Variant report

Variant	rs6918626
Chromosome Location	chr6:4810410-4810411
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:4804953..4807169-chr6:4808675..4810449,2	MCF-7	breast:
2	chr6:4800467..4802843-chr6:4809432..4811722,2	MCF-7	breast:
3	chr6:4809930..4812317-chr6:4814309..4817023,2	K562	blood:
4	chr6:4804785..4806447-chr6:4808370..4810719,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1016877	0.88[EUR][1000 genomes]
rs11967994	0.86[CEU][hapmap];0.92[GIH][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes]
rs11968021	0.86[CEU][hapmap];0.84[EUR][1000 genomes]
rs1265332	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs1265333	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs1265334	0.84[EUR][1000 genomes]
rs1265335	0.86[CEU][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs17138856	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs184588	0.86[CEU][hapmap];0.92[GIH][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs2179269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2179270	0.85[EUR][1000 genomes]
rs233476	0.86[CEU][hapmap];0.84[EUR][1000 genomes]
rs3748078	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs61610972	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62384662	0.84[AMR][1000 genomes]
rs62384663	0.84[AMR][1000 genomes]
rs62386571	0.81[ASN][1000 genomes]
rs62386574	0.84[EUR][1000 genomes]
rs62386575	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62386576	0.85[EUR][1000 genomes]
rs62386577	0.85[EUR][1000 genomes]
rs62386578	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62386582	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62386584	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386585	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386587	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386590	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386591	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386593	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386594	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386612	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62386614	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6910368	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[TSI][hapmap];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6924037	0.89[AMR][1000 genomes]
rs73362560	0.85[EUR][1000 genomes]
rs808608	0.83[EUR][1000 genomes]
rs9378917	0.84[AMR][1000 genomes]
rs9378919	0.89[AMR][1000 genomes]
rs9392640	0.89[AMR][1000 genomes]
rs9405786	0.89[AMR][1000 genomes]
rs9504254	0.86[CEU][hapmap];0.85[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	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1015888	chr6:4787784-4883663	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4794800-4818800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:4801800-4811600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr6:4802200-4811200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:4802400-4812000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr6:4802400-4818800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:4803400-4814600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr6:4803600-4810800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr6:4804600-4810800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:4804600-4812000	Weak transcription	Pancreas	Pancrea
10	chr6:4804600-4812200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:4804600-4812200	Weak transcription	HSMMtube	muscle
12	chr6:4806400-4812000	Weak transcription	Esophagus	oesophagus
13	chr6:4806400-4812000	Weak transcription	Gastric	stomach
14	chr6:4806400-4812600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr6:4806600-4810800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:4806600-4812200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:4806800-4814000	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr6:4806800-4819800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:4806800-4820200	Weak transcription	NHLF	lung
20	chr6:4806800-4820400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr6:4806800-4829400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:4807000-4812200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:4807000-4817400	Weak transcription	Brain Anterior Caudate	brain
24	chr6:4807000-4821200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr6:4807200-4810800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:4807200-4810800	Weak transcription	Spleen	Spleen
27	chr6:4807200-4819800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr6:4807200-4827800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:4807400-4810600	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr6:4807400-4810800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:4807400-4810800	Weak transcription	Colonic Mucosa	Colon
32	chr6:4807400-4810800	Weak transcription	Left Ventricle	heart
33	chr6:4807400-4810800	Weak transcription	Lung	lung
34	chr6:4807400-4810800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr6:4807400-4811000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr6:4807400-4811200	Weak transcription	Right Ventricle	heart
37	chr6:4807400-4812000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:4807400-4812000	Weak transcription	Right Atrium	heart
39	chr6:4807400-4812200	Weak transcription	Fetal Thymus	thymus
40	chr6:4807400-4813400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:4807600-4810600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:4807600-4810800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr6:4807600-4811200	Weak transcription	Colon Smooth Muscle	Colon
44	chr6:4807600-4812400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr6:4807600-4814600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr6:4807600-4817000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr6:4808200-4811400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:4808600-4812600	Enhancers	HepG2	liver
49	chr6:4808800-4818800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:4809000-4810800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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