Variant report

Variant	rs1515813
Chromosome Location	chr2:172543000-172543001
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13385135	1.00[AMR][1000 genomes]
rs2176148	1.00[AMR][1000 genomes]
rs312923	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4668408	1.00[AMR][1000 genomes]
rs4668409	1.00[AMR][1000 genomes]
rs61384579	1.00[AMR][1000 genomes]
rs6746051	1.00[AMR][1000 genomes]
rs73976508	1.00[AMR][1000 genomes]
rs73976515	1.00[AMR][1000 genomes]
rs73976519	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	nsv997638	chr2:172442205-172560406	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172539400-172543600	Weak transcription	K562	blood

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

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