Variant report

Variant	nsv598960
Chromosome Location	chr5:94975592-94988482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1180)
CpG islands
(count:857)
Chromatin interactive
region (count:43)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1180 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:94985110-94986146	K562	blood:	n/a	n/a
2	ARID3A	chr5:94977503-94977803	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:94980021-94980333	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:94982140-94982992	K562	blood:	n/a	n/a
5	ARID3A	chr5:94982148-94983083	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:94983416-94984826	K562	blood:	n/a	n/a
7	ARID3A	chr5:94980090-94980576	K562	blood:	n/a	n/a
8	ATF1	chr5:94982279-94983087	K562	blood:	n/a	n/a
9	ATF1	chr5:94983551-94983924	K562	blood:	n/a	n/a
10	ATF2	chr5:94982321-94982928	GM12878	blood:	n/a	n/a
11	ATF3	chr5:94982217-94982685	H1-hESC	embryonic stem cell:	n/a	chr5:94982545-94982554 chr5:94982399-94982408 chr5:94982612-94982621 chr5:94982435-94982444
12	ATF3	chr5:94983525-94983881	K562	blood:	n/a	n/a
13	ATF3	chr5:94982142-94982818	GM12878	blood:	n/a	chr5:94982545-94982554 chr5:94982399-94982408 chr5:94982612-94982621 chr5:94982435-94982444
14	ATF3	chr5:94982248-94982626	K562	blood:	n/a	chr5:94982545-94982554 chr5:94982399-94982408 chr5:94982612-94982621 chr5:94982435-94982444
15	BACH1	chr5:94983079-94983271	K562	blood:	n/a	n/a
16	BACH1	chr5:94982258-94982653	K562	blood:	n/a	n/a
17	BACH1	chr5:94982357-94982795	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:94987688-94987825	K562	blood:	n/a	n/a
19	BACH1	chr5:94983513-94984025	K562	blood:	n/a	n/a
20	BCL3	chr5:94982469-94983201	A549	lung:	n/a	chr5:94982617-94982630 chr5:94982576-94982589 chr5:94982849-94982862 chr5:94982616-94982629
21	BCL3	chr5:94982327-94982778	GM12878	blood:	n/a	chr5:94982617-94982630 chr5:94982576-94982589 chr5:94982616-94982629
22	BCL3	chr5:94982173-94982997	A549	lung:	n/a	chr5:94982617-94982630 chr5:94982576-94982589 chr5:94982849-94982862 chr5:94982616-94982629
23	BCLAF1	chr5:94982264-94983085	K562	blood:	n/a	chr5:94982617-94982630 chr5:94982576-94982589 chr5:94982849-94982862 chr5:94982616-94982629
24	BCLAF1	chr5:94983451-94984026	K562	blood:	n/a	chr5:94983658-94983667
25	BCLAF1	chr5:94983403-94984610	K562	blood:	n/a	chr5:94984181-94984190 chr5:94983658-94983667
26	BCLAF1	chr5:94982176-94982931	GM12878	blood:	n/a	chr5:94982617-94982630 chr5:94982576-94982589 chr5:94982849-94982862 chr5:94982616-94982629
27	BCLAF1	chr5:94982352-94982759	GM12878	blood:	n/a	chr5:94982617-94982630 chr5:94982576-94982589 chr5:94982616-94982629
28	BHLHE40	chr5:94983660-94983864	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:94982176-94983153	K562	blood:	n/a	chr5:94982619-94982635
30	BHLHE40	chr5:94983474-94984400	K562	blood:	n/a	n/a
31	BHLHE40	chr5:94982275-94982982	A549	lung:	n/a	chr5:94982619-94982635
32	BHLHE40	chr5:94982230-94983133	GM12878	blood:	n/a	chr5:94982619-94982635
33	BHLHE40	chr5:94982173-94983079	HepG2	liver:	n/a	chr5:94982619-94982635
34	BHLHE40	chr5:94979973-94980443	K562	blood:	n/a	n/a
35	BHLHE40	chr5:94982274-94982673	HepG2	liver:	n/a	chr5:94982619-94982635
36	BHLHE40	chr5:94981335-94981503	K562	blood:	n/a	n/a
37	BRCA1	chr5:94982452-94982499	HepG2	liver:	n/a	n/a
38	BRCA1	chr5:94982680-94982683	GM12878	blood:	n/a	n/a
39	BRCA1	chr5:94983133-94983217	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr5:94982313-94982835	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr5:94983398-94983904	K562	blood:	n/a	n/a
42	CBX3	chr5:94982051-94982441	K562	blood:	n/a	n/a
43	CBX3	chr5:94981910-94983105	K562	blood:	n/a	n/a
44	CCNT2	chr5:94984230-94984498	K562	blood:	n/a	n/a
45	CCNT2	chr5:94983612-94983909	K562	blood:	n/a	n/a
46	CCNT2	chr5:94982149-94982992	K562	blood:	n/a	chr5:94982435-94982444
47	CEBPB	chr5:94986799-94987122	K562	blood:	n/a	chr5:94986976-94986987 chr5:94986921-94986934 chr5:94986975-94986988
48	CEBPB	chr5:94982863-94983860	K562	blood:	n/a	n/a
49	CEBPB	chr5:94982771-94984560	K562	blood:	n/a	n/a
50	CEBPB	chr5:94982191-94983307	Hela-S3	cervix:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:94982715-94982765	GM12878	blood:	n/a
2	chr5:94980227-94980277	AoSMC	blood vessel:	n/a
3	chr5:94982685-94982735	AG04450	lung:	fetal
4	chr5:94982715-94982765	GM12878	blood:	n/a
5	chr5:94980227-94980277	AoSMC	blood vessel:	n/a
6	chr5:94982685-94982735	AG04450	lung:	fetal
7	chr5:94983049-94983099	PANC-1	pancreas:	n/a
8	chr5:94982375-94982425	GM06990	blood:	n/a
9	chr5:94982558-94982608	HRE	kidney:	n/a
10	chr5:94980227-94980277	U87	brain:	n/a
11	chr5:94982404-94982454	HAEpiC	amniotic membrane:	n/a
12	chr5:94982715-94982765	HNPCEpiC	eye:	n/a
13	chr5:94982685-94982735	HCM	heart:	n/a
14	chr5:94982404-94982454	HEEpiC	esophagus:	n/a
15	chr5:94983049-94983099	K562	blood:	n/a
16	chr5:94982404-94982454	Jurkat	blood:	n/a
17	chr5:94982427-94982477	AG09309	skin:	n/a
18	chr5:94982330-94982380	AoSMC	blood vessel:	n/a
19	chr5:94982427-94982477	AG04450	lung:	fetal
20	chr5:94983049-94983099	ECC-1	luminal epithelium:	n/a
21	chr5:94982163-94982213	PANC-1	pancreas:	n/a
22	chr5:94982558-94982608	RPTEC	kidney:	n/a
23	chr5:94980227-94980277	GM19239	blood:	n/a
24	chr5:94982427-94982477	NB4	blood:	n/a
25	chr5:94982715-94982765	Jurkat	blood:	n/a
26	chr5:94986485-94986535	AG10803	skin:	n/a
27	chr5:94982685-94982735	GM19239	blood:	n/a
28	chr5:94982715-94982765	NH-A	brain:	n/a
29	chr5:94982433-94982483	GM12892	blood:	n/a
30	chr5:94982558-94982608	HNPCEpiC	eye:	n/a
31	chr5:94982404-94982454	CMK	blood:	n/a
32	chr5:94982163-94982213	AG09309	skin:	n/a
33	chr5:94982685-94982735	AG10803	skin:	n/a
34	chr5:94982211-94982261	AoSMC	blood vessel:	n/a
35	chr5:94982163-94982213	SK-N-SH_RA	brain:	n/a
36	chr5:94982375-94982425	AoSMC	blood vessel:	n/a
37	chr5:94982330-94982380	T-47D	breast:	n/a
38	chr5:94982211-94982261	IMR90	lung:	fetal
39	chr5:94982558-94982608	U87	brain:	n/a
40	chr5:94980227-94980277	NH-A	brain:	n/a
41	chr5:94982715-94982765	HCF	heart:	n/a
42	chr5:94983049-94983099	NHDF-neo	bronchial:	n/a
43	chr5:94982433-94982483	RPTEC	kidney:	n/a
44	chr5:94980227-94980277	Caco-2	colon:	n/a
45	chr5:94982427-94982477	HCM	heart:	n/a
46	chr5:94980227-94980277	HL-60	blood:	n/a
47	chr5:94982715-94982765	GM06990	blood:	n/a
48	chr5:94982161-94982211	GM12878	blood:	n/a
49	chr5:94982685-94982735	NT2-D1	testis:	n/a
50	chr5:94982211-94982261	BJ	skin:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:94979759..94980687-chr5:95182790..95183359,3	MCF-7	breast:
2	chr5:94982379..94987076-chr5:95045372..95049493,6	K562	blood:
3	chr5:94977888..94979962-chr5:95065955..95067662,2	K562	blood:
4	chr5:94979687..94980466-chr5:95178591..95179270,3	K562	blood:
5	chr5:94979518..94982436-chr5:95080869..95082973,2	K562	blood:
6	chr5:94980020..94983633-chr5:95104411..95107623,3	K562	blood:
7	chr5:94890034..94891866-chr5:94974819..94976778,2	MCF-7	breast:
8	chr5:90676216..90679010-chr5:94981409..94984145,2	K562	blood:
9	chr5:94889492..94895025-chr5:94981557..94985063,8	K562	blood:
10	chr5:94981172..94985318-chr5:95169805..95176246,5	MCF-7	breast:
11	chr5:94984590..94987808-chr5:95181177..95184579,4	K562	blood:
12	chr5:94979766..94982277-chr5:95116115..95117894,2	MCF-7	breast:
13	chr5:94979878..94983810-chr5:95295717..95298674,4	K562	blood:
14	chr5:94978656..94980473-chr5:94982284..94983873,2	MCF-7	breast:
15	chr5:94981556..94984192-chr5:95101303..95104225,2	MCF-7	breast:
16	chr5:94978554..94980153-chr5:95176537..95179055,2	MCF-7	breast:
17	chr5:94980151..94980688-chr5:95116443..95117184,2	K562	blood:
18	chr5:94977116..95012475-chr5:95055682..95079552,215	K562	blood:
19	chr5:94890206..94891833-chr5:94987250..94989208,2	K562	blood:
20	chr5:94979741..94980745-chr5:95182392..95183367,12	K562	blood:
21	chr5:94985857..94987927-chr5:95082839..95085135,3	K562	blood:
22	chr5:94980512..95018354-chr5:95057997..95080764,228	K562	blood:
23	chr5:94978692..94981484-chr5:95178419..95181281,2	MCF-7	breast:
24	chr5:94890837..94891363-chr5:94979846..94980667,2	MCF-7	breast:
25	chr5:94981287..94984175-chr5:95296229..95298674,3	K562	blood:
26	chr5:94980861..94985410-chr5:95067178..95071099,5	MCF-7	breast:
27	chr5:94979527..94980403-chr5:95178510..95179271,2	MCF-7	breast:
28	chr5:94979775..94980600-chr5:95178574..95179492,2	MCF-7	breast:
29	chr5:94893117..94894866-chr5:94974664..94977618,2	K562	blood:
30	chr5:94981340..94984731-chr5:95103817..95108133,4	K562	blood:
31	chr5:94979432..94984462-chr5:95062276..95069972,15	MCF-7	breast:
32	chr5:94974928..94977008-chr5:95297075..95299326,2	K562	blood:
33	chr5:94953878..94956024-chr5:94981084..94983825,2	K562	blood:
34	chr5:94985102..94989085-chr5:95082725..95085350,5	K562	blood:
35	chr5:94979988..94984168-chr5:95032454..95035928,4	MCF-7	breast:
36	chr5:94888891..94893786-chr5:94981389..94987516,11	K562	blood:
37	chr5:94984626..94986883-chr5:94989979..94992621,3	MCF-7	breast:
38	chr5:94967847..94971625-chr5:94973983..94977382,3	K562	blood:
39	chr5:94974397..94976527-chr5:94981927..94983725,2	K562	blood:
40	chr5:94981368..94988467-chr5:95046173..95051252,17	K562	blood:
41	chr5:94982383..94984588-chr5:95046353..95049787,5	MCF-7	breast:
42	chr5:94986771..94989176-chr5:94992934..94994549,2	MCF-7	breast:
43	chr5:94979762..94980497-chr5:95182499..95183331,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR150-1	chr5:94983749-94983778	NONHSAT102854
2	lnc-GPR150-1	chr5:94982481-94982521	NONHSAT102853
3	lnc-GPR150-1	chr5:94987841-94988567	NONHSAT102854
4	lnc-GPR150-1	chr5:94987841-94988519	NONHSAT102853

No data

Variant related genes	Relation type
RFESD	TF binding region
RFESD	CpG island
ENSG00000251000	chromatin interactions
ENSG00000175449	chromatin interactions
ENSG00000178015	chromatin interactions
ENSG00000198677	chromatin interactions
ENSG00000145757	chromatin interactions
ENSG00000250240	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000164291	chromatin interactions
ENSG00000251314	chromatin interactions
ENSG00000164292	chromatin interactions
ENSG00000118985	chromatin interactions
ENSG00000251348	chromatin interactions

Extended variants
information (count: 440 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6890832	chr5:94975592-94975593	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575109786	chr5:94975615-94975616	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs6890842	chr5:94975616-94975617	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs17211585	chr5:94975617-94975618	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs577514276	chr5:94975628-94975629	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs60323781	chr5:94975665-94975666	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs559838211	chr5:94975669-94975670	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs577078288	chr5:94975670-94975671	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs528471603	chr5:94975700-94975701	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs189391450	chr5:94975736-94975737	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs149367901	chr5:94975745-94975746	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs530684524	chr5:94975815-94975816	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs566471630	chr5:94975832-94975833	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs111960481	chr5:94975860-94975861	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs530758917	chr5:94975863-94975864	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs532971667	chr5:94975939-94975940	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs551923994	chr5:94975950-94975951	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs546283770	chr5:94976008-94976009	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs79209551	chr5:94976057-94976058	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs550496423	chr5:94976069-94976070	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs138172587	chr5:94976070-94976071	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs567590913	chr5:94976093-94976094	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs180926419	chr5:94976118-94976119	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs568779947	chr5:94976128-94976129	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs6892026	chr5:94976140-94976141	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs201919666	chr5:94976150-94976151	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs557693766	chr5:94976174-94976175	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs373889869	chr5:94976192-94976193	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs11952880	chr5:94976253-94976254	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs6865873	chr5:94976254-94976255	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs185588553	chr5:94976281-94976282	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs536116377	chr5:94976367-94976368	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs142775382	chr5:94976415-94976416	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs146150810	chr5:94976416-94976417	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs562086886	chr5:94976445-94976446	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs575239062	chr5:94976466-94976467	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs368264633	chr5:94976475-94976476	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs140206826	chr5:94976480-94976481	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs532961032	chr5:94976570-94976571	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs112578679	chr5:94976584-94976585	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs115925044	chr5:94976596-94976597	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs560102535	chr5:94976623-94976624	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs11747129	chr5:94976651-94976652	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548806263	chr5:94976673-94976674	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs568827925	chr5:94976750-94976751	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs141510893	chr5:94976770-94976771	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs190249702	chr5:94976786-94976787	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs60010299	chr5:94976955-94976956	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553405865	chr5:94976982-94976983	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540022293	chr5:94977000-94977001	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94968200-94979800	Weak transcription	Primary T cells from cord blood	blood
2	chr5:94969600-94976600	Weak transcription	Fetal Intestine Large	intestine
3	chr5:94973200-94975600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:94974800-94979800	Weak transcription	GM12878-XiMat	blood
5	chr5:94975200-94979200	Enhancers	Pancreas	Pancrea
6	chr5:94975600-94977400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:94976000-94982400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:94976600-94976800	Enhancers	Gastric	stomach
9	chr5:94976600-94977000	Enhancers	Right Atrium	heart
10	chr5:94976600-94977400	Enhancers	HepG2	liver
11	chr5:94976600-94978200	Enhancers	Fetal Intestine Small	intestine
12	chr5:94976600-94978600	Enhancers	Fetal Intestine Large	intestine
13	chr5:94976800-94977400	Weak transcription	Gastric	stomach
14	chr5:94976800-94978200	Enhancers	Stomach Mucosa	stomach
15	chr5:94976800-94978400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr5:94976800-94982200	Enhancers	Liver	Liver
17	chr5:94977000-94977400	Weak transcription	Right Atrium	heart
18	chr5:94977000-94977600	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr5:94977000-94977800	Enhancers	Duodenum Mucosa	Duodenum
20	chr5:94977200-94977800	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr5:94977200-94978000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:94977400-94977600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:94977400-94977600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr5:94977400-94977600	Enhancers	Gastric	stomach
25	chr5:94977400-94977600	Enhancers	Left Ventricle	heart
26	chr5:94977400-94977600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr5:94977400-94977600	Enhancers	Right Atrium	heart
28	chr5:94977400-94977600	Enhancers	HSMM	muscle
29	chr5:94977400-94977600	Enhancers	NHLF	lung
30	chr5:94977400-94977800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:94977400-94977800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr5:94977400-94977800	Flanking Active TSS	HepG2	liver
33	chr5:94977400-94978000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr5:94977400-94978200	Enhancers	K562	blood
35	chr5:94977400-94978400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:94977600-94977800	Enhancers	Aorta	Aorta
37	chr5:94977600-94977800	Enhancers	NHEK	skin
38	chr5:94977600-94979800	Weak transcription	NHLF	lung
39	chr5:94977600-94980400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr5:94977600-94982200	Weak transcription	Right Atrium	heart
41	chr5:94977600-94982200	Weak transcription	HSMM	muscle
42	chr5:94977800-94979800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr5:94977800-94979800	Enhancers	HepG2	liver
44	chr5:94977800-94979800	Weak transcription	NHEK	skin
45	chr5:94977800-94982000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:94977800-94982000	Weak transcription	Duodenum Mucosa	Duodenum
47	chr5:94977800-94982600	Weak transcription	Left Ventricle	heart
48	chr5:94978000-94979800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr5:94978000-94982200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:94978000-94982600	Weak transcription	Aorta	Aorta

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