Variant report

Variant	rs34219471
Chromosome Location	chr6:150808836-150808837
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:150807751..150809812-chr6:150811234..150814298,3	K562	blood:
2	chr6:150783745..150786487-chr6:150807804..150809772,2	K562	blood:
3	chr6:150806855..150809448-chr6:150811234..150813450,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10499263	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes]
rs10499264	0.86[EUR][1000 genomes]
rs11964142	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13193322	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13196518	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13197203	0.87[EUR][1000 genomes]
rs13199757	0.86[EUR][1000 genomes]
rs13206793	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13217733	0.85[EUR][1000 genomes]
rs13218019	0.88[EUR][1000 genomes]
rs17079805	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17079846	0.87[EUR][1000 genomes]
rs17079852	0.87[EUR][1000 genomes]
rs17079861	0.87[EUR][1000 genomes]
rs33951563	0.88[EUR][1000 genomes]
rs34120777	0.85[EUR][1000 genomes]
rs34393000	0.86[EUR][1000 genomes]
rs34537150	0.95[EUR][1000 genomes]
rs34597508	0.86[EUR][1000 genomes]
rs34713924	0.87[EUR][1000 genomes]
rs34779574	0.86[EUR][1000 genomes]
rs34782866	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35046394	0.87[EUR][1000 genomes]
rs35260192	0.87[EUR][1000 genomes]
rs4075592	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4323319	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes]
rs4566894	0.88[EUR][1000 genomes]
rs55673001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55708277	0.85[EUR][1000 genomes]
rs59435275	0.85[EUR][1000 genomes]
rs67925488	0.87[EUR][1000 genomes]
rs6924786	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73002876	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7774671	0.87[EUR][1000 genomes]
rs9384545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9398002	0.83[EUR][1000 genomes]
rs9398004	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9688466	0.86[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	nsv1020067	chr6:150730783-150870708	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886772	chr6:150743364-151024280	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr6:150808000-150811400	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:150808000-150812200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:150808000-150812400	Weak transcription	HUVEC	blood vessel
4	chr6:150808200-150811200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:150808200-150811200	Weak transcription	Fetal Thymus	thymus
6	chr6:150808200-150811400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:150808800-150809200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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