Variant report

Variant	rs10422372
Chromosome Location	chr19:55867037-55867038
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:10)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:10 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr19:55866865-55867120	MCF10A-Er-Src	breast:	n/a	n/a
2	STAT3	chr19:55866786-55867263	MCF10A-Er-Src	breast:	n/a	n/a
3	FOS	chr19:55866838-55867396	MCF10A-Er-Src	breast:	n/a	n/a
4	MYC	chr19:55866811-55867255	MCF10A-Er-Src	breast:	n/a	n/a
5	STAT3	chr19:55866826-55867285	MCF10A-Er-Src	breast:	n/a	n/a
6	MYC	chr19:55866932-55867262	MCF10A-Er-Src	breast:	n/a	n/a
7	STAT3	chr19:55866806-55867338	MCF10A-Er-Src	breast:	n/a	n/a
8	STAT3	chr19:55866915-55867128	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr19:55866888-55867263	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr19:55866809-55867232	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:55864929..55868342-chr19:55869494..55871064,3	MCF-7	breast:
2	chr19:55865530..55867437-chr19:55869222..55871050,2	K562	blood:
3	chr19:55864955..55867658-chr19:55880222..55883231,3	MCF-7	breast:
4	chr19:55865626..55867203-chr19:55869204..55871320,2	K562	blood:
5	chr19:55864065..55867080-chr19:55895058..55897568,4	K562	blood:
6	chr19:55865908..55868131-chr19:55880960..55883611,2	MCF-7	breast:
7	chr19:55865213..55868465-chr19:55868824..55871801,4	MCF-7	breast:
8	chr19:55864307..55867114-chr19:56165229..56167152,3	K562	blood:
9	chr19:55866844..55868519-chr19:55877122..55879184,2	K562	blood:
10	chr19:55862642..55868480-chr19:55895176..55899926,10	K562	blood:
11	chr19:55865425..55868489-chr19:55917598..55920755,3	MCF-7	breast:
12	chr19:55853470..55856275-chr19:55866568..55868839,2	MCF-7	breast:

No data

Variant related genes	Relation type
COX6B2	TF binding region
ENSG00000108107	Chromatin interaction
ENSG00000095752	Chromatin interaction
ENSG00000267706	Chromatin interaction
ENSG00000233493	Chromatin interaction
ENSG00000133247	Chromatin interaction
ENSG00000108106	Chromatin interaction
ENSG00000063244	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10426501	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1126760	1.00[JPT][hapmap]
rs12460416	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12609732	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12611363	0.82[JPT][hapmap]
rs12974819	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12974907	0.96[ASN][1000 genomes]
rs12976922	1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];0.96[ASN][1000 genomes]
rs1466304	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2124918	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2305787	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2305788	0.82[JPT][hapmap]
rs897799	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1816335	chr19:55683977-55901099	Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1065760	chr19:55721521-55929740	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
3	nsv912455	chr19:55725410-55879872	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv912456	chr19:55725410-55925500	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
5	nsv912457	chr19:55725410-56019597	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	228 gene(s)	inside rSNPs	diseases
6	nsv432086	chr19:55807586-56050844	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	220 gene(s)	inside rSNPs	diseases
7	nsv912460	chr19:55814881-55897327	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv912461	chr19:55845386-55897327	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
9	nsv470162	chr19:55845386-55902257	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
10	nsv912462	chr19:55845386-55925500	Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
11	nsv912463	chr19:55845386-56004901	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
12	nsv912464	chr19:55850269-55921164	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
13	esv1799638	chr19:55850652-55883879	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
14	nsv516199	chr19:55854313-55901099	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
15	nsv912465	chr19:55854313-55935184	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
16	esv3430654	chr19:55864590-55867488	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	esv3405241	chr19:55865165-55868013	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	nsv912466	chr19:55867037-55876074	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10422372	CUZD1	trans	lymphoblastoid	seeQTL

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55865800-55867400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:55865800-55867800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr19:55866000-55867200	Bivalent Enhancer	Fetal Stomach	stomach
4	chr19:55866000-55867400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr19:55866000-55867400	Enhancers	HMEC	breast
6	chr19:55866000-55867400	Enhancers	NHEK	skin
7	chr19:55866200-55880600	Weak transcription	Right Atrium	heart
8	chr19:55866400-55867200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr19:55866400-55867400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr19:55866400-55867600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:55866400-55867800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr19:55866800-55867200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
13	chr19:55866800-55867200	Bivalent Enhancer	HSMM	muscle
14	chr19:55866800-55867400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:55866800-55867400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:55866800-55867400	Bivalent Enhancer	Esophagus	oesophagus
17	chr19:55867000-55867200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr19:55867000-55867200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
19	chr19:55867000-55867200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

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