Variant report

Variant	rs57137296
Chromosome Location	chr7:79712965-79712966
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10231925	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10237290	0.83[AMR][1000 genomes]
rs10237415	0.83[AMR][1000 genomes]
rs10238912	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10242482	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10247323	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10260857	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11974166	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11977309	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11977332	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12333681	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs28630699	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs34872162	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs35802637	0.90[AFR][1000 genomes]
rs55687904	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56330158	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56361294	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56761500	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57082352	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57291254	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs58876952	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs59312847	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61390031	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61586173	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73374533	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73374541	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73374589	0.83[AFR][1000 genomes]
rs73374591	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73376508	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73376538	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73376541	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73376565	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73378605	1.00[AMR][1000 genomes]
rs73708417	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73708491	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708493	0.94[AFR][1000 genomes];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	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv607678	chr7:79665817-79726578	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1027494	chr7:79693976-79760332	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79707600-79716600	Weak transcription	Brain Substantia Nigra	brain
2	chr7:79708000-79716800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:79708400-79716400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:79708400-79716800	Weak transcription	NHEK	skin
5	chr7:79712200-79716400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:79712800-79713800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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