Variant report

Variant	nsv909600
Chromosome Location	chr18:44294722-44396246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:856)
Chromatin interactive
region (count:8)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44343741-44343800	HepG2	liver:	n/a	n/a
2	BACH1	chr18:44336050-44336250	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:44335079-44335249	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr18:44367638-44367984	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:44334478-44334576	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:44299297-44299305	K562	blood:	n/a	n/a
7	BRCA1	chr18:44318689-44318719	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr18:44298913-44299496	HCT-116	colon:	n/a	n/a
9	CEBPB	chr18:44376072-44376254	A549	lung:	n/a	n/a
10	CEBPB	chr18:44380339-44380513	HepG2	liver:	n/a	chr18:44380462-44380473
11	CEBPB	chr18:44346904-44347188	K562	blood:	n/a	n/a
12	CEBPB	chr18:44299061-44299279	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr18:44331573-44331857	HepG2	liver:	n/a	chr18:44331721-44331732
14	CEBPB	chr18:44298198-44298374	K562	blood:	n/a	n/a
15	CEBPB	chr18:44376072-44376263	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr18:44307201-44307385	HepG2	liver:	n/a	n/a
17	CEBPB	chr18:44369682-44369880	HepG2	liver:	n/a	chr18:44369709-44369720
18	CEBPB	chr18:44376035-44376269	IMR90	lung:	n/a	n/a
19	CEBPB	chr18:44298091-44298404	IMR90	lung:	n/a	n/a
20	CHD1	chr18:44336734-44336908	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr18:44336861-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44337023-44337033
22	CHD2	chr18:44334253-44334329	GM12878	blood:	n/a	n/a
23	CTBP2	chr18:44336144-44337128	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr18:44335100-44335250	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr18:44352440-44352590	GM12875	blood:	n/a	chr18:44352478-44352499
27	CTCF	chr18:44352547-44352559	GM12878	blood:	n/a	n/a
28	CTCF	chr18:44352367-44352665	GM12878	blood:	n/a	chr18:44352478-44352499
29	CTCF	chr18:44373700-44373850	MCF-7	breast:	n/a	chr18:44373713-44373720
30	CTCF	chr18:44342389-44342461	LNCaP	prostate:	n/a	n/a
31	CTCF	chr18:44373640-44373790	AG04450	lung:	n/a	chr18:44373713-44373720
32	CTCF	chr18:44324641-44324687	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr18:44352360-44352510	WERI-Rb-1	eye:	n/a	chr18:44352478-44352499
34	CTCF	chr18:44373720-44373870	GM12872	blood:	n/a	n/a
35	CTCF	chr18:44335020-44335170	HAc	cerebellar:	n/a	n/a
36	CTCF	chr18:44335040-44335190	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr18:44373620-44373770	GM12868	blood:	n/a	chr18:44373713-44373720
38	CTCF	chr18:44373620-44373770	GM12874	blood:	n/a	chr18:44373713-44373720
39	CTCF	chr18:44295207-44295298	GM19240	blood:	n/a	n/a
40	CTCF	chr18:44295159-44295354	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr18:44352480-44352564	MCF-7	breast:	n/a	n/a
42	CTCF	chr18:44352432-44352587	MCF-7	breast:	n/a	chr18:44352478-44352499
43	CTCF	chr18:44352419-44352532	GM13977	blood:	n/a	chr18:44352478-44352499
44	CTCF	chr18:44295062-44295357	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr18:44373660-44373810	AG10803	skin:	n/a	chr18:44373713-44373720
46	CTCF	chr18:44361192-44361251	GM10266	blood:	n/a	n/a
47	CTCF	chr18:44352433-44352568	K562	blood:	n/a	chr18:44352478-44352499
48	CTCF	chr18:44373620-44373770	HRPEpiC	eye:	n/a	chr18:44373713-44373720
49	CTCF	chr18:44334955-44335270	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr18:44373700-44373850	NB4	blood:	n/a	chr18:44373713-44373720

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44338147-44338197	Hela-S3	cervix:	n/a
2	chr18:44337853-44337903	AG04449	skin:	fetal
3	chr18:44338147-44338197	Hela-S3	cervix:	n/a
4	chr18:44337853-44337903	AG04449	skin:	fetal
5	chr18:44339513-44339563	SAEC	small airway:	n/a
6	chr18:44340177-44340227	HIPEpiC	eye:	n/a
7	chr18:44338099-44338149	NHDF-neo	bronchial:	n/a
8	chr18:44340177-44340227	PANC-1	pancreas:	n/a
9	chr18:44392124-44392174	Hela-S3	cervix:	n/a
10	chr18:44339513-44339563	Hepatocyte	liver:	n/a
11	chr18:44334713-44334763	GM19239	blood:	n/a
12	chr18:44333130-44333180	HRPEpiC	eye:	n/a
13	chr18:44340177-44340227	SKMC	muscle:	n/a
14	chr18:44334713-44334763	AG10803	skin:	n/a
15	chr18:44333130-44333180	Hela-S3	cervix:	n/a
16	chr18:44337099-44337149	SK-N-SH	brain:	n/a
17	chr18:44337922-44337972	PrEC	prostate:	n/a
18	chr18:44334713-44334763	PrEC	prostate:	n/a
19	chr18:44336399-44336449	GM06990	blood:	n/a
20	chr18:44337853-44337903	ECC-1	luminal epithelium:	n/a
21	chr18:44333130-44333180	HPAEpiC	pulmonary alveolar:	n/a
22	chr18:44340177-44340227	AG04450	lung:	fetal
23	chr18:44337910-44337960	AG10803	skin:	n/a
24	chr18:44340177-44340227	A549	lung:	n/a
25	chr18:44338099-44338149	PANC-1	pancreas:	n/a
26	chr18:44336399-44336449	Hela-S3	cervix:	n/a
27	chr18:44338147-44338197	HEEpiC	esophagus:	n/a
28	chr18:44335109-44335159	GM19239	blood:	n/a
29	chr18:44337853-44337903	IMR90	lung:	fetal
30	chr18:44338147-44338197	HRCEpiC	kidney:	n/a
31	chr18:44333130-44333180	AG04450	lung:	fetal
32	chr18:44337910-44337960	SAEC	small airway:	n/a
33	chr18:44335109-44335159	HCPEpiC	choroid plexus:	n/a
34	chr18:44339513-44339563	HPAEpiC	pulmonary alveolar:	n/a
35	chr18:44340177-44340227	U87	brain:	n/a
36	chr18:44339513-44339563	HEK293	kidney:	embryo
37	chr18:44337922-44337972	RPTEC	kidney:	n/a
38	chr18:44335109-44335159	RPTEC	kidney:	n/a
39	chr18:44333130-44333180	GM06990	blood:	n/a
40	chr18:44333130-44333180	MCF10A-Er-Src	breast:	n/a
41	chr18:44335109-44335159	HL-60	blood:	n/a
42	chr18:44392124-44392174	NH-A	brain:	n/a
43	chr18:44334713-44334763	NT2-D1	testis:	n/a
44	chr18:44337664-44337714	ECC-1	luminal epithelium:	n/a
45	chr18:44337099-44337149	IMR90	lung:	fetal
46	chr18:44337910-44337960	PrEC	prostate:	n/a
47	chr18:44392124-44392174	RPTEC	kidney:	n/a
48	chr18:44338147-44338197	NHBE	bronchial:	n/a
49	chr18:44338099-44338149	GM12878	blood:	n/a
50	chr18:44337910-44337960	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
2	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:
3	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
4	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:
5	chr18:44339087..44341037-chr18:44341994..44343919,2	K562	blood:
6	chr18:44290160..44292978-chr18:44295020..44296704,2	K562	blood:
7	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
8	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-1	chr18:44339687-44344371	NONHSAT059142
2	lnc-KATNAL2-1	chr18:44338415-44338422	XLOC_012667
3	lnc-KATNAL2-1	chr18:44339972-44340204	XLOC_012667
4	lnc-KATNAL2-7	chr18:44383140-44387340	NONHSAT059143
5	lnc-KATNAL2-10	chr18:44302938-44303186	NONHSAT059136
6	lnc-KATNAL2-1	chr18:44336896-44336994	ENSG00000270112.2
7	lnc-KATNAL2-1	chr18:44339774-44340307	ENSG00000270112.2
8	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
9	lnc-KATNAL2-1	chr18:44336450-44336587	ENSG00000270112.2
10	lnc-KATNAL2-1	chr18:44338764-44339028	NONHSAT059140
11	lnc-KATNAL2-1	chr18:44336746-44337039	ENSG00000270112.2
12	lnc-PIAS2-1	chr18:44383187-44383857	ENSG00000267167.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIAS2	hsa-miR-26b-5p	chr18:44392379-44392395

Variant related genes	Relation type
ENSG00000270112	TF binding region
ST8SIA5	TF binding region
ENSG00000240983	TF binding region
ENSG00000267167	TF binding region
ENSG00000270112	CpG island
ST8SIA5	CpG island
ENSG00000240983	CpG island
ENSG00000267167	CpG island
ENSG00000101638	chromatin interactions

Extended variants
information (count: 3680 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3680 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9950834	chr18:44294722-44294723	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149849353	chr18:44294764-44294765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570396258	chr18:44294766-44294767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539364364	chr18:44294770-44294771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537798968	chr18:44294874-44294875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553062527	chr18:44294915-44294916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112101003	chr18:44294970-44294971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535521928	chr18:44295063-44295064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12455864	chr18:44295074-44295075	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs575678017	chr18:44295116-44295117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544804321	chr18:44295120-44295121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564687312	chr18:44295138-44295139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189795064	chr18:44295172-44295173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540932823	chr18:44295251-44295252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547883835	chr18:44295255-44295256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568309070	chr18:44295265-44295266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75590111	chr18:44295266-44295267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559048586	chr18:44295289-44295290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375508049	chr18:44295294-44295295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547920790	chr18:44295312-44295313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78074459	chr18:44295328-44295329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533863568	chr18:44295330-44295331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34953341	chr18:44295403-44295404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34762283	chr18:44295405-44295406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11082552	chr18:44295413-44295414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530553704	chr18:44295414-44295415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111711830	chr18:44295465-44295466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76463281	chr18:44295516-44295517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs36007614	chr18:44295517-44295518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs398041369	chr18:44295531-44295532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4890337	chr18:44295546-44295547	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs35047631	chr18:44295593-44295594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539301003	chr18:44295637-44295638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113241743	chr18:44295706-44295707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202220738	chr18:44295708-44295709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566701949	chr18:44295751-44295752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535820558	chr18:44295833-44295834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555513144	chr18:44295841-44295842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143722557	chr18:44295844-44295845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538367087	chr18:44295904-44295905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558337699	chr18:44295920-44295921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs578225224	chr18:44295944-44295945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9956677	chr18:44296001-44296002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182687117	chr18:44296013-44296014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377209912	chr18:44296049-44296050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200086260	chr18:44296050-44296051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9956435	chr18:44296053-44296054	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs35206411	chr18:44296057-44296058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141819059	chr18:44296067-44296068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548860593	chr18:44296069-44296070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44286800-44298800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:44287800-44298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr18:44290000-44295400	Enhancers	Fetal Muscle Leg	muscle
4	chr18:44291800-44295200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:44292000-44295000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr18:44292800-44297000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr18:44293000-44295200	Weak transcription	Right Ventricle	heart
8	chr18:44293000-44296600	Weak transcription	Brain Hippocampus Middle	brain
9	chr18:44293000-44296600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr18:44293000-44298400	Weak transcription	Ovary	ovary
11	chr18:44293000-44298800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr18:44293200-44296600	Weak transcription	Right Atrium	heart
13	chr18:44293200-44296800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr18:44293200-44296800	Weak transcription	Brain Substantia Nigra	brain
15	chr18:44293200-44298400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr18:44293200-44298400	Weak transcription	Osteobl	bone
17	chr18:44293200-44298800	Weak transcription	NHLF	lung
18	chr18:44293400-44298400	Weak transcription	HSMM	muscle
19	chr18:44293400-44298600	Weak transcription	NHDF-Ad	bronchial
20	chr18:44293600-44295800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr18:44293600-44296800	Weak transcription	Brain Angular Gyrus	brain
22	chr18:44293600-44298600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr18:44293600-44298800	Weak transcription	Left Ventricle	heart
24	chr18:44293600-44298800	Weak transcription	Psoas Muscle	Psoas
25	chr18:44293800-44296800	Weak transcription	HSMMtube	muscle
26	chr18:44293800-44298400	Weak transcription	Fetal Heart	heart
27	chr18:44294000-44296800	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr18:44294400-44294800	Enhancers	Fetal Muscle Trunk	muscle
29	chr18:44294400-44297000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr18:44294400-44298400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr18:44294400-44298800	Weak transcription	Brain Germinal Matrix	brain
32	chr18:44294600-44299000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr18:44294800-44295000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr18:44294800-44295200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr18:44295000-44295400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr18:44295000-44295600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr18:44295000-44295800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr18:44295000-44296400	Enhancers	Fetal Muscle Trunk	muscle
39	chr18:44295200-44295400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:44295200-44295400	Enhancers	Right Ventricle	heart
41	chr18:44295200-44295800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr18:44295200-44299000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr18:44295400-44298400	Weak transcription	Right Ventricle	heart
44	chr18:44295400-44298800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr18:44295800-44296000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr18:44295800-44297200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr18:44296000-44296400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr18:44296200-44296400	Enhancers	HUVEC	blood vessel
49	chr18:44296400-44296800	Enhancers	Spleen	Spleen
50	chr18:44296400-44297200	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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