Variant report

Variant	rs62158991
Chromosome Location	chr2:114411222-114411223
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	FOS	chr2:114411144-114411318	MCF10A-Er-Src	breast:	n/a	n/a
2	FOSL2	chr2:114410557-114411316	HepG2	liver:	n/a	chr2:114410892-114410903 chr2:114410943-114410954
3	FOSL2	chr2:114411117-114411359	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:114411198-114411222	HepG2	liver:	n/a	n/a
5	POLR2A	chr2:114411121-114411348	H1-hESC	embryonic stem cell:	n/a	n/a
6	FOS	chr2:114411148-114411318	MCF10A-Er-Src	breast:	n/a	n/a
7	FOSL2	chr2:114411165-114411397	A549	lung:	n/a	n/a
8	FOS	chr2:114411121-114411325	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr2:114411144-114411321	H1-hESC	embryonic stem cell:	n/a	n/a
10	PBX3	chr2:114411145-114411280	GM12878	blood:	n/a	n/a
11	POLR2A	chr2:114411219-114411287	ProgFib	skin:	n/a	n/a
12	FOSL2	chr2:114411203-114411300	A549	lung:	n/a	n/a

Variant related genes	Relation type
ENSG00000144158	TF binding region

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10169190	0.81[ASN][1000 genomes]
rs10197009	0.81[ASN][1000 genomes]
rs10199515	0.81[ASN][1000 genomes]
rs10208651	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11123202	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11123203	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11677168	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12329244	0.81[ASN][1000 genomes]
rs12711781	0.81[ASN][1000 genomes]
rs12986781	0.81[ASN][1000 genomes]
rs13003858	0.81[ASN][1000 genomes]
rs13025042	0.81[ASN][1000 genomes]
rs13028979	0.87[ASN][1000 genomes]
rs13389017	0.87[ASN][1000 genomes]
rs13393247	0.81[ASN][1000 genomes]
rs13395272	0.81[ASN][1000 genomes]
rs13408264	0.81[ASN][1000 genomes]
rs13410586	0.81[ASN][1000 genomes]
rs13417896	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13424899	0.81[ASN][1000 genomes]
rs13428433	0.81[ASN][1000 genomes]
rs17048299	0.81[ASN][1000 genomes]
rs17048506	0.81[ASN][1000 genomes]
rs34026450	0.81[ASN][1000 genomes]
rs34451679	0.81[ASN][1000 genomes]
rs35073956	0.81[ASN][1000 genomes]
rs35255260	0.81[ASN][1000 genomes]
rs62170066	0.81[ASN][1000 genomes]
rs6722177	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759085	chr2:114074949-114428678	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
2	nsv428062	chr2:114251945-114428678	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
3	esv2757827	chr2:114253780-114428678	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
4	nsv1001195	chr2:114362003-114506330	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv508163	chr2:114364609-114431004	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv961495	chr2:114381866-114415806	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv962001	chr2:114390234-114415806	Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv3460333	chr2:114406582-114412880	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3460334	chr2:114406582-114412880	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv820374	chr2:114407510-114411465	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv3333700	chr2:114407582-114412280	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	esv21338	chr2:114408195-114411286	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv3343358	chr2:114409382-114412280	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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