Variant report

Variant	rs2166751
Chromosome Location	chr14:42111079-42111080
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1111179	0.85[JPT][hapmap]
rs11157242	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1117723	1.00[CEU][hapmap];0.94[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs12100476	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs12100840	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12100891	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs12587520	0.85[ASN][1000 genomes]
rs12589180	0.93[ASN][1000 genomes]
rs12590527	0.93[ASN][1000 genomes]
rs17092256	0.85[ASN][1000 genomes]
rs17112133	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[ASN][1000 genomes]
rs17112137	0.84[ASN][1000 genomes]
rs17112148	0.93[ASN][1000 genomes]
rs1950831	0.90[ASN][1000 genomes]
rs1950835	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs1950838	0.81[ASN][1000 genomes]
rs1956446	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1956447	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1998126	0.84[ASN][1000 genomes]
rs2077067	0.85[ASN][1000 genomes]
rs28755010	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2899928	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs59063354	0.93[ASN][1000 genomes]
rs59937937	0.93[ASN][1000 genomes]
rs6572097	0.94[CHB][hapmap];0.86[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap]
rs6572099	0.82[ASN][1000 genomes]
rs8003822	0.88[ASN][1000 genomes]
rs8007172	0.82[ASN][1000 genomes]
rs8013655	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047300	chr14:41671653-42361098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv533968	chr14:41882101-42327882	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1042078	chr14:41993985-42120143	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2758353	chr14:42045873-42259511	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2759983	chr14:42045873-42259511	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription 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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42106400-42111200	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr14:42107200-42111400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:42110200-42112400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr14:42111000-42111400	Enhancers	HUES6 Cell Line	embryonic stem cell

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