Variant report

Variant	rs751529
Chromosome Location	chr6:15730827-15730828
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	chr6:15729983..15731869-chr6:16128035..16130955,3	K562	blood:
2	chr6:15723984..15726678-chr6:15729144..15731299,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000007944	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10484353	0.94[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs10949310	0.87[ASN][1000 genomes]
rs10949311	0.92[ASN][1000 genomes]
rs12197897	1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs12204417	0.89[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs12210613	1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs12211903	0.96[ASN][1000 genomes]
rs12660578	0.91[ASN][1000 genomes]
rs12662373	0.90[ASN][1000 genomes]
rs13190958	0.92[ASN][1000 genomes]
rs13201966	1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs13202253	0.92[ASN][1000 genomes]
rs13203504	0.89[ASN][1000 genomes]
rs13205159	1.00[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs13205914	0.92[ASN][1000 genomes]
rs13219203	1.00[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs2022348	1.00[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs2023428	0.88[CEU][hapmap]
rs2031818	0.89[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs2031819	0.84[CEU][hapmap]
rs4623247	0.86[JPT][hapmap]
rs6939629	0.83[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs737072	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs737073	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7450621	1.00[CHB][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs7740240	0.82[ASN][1000 genomes]
rs7745707	0.92[ASN][1000 genomes]
rs7752961	0.84[CEU][hapmap]
rs7759940	0.81[ASN][1000 genomes]
rs7761926	0.84[CEU][hapmap]
rs9476895	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9476896	0.84[AMR][1000 genomes]
rs9476899	0.81[YRI][hapmap]
rs9766154	0.85[ASN][1000 genomes]
rs9766732	0.85[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	nsv428136	chr6:15595640-15781241	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2755670	chr6:15624762-15736008	Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr6:15721200-15736200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:15728800-15733400	Weak transcription	Fetal Heart	heart
3	chr6:15729600-15731200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:15730000-15731800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:15730400-15731200	Flanking Active TSS	K562	blood
6	chr6:15730600-15731800	Enhancers	Fetal Intestine Small	intestine
7	chr6:15730800-15731200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:15730800-15731400	Enhancers	Fetal Intestine Large	intestine

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