Variant report

Variant	rs10415229
Chromosome Location	chr19:56991687-56991688
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10403163	1.00[EUR][1000 genomes]
rs10412827	1.00[EUR][1000 genomes]
rs10416247	1.00[EUR][1000 genomes]
rs16987281	1.00[EUR][1000 genomes]
rs16987283	1.00[EUR][1000 genomes]
rs16987287	1.00[EUR][1000 genomes]
rs16987292	0.83[AMR][1000 genomes]
rs61739893	1.00[EUR][1000 genomes]
rs7253007	1.00[EUR][1000 genomes]
rs8102264	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949121	chr19:56754719-57591038	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1062341	chr19:56794070-57273332	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv544094	chr19:56794070-57273332	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
4	nsv1056713	chr19:56799151-57265682	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
5	nsv544095	chr19:56799151-57265682	Strong transcription ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv580385	chr19:56918598-57072433	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv1057240	chr19:56919831-57153659	Flanking Active TSS Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv544097	chr19:56919831-57153659	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv580386	chr19:56924761-57072433	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv1055357	chr19:56933632-57190007	ZNF genes & repeats Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56987400-56992400	ZNF genes & repeats	Lung	lung
2	chr19:56990200-56991800	Weak transcription	Aorta	Aorta
3	chr19:56990400-56991800	Weak transcription	Pancreas	Pancrea
4	chr19:56990400-56994000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
5	chr19:56990400-56994200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr19:56990400-56996000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr19:56990600-56992000	Weak transcription	Left Ventricle	heart
8	chr19:56990600-56992200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:56990600-56992200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr19:56990600-56992400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr19:56990600-56992400	Enhancers	Right Ventricle	heart
12	chr19:56990600-56993400	Weak transcription	HSMM	muscle
13	chr19:56990600-56993600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr19:56990600-56994200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:56990800-56991800	Weak transcription	Fetal Muscle Leg	muscle
16	chr19:56990800-56992800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr19:56990800-56992800	Weak transcription	Fetal Kidney	kidney
18	chr19:56990800-57010000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:56991000-56991800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr19:56991000-56992000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr19:56991000-56992000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr19:56991000-56992400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:56991000-56993400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr19:56991000-56993800	Weak transcription	Brain Anterior Caudate	brain
25	chr19:56991000-56998400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:56991000-57005400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:56991200-56991800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr19:56991200-56992000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr19:56991200-56992200	Weak transcription	Brain Hippocampus Middle	brain
30	chr19:56991200-56992400	ZNF genes & repeats	Fetal Stomach	stomach
31	chr19:56991200-56994200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr19:56991200-56994600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
33	chr19:56991200-57001400	Weak transcription	Fetal Heart	heart
34	chr19:56991200-57006800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr19:56991200-57006800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:56991400-56993200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
37	chr19:56991400-56993400	Weak transcription	Osteobl	bone
38	chr19:56991600-56992400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:56991600-56993200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr19:56991600-56997600	ZNF genes & repeats	Fetal Brain Female	brain
41	chr19:56991600-56997800	ZNF genes & repeats	Ovary	ovary

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