Variant report

Variant	nsv1056726
Chromosome Location	chr18:28978180-29049614
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	chr18:29004374-29004617	K562	blood:	n/a	n/a
2	ARID3A	chr18:28979641-28979993	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:28980698-28982615	HepG2	liver:	n/a	chr18:28980825-28980841
5	ARID3A	chr18:29003292-29003573	HepG2	liver:	n/a	n/a
6	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
7	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
8	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
9	ATF2	chr18:28987581-28988048	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	chr18:29018346-29018766	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	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
16	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
17	BCL3	chr18:28987645-28987967	GM12878	blood:	n/a	n/a
18	BCLAF1	chr18:29004430-29004706	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:28981449-28982362	HepG2	liver:	n/a	n/a
20	BHLHE40	chr18:29004365-29004713	GM12878	blood:	n/a	n/a
21	BHLHE40	chr18:29003291-29003573	HepG2	liver:	n/a	n/a
22	BHLHE40	chr18:28979771-28979805	K562	blood:	n/a	n/a
23	BHLHE40	chr18:29004475-29004621	K562	blood:	n/a	n/a
24	BHLHE40	chr18:29004392-29004670	HepG2	liver:	n/a	n/a
25	BHLHE40	chr18:28990641-28990701	K562	blood:	n/a	n/a
26	CBX3	chr18:28979137-28980554	HCT-116	colon:	n/a	n/a
27	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
29	CCNT2	chr18:28999563-28999620	K562	blood:	n/a	n/a
30	CEBPB	chr18:28981969-28982182	A549	lung:	n/a	n/a
31	CEBPB	chr18:28981474-28982350	HepG2	liver:	n/a	n/a
32	CEBPB	chr18:28979724-28979929	HepG2	liver:	n/a	n/a
33	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
34	CEBPB	chr18:28979105-28980269	HCT-116	colon:	n/a	n/a
35	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
36	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
37	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
38	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
39	CEBPB	chr18:28979290-28980148	HCT-116	colon:	n/a	n/a
40	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
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	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
44	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
45	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
46	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
47	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
48	CHD2	chr18:29018582-29018611	GM12878	blood:	n/a	n/a
49	CTCF	chr18:28999492-28999557	NHEK	skin:	n/a	n/a
50	CTCF	chr18:29004404-29004649	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29026303-29026353	ECC-1	luminal epithelium:	n/a
2	chr18:29027701-29027751	SAEC	small airway:	n/a
3	chr18:29026301-29026351	Jurkat	blood:	n/a
4	chr18:29027885-29027935	HRE	kidney:	n/a
5	chr18:29026301-29026351	BJ	skin:	n/a
6	chr18:29027745-29027795	PFSK-1	brain:	n/a
7	chr18:29026303-29026353	NH-A	brain:	n/a
8	chr18:29027745-29027795	HIPEpiC	eye:	n/a
9	chr18:29026303-29026353	LNCaP	prostate:	n/a
10	chr18:29026303-29026353	U87	brain:	n/a
11	chr18:29026303-29026353	HUVEC	blood vessel:	n/a
12	chr18:29026303-29026353	HCF	heart:	n/a
13	chr18:29027658-29027708	Hela-S3	cervix:	n/a
14	chr18:29026303-29026353	T-47D	breast:	n/a
15	chr18:29027701-29027751	Jurkat	blood:	n/a
16	chr18:29027745-29027795	K562	blood:	n/a
17	chr18:29026303-29026353	AG10803	skin:	n/a
18	chr18:29027885-29027935	H1-hESC	embryonic stem cell:	embryo
19	chr18:29026303-29026353	HEEpiC	esophagus:	n/a
20	chr18:29027658-29027708	BE2_C	brain:	n/a
21	chr18:29027745-29027795	PANC-1	pancreas:	n/a
22	chr18:29027885-29027935	GM12892	blood:	n/a
23	chr18:29027658-29027708	NB4	blood:	n/a
24	chr18:29027701-29027751	PFSK-1	brain:	n/a
25	chr18:29027658-29027708	HCM	heart:	n/a
26	chr18:29026301-29026351	SKMC	muscle:	n/a
27	chr18:29027658-29027708	HEK293	kidney:	embryo
28	chr18:29026303-29026353	GM12878	blood:	n/a
29	chr18:29027658-29027708	RPTEC	kidney:	n/a
30	chr18:29026301-29026351	NH-A	brain:	n/a
31	chr18:29027745-29027795	ovcar-3	ovarian:	n/a
32	chr18:29027885-29027935	GM12878	blood:	n/a
33	chr18:29027885-29027935	HEEpiC	esophagus:	n/a
34	chr18:29026303-29026353	SK-N-SH	brain:	n/a
35	chr18:29027701-29027751	MCF10A-Er-Src	breast:	n/a
36	chr18:29027701-29027751	HMEC	breast:	n/a
37	chr18:29027885-29027935	AG04449	skin:	fetal
38	chr18:29026303-29026353	HepG2	liver:	n/a
39	chr18:29026301-29026351	A549	lung:	n/a
40	chr18:29026303-29026353	GM12891	blood:	n/a
41	chr18:29026303-29026353	IMR90	lung:	fetal
42	chr18:29026301-29026351	MCF-7	breast:	n/a
43	chr18:29026303-29026353	H1-hESC	embryonic stem cell:	embryo
44	chr18:29027885-29027935	CMK	blood:	n/a
45	chr18:29026301-29026351	SK-N-MC	brain:	n/a
46	chr18:29026301-29026351	SK-N-SH_RA	brain:	n/a
47	chr18:29027885-29027935	HRCEpiC	kidney:	n/a
48	chr18:29026303-29026353	AG09319	gingival:	n/a
49	chr18:29027745-29027795	SK-N-SH_RA	brain:	n/a
50	chr18:29027701-29027751	IMR90	lung:	fetal

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

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
ENSG00000266729	chromatin interactions
ENSG00000266521	chromatin interactions
ENSG00000046604	chromatin interactions

Extended variants
information (count: 3000 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3000 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546711192	chr18:28978191-28978192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141719365	chr18:28978225-28978226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532434639	chr18:28978245-28978246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78064428	chr18:28978271-28978272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562020474	chr18:28978274-28978275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148763193	chr18:28978279-28978280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555258989	chr18:28978284-28978285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7229349	chr18:28978312-28978313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534364538	chr18:28978320-28978321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558385743	chr18:28978459-28978460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576858133	chr18:28978471-28978472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142459564	chr18:28978545-28978546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17660066	chr18:28978567-28978568	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs372350477	chr18:28978604-28978605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372957230	chr18:28978605-28978606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528499899	chr18:28978620-28978621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369383765	chr18:28978633-28978634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186472877	chr18:28978652-28978653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12956534	chr18:28978691-28978692	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs533401047	chr18:28978692-28978693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199938325	chr18:28978697-28978698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550971924	chr18:28978701-28978702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150893959	chr18:28978705-28978706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571924955	chr18:28978706-28978707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191723970	chr18:28978721-28978722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565261707	chr18:28978731-28978732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183953407	chr18:28978764-28978765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550736517	chr18:28978775-28978776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145544683	chr18:28978790-28978791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189121936	chr18:28978895-28978896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1460594	chr18:28978926-28978927	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534431346	chr18:28979002-28979003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116329753	chr18:28979003-28979004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113890857	chr18:28979004-28979005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115687518	chr18:28979011-28979012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370825015	chr18:28979049-28979050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555945683	chr18:28979056-28979057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7235376	chr18:28979068-28979069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567239911	chr18:28979073-28979074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535047774	chr18:28979077-28979078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553683954	chr18:28979095-28979096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571986162	chr18:28979100-28979101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370600979	chr18:28979121-28979122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111746234	chr18:28979135-28979136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545724872	chr18:28979145-28979146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140183798	chr18:28979171-28979172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368181590	chr18:28979185-28979186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576113919	chr18:28979187-28979188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369018054	chr18:28979246-28979247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs112376128	chr18:28979254-28979255	Weak transcription Enhancers 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:306 , 50 per page) page: 1 2 3 4 5 6 7

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	chr18:28976600-28978400	Enhancers	Small Intestine	intestine
5	chr18:28976600-28979400	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr18:28976800-28980200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr18:28977000-28979400	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr18:28977200-28979200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr18:28977400-28979200	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr18:28977400-28980600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr18:28977400-28981200	Enhancers	HepG2	liver
12	chr18:28977400-28981600	Weak transcription	Fetal Kidney	kidney
13	chr18:28977600-28979200	Weak transcription	Stomach Mucosa	stomach
14	chr18:28977600-28980000	Weak transcription	Liver	Liver
15	chr18:28977600-28980200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr18:28977800-28979200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr18:28977800-28979200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr18:28977800-28979600	Weak transcription	A549	lung
19	chr18:28977800-28981200	Weak transcription	Fetal Lung	lung
20	chr18:28978000-28979200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr18:28978000-28981600	Enhancers	Duodenum Mucosa	Duodenum
22	chr18:28978400-28983200	Weak transcription	Small Intestine	intestine
23	chr18:28979200-28979400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr18:28979200-28979400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr18:28979200-28979400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr18:28979200-28980200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr18:28979200-28980200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr18:28979200-28980200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr18:28979200-28980200	Enhancers	Colon Smooth Muscle	Colon
30	chr18:28979200-28980200	Enhancers	Stomach Mucosa	stomach
31	chr18:28979200-28980600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr18:28979400-28979800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr18:28979400-28980200	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr18:28979400-28980200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr18:28979400-28980400	Enhancers	HMEC	breast
36	chr18:28979600-28979800	Bivalent Enhancer	NH-A	brain
37	chr18:28979600-28980400	Enhancers	Primary hematopoietic stem cells	blood
38	chr18:28979600-28980600	Enhancers	A549	lung
39	chr18:28979800-28980000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr18:28979800-28980600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr18:28979800-28980600	Enhancers	NH-A	brain
42	chr18:28980000-28981400	Enhancers	Liver	Liver
43	chr18:28980200-28980400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr18:28980200-28980400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr18:28980200-28980400	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr18:28980200-28981200	Weak transcription	Colon Smooth Muscle	Colon
47	chr18:28980200-28981200	Weak transcription	Stomach Mucosa	stomach
48	chr18:28980200-28982400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr18:28980400-28981000	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr18:28980400-28981600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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