Variant report

Variant	nsv1061071
Chromosome Location	chr18:28979237-29048429
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	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
4	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29004374-29004617	K562	blood:	n/a	n/a
6	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
7	ATF2	chr18:28987581-28988048	GM12878	blood:	n/a	n/a
8	ATF2	chr18:29018291-29018807	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	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
14	BATF	chr18:29018420-29018737	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	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
21	BHLHE40	chr18:29004475-29004621	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	chr18:28990641-28990701	K562	blood:	n/a	n/a
25	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
26	CBX3	chr18:28979137-28980554	HCT-116	colon:	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	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
30	CEBPB	chr18:29034023-29034597	HCT-116	colon:	n/a	chr18:29034579-29034590
31	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
32	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
33	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
34	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
35	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
36	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
37	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
38	CEBPB	chr18:28981474-28982350	HepG2	liver:	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	chr18:28979105-28980269	HCT-116	colon:	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	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
43	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
44	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
45	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
46	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
47	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
48	CHD2	chr18:29018582-29018611	GM12878	blood:	n/a	n/a
49	CTCF	chr18:29016957-29017069	GM12878	blood:	n/a	n/a
50	CTCF	chr18:29004388-29004689	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29026301-29026351	NB4	blood:	n/a
2	chr18:29027885-29027935	AoSMC	blood vessel:	n/a
3	chr18:29026303-29026353	AoSMC	blood vessel:	n/a
4	chr18:29027658-29027708	HNPCEpiC	eye:	n/a
5	chr18:29027745-29027795	GM12878	blood:	n/a
6	chr18:29026303-29026353	GM12878	blood:	n/a
7	chr18:29027701-29027751	MCF10A-Er-Src	breast:	n/a
8	chr18:29027885-29027935	PrEC	prostate:	n/a
9	chr18:29027885-29027935	MCF-7	breast:	n/a
10	chr18:29027658-29027708	AG04450	lung:	fetal
11	chr18:29026301-29026351	GM06990	blood:	n/a
12	chr18:29027745-29027795	HL-60	blood:	n/a
13	chr18:29027885-29027935	HNPCEpiC	eye:	n/a
14	chr18:29026301-29026351	NHBE	bronchial:	n/a
15	chr18:29027745-29027795	SKMC	muscle:	n/a
16	chr18:29027658-29027708	HAEpiC	amniotic membrane:	n/a
17	chr18:29027658-29027708	K562	blood:	n/a
18	chr18:29026301-29026351	HCF	heart:	n/a
19	chr18:29027745-29027795	K562	blood:	n/a
20	chr18:29026301-29026351	CMK	blood:	n/a
21	chr18:29026303-29026353	T-47D	breast:	n/a
22	chr18:29027701-29027751	SAEC	small airway:	n/a
23	chr18:29027745-29027795	SK-N-SH	brain:	n/a
24	chr18:29026303-29026353	Hela-S3	cervix:	n/a
25	chr18:29027701-29027751	GM12891	blood:	n/a
26	chr18:29026303-29026353	HCM	heart:	n/a
27	chr18:29027658-29027708	Jurkat	blood:	n/a
28	chr18:29026301-29026351	HIPEpiC	eye:	n/a
29	chr18:29027701-29027751	HNPCEpiC	eye:	n/a
30	chr18:29027885-29027935	AG04450	lung:	fetal
31	chr18:29027701-29027751	MCF-7	breast:	n/a
32	chr18:29027658-29027708	A549	lung:	n/a
33	chr18:29027745-29027795	Hepatocyte	liver:	n/a
34	chr18:29027701-29027751	ProgFib	skin:	n/a
35	chr18:29027701-29027751	Caco-2	colon:	n/a
36	chr18:29027745-29027795	NHBE	bronchial:	n/a
37	chr18:29027885-29027935	PANC-1	pancreas:	n/a
38	chr18:29027701-29027751	H1-hESC	embryonic stem cell:	embryo
39	chr18:29027701-29027751	HRPEpiC	eye:	n/a
40	chr18:29027885-29027935	Hepatocyte	liver:	n/a
41	chr18:29026301-29026351	HRCEpiC	kidney:	n/a
42	chr18:29026303-29026353	PANC-1	pancreas:	n/a
43	chr18:29027745-29027795	AG09309	skin:	n/a
44	chr18:29027658-29027708	U87	brain:	n/a
45	chr18:29027701-29027751	T-47D	breast:	n/a
46	chr18:29026303-29026353	HUVEC	blood vessel:	n/a
47	chr18:29027658-29027708	GM06990	blood:	n/a
48	chr18:29027658-29027708	HCF	heart:	n/a
49	chr18:29027658-29027708	ovcar-3	ovarian:	n/a
50	chr18:29027745-29027795	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
2	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
3	chr18:29042545..29045965-chr18:29077171..29079744,3	K562	blood:
4	chr18:28980664..28983039-chr18:28984918..28986737,2	MCF-7	breast:
5	chr18:29001628..29005715-chr18:29006148..29009419,4	K562	blood:
6	chr18:29002388..29006763-chr18:29077410..29081754,4	K562	blood:
7	chr18:29003549..29006106-chr18:29084281..29086820,2	MCF-7	breast:
8	chr18:29046909..29049478-chr18:29076853..29079838,2	K562	blood:
9	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
10	chr18:29004062..29004974-chr18:29135505..29136292,3	MCF-7	breast:
11	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
12	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
13	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
14	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
15	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
16	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
17	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
18	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
19	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
20	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
21	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
22	chr18:28821484..28823254-chr18:29002472..29004133,2	K562	blood:
23	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
24	chr18:29004154..29005000-chr18:29143490..29144004,2	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
DSG3	TF binding region
ENSG00000266729	TF binding region
DSG3	CpG island
ENSG00000266729	CpG island
ENSG00000266729	chromatin interactions
ENSG00000266521	chromatin interactions
ENSG00000046604	chromatin interactions

Extended variants
information (count: 2908 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2908 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369018054	chr18:28979246-28979247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs112376128	chr18:28979254-28979255	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs148911860	chr18:28979257-28979258	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs200590887	chr18:28979309-28979310	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs372942507	chr18:28979310-28979311	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs192864615	chr18:28979318-28979319	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs530136665	chr18:28979330-28979331	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs76349777	chr18:28979331-28979332	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201719326	chr18:28979347-28979348	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs202014315	chr18:28979354-28979355	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs143590546	chr18:28979357-28979358	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs145078681	chr18:28979366-28979367	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs373813561	chr18:28979378-28979379	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs527985044	chr18:28979390-28979391	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs552538448	chr18:28979391-28979392	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200596561	chr18:28979398-28979399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs199759391	chr18:28979408-28979409	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190458670	chr18:28979409-28979410	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs369125321	chr18:28979412-28979413	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs35378785	chr18:28979427-28979428	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs201015162	chr18:28979428-28979429	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs199903416	chr18:28979437-28979438	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs376174057	chr18:28979439-28979440	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs371158987	chr18:28979446-28979447	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs373405894	chr18:28979470-28979471	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147025179	chr18:28979493-28979494	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs377436125	chr18:28979528-28979529	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182199389	chr18:28979532-28979533	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs142081049	chr18:28979558-28979559	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558207248	chr18:28979567-28979568	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs113083176	chr18:28979585-28979586	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs78725993	chr18:28979591-28979592	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185343873	chr18:28979643-28979644	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs576535863	chr18:28979724-28979725	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs376952808	chr18:28979771-28979772	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs576204700	chr18:28979814-28979815	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs543220971	chr18:28979815-28979816	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs149684660	chr18:28979828-28979829	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556732283	chr18:28979830-28979831	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs574967200	chr18:28979836-28979837	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs188240079	chr18:28979839-28979840	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs6506920	chr18:28979847-28979848	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs181420765	chr18:28979884-28979885	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs541615737	chr18:28979907-28979908	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546479729	chr18:28979923-28979924	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs564596356	chr18:28980046-28980047	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs113871540	chr18:28980102-28980103	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs559481963	chr18:28980137-28980138	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs185617602	chr18:28980147-28980148	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549939854	chr18:28980198-28980199	Weak transcription Enhancers Active TSS Flanking Active TSS	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:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28973600-28989400	Weak transcription	Esophagus	oesophagus
2	chr18:28975000-28983400	Enhancers	Fetal Intestine Large	intestine
3	chr18:28976200-28983600	Enhancers	Fetal Intestine Small	intestine
4	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr18:28976800-28980200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr18:28977000-28979400	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr18:28977400-28980600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr18:28977400-28981200	Enhancers	HepG2	liver
9	chr18:28977400-28981600	Weak transcription	Fetal Kidney	kidney
10	chr18:28977600-28980000	Weak transcription	Liver	Liver
11	chr18:28977600-28980200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr18:28977800-28979600	Weak transcription	A549	lung
13	chr18:28977800-28981200	Weak transcription	Fetal Lung	lung
14	chr18:28978000-28981600	Enhancers	Duodenum Mucosa	Duodenum
15	chr18:28978400-28983200	Weak transcription	Small Intestine	intestine
16	chr18:28979200-28979400	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr18:28979200-28979400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr18:28979200-28979400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr18:28979200-28980200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr18:28979200-28980200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr18:28979200-28980200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr18:28979200-28980200	Enhancers	Colon Smooth Muscle	Colon
23	chr18:28979200-28980200	Enhancers	Stomach Mucosa	stomach
24	chr18:28979200-28980600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr18:28979400-28979800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr18:28979400-28980200	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr18:28979400-28980200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
28	chr18:28979400-28980400	Enhancers	HMEC	breast
29	chr18:28979600-28979800	Bivalent Enhancer	NH-A	brain
30	chr18:28979600-28980400	Enhancers	Primary hematopoietic stem cells	blood
31	chr18:28979600-28980600	Enhancers	A549	lung
32	chr18:28979800-28980000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr18:28979800-28980600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr18:28979800-28980600	Enhancers	NH-A	brain
35	chr18:28980000-28981400	Enhancers	Liver	Liver
36	chr18:28980200-28980400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr18:28980200-28980400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr18:28980200-28980400	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr18:28980200-28981200	Weak transcription	Colon Smooth Muscle	Colon
40	chr18:28980200-28981200	Weak transcription	Stomach Mucosa	stomach
41	chr18:28980200-28982400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr18:28980400-28981000	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr18:28980400-28981600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr18:28980600-28981000	Weak transcription	A549	lung
45	chr18:28980800-28981200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr18:28981000-28981200	Enhancers	A549	lung
47	chr18:28981000-28982600	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr18:28981200-28981400	Enhancers	Colon Smooth Muscle	Colon
49	chr18:28981200-28981600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr18:28981200-28981600	Flanking Active TSS	HepG2	liver

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