Variant report

Variant	rs10992168
Chromosome Location	chr9:94690621-94690622
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94689308..94690973-chr9:94691805..94694661,2	K562	blood:
2	chr9:94688039..94689556-chr9:94689805..94691664,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10820916	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10820917	0.84[AMR][1000 genomes]
rs10820919	0.82[AMR][1000 genomes]
rs10820921	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10820922	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10820928	0.92[EUR][1000 genomes]
rs10992161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10992162	0.82[AMR][1000 genomes]
rs10992165	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10992166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1892263	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1919101	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs3932420	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56013831	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56272949	0.91[EUR][1000 genomes]
rs56280154	0.92[EUR][1000 genomes]
rs56309039	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62565755	0.93[EUR][1000 genomes]
rs62567925	0.81[EUR][1000 genomes]
rs72746299	0.94[EUR][1000 genomes]
rs7862013	0.84[AMR][1000 genomes]
rs7866775	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]

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	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv530946	chr9:94633154-94715023	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv1046733	chr9:94690622-95138564	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94681400-94691400	Weak transcription	Pancreas	Pancrea
2	chr9:94683600-94691800	Weak transcription	Fetal Lung	lung
3	chr9:94683600-94692000	Weak transcription	K562	blood
4	chr9:94686400-94692400	Weak transcription	Colon Smooth Muscle	Colon
5	chr9:94686600-94690800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:94686600-94696000	Weak transcription	Ovary	ovary
7	chr9:94688600-94690800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:94690200-94690800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr9:94690200-94690800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:94690200-94693000	ZNF genes & repeats	Fetal Stomach	stomach
11	chr9:94690400-94691200	Enhancers	Stomach Smooth Muscle	stomach
12	chr9:94690400-94692400	ZNF genes & repeats	Fetal Intestine Small	intestine
13	chr9:94690600-94690800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:94690600-94692200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr9:94690600-94692600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung

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