Variant report

Variant	rs16943888
Chromosome Location	chr18:25217902-25217903
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1420941	1.00[AMR][1000 genomes]
rs1519131	1.00[AMR][1000 genomes]
rs1861781	1.00[AMR][1000 genomes]
rs2714375	1.00[AMR][1000 genomes]
rs28404348	1.00[AMR][1000 genomes]
rs3110549	1.00[AMR][1000 genomes]
rs3110550	1.00[AMR][1000 genomes]
rs4261622	1.00[AMR][1000 genomes]
rs56774619	1.00[AMR][1000 genomes]
rs7230612	1.00[AMR][1000 genomes]
rs7242276	1.00[AMR][1000 genomes]
rs8083675	1.00[AMR][1000 genomes]
rs8094042	1.00[AMR][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	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1061993	chr18:25211720-25239455	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1067348	chr18:25213808-25239455	Weak transcription Enhancers Flanking Active TSS Active TSS	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	chr18:25216400-25223000	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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