Variant report

Variant	nsv909588
Chromosome Location	chr18:43474795-43554371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1446)
CpG islands
(count:916)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:43547271-43547530	K562	blood:	n/a	n/a
2	ARID3A	chr18:43542471-43542768	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:43554131-43554486	K562	blood:	n/a	n/a
4	ARID3A	chr18:43515587-43515954	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:43554133-43554483	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:43547067-43547601	HepG2	liver:	n/a	n/a
7	ATF2	chr18:43547052-43547554	GM12878	blood:	n/a	chr18:43547216-43547230
8	ATF3	chr18:43547151-43547412	HepG2	liver:	n/a	chr18:43547402-43547411 chr18:43547289-43547298
9	ATF3	chr18:43547146-43547404	K562	blood:	n/a	chr18:43547289-43547298
10	ATF3	chr18:43547202-43547470	K562	blood:	n/a	chr18:43547402-43547411 chr18:43547289-43547298
11	BATF	chr18:43475673-43475919	GM12878	blood:	n/a	chr18:43475798-43475809
12	BHLHE40	chr18:43547126-43547638	GM12878	blood:	n/a	n/a
13	BHLHE40	chr18:43554153-43554442	K562	blood:	n/a	n/a
14	BHLHE40	chr18:43515524-43515796	HepG2	liver:	n/a	n/a
15	BHLHE40	chr18:43542269-43542831	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:43490476-43490676	GM12878	blood:	n/a	n/a
17	BHLHE40	chr18:43542507-43542775	K562	blood:	n/a	n/a
18	BHLHE40	chr18:43518440-43518844	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:43554090-43554382	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:43546956-43547568	HepG2	liver:	n/a	n/a
21	BHLHE40	chr18:43547082-43547484	K562	blood:	n/a	n/a
22	BRCA1	chr18:43547511-43547695	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr18:43547169-43547446	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr18:43490563-43490599	GM12878	blood:	n/a	n/a
25	CBX3	chr18:43547044-43547492	K562	blood:	n/a	n/a
26	CCNT2	chr18:43547035-43547689	K562	blood:	n/a	chr18:43547427-43547436
27	CEBPB	chr18:43531372-43531614	HepG2	liver:	n/a	chr18:43531480-43531491
28	CEBPB	chr18:43531267-43531778	HCT-116	colon:	n/a	chr18:43531480-43531491
29	CEBPB	chr18:43533998-43534718	IMR90	lung:	n/a	n/a
30	CEBPB	chr18:43531378-43531578	H1-hESC	embryonic stem cell:	n/a	chr18:43531480-43531491
31	CEBPB	chr18:43531175-43531743	A549	lung:	n/a	chr18:43531480-43531491
32	CEBPB	chr18:43538024-43538392	K562	blood:	n/a	n/a
33	CEBPB	chr18:43538062-43538370	A549	lung:	n/a	n/a
34	CEBPB	chr18:43547169-43547566	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr18:43538050-43538352	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr18:43531249-43531822	IMR90	lung:	n/a	chr18:43531480-43531491
37	CEBPB	chr18:43528425-43528653	A549	lung:	n/a	n/a
38	CEBPB	chr18:43537265-43537291	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr18:43531345-43531561	ECC-1	luminal epithelium:	n/a	chr18:43531480-43531491
40	CEBPB	chr18:43554187-43554548	HepG2	liver:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
41	CEBPB	chr18:43554127-43554559	A549	lung:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
42	CEBPB	chr18:43554135-43554521	K562	blood:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
43	CEBPB	chr18:43542824-43543191	IMR90	lung:	n/a	n/a
44	CEBPB	chr18:43531320-43531649	Hela-S3	cervix:	n/a	chr18:43531480-43531491
45	CEBPB	chr18:43538031-43538378	HepG2	liver:	n/a	n/a
46	CEBPB	chr18:43554165-43554526	H1-hESC	embryonic stem cell:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
47	CEBPB	chr18:43538041-43538308	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr18:43540192-43540441	IMR90	lung:	n/a	n/a
49	CEBPB	chr18:43554102-43554549	Hela-S3	cervix:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
50	CEBPB	chr18:43531059-43531841	HCT-116	colon:	n/a	chr18:43531480-43531491

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:43548144-43548194	BE2_C	brain:	n/a
2	chr18:43548144-43548194	BE2_C	brain:	n/a
3	chr18:43547806-43547856	ECC-1	luminal epithelium:	n/a
4	chr18:43547351-43547401	NH-A	brain:	n/a
5	chr18:43547356-43547406	HRPEpiC	eye:	n/a
6	chr18:43547530-43547580	HUVEC	blood vessel:	n/a
7	chr18:43498793-43498843	HEEpiC	esophagus:	n/a
8	chr18:43547252-43547302	GM12891	blood:	n/a
9	chr18:43547177-43547227	HCM	heart:	n/a
10	chr18:43547806-43547856	GM12878	blood:	n/a
11	chr18:43547177-43547227	U87	brain:	n/a
12	chr18:43547338-43547388	GM12892	blood:	n/a
13	chr18:43545025-43545075	U87	brain:	n/a
14	chr18:43551416-43551466	HCM	heart:	n/a
15	chr18:43547356-43547406	AG10803	skin:	n/a
16	chr18:43545025-43545075	NB4	blood:	n/a
17	chr18:43547701-43547751	H1-hESC	embryonic stem cell:	embryo
18	chr18:43547806-43547856	AG09319	gingival:	n/a
19	chr18:43545025-43545075	PANC-1	pancreas:	n/a
20	chr18:43547530-43547580	GM12891	blood:	n/a
21	chr18:43547252-43547302	Caco-2	colon:	n/a
22	chr18:43547252-43547302	HCT-116	colon:	n/a
23	chr18:43547177-43547227	RPTEC	kidney:	n/a
24	chr18:43547335-43547385	HCM	heart:	n/a
25	chr18:43547356-43547406	HL-60	blood:	n/a
26	chr18:43545025-43545075	NH-A	brain:	n/a
27	chr18:43547335-43547385	HAEpiC	amniotic membrane:	n/a
28	chr18:43497533-43497583	PFSK-1	brain:	n/a
29	chr18:43548144-43548194	HIPEpiC	eye:	n/a
30	chr18:43547252-43547302	HCPEpiC	choroid plexus:	n/a
31	chr18:43545025-43545075	ovcar-3	ovarian:	n/a
32	chr18:43547338-43547388	HAEpiC	amniotic membrane:	n/a
33	chr18:43547530-43547580	Hepatocyte	liver:	n/a
34	chr18:43547356-43547406	NHDF-neo	bronchial:	n/a
35	chr18:43547177-43547227	HRCEpiC	kidney:	n/a
36	chr18:43551416-43551466	NHBE	bronchial:	n/a
37	chr18:43546845-43546895	HCPEpiC	choroid plexus:	n/a
38	chr18:43547335-43547385	T-47D	breast:	n/a
39	chr18:43545025-43545075	HIPEpiC	eye:	n/a
40	chr18:43547701-43547751	HRPEpiC	eye:	n/a
41	chr18:43547701-43547751	SK-N-MC	brain:	n/a
42	chr18:43498793-43498843	RPTEC	kidney:	n/a
43	chr18:43547701-43547751	SK-N-SH_RA	brain:	n/a
44	chr18:43547701-43547751	Caco-2	colon:	n/a
45	chr18:43548144-43548194	HCT-116	colon:	n/a
46	chr18:43546845-43546895	HL-60	blood:	n/a
47	chr18:43498793-43498843	HL-60	blood:	n/a
48	chr18:43498793-43498843	HRE	kidney:	n/a
49	chr18:43547335-43547385	HRE	kidney:	n/a
50	chr18:43547252-43547302	ProgFib	skin:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:99569233..99570111-chr18:43506262..43506956,2	MCF-7	breast:
2	chr18:43504494..43505026-chr18:43554152..43554693,2	MCF-7	breast:
3	chr18:43485515..43488498-chr18:43492379..43494809,3	K562	blood:
4	chr18:43200584..43201546-chr18:43553704..43554682,3	K562	blood:
5	chr18:43524994..43527473-chr18:43527647..43529739,3	K562	blood:
6	chr18:43244782..43245689-chr18:43490131..43490993,3	K562	blood:
7	chr18:43524994..43527473-chr18:43527647..43529739,3	K562	blood:
8	chr18:43541351..43543380-chr18:43545435..43548099,2	K562	blood:
9	chr18:43521496..43524399-chr18:43525900..43528243,2	MCF-7	breast:
10	chr18:43509938..43512714-chr18:43514882..43516799,2	MCF-7	breast:
11	chr18:43495972..43498114-chr18:43498517..43500327,2	MCF-7	breast:
12	chr18:43245041..43246004-chr18:43489940..43490676,4	MCF-7	breast:
13	chr18:43485515..43488498-chr18:43492379..43494809,3	K562	blood:
14	chr18:43548996..43552453-chr18:43650910..43654147,4	MCF-7	breast:
15	chr18:43509938..43512714-chr18:43514882..43516799,2	MCF-7	breast:
16	chr18:43553826..43554616-chr18:43653485..43654035,3	MCF-7	breast:
17	chr18:43496478..43498103-chr18:43499621..43501282,2	K562	blood:
18	chr18:43498961..43501457-chr18:43650266..43652606,2	MCF-7	breast:
19	chr18:43470261..43474008-chr18:43474596..43477449,3	K562	blood:
20	chr18:43504494..43505026-chr18:43554152..43554693,2	MCF-7	breast:
21	chr18:43521496..43524399-chr18:43525900..43528243,2	MCF-7	breast:
22	chr18:43245206..43245747-chr18:43553737..43554546,2	K562	blood:
23	chr18:43525078..43527473-chr18:43527531..43529739,4	K562	blood:
24	chr18:43545858..43548536-chr18:43676652..43678402,2	MCF-7	breast:
25	chr18:43525078..43527473-chr18:43527531..43529739,4	K562	blood:
26	chr18:43271019..43271564-chr18:43490221..43490788,2	MCF-7	breast:
27	chr18:43553938..43554665-chr18:43653434..43654381,2	MCF-7	breast:

No data

Variant related genes	Relation type
EPG5	TF binding region
EPG5	CpG island
ENSG00000152223	chromatin interactions
ENSG00000152234	chromatin interactions
ENSG00000152229	chromatin interactions

Extended variants
information (count: 3186 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3186 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1440823	chr18:43474795-43474796	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149467278	chr18:43474798-43474799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542368456	chr18:43474816-43474817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561081548	chr18:43474817-43474818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185767417	chr18:43474823-43474824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189643688	chr18:43474848-43474849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1115698	chr18:43474923-43474924	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs533461694	chr18:43474931-43474932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74513262	chr18:43474988-43474989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566725029	chr18:43475032-43475033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143881594	chr18:43475037-43475038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1115699	chr18:43475042-43475043	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138464562	chr18:43475149-43475150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181540883	chr18:43475184-43475185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537826479	chr18:43475231-43475232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34568342	chr18:43475233-43475234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143064238	chr18:43475267-43475268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114519055	chr18:43475271-43475272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186268486	chr18:43475357-43475358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191219500	chr18:43475365-43475366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146109800	chr18:43475366-43475367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140151500	chr18:43475389-43475390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62095408	chr18:43475402-43475403	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs34004717	chr18:43475410-43475411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs397723508	chr18:43475418-43475419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141467793	chr18:43475439-43475440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566452520	chr18:43475444-43475445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538669287	chr18:43475516-43475517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28450604	chr18:43475552-43475553	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs150860079	chr18:43475567-43475568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533399160	chr18:43475601-43475602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551665517	chr18:43475630-43475631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560453412	chr18:43475650-43475651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528528515	chr18:43475656-43475657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79375094	chr18:43475737-43475738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111467546	chr18:43475745-43475746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182117220	chr18:43475749-43475750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139314221	chr18:43475807-43475808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550169143	chr18:43475983-43475984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571680004	chr18:43475986-43475987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149976006	chr18:43476008-43476009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554107424	chr18:43476085-43476086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147668279	chr18:43476102-43476103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs8085679	chr18:43476110-43476111	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs140566315	chr18:43476120-43476121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9957999	chr18:43476121-43476122	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs4890305	chr18:43476143-43476144	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs34891638	chr18:43476184-43476185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564499461	chr18:43476186-43476187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113952951	chr18:43476200-43476201	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2677 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43420200-43491800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr18:43440600-43489600	Weak transcription	Small Intestine	intestine
3	chr18:43442400-43500200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr18:43445600-43478000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr18:43445800-43483800	Weak transcription	K562	blood
6	chr18:43446200-43479400	Weak transcription	Fetal Brain Male	brain
7	chr18:43447000-43478400	Weak transcription	Stomach Mucosa	stomach
8	chr18:43447000-43491800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr18:43450800-43478000	Weak transcription	Right Ventricle	heart
10	chr18:43451800-43519600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr18:43452000-43479000	Weak transcription	HMEC	breast
12	chr18:43455400-43511400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr18:43455600-43476400	Strong transcription	Primary T cells from cord blood	blood
14	chr18:43456400-43490200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr18:43456400-43498000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr18:43456400-43500400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr18:43457200-43479200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr18:43459200-43478400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr18:43459200-43479200	Weak transcription	Psoas Muscle	Psoas
20	chr18:43460600-43476000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr18:43460800-43500200	Strong transcription	Osteobl	bone
22	chr18:43460800-43500400	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr18:43461000-43478000	Weak transcription	Pancreas	Pancrea
24	chr18:43462200-43478000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr18:43462200-43492000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr18:43462400-43477800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr18:43464800-43475200	Weak transcription	Fetal Kidney	kidney
28	chr18:43464800-43477800	Weak transcription	Brain Hippocampus Middle	brain
29	chr18:43464800-43478000	Weak transcription	Brain Anterior Caudate	brain
30	chr18:43464800-43478000	Weak transcription	Esophagus	oesophagus
31	chr18:43464800-43478000	Weak transcription	Gastric	stomach
32	chr18:43464800-43478200	Weak transcription	Ovary	ovary
33	chr18:43464800-43478200	Weak transcription	GM12878-XiMat	blood
34	chr18:43464800-43479800	Weak transcription	Hela-S3	cervix
35	chr18:43465400-43476800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr18:43465800-43475800	Strong transcription	Dnd41	blood
37	chr18:43466200-43475200	Strong transcription	Fetal Thymus	thymus
38	chr18:43466400-43498400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr18:43466800-43476000	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr18:43467000-43474800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr18:43467800-43477800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr18:43467800-43478000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr18:43467800-43478000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr18:43468000-43474800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr18:43468000-43478000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr18:43469200-43478000	Weak transcription	Spleen	Spleen
47	chr18:43469400-43476200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr18:43469400-43478000	Weak transcription	Aorta	Aorta
49	chr18:43469400-43478000	Weak transcription	Lung	lung
50	chr18:43469400-43487600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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