Variant report

Variant	rs2073300
Chromosome Location	chr20:23471681-23471682
allele	A/C
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	CEBPB	chr20:23471614-23471730	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
CST8	TF binding region

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs12625160	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs12625999	1.00[CEU][hapmap];0.81[GIH][hapmap];0.90[TSI][hapmap];0.83[EUR][1000 genomes]
rs12626013	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17830565	0.81[EUR][1000 genomes]
rs2207988	0.81[EUR][1000 genomes]
rs2207989	0.81[EUR][1000 genomes]
rs28407103	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34449811	0.80[EUR][1000 genomes]
rs34740966	0.81[EUR][1000 genomes]
rs35810824	0.83[EUR][1000 genomes]
rs57021299	0.84[EUR][1000 genomes]
rs6036423	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6036424	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6048803	1.00[CEU][hapmap];0.81[GIH][hapmap]
rs6048810	0.81[EUR][1000 genomes]
rs6048811	0.81[EUR][1000 genomes]
rs6048813	0.81[EUR][1000 genomes]
rs6048814	0.81[EUR][1000 genomes]
rs6048820	0.83[EUR][1000 genomes]
rs6048822	1.00[CEU][hapmap]
rs6083135	1.00[CEU][hapmap]
rs6106656	0.81[EUR][1000 genomes]
rs6106667	0.83[EUR][1000 genomes]
rs6106669	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6114094	1.00[CEU][hapmap]
rs6114098	0.81[EUR][1000 genomes]
rs6114100	0.83[EUR][1000 genomes]
rs6114101	0.81[EUR][1000 genomes]
rs6114141	1.00[CEU][hapmap]
rs6114142	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6114144	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6132620	1.00[CEU][hapmap]
rs6132621	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6132622	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6132623	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6132626	0.83[EUR][1000 genomes]
rs6132628	0.83[EUR][1000 genomes]
rs6132631	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6137957	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs6137959	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6137960	0.83[EUR][1000 genomes]
rs6137961	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6137962	0.83[EUR][1000 genomes]
rs6137963	0.83[EUR][1000 genomes]
rs6137964	0.83[EUR][1000 genomes]
rs6137967	0.81[EUR][1000 genomes]
rs6137971	0.89[EUR][1000 genomes]
rs6137975	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap]
rs6137976	0.86[EUR][1000 genomes]
rs6137977	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6137980	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6137982	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6137983	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6137984	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063655	chr20:23396649-23489730	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv912818	chr20:23406519-23567838	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv912819	chr20:23406519-23569400	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv912820	chr20:23406519-23578148	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1065390	chr20:23412890-23569238	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv1065719	chr20:23415029-23565333	Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv544214	chr20:23415029-23565333	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv470544	chr20:23424638-23569400	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv585722	chr20:23424638-23569400	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
10	nsv458949	chr20:23426648-23569400	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv585723	chr20:23426648-23569400	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv1057992	chr20:23430887-23565333	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv544215	chr20:23430887-23565333	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
14	nsv491876	chr20:23436633-24031374	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
15	esv3380178	chr20:23469952-23472150	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
16	esv3436842	chr20:23470252-23471750	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 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	chr20:23469600-23473200	Weak transcription	Gastric	stomach
2	chr20:23471600-23471800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr20:23471600-23472200	Enhancers	K562	blood
4	chr20:23471600-23472400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:23471600-23473400	Bivalent Enhancer	HepG2	liver

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