Variant report

Variant	rs12638345
Chromosome Location	chr3:24898233-24898234
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10865798	1.00[ASN][1000 genomes]
rs12495571	0.85[ASN][1000 genomes]
rs1319984	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1994905	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1994906	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2362767	1.00[ASN][1000 genomes]
rs2885594	0.88[EUR][1000 genomes]
rs937262	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9864319	1.00[ASN][1000 genomes]
rs9880358	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757862	chr3:24652513-24942926	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759135	chr3:24652513-24942926	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv834643	chr3:24779627-24942886	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv3734	chr3:24861568-24906866	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1011730	chr3:24892941-24912030	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24897600-24898800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr3:24897800-24898600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:24897800-24898600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:24897800-24898800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:24898000-24898600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr3:24898200-24898600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr3:24898200-24898800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:24898200-24899600	Weak transcription	ES-I3 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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