Variant report

Variant	rs35272495
Chromosome Location	chr19:42473665-42473666
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1205964	1.00[EUR][1000 genomes]
rs1685562	1.00[EUR][1000 genomes]
rs61733017	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7255488	1.00[ASW][hapmap]
rs73552843	1.00[EUR][1000 genomes]
rs73552847	1.00[EUR][1000 genomes]
rs874013	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv911777	chr19:42357455-42521108	Bivalent/Poised TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	esv1805469	chr19:42367635-42798851	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv911780	chr19:42398450-42521108	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv911781	chr19:42398450-42542999	Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42464000-42482000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:42464000-42485400	Weak transcription	Primary T cells from cord blood	blood
3	chr19:42464000-42485400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr19:42464000-42486600	Weak transcription	Right Atrium	heart
5	chr19:42464000-42495000	Weak transcription	Fetal Brain Male	brain
6	chr19:42464200-42473800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr19:42464200-42473800	Weak transcription	Brain Anterior Caudate	brain
8	chr19:42464200-42479600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr19:42464200-42485400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:42464200-42485400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr19:42464200-42489400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr19:42464200-42491000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr19:42464200-42491200	Weak transcription	Fetal Heart	heart
14	chr19:42464200-42493800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr19:42464200-42495000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr19:42464200-42497400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:42464200-42497400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr19:42467600-42475600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:42470000-42487200	Strong transcription	Fetal Brain Female	brain
20	chr19:42470200-42475600	Strong transcription	Left Ventricle	heart
21	chr19:42470200-42484400	Strong transcription	Dnd41	blood
22	chr19:42470200-42487200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr19:42470400-42475800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr19:42470400-42487200	Strong transcription	Brain Germinal Matrix	brain
25	chr19:42471400-42476000	Strong transcription	Right Ventricle	heart
26	chr19:42471600-42476000	Strong transcription	Brain Inferior Temporal Lobe	brain
27	chr19:42471600-42479000	Weak transcription	Thymus	Thymus
28	chr19:42471800-42490000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr19:42472000-42474000	Strong transcription	Brain Angular Gyrus	brain
30	chr19:42472000-42490000	Weak transcription	Spleen	Spleen
31	chr19:42472200-42481800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr19:42472400-42474600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:42472400-42497400	Weak transcription	Fetal Thymus	thymus
34	chr19:42472600-42474800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
35	chr19:42472800-42473800	Enhancers	Fetal Intestine Large	intestine
36	chr19:42472800-42474000	Enhancers	Fetal Intestine Small	intestine
37	chr19:42472800-42493400	Weak transcription	Brain Hippocampus Middle	brain
38	chr19:42473200-42474000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr19:42473200-42474400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr19:42473400-42474200	Weak transcription	H9 Cell Line	embryonic stem cell

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