Variant report

Variant	rs9429508
Chromosome Location	chr1:113594263-113594264
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:113593498..113596289-chr1:113632655..113634633,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11102573	0.89[EUR][1000 genomes]
rs11102574	0.86[EUR][1000 genomes]
rs11102575	0.86[EUR][1000 genomes]
rs11102576	0.86[EUR][1000 genomes]
rs11102577	0.84[EUR][1000 genomes]
rs11102578	0.87[EUR][1000 genomes]
rs11584099	0.86[EUR][1000 genomes]
rs11584535	0.86[EUR][1000 genomes]
rs11588345	0.86[EUR][1000 genomes]
rs11590170	0.86[EUR][1000 genomes]
rs11590174	0.86[EUR][1000 genomes]
rs12066274	0.81[EUR][1000 genomes]
rs12129863	0.89[EUR][1000 genomes]
rs12140104	0.84[EUR][1000 genomes]
rs1216766	0.88[EUR][1000 genomes]
rs1216772	0.89[EUR][1000 genomes]
rs1216773	0.89[EUR][1000 genomes]
rs1216775	0.89[EUR][1000 genomes]
rs1216779	0.83[EUR][1000 genomes]
rs1216783	0.90[EUR][1000 genomes]
rs1216784	0.90[EUR][1000 genomes]
rs1216785	0.90[EUR][1000 genomes]
rs1216790	0.88[EUR][1000 genomes]
rs12184285	0.89[EUR][1000 genomes]
rs12354228	0.86[EUR][1000 genomes]
rs12740564	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12745675	0.86[EUR][1000 genomes]
rs12746771	0.84[EUR][1000 genomes]
rs1419136	0.88[EUR][1000 genomes]
rs1544227	0.87[EUR][1000 genomes]
rs17014850	0.89[EUR][1000 genomes]
rs17030901	0.89[EUR][1000 genomes]
rs17030905	0.89[EUR][1000 genomes]
rs1766866	0.81[EUR][1000 genomes]
rs2798687	0.88[EUR][1000 genomes]
rs2798689	0.85[EUR][1000 genomes]
rs2798691	0.89[EUR][1000 genomes]
rs2798692	0.87[EUR][1000 genomes]
rs34233065	0.84[EUR][1000 genomes]
rs34565381	0.83[EUR][1000 genomes]
rs3889656	0.85[EUR][1000 genomes]
rs3951437	0.87[EUR][1000 genomes]
rs4838975	0.85[EUR][1000 genomes]
rs61818171	0.84[EUR][1000 genomes]
rs61818172	0.89[EUR][1000 genomes]
rs61818173	0.88[EUR][1000 genomes]
rs61818174	0.87[EUR][1000 genomes]
rs6656041	0.86[EUR][1000 genomes]
rs6656311	0.85[EUR][1000 genomes]
rs773440	0.85[EUR][1000 genomes]
rs9429509	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9429713	0.81[EUR][1000 genomes]
rs9787311	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
5	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
7	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
8	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
9	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv1007045	chr1:113425222-113839910	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv946146	chr1:113567302-113640814	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv427719	chr1:113570229-114078388	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv508537	chr1:113590343-113635803	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv437002	chr1:113592588-113658887	Weak transcription Flanking Active TSS Strong transcription Enhancers 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	13 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	chr1:113585600-113599200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:113585600-113601800	Weak transcription	Fetal Stomach	stomach
3	chr1:113586600-113599600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:113587400-113599600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:113588000-113596200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:113589400-113596400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:113589800-113595600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:113590000-113596400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr1:113590000-113601400	Weak transcription	Right Atrium	heart
10	chr1:113591000-113596200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:113591000-113596400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr1:113591200-113595800	Weak transcription	Fetal Intestine Small	intestine
13	chr1:113591800-113596200	Weak transcription	HepG2	liver
14	chr1:113592000-113596200	Weak transcription	Fetal Intestine Large	intestine
15	chr1:113593600-113594400	Enhancers	Primary T cells fromperipheralblood	blood
16	chr1:113594000-113594400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:113594000-113594600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:113594200-113595800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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