Variant report

Variant	rs7483783
Chromosome Location	chr11:45312750-45312751
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10501312	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs16926615	0.89[AFR][1000 genomes]
rs16938206	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs2863177	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs2902431	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs4462326	0.81[AFR][1000 genomes]
rs6485610	0.97[AFR][1000 genomes]
rs6485611	0.97[AFR][1000 genomes]
rs7394569	0.97[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	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45311400-45314800	Weak transcription	A549	lung
2	chr11:45312400-45312800	Enhancers	Fetal Intestine Large	intestine
3	chr11:45312400-45313000	Enhancers	Fetal Intestine Small	intestine

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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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