Variant report

Variant	rs2079305
Chromosome Location	chr14:71648045-71648046
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:71647954-71648314	K562	blood:	n/a	n/a
2	USF1	chr14:71647966-71648268	K562	blood:	n/a	n/a
3	NFYB	chr14:71647999-71648539	K562	blood:	n/a	n/a
4	MYC	chr14:71647925-71648226	K562	blood:	n/a	n/a
5	E2F6	chr14:71647982-71648220	K562	blood:	n/a	n/a
6	MAX	chr14:71648005-71648234	K562	blood:	n/a	n/a
7	MAX	chr14:71647937-71648276	K562	blood:	n/a	n/a
8	MAX	chr14:71647985-71648221	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:71647115..71649453-chr14:71786412..71788278,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259907	TF binding region
ENSG00000197555	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10162332	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10162513	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1017023	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1017024	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11158894	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11158895	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11622578	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11628267	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12433285	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12433881	0.81[ASN][1000 genomes]
rs12433971	0.81[ASN][1000 genomes]
rs12436140	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12436994	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12437099	0.81[ASN][1000 genomes]
rs12586505	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12591005	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17177802	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17767137	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2003488	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2240535	1.00[JPT][hapmap]
rs55831429	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55968807	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55979041	0.87[AMR][1000 genomes]
rs56369736	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7144242	0.81[ASN][1000 genomes]
rs7152112	0.81[ASN][1000 genomes]
rs72726621	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72726627	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72726634	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs740069	0.81[ASN][1000 genomes]
rs740070	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs740071	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs740072	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs917063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1038007	chr14:71269747-71667680	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv1036929	chr14:71469148-71683412	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71634600-71648200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:71638600-71654600	Weak transcription	Pancreas	Pancrea
3	chr14:71642400-71648200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:71648000-71648600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr14:71648000-71648600	Enhancers	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links