Variant report

Variant	rs61990342
Chromosome Location	chr14:42188351-42188352
allele	C/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]
rs1597049	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1597050	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17112192	0.82[ASN][1000 genomes]
rs17181601	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17181608	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17181615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17181622	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17181636	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17781361	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs41319550	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4584739	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4586337	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4603462	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4624078	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58373729	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58844543	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59082466	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61990335	0.82[ASN][1000 genomes]
rs61990337	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61990338	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61990339	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61990343	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61990345	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61990346	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61990347	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61990349	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61992404	0.88[ASN][1000 genomes]
rs72686527	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72686528	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[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	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
4	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
5	nsv901738	chr14:42145461-42302552	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42185400-42192800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:42187400-42188400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr14:42187400-42188400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr14:42187400-42188400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:42187400-42188800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr14:42187800-42188400	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr14:42187800-42188400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr14:42187800-42188400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr14:42187800-42188400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr14:42187800-42188400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr14:42188000-42188400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr14:42188200-42188400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr14:42188200-42197000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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