Variant report

Variant	esv3471240
Chromosome Location	chr5:43541792-43587904
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1184)
CpG islands
(count:917)
Chromatin interactive
region (count:109)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1184 , 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	chr5:43557047-43557889	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:43557062-43557257	K562	blood:	n/a	n/a
3	ATF2	chr5:43585225-43585577	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:43556806-43557303	GM12878	blood:	n/a	n/a
5	ATF2	chr5:43556120-43556746	GM12878	blood:	n/a	n/a
6	ATF3	chr5:43556815-43557087	K562	blood:	n/a	n/a
7	BACH1	chr5:43557017-43557725	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:43556361-43556700	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr5:43568081-43568396	GM12878	blood:	n/a	n/a
10	BATF	chr5:43581546-43581832	GM12878	blood:	n/a	n/a
11	BATF	chr5:43581575-43581836	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:43585193-43585529	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr5:43556752-43557673	GM12878	blood:	n/a	chr5:43557213-43557226 chr5:43557356-43557369 chr5:43557300-43557313 chr5:43557038-43557047 chr5:43557301-43557314 chr5:43557069-43557082 chr5:43557073-43557086 chr5:43557396-43557409 chr5:43557293-43557306 chr5:43557019-43557032 chr5:43556980-43556993
14	BCLAF1	chr5:43556730-43557432	GM12878	blood:	n/a	chr5:43557213-43557226 chr5:43557356-43557369 chr5:43557300-43557313 chr5:43557038-43557047 chr5:43557301-43557314 chr5:43557069-43557082 chr5:43557073-43557086 chr5:43557396-43557409 chr5:43557293-43557306 chr5:43557019-43557032 chr5:43556980-43556993
15	BCLAF1	chr5:43556772-43557451	K562	blood:	n/a	chr5:43557213-43557226 chr5:43557356-43557369 chr5:43557300-43557313 chr5:43557038-43557047 chr5:43557301-43557314 chr5:43557069-43557082 chr5:43557073-43557086 chr5:43557396-43557409 chr5:43557293-43557306 chr5:43557019-43557032 chr5:43556980-43556993
16	BCLAF1	chr5:43556185-43556696	GM12878	blood:	n/a	chr5:43556474-43556487
17	BHLHE40	chr5:43556416-43557674	GM12878	blood:	n/a	chr5:43556977-43556993
18	BHLHE40	chr5:43556348-43557796	K562	blood:	n/a	chr5:43556977-43556993
19	BRCA1	chr5:43556364-43556573	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr5:43556868-43557633	GM12878	blood:	n/a	n/a
21	BRCA1	chr5:43579329-43579425	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr5:43555943-43556500	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr5:43556856-43557297	HepG2	liver:	n/a	n/a
24	BRCA1	chr5:43556874-43557303	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr5:43556842-43557430	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr5:43556778-43557411	K562	blood:	n/a	n/a
27	CCNT2	chr5:43556342-43557649	K562	blood:	n/a	chr5:43556582-43556591 chr5:43557523-43557532 chr5:43556469-43556478
28	CEBPB	chr5:43571432-43571679	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr5:43571286-43571756	K562	blood:	n/a	n/a
30	CEBPB	chr5:43557686-43557903	K562	blood:	n/a	n/a
31	CEBPB	chr5:43559538-43559824	K562	blood:	n/a	chr5:43559655-43559666
32	CEBPB	chr5:43571521-43571599	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:43571439-43571627	K562	blood:	n/a	n/a
34	CEBPB	chr5:43557130-43557391	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:43559594-43559835	HepG2	liver:	n/a	chr5:43559655-43559666
36	CEBPB	chr5:43571366-43571737	K562	blood:	n/a	n/a
37	CEBPB	chr5:43573205-43573578	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:43571372-43571717	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:43571369-43571731	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:43571458-43571687	A549	lung:	n/a	n/a
41	CEBPD	chr5:43557178-43557451	HepG2	liver:	n/a	n/a
42	CEBPD	chr5:43556785-43557607	K562	blood:	n/a	n/a
43	CEBPD	chr5:43556809-43557172	HepG2	liver:	n/a	n/a
44	CEBPD	chr5:43556790-43557537	K562	blood:	n/a	n/a
45	CHD1	chr5:43556374-43557560	GM12878	blood:	n/a	chr5:43556469-43556479 chr5:43557522-43557532
46	CHD1	chr5:43555890-43556767	H1-hESC	embryonic stem cell:	n/a	chr5:43556469-43556479
47	CHD2	chr5:43585289-43585636	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr5:43556450-43557740	HepG2	liver:	n/a	chr5:43556469-43556479 chr5:43557522-43557532
49	CHD2	chr5:43556242-43557753	GM12878	blood:	n/a	chr5:43556469-43556479 chr5:43557522-43557532
50	CHD2	chr5:43564418-43564679	K562	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:43557653-43557703	HIPEpiC	eye:	n/a
2	chr5:43557602-43557652	NB4	blood:	n/a
3	chr5:43557653-43557703	HIPEpiC	eye:	n/a
4	chr5:43557602-43557652	NB4	blood:	n/a
5	chr5:43557521-43557571	RPTEC	kidney:	n/a
6	chr5:43557602-43557652	HCPEpiC	choroid plexus:	n/a
7	chr5:43557435-43557485	HCPEpiC	choroid plexus:	n/a
8	chr5:43556361-43556411	GM12892	blood:	n/a
9	chr5:43557644-43557694	HMEC	breast:	n/a
10	chr5:43557751-43557801	MCF-7	breast:	n/a
11	chr5:43557435-43557485	GM12891	blood:	n/a
12	chr5:43557482-43557532	ovcar-3	ovarian:	n/a
13	chr5:43557583-43557633	HRE	kidney:	n/a
14	chr5:43558398-43558448	CMK	blood:	n/a
15	chr5:43557435-43557485	HEK293	kidney:	embryo
16	chr5:43557521-43557571	IMR90	lung:	fetal
17	chr5:43557583-43557633	AoSMC	blood vessel:	n/a
18	chr5:43559688-43559738	SKMC	muscle:	n/a
19	chr5:43557135-43557185	AG10803	skin:	n/a
20	chr5:43557135-43557185	GM12891	blood:	n/a
21	chr5:43558398-43558448	HCT-116	colon:	n/a
22	chr5:43557435-43557485	SK-N-SH	brain:	n/a
23	chr5:43556691-43556741	LNCaP	prostate:	n/a
24	chr5:43558398-43558448	BJ	skin:	n/a
25	chr5:43552780-43552830	HEEpiC	esophagus:	n/a
26	chr5:43557435-43557485	MCF-7	breast:	n/a
27	chr5:43556361-43556411	HCF	heart:	n/a
28	chr5:43558398-43558448	A549	lung:	n/a
29	chr5:43557482-43557532	AG10803	skin:	n/a
30	chr5:43558859-43558909	HMEC	breast:	n/a
31	chr5:43557751-43557801	IMR90	lung:	fetal
32	chr5:43557135-43557185	HCT-116	colon:	n/a
33	chr5:43557653-43557703	GM12892	blood:	n/a
34	chr5:43557135-43557185	Jurkat	blood:	n/a
35	chr5:43556361-43556411	SKMC	muscle:	n/a
36	chr5:43559688-43559738	GM06990	blood:	n/a
37	chr5:43557583-43557633	ECC-1	luminal epithelium:	n/a
38	chr5:43556691-43556741	NHDF-neo	bronchial:	n/a
39	chr5:43556361-43556411	MCF-7	breast:	n/a
40	chr5:43557583-43557633	HUVEC	blood vessel:	n/a
41	chr5:43557482-43557532	HRPEpiC	eye:	n/a
42	chr5:43556361-43556411	MCF10A-Er-Src	breast:	n/a
43	chr5:43557482-43557532	SK-N-MC	brain:	n/a
44	chr5:43552780-43552830	ECC-1	luminal epithelium:	n/a
45	chr5:43557583-43557633	Hela-S3	cervix:	n/a
46	chr5:43557435-43557485	T-47D	breast:	n/a
47	chr5:43557135-43557185	LNCaP	prostate:	n/a
48	chr5:43557644-43557694	HEK293	kidney:	embryo
49	chr5:43557751-43557801	K562	blood:	n/a
50	chr5:43556691-43556741	SAEC	small airway:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:43512478..43519226-chr5:43552704..43558861,10	MCF-7	breast:
2	chr5:43505801..43507815-chr5:43555939..43557727,2	MCF-7	breast:
3	chr5:43555603..43557203-chr5:43575638..43578155,2	K562	blood:
4	chr5:43555487..43559521-chr5:43598404..43605405,16	K562	blood:
5	chr5:43563244..43565362-chr5:43568381..43570262,2	K562	blood:
6	chr5:43557377..43557920-chr6:26123924..26124717,2	Hela-S3	cervix:
7	chr5:43541229..43543256-chr5:43600683..43602539,2	K562	blood:
8	chr22:17639626..17640361-chr5:43556833..43557442,2	HCT-116	colon:
9	chr5:43556013..43559876-chr5:43586120..43588801,3	K562	blood:
10	chr5:43505282..43507808-chr5:43556089..43557593,2	K562	blood:
11	chr5:43557091..43557731-chr5:43602959..43603556,2	MCF-7	breast:
12	chr5:43540433..43542729-chr5:43600683..43602719,2	K562	blood:
13	chr5:43504115..43506398-chr5:43542097..43545068,2	MCF-7	breast:
14	chr5:43513876..43516684-chr5:43553510..43558785,6	MCF-7	breast:
15	chr5:43564714..43567873-chr5:43601188..43604304,3	K562	blood:
16	chr2:98280019..98280550-chr5:43556723..43557699,2	Hela-S3	cervix:
17	chr5:43481238..43485996-chr5:43553681..43560344,12	K562	blood:
18	chr5:43482505..43485566-chr5:43554663..43558409,7	MCF-7	breast:
19	chr5:43580034..43581980-chr5:43601875..43603679,2	MCF-7	breast:
20	chr5:43556567..43558867-chr5:43579199..43581062,3	MCF-7	breast:
21	chr5:43483908..43484590-chr5:43556767..43557347,2	K562	blood:
22	chr5:43483169..43485499-chr5:43549794..43552040,2	MCF-7	breast:
23	chr5:43545437..43548284-chr5:43610055..43612795,2	K562	blood:
24	chr5:43481891..43486310-chr5:43553986..43559337,13	K562	blood:
25	chr5:43395337..43397260-chr5:43554283..43555898,2	MCF-7	breast:
26	chr5:43566373..43570038-chr5:43599893..43602969,4	K562	blood:
27	chr5:43558159..43559976-chr5:43570027..43571651,2	K562	blood:
28	chr5:43063931..43068016-chr5:43554200..43557480,3	K562	blood:
29	chr5:43536689..43538647-chr5:43540263..43543098,2	K562	blood:
30	chr5:43565730..43567318-chr5:43568871..43570663,2	K562	blood:
31	chr12:6861979..6862810-chr5:43556567..43557310,2	Hela-S3	cervix:
32	chr5:43556502..43558456-chr5:43583768..43585773,2	K562	blood:
33	chr5:43554204..43556115-chr6:30581283..30584220,2	K562	blood:
34	chr5:43562817..43565608-chr5:43599983..43604180,4	MCF-7	breast:
35	chr5:43552832..43560830-chr5:43598877..43605844,26	MCF-7	breast:
36	chr5:43555808..43557395-chr5:43575141..43577121,3	MCF-7	breast:
37	chr1:114471689..114472657-chr5:43557087..43557874,2	Hela-S3	cervix:
38	chr5:43552178..43554497-chr5:43589226..43592032,2	K562	blood:
39	chr1:161735480..161736094-chr5:43556295..43557137,2	Hela-S3	cervix:
40	chr5:43568689..43571180-chr5:43594322..43596361,2	MCF-7	breast:
41	chr5:43553205..43562648-chr5:43565710..43576086,17	K562	blood:
42	chr11:47236058..47237053-chr5:43556605..43557161,2	Hela-S3	cervix:
43	chr17:27717266..27717817-chr5:43556542..43557111,2	Hela-S3	cervix:
44	chr17:27055082..27056024-chr5:43556763..43557563,2	Hela-S3	cervix:
45	chr5:43557000..43557782-chr5:176730254..176730958,2	NB4	blood:
46	chr5:43513317..43518816-chr5:43554982..43559074,7	K562	blood:
47	chr5:43571687..43573439-chr5:43598421..43600933,2	MCF-7	breast:
48	chr5:43556596..43557400-chr8:33370799..33371471,2	HCT-116	colon:
49	chr5:43563244..43565362-chr5:43568381..43570262,2	K562	blood:
50	chr5:43556013..43559876-chr5:43586120..43588801,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NNT-5	chr5:43571510-43577741	NONHSAT101320

No data

Variant related genes	Relation type
PAIP1	TF binding region
PAIP1	CpG island
ENSG00000226889	chromatin interactions
ENSG00000239039	chromatin interactions
ENSG00000226419	chromatin interactions
ENSG00000053501	chromatin interactions
ENSG00000134574	chromatin interactions
ENSG00000159176	chromatin interactions
ENSG00000169230	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000264808	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000185837	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000160551	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000248240	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000112992	chromatin interactions
ENSG00000165775	chromatin interactions
ENSG00000118217	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000249286	chromatin interactions
ENSG00000186298	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000116874	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000172239	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000169228	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000177738	chromatin interactions
ENSG00000231365	chromatin interactions
ENSG00000069998	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000224536	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000263719	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000248092	chromatin interactions
ENSG00000089693	chromatin interactions
ENSG00000160602	chromatin interactions

Extended variants
information (count: 1687 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1687 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79649443	chr5:43541804-43541805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74886755	chr5:43541805-43541806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528999346	chr5:43541813-43541814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13436879	chr5:43541824-43541825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
5	rs193176690	chr5:43541840-43541841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560916940	chr5:43541856-43541857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534559549	chr5:43541884-43541885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150273449	chr5:43542004-43542005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571597600	chr5:43542005-43542006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537319850	chr5:43542017-43542018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371576384	chr5:43542044-43542045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375050592	chr5:43542049-43542050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370759085	chr5:43542060-43542061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372963792	chr5:43542074-43542075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557409778	chr5:43542077-43542078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573914089	chr5:43542148-43542149	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543114061	chr5:43542172-43542173	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs13436939	chr5:43542205-43542206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200165278	chr5:43542234-43542235	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201030766	chr5:43542252-43542253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185038543	chr5:43542277-43542278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs6868426	chr5:43542296-43542297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
23	rs545232288	chr5:43542346-43542347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201748730	chr5:43542393-43542394	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574671098	chr5:43542455-43542456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565116085	chr5:43542456-43542457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs202145737	chr5:43542460-43542461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531130236	chr5:43542462-43542463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190682935	chr5:43542490-43542491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181781912	chr5:43542491-43542492	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528835602	chr5:43542503-43542504	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186434794	chr5:43542505-43542506	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs4866835	chr5:43542511-43542512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs149462655	chr5:43542579-43542580	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35477434	chr5:43542607-43542608	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35220672	chr5:43542636-43542637	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs397964966	chr5:43542652-43542653	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145929318	chr5:43542703-43542704	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565509095	chr5:43542726-43542727	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74829374	chr5:43542730-43542731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551628544	chr5:43542764-43542765	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571434358	chr5:43542868-43542869	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537354765	chr5:43542880-43542881	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539532179	chr5:43542900-43542901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557248942	chr5:43542944-43542945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567550971	chr5:43542947-43542948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536292650	chr5:43542957-43542958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79581612	chr5:43542990-43542991	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs374594613	chr5:43543093-43543094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530277242	chr5:43543114-43543115	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21569311	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1328 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43523200-43550600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:43523200-43551600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr5:43523200-43551800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:43523200-43552200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:43523400-43551000	Strong transcription	Liver	Liver
6	chr5:43523400-43553600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:43523400-43554600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr5:43523600-43551000	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr5:43523600-43554200	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr5:43524000-43555200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:43524200-43553600	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:43524800-43553600	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:43525000-43552400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:43525200-43548600	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr5:43525400-43553400	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:43525600-43541800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:43526000-43553200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:43526000-43554200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:43527200-43543400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:43527200-43543400	Strong transcription	Adipose Nuclei	Adipose
21	chr5:43527200-43548200	Strong transcription	HUVEC	blood vessel
22	chr5:43527200-43550400	Strong transcription	Dnd41	blood
23	chr5:43527200-43552000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr5:43527200-43552400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:43527400-43552400	Strong transcription	Hela-S3	cervix
26	chr5:43527400-43554200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:43527600-43548800	Strong transcription	HSMM	muscle
28	chr5:43527600-43550400	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr5:43527600-43550800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr5:43527600-43550800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr5:43527600-43553200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr5:43527600-43554400	Strong transcription	Primary B cells from peripheral blood	blood
33	chr5:43527600-43555600	Strong transcription	Fetal Thymus	thymus
34	chr5:43527600-43556000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:43527800-43549000	Strong transcription	Osteobl	bone
36	chr5:43527800-43552400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:43528000-43554800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr5:43530200-43552000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr5:43532200-43552200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr5:43532400-43548800	Strong transcription	Placenta	Placenta
41	chr5:43532800-43552400	Strong transcription	Fetal Intestine Large	intestine
42	chr5:43532800-43554000	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr5:43533000-43549000	Strong transcription	Fetal Muscle Trunk	muscle
44	chr5:43533000-43551400	Strong transcription	Fetal Lung	lung
45	chr5:43534200-43550600	Weak transcription	Fetal Heart	heart
46	chr5:43534400-43548000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr5:43534400-43550400	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr5:43534600-43546800	Weak transcription	Gastric	stomach
49	chr5:43534600-43554400	Weak transcription	Aorta	Aorta
50	chr5:43534800-43542000	Weak transcription	Esophagus	oesophagus

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