Variant report

Variant	rs2636612
Chromosome Location	chr6:133938613-133938614
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11154736	0.85[ASN][1000 genomes]
rs1320113	0.88[EUR][1000 genomes]
rs1320114	0.85[ASN][1000 genomes]
rs1878550	0.83[ASN][1000 genomes]
rs2251873	0.94[ASN][1000 genomes]
rs2256702	0.87[ASN][1000 genomes]
rs2459697	0.98[ASN][1000 genomes]
rs2636590	0.98[ASN][1000 genomes]
rs2636591	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2636606	0.88[EUR][1000 genomes]
rs2636611	0.86[ASN][1000 genomes]
rs2636614	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2636615	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2636617	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2636619	0.97[ASN][1000 genomes]
rs2636623	0.96[ASN][1000 genomes]
rs2636626	0.94[ASN][1000 genomes]
rs2677812	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2677825	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2677827	0.98[ASN][1000 genomes]
rs2677829	0.98[ASN][1000 genomes]
rs2677832	0.97[ASN][1000 genomes]
rs2677835	0.93[ASN][1000 genomes]
rs2677836	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3021401	0.85[ASN][1000 genomes]
rs4410743	0.89[ASN][1000 genomes]
rs62427499	0.83[EUR][1000 genomes]
rs62427502	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6922365	0.82[ASN][1000 genomes]
rs7452066	0.83[AFR][1000 genomes]
rs7746271	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9375970	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9385655	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9385656	0.85[ASN][1000 genomes]
rs9385657	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9402519	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9493660	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	nsv886682	chr6:133892208-133943732	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1019267	chr6:133912335-133975187	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133932200-133944200	Weak transcription	NH-A	brain
2	chr6:133936200-133942400	Weak transcription	Fetal Stomach	stomach
3	chr6:133936200-133942600	Weak transcription	Ovary	ovary
4	chr6:133937000-133942800	Weak transcription	A549	lung

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