Variant report

Variant	rs2711887
Chromosome Location	chr7:103139301-103139302
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:103138361..103141055-chr7:103143694..103145615,2	K562	blood:
2	chr7:103139301..103141097-chr7:103143967..103145942,2	MCF-7	breast:
3	chr7:103131065..103134051-chr7:103136499..103139382,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10085736	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1024559	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11979750	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11979752	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11983689	0.82[ASN][1000 genomes]
rs12705123	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13229533	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13232021	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13235135	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13239318	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17150781	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17152161	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2079469	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2528872	0.83[AMR][1000 genomes]
rs2528873	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2528875	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2711882	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2711883	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34079239	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34953117	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35246772	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35603368	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3823990	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62480384	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7804453	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7808106	0.95[EUR][1000 genomes];0.89[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	nsv1030446	chr7:102932689-103221638	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103122800-103141000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:103130800-103155000	Weak transcription	Brain Substantia Nigra	brain
3	chr7:103130800-103163600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:103131200-103145000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:103136200-103139800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:103137400-103164400	Weak transcription	Brain Anterior Caudate	brain
7	chr7:103138000-103144200	Strong transcription	HepG2	liver
8	chr7:103138800-103142800	Weak transcription	K562	blood

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