Variant report

Variant	rs35356792
Chromosome Location	chr19:53014787-53014788
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF83-7	chr19:53014535-53015246	ENSG00000269349.1

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12461522	1.00[ASN][1000 genomes]
rs12462080	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12971372	1.00[ASN][1000 genomes]
rs12977988	1.00[ASN][1000 genomes]
rs12985487	1.00[ASN][1000 genomes]
rs12986137	1.00[ASN][1000 genomes]
rs16983943	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2061355	1.00[ASN][1000 genomes]
rs28570374	1.00[ASN][1000 genomes]
rs329948	1.00[ASN][1000 genomes]
rs329949	1.00[ASN][1000 genomes]
rs34106830	1.00[ASN][1000 genomes]
rs34203482	1.00[ASN][1000 genomes]
rs34316627	1.00[ASN][1000 genomes]
rs34529833	1.00[ASN][1000 genomes]
rs34724169	1.00[ASN][1000 genomes]
rs34747259	1.00[ASN][1000 genomes]
rs34942135	1.00[ASN][1000 genomes]
rs35591322	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35888888	1.00[ASN][1000 genomes]
rs35895760	1.00[ASN][1000 genomes]
rs35904532	1.00[ASN][1000 genomes]
rs36089907	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs382838	1.00[ASN][1000 genomes]
rs436426	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs557496	1.00[ASN][1000 genomes]
rs58067500	1.00[ASN][1000 genomes]
rs71358875	1.00[ASN][1000 genomes]
rs71358876	1.00[ASN][1000 genomes]
rs71358877	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71358878	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71358879	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71358884	1.00[ASN][1000 genomes]
rs7252479	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7257799	0.83[AMR][1000 genomes]
rs7257824	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73578236	1.00[ASN][1000 genomes]
rs73578252	1.00[ASN][1000 genomes]
rs8104197	1.00[ASN][1000 genomes]
rs811920	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066537	chr19:52794424-53044977	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv544060	chr19:52794424-53044977	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv580026	chr19:52937100-53059872	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1063648	chr19:52938131-53041119	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1057296	chr19:52950339-53396986	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv978841	chr19:52983057-53088237	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	esv3404701	chr19:52986895-53035152	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1058567	chr19:52992455-53021505	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3440535	chr19:52993529-53035203	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1066717	chr19:52993620-53041995	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1064342	chr19:52996710-53041119	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1055825	chr19:53001299-53037378	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers 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	3 gene(s)	inside rSNPs	diseases
13	nsv1055859	chr19:53001299-53041119	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1060656	chr19:53001299-53041995	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53002600-53021400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:53003000-53014800	Weak transcription	Brain Germinal Matrix	brain
3	chr19:53003400-53022600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:53003800-53015000	Weak transcription	Fetal Lung	lung
5	chr19:53003800-53017600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr19:53004400-53014800	Weak transcription	Brain Angular Gyrus	brain
7	chr19:53004600-53015800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr19:53005400-53015800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr19:53006400-53021200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr19:53006400-53021400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr19:53006600-53014800	Weak transcription	Brain Anterior Caudate	brain
12	chr19:53006600-53015600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr19:53006600-53016200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr19:53006800-53015000	Weak transcription	Fetal Brain Female	brain
15	chr19:53006800-53021400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr19:53007000-53015000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr19:53007000-53021400	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr19:53007400-53015200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr19:53008400-53015600	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr19:53009000-53022600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr19:53010000-53014800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr19:53011000-53017800	Weak transcription	Right Ventricle	heart
23	chr19:53012200-53016000	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr19:53012400-53015200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr19:53012400-53016200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr19:53012600-53015800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr19:53012800-53015600	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr19:53013000-53016000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr19:53013000-53016200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr19:53013000-53016200	Weak transcription	Fetal Stomach	stomach
31	chr19:53013200-53015000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr19:53013200-53015200	Strong transcription	HSMMtube	muscle
33	chr19:53013200-53021800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr19:53013400-53015200	ZNF genes & repeats	Stomach Smooth Muscle	stomach
35	chr19:53013400-53016400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr19:53013600-53015600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr19:53013800-53015000	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr19:53013800-53015400	ZNF genes & repeats	Liver	Liver
39	chr19:53013800-53015800	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr19:53013800-53018200	Strong transcription	Fetal Muscle Leg	muscle
41	chr19:53014000-53014800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr19:53014000-53015000	Strong transcription	Left Ventricle	heart
43	chr19:53014000-53015400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:53014000-53015400	Strong transcription	Dnd41	blood
45	chr19:53014000-53015600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
46	chr19:53014000-53015600	Strong transcription	Fetal Kidney	kidney
47	chr19:53014000-53015800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr19:53014200-53015600	Strong transcription	Aorta	Aorta
49	chr19:53014200-53016000	Strong transcription	Ovary	ovary
50	chr19:53014400-53015600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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