Variant report

Variant	nsv2244
Chromosome Location	chr18:28635554-28666380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:28638602-28639276	HepG2	liver:	n/a	n/a
2	ATF2	chr18:28644069-28644441	GM12878	blood:	n/a	n/a
3	ATF2	chr18:28643982-28644530	GM12878	blood:	n/a	n/a
4	ATF2	chr18:28641762-28642485	GM12878	blood:	n/a	n/a
5	ATF2	chr18:28641878-28642432	GM12878	blood:	n/a	n/a
6	BACH1	chr18:28654125-28654223	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr18:28644099-28644529	GM12878	blood:	n/a	chr18:28644282-28644293
8	BATF	chr18:28644079-28644420	GM12878	blood:	n/a	chr18:28644282-28644293
9	BCL11A	chr18:28644099-28644453	GM12878	blood:	n/a	n/a
10	BCL3	chr18:28644069-28644521	GM12878	blood:	n/a	n/a
11	BCL3	chr18:28641839-28642386	GM12878	blood:	n/a	n/a
12	BCL3	chr18:28644087-28644381	GM12878	blood:	n/a	n/a
13	BCLAF1	chr18:28644038-28644550	GM12878	blood:	n/a	n/a
14	BHLHE40	chr18:28643724-28643732	GM12878	blood:	n/a	n/a
15	BHLHE40	chr18:28644116-28644316	GM12878	blood:	n/a	n/a
16	CEBPB	chr18:28638538-28639284	HepG2	liver:	n/a	chr18:28639221-28639234
17	CEBPB	chr18:28638583-28639275	HepG2	liver:	n/a	chr18:28639221-28639234
18	CEBPB	chr18:28637017-28637308	HepG2	liver:	n/a	chr18:28637161-28637172
19	CEBPB	chr18:28637109-28637335	A549	lung:	n/a	chr18:28637161-28637172
20	CEBPB	chr18:28639017-28639155	HepG2	liver:	n/a	n/a
21	CUX1	chr18:28642079-28642334	GM12878	blood:	n/a	n/a
22	E2F4	chr18:28650025-28650606	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr18:28644200-28644792	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr18:28645131-28645159	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr18:28644091-28644296	GM12878	blood:	n/a	n/a
26	EBF1	chr18:28640278-28640433	GM12878	blood:	n/a	chr18:28640369-28640380 chr18:28640368-28640381 chr18:28640370-28640379 chr18:28640370-28640380
27	EBF1	chr18:28641932-28642416	GM12878	blood:	n/a	n/a
28	EGR1	chr18:28644158-28644362	GM12878	blood:	n/a	chr18:28644261-28644275
29	EGR1	chr18:28644135-28644342	K562	blood:	n/a	chr18:28644261-28644275
30	EGR1	chr18:28644144-28644373	K562	blood:	n/a	chr18:28644261-28644275
31	EGR1	chr18:28644144-28644322	GM12878	blood:	n/a	chr18:28644261-28644275
32	EGR1	chr18:28644052-28644390	HCT-116	colon:	n/a	chr18:28644261-28644275
33	ELF1	chr18:28657877-28658171	K562	blood:	n/a	chr18:28658054-28658067 chr18:28658022-28658035 chr18:28658023-28658034
34	EP300	chr18:28644106-28644433	GM12878	blood:	n/a	n/a
35	EP300	chr18:28638775-28639136	HepG2	liver:	n/a	chr18:28638846-28638854
36	EP300	chr18:28638847-28639227	HepG2	liver:	n/a	n/a
37	EP300	chr18:28644385-28644406	GM12878	blood:	n/a	n/a
38	FOS	chr18:28650249-28650661	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr18:28650177-28650612	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr18:28644085-28644505	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr18:28644092-28644465	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr18:28640067-28640074	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr18:28636982-28637237	MCF10A-Er-Src	breast:	n/a	chr18:28636985-28636997
44	FOS	chr18:28637021-28637295	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr18:28650229-28650612	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr18:28644089-28644446	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr18:28644104-28644458	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr18:28645104-28645246	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr18:28652291-28652367	MCF10A-Er-Src	breast:	n/a	chr18:28652331-28652342 chr18:28652332-28652341
50	FOS	chr18:28650189-28650629	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:28658043-28658093	AG09309	skin:	n/a
2	chr18:28658043-28658093	A549	lung:	n/a
3	chr18:28658043-28658093	HEEpiC	esophagus:	n/a
4	chr18:28658043-28658093	PFSK-1	brain:	n/a
5	chr18:28658043-28658093	NH-A	brain:	n/a
6	chr18:28658043-28658093	SK-N-MC	brain:	n/a
7	chr18:28658043-28658093	GM12878	blood:	n/a
8	chr18:28658043-28658093	HNPCEpiC	eye:	n/a
9	chr18:28658043-28658093	ovcar-3	ovarian:	n/a
10	chr18:28658043-28658093	SK-N-SH_RA	brain:	n/a
11	chr18:28658043-28658093	RPTEC	kidney:	n/a
12	chr18:28658043-28658093	MCF10A-Er-Src	breast:	n/a
13	chr18:28658043-28658093	NT2-D1	testis:	n/a
14	chr18:28658043-28658093	ProgFib	skin:	n/a
15	chr18:28658043-28658093	HPAEpiC	pulmonary alveolar:	n/a
16	chr18:28658043-28658093	AG04450	lung:	fetal
17	chr18:28658043-28658093	AG09319	gingival:	n/a
18	chr18:28658043-28658093	GM12891	blood:	n/a
19	chr18:28658043-28658093	HEK293	kidney:	embryo
20	chr18:28658043-28658093	SAEC	small airway:	n/a
21	chr18:28658043-28658093	NHBE	bronchial:	n/a
22	chr18:28658043-28658093	HRPEpiC	eye:	n/a
23	chr18:28658043-28658093	T-47D	breast:	n/a
24	chr18:28658043-28658093	IMR90	lung:	fetal
25	chr18:28658043-28658093	SK-N-SH	brain:	n/a
26	chr18:28658043-28658093	AG10803	skin:	n/a
27	chr18:28658043-28658093	GM12892	blood:	n/a
28	chr18:28658043-28658093	CMK	blood:	n/a
29	chr18:28658043-28658093	GM19239	blood:	n/a
30	chr18:28658043-28658093	K562	blood:	n/a
31	chr18:28658043-28658093	HIPEpiC	eye:	n/a
32	chr18:28658043-28658093	HCT-116	colon:	n/a
33	chr18:28658043-28658093	HRCEpiC	kidney:	n/a
34	chr18:28658043-28658093	H1-hESC	embryonic stem cell:	embryo
35	chr18:28658043-28658093	HepG2	liver:	n/a
36	chr18:28658043-28658093	HMEC	breast:	n/a
37	chr18:28658043-28658093	HL-60	blood:	n/a
38	chr18:28658043-28658093	HCPEpiC	choroid plexus:	n/a
39	chr18:28658043-28658093	LNCaP	prostate:	n/a
40	chr18:28658043-28658093	HCF	heart:	n/a
41	chr18:28658043-28658093	AoSMC	blood vessel:	n/a
42	chr18:28658043-28658093	MCF-7	breast:	n/a
43	chr18:28658043-28658093	HCM	heart:	n/a
44	chr18:28658043-28658093	PANC-1	pancreas:	n/a
45	chr18:28658043-28658093	ECC-1	luminal epithelium:	n/a
46	chr18:28658043-28658093	Hepatocyte	liver:	n/a
47	chr18:28658043-28658093	GM06990	blood:	n/a
48	chr18:28658043-28658093	SKMC	muscle:	n/a
49	chr18:28658043-28658093	BE2_C	brain:	n/a
50	chr18:28658043-28658093	PrEC	prostate:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr18:28641189..28643310-chr18:28664453..28667293,2	K562	blood:
2	chr18:28635379..28636910-chr18:28640103..28642394,2	K562	blood:
3	chr18:28641189..28643310-chr18:28664453..28667293,2	K562	blood:
4	chr18:28633421..28635335-chr18:28642535..28645515,2	K562	blood:
5	chr18:28663717..28665312-chr18:28679601..28681471,2	K562	blood:
6	chr18:28655509..28657780-chr18:28673533..28675759,2	K562	blood:
7	chr18:28663646..28666482-chr18:28680047..28681703,2	K562	blood:
8	chr18:28642756..28645487-chr18:28647010..28648822,3	K562	blood:
9	chr18:28660094..28661732-chr18:28665344..28667098,2	K562	blood:
10	chr18:28653486..28654988-chr18:28657389..28659058,2	K562	blood:
11	chr18:28653486..28654988-chr18:28657389..28659058,2	K562	blood:
12	chr18:28635410..28637896-chr18:28640436..28642394,2	K562	blood:
13	chr18:28651842..28653529-chr18:28655723..28658009,2	MCF-7	breast:
14	chr18:28635410..28637896-chr18:28640436..28642394,2	K562	blood:
15	chr18:28642756..28645487-chr18:28647010..28648822,3	K562	blood:
16	chr18:28638090..28639722-chr18:28640416..28641974,2	K562	blood:
17	chr18:28652833..28654483-chr18:28679672..28682007,2	K562	blood:
18	chr18:28662932..28665647-chr18:28680801..28683463,2	MCF-7	breast:
19	chr18:28627195..28629881-chr18:28637008..28639341,2	MCF-7	breast:
20	chr18:28640728..28642575-chr18:28644774..28647318,2	K562	blood:
21	chr18:28620876..28623818-chr18:28658735..28661003,2	K562	blood:
22	chr18:28660094..28661732-chr18:28665344..28667098,2	K562	blood:
23	chr18:28640728..28642575-chr18:28644774..28647318,2	K562	blood:
24	chr18:28640333..28642657-chr18:28648234..28652025,3	K562	blood:
25	chr18:28637499..28640163-chr18:28647964..28650502,2	K562	blood:
26	chr18:28635379..28636910-chr18:28640103..28642394,2	K562	blood:
27	chr18:28606623..28609017-chr18:28636811..28638702,2	K562	blood:
28	chr18:28665512..28667530-chr18:28670151..28672364,2	K562	blood:
29	chr18:28652105..28654902-chr18:28682018..28683959,2	K562	blood:
30	chr18:28640333..28642657-chr18:28648234..28652025,3	K562	blood:
31	chr18:28636549..28638858-chr18:28710603..28713057,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSC2-1	chr18:28638806-28639359	ENSG00000261521.1

No data

Variant related genes	Relation type
ENSG00000261521	TF binding region
ENSG00000238376	TF binding region
ENSG00000261521	CpG island
ENSG00000238376	CpG island
ENSG00000261521	chromatin interactions
ENSG00000265888	chromatin interactions
ENSG00000134762	chromatin interactions
ENSG00000238376	chromatin interactions
ENSG00000134755	chromatin interactions
ENSG00000263698	chromatin interactions

Extended variants
information (count: 1154 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372359048	chr18:28635566-28635567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115936997	chr18:28635595-28635596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs80148345	chr18:28635605-28635606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539939469	chr18:28635624-28635625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113968526	chr18:28635630-28635631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577017796	chr18:28635640-28635641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544190315	chr18:28635679-28635680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193096269	chr18:28635680-28635681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529990478	chr18:28635705-28635706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548493024	chr18:28635725-28635726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145151425	chr18:28635732-28635733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149165193	chr18:28635740-28635741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546775819	chr18:28635748-28635749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11081678	chr18:28635776-28635777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs75026216	chr18:28635790-28635791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142376777	chr18:28635792-28635793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145677534	chr18:28635846-28635847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1790696	chr18:28635877-28635878	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs184653693	chr18:28635937-28635938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567018352	chr18:28635947-28635948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566061501	chr18:28635991-28635992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374829407	chr18:28636000-28636001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1866104	chr18:28636005-28636006	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs199986378	chr18:28636013-28636014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74402430	chr18:28636027-28636028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151272400	chr18:28636080-28636081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558896916	chr18:28636111-28636112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577579964	chr18:28636127-28636128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1893964	chr18:28636224-28636225	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs117851818	chr18:28636267-28636268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562449318	chr18:28636274-28636275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147083337	chr18:28636285-28636286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541748551	chr18:28636347-28636348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138564298	chr18:28636369-28636370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537154654	chr18:28636385-28636386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527594387	chr18:28636411-28636412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs16961152	chr18:28636506-28636507	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs78150665	chr18:28636533-28636534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189117415	chr18:28636540-28636541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555209250	chr18:28636543-28636544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550694897	chr18:28636548-28636549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568898944	chr18:28636558-28636559	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530152639	chr18:28636566-28636567	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548292863	chr18:28636587-28636588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1658101	chr18:28636616-28636617	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs142604453	chr18:28636618-28636619	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559082136	chr18:28636628-28636629	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs180755546	chr18:28636631-28636632	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150090483	chr18:28636647-28636648	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534839003	chr18:28636655-28636656	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28631200-28640400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr18:28634000-28636200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr18:28634400-28636200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr18:28634400-28641800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr18:28635600-28637000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr18:28635800-28636600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr18:28635800-28636600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr18:28635800-28636800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr18:28635800-28637200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr18:28635800-28637800	Enhancers	NHEK	skin
11	chr18:28636000-28636800	Enhancers	Fetal Lung	lung
12	chr18:28636000-28637000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr18:28636000-28637000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr18:28636000-28637000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr18:28636000-28637400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr18:28636200-28636400	Enhancers	Fetal Intestine Large	intestine
17	chr18:28636200-28636600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr18:28636200-28636600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr18:28636200-28637200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr18:28636200-28637400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr18:28636400-28645000	Weak transcription	Fetal Intestine Large	intestine
22	chr18:28636600-28640600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr18:28636600-28644800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr18:28636600-28645200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr18:28636800-28637200	Weak transcription	Fetal Lung	lung
26	chr18:28636800-28641800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr18:28637000-28637800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr18:28637000-28643800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr18:28637000-28645000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr18:28637000-28647400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr18:28637200-28637600	Active TSS	Fetal Brain Male	brain
32	chr18:28637200-28637800	Enhancers	Fetal Lung	lung
33	chr18:28637200-28649000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr18:28637400-28637800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr18:28637400-28638400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr18:28637800-28638000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr18:28637800-28638400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr18:28637800-28641800	Weak transcription	Fetal Lung	lung
39	chr18:28638000-28638200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr18:28638000-28639400	Enhancers	HepG2	liver
41	chr18:28638000-28647400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr18:28638200-28649000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr18:28638400-28639000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr18:28638400-28645400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr18:28639000-28639200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr18:28639000-28639200	Enhancers	Pancreas	Pancrea
47	chr18:28639000-28647400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr18:28639200-28647600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr18:28639200-28648600	Weak transcription	Pancreas	Pancrea
50	chr18:28639400-28646800	Weak transcription	HepG2	liver

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