Variant report

Variant	nsv1056007
Chromosome Location	chr18:29711974-29899564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1602)
CpG islands
(count:244)
Chromatin interactive
region (count:52)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1602 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29869475-29869822	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29851724-29851986	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29738032-29738318	K562	blood:	n/a	n/a
4	ARID3A	chr18:29897304-29897515	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29899090-29899515	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29737989-29738329	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29858231-29858695	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:29718269-29718808	K562	blood:	n/a	n/a
9	ATF1	chr18:29718320-29718556	K562	blood:	n/a	n/a
10	ATF3	chr18:29897037-29897612	HCT-116	colon:	n/a	n/a
11	BACH1	chr18:29818854-29819068	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr18:29897394-29897429	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr18:29732998-29733377	GM12878	blood:	n/a	n/a
14	BATF	chr18:29733064-29733348	GM12878	blood:	n/a	n/a
15	BATF	chr18:29881951-29882288	GM12878	blood:	n/a	n/a
16	BHLHE40	chr18:29860244-29860325	K562	blood:	n/a	chr18:29860277-29860286 chr18:29860275-29860288 chr18:29860276-29860285 chr18:29860277-29860286
17	BHLHE40	chr18:29737978-29738337	K562	blood:	n/a	n/a
18	BRCA1	chr18:29737994-29738352	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr18:29738003-29738319	H1-hESC	embryonic stem cell:	n/a	n/a
20	CCNT2	chr18:29714207-29714511	K562	blood:	n/a	n/a
21	CEBPB	chr18:29738975-29739253	IMR90	lung:	n/a	chr18:29739135-29739146
22	CEBPB	chr18:29741075-29741341	IMR90	lung:	n/a	n/a
23	CEBPB	chr18:29883372-29883601	A549	lung:	n/a	n/a
24	CEBPB	chr18:29741107-29741358	MCF-7	breast:	n/a	n/a
25	CEBPB	chr18:29739070-29739217	HepG2	liver:	n/a	chr18:29739135-29739146
26	CEBPB	chr18:29753231-29753468	A549	lung:	n/a	n/a
27	CEBPB	chr18:29790666-29790775	HepG2	liver:	n/a	chr18:29790714-29790725 chr18:29790713-29790726
28	CEBPB	chr18:29897141-29897528	HepG2	liver:	n/a	chr18:29897318-29897329
29	CEBPB	chr18:29736923-29737226	HepG2	liver:	n/a	chr18:29737041-29737052 chr18:29737042-29737053
30	CEBPB	chr18:29793645-29794053	HepG2	liver:	n/a	n/a
31	CEBPB	chr18:29897055-29897657	HCT-116	colon:	n/a	chr18:29897612-29897625 chr18:29897612-29897625 chr18:29897318-29897329
32	CEBPB	chr18:29881892-29882450	IMR90	lung:	n/a	n/a
33	CEBPB	chr18:29897127-29897563	ECC-1	luminal epithelium:	n/a	chr18:29897318-29897329
34	CEBPB	chr18:29858469-29858713	HepG2	liver:	n/a	n/a
35	CEBPB	chr18:29824093-29824400	IMR90	lung:	n/a	chr18:29824260-29824271 chr18:29824260-29824269 chr18:29824258-29824269 chr18:29824260-29824269 chr18:29824260-29824269 chr18:29824260-29824269
36	CEBPB	chr18:29883349-29883685	IMR90	lung:	n/a	n/a
37	CEBPB	chr18:29817112-29817385	HepG2	liver:	n/a	chr18:29817219-29817230
38	CEBPB	chr18:29803060-29803357	K562	blood:	n/a	n/a
39	CEBPB	chr18:29897141-29897612	Hela-S3	cervix:	n/a	chr18:29897318-29897329
40	CEBPB	chr18:29824090-29824387	A549	lung:	n/a	chr18:29824260-29824271 chr18:29824260-29824269 chr18:29824258-29824269 chr18:29824260-29824269 chr18:29824260-29824269 chr18:29824260-29824269
41	CEBPB	chr18:29791674-29791964	HepG2	liver:	n/a	chr18:29791815-29791828 chr18:29791816-29791827 chr18:29791815-29791826 chr18:29791815-29791828
42	CEBPB	chr18:29897105-29897728	HCT-116	colon:	n/a	chr18:29897612-29897625 chr18:29897612-29897625 chr18:29897318-29897329
43	CEBPB	chr18:29897154-29897562	A549	lung:	n/a	chr18:29897318-29897329
44	CEBPB	chr18:29841166-29841171	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr18:29829486-29829738	A549	lung:	n/a	n/a
46	CEBPB	chr18:29897149-29897454	HepG2	liver:	n/a	chr18:29897318-29897329
47	CEBPB	chr18:29747952-29748206	MCF-7	breast:	n/a	n/a
48	CEBPB	chr18:29829543-29829686	IMR90	lung:	n/a	n/a
49	CEBPB	chr18:29791686-29791919	IMR90	lung:	n/a	chr18:29791815-29791828 chr18:29791816-29791827 chr18:29791815-29791826 chr18:29791815-29791828
50	CEBPB	chr18:29799742-29799841	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29769853-29769903	HNPCEpiC	eye:	n/a
2	chr18:29769853-29769903	HMEC	breast:	n/a
3	chr18:29770081-29770131	AG09319	gingival:	n/a
4	chr18:29847791-29847841	AG10803	skin:	n/a
5	chr18:29770081-29770131	HNPCEpiC	eye:	n/a
6	chr18:29770081-29770131	CMK	blood:	n/a
7	chr18:29769853-29769903	GM19239	blood:	n/a
8	chr18:29847791-29847841	Jurkat	blood:	n/a
9	chr18:29847791-29847841	SK-N-SH	brain:	n/a
10	chr18:29769853-29769903	PFSK-1	brain:	n/a
11	chr18:29769853-29769903	HPAEpiC	pulmonary alveolar:	n/a
12	chr18:29769853-29769903	Hepatocyte	liver:	n/a
13	chr18:29769853-29769903	HUVEC	blood vessel:	n/a
14	chr18:29847791-29847841	NT2-D1	testis:	n/a
15	chr18:29847791-29847841	BJ	skin:	n/a
16	chr18:29769853-29769903	BE2_C	brain:	n/a
17	chr18:29770081-29770131	HCPEpiC	choroid plexus:	n/a
18	chr18:29769853-29769903	SKMC	muscle:	n/a
19	chr18:29847791-29847841	SK-N-SH_RA	brain:	n/a
20	chr18:29847791-29847841	ProgFib	skin:	n/a
21	chr18:29770081-29770131	HMEC	breast:	n/a
22	chr18:29770081-29770131	HUVEC	blood vessel:	n/a
23	chr18:29769853-29769903	ECC-1	luminal epithelium:	n/a
24	chr18:29847791-29847841	SAEC	small airway:	n/a
25	chr18:29769532-29769582	GM06990	blood:	n/a
26	chr18:29847791-29847841	HAEpiC	amniotic membrane:	n/a
27	chr18:29769853-29769903	HAEpiC	amniotic membrane:	n/a
28	chr18:29770081-29770131	Hepatocyte	liver:	n/a
29	chr18:29770081-29770131	Hela-S3	cervix:	n/a
30	chr18:29847791-29847841	HRPEpiC	eye:	n/a
31	chr18:29770081-29770131	NB4	blood:	n/a
32	chr18:29847791-29847841	Hepatocyte	liver:	n/a
33	chr18:29769532-29769582	Jurkat	blood:	n/a
34	chr18:29847791-29847841	SK-N-MC	brain:	n/a
35	chr18:29770081-29770131	Caco-2	colon:	n/a
36	chr18:29770081-29770131	BE2_C	brain:	n/a
37	chr18:29769532-29769582	SK-N-SH	brain:	n/a
38	chr18:29847791-29847841	H1-hESC	embryonic stem cell:	embryo
39	chr18:29769853-29769903	A549	lung:	n/a
40	chr18:29769853-29769903	LNCaP	prostate:	n/a
41	chr18:29769853-29769903	K562	blood:	n/a
42	chr18:29769853-29769903	HRPEpiC	eye:	n/a
43	chr18:29847791-29847841	AG04450	lung:	fetal
44	chr18:29847791-29847841	Hela-S3	cervix:	n/a
45	chr18:29770081-29770131	HRPEpiC	eye:	n/a
46	chr18:29847791-29847841	GM19239	blood:	n/a
47	chr18:29770081-29770131	HCF	heart:	n/a
48	chr18:29769853-29769903	CMK	blood:	n/a
49	chr18:29770081-29770131	GM12878	blood:	n/a
50	chr18:29847791-29847841	HRE	kidney:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:29868718..29871349-chr18:30049265..30052223,3	MCF-7	breast:
2	chr18:29843865..29846147-chr18:30049369..30051018,2	MCF-7	breast:
3	chr18:29851628..29852386-chr18:30132192..30133063,2	MCF-7	breast:
4	chr18:29891994..29893877-chr18:29897571..29900006,2	MCF-7	breast:
5	chr18:29737731..29738647-chr18:30131030..30131759,2	MCF-7	breast:
6	chr18:29737793..29738341-chr18:30132122..30132837,2	MCF-7	breast:
7	chr18:29869308..29870117-chr18:30050651..30051625,5	MCF-7	breast:
8	chr18:29895037..29897248-chr18:29897872..29900366,2	K562	blood:
9	chr18:29869178..29870066-chr18:30128854..30129812,2	MCF-7	breast:
10	chr18:29895037..29897248-chr18:29897872..29900366,2	K562	blood:
11	chr18:29856972..29858473-chr18:30049654..30051815,2	MCF-7	breast:
12	chr18:29703952..29707950-chr18:29710554..29715618,4	K562	blood:
13	chr18:29851552..29852413-chr18:30132133..30133147,4	MCF-7	breast:
14	chr18:29737713..29738256-chr18:30129386..30129926,2	MCF-7	breast:
15	chr18:29737699..29739046-chr18:30132133..30133008,6	MCF-7	breast:
16	chr18:29737720..29738653-chr18:30132086..30132779,5	K562	blood:
17	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
18	chr18:29839871..29842778-chr18:29859077..29861521,2	K562	blood:
19	chr18:29746021..29748182-chr18:30119700..30121439,2	K562	blood:
20	chr18:29737738..29738425-chr18:30129431..30129978,2	MCF-7	breast:
21	chr18:29837235..29838765-chr18:29839489..29841604,2	MCF-7	breast:
22	chr18:29869293..29870126-chr18:30132476..30133178,2	MCF-7	breast:
23	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
24	chr18:29867305..29869453-chr18:30048858..30050694,2	MCF-7	breast:
25	chr18:29877540..29879536-chr18:29882707..29884848,2	MCF-7	breast:
26	chr18:29851159..29852631-chr18:30128814..30129900,6	MCF-7	breast:
27	chr18:29873261..29875337-chr18:30049350..30051070,2	MCF-7	breast:
28	chr18:29877540..29879536-chr18:29882707..29884848,2	MCF-7	breast:
29	chr18:29869255..29869847-chr18:30050643..30051337,3	MCF-7	breast:
30	chr18:29847813..29851392-chr18:29854747..29858581,3	MCF-7	breast:
31	chr18:29839871..29842778-chr18:29859077..29861521,2	K562	blood:
32	chr18:29852094..29854619-chr18:29865481..29868899,3	K562	blood:
33	chr18:29896360..29897935-chr18:29901825..29904220,2	K562	blood:
34	chr18:29703390..29707950-chr18:29711661..29715023,4	K562	blood:
35	chr18:29851409..29852190-chr18:30050752..30051380,2	MCF-7	breast:
36	chr18:29851378..29852356-chr18:30050569..30051553,4	MCF-7	breast:
37	chr18:29671851..29673627-chr18:29753995..29756065,2	MCF-7	breast:
38	chr18:29887452..29890348-chr18:30046410..30049276,2	MCF-7	breast:
39	chr18:29714493..29716790-chr18:29718511..29720452,2	K562	blood:
40	chr18:29671748..29674149-chr18:29717324..29719515,2	K562	blood:
41	chr18:29891994..29893877-chr18:29897571..29900006,2	MCF-7	breast:
42	chr11:122010055..122011576-chr18:29727676..29729176,2	MCF-7	breast:
43	chr18:29854965..29857562-chr18:29891190..29893119,2	K562	blood:
44	chr18:29714493..29716790-chr18:29718511..29720452,2	K562	blood:
45	chr18:29837235..29838765-chr18:29839489..29841604,2	MCF-7	breast:
46	chr18:29777158..29779490-chr18:29781970..29783984,2	MCF-7	breast:
47	chr18:29854965..29857562-chr18:29891190..29893119,2	K562	blood:
48	chr18:29847813..29851392-chr18:29854747..29858581,3	MCF-7	breast:
49	chr18:29851742..29852316-chr18:30263045..30263644,2	MCF-7	breast:
50	chr18:29777158..29779490-chr18:29781970..29783984,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEP1B-3	chr18:29898404-29898738	NONHSAT058862
2	lnc-FAM59A-1	chr18:29828719-29828995	ENSG00000263904.1
3	lnc-MEP1B-3	chr18:29891709-29891919	NONHSAT058862
4	lnc-FAM59A-1	chr18:29825909-29826099	ENSG00000263904.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM59A	hsa-miR-186-5p	chr18:29843701-29843695

Variant related genes	Relation type
RNA5SP453	TF binding region
ENSG00000265279	TF binding region
ENSG00000263904	TF binding region
GAREM	TF binding region
ENSG00000222395	TF binding region
MEP1B	TF binding region
ENSG00000264982	TF binding region
RNA5SP453	CpG island
ENSG00000265279	CpG island
ENSG00000263904	CpG island
GAREM	CpG island
ENSG00000222395	CpG island
MEP1B	CpG island
ENSG00000264982	CpG island
ENSG00000265008	chromatin interactions
ENSG00000264982	chromatin interactions
ENSG00000263393	chromatin interactions
ENSG00000141441	chromatin interactions
ENSG00000134758	chromatin interactions

Extended variants
information (count: 5825 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:5825 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140085127	chr18:29711986-29711987	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs12965536	chr18:29712119-29712120	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs193299260	chr18:29712156-29712157	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs8094028	chr18:29712171-29712172	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs185126134	chr18:29712186-29712187	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs76729610	chr18:29712192-29712193	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189066792	chr18:29712290-29712291	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552231339	chr18:29712301-29712302	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570423358	chr18:29712326-29712327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs79312438	chr18:29712341-29712342	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557233335	chr18:29712355-29712356	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs76325464	chr18:29712358-29712359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536537657	chr18:29712426-29712427	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554576641	chr18:29712438-29712439	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs3980845	chr18:29712450-29712451	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572879547	chr18:29712460-29712461	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs3980846	chr18:29712504-29712505	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs1895623	chr18:29712505-29712506	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs4399611	chr18:29712527-29712528	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs577226606	chr18:29712554-29712555	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs62095574	chr18:29712569-29712570	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs548355370	chr18:29712570-29712571	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs35364812	chr18:29712571-29712572	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75033834	chr18:29712572-29712573	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs544397497	chr18:29712600-29712601	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs143989162	chr18:29712633-29712634	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530058241	chr18:29712703-29712704	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561081941	chr18:29712710-29712711	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs548488579	chr18:29712751-29712752	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs528595940	chr18:29712752-29712753	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs527305876	chr18:29712754-29712755	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs551856298	chr18:29712763-29712764	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540298018	chr18:29712831-29712832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs3980847	chr18:29712851-29712852	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570539514	chr18:29712856-29712857	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537499674	chr18:29712902-29712903	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191580851	chr18:29712916-29712917	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs147336575	chr18:29712928-29712929	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536574754	chr18:29712940-29712941	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs117988689	chr18:29712997-29712998	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs573165839	chr18:29713016-29713017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs534207188	chr18:29713042-29713043	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184062662	chr18:29713049-29713050	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs632468	chr18:29713095-29713096	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs200330916	chr18:29713107-29713108	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577313391	chr18:29713108-29713109	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs635978	chr18:29713118-29713119	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544371908	chr18:29713146-29713147	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368917274	chr18:29713149-29713150	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs562708068	chr18:29713168-29713169	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	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
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29673400-29713800	Weak transcription	Spleen	Spleen
2	chr18:29673800-29714000	Weak transcription	Esophagus	oesophagus
3	chr18:29673800-29714200	Weak transcription	Ovary	ovary
4	chr18:29673800-29715200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr18:29673800-29715200	Weak transcription	Lung	lung
6	chr18:29673800-29715800	Weak transcription	Colonic Mucosa	Colon
7	chr18:29673800-29717000	Weak transcription	HSMMtube	muscle
8	chr18:29674000-29712000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr18:29675000-29717200	Weak transcription	NH-A	brain
10	chr18:29676800-29717200	Weak transcription	Brain Germinal Matrix	brain
11	chr18:29677000-29713800	Weak transcription	Small Intestine	intestine
12	chr18:29677000-29715600	Weak transcription	Fetal Heart	heart
13	chr18:29677000-29717000	Weak transcription	Aorta	Aorta
14	chr18:29687200-29713600	Strong transcription	Dnd41	blood
15	chr18:29688200-29712400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:29689400-29713600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr18:29689800-29713200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr18:29691000-29712400	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr18:29691000-29712600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr18:29691200-29713600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr18:29691400-29715000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr18:29691600-29713000	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr18:29691800-29712400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:29695200-29713200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr18:29695800-29715200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr18:29695800-29717600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr18:29696800-29712000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr18:29697000-29714200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr18:29699600-29715400	Weak transcription	Left Ventricle	heart
30	chr18:29701000-29712400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr18:29701800-29712400	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr18:29702200-29712200	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr18:29702200-29712200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr18:29702200-29712400	Strong transcription	Liver	Liver
35	chr18:29702200-29712600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr18:29702200-29713600	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr18:29702400-29712400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr18:29702800-29712400	Strong transcription	Primary hematopoietic stem cells	blood
39	chr18:29702800-29712400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr18:29703200-29712400	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr18:29704000-29712200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr18:29704000-29713600	Strong transcription	Primary B cells from cord blood	blood
43	chr18:29704200-29714600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr18:29705400-29713800	Weak transcription	Brain Anterior Caudate	brain
45	chr18:29705400-29714000	Weak transcription	Brain Hippocampus Middle	brain
46	chr18:29705400-29714200	Weak transcription	HUVEC	blood vessel
47	chr18:29705400-29715400	Weak transcription	Fetal Kidney	kidney
48	chr18:29705400-29716400	Weak transcription	Stomach Smooth Muscle	stomach
49	chr18:29705400-29717800	Weak transcription	A549	lung
50	chr18:29705600-29713800	Weak transcription	Skeletal Muscle Male	skeletal muscle

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