Variant report

Variant	rs13427703
Chromosome Location	chr2:234247508-234247509
allele	C/G
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	BCL3	chr2:234247428-234247832	GM12878	blood:	n/a	chr2:234247800-234247809

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234159356..234161467-chr2:234246206..234249085,2	MCF-7	breast:
2	chr2:234242293..234245038-chr2:234245423..234247780,3	MCF-7	breast:

Variant related genes	Relation type
SAG	TF binding region
ENSG00000085978	Chromatin interaction
ENSG00000130561	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10153945	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10168367	1.00[JPT][hapmap]
rs10168794	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs10185174	0.84[ASN][1000 genomes]
rs10199833	1.00[CHB][hapmap]
rs11892545	1.00[CHB][hapmap]
rs13384932	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs13400563	1.00[CHB][hapmap]
rs13416292	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13420976	0.84[ASN][1000 genomes]
rs2124045	1.00[CHB][hapmap]
rs2289473	1.00[CHB][hapmap];0.83[CHD][hapmap];0.92[ASN][1000 genomes]
rs2304773	1.00[JPT][hapmap]
rs28437319	0.84[ASN][1000 genomes]
rs28605452	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28657808	0.84[ASN][1000 genomes]
rs2971865	1.00[CHB][hapmap]
rs3762586	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3792095	1.00[ASN][1000 genomes]
rs3792104	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[YRI][hapmap];0.92[ASN][1000 genomes]
rs3792105	1.00[CHB][hapmap]
rs56871749	0.84[ASN][1000 genomes]
rs57712949	0.84[ASN][1000 genomes]
rs58222850	0.84[ASN][1000 genomes]
rs6431282	0.92[ASN][1000 genomes]
rs6716988	1.00[CHB][hapmap]
rs6745134	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs73106630	0.84[ASN][1000 genomes]
rs73998327	0.92[ASN][1000 genomes]
rs7422734	1.00[CHB][hapmap]
rs7588509	1.00[CHB][hapmap]
rs838557	1.00[CHB][hapmap]
rs838558	1.00[CHB][hapmap]
rs838561	1.00[CHB][hapmap]
rs838562	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv584699	chr2:234182240-234255547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv584700	chr2:234199401-234364426	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1002075	chr2:234225979-234277508	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv460135	chr2:234242347-234288048	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv584701	chr2:234242347-234288048	ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv460136	chr2:234244395-234288048	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv584702	chr2:234244395-234288048	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234237400-234249800	Enhancers	Primary B cells from peripheral blood	blood
2	chr2:234241000-234249600	Enhancers	Primary B cells from cord blood	blood
3	chr2:234243000-234247800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:234244200-234247600	Weak transcription	GM12878-XiMat	blood
5	chr2:234244600-234247600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr2:234244600-234257800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr2:234245600-234247600	Weak transcription	Small Intestine	intestine
8	chr2:234245800-234247600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr2:234246000-234247600	Weak transcription	Fetal Intestine Large	intestine
10	chr2:234246600-234249400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr2:234247000-234248200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr2:234247000-234248400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr2:234247000-234249200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr2:234247000-234249400	Enhancers	Hela-S3	cervix
15	chr2:234247200-234247800	Enhancers	Fetal Intestine Small	intestine
16	chr2:234247200-234248400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr2:234247200-234249400	Enhancers	HepG2	liver
18	chr2:234247400-234247600	Enhancers	Spleen	Spleen
19	chr2:234247400-234247800	Enhancers	Gastric	stomach
20	chr2:234247400-234247800	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr2:234247400-234249200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:234247400-234249200	Enhancers	Stomach Mucosa	stomach
23	chr2:234247400-234251400	Weak transcription	K562	blood

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