Variant report

Variant	rs509966
Chromosome Location	chr15:40236835-40236836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:40226451..40228182-chr15:40236413..40239026,2	MCF-7	breast:
2	chr15:40227974..40230444-chr15:40236467..40239295,4	K562	blood:
3	chr15:40225075..40228327-chr15:40235171..40238770,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128829	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12050584	1.00[AMR][1000 genomes]
rs2412455	1.00[AMR][1000 genomes]
rs2412461	1.00[AMR][1000 genomes]
rs2640644	1.00[AMR][1000 genomes]
rs2898983	1.00[AMR][1000 genomes]
rs2917838	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2934195	1.00[AMR][1000 genomes]
rs472530	1.00[AMR][1000 genomes]
rs503775	1.00[AMR][1000 genomes]
rs508280	1.00[AMR][1000 genomes]
rs514394	1.00[AMR][1000 genomes]
rs535400	1.00[AMR][1000 genomes]
rs544070	1.00[AMR][1000 genomes]
rs571256	1.00[AMR][1000 genomes]
rs578429	1.00[AMR][1000 genomes]
rs581167	1.00[AMR][1000 genomes]
rs7165452	1.00[AMR][1000 genomes]
rs7173708	1.00[AMR][1000 genomes]
rs7174465	1.00[AMR][1000 genomes]
rs8042413	1.00[AMR][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	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv832983	chr15:40098766-40248839	Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40227200-40247800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:40227200-40248200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:40227200-40268400	Weak transcription	Esophagus	oesophagus
4	chr15:40227400-40237600	Weak transcription	Fetal Brain Male	brain
5	chr15:40227400-40283400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr15:40227800-40237600	Weak transcription	Gastric	stomach
7	chr15:40227800-40247000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:40227800-40268400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:40228000-40238400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr15:40228200-40323800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr15:40228600-40239800	Weak transcription	Stomach Mucosa	stomach
12	chr15:40228600-40246000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr15:40230000-40263000	Strong transcription	Fetal Muscle Trunk	muscle
14	chr15:40230200-40255600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:40230400-40240000	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr15:40230400-40261600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr15:40230600-40237400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr15:40230600-40252400	Weak transcription	Right Atrium	heart
19	chr15:40230800-40239600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:40230800-40240000	Strong transcription	Fetal Stomach	stomach
21	chr15:40231000-40237600	Weak transcription	Spleen	Spleen
22	chr15:40231000-40268400	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr15:40231400-40243400	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr15:40231800-40238800	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr15:40231800-40239000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr15:40231800-40240200	Strong transcription	Fetal Muscle Leg	muscle
27	chr15:40231800-40243400	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr15:40231800-40252600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr15:40232000-40240000	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr15:40232000-40240400	Strong transcription	Primary B cells from cord blood	blood
31	chr15:40232000-40261400	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr15:40232000-40262600	Strong transcription	Liver	Liver
33	chr15:40232200-40237000	Strong transcription	Primary hematopoietic stem cells	blood
34	chr15:40232200-40237600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr15:40232200-40237800	Weak transcription	Fetal Heart	heart
36	chr15:40232200-40238800	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr15:40232200-40239000	Strong transcription	HepG2	liver
38	chr15:40232200-40239400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr15:40232200-40239400	Strong transcription	Fetal Intestine Large	intestine
40	chr15:40232200-40239600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr15:40232200-40239800	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr15:40232200-40240000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr15:40232200-40240000	Strong transcription	Stomach Smooth Muscle	stomach
44	chr15:40232200-40240200	Strong transcription	Fetal Thymus	thymus
45	chr15:40232200-40241600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:40232200-40244600	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr15:40232200-40250200	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr15:40232200-40252400	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr15:40232400-40238600	Strong transcription	Lung	lung
50	chr15:40232400-40240000	Strong transcription	H9 Cell Line	embryonic stem cell

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