Variant report

Variant	rs7651091
Chromosome Location	chr3:43300612-43300613
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10212591	0.85[AFR][1000 genomes]
rs11129997	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11129998	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1120779	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11713302	1.00[AMR][1000 genomes]
rs12632805	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1320157	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1320159	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1472807	1.00[AMR][1000 genomes]
rs1506618	1.00[AMR][1000 genomes]
rs1996496	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2036616	0.85[AFR][1000 genomes]
rs2135510	1.00[AMR][1000 genomes]
rs2372353	1.00[AMR][1000 genomes]
rs2372357	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2372358	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2372359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2888311	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4234427	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4234466	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4339089	1.00[AMR][1000 genomes]
rs4346523	1.00[AMR][1000 genomes]
rs4405884	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4420837	1.00[AMR][1000 genomes]
rs4425230	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4470482	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4569634	1.00[AMR][1000 genomes]
rs4618196	1.00[AMR][1000 genomes]
rs4642093	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4682673	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4682674	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4682681	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4682684	1.00[AMR][1000 genomes]
rs4682884	1.00[AMR][1000 genomes]
rs4682889	1.00[AMR][1000 genomes]
rs4683365	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4683368	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6441771	0.85[AFR][1000 genomes]
rs6442145	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6765835	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6766825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6767741	1.00[AMR][1000 genomes]
rs6775392	1.00[AMR][1000 genomes]
rs6784075	1.00[AMR][1000 genomes]
rs6791682	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6793755	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7616072	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7636644	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7648023	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs906156	1.00[AMR][1000 genomes]
rs906157	1.00[AMR][1000 genomes]
rs906158	1.00[AMR][1000 genomes]
rs937827	1.00[AMR][1000 genomes]
rs9755005	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs984345	1.00[AMR][1000 genomes]
rs9859465	0.86[AFR][1000 genomes];1.00[AMR][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	nsv834672	chr3:43132722-43306272	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2752008	chr3:43285369-43360879	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1009102	chr3:43285369-43369712	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43290800-43300800	Weak transcription	Brain Anterior Caudate	brain
2	chr3:43294200-43300800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:43296800-43305800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:43297800-43301000	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:43299400-43303400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:43299800-43300800	Weak transcription	Esophagus	oesophagus
7	chr3:43299800-43301000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr3:43299800-43306400	Weak transcription	Spleen	Spleen
9	chr3:43299800-43308200	Weak transcription	Right Atrium	heart
10	chr3:43300200-43301200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr3:43300400-43301800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr3:43300400-43302000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:43300400-43302200	Enhancers	NHEK	skin
14	chr3:43300400-43305800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr3:43300400-43305800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:43300600-43301000	Enhancers	Lung	lung
17	chr3:43300600-43301800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:43300600-43302200	Enhancers	HMEC	breast
19	chr3:43300600-43302400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:43300600-43305800	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr3:43300600-43306000	Weak transcription	Primary monocytes fromperipheralblood	blood

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