Variant report

Variant	nsv1062970
Chromosome Location	chr18:28976790-29049614
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	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:28976731-28977863	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29004374-29004617	K562	blood:	n/a	n/a
5	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
7	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
8	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
9	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
10	ATF2	chr18:29018383-29018706	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	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
14	BATF	chr18:28989277-28989486	GM12878	blood:	n/a	n/a
15	BATF	chr18:28987665-28987980	GM12878	blood:	n/a	chr18:28987834-28987845
16	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
17	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
18	BCL3	chr18:29018340-29018768	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	chr18:28990641-28990701	K562	blood:	n/a	n/a
22	BHLHE40	chr18:29003291-29003573	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
25	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
27	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
29	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
30	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
31	CEBPB	chr18:29027821-29028120	IMR90	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
32	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
33	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
34	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
35	CEBPB	chr18:29034023-29034597	HCT-116	colon:	n/a	chr18:29034579-29034590
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	chr18:29027491-29028085	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
38	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
39	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
40	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
41	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
42	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
43	CEBPB	chr18:28979105-28980269	HCT-116	colon:	n/a	n/a
44	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
45	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
46	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
47	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
48	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
49	CHD2	chr18:29018582-29018611	GM12878	blood:	n/a	n/a
50	CHD2	chr18:28977252-28977482	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29027658-29027708	AG09319	gingival:	n/a
2	chr18:29026301-29026351	MCF-7	breast:	n/a
3	chr18:29027658-29027708	Hepatocyte	liver:	n/a
4	chr18:29026303-29026353	HRPEpiC	eye:	n/a
5	chr18:29027701-29027751	HUVEC	blood vessel:	n/a
6	chr18:29027701-29027751	GM12878	blood:	n/a
7	chr18:29027745-29027795	HEEpiC	esophagus:	n/a
8	chr18:29027701-29027751	Hela-S3	cervix:	n/a
9	chr18:29026301-29026351	PrEC	prostate:	n/a
10	chr18:29027745-29027795	RPTEC	kidney:	n/a
11	chr18:29026301-29026351	SKMC	muscle:	n/a
12	chr18:29026303-29026353	HMEC	breast:	n/a
13	chr18:29026303-29026353	GM06990	blood:	n/a
14	chr18:29026303-29026353	SK-N-SH_RA	brain:	n/a
15	chr18:29027745-29027795	AG04449	skin:	fetal
16	chr18:29027701-29027751	A549	lung:	n/a
17	chr18:29027885-29027935	AoSMC	blood vessel:	n/a
18	chr18:29027745-29027795	NHBE	bronchial:	n/a
19	chr18:29027745-29027795	GM12891	blood:	n/a
20	chr18:29026303-29026353	HepG2	liver:	n/a
21	chr18:29027701-29027751	HCPEpiC	choroid plexus:	n/a
22	chr18:29027658-29027708	MCF10A-Er-Src	breast:	n/a
23	chr18:29026301-29026351	HRCEpiC	kidney:	n/a
24	chr18:29027701-29027751	HCF	heart:	n/a
25	chr18:29027745-29027795	U87	brain:	n/a
26	chr18:29027658-29027708	NHDF-neo	bronchial:	n/a
27	chr18:29027701-29027751	AG10803	skin:	n/a
28	chr18:29027658-29027708	LNCaP	prostate:	n/a
29	chr18:29027701-29027751	SK-N-SH_RA	brain:	n/a
30	chr18:29026303-29026353	HCT-116	colon:	n/a
31	chr18:29027745-29027795	Caco-2	colon:	n/a
32	chr18:29027745-29027795	Jurkat	blood:	n/a
33	chr18:29026301-29026351	T-47D	breast:	n/a
34	chr18:29027885-29027935	MCF10A-Er-Src	breast:	n/a
35	chr18:29027701-29027751	HepG2	liver:	n/a
36	chr18:29027701-29027751	LNCaP	prostate:	n/a
37	chr18:29027745-29027795	GM19239	blood:	n/a
38	chr18:29027701-29027751	GM19239	blood:	n/a
39	chr18:29027701-29027751	AG09309	skin:	n/a
40	chr18:29027745-29027795	PANC-1	pancreas:	n/a
41	chr18:29027885-29027935	AG09309	skin:	n/a
42	chr18:29027701-29027751	HRPEpiC	eye:	n/a
43	chr18:29027701-29027751	GM06990	blood:	n/a
44	chr18:29026301-29026351	NB4	blood:	n/a
45	chr18:29026303-29026353	AoSMC	blood vessel:	n/a
46	chr18:29027658-29027708	HRE	kidney:	n/a
47	chr18:29027885-29027935	HCF	heart:	n/a
48	chr18:29027701-29027751	HRE	kidney:	n/a
49	chr18:29026303-29026353	NB4	blood:	n/a
50	chr18:29027885-29027935	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
2	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
3	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
4	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
5	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
6	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
7	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
8	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
9	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
10	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
11	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
12	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
13	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
14	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
15	chr18:29046909..29049478-chr18:29076853..29079838,2	K562	blood:
16	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
17	chr18:28971505..28973722-chr18:28976105..28978957,2	K562	blood:
18	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
19	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
20	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
21	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
22	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
23	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
24	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
25	chr18:29042545..29045965-chr18:29077171..29079744,3	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
ENSG00000266521	chromatin interactions

Extended variants
information (count: 3052 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3052 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565203917	chr18:28976790-28976791	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs532299149	chr18:28976812-28976813	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs542483548	chr18:28976816-28976817	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs77163042	chr18:28976817-28976818	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs10775448	chr18:28976882-28976883	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs190249759	chr18:28976899-28976900	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs549089493	chr18:28976902-28976903	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567390197	chr18:28976906-28976907	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs534732019	chr18:28976939-28976940	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs114687568	chr18:28976943-28976944	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs35170048	chr18:28976996-28976997	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs71383036	chr18:28976998-28976999	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs578229150	chr18:28977067-28977068	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs150363228	chr18:28977082-28977083	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs182522682	chr18:28977089-28977090	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs922184	chr18:28977128-28977129	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186241625	chr18:28977138-28977139	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs543208150	chr18:28977177-28977178	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs191555854	chr18:28977279-28977280	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs560997826	chr18:28977365-28977366	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs34269995	chr18:28977388-28977389	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs184161062	chr18:28977392-28977393	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs540274848	chr18:28977410-28977411	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs138725232	chr18:28977436-28977437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs112422655	chr18:28977451-28977452	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs72929918	chr18:28977482-28977483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs562776855	chr18:28977549-28977550	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs188711940	chr18:28977583-28977584	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs547967931	chr18:28977586-28977587	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs577995080	chr18:28977599-28977600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs539844141	chr18:28977646-28977647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528562400	chr18:28977679-28977680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546631233	chr18:28977704-28977705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146300648	chr18:28977732-28977733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538995410	chr18:28977762-28977763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557384970	chr18:28977774-28977775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569517095	chr18:28977805-28977806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs118025013	chr18:28977858-28977859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555195930	chr18:28977912-28977913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573012888	chr18:28977920-28977921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540337804	chr18:28977929-28977930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs193218140	chr18:28977933-28977934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111361453	chr18:28977934-28977935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142838073	chr18:28977985-28977986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs58782598	chr18:28978011-28978012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58572396	chr18:28978012-28978013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562676777	chr18:28978015-28978016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1299714	chr18:28978086-28978087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529917734	chr18:28978151-28978152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182268864	chr18:28978161-28978162	Weak transcription Enhancers	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:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28972800-28976800	Weak transcription	Fetal Kidney	kidney
2	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
3	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
4	chr18:28975400-28977000	Enhancers	HepG2	liver
5	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
6	chr18:28976400-28976800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr18:28976400-28977000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
8	chr18:28976400-28977800	Enhancers	Left Ventricle	heart
9	chr18:28976600-28976800	Active TSS	Adipose Nuclei	Adipose
10	chr18:28976600-28977000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr18:28976600-28977000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
12	chr18:28976600-28977400	Enhancers	Right Atrium	heart
13	chr18:28976600-28977600	Enhancers	Liver	Liver
14	chr18:28976600-28977600	Enhancers	Duodenum Mucosa	Duodenum
15	chr18:28976600-28977600	Enhancers	Stomach Mucosa	stomach
16	chr18:28976600-28978400	Enhancers	Small Intestine	intestine
17	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr18:28976800-28977000	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr18:28976800-28977000	Enhancers	Colon Smooth Muscle	Colon
20	chr18:28976800-28977400	Enhancers	Fetal Kidney	kidney
21	chr18:28976800-28977400	Enhancers	Gastric	stomach
22	chr18:28976800-28977600	Enhancers	Fetal Stomach	stomach
23	chr18:28976800-28977600	Enhancers	Hela-S3	cervix
24	chr18:28976800-28977800	Enhancers	Fetal Heart	heart
25	chr18:28976800-28977800	Enhancers	Fetal Lung	lung
26	chr18:28976800-28978000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr18:28976800-28980200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr18:28977000-28977200	Active TSS	Adipose Nuclei	Adipose
29	chr18:28977000-28977400	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr18:28977000-28977400	Flanking Active TSS	HepG2	liver
31	chr18:28977000-28979400	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr18:28977200-28977400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr18:28977200-28977600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr18:28977200-28977600	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr18:28977200-28977800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr18:28977200-28977800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr18:28977200-28977800	Enhancers	A549	lung
38	chr18:28977200-28979200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr18:28977400-28979200	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr18:28977400-28980600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr18:28977400-28981200	Enhancers	HepG2	liver
42	chr18:28977400-28981600	Weak transcription	Fetal Kidney	kidney
43	chr18:28977600-28977800	Enhancers	Adipose Nuclei	Adipose
44	chr18:28977600-28978000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr18:28977600-28979200	Weak transcription	Stomach Mucosa	stomach
46	chr18:28977600-28980000	Weak transcription	Liver	Liver
47	chr18:28977600-28980200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr18:28977800-28979200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr18:28977800-28979200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr18:28977800-28979600	Weak transcription	A549	lung

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