Variant report

Variant	rs549361767
Chromosome Location	chr1:45483629-45483630
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	chr1:45483205..45483889-chr1:45765728..45766395,2	MCF-7	breast:
2	chr1:45483104..45484724-chr1:45490873..45492941,2	K562	blood:
3	chr1:45483477..45484967-chr1:45765750..45766657,4	K562	blood:
4	chr1:45483011..45483657-chr1:45764134..45764928,2	K562	blood:
5	chr1:45476357..45485239-chr1:45761850..45773601,48	K562	blood:
6	chr1:45482345..45484376-chr1:45808953..45810497,2	K562	blood:
7	chr1:45265945..45268277-chr1:45482213..45483730,2	K562	blood:
8	chr1:45475929..45480621-chr1:45481195..45486078,6	MCF-7	breast:
9	chr1:45482594..45485585-chr1:45656946..45658548,2	K562	blood:
10	chr1:45185920..45189252-chr1:45480937..45484378,4	K562	blood:
11	chr1:45483402..45485551-chr1:45804133..45806888,2	K562	blood:
12	chr1:45285085..45286788-chr1:45483316..45485098,2	K562	blood:
13	chr1:45480075..45485962-chr1:45670647..45674355,5	MCF-7	breast:
14	chr1:45483055..45484838-chr1:45740397..45743390,2	K562	blood:
15	chr1:45252618..45255680-chr1:45481014..45484053,3	K562	blood:
16	chr1:45265885..45267445-chr1:45480826..45483713,2	K562	blood:
17	chr1:45483202..45484788-chr1:45677331..45680052,2	K562	blood:
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
ENSG00000132781	Chromatin interaction
ENSG00000126107	Chromatin interaction
ENSG00000162415	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000202444	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000142959	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000199377	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45478600-45500000	Weak transcription	Aorta	Aorta
2	chr1:45478800-45484000	Weak transcription	Right Atrium	heart
3	chr1:45479000-45484200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:45479000-45484200	Weak transcription	Esophagus	oesophagus
5	chr1:45479000-45485200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr1:45479000-45493000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:45479200-45484200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr1:45479400-45484200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:45479600-45484000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:45479600-45484200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr1:45479600-45484400	Weak transcription	Right Ventricle	heart
12	chr1:45480600-45484200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:45480600-45484200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr1:45480800-45484000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:45480800-45484000	Weak transcription	Pancreas	Pancrea
16	chr1:45480800-45484200	Weak transcription	Brain Angular Gyrus	brain
17	chr1:45480800-45484200	Weak transcription	Brain Substantia Nigra	brain
18	chr1:45480800-45484200	Weak transcription	Fetal Heart	heart
19	chr1:45480800-45486000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:45480800-45500000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:45480800-45500600	Weak transcription	HepG2	liver
22	chr1:45480800-45501200	Weak transcription	Fetal Brain Male	brain
23	chr1:45480800-45510400	Weak transcription	Colon Smooth Muscle	Colon
24	chr1:45481000-45484200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr1:45481000-45484400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:45481000-45484600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr1:45481200-45483800	Weak transcription	Gastric	stomach
28	chr1:45481200-45483800	Weak transcription	Thymus	Thymus
29	chr1:45481200-45484000	Weak transcription	HSMMtube	muscle
30	chr1:45481200-45484200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:45481200-45484200	Weak transcription	Brain Anterior Caudate	brain
32	chr1:45481200-45484200	Weak transcription	Fetal Intestine Small	intestine
33	chr1:45481200-45484200	Weak transcription	GM12878-XiMat	blood
34	chr1:45481200-45484400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr1:45481200-45504600	Weak transcription	Colonic Mucosa	Colon
36	chr1:45481200-45510200	Weak transcription	Lung	lung
37	chr1:45481200-45525000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr1:45481200-45527400	Weak transcription	Left Ventricle	heart
39	chr1:45481400-45483800	Weak transcription	HMEC	breast
40	chr1:45481400-45484000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:45481400-45484000	Weak transcription	Liver	Liver
42	chr1:45481400-45484000	Weak transcription	Ovary	ovary
43	chr1:45481400-45484000	Weak transcription	NHLF	lung
44	chr1:45481400-45484200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:45481400-45484200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:45481400-45484200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr1:45481400-45484200	Weak transcription	HSMM	muscle
48	chr1:45481400-45488000	Weak transcription	Fetal Kidney	kidney
49	chr1:45481400-45500000	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr1:45481600-45483800	Weak transcription	Muscle Satellite Cultured Cells	--

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