Variant report

Variant	rs34575766
Chromosome Location	chr11:71909987-71909988
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12807696	1.00[AFR][1000 genomes]
rs35437876	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs71477715	1.00[AFR][1000 genomes]
rs71477720	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71906200-71912200	Enhancers	Placenta	Placenta
2	chr11:71907400-71911200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:71909800-71910600	Enhancers	Hela-S3	cervix
4	chr11:71909800-71910600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr11:71909800-71911000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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