Variant report

Variant	rs7953992
Chromosome Location	chr12:44693604-44693605
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10506243	1.00[EUR][1000 genomes]
rs10506244	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10506245	0.92[EUR][1000 genomes]
rs11182470	0.92[EUR][1000 genomes]
rs11182477	0.92[EUR][1000 genomes]
rs12300292	1.00[EUR][1000 genomes]
rs1527315	0.92[EUR][1000 genomes]
rs17094382	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17094386	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17094396	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17094401	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094405	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094408	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094412	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094421	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094423	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094437	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094458	1.00[EUR][1000 genomes]
rs17094465	0.92[EUR][1000 genomes]
rs17094473	0.92[EUR][1000 genomes]
rs17094505	0.92[EUR][1000 genomes]
rs17094509	0.92[EUR][1000 genomes]
rs17094532	0.92[EUR][1000 genomes]
rs17094560	0.92[EUR][1000 genomes]
rs1716605	1.00[EUR][1000 genomes]
rs1726889	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1948424	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2080876	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3858725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4307772	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4544066	0.92[EUR][1000 genomes]
rs4573751	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7296406	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73276261	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74084494	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7953537	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7966220	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7975491	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs840774	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv686	chr12:44671240-44696910	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	lncRNA	n/a	inside rSNPs	n/a
3	nsv1038498	chr12:44679455-44816572	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44676600-44697800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:44682000-44698600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:44685000-44695400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:44688800-44702000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:44690400-44697800	Weak transcription	HSMMtube	muscle
6	chr12:44690400-44698000	Weak transcription	Liver	Liver
7	chr12:44690400-44698600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:44690600-44697800	Weak transcription	Aorta	Aorta
9	chr12:44690600-44697800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr12:44690800-44694800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr12:44690800-44696000	Weak transcription	Pancreas	Pancrea
12	chr12:44690800-44698000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr12:44690800-44698000	Weak transcription	Esophagus	oesophagus
14	chr12:44690800-44701400	Weak transcription	Left Ventricle	heart
15	chr12:44691400-44701400	Weak transcription	Psoas Muscle	Psoas
16	chr12:44693200-44694200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr12:44693200-44694200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:44693200-44694200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr12:44693200-44694200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:44693200-44694200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr12:44693200-44694400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:44693400-44694400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:44693600-44694000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr12:44693600-44694400	Enhancers	Fetal Brain Male	brain
25	chr12:44693600-44697800	Weak transcription	Fetal Intestine Small	intestine
26	chr12:44693600-44698600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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