Variant report

Variant	rs57059254
Chromosome Location	chr10:26466333-26466334
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10508716	1.00[EUR][1000 genomes]
rs11015010	1.00[EUR][1000 genomes]
rs12253114	1.00[EUR][1000 genomes]
rs16926523	1.00[EUR][1000 genomes]
rs16926634	1.00[EUR][1000 genomes]
rs16926866	1.00[EUR][1000 genomes]
rs61322866	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7068224	1.00[EUR][1000 genomes]
rs74126456	1.00[EUR][1000 genomes]
rs74126457	1.00[EUR][1000 genomes]
rs74126459	1.00[EUR][1000 genomes]
rs74126460	1.00[EUR][1000 genomes]
rs74126461	1.00[EUR][1000 genomes]
rs74126462	1.00[EUR][1000 genomes]
rs74126465	1.00[EUR][1000 genomes]
rs74126466	1.00[EUR][1000 genomes]
rs7476345	1.00[EUR][1000 genomes]
rs7897279	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7922748	1.00[EUR][1000 genomes]
rs8190585	1.00[EUR][1000 genomes]
rs8190593	1.00[EUR][1000 genomes]
rs8190689	1.00[EUR][1000 genomes]
rs8190714	1.00[EUR][1000 genomes]
rs8190720	1.00[EUR][1000 genomes]
rs8190807	1.00[EUR][1000 genomes]
rs8190815	1.00[EUR][1000 genomes]
rs928198	1.00[EUR][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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26440800-26473400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26453800-26466800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:26459400-26466800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr10:26461400-26466800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:26464600-26478000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:26465000-26466800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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