Variant report

Variant	nsv1056985
Chromosome Location	chr18:30486272-30540347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:30510663-30511023	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:30501452-30501739	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:30499794-30500195	HepG2	liver:	n/a	n/a
4	ATF1	chr18:30510749-30510935	K562	blood:	n/a	n/a
5	ATF2	chr18:30502920-30503305	GM12878	blood:	n/a	n/a
6	BACH1	chr18:30516693-30517043	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr18:30510763-30510997	GM12878	blood:	n/a	n/a
8	BHLHE40	chr18:30503054-30503254	GM12878	blood:	n/a	n/a
9	CCNT2	chr18:30486329-30486420	K562	blood:	n/a	n/a
10	CEBPB	chr18:30500757-30501119	HepG2	liver:	n/a	chr18:30500944-30500955
11	CEBPB	chr18:30526711-30526869	HepG2	liver:	n/a	n/a
12	CEBPB	chr18:30500836-30501105	A549	lung:	n/a	chr18:30500944-30500955
13	CEBPB	chr18:30510693-30510988	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr18:30499850-30500111	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr18:30518996-30519140	HepG2	liver:	n/a	n/a
16	CEBPB	chr18:30501563-30501737	HepG2	liver:	n/a	chr18:30501659-30501670
17	CEBPB	chr18:30516859-30517065	H1-hESC	embryonic stem cell:	n/a	chr18:30516952-30516965
18	CEBPB	chr18:30501453-30501831	IMR90	lung:	n/a	chr18:30501659-30501670
19	CEBPB	chr18:30501420-30502206	Hela-S3	cervix:	n/a	chr18:30501659-30501670
20	CEBPB	chr18:30500870-30501015	HepG2	liver:	n/a	chr18:30500944-30500955
21	CEBPB	chr18:30526622-30526902	HepG2	liver:	n/a	n/a
22	CEBPB	chr18:30499791-30500141	HepG2	liver:	n/a	n/a
23	CEBPB	chr18:30501423-30501831	ECC-1	luminal epithelium:	n/a	chr18:30501659-30501670
24	CEBPB	chr18:30490199-30490413	HepG2	liver:	n/a	chr18:30490237-30490245
25	CEBPB	chr18:30501501-30501761	A549	lung:	n/a	chr18:30501659-30501670
26	CEBPB	chr18:30526628-30526917	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr18:30501473-30501857	ECC-1	luminal epithelium:	n/a	chr18:30501659-30501670
28	CEBPB	chr18:30501471-30501840	HepG2	liver:	n/a	chr18:30501659-30501670
29	CEBPB	chr18:30490164-30490541	HepG2	liver:	n/a	chr18:30490237-30490245
30	CEBPB	chr18:30501416-30501805	HCT-116	colon:	n/a	chr18:30501659-30501670
31	CEBPB	chr18:30510683-30510966	HepG2	liver:	n/a	n/a
32	CTCF	chr18:30536640-30536790	AG04450	lung:	n/a	n/a
33	CTCF	chr18:30510745-30510995	Medullo	brain:	n/a	n/a
34	CTCF	chr18:30499880-30500030	GM12870	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
35	CTCF	chr18:30510780-30510930	GM12872	blood:	n/a	n/a
36	CTCF	chr18:30499548-30500222	HepG2	liver:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
37	CTCF	chr18:30499849-30500111	NHEK	skin:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
38	CTCF	chr18:30536680-30536830	HMEC	breast:	n/a	n/a
39	CTCF	chr18:30536580-30536730	RPTEC	kidney:	n/a	n/a
40	CTCF	chr18:30499857-30500082	HUVEC	blood vessel:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
41	CTCF	chr18:30499920-30500070	HRE	kidney:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
42	CTCF	chr18:30510780-30510930	HVMF	connective:	n/a	n/a
43	CTCF	chr18:30499650-30500192	A549	lung:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
44	CTCF	chr18:30499880-30500030	HRE	kidney:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
45	CTCF	chr18:30510783-30510953	GM20000	blood:	n/a	n/a
46	CTCF	chr18:30510780-30510930	AG04450	lung:	n/a	n/a
47	CTCF	chr18:30499900-30500050	HepG2	liver:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
48	CTCF	chr18:30510780-30510930	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr18:30499860-30500010	HCM	heart:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
50	CTCF	chr18:30510780-30510930	GM12873	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:30517666-30517716	HUVEC	blood vessel:	n/a
2	chr18:30517666-30517716	AoSMC	blood vessel:	n/a
3	chr18:30517666-30517716	CMK	blood:	n/a
4	chr18:30517666-30517716	HPAEpiC	pulmonary alveolar:	n/a
5	chr18:30517666-30517716	GM06990	blood:	n/a
6	chr18:30517666-30517716	HepG2	liver:	n/a
7	chr18:30517666-30517716	Hela-S3	cervix:	n/a
8	chr18:30517666-30517716	AG09319	gingival:	n/a
9	chr18:30517666-30517716	HMEC	breast:	n/a
10	chr18:30517666-30517716	HCT-116	colon:	n/a
11	chr18:30517666-30517716	MCF10A-Er-Src	breast:	n/a
12	chr18:30517666-30517716	GM12892	blood:	n/a
13	chr18:30517666-30517716	GM12878	blood:	n/a
14	chr18:30517666-30517716	NHDF-neo	bronchial:	n/a
15	chr18:30517666-30517716	ECC-1	luminal epithelium:	n/a
16	chr18:30517666-30517716	SK-N-SH	brain:	n/a
17	chr18:30517666-30517716	GM19239	blood:	n/a
18	chr18:30517666-30517716	PrEC	prostate:	n/a
19	chr18:30517666-30517716	Caco-2	colon:	n/a
20	chr18:30517666-30517716	AG10803	skin:	n/a
21	chr18:30517666-30517716	Jurkat	blood:	n/a
22	chr18:30517666-30517716	HRPEpiC	eye:	n/a
23	chr18:30517666-30517716	HCPEpiC	choroid plexus:	n/a
24	chr18:30517666-30517716	K562	blood:	n/a
25	chr18:30517666-30517716	NT2-D1	testis:	n/a
26	chr18:30517666-30517716	MCF-7	breast:	n/a
27	chr18:30517666-30517716	AG04449	skin:	fetal
28	chr18:30517666-30517716	AG09309	skin:	n/a
29	chr18:30517666-30517716	NB4	blood:	n/a
30	chr18:30517666-30517716	GM12891	blood:	n/a
31	chr18:30517666-30517716	HCM	heart:	n/a
32	chr18:30517666-30517716	HAEpiC	amniotic membrane:	n/a
33	chr18:30517666-30517716	HEK293	kidney:	embryo
34	chr18:30517666-30517716	ovcar-3	ovarian:	n/a
35	chr18:30517666-30517716	AG04450	lung:	fetal
36	chr18:30517666-30517716	HEEpiC	esophagus:	n/a
37	chr18:30517666-30517716	H1-hESC	embryonic stem cell:	embryo
38	chr18:30517666-30517716	HRCEpiC	kidney:	n/a
39	chr18:30517666-30517716	SAEC	small airway:	n/a
40	chr18:30517666-30517716	NH-A	brain:	n/a
41	chr18:30517666-30517716	SKMC	muscle:	n/a
42	chr18:30517666-30517716	IMR90	lung:	fetal
43	chr18:30517666-30517716	PANC-1	pancreas:	n/a
44	chr18:30517666-30517716	HIPEpiC	eye:	n/a
45	chr18:30517666-30517716	BE2_C	brain:	n/a
46	chr18:30517666-30517716	BJ	skin:	n/a
47	chr18:30517666-30517716	HL-60	blood:	n/a
48	chr18:30517666-30517716	RPTEC	kidney:	n/a
49	chr18:30517666-30517716	HNPCEpiC	eye:	n/a
50	chr18:30517666-30517716	SK-N-MC	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:30492146..30494495-chr18:30497517..30499760,2	K562	blood:
2	chr18:30294450..30295198-chr18:30499539..30500758,7	MCF-7	breast:
3	chr18:30479533..30480412-chr18:30499540..30500172,2	MCF-7	breast:
4	chr18:30492890..30494424-chr18:30498589..30500639,2	MCF-7	breast:
5	chr18:30517553..30519382-chr18:30521482..30523955,2	MCF-7	breast:
6	chr18:30293724..30294417-chr18:30499835..30500382,2	MCF-7	breast:
7	chr18:30294270..30295293-chr18:30499582..30500548,5	MCF-7	breast:
8	chr18:30492890..30494424-chr18:30498589..30500639,2	MCF-7	breast:
9	chr18:30487680..30490056-chr18:30492113..30494145,2	K562	blood:
10	chr18:30487680..30490056-chr18:30492113..30494145,2	K562	blood:
11	chr18:30505715..30508318-chr18:30511122..30512749,2	MCF-7	breast:
12	chr18:30479602..30480672-chr18:30499517..30500435,5	MCF-7	breast:
13	chr18:30517553..30519382-chr18:30521482..30523955,2	MCF-7	breast:
14	chr18:30505715..30508318-chr18:30511122..30512749,2	MCF-7	breast:
15	chr18:30155970..30156491-chr18:30499440..30500054,2	MCF-7	breast:
16	chr18:30492146..30494495-chr18:30497517..30499760,2	K562	blood:
17	chr18:30482192..30483831-chr18:30485480..30487269,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC012123.1.1-2	chr18:30537736-30537962	ENSG00000263450.1
2	lnc-AC012123.1.1-2	chr18:30534039-30534050	ENSG00000263450.1
3	lnc-AC012123.1.1-1	chr18:30517950-30518280	ENSG00000263765.1
4	lnc-AC012123.1.1-1	chr18:30492858-30492929	NONHSAT058876
5	lnc-AC012123.1.1-2	chr18:30536598-30536774	ENSG00000263450.1
6	lnc-AC012123.1.1-1	chr18:30492797-30492928	ENSG00000263765.1
7	lnc-AC012123.1.1-1	chr18:30492797-30492821	NONHSAT058872
8	lnc-AC012123.1.1-2	chr18:30534470-30534611	ENSG00000263450.1

No data

Variant related genes	Relation type
ENSG00000263450	TF binding region
ENSG00000263450	CpG island

Extended variants
information (count: 1233 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539726439	chr18:30486272-30486273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557954455	chr18:30486353-30486354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112191542	chr18:30486355-30486356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374766180	chr18:30486362-30486363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115444745	chr18:30486380-30486381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184689318	chr18:30486381-30486382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573953907	chr18:30486382-30486383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541407957	chr18:30486415-30486416	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs562811780	chr18:30486474-30486475	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs187007295	chr18:30486492-30486493	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs578025769	chr18:30486552-30486553	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs545302353	chr18:30486585-30486586	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs34031354	chr18:30486596-30486597	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs369021835	chr18:30486607-30486608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370612745	chr18:30486610-30486611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79829186	chr18:30486614-30486615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538253019	chr18:30486629-30486630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78577566	chr18:30486663-30486664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146432344	chr18:30486674-30486675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75186797	chr18:30486709-30486710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528099852	chr18:30486712-30486713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546222569	chr18:30486768-30486769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373482277	chr18:30486802-30486803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11081789	chr18:30486809-30486810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs191788973	chr18:30486821-30486822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144082770	chr18:30486851-30486852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184171054	chr18:30486853-30486854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116421446	chr18:30486879-30486880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537678851	chr18:30486900-30486901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537604273	chr18:30486907-30486908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189397916	chr18:30486919-30486920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574146386	chr18:30486979-30486980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535107873	chr18:30486985-30486986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568829184	chr18:30486989-30486990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553432471	chr18:30486996-30486997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs180984398	chr18:30487005-30487006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545362256	chr18:30487009-30487010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563561328	chr18:30487024-30487025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28691632	chr18:30487059-30487060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28398144	chr18:30487061-30487062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369700870	chr18:30487077-30487078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572987773	chr18:30487079-30487080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560837698	chr18:30487095-30487096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528197903	chr18:30487097-30487098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546283922	chr18:30487112-30487113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368774774	chr18:30487138-30487139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185676743	chr18:30487142-30487143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553236395	chr18:30487169-30487170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533851639	chr18:30487193-30487194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190558014	chr18:30487224-30487225	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30483200-30486600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr18:30485400-30487600	Enhancers	Fetal Brain Male	brain
3	chr18:30485600-30489200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr18:30485800-30486800	Weak transcription	Ovary	ovary
5	chr18:30485800-30489800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr18:30486000-30486800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr18:30486000-30487000	Enhancers	HMEC	breast
8	chr18:30486200-30487200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr18:30486400-30486600	Bivalent Enhancer	HepG2	liver
10	chr18:30486600-30487000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr18:30486600-30487000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr18:30486600-30487000	Enhancers	Adipose Nuclei	Adipose
13	chr18:30486600-30488000	Enhancers	Primary B cells from peripheral blood	blood
14	chr18:30486800-30487000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr18:30486800-30487000	Enhancers	Ovary	ovary
16	chr18:30486800-30487400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr18:30487000-30487600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr18:30487000-30487800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr18:30487000-30490400	Weak transcription	HMEC	breast
20	chr18:30487200-30487600	Enhancers	Brain Hippocampus Middle	brain
21	chr18:30487200-30490400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr18:30487400-30487600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr18:30487400-30487600	Enhancers	Primary B cells from cord blood	blood
24	chr18:30487400-30487800	Enhancers	HepG2	liver
25	chr18:30487400-30488000	Enhancers	Brain Cingulate Gyrus	brain
26	chr18:30487400-30489800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr18:30487600-30487800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr18:30487600-30487800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr18:30487600-30488000	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr18:30487600-30488400	Weak transcription	Primary B cells from cord blood	blood
31	chr18:30487800-30489800	Weak transcription	HepG2	liver
32	chr18:30487800-30490800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr18:30487800-30490800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr18:30488000-30488400	Weak transcription	Primary B cells from peripheral blood	blood
35	chr18:30488400-30488600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr18:30488400-30491200	Enhancers	Primary B cells from peripheral blood	blood
37	chr18:30488400-30492200	Enhancers	Primary B cells from cord blood	blood
38	chr18:30489200-30489600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr18:30489400-30491800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr18:30489600-30491000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr18:30489800-30490000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr18:30489800-30490600	Enhancers	NH-A	brain
43	chr18:30489800-30490800	Enhancers	HepG2	liver
44	chr18:30489800-30491000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr18:30490000-30490400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr18:30490200-30491000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr18:30490200-30491200	Enhancers	Fetal Muscle Leg	muscle
48	chr18:30490200-30492200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr18:30490400-30491200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr18:30490400-30491600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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