Variant report

Variant	nsv1060428
Chromosome Location	chr18:252297-322289
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	chr18:268051-268209	K562	blood:	n/a	n/a
2	ARID3A	chr18:286488-286736	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:267953-268346	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:269422-269886	HepG2	liver:	n/a	n/a
5	ATF1	chr18:267856-268252	K562	blood:	n/a	n/a
6	ATF2	chr18:267573-268458	GM12878	blood:	n/a	n/a
7	ATF2	chr18:267806-268299	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr18:267857-268299	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr18:267677-268450	GM12878	blood:	n/a	n/a
10	ATF3	chr18:267842-268358	GM12878	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
11	ATF3	chr18:267910-268154	H1-hESC	embryonic stem cell:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
12	ATF3	chr18:267854-268179	HepG2	liver:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
13	ATF3	chr18:267904-268183	GM12878	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
14	ATF3	chr18:267819-268244	K562	blood:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
15	ATF3	chr18:267636-268296	H1-hESC	embryonic stem cell:	n/a	chr18:268062-268075 chr18:268064-268072 chr18:268065-268072 chr18:268061-268076 chr18:268062-268075 chr18:268062-268072 chr18:268061-268074 chr18:268062-268072 chr18:268053-268073 chr18:268061-268072 chr18:268062-268073
16	BACH1	chr18:267979-268355	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr18:267919-268509	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:267902-268405	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
19	BCL3	chr18:267887-268393	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
20	BCL3	chr18:267793-268331	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
21	BCL3	chr18:267839-268276	A549	lung:	n/a	chr18:268153-268162 chr18:268049-268062
22	BCLAF1	chr18:267804-269077	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
23	BCLAF1	chr18:267773-268502	GM12878	blood:	n/a	chr18:268153-268162 chr18:268049-268062
24	BHLHE40	chr18:267842-268511	GM12878	blood:	n/a	chr18:268046-268062 chr18:268047-268063
25	BHLHE40	chr18:268183-268376	A549	lung:	n/a	n/a
26	BHLHE40	chr18:302234-302299	K562	blood:	n/a	n/a
27	BHLHE40	chr18:267852-268323	HepG2	liver:	n/a	chr18:268046-268062 chr18:268047-268063
28	BHLHE40	chr18:267862-268321	K562	blood:	n/a	chr18:268046-268062 chr18:268047-268063
29	BRCA1	chr18:267916-268222	HepG2	liver:	n/a	n/a
30	BRCA1	chr18:267927-268244	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr18:267974-268246	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr18:268653-269146	K562	blood:	n/a	n/a
33	CBX3	chr18:267877-268270	K562	blood:	n/a	n/a
34	CBX3	chr18:267701-268641	K562	blood:	n/a	n/a
35	CBX3	chr18:271857-272187	K562	blood:	n/a	n/a
36	CCNT2	chr18:306762-306890	K562	blood:	n/a	n/a
37	CCNT2	chr18:267628-268513	K562	blood:	n/a	n/a
38	CEBPB	chr18:267829-268561	GM12878	blood:	n/a	n/a
39	CEBPB	chr18:267818-268289	K562	blood:	n/a	n/a
40	CEBPB	chr18:268092-268184	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr18:269678-269795	K562	blood:	n/a	n/a
42	CEBPB	chr18:269538-269869	K562	blood:	n/a	n/a
43	CEBPD	chr18:306669-307002	K562	blood:	n/a	n/a
44	CEBPD	chr18:267595-268288	HepG2	liver:	n/a	n/a
45	CEBPD	chr18:267772-268726	K562	blood:	n/a	n/a
46	CHD1	chr18:267960-268495	GM12878	blood:	n/a	chr18:268135-268145
47	CHD1	chr18:268180-268771	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr18:267987-268408	K562	blood:	n/a	chr18:268135-268145
49	CHD2	chr18:267821-268371	H1-hESC	embryonic stem cell:	n/a	chr18:268135-268145
50	CHD2	chr18:308135-308422	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:319786-319836	GM12891	blood:	n/a
2	chr18:268031-268081	GM19239	blood:	n/a
3	chr18:268601-268651	NHBE	bronchial:	n/a
4	chr18:267711-267761	HRCEpiC	kidney:	n/a
5	chr18:268068-268118	AoSMC	blood vessel:	n/a
6	chr18:268184-268234	PFSK-1	brain:	n/a
7	chr18:271673-271723	HCF	heart:	n/a
8	chr18:264576-264626	PrEC	prostate:	n/a
9	chr18:268131-268181	A549	lung:	n/a
10	chr18:268166-268216	PANC-1	pancreas:	n/a
11	chr18:268068-268118	HIPEpiC	eye:	n/a
12	chr18:268381-268431	ProgFib	skin:	n/a
13	chr18:268068-268118	HNPCEpiC	eye:	n/a
14	chr18:271673-271723	BJ	skin:	n/a
15	chr18:268256-268306	LNCaP	prostate:	n/a
16	chr18:268601-268651	HCPEpiC	choroid plexus:	n/a
17	chr18:264576-264626	MCF10A-Er-Src	breast:	n/a
18	chr18:268068-268118	NHBE	bronchial:	n/a
19	chr18:268256-268306	BJ	skin:	n/a
20	chr18:268601-268651	HCT-116	colon:	n/a
21	chr18:319786-319836	HRE	kidney:	n/a
22	chr18:268381-268431	HEK293	kidney:	embryo
23	chr18:271673-271723	K562	blood:	n/a
24	chr18:268256-268306	NHDF-neo	bronchial:	n/a
25	chr18:268131-268181	PrEC	prostate:	n/a
26	chr18:268184-268234	AG09309	skin:	n/a
27	chr18:268131-268181	HIPEpiC	eye:	n/a
28	chr18:268381-268431	HMEC	breast:	n/a
29	chr18:268131-268181	GM06990	blood:	n/a
30	chr18:268131-268181	AG04449	skin:	fetal
31	chr18:268278-268328	AG09319	gingival:	n/a
32	chr18:319786-319836	Jurkat	blood:	n/a
33	chr18:268601-268651	HL-60	blood:	n/a
34	chr18:268166-268216	K562	blood:	n/a
35	chr18:268278-268328	HRPEpiC	eye:	n/a
36	chr18:268278-268328	PANC-1	pancreas:	n/a
37	chr18:264576-264626	HRE	kidney:	n/a
38	chr18:267637-267687	HCT-116	colon:	n/a
39	chr18:268135-268185	SKMC	muscle:	n/a
40	chr18:268256-268306	GM19239	blood:	n/a
41	chr18:268278-268328	HMEC	breast:	n/a
42	chr18:267711-267761	HCM	heart:	n/a
43	chr18:268135-268185	GM12892	blood:	n/a
44	chr18:319786-319836	Caco-2	colon:	n/a
45	chr18:271673-271723	ProgFib	skin:	n/a
46	chr18:267637-267687	HL-60	blood:	n/a
47	chr18:264576-264626	AG09309	skin:	n/a
48	chr18:268166-268216	AG10803	skin:	n/a
49	chr18:268131-268181	PFSK-1	brain:	n/a
50	chr18:268131-268181	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:251595..253868-chr18:269090..271217,2	K562	blood:
2	chr18:273600..276346-chr18:278461..281773,3	MCF-7	breast:
3	chr18:302419..306527-chr18:308522..311824,4	K562	blood:
4	chr18:258780..260589-chr18:262458..263959,2	MCF-7	breast:
5	chr18:286191..286695-chr18:468859..469735,2	MCF-7	breast:
6	chr18:263619..266135-chr18:272357..275080,2	MCF-7	breast:
7	chr18:269547..271961-chr18:280130..281760,2	K562	blood:
8	chr18:295698..298491-chr18:306221..309182,2	MCF-7	breast:
9	chr18:240829..243989-chr18:256150..258223,3	K562	blood:
10	chr18:305775..308691-chr18:309654..313982,3	K562	blood:
11	chr18:257542..263185-chr18:266000..270349,8	MCF-7	breast:
12	chr18:267452..268053-chr9:134269416..134270075,2	Hela-S3	cervix:
13	chr18:248314..250346-chr18:271820..273799,2	K562	blood:
14	chr18:229127..231742-chr18:269257..272237,2	K562	blood:
15	chr18:224129..226932-chr18:263404..265975,2	K562	blood:
16	chr18:158336..160794-chr18:268769..270393,2	K562	blood:
17	chr18:250843..253350-chr18:266351..269442,3	MCF-7	breast:
18	chr18:294145..296995-chr18:298267..301076,2	K562	blood:
19	chr18:273825..276341-chr18:276906..279543,2	K562	blood:
20	chr18:273687..277951-chr18:283700..285982,3	K562	blood:
21	chr18:277729..280050-chr18:615244..618128,2	MCF-7	breast:
22	chr18:254095..260758-chr18:263922..270842,11	K562	blood:
23	chr18:157295..159730-chr18:266988..268701,2	MCF-7	breast:
24	chr18:286089..286649-chr18:19535847..19536611,2	K562	blood:
25	chr18:286401..287237-chr18:477304..478254,5	MCF-7	breast:
26	chr18:267932..269522-chr18:657904..660311,2	K562	blood:
27	chr18:269653..272578-chr18:297355..299675,2	K562	blood:
28	chr18:292073..293974-chr18:294604..297450,2	K562	blood:
29	chr18:250566..253483-chr18:259670..262820,3	K562	blood:
30	chr18:257542..263185-chr18:266000..270349,8	MCF-7	breast:
31	chr18:266762..268550-chr18:321925..324261,2	K562	blood:
32	chr18:273825..276341-chr18:276906..279543,2	K562	blood:
33	chr18:267782..268602-chr2:228189553..228190377,2	Hela-S3	cervix:
34	chr18:249334..252987-chr18:265974..268103,4	MCF-7	breast:
35	chr18:286219..287016-chr18:477377..477880,2	MCF-7	breast:
36	chr18:286140..286815-chr18:616539..617291,2	MCF-7	breast:
37	chr18:293551..294215-chr18:616120..617138,3	MCF-7	breast:
38	chr18:254095..260758-chr18:263922..270842,11	K562	blood:
39	chr18:266563..269513-chr18:596555..599263,2	K562	blood:
40	chr18:158012..160007-chr18:265808..268303,2	MCF-7	breast:
41	chr18:253259..255595-chr18:265697..268644,2	K562	blood:
42	chr18:250537..252163-chr18:257039..259067,2	MCF-7	breast:
43	chr18:250843..253350-chr18:266351..269442,3	MCF-7	breast:
44	chr18:273687..277951-chr18:283700..285982,3	K562	blood:
45	chr18:251747..253552-chr18:262672..265291,2	K562	blood:
46	chr18:305775..308691-chr18:309654..313982,3	K562	blood:
47	chr18:293279..294017-chr18:477353..478290,2	MCF-7	breast:
48	chr18:269653..272578-chr18:297355..299675,2	K562	blood:
49	chr18:264152..266955-chr18:267576..271730,4	MCF-7	breast:
50	chr18:272315..274100-chr18:321177..323834,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP14-4	chr18:317866-318033	XLOC_012601
2	lnc-COLEC12-1	chr18:317099-317366	ENSG00000264433.1
3	lnc-USP14-4	chr18:314887-317129	XLOC_012601
4	lnc-USP14-4	chr18:318868-319165	ENSG00000264514.1
5	lnc-USP14-4	chr18:316737-316986	ENSG00000264514.1
6	lnc-USP14-6	chr18:270815-271054	NONHSAT056835
7	lnc-USP14-3	chr18:268148-270278	ENSG00000263884.1
8	lnc-COLEC12-1	chr18:316740-316963	ENSG00000264433.1
9	lnc-COLEC12-6	chr18:253324-253897	expReg_chr18_62_-

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

Variant related genes	Relation type
THOC1	TF binding region
ENSG00000264433	TF binding region
ENSG00000264514	TF binding region
ENSG00000263884	TF binding region
THOC1	CpG island
ENSG00000264433	CpG island
ENSG00000264514	CpG island
ENSG00000263884	CpG island
ENSG00000079134	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000130723	chromatin interactions
ENSG00000101557	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000263006	chromatin interactions
ENSG00000263884	chromatin interactions
ENSG00000168958	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000132199	chromatin interactions
ENSG00000236432	chromatin interactions
ENSG00000202408	chromatin interactions

Extended variants
information (count: 2445 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529491141	chr18:252322-252323	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs536769662	chr18:252347-252348	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs77154435	chr18:252436-252437	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573337903	chr18:252456-252457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs57133883	chr18:252472-252473	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs367587767	chr18:252486-252487	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540618016	chr18:252490-252491	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs370337805	chr18:252495-252496	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559649195	chr18:252506-252507	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs577864076	chr18:252510-252511	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374306142	chr18:252517-252518	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368194949	chr18:252519-252520	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs657138	chr18:252559-252560	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs563042825	chr18:252571-252572	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374729355	chr18:252598-252599	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs370978327	chr18:252629-252630	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368793737	chr18:252634-252635	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530696555	chr18:252655-252656	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550331973	chr18:252710-252711	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531307104	chr18:252761-252762	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs529352604	chr18:252763-252764	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs185499768	chr18:252769-252770	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs199766127	chr18:252770-252771	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs149696032	chr18:252778-252779	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs375981567	chr18:252787-252788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs16977200	chr18:252795-252796	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552020718	chr18:252842-252843	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371754738	chr18:252891-252892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533847789	chr18:252893-252894	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs202147876	chr18:252925-252926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs189816034	chr18:252970-252971	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72856271	chr18:252998-252999	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs567457254	chr18:253043-253044	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534668704	chr18:253058-253059	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552702915	chr18:253103-253104	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577533151	chr18:253104-253105	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs544997430	chr18:253129-253130	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs563558655	chr18:253139-253140	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182610220	chr18:253216-253217	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs563245746	chr18:253252-253253	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187299682	chr18:253265-253266	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147821753	chr18:253305-253306	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs547831999	chr18:253311-253312	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs559507374	chr18:253321-253322	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs533336086	chr18:253334-253335	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs143774226	chr18:253336-253337	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs570006241	chr18:253376-253377	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs537296711	chr18:253416-253417	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs9946523	chr18:253506-253507	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs192145786	chr18:253578-253579	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	21865298	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:212000-256400	Weak transcription	Gastric	stomach
2	chr18:218000-267400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:218600-261400	Weak transcription	Pancreas	Pancrea
4	chr18:218600-267200	Weak transcription	Stomach Mucosa	stomach
5	chr18:219000-267200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr18:219000-267200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr18:225200-254600	Weak transcription	Right Ventricle	heart
8	chr18:238000-265800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr18:238000-266200	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr18:238200-265000	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr18:238400-265800	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr18:239600-258200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr18:239600-265200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr18:239600-265200	Strong transcription	Liver	Liver
15	chr18:239800-265800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr18:240000-265200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr18:240200-265200	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr18:240200-265200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr18:240200-265400	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr18:240600-255400	Weak transcription	Fetal Heart	heart
21	chr18:240600-258600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr18:240600-266200	Strong transcription	Primary B cells from cord blood	blood
23	chr18:241000-260800	Strong transcription	Primary B cells from peripheral blood	blood
24	chr18:241200-253400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr18:241200-265400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr18:241400-259800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr18:241600-255000	Weak transcription	Spleen	Spleen
28	chr18:241600-259400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr18:241600-261400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr18:241600-265600	Strong transcription	Fetal Thymus	thymus
31	chr18:242600-260000	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr18:243000-262200	Strong transcription	HepG2	liver
33	chr18:243200-265600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr18:243600-265000	Strong transcription	Adipose Nuclei	Adipose
35	chr18:243800-262000	Strong transcription	HSMM	muscle
36	chr18:243800-265600	Strong transcription	Fetal Intestine Large	intestine
37	chr18:244200-260400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr18:244200-265600	Strong transcription	Dnd41	blood
39	chr18:244400-259800	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr18:244400-259800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr18:244400-265000	Strong transcription	Rectal Mucosa Donor 29	rectum
42	chr18:244400-265400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr18:244400-265400	Strong transcription	Placenta	Placenta
44	chr18:244600-253400	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr18:244600-257400	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr18:244600-265000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr18:245000-265800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr18:245200-253000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr18:245200-265800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr18:245400-266200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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