Variant report

Variant	rs6882601
Chromosome Location	chr5:114180957-114180958
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10055666	0.83[AMR][1000 genomes]
rs10067801	0.83[AMR][1000 genomes]
rs10070575	0.83[AMR][1000 genomes]
rs10071942	0.83[AMR][1000 genomes]
rs57315626	0.85[EUR][1000 genomes]
rs6594841	0.83[AMR][1000 genomes]
rs6594842	0.83[AMR][1000 genomes]
rs6594843	0.83[AMR][1000 genomes]
rs6594844	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6594848	0.83[AMR][1000 genomes]
rs6859066	0.83[AMR][1000 genomes]
rs6863152	0.83[AMR][1000 genomes]
rs6875825	0.82[AMR][1000 genomes]
rs6876195	0.83[AMR][1000 genomes]
rs6876229	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6877494	0.83[AMR][1000 genomes]
rs6882425	0.83[AMR][1000 genomes]
rs6884508	0.83[AMR][1000 genomes]
rs6885177	0.83[AMR][1000 genomes]
rs6885466	0.83[AMR][1000 genomes]
rs6885627	0.83[AMR][1000 genomes]
rs6889672	0.83[AMR][1000 genomes]
rs6889860	0.83[AMR][1000 genomes]
rs6890974	0.83[AMR][1000 genomes]
rs6894130	0.83[AMR][1000 genomes]
rs6897194	0.83[AMR][1000 genomes]
rs73259504	0.83[AMR][1000 genomes]
rs73259509	0.83[AMR][1000 genomes]
rs7700555	0.83[AMR][1000 genomes]
rs7703133	0.83[AMR][1000 genomes]
rs7706010	0.85[EUR][1000 genomes]
rs7706222	0.83[AMR][1000 genomes]
rs7711594	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7730893	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020798	chr5:113821828-114392727	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537867	chr5:113821828-114392727	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv981027	chr5:114143849-114191806	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114180400-114181000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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