Variant report

Variant	rs34011966
Chromosome Location	chr4:110225384-110225385
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs13141018	0.94[EUR][1000 genomes]
rs13147221	0.94[EUR][1000 genomes]
rs13147935	0.86[EUR][1000 genomes]
rs17040388	0.97[EUR][1000 genomes]
rs17040390	0.97[EUR][1000 genomes]
rs34286241	0.91[EUR][1000 genomes]
rs34839743	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35525444	0.94[EUR][1000 genomes]
rs66650623	0.94[EUR][1000 genomes]
rs6826810	0.92[EUR][1000 genomes]
rs6854151	0.97[EUR][1000 genomes]
rs714586	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7681671	0.97[EUR][1000 genomes]
rs7691652	0.92[EUR][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	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv515893	chr4:110222845-110254841	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:110224600-110225600	Weak transcription	Psoas Muscle	Psoas
2	chr4:110224800-110225600	Weak transcription	Hela-S3	cervix

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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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