131262000-131271600	Weak transcription	Primary B cells from cord blood	blood
15	chr8:131262200-131270800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:131262200-131276200	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr8:131262800-131271400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr8:131263000-131275800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr8:131263000-131276000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr8:131263200-131270600	Weak transcription	GM12878-XiMat	blood
21	chr8:131263800-131270800	Weak transcription	Brain Germinal Matrix	brain
22	chr8:131264400-131276200	Weak transcription	Fetal Heart	heart
23	chr8:131264800-131271400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr8:131265600-131270600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:131265600-131270600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr8:131265600-131271000	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr8:131265600-131271000	Weak transcription	HMEC	breast
28	chr8:131266400-131271400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr8:131266800-131270600	Enhancers	Liver	Liver
30	chr8:131267000-131270600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:131267000-131272200	Enhancers	HepG2	liver
32	chr8:131267600-131275800	Weak transcription	Primary T cells from cord blood	blood
33	chr8:131267800-131271000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr8:131268200-131270800	Weak transcription	Adipose Nuclei	Adipose
35	chr8:131268400-131270800	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr8:131268400-131271000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:131268400-131276000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr8:131268400-131281600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:131268400-131291400	Weak transcription	Fetal Intestine Large	intestine
40	chr8:131268600-131270600	Weak transcription	HSMMtube	muscle
41	chr8:131268600-131270800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr8:131268600-131270800	Weak transcription	Brain Anterior Caudate	brain
43	chr8:131268600-131271000	Weak transcription	Brain Hippocampus Middle	brain
44	chr8:131268600-131271000	Weak transcription	Colon Smooth Muscle	Colon
45	chr8:131268600-131271400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:131268600-131271600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:131268600-131271600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr8:131268600-131271800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr8:131268600-131271800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr8:131268600-131275200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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