Variant report

Variant	rs10439586
Chromosome Location	chr20:13564592-13564593
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs2180570	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6033774	0.87[AFR][1000 genomes]
rs6033782	0.87[AFR][1000 genomes]
rs6033784	0.82[AFR][1000 genomes]
rs6042233	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042234	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042237	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042241	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042242	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042243	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042246	0.87[AFR][1000 genomes]
rs6042247	0.87[AFR][1000 genomes]
rs6042248	0.87[AFR][1000 genomes]
rs6042249	0.87[AFR][1000 genomes]
rs6042252	0.87[AFR][1000 genomes]
rs6042265	0.87[AFR][1000 genomes]
rs6042267	0.87[AFR][1000 genomes]
rs6109967	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6109968	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6109972	0.83[AFR][1000 genomes]
rs6109973	0.87[AFR][1000 genomes]
rs6109985	0.87[AFR][1000 genomes]
rs73268992	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061303	chr20:13395546-13810990	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv585435	chr20:13410638-13582476	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv916202	chr20:13421724-14043615	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1059817	chr20:13422602-13807968	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv458871	chr20:13447896-13573415	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv585436	chr20:13447896-13573415	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1066810	chr20:13451869-14432454	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv912687	chr20:13507057-13591596	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv1797514	chr20:13541011-13610424	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv912688	chr20:13546903-13589682	ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv1061323	chr20:13551004-13746346	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:13492200-13567000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr20:13515000-13605600	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr20:13526800-13613800	Weak transcription	Hela-S3	cervix
4	chr20:13535600-13608000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr20:13538200-13571800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr20:13541200-13578000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr20:13545000-13567000	Strong transcription	Dnd41	blood
8	chr20:13546200-13594200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr20:13546800-13574000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr20:13547600-13565600	Weak transcription	Osteobl	bone
11	chr20:13548000-13568600	Weak transcription	Brain Angular Gyrus	brain
12	chr20:13548600-13566200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr20:13548600-13568800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr20:13548600-13584600	Weak transcription	Gastric	stomach
15	chr20:13554000-13568400	Weak transcription	Fetal Brain Male	brain
16	chr20:13554600-13577400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr20:13554800-13567000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr20:13556000-13565600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr20:13556200-13618800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr20:13556600-13565400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr20:13556600-13567000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr20:13556600-13567000	Weak transcription	Psoas Muscle	Psoas
23	chr20:13556600-13567800	Weak transcription	Liver	Liver
24	chr20:13556800-13566200	Weak transcription	Brain Hippocampus Middle	brain
25	chr20:13556800-13566400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr20:13557200-13566800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr20:13557600-13564600	Strong transcription	Primary B cells from cord blood	blood
28	chr20:13557800-13566400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr20:13561200-13566200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr20:13561600-13566000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr20:13561800-13567000	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr20:13562600-13565000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr20:13563400-13564600	Strong transcription	Primary B cells from peripheral blood	blood
34	chr20:13563400-13564600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr20:13563400-13564600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr20:13563400-13564600	Strong transcription	Thymus	Thymus
37	chr20:13563400-13564800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr20:13563400-13565000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:13563400-13565400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr20:13563400-13567200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr20:13563400-13571200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr20:13563600-13564600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr20:13563600-13564800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr20:13563600-13564800	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr20:13563600-13564800	ZNF genes & repeats	Fetal Stomach	stomach
46	chr20:13563800-13566400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr20:13563800-13568400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr20:13563800-13619000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr20:13564000-13564800	Strong transcription	Fetal Thymus	thymus
50	chr20:13564000-13565600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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