Variant report

Variant	rs28897765
Chromosome Location	chr3:142280108-142280109
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs28897764	1.00[GIH][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28910270	0.83[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28910271	0.87[LWK][hapmap];1.00[MKK][hapmap];0.83[TSI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28910272	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34104088	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs34213965	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34383865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34678750	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34686786	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35264204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35363608	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35404216	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35440390	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35988759	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35993426	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36090479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7618253	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877556	chr3:141898980-142331360	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv877558	chr3:142123841-142331360	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv877559	chr3:142132749-142331360	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers 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	35 gene(s)	inside rSNPs	diseases
4	nsv877560	chr3:142132749-142362179	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv877561	chr3:142152925-142331360	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
6	nsv932989	chr3:142204208-142423305	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv933680	chr3:142211643-142287189	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv591919	chr3:142219542-142308070	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28897765	PLS1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142204200-142281400	Weak transcription	Colonic Mucosa	Colon
2	chr3:142226000-142287200	Weak transcription	Right Ventricle	heart
3	chr3:142231600-142295800	Weak transcription	Small Intestine	intestine
4	chr3:142240800-142281600	Weak transcription	Fetal Brain Male	brain
5	chr3:142241000-142280800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr3:142244400-142295600	Weak transcription	Fetal Heart	heart
7	chr3:142248400-142287400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:142253400-142284800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:142253400-142284800	Weak transcription	Brain Substantia Nigra	brain
10	chr3:142253800-142296400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr3:142256200-142283600	Weak transcription	Aorta	Aorta
12	chr3:142259800-142285600	Strong transcription	Dnd41	blood
13	chr3:142263000-142285400	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr3:142263400-142286200	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr3:142263600-142288000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:142263800-142285600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:142263800-142286600	Strong transcription	Liver	Liver
18	chr3:142264000-142285200	Strong transcription	Fetal Thymus	thymus
19	chr3:142265200-142285000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr3:142265200-142287600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:142265400-142283600	Weak transcription	HSMMtube	muscle
22	chr3:142266400-142285600	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr3:142267000-142286600	Strong transcription	Primary B cells from cord blood	blood
24	chr3:142267600-142282000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr3:142267800-142285200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr3:142268800-142284200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr3:142269200-142292600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr3:142270000-142287200	Weak transcription	Pancreas	Pancrea
29	chr3:142270200-142285000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:142270800-142285200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:142270800-142286400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:142271000-142285400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:142271800-142282200	Weak transcription	Fetal Kidney	kidney
34	chr3:142271800-142285200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:142272200-142286200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:142272400-142282200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:142272600-142280200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr3:142272600-142282000	Weak transcription	Rectal Smooth Muscle	rectum
39	chr3:142272600-142283600	Weak transcription	Fetal Brain Female	brain
40	chr3:142272600-142284800	Weak transcription	HepG2	liver
41	chr3:142272600-142287400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr3:142272600-142296200	Weak transcription	Brain Angular Gyrus	brain
43	chr3:142272600-142296200	Weak transcription	Psoas Muscle	Psoas
44	chr3:142272800-142293400	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr3:142274000-142284800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr3:142274000-142285200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:142274000-142286600	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr3:142274000-142287200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr3:142274000-142287400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr3:142274000-142287400	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links