Variant report

Variant	rs6790703
Chromosome Location	chr3:138840080-138840081
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:138839775..138842671-chr3:138939843..138942396,2	K562	blood:
2	chr3:138836042..138841722-chr3:138842580..138845228,5	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1105251	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030471	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2737735	0.82[EUR][1000 genomes]
rs595352	0.83[EUR][1000 genomes]
rs646315	0.95[ASN][1000 genomes]
rs661149	0.84[EUR][1000 genomes]
rs673174	0.84[EUR][1000 genomes]
rs685220	0.80[EUR][1000 genomes]
rs688964	0.83[EUR][1000 genomes]
rs939646	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs940187	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs940188	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs940189	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs940191	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868955	chr3:138248190-138848947	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv829736	chr3:138737352-138934758	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138835800-138843200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr3:138836200-138843400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:138836400-138841600	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr3:138836600-138843400	Enhancers	HSMM	muscle
5	chr3:138836600-138846800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:138837600-138841800	Enhancers	Pancreas	Pancrea
7	chr3:138838200-138843000	Enhancers	Primary hematopoietic stem cells	blood
8	chr3:138838400-138840400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr3:138838600-138840400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:138838600-138840800	Enhancers	Hela-S3	cervix
11	chr3:138838600-138841000	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr3:138838600-138841200	Enhancers	Fetal Intestine Large	intestine
13	chr3:138838600-138841800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr3:138838600-138842200	Enhancers	HSMMtube	muscle
15	chr3:138838600-138842600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:138838600-138842600	Enhancers	NHDF-Ad	bronchial
17	chr3:138838600-138842800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:138838800-138840400	Enhancers	Fetal Intestine Small	intestine
19	chr3:138838800-138841600	Enhancers	Osteobl	bone
20	chr3:138838800-138841800	Enhancers	NHLF	lung
21	chr3:138839000-138841200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr3:138839000-138841400	Enhancers	A549	lung
23	chr3:138839000-138842600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:138839200-138840400	Enhancers	Right Atrium	heart
25	chr3:138839200-138840600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr3:138839200-138840600	Enhancers	Stomach Mucosa	stomach
27	chr3:138839200-138841000	Enhancers	Small Intestine	intestine
28	chr3:138839200-138841200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr3:138839200-138841600	Enhancers	Liver	Liver
30	chr3:138839400-138840400	Enhancers	Colonic Mucosa	Colon
31	chr3:138839400-138840800	Enhancers	Gastric	stomach
32	chr3:138839400-138841200	Enhancers	Placenta	Placenta
33	chr3:138839400-138849200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:138839600-138840200	Enhancers	Lung	lung
35	chr3:138839600-138840600	Enhancers	Duodenum Mucosa	Duodenum
36	chr3:138839800-138840800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:138839800-138840800	Enhancers	HepG2	liver
38	chr3:138839800-138841800	Enhancers	Ovary	ovary
39	chr3:138839800-138842400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:138839800-138843000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr3:138839800-138843000	Weak transcription	Spleen	Spleen
42	chr3:138839800-138843400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr3:138839800-138843600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr3:138839800-138847200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr3:138840000-138840200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr3:138840000-138840400	Enhancers	K562	blood

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