Variant report

Variant	rs73513396
Chromosome Location	chr9:118434072-118434073
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs59774155	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6478200	1.00[AMR][1000 genomes]
rs7031379	0.84[AFR][1000 genomes]
rs73513369	0.81[AFR][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	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats 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	11 gene(s)	inside rSNPs	diseases
2	nsv948346	chr9:118107565-118718197	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1046948	chr9:118185587-118926891	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv916622	chr9:118206309-118952390	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv540207	chr9:118206311-118920304	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv491661	chr9:118206312-118802177	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv831698	chr9:118284259-118446456	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1047164	chr9:118286742-118456851	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118425000-118434800	Weak transcription	Aorta	Aorta
2	chr9:118429200-118436600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:118429400-118434800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:118430000-118434800	Enhancers	NHDF-Ad	bronchial
5	chr9:118430200-118434800	Enhancers	Hela-S3	cervix
6	chr9:118430800-118434200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:118431800-118434400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:118431800-118434600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr9:118432400-118436200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr9:118432400-118436600	Enhancers	NHEK	skin
11	chr9:118432600-118434800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:118432600-118436600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:118433200-118434600	Enhancers	HSMM	muscle
14	chr9:118433200-118434800	Enhancers	HSMMtube	muscle
15	chr9:118433200-118434800	Enhancers	NHLF	lung
16	chr9:118433400-118434400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr9:118433400-118434400	Enhancers	NH-A	brain
18	chr9:118433400-118434800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr9:118433400-118434800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:118433400-118434800	Enhancers	Osteobl	bone
21	chr9:118433600-118436600	Enhancers	HMEC	breast
22	chr9:118433800-118434400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:118433800-118434600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:118434000-118434200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr9:118434000-118434600	Enhancers	A549	lung
26	chr9:118434000-118434800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:118434000-118436200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr9:118434000-118436600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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