Variant report

Variant	rs6690278
Chromosome Location	chr1:186946010-186946011
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10157406	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10798077	1.00[EUR][1000 genomes]
rs10911978	1.00[EUR][1000 genomes]
rs1555202	1.00[GIH][hapmap]
rs1555205	1.00[EUR][1000 genomes]
rs2016991	1.00[EUR][1000 genomes]
rs2307198	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2383557	0.92[EUR][1000 genomes]
rs4650711	1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[EUR][1000 genomes]
rs4650712	0.96[EUR][1000 genomes]
rs4650713	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.96[EUR][1000 genomes]
rs4650714	1.00[EUR][1000 genomes]
rs6672835	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6674263	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[EUR][1000 genomes]
rs6683363	1.00[GIH][hapmap]
rs6696994	1.00[EUR][1000 genomes]
rs6700651	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs981581	1.00[EUR][1000 genomes]
rs9970500	0.87[EUR][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	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv548407	chr1:186875459-186951429	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186881800-186951200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr1:186923400-186958800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr1:186926800-186951200	Weak transcription	Fetal Intestine Small	intestine
4	chr1:186935000-186950800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr1:186935800-186947400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr1:186936000-186949400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr1:186936200-186948000	Weak transcription	Hela-S3	cervix
8	chr1:186936600-186947000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr1:186937400-186946400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:186939200-186950000	Weak transcription	A549	lung
11	chr1:186939800-186947600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:186943400-186946800	Enhancers	NH-A	brain
13	chr1:186943400-186947200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:186943600-186948400	Enhancers	Colon Smooth Muscle	Colon
15	chr1:186943600-186948400	Enhancers	Rectal Smooth Muscle	rectum
16	chr1:186943800-186948400	Enhancers	NHDF-Ad	bronchial
17	chr1:186944000-186947600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:186944200-186946800	Enhancers	Stomach Smooth Muscle	stomach
19	chr1:186944200-186947800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:186944400-186947400	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr1:186944400-186951600	Weak transcription	Adipose Nuclei	Adipose
22	chr1:186944600-186946400	Enhancers	HUVEC	blood vessel
23	chr1:186944600-186946800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:186944800-186947000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr1:186945000-186947600	Weak transcription	Osteobl	bone
26	chr1:186945000-186948000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:186945000-186949200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:186945000-186952200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:186945200-186947200	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr1:186945800-186947600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:186946000-186946200	Enhancers	Fetal Stomach	stomach
32	chr1:186946000-186948000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:186946000-186948000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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