Variant report

Variant	rs13113741
Chromosome Location	chr4:130959296-130959297
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10021589	0.89[EUR][1000 genomes]
rs1022005	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1022007	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11729475	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs13112908	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17469824	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2135927	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35211914	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35595889	0.93[EUR][1000 genomes]
rs60016092	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6534761	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs67881292	0.98[EUR][1000 genomes]
rs6828230	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6850077	0.87[EUR][1000 genomes]
rs72926839	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9307620	0.81[EUR][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	nsv1019516	chr4:130754819-130976202	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1017270	chr4:130853337-130982586	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv879936	chr4:130941492-130981535	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130946600-130959600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:130950800-130959600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr4:130952600-130965000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:130954600-130960600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:130954800-130966000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:130954800-130966200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr4:130954800-130966600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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