Variant report

Variant	nsv1060592
Chromosome Location	chr18:28965770-29042332
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	chr18:29004374-29004617	K562	blood:	n/a	n/a
2	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
3	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
7	ATF2	chr18:29018291-29018807	GM12878	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	BACH1	chr18:28982605-28982714	K562	blood:	n/a	n/a
11	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
12	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
13	BATF	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
14	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
15	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
16	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
17	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
18	BCLAF1	chr18:29004430-29004706	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:28990641-28990701	K562	blood:	n/a	n/a
20	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
21	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
22	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
23	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:29003291-29003573	HepG2	liver:	n/a	n/a
26	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
27	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
29	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
30	CEBPB	chr18:28966671-28966959	HepG2	liver:	n/a	chr18:28966789-28966800
31	CEBPB	chr18:28966630-28966940	K562	blood:	n/a	chr18:28966789-28966800
32	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
33	CEBPB	chr18:28974947-28975271	K562	blood:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
34	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
35	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
36	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
37	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
38	CEBPB	chr18:28966625-28966965	ECC-1	luminal epithelium:	n/a	chr18:28966789-28966800
39	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
40	CEBPB	chr18:28974940-28975186	A549	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
41	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
42	CEBPB	chr18:29034023-29034597	HCT-116	colon:	n/a	chr18:29034579-29034590
43	CEBPB	chr18:28972607-28972963	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
45	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
46	CEBPB	chr18:28975048-28975251	H1-hESC	embryonic stem cell:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
47	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
48	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
49	CEBPB	chr18:28974953-28975247	IMR90	lung:	n/a	chr18:28975103-28975114 chr18:28975103-28975116
50	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29027658-29027708	K562	blood:	n/a
2	chr18:29027701-29027751	HCT-116	colon:	n/a
3	chr18:29027658-29027708	PANC-1	pancreas:	n/a
4	chr18:29027745-29027795	AG04450	lung:	fetal
5	chr18:29026301-29026351	HEK293	kidney:	embryo
6	chr18:29026303-29026353	SK-N-SH_RA	brain:	n/a
7	chr18:29027885-29027935	GM06990	blood:	n/a
8	chr18:29027658-29027708	AG04449	skin:	fetal
9	chr18:29026303-29026353	HCPEpiC	choroid plexus:	n/a
10	chr18:29027885-29027935	HepG2	liver:	n/a
11	chr18:29027885-29027935	HRCEpiC	kidney:	n/a
12	chr18:29026301-29026351	AG04450	lung:	fetal
13	chr18:29027658-29027708	BJ	skin:	n/a
14	chr18:29027701-29027751	HRCEpiC	kidney:	n/a
15	chr18:29026303-29026353	HCM	heart:	n/a
16	chr18:29027885-29027935	HIPEpiC	eye:	n/a
17	chr18:29026301-29026351	MCF10A-Er-Src	breast:	n/a
18	chr18:29027745-29027795	GM12892	blood:	n/a
19	chr18:29027701-29027751	HPAEpiC	pulmonary alveolar:	n/a
20	chr18:29026301-29026351	SAEC	small airway:	n/a
21	chr18:29027745-29027795	HRCEpiC	kidney:	n/a
22	chr18:29026303-29026353	U87	brain:	n/a
23	chr18:29027701-29027751	HEEpiC	esophagus:	n/a
24	chr18:29027745-29027795	IMR90	lung:	fetal
25	chr18:29026303-29026353	ovcar-3	ovarian:	n/a
26	chr18:29027745-29027795	SAEC	small airway:	n/a
27	chr18:29027745-29027795	AG04449	skin:	fetal
28	chr18:29027658-29027708	HCM	heart:	n/a
29	chr18:29027701-29027751	Hepatocyte	liver:	n/a
30	chr18:29027658-29027708	LNCaP	prostate:	n/a
31	chr18:29027885-29027935	PANC-1	pancreas:	n/a
32	chr18:29027658-29027708	HIPEpiC	eye:	n/a
33	chr18:29026303-29026353	HL-60	blood:	n/a
34	chr18:29027701-29027751	BE2_C	brain:	n/a
35	chr18:29027745-29027795	HRPEpiC	eye:	n/a
36	chr18:29027658-29027708	HL-60	blood:	n/a
37	chr18:29027658-29027708	HUVEC	blood vessel:	n/a
38	chr18:29026303-29026353	AG09309	skin:	n/a
39	chr18:29026303-29026353	HAEpiC	amniotic membrane:	n/a
40	chr18:29026301-29026351	HMEC	breast:	n/a
41	chr18:29027701-29027751	MCF10A-Er-Src	breast:	n/a
42	chr18:29027885-29027935	HRE	kidney:	n/a
43	chr18:29026301-29026351	MCF-7	breast:	n/a
44	chr18:29026301-29026351	SKMC	muscle:	n/a
45	chr18:29027701-29027751	T-47D	breast:	n/a
46	chr18:29027701-29027751	K562	blood:	n/a
47	chr18:29026303-29026353	Hepatocyte	liver:	n/a
48	chr18:29027658-29027708	MCF-7	breast:	n/a
49	chr18:29026301-29026351	HRE	kidney:	n/a
50	chr18:29027745-29027795	HNPCEpiC	eye:	n/a

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

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

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

Extended variants
information (count: 3206 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3206 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536667496	chr18:28965773-28965774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554653031	chr18:28965886-28965887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573507451	chr18:28965900-28965901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534219968	chr18:28965901-28965902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs8086756	chr18:28965921-28965922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184888275	chr18:28965930-28965931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544770288	chr18:28965952-28965953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78001110	chr18:28965987-28965988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574414883	chr18:28965994-28965995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9304094	chr18:28966036-28966037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371270064	chr18:28966047-28966048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559891046	chr18:28966090-28966091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550573444	chr18:28966119-28966120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552063808	chr18:28966142-28966143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188476401	chr18:28966158-28966159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111660519	chr18:28966168-28966169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549532658	chr18:28966182-28966183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113031910	chr18:28966186-28966187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111797626	chr18:28966205-28966206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548608933	chr18:28966211-28966212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs137864509	chr18:28966254-28966255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs60353862	chr18:28966278-28966279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1460596	chr18:28966284-28966285	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs559296103	chr18:28966294-28966295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577583970	chr18:28966296-28966297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111377873	chr18:28966333-28966334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556777566	chr18:28966335-28966336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180790047	chr18:28966337-28966338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541552489	chr18:28966394-28966395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560153887	chr18:28966411-28966412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184163288	chr18:28966413-28966414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143911363	chr18:28966429-28966430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545368001	chr18:28966458-28966459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189924464	chr18:28966467-28966468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181083653	chr18:28966476-28966477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549595681	chr18:28966487-28966488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561727985	chr18:28966493-28966494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1460597	chr18:28966518-28966519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs369211300	chr18:28966608-28966609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372495403	chr18:28966631-28966632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201146453	chr18:28966666-28966667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139940348	chr18:28966679-28966680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370177706	chr18:28966723-28966724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200219673	chr18:28966732-28966733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149672864	chr18:28966738-28966739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527707261	chr18:28966742-28966743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374462685	chr18:28966758-28966759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552571097	chr18:28966805-28966806	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148248471	chr18:28966826-28966827	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538517136	chr18:28966847-28966848	Active TSS 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:357 , 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	chr18:28966800-28967000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:28966800-28967200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr18:28967000-28967200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr18:28967000-28968000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr18:28968000-28968400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr18:28968000-28968400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr18:28968000-28968400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr18:28968000-28968400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr18:28968000-28968400	Enhancers	HepG2	liver
12	chr18:28968000-28968600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr18:28968400-28973400	Weak transcription	HepG2	liver
14	chr18:28972000-28976400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr18:28972400-28972800	Enhancers	Fetal Kidney	kidney
16	chr18:28972800-28976800	Weak transcription	Fetal Kidney	kidney
17	chr18:28973400-28973600	Enhancers	Duodenum Mucosa	Duodenum
18	chr18:28973400-28973600	ZNF genes & repeats	Esophagus	oesophagus
19	chr18:28973400-28973600	Enhancers	Small Intestine	intestine
20	chr18:28973400-28973600	Enhancers	HepG2	liver
21	chr18:28973400-28976600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr18:28973600-28974000	Weak transcription	HepG2	liver
23	chr18:28973600-28975600	Weak transcription	Duodenum Mucosa	Duodenum
24	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
25	chr18:28974000-28974200	Enhancers	HepG2	liver
26	chr18:28974200-28975400	Weak transcription	HepG2	liver
27	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
28	chr18:28975400-28975600	Enhancers	Fetal Intestine Small	intestine
29	chr18:28975400-28977000	Enhancers	HepG2	liver
30	chr18:28975600-28975800	Enhancers	Duodenum Mucosa	Duodenum
31	chr18:28975600-28975800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr18:28975600-28976200	Weak transcription	Fetal Intestine Small	intestine
33	chr18:28975800-28976400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr18:28975800-28976600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr18:28975800-28976600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
37	chr18:28976400-28976600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr18:28976400-28976800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr18:28976400-28977000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr18:28976400-28977800	Enhancers	Left Ventricle	heart
41	chr18:28976600-28976800	Active TSS	Adipose Nuclei	Adipose
42	chr18:28976600-28977000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr18:28976600-28977000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
44	chr18:28976600-28977400	Enhancers	Right Atrium	heart
45	chr18:28976600-28977600	Enhancers	Liver	Liver
46	chr18:28976600-28977600	Enhancers	Duodenum Mucosa	Duodenum
47	chr18:28976600-28977600	Enhancers	Stomach Mucosa	stomach
48	chr18:28976600-28978400	Enhancers	Small Intestine	intestine
49	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr18:28976800-28977000	Flanking Active TSS	Adipose Nuclei	Adipose

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