Variant report

Variant	nsv528397
Chromosome Location	chr18:30498621-30556985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	BATF	chr18:30554611-30554999	GM12878	blood:	n/a	n/a
8	BHLHE40	chr18:30510763-30510997	GM12878	blood:	n/a	n/a
9	BHLHE40	chr18:30503054-30503254	GM12878	blood:	n/a	n/a
10	CEBPB	chr18:30501423-30501831	ECC-1	luminal epithelium:	n/a	chr18:30501659-30501670
11	CEBPB	chr18:30501416-30501805	HCT-116	colon:	n/a	chr18:30501659-30501670
12	CEBPB	chr18:30500836-30501105	A549	lung:	n/a	chr18:30500944-30500955
13	CEBPB	chr18:30501420-30502206	Hela-S3	cervix:	n/a	chr18:30501659-30501670
14	CEBPB	chr18:30500757-30501119	HepG2	liver:	n/a	chr18:30500944-30500955
15	CEBPB	chr18:30501453-30501831	IMR90	lung:	n/a	chr18:30501659-30501670
16	CEBPB	chr18:30499791-30500141	HepG2	liver:	n/a	n/a
17	CEBPB	chr18:30501501-30501761	A549	lung:	n/a	chr18:30501659-30501670
18	CEBPB	chr18:30500870-30501015	HepG2	liver:	n/a	chr18:30500944-30500955
19	CEBPB	chr18:30526622-30526902	HepG2	liver:	n/a	n/a
20	CEBPB	chr18:30510683-30510966	HepG2	liver:	n/a	n/a
21	CEBPB	chr18:30548180-30548638	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr18:30510693-30510988	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr18:30516859-30517065	H1-hESC	embryonic stem cell:	n/a	chr18:30516952-30516965
24	CEBPB	chr18:30501473-30501857	ECC-1	luminal epithelium:	n/a	chr18:30501659-30501670
25	CEBPB	chr18:30518996-30519140	HepG2	liver:	n/a	n/a
26	CEBPB	chr18:30501563-30501737	HepG2	liver:	n/a	chr18:30501659-30501670
27	CEBPB	chr18:30501471-30501840	HepG2	liver:	n/a	chr18:30501659-30501670
28	CEBPB	chr18:30526628-30526917	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr18:30526711-30526869	HepG2	liver:	n/a	n/a
30	CEBPB	chr18:30499850-30500111	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr18:30499869-30500109	GM12892	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
32	CTCF	chr18:30499920-30500070	GM12869	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
33	CTCF	chr18:30536640-30536790	HCFaa	heart:	n/a	n/a
34	CTCF	chr18:30499880-30500030	HAc	cerebellar:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
35	CTCF	chr18:30499880-30500030	GM12874	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
36	CTCF	chr18:30510800-30510950	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr18:30499867-30500063	A549	lung:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
38	CTCF	chr18:30499845-30500122	GM19238	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
39	CTCF	chr18:30499900-30500050	HMF	breast:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
40	CTCF	chr18:30536561-30536790	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr18:30510741-30510980	LNCaP	prostate:	n/a	n/a
42	CTCF	chr18:30499880-30500030	GM12872	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
43	CTCF	chr18:30510824-30510923	Lung_OC	lung:	n/a	n/a
44	CTCF	chr18:30536640-30536790	AG04450	lung:	n/a	n/a
45	CTCF	chr18:30536620-30536770	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr18:30510780-30510930	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr18:30510745-30510995	Medullo	brain:	n/a	n/a
48	CTCF	chr18:30499892-30500064	Pancreas_OC	pancreas:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
49	CTCF	chr18:30499880-30500030	SAEC	small airway:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
50	CTCF	chr18:30499480-30499630	GM12875	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	Jurkat	blood:	n/a
2	chr18:30517666-30517716	ovcar-3	ovarian:	n/a
3	chr18:30517666-30517716	BE2_C	brain:	n/a
4	chr18:30517666-30517716	HAEpiC	amniotic membrane:	n/a
5	chr18:30517666-30517716	ECC-1	luminal epithelium:	n/a
6	chr18:30517666-30517716	HRE	kidney:	n/a
7	chr18:30517666-30517716	SK-N-MC	brain:	n/a
8	chr18:30517666-30517716	AG04449	skin:	fetal
9	chr18:30517666-30517716	IMR90	lung:	fetal
10	chr18:30517666-30517716	NB4	blood:	n/a
11	chr18:30517666-30517716	GM19239	blood:	n/a
12	chr18:30517666-30517716	GM06990	blood:	n/a
13	chr18:30517666-30517716	HL-60	blood:	n/a
14	chr18:30517666-30517716	SAEC	small airway:	n/a
15	chr18:30517666-30517716	BJ	skin:	n/a
16	chr18:30517666-30517716	HMEC	breast:	n/a
17	chr18:30517666-30517716	HCM	heart:	n/a
18	chr18:30517666-30517716	HIPEpiC	eye:	n/a
19	chr18:30517666-30517716	HCPEpiC	choroid plexus:	n/a
20	chr18:30517666-30517716	HepG2	liver:	n/a
21	chr18:30517666-30517716	AG09309	skin:	n/a
22	chr18:30517666-30517716	HRCEpiC	kidney:	n/a
23	chr18:30517666-30517716	NH-A	brain:	n/a
24	chr18:30517666-30517716	HCT-116	colon:	n/a
25	chr18:30517666-30517716	SK-N-SH	brain:	n/a
26	chr18:30517666-30517716	NHBE	bronchial:	n/a
27	chr18:30517666-30517716	LNCaP	prostate:	n/a
28	chr18:30517666-30517716	HCF	heart:	n/a
29	chr18:30517666-30517716	AG09319	gingival:	n/a
30	chr18:30517666-30517716	HUVEC	blood vessel:	n/a
31	chr18:30517666-30517716	SKMC	muscle:	n/a
32	chr18:30517666-30517716	MCF10A-Er-Src	breast:	n/a
33	chr18:30517666-30517716	HEEpiC	esophagus:	n/a
34	chr18:30517666-30517716	SK-N-SH_RA	brain:	n/a
35	chr18:30517666-30517716	AG10803	skin:	n/a
36	chr18:30517666-30517716	Hepatocyte	liver:	n/a
37	chr18:30517666-30517716	GM12892	blood:	n/a
38	chr18:30517666-30517716	RPTEC	kidney:	n/a
39	chr18:30517666-30517716	H1-hESC	embryonic stem cell:	embryo
40	chr18:30517666-30517716	HPAEpiC	pulmonary alveolar:	n/a
41	chr18:30517666-30517716	CMK	blood:	n/a
42	chr18:30517666-30517716	GM12878	blood:	n/a
43	chr18:30517666-30517716	A549	lung:	n/a
44	chr18:30517666-30517716	GM12891	blood:	n/a
45	chr18:30517666-30517716	HRPEpiC	eye:	n/a
46	chr18:30517666-30517716	PANC-1	pancreas:	n/a
47	chr18:30517666-30517716	U87	brain:	n/a
48	chr18:30517666-30517716	K562	blood:	n/a
49	chr18:30517666-30517716	NT2-D1	testis:	n/a
50	chr18:30517666-30517716	HNPCEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

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

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC012123.1.1-1	chr18:30517950-30518280	ENSG00000263765.1
2	lnc-AC012123.1.1-2	chr18:30534039-30534050	ENSG00000263450.1
3	lnc-AC012123.1.1-2	chr18:30534470-30534611	ENSG00000263450.1
4	lnc-AC012123.1.1-2	chr18:30536598-30536774	ENSG00000263450.1
5	lnc-AC012123.1.1-2	chr18:30537736-30537962	ENSG00000263450.1

No data

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

Extended variants
information (count: 874 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1941265	chr18:30498621-30498622	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62090726	chr18:30498678-30498679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547730917	chr18:30498842-30498843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559908442	chr18:30498843-30498844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533332599	chr18:30498860-30498861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9961243	chr18:30498878-30498879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371924664	chr18:30498923-30498924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182195929	chr18:30498928-30498929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549439640	chr18:30498988-30498989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367977603	chr18:30498989-30498990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6506997	chr18:30498997-30498998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs187627341	chr18:30499011-30499012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577783333	chr18:30499030-30499031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543569552	chr18:30499079-30499080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28540251	chr18:30499129-30499130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs575027840	chr18:30499152-30499153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542303598	chr18:30499163-30499164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146823018	chr18:30499166-30499167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140479460	chr18:30499191-30499192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564384236	chr18:30499203-30499204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541728857	chr18:30499236-30499237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559769876	chr18:30499237-30499238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191483696	chr18:30499241-30499242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552039810	chr18:30499256-30499257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374343544	chr18:30499323-30499324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150464831	chr18:30499336-30499337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113153379	chr18:30499337-30499338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs8094462	chr18:30499432-30499433	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs116699424	chr18:30499447-30499448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371393296	chr18:30499493-30499494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182166231	chr18:30499505-30499506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568290408	chr18:30499547-30499548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79533586	chr18:30499573-30499574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575089585	chr18:30499584-30499585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535954540	chr18:30499644-30499645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185426735	chr18:30499762-30499763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138258340	chr18:30499770-30499771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113339285	chr18:30499804-30499805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558510670	chr18:30499819-30499820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578218444	chr18:30499829-30499830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545713587	chr18:30499889-30499890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1941264	chr18:30499899-30499900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531085483	chr18:30499912-30499913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149230268	chr18:30499934-30499935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190132477	chr18:30499953-30499954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114448483	chr18:30499957-30499958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375487649	chr18:30499989-30499990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528563873	chr18:30500005-30500006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146902516	chr18:30500023-30500024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182049869	chr18:30500025-30500026	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:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30496400-30499800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr18:30497600-30500200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr18:30498400-30500400	Enhancers	Primary B cells from cord blood	blood
4	chr18:30498600-30499200	Enhancers	Fetal Brain Male	brain
5	chr18:30498600-30500200	Enhancers	Primary B cells from peripheral blood	blood
6	chr18:30498800-30500000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr18:30499600-30502000	Enhancers	HepG2	liver
8	chr18:30499800-30500000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr18:30499800-30501000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr18:30500000-30500200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr18:30500000-30502200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr18:30500000-30502800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr18:30500000-30503200	Enhancers	NHEK	skin
14	chr18:30500200-30500600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr18:30500200-30500800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr18:30500200-30501000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr18:30500200-30502000	Weak transcription	Primary B cells from peripheral blood	blood
18	chr18:30500200-30502200	Enhancers	HMEC	breast
19	chr18:30500400-30502400	Weak transcription	Primary B cells from cord blood	blood
20	chr18:30500400-30504000	Enhancers	HSMM	muscle
21	chr18:30500600-30502200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr18:30500600-30502400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr18:30500600-30503800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr18:30500800-30501000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr18:30500800-30501000	Enhancers	NH-A	brain
26	chr18:30500800-30502200	Enhancers	Hela-S3	cervix
27	chr18:30500800-30502200	Enhancers	HUVEC	blood vessel
28	chr18:30500800-30503400	Enhancers	Osteobl	bone
29	chr18:30500800-30503600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr18:30500800-30503600	Enhancers	HSMMtube	muscle
31	chr18:30501000-30501200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr18:30501000-30501200	Flanking Active TSS	NHDF-Ad	bronchial
33	chr18:30501000-30501400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr18:30501000-30501400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr18:30501000-30501400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr18:30501000-30501400	Flanking Active TSS	NH-A	brain
37	chr18:30501000-30501600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr18:30501000-30502000	Enhancers	Dnd41	blood
39	chr18:30501000-30502200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr18:30501000-30502400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr18:30501200-30501400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr18:30501200-30502000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr18:30501200-30502000	Enhancers	NHDF-Ad	bronchial
44	chr18:30501200-30502200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr18:30501200-30503200	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr18:30501400-30501800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr18:30501400-30501800	Active TSS	NH-A	brain
48	chr18:30501400-30502400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr18:30501400-30503000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr18:30501600-30503600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links