Variant report

Variant	rs10204718
Chromosome Location	chr2:149370840-149370841
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:149366818..149368565-chr2:149369705..149372516,2	MCF-7	breast:
2	chr2:149370215..149372318-chr2:149401556..149403529,3	K562	blood:
3	chr2:149368855..149371718-chr2:149401753..149403322,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000135999	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10165986	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10171728	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10177983	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10181555	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10181614	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10190474	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10200061	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10497035	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10928401	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10928402	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10928408	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11687034	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11687783	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11688979	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12691801	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13016446	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13407240	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13427633	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16828908	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16828910	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2382230	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28533220	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3936439	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4450539	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4624325	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4972282	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4972374	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6430322	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6430326	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6716704	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6736226	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6736270	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6736369	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6739607	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6747262	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6750878	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7574168	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7574666	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs769079	0.86[ASN][1000 genomes]
rs921242	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs921243	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9636222	0.87[EUR][1000 genomes];0.86[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	esv2751831	chr2:149151358-150105603	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv868861	chr2:149198443-149434604	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv917109	chr2:149198443-149948302	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1004663	chr2:149214090-149373061	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv1827161	chr2:149352353-149475737	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149366000-149371000	Weak transcription	Placenta	Placenta
2	chr2:149366000-149371000	Weak transcription	Hela-S3	cervix
3	chr2:149368200-149371400	Weak transcription	Fetal Heart	heart
4	chr2:149368200-149371600	Weak transcription	Right Atrium	heart
5	chr2:149368400-149372000	Weak transcription	Pancreas	Pancrea
6	chr2:149370000-149371200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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