Variant report

Variant	rs73300587
Chromosome Location	chr7:15668186-15668187
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs58299352	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58533838	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61306199	1.00[AMR][1000 genomes]
rs73288136	1.00[AMR][1000 genomes]
rs73288148	1.00[AMR][1000 genomes]
rs73290166	1.00[AMR][1000 genomes]
rs73296558	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296572	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73298571	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932168	chr7:15573437-15895294	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription 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	10 gene(s)	inside rSNPs	diseases
2	nsv523199	chr7:15582208-16042596	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv887735	chr7:15625992-15698178	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
4	nsv830911	chr7:15666307-15817662	Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv428501	chr7:15666307-15817662	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15645400-15668200	Weak transcription	Right Ventricle	heart
2	chr7:15652000-15683400	Weak transcription	Adipose Nuclei	Adipose
3	chr7:15657400-15673000	Weak transcription	Psoas Muscle	Psoas
4	chr7:15660800-15668200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:15665000-15668200	Weak transcription	NHLF	lung
6	chr7:15666400-15668200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:15666600-15682600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr7:15666800-15668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:15667800-15669600	Enhancers	Osteobl	bone
10	chr7:15667800-15670000	Enhancers	NHDF-Ad	bronchial
11	chr7:15668000-15668400	Flanking Bivalent TSS/Enh	Fetal Lung	lung
12	chr7:15668000-15668400	Enhancers	Left Ventricle	heart
13	chr7:15668000-15668400	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr7:15668000-15668600	Enhancers	Fetal Muscle Leg	muscle
15	chr7:15668000-15669200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:15668000-15669200	Enhancers	Fetal Stomach	stomach
17	chr7:15668000-15669400	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:15668000-15670600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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