Variant report

Variant	rs6453845
Chromosome Location	chr6:76576527-76576528
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:76458966..76460939-chr6:76574214..76577179,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196586	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1280039	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1280044	0.93[CEU][hapmap];0.90[CHB][hapmap];0.85[GIH][hapmap];0.90[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1280047	0.93[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1280048	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1321161	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs1321162	0.85[CHB][hapmap];0.85[JPT][hapmap];0.91[MEX][hapmap]
rs2038624	1.00[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2038625	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.94[TSI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2748955	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs276697	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs276698	1.00[CEU][hapmap];0.89[CHB][hapmap];0.80[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3798439	1.00[ASW][hapmap];0.93[CEU][hapmap];0.97[GIH][hapmap];0.89[JPT][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3822957	1.00[ASW][hapmap];0.93[CEU][hapmap];0.90[CHB][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3857468	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6905047	0.93[CEU][hapmap];0.85[CHB][hapmap];0.85[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6906615	0.93[CEU][hapmap];0.85[CHB][hapmap];0.80[GIH][hapmap];0.85[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6938349	1.00[CEU][hapmap];0.85[CHB][hapmap];0.85[JPT][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6942367	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs721264	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs9359139	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9443189	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019328	chr6:76154751-76604197	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	nsv538314	chr6:76154751-76604197	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
3	nsv1021090	chr6:76306100-76759397	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv538318	chr6:76306100-76759397	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv1032961	chr6:76343575-76788852	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv932201	chr6:76365548-77219650	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
7	nsv1028340	chr6:76410921-76960225	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv538319	chr6:76410921-76960225	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76541000-76590600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr6:76543000-76615000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:76544000-76583200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr6:76544400-76603800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:76552200-76592400	Weak transcription	HSMM	muscle
6	chr6:76552600-76592400	Weak transcription	Psoas Muscle	Psoas
7	chr6:76560000-76585800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:76560400-76583200	Weak transcription	Osteobl	bone
9	chr6:76562400-76599800	Weak transcription	Fetal Muscle Leg	muscle
10	chr6:76562800-76583400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr6:76563000-76580200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr6:76563000-76585400	Weak transcription	NHDF-Ad	bronchial
13	chr6:76563400-76602800	Weak transcription	Small Intestine	intestine
14	chr6:76566200-76604600	Weak transcription	Right Ventricle	heart
15	chr6:76567000-76604400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr6:76567400-76577400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:76567600-76584000	Weak transcription	Fetal Heart	heart
18	chr6:76567600-76598600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr6:76567600-76604200	Weak transcription	NHLF	lung
20	chr6:76568800-76577600	Strong transcription	Duodenum Mucosa	Duodenum
21	chr6:76569200-76577200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr6:76569200-76577600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:76569400-76577200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:76569600-76577800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:76570400-76577400	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr6:76570400-76580400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:76570600-76577400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:76571200-76592400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:76571400-76582200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:76571400-76583400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr6:76571600-76577200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:76572600-76577200	Strong transcription	Lung	lung
33	chr6:76573000-76577000	Weak transcription	NHEK	skin
34	chr6:76573000-76583400	Weak transcription	Aorta	Aorta
35	chr6:76573000-76584000	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr6:76573000-76597800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:76573000-76624000	Weak transcription	Placenta	Placenta
38	chr6:76573200-76604200	Weak transcription	Colonic Mucosa	Colon
39	chr6:76573400-76592800	Weak transcription	Stomach Mucosa	stomach
40	chr6:76573600-76583000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr6:76573600-76606200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:76573800-76576800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:76573800-76583400	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr6:76573800-76607200	Weak transcription	Gastric	stomach
45	chr6:76573800-76608400	Weak transcription	Esophagus	oesophagus
46	chr6:76574000-76583400	Weak transcription	NH-A	brain
47	chr6:76574000-76584600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:76574200-76583200	Weak transcription	Brain Angular Gyrus	brain
49	chr6:76574400-76577000	Weak transcription	Brain Hippocampus Middle	brain
50	chr6:76574400-76583000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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