Variant report

Variant	rs7675845
Chromosome Location	chr4:87383276-87383277
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10008165	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs10023787	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs10029671	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs10031843	0.84[CHB][hapmap];0.81[JPT][hapmap]
rs1021101	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs11097110	1.00[YRI][hapmap]
rs11097115	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs11947775	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12507758	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs1481833	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs17011924	0.94[ASN][1000 genomes]
rs17418221	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17418531	0.91[ASN][1000 genomes]
rs17418801	0.89[ASN][1000 genomes]
rs17418878	0.87[ASN][1000 genomes]
rs17419295	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs17452467	0.91[ASN][1000 genomes]
rs17452556	0.89[ASN][1000 genomes]
rs28483710	0.80[ASN][1000 genomes]
rs4235081	0.88[ASN][1000 genomes]
rs4404513	0.91[ASN][1000 genomes]
rs4405982	0.87[ASN][1000 genomes]
rs4407468	0.85[ASN][1000 genomes]
rs4452393	0.84[ASN][1000 genomes]
rs4466012	0.85[ASN][1000 genomes]
rs4511966	0.84[ASN][1000 genomes]
rs4513526	0.80[ASN][1000 genomes]
rs4529013	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs4552430	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4607180	0.85[ASN][1000 genomes]
rs4622964	0.87[ASN][1000 genomes]
rs4640633	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4693147	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs4693771	0.98[AFR][1000 genomes]
rs4693772	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4693776	0.85[ASN][1000 genomes]
rs4693777	0.84[ASN][1000 genomes]
rs55653332	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs55660529	0.87[ASN][1000 genomes]
rs55722156	0.89[ASN][1000 genomes]
rs55814693	0.81[ASN][1000 genomes]
rs55842318	0.85[ASN][1000 genomes]
rs55872468	0.85[ASN][1000 genomes]
rs55881335	0.89[ASN][1000 genomes]
rs55908925	0.85[ASN][1000 genomes]
rs55930543	0.85[ASN][1000 genomes]
rs55969415	0.91[ASN][1000 genomes]
rs55982489	0.85[ASN][1000 genomes]
rs56009992	0.85[ASN][1000 genomes]
rs56164000	0.88[ASN][1000 genomes]
rs56178389	0.80[ASN][1000 genomes]
rs56222033	0.87[ASN][1000 genomes]
rs56353461	0.88[ASN][1000 genomes]
rs59644743	0.87[ASN][1000 genomes]
rs61152200	0.87[ASN][1000 genomes]
rs6531932	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs67341369	0.80[ASN][1000 genomes]
rs67928053	0.80[ASN][1000 genomes]
rs6822396	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6838659	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6847139	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs72664002	0.90[ASN][1000 genomes]
rs72665711	0.92[ASN][1000 genomes]
rs72665712	0.92[ASN][1000 genomes]
rs72665714	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72665719	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72665722	0.86[ASN][1000 genomes]
rs72665724	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72665725	0.86[ASN][1000 genomes]
rs72665729	0.85[ASN][1000 genomes]
rs72665734	0.85[ASN][1000 genomes]
rs72665736	0.85[ASN][1000 genomes]
rs72665737	0.85[ASN][1000 genomes]
rs72665738	0.85[ASN][1000 genomes]
rs72665740	0.88[ASN][1000 genomes]
rs72665744	0.85[ASN][1000 genomes]
rs72665746	0.88[ASN][1000 genomes]
rs72665752	0.85[ASN][1000 genomes]
rs72665753	0.84[ASN][1000 genomes]
rs72665756	0.84[ASN][1000 genomes]
rs7435744	0.84[ASN][1000 genomes]
rs7673698	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7679269	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7694723	0.82[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap]
rs7695011	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7697819	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9307020	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs9683663	0.89[ASN][1000 genomes]
rs9993042	0.89[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594786	chr4:87076360-87609320	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv999470	chr4:87165663-87514552	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537164	chr4:87165663-87514552	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv594787	chr4:87221827-87888667	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv1012836	chr4:87279206-87643558	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87381200-87383600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:87382400-87383600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:87382600-87383600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:87382600-87384200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr4:87382600-87385000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:87382600-87387800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:87382800-87384000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:87382800-87393400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:87383000-87383800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr4:87383000-87384400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:87383000-87384400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:87383000-87384400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:87383000-87384600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:87383200-87383800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links