Variant report

Variant	rs4669148
Chromosome Location	chr2:7334962-7334963
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:7333942..7335730-chr2:8825040..8827834,2	MCF-7	breast:
2	chr2:7334770..7337311-chr2:7337607..7339692,2	K562	blood:
3	chr2:7330725..7333657-chr2:7333775..7335694,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1016515	0.83[ASN][1000 genomes]
rs11676725	0.85[ASN][1000 genomes]
rs11680346	0.87[ASN][1000 genomes]
rs11695715	0.84[ASN][1000 genomes]
rs12474153	0.85[AFR][1000 genomes]
rs12612703	0.84[ASN][1000 genomes]
rs12621585	0.84[ASN][1000 genomes]
rs12623613	0.84[ASN][1000 genomes]
rs13002545	0.84[ASN][1000 genomes]
rs13007890	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13023691	0.84[ASN][1000 genomes]
rs13035063	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404841	0.99[ASN][1000 genomes]
rs1404842	0.98[ASN][1000 genomes]
rs1404843	0.99[ASN][1000 genomes]
rs1404844	0.99[ASN][1000 genomes]
rs1464879	0.85[ASN][1000 genomes]
rs1473656	0.88[ASN][1000 genomes]
rs1474401	0.99[ASN][1000 genomes]
rs1474402	0.99[ASN][1000 genomes]
rs1474403	0.99[ASN][1000 genomes]
rs1525491	0.85[ASN][1000 genomes]
rs1581562	0.85[ASN][1000 genomes]
rs17672986	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1880604	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1917675	0.85[ASN][1000 genomes]
rs1917676	0.85[ASN][1000 genomes]
rs1917677	0.85[ASN][1000 genomes]
rs1917680	1.00[ASN][1000 genomes]
rs2352711	0.99[ASN][1000 genomes]
rs2352713	0.83[ASN][1000 genomes]
rs34130652	0.84[ASN][1000 genomes]
rs36034588	0.85[ASN][1000 genomes]
rs4356635	0.85[ASN][1000 genomes]
rs4362529	0.85[ASN][1000 genomes]
rs4362530	0.85[ASN][1000 genomes]
rs4668526	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4668527	0.87[ASN][1000 genomes]
rs4669147	0.99[ASN][1000 genomes]
rs4669149	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4669150	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4669154	0.91[ASN][1000 genomes]
rs4669155	0.91[ASN][1000 genomes]
rs4669157	0.89[ASN][1000 genomes]
rs4669162	0.85[ASN][1000 genomes]
rs4669163	0.87[ASN][1000 genomes]
rs55914055	0.86[ASN][1000 genomes]
rs6719090	0.99[ASN][1000 genomes]
rs6732488	0.83[ASN][1000 genomes]
rs6738582	0.81[ASN][1000 genomes]
rs6739202	0.88[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6744969	0.99[ASN][1000 genomes]
rs6745122	0.99[ASN][1000 genomes]
rs7557233	0.99[ASN][1000 genomes]
rs7607300	0.99[ASN][1000 genomes]
rs870863	0.85[ASN][1000 genomes]
rs960793	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7331000-7341800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:7332800-7335400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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