Variant report

Variant	rs7046222
Chromosome Location	chr9:93760930-93760931
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:93760587..93764673-chr9:93765338..93768530,4	MCF-7	breast:
2	chr9:93759880..93762736-chr9:93764268..93766103,2	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1585456	0.86[AFR][1000 genomes]
rs1585457	0.96[AFR][1000 genomes]
rs1585458	0.96[AFR][1000 genomes]
rs1585459	0.96[AFR][1000 genomes]
rs55796701	0.91[AFR][1000 genomes]
rs55837511	0.96[AFR][1000 genomes]
rs56215441	0.96[AFR][1000 genomes]
rs56286690	0.95[AFR][1000 genomes]
rs56413001	1.00[AMR][1000 genomes]
rs57135918	0.81[AMR][1000 genomes]
rs57191437	1.00[AMR][1000 genomes]
rs57595048	1.00[AMR][1000 genomes]
rs57619886	1.00[AMR][1000 genomes]
rs57756037	0.95[AFR][1000 genomes]
rs57874603	0.95[AFR][1000 genomes]
rs58087771	0.96[AFR][1000 genomes]
rs58145618	0.96[AFR][1000 genomes]
rs58968598	0.92[AFR][1000 genomes]
rs59101625	1.00[AMR][1000 genomes]
rs59262734	0.96[AFR][1000 genomes]
rs59306422	0.91[AFR][1000 genomes]
rs59874266	0.95[AFR][1000 genomes]
rs60129254	0.96[AFR][1000 genomes]
rs60691320	0.96[AFR][1000 genomes]
rs61052452	1.00[AMR][1000 genomes]
rs61647505	0.96[AFR][1000 genomes]
rs7020346	0.96[AFR][1000 genomes]
rs7024221	0.94[AFR][1000 genomes]
rs7032345	0.94[AFR][1000 genomes]
rs7034744	0.96[AFR][1000 genomes]
rs7035409	0.96[AFR][1000 genomes]
rs7039162	0.96[AFR][1000 genomes]
rs7039179	0.96[AFR][1000 genomes]
rs7039199	0.96[AFR][1000 genomes]
rs7042057	1.00[AMR][1000 genomes]
rs7042483	0.99[AFR][1000 genomes]
rs7047670	0.96[AFR][1000 genomes]
rs73490578	0.89[AMR][1000 genomes]
rs73490596	1.00[AMR][1000 genomes]
rs73492503	1.00[AMR][1000 genomes]
rs73492505	1.00[AMR][1000 genomes]
rs73492518	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492522	0.96[AFR][1000 genomes]
rs73492530	0.96[AFR][1000 genomes]
rs73492532	0.96[AFR][1000 genomes]
rs73492542	0.92[AFR][1000 genomes]
rs73492545	0.94[AFR][1000 genomes]
rs73492551	0.99[AFR][1000 genomes]
rs73653521	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73653522	0.96[AFR][1000 genomes]
rs7854507	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7854907	0.96[AFR][1000 genomes]
rs7855222	0.96[AFR][1000 genomes]
rs7855269	0.96[AFR][1000 genomes]
rs7856489	0.96[AFR][1000 genomes]
rs7856691	0.96[AFR][1000 genomes]
rs7859976	0.89[AFR][1000 genomes]
rs7860957	1.00[AMR][1000 genomes]
rs7867663	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93754800-93763400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:93755000-93761000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:93755600-93761200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:93755600-93763200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:93758800-93762800	Weak transcription	NHDF-Ad	bronchial
6	chr9:93758800-93763600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:93760200-93763200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr9:93760400-93761000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:93760600-93761400	Enhancers	HUVEC	blood vessel
10	chr9:93760600-93763400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr9:93760600-93764000	Enhancers	Hela-S3	cervix
12	chr9:93760800-93761000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:93760800-93761200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr9:93760800-93761200	Enhancers	Fetal Muscle Trunk	muscle
15	chr9:93760800-93761400	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr9:93760800-93761400	Enhancers	K562	blood
17	chr9:93760800-93762000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:93760800-93762000	Enhancers	NHEK	skin
19	chr9:93760800-93762400	Enhancers	Esophagus	oesophagus
20	chr9:93760800-93762400	Enhancers	Fetal Muscle Leg	muscle
21	chr9:93760800-93762400	Enhancers	Osteobl	bone
22	chr9:93760800-93762600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:93760800-93762800	Enhancers	Placenta	Placenta
24	chr9:93760800-93763000	Enhancers	Adipose Nuclei	Adipose
25	chr9:93760800-93763400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:93760800-93763600	Enhancers	Liver	Liver
27	chr9:93760800-93764000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr9:93760800-93764000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:93760800-93764200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:93760800-93764200	Enhancers	HMEC	breast

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