Variant report

Variant	rs915056
Chromosome Location	chr14:66911129-66911130
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10133769	0.83[CHB][hapmap]
rs10134043	0.83[CHB][hapmap]
rs10134278	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs10144449	0.83[CHB][hapmap]
rs10148290	0.83[CHB][hapmap]
rs10148418	0.83[CHB][hapmap]
rs11158627	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13379248	0.83[CHB][hapmap]
rs1379413	0.83[CHB][hapmap]
rs1457419	0.83[CHB][hapmap]
rs1457420	0.83[CHB][hapmap]
rs1457422	0.83[CHB][hapmap]
rs1457423	0.83[CHB][hapmap]
rs1457424	0.82[CHB][hapmap]
rs17182710	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17827735	0.83[CHB][hapmap]
rs17827741	0.83[CHB][hapmap]
rs17827790	0.82[CHB][hapmap]
rs1952070	0.83[CHB][hapmap]
rs1958001	0.83[CHB][hapmap]
rs2297620	0.83[CHB][hapmap]
rs2319387	0.83[CHB][hapmap]
rs2319389	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3737160	0.83[CHB][hapmap]
rs3737161	0.83[CHB][hapmap]
rs3818770	0.83[CHB][hapmap]
rs4899198	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6573680	0.82[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7140281	0.83[CHB][hapmap]
rs7140509	0.83[CHB][hapmap]
rs7142097	0.83[CHB][hapmap]
rs7143823	0.83[CHB][hapmap]
rs7145556	0.83[CHB][hapmap]
rs7146723	0.83[CHB][hapmap]
rs7147360	0.83[CHB][hapmap]
rs7149265	0.84[ASN][1000 genomes]
rs7149352	0.83[CHB][hapmap]
rs7149668	0.83[CHB][hapmap]
rs7151102	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs7154154	0.83[CHB][hapmap]
rs7155112	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7155944	0.83[CHB][hapmap]
rs7156737	0.83[CHB][hapmap]
rs7157060	0.83[CHB][hapmap]
rs7159473	0.83[CHB][hapmap]
rs7159796	0.81[CHB][hapmap]
rs7160183	0.83[CHB][hapmap]
rs7160519	0.83[CHB][hapmap]
rs8004779	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8018444	0.83[CHB][hapmap]
rs928553	0.83[CHB][hapmap]
rs9323473	0.83[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	esv3385263	chr14:66514718-67511481	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv983837	chr14:66619600-67014519	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv933275	chr14:66649843-67024881	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv1054056	chr14:66848234-66946135	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv525460	chr14:66851185-67626594	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	esv2755038	chr14:66869437-67041440	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
12	nsv521739	chr14:66880362-66930258	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs915056	FAM71D	cis	cerebellum	SCAN
rs915056	EIF2S1	cis	lymphoblastoid	seeQTL

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66908800-66913200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:66908800-66913400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr14:66909000-66913200	Enhancers	Fetal Brain Female	brain
4	chr14:66909200-66911800	Enhancers	Fetal Stomach	stomach
5	chr14:66909200-66913000	Enhancers	Brain Germinal Matrix	brain
6	chr14:66909200-66914000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:66909600-66911800	Enhancers	Adipose Nuclei	Adipose
8	chr14:66909800-66911600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr14:66910000-66911200	Weak transcription	Fetal Muscle Leg	muscle
10	chr14:66910200-66911200	Weak transcription	Fetal Kidney	kidney
11	chr14:66910400-66911400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr14:66910600-66912600	Weak transcription	Fetal Brain Male	brain
13	chr14:66911000-66911600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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