Variant report

Variant	rs35465473
Chromosome Location	chr3:45998867-45998868
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:55)

rs_ID	r²[population]
rs1072755	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11130080	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12630101	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12635494	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12635657	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12639598	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13066048	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13091821	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13091979	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1392291	0.83[ASN][1000 genomes]
rs1532071	0.98[ASN][1000 genomes]
rs1552489	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1552490	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1601867	1.00[ASN][1000 genomes]
rs17078495	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1994488	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1994489	0.98[ASN][1000 genomes]
rs1994490	0.88[ASN][1000 genomes]
rs2054866	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2171530	0.80[ASN][1000 genomes]
rs2234358	0.99[ASN][1000 genomes]
rs2248228	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2291470	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35537559	0.81[ASN][1000 genomes]
rs3733100	0.88[ASN][1000 genomes]
rs3733103	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3774634	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3774635	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3774639	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3796373	0.82[ASN][1000 genomes]
rs3796375	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3821884	0.84[ASN][1000 genomes]
rs4535265	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4682799	0.98[ASN][1000 genomes]
rs4682800	0.98[ASN][1000 genomes]
rs4683148	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4683149	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4683152	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4683154	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4683156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4683157	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59226168	0.81[ASN][1000 genomes]
rs62242796	0.81[ASN][1000 genomes]
rs67044455	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6778896	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7129	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs730983	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs737452	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs751552	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs751553	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9311380	0.98[ASN][1000 genomes]
rs931704	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs936938	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9824253	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9831315	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][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	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv834678	chr3:45804294-46010256	Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv876736	chr3:45900621-46027410	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:45959400-46009800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:45980800-46013400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:45981000-45999400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr3:45981600-46025000	Strong transcription	Fetal Intestine Large	intestine
5	chr3:45982200-45999800	Strong transcription	Stomach Smooth Muscle	stomach
6	chr3:45982800-46000800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:45983200-46012400	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr3:45984400-46000800	Weak transcription	Psoas Muscle	Psoas
9	chr3:45986200-46006800	Strong transcription	Fetal Intestine Small	intestine
10	chr3:45986200-46007600	Strong transcription	Fetal Stomach	stomach
11	chr3:45986400-46001400	Weak transcription	A549	lung
12	chr3:45986400-46006200	Strong transcription	Fetal Muscle Leg	muscle
13	chr3:45986400-46006800	Strong transcription	Fetal Muscle Trunk	muscle
14	chr3:45986400-46007600	Strong transcription	Duodenum Smooth Muscle	Duodenum
15	chr3:45986400-46012200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr3:45986400-46026600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:45986600-46009000	Strong transcription	Primary B cells from cord blood	blood
18	chr3:45986600-46012000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr3:45986600-46026800	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr3:45986800-46012200	Strong transcription	Primary B cells from peripheral blood	blood
21	chr3:45987200-46013600	Strong transcription	Primary hematopoietic stem cells	blood
22	chr3:45987200-46027200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:45987400-46026600	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr3:45987600-46002000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:45987600-46007800	Strong transcription	K562	blood
26	chr3:45987800-46001400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:45987800-46012200	Strong transcription	HepG2	liver
28	chr3:45987800-46026400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr3:45987800-46026800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:45987800-46027200	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr3:45988000-45999400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:45988000-46012000	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr3:45988000-46026600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:45988200-46009800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr3:45988200-46012000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:45988800-46011800	Strong transcription	Lung	lung
37	chr3:45989000-45999800	Weak transcription	Right Atrium	heart
38	chr3:45989400-45999800	Weak transcription	NH-A	brain
39	chr3:45989400-46013800	Strong transcription	Dnd41	blood
40	chr3:45990600-45999000	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr3:45990600-45999200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr3:45990600-45999800	Strong transcription	Rectal Smooth Muscle	rectum
43	chr3:45990600-46017200	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr3:45991200-46006800	Strong transcription	HSMMtube	muscle
45	chr3:45991200-46012000	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr3:45991200-46017400	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr3:45991400-45999800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr3:45991400-46009800	Strong transcription	Aorta	Aorta
49	chr3:45991400-46009800	Strong transcription	NHLF	lung
50	chr3:45991600-46003200	Strong transcription	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links