Variant report

Variant	nsv524890
Chromosome Location	chr18:28967410-29056465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
6	ARID3A	chr18:29004374-29004617	K562	blood:	n/a	n/a
7	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
8	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
9	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
10	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
11	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
12	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
13	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
14	BATF	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
15	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
16	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
17	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
18	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
19	BCLAF1	chr18:29004430-29004706	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
21	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
22	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
23	BHLHE40	chr18:28990641-28990701	K562	blood:	n/a	n/a
24	BHLHE40	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:29003291-29003573	HepG2	liver:	n/a	n/a
27	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
29	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
30	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
31	CEBPB	chr18:28974932-28975260	HepG2	liver:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
32	CEBPB	chr18:29026954-29028137	K562	blood:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027139-29027150 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027139-29027150 chr18:29027957-29027970
33	CEBPB	chr18:29027614-29028137	HepG2	liver:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
34	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
35	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
36	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
37	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
38	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
39	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
40	CEBPB	chr18:28974940-28975186	A549	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
41	CEBPB	chr18:29027824-29028093	A549	lung:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
42	CEBPB	chr18:28974947-28975271	K562	blood:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
43	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
44	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
45	CEBPB	chr18:28972607-28972963	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr18:29027491-29028085	H1-hESC	embryonic stem cell:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
47	CEBPB	chr18:29027850-29028050	Hela-S3	cervix:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
48	CEBPB	chr18:29049774-29049964	HepG2	liver:	n/a	chr18:29049873-29049884
49	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
50	CEBPB	chr18:28974953-28975247	IMR90	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29027885-29027935	HCM	heart:	n/a
2	chr18:29026301-29026351	PrEC	prostate:	n/a
3	chr18:29027745-29027795	NT2-D1	testis:	n/a
4	chr18:29027658-29027708	SK-N-MC	brain:	n/a
5	chr18:29026303-29026353	MCF-7	breast:	n/a
6	chr18:29026301-29026351	K562	blood:	n/a
7	chr18:29026303-29026353	HCM	heart:	n/a
8	chr18:29027745-29027795	HIPEpiC	eye:	n/a
9	chr18:29027745-29027795	AG04450	lung:	fetal
10	chr18:29027658-29027708	HUVEC	blood vessel:	n/a
11	chr18:29027701-29027751	HEEpiC	esophagus:	n/a
12	chr18:29027745-29027795	SKMC	muscle:	n/a
13	chr18:29027745-29027795	GM12891	blood:	n/a
14	chr18:29026303-29026353	SK-N-MC	brain:	n/a
15	chr18:29027658-29027708	GM12878	blood:	n/a
16	chr18:29027885-29027935	AoSMC	blood vessel:	n/a
17	chr18:29027745-29027795	HEEpiC	esophagus:	n/a
18	chr18:29027701-29027751	Jurkat	blood:	n/a
19	chr18:29027885-29027935	Hepatocyte	liver:	n/a
20	chr18:29027658-29027708	ECC-1	luminal epithelium:	n/a
21	chr18:29027885-29027935	AG04450	lung:	fetal
22	chr18:29026301-29026351	BJ	skin:	n/a
23	chr18:29027885-29027935	MCF10A-Er-Src	breast:	n/a
24	chr18:29027745-29027795	HepG2	liver:	n/a
25	chr18:29026301-29026351	U87	brain:	n/a
26	chr18:29027885-29027935	AG09309	skin:	n/a
27	chr18:29027658-29027708	GM12891	blood:	n/a
28	chr18:29027885-29027935	HNPCEpiC	eye:	n/a
29	chr18:29027885-29027935	HEEpiC	esophagus:	n/a
30	chr18:29027701-29027751	GM12892	blood:	n/a
31	chr18:29026301-29026351	AG04450	lung:	fetal
32	chr18:29027885-29027935	HUVEC	blood vessel:	n/a
33	chr18:29027658-29027708	A549	lung:	n/a
34	chr18:29027658-29027708	SAEC	small airway:	n/a
35	chr18:29027745-29027795	HRCEpiC	kidney:	n/a
36	chr18:29026301-29026351	ProgFib	skin:	n/a
37	chr18:29027701-29027751	HPAEpiC	pulmonary alveolar:	n/a
38	chr18:29026301-29026351	HEEpiC	esophagus:	n/a
39	chr18:29027745-29027795	H1-hESC	embryonic stem cell:	embryo
40	chr18:29027745-29027795	NH-A	brain:	n/a
41	chr18:29027658-29027708	GM19239	blood:	n/a
42	chr18:29026303-29026353	GM19239	blood:	n/a
43	chr18:29026303-29026353	AG09319	gingival:	n/a
44	chr18:29027701-29027751	HCT-116	colon:	n/a
45	chr18:29027658-29027708	IMR90	lung:	fetal
46	chr18:29026301-29026351	ovcar-3	ovarian:	n/a
47	chr18:29027885-29027935	GM06990	blood:	n/a
48	chr18:29027885-29027935	PANC-1	pancreas:	n/a
49	chr18:29027701-29027751	H1-hESC	embryonic stem cell:	embryo
50	chr18:29027701-29027751	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
2	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
3	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
4	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
5	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
6	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
7	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
8	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
9	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
10	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
11	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
12	chr18:29056016..29057570-chr18:29059465..29061281,2	K562	blood:
13	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
14	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
15	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
16	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
17	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
18	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
19	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
20	chr18:29046909..29049478-chr18:29076853..29079838,2	K562	blood:
21	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
22	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
23	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
24	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
25	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
26	chr18:29042545..29045965-chr18:29077171..29079744,3	K562	blood:
27	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSC1-1	chr18:29006796-29006951	ENSG00000266729.1
2	lnc-DSC1-1	chr18:29006796-29006890	ENSG00000266729.1

Variant related genes	Relation type
ENSG00000266729	TF binding region
DSG3	TF binding region
ENSG00000266729	CpG island
DSG3	CpG island
ENSG00000266729	chromatin interactions
ENSG00000046604	chromatin interactions
ENSG00000266521	chromatin interactions

Extended variants
information (count: 3748 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3748 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8092320	chr18:28967410-28967411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369432897	chr18:28967473-28967474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147462089	chr18:28967483-28967484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566074327	chr18:28967484-28967485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572998182	chr18:28967515-28967516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370669997	chr18:28967542-28967543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139240450	chr18:28967611-28967612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150010533	chr18:28967613-28967614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575639904	chr18:28967677-28967678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549563339	chr18:28967679-28967680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144050233	chr18:28967684-28967685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538505057	chr18:28967713-28967714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145226441	chr18:28967729-28967730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573844447	chr18:28967772-28967773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540902984	chr18:28967776-28967777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376504822	chr18:28967780-28967781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527832040	chr18:28967793-28967794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9951411	chr18:28967794-28967795	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564527020	chr18:28967821-28967822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142418042	chr18:28967905-28967906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531761204	chr18:28967929-28967930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550115420	chr18:28967967-28967968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574375852	chr18:28967971-28967972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529571800	chr18:28967979-28967980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146841822	chr18:28968000-28968001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190461452	chr18:28968028-28968029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140725468	chr18:28968083-28968084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145872108	chr18:28968090-28968091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74615251	chr18:28968106-28968107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569380892	chr18:28968119-28968120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536662472	chr18:28968120-28968121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555326265	chr18:28968133-28968134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573878756	chr18:28968158-28968159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140661448	chr18:28968166-28968167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73410275	chr18:28968196-28968197	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs577916884	chr18:28968199-28968200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545196049	chr18:28968212-28968213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150084716	chr18:28968232-28968233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182027794	chr18:28968240-28968241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543482376	chr18:28968291-28968292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201790595	chr18:28968297-28968298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201692493	chr18:28968301-28968302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368838232	chr18:28968307-28968308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111309674	chr18:28968316-28968317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145443659	chr18:28968334-28968335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200935383	chr18:28968344-28968345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs36040686	chr18:28968349-28968350	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548077429	chr18:28968357-28968358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145324949	chr18:28968359-28968360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146500402	chr18:28968361-28968362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28960600-28973400	Weak transcription	Esophagus	oesophagus
2	chr18:28966200-28968200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr18:28967000-28968000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:28968000-28968400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr18:28968000-28968400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr18:28968000-28968400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr18:28968000-28968400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr18:28968000-28968400	Enhancers	HepG2	liver
9	chr18:28968000-28968600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr18:28968400-28973400	Weak transcription	HepG2	liver
11	chr18:28972000-28976400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr18:28972400-28972800	Enhancers	Fetal Kidney	kidney
13	chr18:28972800-28976800	Weak transcription	Fetal Kidney	kidney
14	chr18:28973400-28973600	Enhancers	Duodenum Mucosa	Duodenum
15	chr18:28973400-28973600	ZNF genes & repeats	Esophagus	oesophagus
16	chr18:28973400-28973600	Enhancers	Small Intestine	intestine
17	chr18:28973400-28973600	Enhancers	HepG2	liver
18	chr18:28973400-28976600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr18:28973600-28974000	Weak transcription	HepG2	liver
20	chr18:28973600-28975600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
22	chr18:28974000-28974200	Enhancers	HepG2	liver
23	chr18:28974200-28975400	Weak transcription	HepG2	liver
24	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
25	chr18:28975400-28975600	Enhancers	Fetal Intestine Small	intestine
26	chr18:28975400-28977000	Enhancers	HepG2	liver
27	chr18:28975600-28975800	Enhancers	Duodenum Mucosa	Duodenum
28	chr18:28975600-28975800	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr18:28975600-28976200	Weak transcription	Fetal Intestine Small	intestine
30	chr18:28975800-28976400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr18:28975800-28976600	Weak transcription	Duodenum Mucosa	Duodenum
32	chr18:28975800-28976600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
34	chr18:28976400-28976600	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr18:28976400-28976800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr18:28976400-28977000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr18:28976400-28977800	Enhancers	Left Ventricle	heart
38	chr18:28976600-28976800	Active TSS	Adipose Nuclei	Adipose
39	chr18:28976600-28977000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr18:28976600-28977000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr18:28976600-28977400	Enhancers	Right Atrium	heart
42	chr18:28976600-28977600	Enhancers	Liver	Liver
43	chr18:28976600-28977600	Enhancers	Duodenum Mucosa	Duodenum
44	chr18:28976600-28977600	Enhancers	Stomach Mucosa	stomach
45	chr18:28976600-28978400	Enhancers	Small Intestine	intestine
46	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr18:28976800-28977000	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr18:28976800-28977000	Enhancers	Colon Smooth Muscle	Colon
49	chr18:28976800-28977400	Enhancers	Fetal Kidney	kidney
50	chr18:28976800-28977400	Enhancers	Gastric	stomach

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