Variant report

Variant	rs9990213
Chromosome Location	chr3:51387647-51387648
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs17051747	0.90[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17051755	0.82[ASW][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55640023	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55699461	1.00[EUR][1000 genomes]
rs55708856	1.00[EUR][1000 genomes]
rs56037427	1.00[EUR][1000 genomes]
rs56254449	1.00[EUR][1000 genomes]
rs56361536	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56870664	1.00[EUR][1000 genomes]
rs56940802	1.00[EUR][1000 genomes]
rs57569631	0.86[AFR][1000 genomes]
rs57742040	1.00[EUR][1000 genomes]
rs58236908	1.00[EUR][1000 genomes]
rs58548979	1.00[EUR][1000 genomes]
rs59019902	1.00[EUR][1000 genomes]
rs59557845	1.00[EUR][1000 genomes]
rs59599274	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59652730	1.00[EUR][1000 genomes]
rs59794491	1.00[EUR][1000 genomes]
rs60166061	1.00[EUR][1000 genomes]
rs60862896	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60973580	1.00[EUR][1000 genomes]
rs61337570	1.00[EUR][1000 genomes]
rs61526358	1.00[EUR][1000 genomes]
rs61570923	1.00[EUR][1000 genomes]
rs6804101	1.00[EUR][1000 genomes]
rs73833980	1.00[EUR][1000 genomes]
rs73833981	1.00[EUR][1000 genomes]
rs73833982	1.00[EUR][1000 genomes]
rs73833985	1.00[EUR][1000 genomes]
rs73833986	1.00[EUR][1000 genomes]
rs73833987	1.00[EUR][1000 genomes]
rs73833989	1.00[EUR][1000 genomes]
rs73833990	1.00[EUR][1000 genomes]
rs73833991	1.00[EUR][1000 genomes]
rs73833992	1.00[EUR][1000 genomes]
rs73833993	1.00[EUR][1000 genomes]
rs73833996	1.00[EUR][1000 genomes]
rs73834257	1.00[EUR][1000 genomes]
rs73837406	1.00[EUR][1000 genomes]
rs73837420	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73837421	1.00[EUR][1000 genomes]
rs73837422	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73837423	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73837425	1.00[EUR][1000 genomes]
rs73837428	1.00[EUR][1000 genomes]
rs73837431	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73837432	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73837433	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73837434	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7630259	0.82[ASW][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7635095	0.82[ASW][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7642077	0.82[ASW][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005858	chr3:51090373-51444027	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv536569	chr3:51090373-51444027	Flanking Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1014464	chr3:51220151-51909780	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	esv20206	chr3:51344873-51415825	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51376800-51391800	Weak transcription	Brain Germinal Matrix	brain
2	chr3:51376800-51392400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:51378000-51399800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr3:51378400-51389800	Weak transcription	Brain Substantia Nigra	brain
5	chr3:51378600-51421000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:51378800-51388000	Weak transcription	Brain Angular Gyrus	brain
7	chr3:51378800-51421400	Weak transcription	Right Ventricle	heart
8	chr3:51379000-51390200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:51379000-51393800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr3:51379000-51414600	Weak transcription	Left Ventricle	heart
11	chr3:51379200-51393600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr3:51379200-51393800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr3:51379200-51399800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr3:51379400-51403400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:51380000-51398400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:51380000-51398400	Weak transcription	Aorta	Aorta
17	chr3:51381400-51392000	Weak transcription	Brain Anterior Caudate	brain
18	chr3:51381800-51392200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr3:51382400-51389800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr3:51382800-51392200	Weak transcription	HSMMtube	muscle
21	chr3:51383000-51391000	Weak transcription	Brain Hippocampus Middle	brain
22	chr3:51384200-51392400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr3:51384200-51393800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr3:51384200-51420600	Weak transcription	Fetal Brain Male	brain
25	chr3:51385400-51405600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr3:51386400-51405400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:51386600-51392200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:51387200-51392400	Strong transcription	Brain Inferior Temporal Lobe	brain
29	chr3:51387400-51388800	Strong transcription	Fetal Brain Female	brain
30	chr3:51387400-51389000	Strong transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links