Variant report

Variant	rs73433190
Chromosome Location	chr11:17507640-17507641
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs58547851	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73429065	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433186	1.00[AMR][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	nsv469895	chr11:17368270-17584220	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr11:17504600-17507800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr11:17505800-17508800	Enhancers	Fetal Intestine Small	intestine
3	chr11:17506200-17508800	Enhancers	Fetal Intestine Large	intestine
4	chr11:17507600-17507800	Enhancers	Gastric	stomach
5	chr11:17507600-17508000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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

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