Variant report

Variant	rs9289042
Chromosome Location	chr3:115788713-115788714
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:115782312..115784390-chr3:115787119..115790072,2	K562	blood:
2	chr3:115784918..115786597-chr3:115787841..115790560,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs11425708	0.88[ASN][1000 genomes]
rs11918080	0.88[ASN][1000 genomes]
rs12695319	0.82[ASN][1000 genomes]
rs13100914	0.85[ASN][1000 genomes]
rs13315058	0.82[ASN][1000 genomes]
rs1344131	0.89[ASN][1000 genomes]
rs17630430	0.84[ASN][1000 genomes]
rs17697994	0.89[ASN][1000 genomes]
rs1920360	0.82[ASN][1000 genomes]
rs1920379	0.88[ASN][1000 genomes]
rs2091669	0.88[ASN][1000 genomes]
rs2222827	0.88[ASN][1000 genomes]
rs2864066	0.90[ASN][1000 genomes]
rs2864067	0.90[ASN][1000 genomes]
rs28735793	0.86[ASN][1000 genomes]
rs33956431	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34523792	0.84[ASN][1000 genomes]
rs34543919	0.82[ASN][1000 genomes]
rs34844901	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34930794	0.89[ASN][1000 genomes]
rs35080450	0.82[ASN][1000 genomes]
rs35242629	0.95[ASN][1000 genomes]
rs35619123	0.95[ASN][1000 genomes]
rs35780065	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35914238	0.88[ASN][1000 genomes]
rs4263291	0.89[ASN][1000 genomes]
rs4831121	0.82[ASN][1000 genomes]
rs4831225	0.82[ASN][1000 genomes]
rs4831226	0.82[ASN][1000 genomes]
rs4831227	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4831228	0.88[ASN][1000 genomes]
rs4831229	0.89[ASN][1000 genomes]
rs4831230	0.89[ASN][1000 genomes]
rs5004406	0.88[ASN][1000 genomes]
rs56121547	0.89[ASN][1000 genomes]
rs62269168	0.89[ASN][1000 genomes]
rs62269170	0.89[ASN][1000 genomes]
rs62271281	0.82[ASN][1000 genomes]
rs66490447	0.88[ASN][1000 genomes]
rs6765355	0.88[ASN][1000 genomes]
rs6772113	0.88[ASN][1000 genomes]
rs73139202	0.88[ASN][1000 genomes]
rs7632265	0.89[ASN][1000 genomes]
rs7637650	0.88[ASN][1000 genomes]
rs9816425	0.88[ASN][1000 genomes]
rs9821040	0.82[ASN][1000 genomes]
rs9821865	0.88[ASN][1000 genomes]
rs9822568	0.88[ASN][1000 genomes]
rs9824605	0.82[ASN][1000 genomes]
rs9836963	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9837276	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9839078	0.88[ASN][1000 genomes]
rs9851643	0.84[ASN][1000 genomes]
rs9854345	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9854711	0.88[ASN][1000 genomes]
rs9855097	0.88[ASN][1000 genomes]
rs9857520	0.88[ASN][1000 genomes]
rs9858539	0.82[ASN][1000 genomes]
rs9866484	0.88[ASN][1000 genomes]
rs9868706	0.82[ASN][1000 genomes]
rs9873576	0.92[ASN][1000 genomes]
rs9877662	0.88[ASN][1000 genomes]
rs9878289	0.81[ASN][1000 genomes]
rs9878559	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931948	chr3:114884574-115802562	Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2760762	chr3:115476222-115807650	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv829685	chr3:115643521-115812913	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1001538	chr3:115746561-115791116	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115766200-115794200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:115780400-115830000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:115780600-115803800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:115787800-115788800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:115787800-115789200	Enhancers	K562	blood
6	chr3:115788000-115789400	Enhancers	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links