Variant report

Variant	rs73044686
Chromosome Location	chr5:16155188-16155189
allele	C/T
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:11)

rs_ID	r²[population]
rs56782886	1.00[AMR][1000 genomes]
rs57228803	1.00[AMR][1000 genomes]
rs6876118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6880397	1.00[AMR][1000 genomes]
rs6897610	1.00[AMR][1000 genomes]
rs73044647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73046507	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830217	chr5:16004704-16225229	Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv1838286	chr5:16150721-16180167	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv1848638	chr5:16150721-16180167	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16153600-16156800	Enhancers	Fetal Heart	heart
2	chr5:16154800-16157600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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