Variant report

Variant	rs12341228
Chromosome Location	chr9:101036007-101036008
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	chr9:101034358..101036194-chr9:101038260..101041518,3	K562	blood:
2	chr9:101034397..101036575-chr9:101039828..101041518,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10156520	0.92[ASN][1000 genomes]
rs10156543	0.91[ASN][1000 genomes]
rs10818728	0.92[ASN][1000 genomes]
rs10985682	0.98[ASN][1000 genomes]
rs10985714	0.98[ASN][1000 genomes]
rs10985747	0.85[ASN][1000 genomes]
rs12339418	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12341227	0.98[ASN][1000 genomes]
rs12343605	0.93[ASN][1000 genomes]
rs12347890	0.95[ASN][1000 genomes]
rs12349672	0.80[ASN][1000 genomes]
rs12350177	0.98[ASN][1000 genomes]
rs12552446	0.95[ASN][1000 genomes]
rs12683370	0.95[ASN][1000 genomes]
rs12683816	0.82[ASN][1000 genomes]
rs12685596	0.98[ASN][1000 genomes]
rs12685597	0.98[ASN][1000 genomes]
rs1435255	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1435258	0.91[ASN][1000 genomes]
rs1435259	0.88[ASN][1000 genomes]
rs1435260	0.91[ASN][1000 genomes]
rs16914443	0.88[AFR][1000 genomes]
rs16914485	0.98[ASN][1000 genomes]
rs1966664	0.88[ASN][1000 genomes]
rs55734037	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55740603	0.97[ASN][1000 genomes]
rs56397452	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56406831	0.94[ASN][1000 genomes]
rs7037857	0.95[ASN][1000 genomes]
rs73488785	0.83[AFR][1000 genomes]
rs73490714	0.88[AFR][1000 genomes]
rs73490718	0.88[AFR][1000 genomes]
rs73490720	0.88[AFR][1000 genomes]
rs73490723	0.88[AFR][1000 genomes]
rs73490727	0.88[AFR][1000 genomes]
rs73657129	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7848351	0.93[ASN][1000 genomes]
rs7848352	0.93[ASN][1000 genomes]
rs7853699	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831663	chr9:100941048-101109492	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1045780	chr9:100943318-101080389	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv540180	chr9:100943318-101080389	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv519818	chr9:101024887-101092316	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	Chromatin interactive region	10 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	chr9:101028200-101037000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:101033400-101036200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr9:101034400-101038600	Weak transcription	K562	blood
4	chr9:101034600-101037000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:101035200-101037200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr9:101036000-101036200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:101036000-101036400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr9:101036000-101037000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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