Variant report

Variant	rs73775515
Chromosome Location	chr5:103387387-103387388
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs17156182	1.00[AMR][1000 genomes]
rs55809362	1.00[AMR][1000 genomes]
rs55842250	1.00[AMR][1000 genomes]
rs56007768	1.00[AMR][1000 genomes]
rs56304324	1.00[AMR][1000 genomes]
rs57146772	1.00[AMR][1000 genomes]
rs57389993	1.00[AMR][1000 genomes]
rs57792971	1.00[AMR][1000 genomes]
rs58162690	1.00[AMR][1000 genomes]
rs59240883	1.00[AMR][1000 genomes]
rs60830179	1.00[AMR][1000 genomes]
rs61009930	1.00[AMR][1000 genomes]
rs73775513	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73775516	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73775521	1.00[AMR][1000 genomes]
rs73775530	1.00[AMR][1000 genomes]
rs73775532	1.00[AMR][1000 genomes]
rs73775550	1.00[AMR][1000 genomes]
rs73775552	1.00[AMR][1000 genomes]
rs73777645	1.00[AMR][1000 genomes]
rs73777647	1.00[AMR][1000 genomes]
rs73777649	1.00[AMR][1000 genomes]
rs73777656	1.00[AMR][1000 genomes]
rs73777658	1.00[AMR][1000 genomes]
rs73777659	1.00[AMR][1000 genomes]
rs73777660	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025859	chr5:102744479-103710290	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537833	chr5:102744479-103710290	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv882524	chr5:103237745-104019292	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1027818	chr5:103318123-103445127	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1019939	chr5:103380722-103770101	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv537836	chr5:103380722-103770101	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1033278	chr5:103383207-103773361	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103386800-103388800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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