Variant report

Variant	rs10410527
Chromosome Location	chr19:42237023-42237024
allele	C/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]
rs10405947	0.83[AMR][1000 genomes]
rs10406719	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10411490	1.00[AMR][1000 genomes]
rs10412753	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10414563	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10417176	1.00[AMR][1000 genomes]
rs13343300	0.82[ASW][hapmap];0.93[MKK][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28366798	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28521200	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8103664	0.94[AFR][1000 genomes];1.00[AMR][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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	esv3425986	chr19:42212540-42259719	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv579615	chr19:42221434-42310388	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42231400-42237800	Weak transcription	Colonic Mucosa	Colon
2	chr19:42234000-42237600	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr19:42234400-42239800	Enhancers	Stomach Mucosa	stomach
4	chr19:42236400-42237800	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr19:42236400-42241800	Enhancers	Fetal Intestine Large	intestine
6	chr19:42237000-42237400	Weak transcription	Fetal Intestine Small	intestine
7	chr19:42237000-42243400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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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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