Variant report

Variant	rs1906677
Chromosome Location	chr4:56500951-56500952
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	TBL1XR1	chr4:56499512-56501926	K562	blood:	n/a	n/a
2	MAZ	chr4:56500668-56501074	K562	blood:	n/a	n/a
3	EP300	chr4:56500854-56500963	GM12878	blood:	n/a	n/a
4	RCOR1	chr4:56500802-56503942	K562	blood:	n/a	n/a
5	REST	chr4:56500830-56504009	H1-neurons	neurons:	n/a	chr4:56502226-56502236
6	CUX1	chr4:56499698-56500972	K562	blood:	n/a	n/a
7	IRF1	chr4:56500752-56501984	K562	blood:	n/a	chr4:56501094-56501106
8	POLR2A	chr4:56499394-56503785	K562	blood:	n/a	n/a
9	POLR2A	chr4:56500485-56503059	Raji	blood:	n/a	n/a
10	UBTF	chr4:56500856-56503073	K562	blood:	n/a	n/a
11	POLR2A	chr4:56500944-56500953	K562	blood:	n/a	n/a
12	POLR2A	chr4:56499543-56503922	K562	blood:	n/a	n/a
13	POLR2A	chr4:56499874-56503767	K562	blood:	n/a	n/a
14	MXI1	chr4:56500616-56503285	SK-N-SH	brain:	n/a	n/a
15	RCOR1	chr4:56500831-56501196	K562	blood:	n/a	n/a
16	POLR2A	chr4:56499478-56502006	K562	blood:	n/a	n/a
17	POLR2A	chr4:56499765-56503986	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:56500129..56502345-chr4:56579313..56582236,2	K562	blood:
2	chr4:56407970..56411777-chr4:56498734..56501001,3	K562	blood:

Variant related genes	Relation type
NMU	TF binding region

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10002268	0.95[ASN][1000 genomes]
rs10003113	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10003211	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10011137	0.93[ASN][1000 genomes]
rs10033028	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10517356	0.95[ASN][1000 genomes]
rs1077103	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1077104	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11133404	0.91[ASN][1000 genomes]
rs11735910	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11931026	0.95[ASN][1000 genomes]
rs11935806	0.93[ASN][1000 genomes]
rs11945558	0.95[ASN][1000 genomes]
rs12498734	0.91[ASN][1000 genomes]
rs12499623	0.91[ASN][1000 genomes]
rs12510588	0.93[ASN][1000 genomes]
rs12512220	0.93[ASN][1000 genomes]
rs13118189	0.89[ASN][1000 genomes]
rs1488939	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1809643	0.93[ASN][1000 genomes]
rs1844219	0.95[ASN][1000 genomes]
rs1844220	0.95[ASN][1000 genomes]
rs1906675	0.82[EUR][1000 genomes]
rs1971991	0.95[ASN][1000 genomes]
rs2087320	0.82[EUR][1000 genomes]
rs2101475	0.82[EUR][1000 genomes]
rs28377791	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28434169	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs28448373	0.95[ASN][1000 genomes]
rs28626806	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28644417	0.95[ASN][1000 genomes]
rs28694060	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4865020	0.97[ASN][1000 genomes]
rs4865021	0.88[ASN][1000 genomes]
rs61072181	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6827359	0.91[ASN][1000 genomes]
rs6839462	0.92[ASN][1000 genomes]
rs7658532	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7680941	0.95[ASN][1000 genomes]
rs7690375	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7690566	0.93[ASN][1000 genomes]
rs7697972	0.93[ASN][1000 genomes]
rs9312664	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9993462	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv10496	chr4:56336946-56841137	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv998179	chr4:56425126-56694339	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv932636	chr4:56438618-56667329	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv879021	chr4:56482750-56648713	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv3393088	chr4:56484073-56503988	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3395811	chr4:56486113-56514675	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56499400-56501000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:56499800-56501000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:56499800-56501400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:56500000-56501200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:56500000-56501600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:56500200-56501000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:56500200-56501000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
8	chr4:56500400-56501000	Active TSS	K562	blood
9	chr4:56500600-56501000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
10	chr4:56500600-56501000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:56500600-56501200	Enhancers	H9 Cell Line	embryonic stem cell
12	chr4:56500600-56501600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
13	chr4:56500600-56501600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
14	chr4:56500600-56501600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
15	chr4:56500600-56501800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
16	chr4:56500800-56501200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr4:56500800-56501600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
18	chr4:56500800-56502600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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