Variant report

Variant	rs2396136
Chromosome Location	chr7:109238303-109238304
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10264734	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12537605	0.96[ASN][1000 genomes]
rs12540076	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1357690	0.92[ASN][1000 genomes]
rs1405065	0.88[ASN][1000 genomes]
rs1464743	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1524280	0.92[ASN][1000 genomes]
rs1568778	0.92[ASN][1000 genomes]
rs1626408	0.99[ASN][1000 genomes]
rs1721418	0.92[ASN][1000 genomes]
rs1721420	0.92[ASN][1000 genomes]
rs1721422	0.96[ASN][1000 genomes]
rs1721424	0.98[ASN][1000 genomes]
rs1721425	0.98[ASN][1000 genomes]
rs1721426	0.97[ASN][1000 genomes]
rs1721428	0.83[ASN][1000 genomes]
rs1721431	0.92[ASN][1000 genomes]
rs1721452	0.92[ASN][1000 genomes]
rs1721454	0.92[ASN][1000 genomes]
rs1721456	0.92[ASN][1000 genomes]
rs1721925	0.86[ASN][1000 genomes]
rs1721934	0.99[ASN][1000 genomes]
rs1721936	0.98[ASN][1000 genomes]
rs1721938	0.97[ASN][1000 genomes]
rs1721941	0.92[ASN][1000 genomes]
rs1721945	0.89[ASN][1000 genomes]
rs1721946	0.92[ASN][1000 genomes]
rs1721950	0.92[ASN][1000 genomes]
rs1721951	0.92[ASN][1000 genomes]
rs1721953	0.92[ASN][1000 genomes]
rs1916913	0.92[ASN][1000 genomes]
rs2250798	0.88[ASN][1000 genomes]
rs2396137	0.98[ASN][1000 genomes]
rs2690352	0.85[ASN][1000 genomes]
rs2690360	0.86[ASN][1000 genomes]
rs2690372	0.93[ASN][1000 genomes]
rs2690376	0.88[ASN][1000 genomes]
rs4730395	0.92[ASN][1000 genomes]
rs6949142	0.92[ASN][1000 genomes]
rs7797247	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[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	nsv1023379	chr7:109003574-109355234	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv608079	chr7:109098364-109862289	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1020761	chr7:109208187-109275700	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109234000-109238600	Active TSS	H1 Cell Line	embryonic stem cell
2	chr7:109237200-109239800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:109237400-109239600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:109237400-109240400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr7:109237600-109238400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr7:109237800-109238600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr7:109237800-109238600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr7:109237800-109238600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr7:109237800-109238600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr7:109238000-109238600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:109238200-109238400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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