Variant report

Variant	rs41324950
Chromosome Location	chr14:84740000-84740001
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs57013094	0.82[AFR][1000 genomes]
rs58718562	0.82[AFR][1000 genomes]
rs59400041	0.82[AFR][1000 genomes]
rs60913366	0.82[AFR][1000 genomes]
rs60939651	0.82[AFR][1000 genomes]
rs73384934	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73384935	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73384937	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73384939	1.00[AMR][1000 genomes]
rs73384941	0.82[AFR][1000 genomes]
rs73384944	0.82[AFR][1000 genomes]
rs73384953	0.82[AFR][1000 genomes]
rs73384955	0.82[AFR][1000 genomes]
rs73386428	0.82[AFR][1000 genomes]
rs73386429	0.82[AFR][1000 genomes]
rs73386433	0.82[AFR][1000 genomes]
rs73386435	0.82[AFR][1000 genomes]
rs73386438	0.82[AFR][1000 genomes]
rs73386441	0.82[AFR][1000 genomes]
rs73386448	0.82[AFR][1000 genomes]
rs73386449	0.82[AFR][1000 genomes]
rs73386453	0.82[AFR][1000 genomes]
rs73386455	0.82[AFR][1000 genomes]
rs73386458	0.82[AFR][1000 genomes]
rs73386461	0.82[AFR][1000 genomes]
rs73386462	0.82[AFR][1000 genomes]
rs73386469	0.82[AFR][1000 genomes]
rs73386471	0.82[AFR][1000 genomes]
rs73386472	0.82[AFR][1000 genomes]
rs73386474	0.82[AFR][1000 genomes]
rs73386477	0.82[AFR][1000 genomes]
rs73386480	0.82[AFR][1000 genomes]
rs73386481	0.82[AFR][1000 genomes]
rs73386491	0.82[AFR][1000 genomes]
rs73386492	0.82[AFR][1000 genomes]
rs73386493	0.82[AFR][1000 genomes]
rs73386495	0.82[AFR][1000 genomes]
rs73386499	0.82[AFR][1000 genomes]
rs73386502	0.82[AFR][1000 genomes]
rs73388313	0.82[AFR][1000 genomes]
rs73388315	0.82[AFR][1000 genomes]
rs73388317	0.82[AFR][1000 genomes]
rs73388318	0.82[AFR][1000 genomes]
rs73388321	0.82[AFR][1000 genomes]
rs73388324	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902161	chr14:84699866-84769903	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84738200-84740000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr14:84738600-84741200	Enhancers	Ovary	ovary
3	chr14:84739200-84740000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr14:84739600-84740200	Enhancers	HUVEC	blood vessel
5	chr14:84740000-84741000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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