Variant report

Variant	rs13234130
Chromosome Location	chr7:13618649-13618650
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10499429	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699509	1.00[ASN][1000 genomes]
rs12699514	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699515	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699521	1.00[ASN][1000 genomes]
rs12699522	1.00[ASN][1000 genomes]
rs12699523	1.00[ASN][1000 genomes]
rs12699526	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12699527	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12699533	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13222945	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13223388	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13223397	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13226153	1.00[ASN][1000 genomes]
rs13226865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13229998	1.00[ASN][1000 genomes]
rs13230082	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13233758	1.00[ASN][1000 genomes]
rs13234879	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13235921	1.00[ASN][1000 genomes]
rs13237232	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13238361	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13243009	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs13243211	1.00[ASN][1000 genomes]
rs1357978	1.00[ASN][1000 genomes]
rs1357979	1.00[ASN][1000 genomes]
rs1525678	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17194917	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34575271	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34817842	1.00[ASN][1000 genomes]
rs35137805	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35519947	1.00[ASN][1000 genomes]
rs35553190	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35657075	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35907373	1.00[ASN][1000 genomes]
rs35907984	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs36068685	1.00[ASN][1000 genomes]
rs4721234	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4721237	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67184261	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6951342	1.00[ASN][1000 genomes]
rs6955662	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6961459	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6978901	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6979071	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7778160	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7789334	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs869552	1.00[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	nsv1023580	chr7:13403531-13624975	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv1815242	chr7:13591076-13633151	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv887690	chr7:13591197-13702169	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1026929	chr7:13597929-13716063	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1023839	chr7:13617615-13735946	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 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	chr7:13617200-13619000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr7:13617200-13619000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr7:13617200-13619200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr7:13617200-13619800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr7:13617400-13619000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:13617600-13619200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr7:13618400-13619000	Enhancers	H9 Cell Line	embryonic stem cell

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