Variant report

Variant	rs73697696
Chromosome Location	chr8:104905554-104905555
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12114257	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12115119	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55738066	1.00[AMR][1000 genomes]
rs60412815	1.00[AMR][1000 genomes]
rs60552383	1.00[AMR][1000 genomes]
rs61042766	1.00[AMR][1000 genomes]
rs61589769	1.00[AMR][1000 genomes]
rs6990477	1.00[AMR][1000 genomes]
rs7004346	1.00[AMR][1000 genomes]
rs7006816	1.00[AMR][1000 genomes]
rs7017687	1.00[AMR][1000 genomes]
rs73697653	1.00[AMR][1000 genomes]
rs73697657	1.00[AMR][1000 genomes]
rs73697662	1.00[AMR][1000 genomes]
rs73697668	1.00[AMR][1000 genomes]
rs73697673	1.00[AMR][1000 genomes]
rs73697683	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697684	1.00[AMR][1000 genomes]
rs73697688	1.00[AMR][1000 genomes]
rs73697690	1.00[AMR][1000 genomes]
rs73697694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73697695	1.00[AMR][1000 genomes]
rs73697698	1.00[AMR][1000 genomes]
rs7826206	1.00[AMR][1000 genomes]
rs7841801	1.00[AMR][1000 genomes]
rs9918740	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	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv2752692	chr8:104520824-105123824	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1016387	chr8:104578389-104931853	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	esv1841024	chr8:104872512-104908099	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104897200-104914200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr8:104898200-104919000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:104899400-104933400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links