Variant report

Variant	rs60197913
Chromosome Location	chr10:45595046-45595047
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11239349	0.85[ASN][1000 genomes]
rs12252994	0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12569983	0.92[ASN][1000 genomes]
rs12570593	0.87[ASN][1000 genomes]
rs28510585	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs34564821	0.82[ASN][1000 genomes]
rs55648726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73291619	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7907860	0.93[ASN][1000 genomes]
rs9663396	0.95[AMR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831848	chr10:45490176-45667670	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	nsv971917	chr10:45547355-45595482	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2750897	chr10:45550145-45820136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45590400-45596400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:45591000-45602000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr10:45591400-45595600	Weak transcription	Brain Germinal Matrix	brain
4	chr10:45591400-45596000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:45591800-45596000	Weak transcription	Fetal Muscle Leg	muscle

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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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