Variant report

Variant	rs28576892
Chromosome Location	chr16:69923843-69923844
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs13329778	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13329812	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13330995	1.00[AMR][1000 genomes]
rs13332544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13336041	1.00[AMR][1000 genomes]
rs13336357	1.00[AMR][1000 genomes]
rs13338911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13339493	1.00[AMR][1000 genomes]
rs28429826	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28502677	1.00[AMR][1000 genomes]
rs28514573	1.00[AMR][1000 genomes]
rs28523536	1.00[AMR][1000 genomes]
rs28583989	1.00[AMR][1000 genomes]
rs28610117	1.00[AMR][1000 genomes]
rs28628240	1.00[AMR][1000 genomes]
rs28651196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28673794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28756357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28803823	1.00[AMR][1000 genomes]
rs28867427	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28882509	1.00[AMR][1000 genomes]
rs9923096	1.00[AMR][1000 genomes]
rs9923471	1.00[AMR][1000 genomes]
rs9924073	1.00[AMR][1000 genomes]
rs9924630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9926382	1.00[AMR][1000 genomes]
rs9928560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9930692	1.00[AMR][1000 genomes]
rs9931243	1.00[AFR][1000 genomes]
rs9931479	1.00[AMR][1000 genomes]
rs9933583	1.00[AMR][1000 genomes]
rs9933606	1.00[AMR][1000 genomes]
rs9933745	1.00[AMR][1000 genomes]
rs9935697	1.00[AMR][1000 genomes]
rs9935973	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9936451	1.00[AMR][1000 genomes]
rs9937762	1.00[AMR][1000 genomes]
rs9938552	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv906823	chr16:69711533-69959223	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1062171	chr16:69854267-70188585	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv542941	chr16:69854267-70188585	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1059249	chr16:69854467-70188446	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv542942	chr16:69854467-70188446	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	esv2758428	chr16:69855122-70313222	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	esv2758652	chr16:69855122-70313222	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69893000-69934800	Weak transcription	Hela-S3	cervix
2	chr16:69900800-69933400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr16:69901800-69924600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:69902600-69924800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:69904200-69951200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr16:69907600-69942600	Weak transcription	Small Intestine	intestine
7	chr16:69908000-69924200	Weak transcription	Colon Smooth Muscle	Colon
8	chr16:69908200-69943000	Weak transcription	Right Ventricle	heart
9	chr16:69910600-69937400	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr16:69911400-69924400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr16:69911400-69970200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr16:69913600-69950400	Weak transcription	A549	lung
13	chr16:69915200-69924000	Weak transcription	NH-A	brain
14	chr16:69915400-69924000	Weak transcription	NHLF	lung
15	chr16:69915400-69924000	Weak transcription	Osteobl	bone
16	chr16:69915400-69924200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr16:69916400-69931600	Strong transcription	Primary B cells from cord blood	blood
18	chr16:69916400-69931600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr16:69917200-69930600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr16:69919800-69932400	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr16:69920600-69928000	Strong transcription	Primary T cells from cord blood	blood
22	chr16:69921200-69924000	Strong transcription	Fetal Intestine Small	intestine
23	chr16:69921400-69938800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr16:69921600-69925000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr16:69921600-69925800	Strong transcription	HepG2	liver
26	chr16:69921600-69932800	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr16:69921800-69924000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr16:69921800-69924400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr16:69921800-69924400	Strong transcription	Fetal Intestine Large	intestine
30	chr16:69921800-69925000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr16:69921800-69925800	Strong transcription	Primary B cells from peripheral blood	blood
32	chr16:69921800-69925800	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr16:69921800-69926000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr16:69921800-69926000	Strong transcription	Thymus	Thymus
35	chr16:69921800-69926400	Strong transcription	Duodenum Mucosa	Duodenum
36	chr16:69921800-69926600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr16:69922000-69924000	Strong transcription	Fetal Stomach	stomach
38	chr16:69922000-69924000	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr16:69922000-69924400	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr16:69922000-69925800	Enhancers	Brain Cingulate Gyrus	brain
41	chr16:69922000-69926000	Enhancers	Brain Substantia Nigra	brain
42	chr16:69922200-69924200	Strong transcription	Primary hematopoietic stem cells	blood
43	chr16:69922200-69924400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr16:69922200-69924600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr16:69922600-69925000	Strong transcription	Fetal Thymus	thymus
46	chr16:69922800-69924000	Strong transcription	NHEK	skin
47	chr16:69923000-69924600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
48	chr16:69923200-69924000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr16:69923200-69924600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr16:69923200-69938600	Weak transcription	Ovary	ovary

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