Variant report

Variant	rs881557
Chromosome Location	chr9:16915644-16915645
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10738467	0.93[ASN][1000 genomes]
rs10738468	0.93[ASN][1000 genomes]
rs10810671	0.98[ASN][1000 genomes]
rs10810672	0.93[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12551173	0.93[ASN][1000 genomes]
rs12552675	0.81[EUR][1000 genomes]
rs1416745	1.00[EUR][1000 genomes]
rs34097600	1.00[EUR][1000 genomes]
rs3814113	0.99[ASN][1000 genomes]
rs3814114	0.93[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4246133	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4246134	0.97[ASN][1000 genomes]
rs4366169	0.93[ASN][1000 genomes]
rs4445329	0.93[ASN][1000 genomes]
rs4465052	0.97[ASN][1000 genomes]
rs4631563	0.97[ASN][1000 genomes]
rs55689948	0.92[ASN][1000 genomes]
rs6475092	0.97[ASN][1000 genomes]
rs6475093	0.97[ASN][1000 genomes]
rs6475094	0.95[ASN][1000 genomes]
rs7032221	0.98[ASN][1000 genomes]
rs7045767	0.91[ASN][1000 genomes]
rs7048397	0.89[ASN][1000 genomes]
rs7866677	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv892650	chr9:16696187-16950860	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv892652	chr9:16843128-16958312	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
4	nsv1018615	chr9:16865804-16960970	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
5	nsv540074	chr9:16865804-16960970	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
6	nsv892654	chr9:16898603-16941006	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
7	esv3693021	chr9:16903446-16929803	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv466266	chr9:16903446-16950860	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
9	nsv471286	chr9:16903446-16950860	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
10	nsv613686	chr9:16903446-16950860	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
11	esv2764141	chr9:16903446-17351711	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	esv2757320	chr9:16903850-16918196	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
13	esv2759674	chr9:16903850-16918196	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
14	nsv1030297	chr9:16913777-16931807	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
15	nsv1021873	chr9:16914412-16931807	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16912800-16921800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr9:16912800-16928000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:16914800-16915800	Enhancers	Osteobl	bone
4	chr9:16915200-16915800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr9:16915400-16915800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:16915400-16915800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:16915400-16915800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:16915400-16915800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:16915400-16915800	Enhancers	Psoas Muscle	Psoas
10	chr9:16915400-16915800	Enhancers	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links