Variant report

Variant	rs61086197
Chromosome Location	chr15:54662173-54662174
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs73415703	0.91[AFR][1000 genomes]
rs73415705	0.91[AFR][1000 genomes]
rs73415710	0.91[AFR][1000 genomes]
rs73415711	0.91[AFR][1000 genomes]
rs73415715	0.81[AFR][1000 genomes]
rs73415722	0.91[AFR][1000 genomes]
rs73415723	0.91[AFR][1000 genomes]
rs73415738	0.91[AFR][1000 genomes]
rs73415762	0.91[AFR][1000 genomes]
rs73415765	0.83[AFR][1000 genomes]
rs73417711	1.00[AFR][1000 genomes]
rs73417732	1.00[AFR][1000 genomes]
rs73417767	0.91[AFR][1000 genomes]
rs73417771	0.91[AFR][1000 genomes]
rs73417779	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1845471	chr15:54556063-54685463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr15:54654600-54664400	Weak transcription	Aorta	Aorta
2	chr15:54654600-54665600	Weak transcription	Fetal Lung	lung
3	chr15:54661400-54662200	Enhancers	HUES48 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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