Variant report

Variant	rs9458012
Chromosome Location	chr6:161130930-161130931
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	chr6:161125304..161127777-chr6:161128271..161131075,2	K562	blood:

Variant related genes	Relation type
ENSG00000122194	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1321197	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13231	0.87[EUR][1000 genomes]
rs1853016	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1853017	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1853018	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1897108	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35513104	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4252066	0.88[EUR][1000 genomes]
rs4252072	0.89[EUR][1000 genomes]
rs4252076	0.89[EUR][1000 genomes]
rs4252078	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4252082	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4252086	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4252087	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4252090	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4252093	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4252096	0.88[EUR][1000 genomes]
rs4252107	0.88[EUR][1000 genomes]
rs4252109	0.88[EUR][1000 genomes]
rs4252114	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4252117	0.86[EUR][1000 genomes]
rs4252120	0.86[EUR][1000 genomes]
rs4252125	0.84[EUR][1000 genomes]
rs4252126	0.84[EUR][1000 genomes]
rs4252130	0.84[EUR][1000 genomes]
rs4252134	0.84[EUR][1000 genomes]
rs4252135	0.84[EUR][1000 genomes]
rs4252151	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4252165	0.84[EUR][1000 genomes]
rs56093624	0.84[EUR][1000 genomes]
rs59614420	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62439804	0.88[EUR][1000 genomes]
rs62439805	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9456578	0.86[EUR][1000 genomes]
rs9458016	0.86[EUR][1000 genomes]
rs9458017	0.84[EUR][1000 genomes]
rs9458019	0.84[EUR][1000 genomes]
rs9458020	0.84[EUR][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	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv605005	chr6:161069941-161152449	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv981222	chr6:161121517-161135479	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1019113	chr6:161127584-161197558	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv969466	chr6:161127758-161135479	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161129200-161131000	Enhancers	HepG2	liver
2	chr6:161130000-161131000	Enhancers	Fetal Intestine Large	intestine
3	chr6:161130400-161131000	Enhancers	Fetal Intestine Small	intestine
4	chr6:161130400-161131200	Transcr. at gene 5' and 3'	Liver	Liver
5	chr6:161130600-161131000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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