Variant report

Variant	rs72782230
Chromosome Location	chr10:25407914-25407915
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs17532593	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17616467	0.93[EUR][1000 genomes]
rs41279898	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56176936	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56281542	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57545487	0.93[EUR][1000 genomes]
rs59098941	0.93[EUR][1000 genomes]
rs60598875	0.93[EUR][1000 genomes]
rs61084611	0.86[AMR][1000 genomes]
rs72782211	0.91[EUR][1000 genomes]
rs72782215	0.89[EUR][1000 genomes]
rs72782216	0.96[EUR][1000 genomes]
rs72782217	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782219	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782220	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782221	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782222	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782223	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782224	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72782225	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72782226	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782227	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782228	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72782229	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72792045	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72792046	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72792047	0.86[AMR][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	nsv894970	chr10:25385858-25522280	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv894971	chr10:25403234-25522280	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25392400-25414200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:25402600-25409600	Weak transcription	Pancreas	Pancrea
3	chr10:25406000-25411600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:25406400-25408400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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Input of quick search could be:

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

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