Variant report

Variant	rs3792099
Chromosome Location	chr2:234234679-234234680
allele	A/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	REST	chr2:234234400-234234855	ECC-1	luminal epithelium:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
2	REST	chr2:234234440-234234848	ECC-1	luminal epithelium:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
3	REST	chr2:234234494-234234812	SK-N-SH	brain:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
4	REST	chr2:234234492-234234798	PFSK-1	brain:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
5	REST	chr2:234234421-234234903	HL-60	blood:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
6	REST	chr2:234234564-234234726	Hela-S3	cervix:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
7	REST	chr2:234234449-234234864	PFSK-1	brain:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
8	REST	chr2:234234420-234234860	PANC-1	pancreas:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
9	REST	chr2:234234571-234234788	H1-hESC	embryonic stem cell:	n/a	chr2:234234649-234234658 chr2:234234643-234234663
10	REST	chr2:234234551-234234793	MCF-7	breast:	n/a	chr2:234234649-234234658 chr2:234234643-234234663

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234226679..234228246-chr2:234234524..234237366,2	K562	blood:

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

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1000548	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11679064	0.81[ASN][1000 genomes]
rs11890330	0.81[ASN][1000 genomes]
rs11890449	0.81[ASN][1000 genomes]
rs2304775	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3792101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55754152	0.81[ASN][1000 genomes]
rs55895356	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56242862	0.81[ASN][1000 genomes]
rs59303693	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6719241	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72976324	0.81[ASN][1000 genomes]
rs72976366	0.81[ASN][1000 genomes]
rs72978306	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72978311	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72978313	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72978315	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72978317	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7564805	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7565275	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7578402	0.81[ASN][1000 genomes]
rs7583380	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7594365	0.81[ASN][1000 genomes]
rs7594781	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234223600-234245400	Weak transcription	Pancreas	Pancrea
2	chr2:234228400-234240000	Weak transcription	Fetal Intestine Small	intestine
3	chr2:234229800-234235000	Enhancers	Primary B cells from cord blood	blood
4	chr2:234229800-234235600	Enhancers	Primary B cells from peripheral blood	blood
5	chr2:234232800-234237800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:234233400-234237600	Weak transcription	Lung	lung
7	chr2:234234400-234234800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:234234400-234239800	Weak transcription	Thymus	Thymus

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