Variant report

Variant	rs1649905
Chromosome Location	chr2:231410947-231410948
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1102957	0.82[AMR][1000 genomes]
rs1104327	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13000851	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1649902	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1649906	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1649907	0.85[ASN][1000 genomes]
rs1649908	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1649909	0.89[AMR][1000 genomes]
rs1649910	0.85[AMR][1000 genomes]
rs1678187	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1678189	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1678190	0.80[AMR][1000 genomes]
rs2434050	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62195461	0.92[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6717269	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6724975	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6740016	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs836236	0.87[ASN][1000 genomes]
rs836237	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs836238	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs836239	0.84[AMR][1000 genomes];0.87[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	esv18000	chr2:231072978-231467847	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv875948	chr2:231380697-231420401	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv584673	chr2:231385231-231433237	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv875949	chr2:231407663-231434272	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231401000-231430200	Weak transcription	Pancreas	Pancrea
2	chr2:231404000-231417200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr2:231404600-231416400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:231405400-231411600	Weak transcription	Placenta	Placenta
5	chr2:231405400-231411800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr2:231405800-231415000	Weak transcription	Gastric	stomach
7	chr2:231406800-231411200	Weak transcription	Aorta	Aorta
8	chr2:231407000-231417200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr2:231407200-231411000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr2:231407200-231417200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:231408000-231415000	Weak transcription	GM12878-XiMat	blood
12	chr2:231408400-231411000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:231408600-231411000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:231408600-231414200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:231408800-231412200	Weak transcription	Left Ventricle	heart
16	chr2:231408800-231413400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr2:231408800-231414400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr2:231408800-231417000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr2:231408800-231417200	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr2:231408800-231417200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr2:231409000-231411600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:231409000-231411800	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr2:231409000-231413400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr2:231409200-231411000	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr2:231409400-231417200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr2:231409600-231411400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr2:231409800-231411400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr2:231409800-231417200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr2:231410200-231412000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr2:231410200-231417000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:231410200-231428800	Weak transcription	Primary B cells from cord blood	blood

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