Variant report

Variant	rs11757882
Chromosome Location	chr6:161447047-161447048
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:161446925..161450155-chr6:161452719..161457291,6	K562	blood:
2	chr6:161447042..161448624-chr6:161451951..161454419,2	MCF-7	breast:
3	chr6:161445425..161447208-chr6:161450821..161452549,2	K562	blood:

Variant related genes	Relation type
ENSG00000085511	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1001421	1.00[CHB][hapmap]
rs1001422	1.00[CHB][hapmap]
rs1001756	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs11751634	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11751688	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11751843	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs11752188	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11753446	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11755042	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11755244	0.83[AMR][1000 genomes]
rs11757223	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757309	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11758794	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11759408	1.00[CHB][hapmap]
rs11962121	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12110827	1.00[CHB][hapmap]
rs1404269	1.00[CHB][hapmap]
rs1464781	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs1534020	1.00[CHB][hapmap]
rs1562025	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17626731	1.00[YRI][hapmap]
rs1807426	1.00[CHB][hapmap]
rs2009830	1.00[CHB][hapmap]
rs2314190	1.00[CHB][hapmap]
rs2314376	1.00[CHB][hapmap]
rs2314377	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs35142900	1.00[ASN][1000 genomes]
rs3778218	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs3778225	1.00[CHB][hapmap]
rs3798916	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs3823057	1.00[CHB][hapmap]
rs57922639	0.83[AMR][1000 genomes]
rs58040353	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59129068	0.83[AMR][1000 genomes]
rs59318837	0.83[AMR][1000 genomes]
rs60649875	1.00[ASN][1000 genomes]
rs6905734	1.00[CHB][hapmap]
rs6940321	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7738423	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7754215	1.00[CHB][hapmap]
rs9365245	1.00[CHB][hapmap]
rs9456635	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9458121	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9458135	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9458141	1.00[CHB][hapmap]

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	nsv1030045	chr6:161359075-161562255	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1023982	chr6:161382188-161549831	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161414200-161458200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:161414400-161469600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:161414600-161457400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:161415600-161450000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr6:161416600-161475200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr6:161417400-161449000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:161418000-161448800	Weak transcription	Lung	lung
8	chr6:161428600-161455800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:161432200-161450000	Weak transcription	HMEC	breast
10	chr6:161432200-161450400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:161432200-161451200	Weak transcription	NHEK	skin
12	chr6:161432600-161455400	Weak transcription	Fetal Intestine Large	intestine
13	chr6:161433000-161449000	Weak transcription	HSMM	muscle
14	chr6:161433000-161458000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:161433200-161448800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr6:161433200-161450000	Weak transcription	Aorta	Aorta
17	chr6:161433200-161459200	Weak transcription	Fetal Stomach	stomach
18	chr6:161433400-161450000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:161433400-161455600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:161433400-161455800	Weak transcription	Fetal Muscle Leg	muscle
21	chr6:161433400-161455800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr6:161433400-161459000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr6:161433600-161458200	Weak transcription	Fetal Brain Female	brain
24	chr6:161433600-161459600	Weak transcription	Brain Germinal Matrix	brain
25	chr6:161433800-161448400	Weak transcription	NH-A	brain
26	chr6:161433800-161451000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:161434000-161449800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr6:161434000-161455600	Weak transcription	Adipose Nuclei	Adipose
29	chr6:161434000-161459000	Weak transcription	Brain Hippocampus Middle	brain
30	chr6:161434200-161450000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr6:161434800-161458200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr6:161435000-161448800	Weak transcription	Gastric	stomach
33	chr6:161435000-161448800	Weak transcription	Pancreas	Pancrea
34	chr6:161435000-161449600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:161435000-161452200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr6:161435000-161458000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr6:161435000-161458800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr6:161435000-161490400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr6:161435200-161450400	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr6:161435200-161454800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr6:161435200-161455800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr6:161435400-161450400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:161436800-161455600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr6:161437000-161451200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr6:161437000-161451600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:161437000-161452800	Weak transcription	Primary T cells from cord blood	blood
47	chr6:161437400-161457600	Weak transcription	Liver	Liver
48	chr6:161437800-161449800	Weak transcription	Colon Smooth Muscle	Colon
49	chr6:161437800-161451200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr6:161438000-161452400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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