Variant report

Variant	rs72764715
Chromosome Location	chr9:118412514-118412515
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12006166	1.00[ASN][1000 genomes]
rs2418404	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62575331	1.00[ASN][1000 genomes]
rs62575332	1.00[ASN][1000 genomes]
rs72764714	1.00[ASN][1000 genomes]
rs72764716	1.00[ASN][1000 genomes]
rs72764717	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72764742	0.91[ASN][1000 genomes]
rs72764744	0.91[ASN][1000 genomes]
rs72764749	0.82[ASN][1000 genomes]
rs72764751	0.85[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	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:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118407200-118429200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:118410800-118415800	Enhancers	HSMM	muscle
3	chr9:118411000-118414600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:118411200-118413200	Enhancers	NHLF	lung
5	chr9:118411600-118413800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:118411600-118414000	Enhancers	NH-A	brain
7	chr9:118411600-118414400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:118411600-118414600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:118411800-118413000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
10	chr9:118411800-118413000	Enhancers	Adipose Nuclei	Adipose
11	chr9:118411800-118413000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr9:118411800-118413400	Enhancers	Fetal Stomach	stomach
13	chr9:118411800-118414600	Enhancers	NHDF-Ad	bronchial
14	chr9:118412000-118412600	Active TSS	Brain Hippocampus Middle	brain
15	chr9:118412000-118412600	Weak transcription	Brain Substantia Nigra	brain
16	chr9:118412000-118412800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:118412000-118414000	Enhancers	Rectal Smooth Muscle	rectum
18	chr9:118412200-118412600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:118412200-118412600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr9:118412200-118412600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:118412200-118412600	Enhancers	Fetal Lung	lung
22	chr9:118412200-118412800	Flanking Active TSS	Osteobl	bone
23	chr9:118412200-118413000	Active TSS	Brain Anterior Caudate	brain
24	chr9:118412200-118413600	Enhancers	NHEK	skin
25	chr9:118412200-118414000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr9:118412400-118412600	Flanking Active TSS	HSMMtube	muscle
27	chr9:118412400-118414000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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