Variant report

Variant	rs1721908
Chromosome Location	chr7:109186754-109186755
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:109186467..109188303-chr7:109189760..109191326,2	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10267307	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10499979	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10953620	0.85[ASN][1000 genomes]
rs11521007	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12536153	0.82[ASN][1000 genomes]
rs12705613	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12705619	0.82[ASN][1000 genomes]
rs13238416	0.82[ASN][1000 genomes]
rs13239845	0.83[ASN][1000 genomes]
rs1357685	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1464744	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1524271	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1524273	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1524277	0.83[ASN][1000 genomes]
rs1616510	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1721445	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1721447	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1721448	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1721898	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1721899	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1721903	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17463939	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17464044	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1880236	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1880237	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2103123	0.82[EUR][1000 genomes]
rs2140585	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2140587	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2396133	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56165817	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62473267	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109186000-109187800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:109186200-109187200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:109186200-109187400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:109186200-109187400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:109186400-109187600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:109186400-109187600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:109186400-109187800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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