Variant report

Variant	rs547945
Chromosome Location	chr19:56641777-56641778
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs12459102	0.81[AMR][1000 genomes]
rs12983086	0.85[JPT][hapmap]
rs2450439	0.89[ASN][1000 genomes]
rs2631625	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2631627	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2631628	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2631631	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2631637	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2631640	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2637088	0.83[AMR][1000 genomes]
rs2637092	0.85[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2637093	0.83[ASN][1000 genomes]
rs2637094	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2637097	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2637114	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2932757	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs473953	0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs478402	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4801676	0.81[JPT][hapmap]
rs481936	0.83[AMR][1000 genomes]
rs490345	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs492078	0.81[AMR][1000 genomes]
rs497453	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs504350	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs506547	1.00[CEU][hapmap];0.85[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs509897	0.85[AMR][1000 genomes]
rs517021	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs517582	0.83[AMR][1000 genomes]
rs521092	0.81[AMR][1000 genomes]
rs522980	0.88[AMR][1000 genomes]
rs524778	0.85[ASN][1000 genomes]
rs524829	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs524988	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs525827	1.00[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs527715	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs530102	1.00[CEU][hapmap]
rs535393	0.82[AMR][1000 genomes]
rs540900	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs544365	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs545570	0.83[AMR][1000 genomes]
rs547002	0.84[AMR][1000 genomes]
rs564973	0.80[ASN][1000 genomes]
rs565879	0.81[AMR][1000 genomes]
rs569310	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs572851	0.97[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs578990	1.00[CEU][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs578991	1.00[CEU][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs582271	0.81[AMR][1000 genomes]
rs583330	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs587702	0.85[AMR][1000 genomes]
rs588574	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs592827	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs599405	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs609736	0.82[JPT][hapmap]
rs619934	0.82[JPT][hapmap];0.83[AMR][1000 genomes]
rs626821	1.00[CEU][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs628090	0.82[ASN][1000 genomes]
rs629544	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs640654	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs642776	0.83[AMR][1000 genomes]
rs643133	1.00[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs643174	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs648352	0.81[AMR][1000 genomes]
rs659424	1.00[CEU][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs662308	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs662763	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs665082	0.97[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs665846	0.81[AMR][1000 genomes]
rs665857	0.85[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs667438	1.00[CEU][hapmap];0.80[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs667523	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs667974	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs669866	0.85[CHB][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs677127	0.85[CHB][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs677142	0.82[AMR][1000 genomes]
rs678540	0.97[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs684653	1.00[CEU][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs685117	1.00[CEU][hapmap];0.81[ASN][1000 genomes]
rs8103672	0.85[JPT][hapmap]
rs9676765	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056598	chr19:56331762-56703428	Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv580354	chr19:56505685-56723492	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
5	nsv523651	chr19:56537528-56707048	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
6	nsv1057820	chr19:56555942-56720262	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	nsv528998	chr19:56578238-56707048	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv517365	chr19:56592286-56674548	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv912513	chr19:56592286-56685463	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
10	nsv521744	chr19:56592286-56686953	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
11	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
12	nsv528361	chr19:56638845-56688570	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56634000-56645400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr19:56637400-56645400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr19:56637800-56643200	Weak transcription	Fetal Stomach	stomach
4	chr19:56637800-56645200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr19:56637800-56647600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:56638600-56643800	Weak transcription	HSMM	muscle
7	chr19:56638600-56643800	Weak transcription	HSMMtube	muscle
8	chr19:56638600-56651200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr19:56638800-56651800	Weak transcription	Spleen	Spleen
10	chr19:56639000-56647600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:56639200-56643200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr19:56639200-56643200	Weak transcription	HepG2	liver
13	chr19:56639200-56643400	Weak transcription	Fetal Muscle Leg	muscle
14	chr19:56639200-56645200	Weak transcription	K562	blood
15	chr19:56639200-56645600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr19:56640800-56644600	Enhancers	Fetal Lung	lung
17	chr19:56640800-56649000	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr19:56641000-56643400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr19:56641600-56643600	Weak transcription	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links