Variant report

Variant	nsv457977
Chromosome Location	chr18:289153-407958
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	chr18:322586-322907	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:323362-323666	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:361954-362757	HepG2	liver:	n/a	chr18:362252-362268
4	ARID3A	chr18:322588-322899	K562	blood:	n/a	n/a
5	ATF1	chr18:322600-322859	K562	blood:	n/a	n/a
6	ATF3	chr18:322457-322909	K562	blood:	n/a	n/a
7	ATF3	chr18:323314-323635	K562	blood:	n/a	n/a
8	ATF3	chr18:322557-322878	K562	blood:	n/a	n/a
9	BACH1	chr18:365039-365067	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr18:322542-322828	GM12878	blood:	n/a	chr18:322737-322747
11	BHLHE40	chr18:302234-302299	K562	blood:	n/a	n/a
12	BHLHE40	chr18:323381-323581	HepG2	liver:	n/a	n/a
13	BHLHE40	chr18:322602-322921	HepG2	liver:	n/a	n/a
14	BHLHE40	chr18:361911-362590	HepG2	liver:	n/a	n/a
15	BHLHE40	chr18:322531-322950	K562	blood:	n/a	n/a
16	CBX3	chr18:322501-322885	K562	blood:	n/a	n/a
17	CBX3	chr18:322440-322947	K562	blood:	n/a	n/a
18	CCNT2	chr18:306762-306890	K562	blood:	n/a	n/a
19	CCNT2	chr18:322607-322880	K562	blood:	n/a	n/a
20	CEBPB	chr18:363510-363890	H1-hESC	embryonic stem cell:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
21	CEBPB	chr18:363424-363967	MCF-7	breast:	n/a	chr18:363694-363707 chr18:363465-363478 chr18:363696-363705 chr18:363467-363478 chr18:363435-363447 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707 chr18:363467-363478
22	CEBPB	chr18:363550-363845	A549	lung:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
23	CEBPB	chr18:362243-362583	HepG2	liver:	n/a	n/a
24	CEBPB	chr18:363567-363824	ECC-1	luminal epithelium:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
25	CEBPB	chr18:366698-366840	HepG2	liver:	n/a	chr18:366758-366769 chr18:366758-366771 chr18:366760-366771
26	CEBPB	chr18:362364-362570	HepG2	liver:	n/a	n/a
27	CEBPB	chr18:363476-363913	MCF-7	breast:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
28	CEBPB	chr18:400522-400833	K562	blood:	n/a	chr18:400567-400578
29	CEBPB	chr18:322515-322975	K562	blood:	n/a	n/a
30	CEBPB	chr18:363524-363873	HepG2	liver:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
31	CEBPB	chr18:361885-362085	HepG2	liver:	n/a	n/a
32	CEBPB	chr18:363498-363854	ECC-1	luminal epithelium:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
33	CEBPB	chr18:323318-323552	HepG2	liver:	n/a	n/a
34	CEBPB	chr18:363586-363807	Hela-S3	cervix:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
35	CEBPB	chr18:363429-363947	A549	lung:	n/a	chr18:363694-363707 chr18:363465-363478 chr18:363696-363705 chr18:363467-363478 chr18:363435-363447 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707 chr18:363467-363478
36	CEBPB	chr18:366695-366826	HepG2	liver:	n/a	chr18:366758-366769 chr18:366758-366771 chr18:366760-366771
37	CEBPB	chr18:323333-323502	HepG2	liver:	n/a	n/a
38	CEBPB	chr18:363514-363891	K562	blood:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
39	CEBPB	chr18:366593-366943	H1-hESC	embryonic stem cell:	n/a	chr18:366758-366769 chr18:366758-366771 chr18:366760-366771
40	CEBPB	chr18:363534-363854	IMR90	lung:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
41	CEBPB	chr18:361910-362057	HepG2	liver:	n/a	n/a
42	CEBPB	chr18:363509-363858	K562	blood:	n/a	chr18:363694-363707 chr18:363696-363705 chr18:363696-363705 chr18:363695-363706 chr18:363696-363705 chr18:363788-363801 chr18:363694-363707
43	CEBPB	chr18:400529-400822	IMR90	lung:	n/a	chr18:400567-400578
44	CEBPD	chr18:306669-307002	K562	blood:	n/a	n/a
45	CEBPD	chr18:362256-362611	HepG2	liver:	n/a	n/a
46	CHD2	chr18:362473-362714	HepG2	liver:	n/a	n/a
47	CHD2	chr18:308135-308422	K562	blood:	n/a	n/a
48	CHD2	chr18:362010-362259	HepG2	liver:	n/a	n/a
49	CTCF	chr18:332553-332908	MCF-7	breast:	n/a	chr18:332755-332773 chr18:332758-332771 chr18:332757-332778
50	CTCF	chr18:390080-390230	GM12871	blood:	n/a	chr18:390150-390159

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:319786-319836	PANC-1	pancreas:	n/a
2	chr18:319786-319836	BE2_C	brain:	n/a
3	chr18:319786-319836	ProgFib	skin:	n/a
4	chr18:319786-319836	Hepatocyte	liver:	n/a
5	chr18:319786-319836	AG04449	skin:	fetal
6	chr18:319786-319836	HUVEC	blood vessel:	n/a
7	chr18:319786-319836	HRE	kidney:	n/a
8	chr18:319786-319836	HRCEpiC	kidney:	n/a
9	chr18:319786-319836	ovcar-3	ovarian:	n/a
10	chr18:319786-319836	HL-60	blood:	n/a
11	chr18:319786-319836	GM12892	blood:	n/a
12	chr18:319786-319836	MCF-7	breast:	n/a
13	chr18:319786-319836	GM19239	blood:	n/a
14	chr18:319786-319836	NB4	blood:	n/a
15	chr18:319786-319836	HPAEpiC	pulmonary alveolar:	n/a
16	chr18:319786-319836	HIPEpiC	eye:	n/a
17	chr18:319786-319836	HEK293	kidney:	embryo
18	chr18:319786-319836	K562	blood:	n/a
19	chr18:319786-319836	CMK	blood:	n/a
20	chr18:319786-319836	NT2-D1	testis:	n/a
21	chr18:319786-319836	Jurkat	blood:	n/a
22	chr18:319786-319836	SK-N-SH	brain:	n/a
23	chr18:319786-319836	HCT-116	colon:	n/a
24	chr18:319786-319836	HCM	heart:	n/a
25	chr18:319786-319836	A549	lung:	n/a
26	chr18:319786-319836	PrEC	prostate:	n/a
27	chr18:319786-319836	HNPCEpiC	eye:	n/a
28	chr18:319786-319836	Caco-2	colon:	n/a
29	chr18:319786-319836	RPTEC	kidney:	n/a
30	chr18:319786-319836	GM12878	blood:	n/a
31	chr18:319786-319836	SAEC	small airway:	n/a
32	chr18:319786-319836	NH-A	brain:	n/a
33	chr18:319786-319836	AG10803	skin:	n/a
34	chr18:319786-319836	HRPEpiC	eye:	n/a
35	chr18:319786-319836	HCPEpiC	choroid plexus:	n/a
36	chr18:319786-319836	NHBE	bronchial:	n/a
37	chr18:319786-319836	ECC-1	luminal epithelium:	n/a
38	chr18:319786-319836	GM06990	blood:	n/a
39	chr18:319786-319836	AG04450	lung:	fetal
40	chr18:319786-319836	HepG2	liver:	n/a
41	chr18:319786-319836	GM12891	blood:	n/a
42	chr18:319786-319836	U87	brain:	n/a
43	chr18:319786-319836	H1-hESC	embryonic stem cell:	embryo
44	chr18:319786-319836	NHDF-neo	bronchial:	n/a
45	chr18:319786-319836	MCF10A-Er-Src	breast:	n/a
46	chr18:319786-319836	SK-N-MC	brain:	n/a
47	chr18:319786-319836	AG09309	skin:	n/a
48	chr18:319786-319836	BJ	skin:	n/a
49	chr18:319786-319836	AoSMC	blood vessel:	n/a
50	chr18:319786-319836	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:305775..308691-chr18:309654..313982,3	K562	blood:
2	chr18:366740..368283-chr18:380460..382795,2	MCF-7	breast:
3	chr18:331361..333834-chr18:339514..341220,2	K562	blood:
4	chr18:387414..389683-chr18:397605..399676,2	MCF-7	breast:
5	chr18:387314..389519-chr18:391582..393434,2	K562	blood:
6	chr18:300482..306131-chr18:306212..309352,5	K562	blood:
7	chr18:302419..306527-chr18:308522..311824,4	K562	blood:
8	chr18:330383..333322-chr18:336315..339343,3	K562	blood:
9	chr18:362806..364833-chr18:392678..394320,2	K562	blood:
10	chr18:373442..375390-chr18:380419..383065,2	K562	blood:
11	chr18:387314..389519-chr18:391582..393434,2	K562	blood:
12	chr18:332464..333064-chr18:469230..470136,2	MCF-7	breast:
13	chr18:293279..294017-chr18:477353..478290,2	MCF-7	breast:
14	chr18:323395..325246-chr18:328726..330644,2	K562	blood:
15	chr18:368265..370725-chr18:373319..375818,2	K562	blood:
16	chr18:292073..293974-chr18:294604..297450,2	K562	blood:
17	chr18:369225..372078-chr18:373724..375818,2	K562	blood:
18	chr18:393515..395021-chr18:401275..403491,2	K562	blood:
19	chr18:368265..370725-chr18:373319..375818,2	K562	blood:
20	chr18:331361..333834-chr18:339514..341220,2	K562	blood:
21	chr18:327014..329682-chr18:339445..341723,2	K562	blood:
22	chr18:369225..372078-chr18:373724..375818,2	K562	blood:
23	chr18:305775..308691-chr18:309654..313982,3	K562	blood:
24	chr18:294145..296995-chr18:298267..301076,2	K562	blood:
25	chr18:387414..389683-chr18:397605..399676,2	MCF-7	breast:
26	chr18:338753..341671-chr18:342175..343994,2	K562	blood:
27	chr18:294145..296995-chr18:298267..301076,2	K562	blood:
28	chr18:385070..387851-chr18:389835..392598,2	MCF-7	breast:
29	chr18:346666..347469-chr18:13539665..13540400,2	MCF-7	breast:
30	chr18:272315..274100-chr18:321177..323834,2	K562	blood:
31	chr18:302419..306527-chr18:308522..311824,4	K562	blood:
32	chr18:398278..401003-chr18:448544..450699,2	MCF-7	breast:
33	chr18:340199..343062-chr18:344360..346781,2	K562	blood:
34	chr18:362806..364833-chr18:392678..394320,2	K562	blood:
35	chr18:323395..325246-chr18:328726..330644,2	K562	blood:
36	chr18:340199..343062-chr18:344360..346781,2	K562	blood:
37	chr18:333834..337765-chr18:338679..342822,4	K562	blood:
38	chr18:401348..404320-chr18:415825..418270,2	K562	blood:
39	chr18:292167..293133-chr18:616102..616665,2	MCF-7	breast:
40	chr18:266762..268550-chr18:321925..324261,2	K562	blood:
41	chr18:300482..306131-chr18:306212..309352,5	K562	blood:
42	chr18:352568..355248-chr18:364215..365961,2	K562	blood:
43	chr18:291631..293957-chr18:611359..613782,2	MCF-7	breast:
44	chr18:343824..347301-chr18:347889..349452,3	MCF-7	breast:
45	chr18:292073..293974-chr18:294604..297450,2	K562	blood:
46	chr18:385070..387851-chr18:389835..392598,2	MCF-7	breast:
47	chr18:327014..329682-chr18:339445..341723,2	K562	blood:
48	chr18:330383..333322-chr18:336315..339343,3	K562	blood:
49	chr18:293551..294215-chr18:616120..617138,3	MCF-7	breast:
50	chr18:248724..251192-chr18:298155..299664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP14-4	chr18:317866-318033	XLOC_012601
2	lnc-USP14-4	chr18:318868-319165	ENSG00000264514.1
3	lnc-COLEC12-1	chr18:316740-316963	ENSG00000264433.1
4	lnc-USP14-4	chr18:316737-316986	ENSG00000264514.1
5	lnc-COLEC12-1	chr18:317099-317366	ENSG00000264433.1
6	lnc-USP14-4	chr18:314887-317129	XLOC_012601

No.	miRNA target gene	miRNA name	Chromosome Location
1	COLEC12	hsa-miR-9-5p	chr18:319479-319497
2	COLEC12	hsa-miR-7-5p	chr18:319760-319781
3	COLEC12	hsa-miR-26b-5p	chr18:319583-319605
4	COLEC12	hsa-miR-9-5p	chr18:319484-319478

Variant related genes	Relation type
ENSG00000264433	TF binding region
ENSG00000264514	TF binding region
ENSG00000264433	CpG island
ENSG00000264514	CpG island
ENSG00000079101	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000263884	chromatin interactions

Extended variants
information (count: 4945 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4945 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs653301	chr18:289153-289154	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571777606	chr18:289193-289194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6506033	chr18:289209-289210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs478096	chr18:289210-289211	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs575389001	chr18:289218-289219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542891549	chr18:289314-289315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375809638	chr18:289327-289328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554594346	chr18:289347-289348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182104748	chr18:289397-289398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572945496	chr18:289400-289401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369983032	chr18:289474-289475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555920215	chr18:289563-289564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144582758	chr18:289589-289590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574709866	chr18:292806-292807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372327250	chr18:292814-292815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71352934	chr18:292821-292822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188568500	chr18:292822-292823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572201954	chr18:292867-292868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545930539	chr18:292893-292894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72857525	chr18:292927-292928	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531559207	chr18:292928-292929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180941165	chr18:292936-292937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12606262	chr18:292939-292940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376740747	chr18:292947-292948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372030492	chr18:292951-292952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544828366	chr18:292966-292967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562030039	chr18:293004-293005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145939484	chr18:293045-293046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547418868	chr18:293058-293059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558429153	chr18:293103-293104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558096702	chr18:293108-293109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs3889144	chr18:293161-293162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138505525	chr18:293164-293165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115263665	chr18:293191-293192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141651326	chr18:293213-293214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76690082	chr18:293240-293241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115216995	chr18:293241-293242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186029200	chr18:293251-293252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575084283	chr18:293338-293339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146203354	chr18:293350-293351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148777069	chr18:293376-293377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs627789	chr18:293384-293385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545869100	chr18:293399-293400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76246191	chr18:293560-293561	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187006746	chr18:293562-293563	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs142393467	chr18:293581-293582	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569743191	chr18:293582-293583	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs150914561	chr18:293594-293595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs374187300	chr18:293655-293656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190501730	chr18:293656-293657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1482 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:288600-289600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr18:288800-289400	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr18:292800-293400	Enhancers	Placenta	Placenta
4	chr18:293000-293400	Enhancers	Pancreas	Pancrea
5	chr18:293600-294000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr18:294000-294200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr18:294200-295000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr18:294600-295000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr18:295000-296600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr18:295200-297000	Enhancers	NHDF-Ad	bronchial
11	chr18:295400-296000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr18:295400-296600	Enhancers	Osteobl	bone
13	chr18:295400-297000	Enhancers	HUVEC	blood vessel
14	chr18:296000-296600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr18:296000-296600	Enhancers	Fetal Muscle Leg	muscle
16	chr18:296000-296600	Enhancers	Fetal Stomach	stomach
17	chr18:296600-297600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr18:297000-297800	Weak transcription	NHDF-Ad	bronchial
19	chr18:297000-301400	Weak transcription	HUVEC	blood vessel
20	chr18:297600-298600	Enhancers	K562	blood
21	chr18:297600-299000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr18:297800-298200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr18:297800-298200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr18:297800-298600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr18:297800-298600	Enhancers	NHDF-Ad	bronchial
26	chr18:298600-302200	Weak transcription	K562	blood
27	chr18:298600-304800	Weak transcription	NHDF-Ad	bronchial
28	chr18:300800-301800	Enhancers	Fetal Lung	lung
29	chr18:301000-301400	Enhancers	Fetal Kidney	kidney
30	chr18:301400-302400	Enhancers	HUVEC	blood vessel
31	chr18:301800-303400	Weak transcription	Fetal Lung	lung
32	chr18:302000-302400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr18:302200-302400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr18:302200-302400	Enhancers	K562	blood
35	chr18:302200-302600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr18:302400-303400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr18:302400-303800	Weak transcription	K562	blood
38	chr18:303200-305800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr18:303400-304600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr18:303400-305600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr18:303400-305600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr18:303400-305600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr18:303400-305600	Enhancers	Fetal Lung	lung
44	chr18:303400-307200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr18:303400-307800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr18:303400-308200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr18:303600-305800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr18:303800-305400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr18:303800-305600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr18:303800-306600	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links