Variant report

Variant	rs73727103
Chromosome Location	chr7:150883613-150883614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10252021	1.00[AMR][1000 genomes]
rs10281455	1.00[AMR][1000 genomes]
rs28650070	1.00[AMR][1000 genomes]
rs28716681	1.00[AMR][1000 genomes]
rs58120976	1.00[AMR][1000 genomes]
rs60681403	1.00[AMR][1000 genomes]
rs6945773	1.00[AMR][1000 genomes]
rs73727105	1.00[AMR][1000 genomes]
rs73727488	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv889476	chr7:150729212-150951819	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
3	nsv889478	chr7:150732812-150889527	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
4	nsv831188	chr7:150735204-150912875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv889486	chr7:150775306-150891641	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
6	nsv609034	chr7:150830015-150893629	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150882600-150883800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr7:150882800-150884400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
3	chr7:150882800-150885000	Active TSS	Left Ventricle	heart
4	chr7:150883000-150884000	Enhancers	Fetal Muscle Leg	muscle
5	chr7:150883200-150884400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr7:150883400-150883800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr7:150883400-150884000	Flanking Active TSS	Right Ventricle	heart
8	chr7:150883400-150885000	Active TSS	Right Atrium	heart
9	chr7:150883400-150885600	Enhancers	Fetal Heart	heart
10	chr7:150883600-150883800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:150883600-150883800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:150883600-150885000	Active TSS	Psoas Muscle	Psoas

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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