Variant report

Variant	rs28444219
Chromosome Location	chr15:43540633-43540634
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:43535426..43538797-chr15:43540482..43544036,3	K562	blood:
2	chr15:43536398..43537938-chr15:43540346..43541943,2	MCF-7	breast:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10048057	1.00[EUR][1000 genomes]
rs10083725	1.00[EUR][1000 genomes]
rs10152237	1.00[EUR][1000 genomes]
rs10220812	1.00[EUR][1000 genomes]
rs1042168	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10438267	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10467909	1.00[EUR][1000 genomes]
rs1078243	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11504654	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11504655	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12324094	1.00[EUR][1000 genomes]
rs12324436	1.00[EUR][1000 genomes]
rs12324573	1.00[EUR][1000 genomes]
rs1474199	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1520519	1.00[EUR][1000 genomes]
rs16957409	1.00[EUR][1000 genomes]
rs16957462	1.00[EUR][1000 genomes]
rs16957499	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16957502	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16957507	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16957739	1.00[EUR][1000 genomes]
rs1863601	1.00[EUR][1000 genomes]
rs2004809	1.00[EUR][1000 genomes]
rs2271964	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2271965	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28539201	1.00[EUR][1000 genomes]
rs3177296	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34222269	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4419035	1.00[EUR][1000 genomes]
rs505276	1.00[EUR][1000 genomes]
rs58059509	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59401274	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59900401	1.00[EUR][1000 genomes]
rs60435696	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60481556	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61268760	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61343376	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61711558	1.00[EUR][1000 genomes]
rs7162620	1.00[EUR][1000 genomes]
rs7162971	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7171797	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7176183	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7182685	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7183024	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8030850	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8035881	1.00[EUR][1000 genomes]
rs8039342	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8040769	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8040960	1.00[EUR][1000 genomes]
rs8041312	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9806236	1.00[EUR][1000 genomes]
rs9806629	1.00[EUR][1000 genomes]
rs9972314	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9972367	1.00[EUR][1000 genomes]
rs999025	1.00[EUR][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	nsv1044522	chr15:43115348-43658417	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv1044508	chr15:43270637-43658417	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43532600-43541600	Weak transcription	K562	blood
2	chr15:43536800-43543400	Weak transcription	Esophagus	oesophagus
3	chr15:43538000-43546600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr15:43539000-43541000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr15:43539000-43541000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr15:43539200-43540800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr15:43540000-43541400	Enhancers	GM12878-XiMat	blood
8	chr15:43540400-43542600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:43540600-43541000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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