Variant report

Variant	rs10082235
Chromosome Location	chr1:153656650-153656651
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	ATF1	chr1:153656426-153656714	K562	blood:	n/a	n/a
2	JUND	chr1:153656410-153656724	K562	blood:	n/a	chr1:153656555-153656564
3	RCOR1	chr1:153656521-153656713	Hela-S3	cervix:	n/a	n/a
4	SMC3	chr1:153656480-153656680	Hela-S3	cervix:	n/a	n/a
5	RAD21	chr1:153656478-153656724	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:153656433-153656722	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:153656480-153656706	K562	blood:	n/a	n/a
8	FOS	chr1:153656503-153656696	MCF10A-Er-Src	breast:	n/a	chr1:153656555-153656564
9	FOS	chr1:153656527-153656703	MCF10A-Er-Src	breast:	n/a	chr1:153656555-153656564

No.	Distal block	Cell Line	Cell type
1	chr1:153651109..153660855-chr1:153698392..153702896,14	MCF-7	breast:
2	chr1:153649941..153652996-chr1:153654947..153657663,3	K562	blood:
3	chr1:153654218..153657204-chr1:153660557..153664055,3	MCF-7	breast:
4	chr1:153648584..153651991-chr1:153654471..153657777,3	MCF-7	breast:
5	chr1:153640859..153647825-chr1:153650423..153657512,10	K562	blood:

Variant related genes	Relation type
NPR1	TF binding region
ENSG00000199565	Chromatin interaction
ENSG00000143624	Chromatin interaction
ENSG00000169418	Chromatin interaction
ENSG00000143621	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11805092	1.00[JPT][hapmap]
rs11808118	0.86[ASN][1000 genomes]
rs12097043	1.00[CHB][hapmap]
rs12097725	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13305995	0.86[ASN][1000 genomes]
rs13305996	0.86[ASN][1000 genomes]
rs13305998	0.86[ASN][1000 genomes]
rs13306004	0.86[ASN][1000 genomes]
rs28437915	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34192791	0.86[ASN][1000 genomes]
rs35240348	0.98[EUR][1000 genomes]
rs3891075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs4073768	1.00[CHB][hapmap]
rs57304273	0.86[ASN][1000 genomes]
rs59770064	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61806716	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6663988	1.00[CHB][hapmap]
rs6665831	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6672371	1.00[CHB][hapmap]
rs6692298	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7520299	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7533987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7536700	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7543790	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv547928	chr1:153612133-153714252	Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	esv2830411	chr1:153613393-153725007	Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv1067771	chr1:153613593-153724866	Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Enhancers Active TSS 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 miRNA target site	48 gene(s)	inside rSNPs	diseases
6	nsv530052	chr1:153613593-153724866	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv1005818	chr1:153613597-153724980	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
8	nsv535173	chr1:153613597-153724980	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	nsv1007835	chr1:153613597-153729959	Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv535174	chr1:153613597-153729959	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
11	nsv1011897	chr1:153613597-153836703	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
12	nsv464028	chr1:153622220-153723037	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv547929	chr1:153622220-153723037	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv999364	chr1:153622634-154419436	Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
15	nsv535175	chr1:153622634-154419436	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
16	nsv1001312	chr1:153622834-153724867	Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv535176	chr1:153622834-153724867	Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153652400-153664600	Weak transcription	Gastric	stomach
2	chr1:153652400-153669800	Weak transcription	Pancreas	Pancrea
3	chr1:153653000-153669800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:153653200-153664000	Weak transcription	Left Ventricle	heart
5	chr1:153653200-153669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:153653400-153663200	Strong transcription	Ovary	ovary
7	chr1:153653600-153656800	Genic enhancers	Adipose Nuclei	Adipose
8	chr1:153653600-153659600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:153653800-153666400	Strong transcription	Lung	lung
10	chr1:153653800-153669400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr1:153654400-153657400	Weak transcription	Right Atrium	heart
12	chr1:153654400-153669200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:153654400-153669400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:153654800-153659400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:153655400-153658000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr1:153655400-153660800	Weak transcription	Spleen	Spleen
17	chr1:153655400-153669800	Weak transcription	Esophagus	oesophagus
18	chr1:153655800-153657800	Strong transcription	Right Ventricle	heart
19	chr1:153656000-153656800	Genic enhancers	Aorta	Aorta
20	chr1:153656000-153657400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:153656000-153657400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:153656200-153656800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:153656200-153659400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr1:153656400-153656800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr1:153656400-153656800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:153656400-153656800	Enhancers	Placenta Amnion	Placenta Amnion
27	chr1:153656400-153656800	Enhancers	A549	lung
28	chr1:153656400-153656800	Enhancers	Hela-S3	cervix
29	chr1:153656400-153656800	Bivalent Enhancer	NHLF	lung
30	chr1:153656400-153657400	Enhancers	Stomach Mucosa	stomach
31	chr1:153656400-153659600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr1:153656400-153659600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:153656600-153656800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:153656600-153657400	Weak transcription	Fetal Muscle Trunk	muscle
35	chr1:153656600-153657800	Enhancers	Fetal Intestine Small	intestine
36	chr1:153656600-153669400	Weak transcription	Fetal Kidney	kidney

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