Variant report

Variant	rs532080559
Chromosome Location	chr1:45484442-45484443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45483655..45486167-chr1:45802201..45804305,2	K562	blood:
2	chr1:45483104..45484724-chr1:45490873..45492941,2	K562	blood:
3	chr1:45483477..45484967-chr1:45765750..45766657,4	K562	blood:
4	chr1:45184531..45187337-chr1:45484420..45488341,4	K562	blood:
5	chr1:45476357..45485239-chr1:45761850..45773601,48	K562	blood:
6	chr1:45484129..45484961-chr1:45769347..45770315,2	K562	blood:
7	chr1:45475929..45480621-chr1:45481195..45486078,6	MCF-7	breast:
8	chr1:45482594..45485585-chr1:45656946..45658548,2	K562	blood:
9	chr1:45483402..45485551-chr1:45804133..45806888,2	K562	blood:
10	chr1:45285085..45286788-chr1:45483316..45485098,2	K562	blood:
11	chr1:45480075..45485962-chr1:45670647..45674355,5	MCF-7	breast:
12	chr1:45483055..45484838-chr1:45740397..45743390,2	K562	blood:
13	chr1:45483996..45486300-chr1:45594488..45596026,2	K562	blood:
14	chr1:45483202..45484788-chr1:45677331..45680052,2	K562	blood:
15	chr1:45484097..45484937-chr1:45766011..45766623,2	MCF-7	breast:
16	chr1:45484177..45484927-chr1:45695999..45696897,4	MCF-7	breast:
17	chr1:45483767..45484830-chr1:45695988..45696895,3	MCF-7	breast:
18	chr1:45184531..45190715-chr1:45481425..45486664,6	K562	blood:
19	chr1:45476265..45486633-chr1:45761064..45774272,63	K562	blood:

No data

Variant related genes	Relation type
ENSG00000202444	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000162415	Chromatin interaction
ENSG00000126107	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
2	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
3	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
5	nsv945916	chr1:45482107-45485685	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
6	nsv945579	chr1:45484262-45485685	Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45478600-45500000	Weak transcription	Aorta	Aorta
2	chr1:45479000-45485200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr1:45479000-45493000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:45480800-45486000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:45480800-45500000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:45480800-45500600	Weak transcription	HepG2	liver
7	chr1:45480800-45501200	Weak transcription	Fetal Brain Male	brain
8	chr1:45480800-45510400	Weak transcription	Colon Smooth Muscle	Colon
9	chr1:45481000-45484600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:45481200-45504600	Weak transcription	Colonic Mucosa	Colon
11	chr1:45481200-45510200	Weak transcription	Lung	lung
12	chr1:45481200-45525000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr1:45481200-45527400	Weak transcription	Left Ventricle	heart
14	chr1:45481400-45488000	Weak transcription	Fetal Kidney	kidney
15	chr1:45481400-45500000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr1:45481600-45489400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:45481600-45491800	Weak transcription	NHDF-Ad	bronchial
18	chr1:45481600-45498600	Weak transcription	Hela-S3	cervix
19	chr1:45481600-45499800	Weak transcription	Fetal Intestine Large	intestine
20	chr1:45481600-45499800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr1:45481800-45489600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr1:45481800-45491400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:45481800-45499800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:45482000-45490600	Weak transcription	Fetal Lung	lung
25	chr1:45482000-45523800	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr1:45483200-45486200	Weak transcription	K562	blood
27	chr1:45483600-45486200	Strong transcription	Fetal Brain Female	brain
28	chr1:45484000-45484600	Strong transcription	Right Atrium	heart
29	chr1:45484000-45484800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:45484000-45484800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr1:45484000-45484800	Enhancers	Liver	Liver
32	chr1:45484000-45484800	Enhancers	Pancreas	Pancrea
33	chr1:45484000-45485800	Strong transcription	Ovary	ovary
34	chr1:45484200-45484600	Enhancers	Primary T cells fromperipheralblood	blood
35	chr1:45484200-45484600	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr1:45484200-45484600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:45484200-45484600	Enhancers	Brain Cingulate Gyrus	brain
38	chr1:45484200-45484800	Enhancers	Brain Angular Gyrus	brain
39	chr1:45484200-45484800	Enhancers	Brain Hippocampus Middle	brain
40	chr1:45484200-45484800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr1:45484200-45484800	Enhancers	Esophagus	oesophagus
42	chr1:45484200-45484800	Enhancers	Gastric	stomach
43	chr1:45484200-45484800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr1:45484200-45485000	Enhancers	Brain Substantia Nigra	brain
45	chr1:45484200-45485400	Genic enhancers	Brain Germinal Matrix	brain
46	chr1:45484200-45486400	Strong transcription	Fetal Intestine Small	intestine
47	chr1:45484200-45499800	Weak transcription	Fetal Stomach	stomach
48	chr1:45484400-45484600	Flanking Active TSS	Brain Anterior Caudate	brain
49	chr1:45484400-45484600	Enhancers	Right Ventricle	heart
50	chr1:45484400-45484600	Enhancers	Skeletal Muscle Male	skeletal muscle

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