Variant report

Variant	rs17005142
Chromosome Location	chr4:82402588-82402589
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10010140	1.00[ASN][1000 genomes]
rs10010394	1.00[ASN][1000 genomes]
rs10012642	0.95[ASN][1000 genomes]
rs10015146	1.00[ASN][1000 genomes]
rs10023826	0.90[ASN][1000 genomes]
rs12500201	1.00[ASN][1000 genomes]
rs12502814	1.00[ASN][1000 genomes]
rs13102560	0.95[ASN][1000 genomes]
rs13111699	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13128387	0.90[ASN][1000 genomes]
rs13131664	0.95[ASN][1000 genomes]
rs16998600	0.97[ASN][1000 genomes]
rs17005144	1.00[ASN][1000 genomes]
rs17005145	1.00[ASN][1000 genomes]
rs28479652	1.00[ASN][1000 genomes]
rs28767523	1.00[ASN][1000 genomes]
rs28827174	1.00[ASN][1000 genomes]
rs34128580	1.00[ASN][1000 genomes]
rs34749111	0.90[ASN][1000 genomes]
rs35010226	0.90[ASN][1000 genomes]
rs35149381	0.95[ASN][1000 genomes]
rs35991185	1.00[ASN][1000 genomes]
rs36026752	1.00[ASN][1000 genomes]
rs41523946	0.90[ASN][1000 genomes]
rs4693274	1.00[ASN][1000 genomes]
rs4693275	0.92[ASN][1000 genomes]
rs4693276	0.92[ASN][1000 genomes]
rs4693277	0.92[ASN][1000 genomes]
rs62303604	1.00[ASN][1000 genomes]
rs6535252	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6819741	1.00[ASN][1000 genomes]
rs6819989	1.00[ASN][1000 genomes]
rs6825177	1.00[ASN][1000 genomes]
rs6834665	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7660392	0.95[ASN][1000 genomes]
rs7678464	0.90[ASN][1000 genomes]
rs7683852	0.90[ASN][1000 genomes]
rs7684580	1.00[ASN][1000 genomes]
rs7688827	0.90[ASN][1000 genomes]
rs7690069	0.95[ASN][1000 genomes]
rs7691170	0.95[ASN][1000 genomes]
rs9307784	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829986	chr4:82345163-82509860	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:82395800-82406400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:82402400-82403200	Enhancers	Monocytes-CD14+_RO01746	blood

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