Variant report

Variant	rs32791
Chromosome Location	chr5:35431383-35431384
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	chr5:35229197..35230970-chr5:35430863..35432528,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000113494	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10041120	0.95[ASN][1000 genomes]
rs10044118	0.94[ASN][1000 genomes]
rs10044161	0.94[ASN][1000 genomes]
rs1508659	0.92[ASN][1000 genomes]
rs1508660	0.98[ASN][1000 genomes]
rs1605689	0.98[ASN][1000 genomes]
rs26197	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs26198	0.88[ASN][1000 genomes]
rs26199	0.88[ASN][1000 genomes]
rs26200	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs26201	0.88[ASN][1000 genomes]
rs26203	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs26204	0.95[ASN][1000 genomes]
rs26205	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs27487	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs27762	0.88[ASN][1000 genomes]
rs27940	0.88[ASN][1000 genomes]
rs28020	0.88[ASN][1000 genomes]
rs284692	0.88[ASN][1000 genomes]
rs284693	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs284694	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs284695	0.88[ASN][1000 genomes]
rs284697	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs284698	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs284750	0.89[EUR][1000 genomes]
rs32733	0.95[ASN][1000 genomes]
rs32754	0.87[ASN][1000 genomes]
rs32755	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs32758	0.88[ASN][1000 genomes]
rs32789	0.91[ASN][1000 genomes]
rs32790	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs39981	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs457255	0.88[ASN][1000 genomes]
rs4703362	0.98[ASN][1000 genomes]
rs4703363	0.98[ASN][1000 genomes]
rs4703401	0.94[ASN][1000 genomes]
rs4703402	0.98[ASN][1000 genomes]
rs58530298	0.92[ASN][1000 genomes]
rs6451200	0.92[ASN][1000 genomes]
rs6865370	0.95[ASN][1000 genomes]
rs6897316	0.98[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35430200-35431400	Enhancers	NHEK	skin
2	chr5:35430200-35431800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:35430400-35431400	Weak transcription	Placenta	Placenta
4	chr5:35430400-35431800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr5:35430600-35431400	Enhancers	Fetal Intestine Small	intestine
6	chr5:35431000-35431800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr5:35431200-35431600	Enhancers	Placenta Amnion	Placenta Amnion

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