Variant report

Variant	nsv833988
Chromosome Location	chr20:41227788-41379921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:369)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr20:41370653-41370853	K562	blood:	n/a	n/a
2	BACH1	chr20:41324497-41324521	K562	blood:	n/a	n/a
3	BACH1	chr20:41307552-41307915	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr20:41362026-41362032	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr20:41378208-41378560	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr20:41262897-41263215	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr20:41371368-41371745	K562	blood:	n/a	n/a
8	BHLHE40	chr20:41355345-41355582	K562	blood:	n/a	n/a
9	CEBPB	chr20:41361593-41361847	HepG2	liver:	n/a	chr20:41361684-41361697 chr20:41361685-41361696
10	CEBPB	chr20:41251310-41251377	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:41240638-41240690	HepG2	liver:	n/a	chr20:41240677-41240688
12	CEBPB	chr20:41378592-41378801	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr20:41372285-41372407	HepG2	liver:	n/a	chr20:41372350-41372361 chr20:41372349-41372362
14	CEBPB	chr20:41341367-41341488	HepG2	liver:	n/a	n/a
15	CEBPB	chr20:41269498-41269701	HepG2	liver:	n/a	chr20:41269631-41269642
16	CEBPB	chr20:41347105-41347193	K562	blood:	n/a	n/a
17	CEBPB	chr20:41282814-41283026	HepG2	liver:	n/a	chr20:41282919-41282930
18	CEBPB	chr20:41274989-41275199	HepG2	liver:	n/a	n/a
19	CEBPB	chr20:41359726-41359923	HepG2	liver:	n/a	n/a
20	CEBPB	chr20:41279055-41279225	H1-hESC	embryonic stem cell:	n/a	chr20:41279114-41279125
21	CEBPB	chr20:41297733-41297951	HepG2	liver:	n/a	chr20:41297799-41297810
22	CEBPB	chr20:41265532-41265732	HepG2	liver:	n/a	chr20:41265590-41265603 chr20:41265591-41265602
23	CEBPB	chr20:41234364-41234717	HepG2	liver:	n/a	n/a
24	CEBPB	chr20:41234470-41234614	K562	blood:	n/a	n/a
25	CTCF	chr20:41307650-41307818	A549	lung:	n/a	n/a
26	CTCF	chr20:41238877-41238939	K562	blood:	n/a	n/a
27	CTCF	chr20:41307640-41307790	GM12864	blood:	n/a	n/a
28	CTCF	chr20:41307660-41307810	Caco-2	colon:	n/a	n/a
29	CTCF	chr20:41307640-41307790	GM12878	blood:	n/a	n/a
30	CTCF	chr20:41307580-41307730	GM12872	blood:	n/a	n/a
31	CTCF	chr20:41307575-41307877	K562	blood:	n/a	n/a
32	CTCF	chr20:41307608-41307865	MCF-7	breast:	n/a	n/a
33	CTCF	chr20:41307660-41307810	BE2_C	brain:	n/a	n/a
34	CTCF	chr20:41307660-41307810	GM12865	blood:	n/a	n/a
35	CTCF	chr20:41307635-41307841	GM19238	blood:	n/a	n/a
36	CTCF	chr20:41238760-41238910	MCF-7	breast:	n/a	n/a
37	CTCF	chr20:41307260-41307410	MCF-7	breast:	n/a	n/a
38	CTCF	chr20:41307640-41307790	GM12873	blood:	n/a	n/a
39	CTCF	chr20:41307680-41307830	HMEC	breast:	n/a	n/a
40	CTCF	chr20:41370151-41370195	GM20000	blood:	n/a	n/a
41	CTCF	chr20:41307640-41307790	GM12867	blood:	n/a	n/a
42	CTCF	chr20:41307658-41307774	Gliobla	brain:	n/a	n/a
43	CTCF	chr20:41307560-41307710	GM06990	blood:	n/a	n/a
44	CTCF	chr20:41307700-41307850	HL-60	blood:	n/a	n/a
45	CTCF	chr20:41307700-41307850	HEK293	kidney:	n/a	n/a
46	CTCF	chr20:41307670-41307780	Fibrobl	skin:	n/a	n/a
47	CTCF	chr20:41238740-41238890	HEK293	kidney:	n/a	n/a
48	CTCF	chr20:41307643-41307849	LNCaP	prostate:	n/a	n/a
49	CTCF	chr20:41307700-41307850	K562	blood:	n/a	n/a
50	CTCF	chr20:41307680-41307830	MCF-7	breast:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr20:41235856..41237826-chr20:41240786..41243321,2	K562	blood:
2	chr20:41352782..41354688-chr20:41355194..41357788,2	K562	blood:
3	chr1:115296501..115298139-chr20:41277950..41280016,2	MCF-7	breast:
4	chr20:41376932..41379314-chr20:41384669..41386890,2	K562	blood:
5	chr20:41238748..41239268-chr20:41307296..41307807,2	MCF-7	breast:
6	chr1:115299061..115301144-chr20:41248782..41252439,3	MCF-7	breast:
7	chr20:41356881..41359207-chr20:41359274..41361954,2	K562	blood:
8	chr20:41232529..41235268-chr20:41239023..41240669,2	MCF-7	breast:
9	chr20:41350902..41352740-chr20:41354249..41356948,2	MCF-7	breast:
10	chr20:41112023..41112867-chr20:41307681..41308188,2	MCF-7	breast:
11	chr20:41356881..41359207-chr20:41359274..41361954,2	K562	blood:
12	chr20:41352782..41354688-chr20:41355194..41357788,2	K562	blood:
13	chr20:41378883..41381522-chr20:41383064..41386046,2	K562	blood:
14	chr20:41238748..41239268-chr20:41307296..41307807,2	MCF-7	breast:
15	chr1:115299122..115302084-chr20:41239351..41241193,2	MCF-7	breast:
16	chr20:41350902..41352740-chr20:41354249..41356948,2	MCF-7	breast:
17	chr20:41235856..41237826-chr20:41240786..41243321,2	K562	blood:
18	chr20:41232529..41235268-chr20:41239023..41240669,2	MCF-7	breast:
19	chr20:41221842..41223467-chr20:41282056..41284683,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRSF6-3	chr20:41314526-41314699	ENSG00000229042.2
2	lnc-SRSF6-3	chr20:41314585-41314699	ENSG00000229042.2
3	lnc-SRSF6-3	chr20:41314788-41314857	ENSG00000229042.2
4	lnc-SRSF6-11	chr20:41236034-41236199	NONHSAT079803
5	lnc-SRSF6-3	chr20:41314123-41314471	ENSG00000229042.2
6	lnc-SRSF6-3	chr20:41314788-41314952	ENSG00000229042
7	lnc-SRSF6-3	chr20:41314123-41314471	ENSG00000229042
8	lnc-SRSF6-3	chr20:41314788-41314952	ENSG00000229042.2
9	lnc-SRSF6-3	chr20:41314585-41314699	ENSG00000229042
10	lnc-SRSF6-3	chr20:41315837-41317202	ENSG00000229042.2
11	lnc-SRSF6-3	chr20:41315837-41316285	ENSG00000229042
12	lnc-SRSF6-3	chr20:41314044-41314372	ENSG00000229042.2
13	lnc-SRSF6-11	chr20:41235334-41235515	NONHSAT079803

No data

Variant related genes	Relation type
ENSG00000229042	TF binding region
ENSG00000229892	TF binding region
ENSG00000009307	chromatin interactions
CIRBP	miRNA target sites
FAHD1	miRNA target sites
RND3	miRNA target sites

Extended variants
information (count: 6329 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6329 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192927369	chr20:41227815-41227816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552839399	chr20:41227847-41227848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566208514	chr20:41227858-41227859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143632417	chr20:41227887-41227888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555110367	chr20:41227906-41227907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575186575	chr20:41227925-41227926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537701947	chr20:41227932-41227933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147181741	chr20:41227951-41227952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371838957	chr20:41228028-41228029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577212022	chr20:41228038-41228039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562479563	chr20:41228043-41228044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138739080	chr20:41228061-41228062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559623010	chr20:41228071-41228072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533002304	chr20:41228091-41228092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573337098	chr20:41228125-41228126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6102925	chr20:41228178-41228179	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs562215795	chr20:41228185-41228186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183161870	chr20:41228196-41228197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551030541	chr20:41228215-41228216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374981100	chr20:41228234-41228235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564797957	chr20:41228334-41228335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62203817	chr20:41228377-41228378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34027202	chr20:41228402-41228403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs150725807	chr20:41228422-41228423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188637114	chr20:41228454-41228455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548770612	chr20:41228483-41228484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139016947	chr20:41228514-41228515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192977044	chr20:41228548-41228549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150071525	chr20:41228555-41228556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577849201	chr20:41228589-41228590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs8123995	chr20:41228600-41228601	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs8119203	chr20:41228652-41228653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs8124013	chr20:41228678-41228679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542301204	chr20:41228685-41228686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6102926	chr20:41228738-41228739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs8123681	chr20:41228763-41228764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs556706058	chr20:41228776-41228777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201422471	chr20:41228782-41228783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544769550	chr20:41228855-41228856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564661576	chr20:41228925-41228926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146155121	chr20:41228928-41228929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546301383	chr20:41228929-41228930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539491030	chr20:41228960-41228961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528966787	chr20:41228970-41228971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548712074	chr20:41228982-41228983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568611425	chr20:41228983-41228984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537675405	chr20:41228986-41228987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201760204	chr20:41228994-41228995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140162462	chr20:41229018-41229019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571470716	chr20:41229021-41229022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian cancer	19193619	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelodysplastic syndrome	17634407	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Cervical cancer	21062161	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41219200-41240200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:41226200-41232400	Weak transcription	Pancreas	Pancrea
3	chr20:41227000-41227800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr20:41227400-41228000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr20:41227400-41228000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr20:41227400-41228200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr20:41228000-41231200	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr20:41231200-41233400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr20:41232400-41232600	Enhancers	Pancreas	Pancrea
10	chr20:41232600-41233000	Weak transcription	Pancreas	Pancrea
11	chr20:41232800-41234400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:41233000-41234800	Enhancers	Pancreas	Pancrea
13	chr20:41233800-41234200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr20:41234200-41234600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr20:41234400-41234800	Enhancers	NHEK	skin
16	chr20:41234800-41236000	Weak transcription	NHEK	skin
17	chr20:41236000-41236600	Enhancers	NHEK	skin
18	chr20:41240000-41241600	Enhancers	Fetal Brain Male	brain
19	chr20:41240000-41242800	Enhancers	Fetal Muscle Leg	muscle
20	chr20:41240200-41240400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr20:41240200-41240800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
22	chr20:41240400-41240600	Bivalent Enhancer	Fetal Brain Female	brain
23	chr20:41240400-41240800	Enhancers	Fetal Muscle Trunk	muscle
24	chr20:41240400-41241400	Enhancers	Fetal Stomach	stomach
25	chr20:41240600-41242200	Enhancers	Fetal Brain Female	brain
26	chr20:41241000-41242200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr20:41241800-41242400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr20:41242800-41243000	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr20:41249200-41249600	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr20:41249200-41249600	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr20:41249200-41249800	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr20:41249200-41249800	Active TSS	Duodenum Mucosa	Duodenum
33	chr20:41251400-41252000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr20:41251400-41253800	Enhancers	NHEK	skin
35	chr20:41251600-41253600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr20:41251800-41252400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr20:41251800-41252600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr20:41253600-41270200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr20:41257000-41258200	Enhancers	Liver	Liver
40	chr20:41263000-41263400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr20:41263000-41264200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr20:41270200-41270800	Enhancers	Pancreas	Pancrea
43	chr20:41270200-41271600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr20:41271600-41300800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr20:41277000-41277400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr20:41278600-41279400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr20:41278800-41279400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr20:41279000-41279400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr20:41281000-41281400	Enhancers	Gastric	stomach
50	chr20:41281200-41281600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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