Variant report

Variant	rs73610350
Chromosome Location	chr10:26034638-26034639
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10128321	1.00[EUR][1000 genomes]
rs10508702	1.00[EUR][1000 genomes]
rs11014730	1.00[EUR][1000 genomes]
rs11014731	1.00[EUR][1000 genomes]
rs12245158	1.00[EUR][1000 genomes]
rs12248899	1.00[EUR][1000 genomes]
rs12254756	1.00[EUR][1000 genomes]
rs12260558	1.00[EUR][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	nsv894973	chr10:26020424-26043071	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
2	nsv894974	chr10:26028530-26322783	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:26031200-26035400	Weak transcription	Brain Germinal Matrix	brain
2	chr10:26034400-26035200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr10:26034600-26036600	Enhancers	NH-A	brain

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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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