Variant report

Variant	rs17600440
Chromosome Location	chr14:38779574-38779575
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs1168419	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168420	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168421	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168422	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168423	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168424	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168425	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168426	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168427	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168428	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168430	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168435	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168460	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1168462	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1168463	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1168466	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1168477	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1168490	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1168495	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1168497	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1168498	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1168500	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1168503	0.91[EUR][1000 genomes]
rs1177558	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1182911	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1182912	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1183880	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1183882	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1183883	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1184553	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1754703	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1763176	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1763177	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2812053	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs928105	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs969305	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs990495	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
2	nsv533235	chr14:38558180-39117391	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv832773	chr14:38612778-38785003	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv530640	chr14:38702117-38927901	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38779000-38780400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr14:38779000-38780400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
3	chr14:38779000-38780600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
4	chr14:38779200-38780000	Flanking Active TSS	HUVEC	blood vessel
5	chr14:38779200-38780400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
6	chr14:38779200-38781200	Enhancers	Hela-S3	cervix
7	chr14:38779200-38781800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr14:38779400-38779600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr14:38779400-38780400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr14:38779400-38780600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr14:38779400-38782800	Weak transcription	Psoas Muscle	Psoas

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