Variant report

Variant	rs74034309
Chromosome Location	chr14:20999962-20999963
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:20999182..21000434-chr14:21077072..21078173,4	K562	blood:
2	chr14:20998943..21000065-chr14:21077252..21078209,3	MCF-7	breast:
3	chr14:20993418..20995873-chr14:20998569..21001480,3	K562	blood:
4	chr14:20868871..20872718-chr14:20998091..21001261,3	MCF-7	breast:
5	chr14:20937509..20939989-chr14:20997994..21000169,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129566	Chromatin interaction
ENSG00000173464	Chromatin interaction
ENSG00000198805	Chromatin interaction
ENSG00000259060	Chromatin interaction
ENSG00000258456	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10162403	1.00[EUR][1000 genomes]
rs12100586	1.00[EUR][1000 genomes]
rs12100598	1.00[EUR][1000 genomes]
rs12100800	1.00[EUR][1000 genomes]
rs12100933	1.00[EUR][1000 genomes]
rs12100943	1.00[EUR][1000 genomes]
rs12101090	1.00[EUR][1000 genomes]
rs12101096	1.00[EUR][1000 genomes]
rs12101201	1.00[EUR][1000 genomes]
rs12101227	1.00[EUR][1000 genomes]
rs17092013	1.00[EUR][1000 genomes]
rs17112807	1.00[EUR][1000 genomes]
rs17112928	1.00[EUR][1000 genomes]
rs17112943	1.00[EUR][1000 genomes]
rs17112951	1.00[EUR][1000 genomes]
rs17113273	1.00[EUR][1000 genomes]
rs2228653	1.00[EUR][1000 genomes]
rs55747318	1.00[EUR][1000 genomes]
rs55795834	1.00[EUR][1000 genomes]
rs55917840	1.00[EUR][1000 genomes]
rs55980661	1.00[EUR][1000 genomes]
rs55987734	1.00[EUR][1000 genomes]
rs56294788	1.00[EUR][1000 genomes]
rs57630159	1.00[EUR][1000 genomes]
rs58957711	1.00[EUR][1000 genomes]
rs58964539	1.00[EUR][1000 genomes]
rs59045719	1.00[EUR][1000 genomes]
rs59612537	1.00[EUR][1000 genomes]
rs59800190	1.00[EUR][1000 genomes]
rs60239610	1.00[EUR][1000 genomes]
rs60292704	1.00[EUR][1000 genomes]
rs60508855	1.00[EUR][1000 genomes]
rs60971353	1.00[EUR][1000 genomes]
rs61626479	1.00[EUR][1000 genomes]
rs7143903	1.00[EUR][1000 genomes]
rs7146539	1.00[EUR][1000 genomes]
rs7152653	1.00[EUR][1000 genomes]
rs7155848	1.00[EUR][1000 genomes]
rs7160116	1.00[EUR][1000 genomes]
rs7161484	1.00[EUR][1000 genomes]
rs73571203	1.00[EUR][1000 genomes]
rs73571209	1.00[EUR][1000 genomes]
rs73571210	1.00[EUR][1000 genomes]
rs73571212	1.00[EUR][1000 genomes]
rs73571302	1.00[EUR][1000 genomes]
rs74034305	1.00[EUR][1000 genomes]
rs74034308	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74037158	1.00[EUR][1000 genomes]
rs74037159	1.00[EUR][1000 genomes]
rs74037160	1.00[EUR][1000 genomes]
rs8003273	1.00[EUR][1000 genomes]
rs8010422	1.00[EUR][1000 genomes]
rs8018216	1.00[EUR][1000 genomes]
rs8022560	1.00[EUR][1000 genomes]
rs8022642	1.00[EUR][1000 genomes]
rs8022887	1.00[EUR][1000 genomes]
rs8022889	1.00[EUR][1000 genomes]
rs8022924	1.00[EUR][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	nsv1043923	chr14:20338742-21336425	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
2	nsv541970	chr14:20338742-21336425	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
3	esv21015	chr14:20800765-21257878	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
4	nsv901468	chr14:20997221-21149785	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 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	chr14:20999200-21002800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:20999400-21003200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links