Variant report

Variant	nsv1060310
Chromosome Location	chr19:43654209-43846382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2986)
CpG islands
(count:1283)
Chromatin interactive
region (count:17)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2986 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
2	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
3	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
4	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
5	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
8	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
9	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
10	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
11	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
12	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
13	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
14	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
15	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
16	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
18	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
21	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
23	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
24	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
26	CEBPB	chr19:43656366-43656852	IMR90	lung:	n/a	chr19:43656521-43656532
27	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
28	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
30	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
31	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
35	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
36	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
37	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
42	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
44	CEBPB	chr19:43656349-43656822	Hela-S3	cervix:	n/a	chr19:43656521-43656532
45	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
49	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr19:43656390-43656701	K562	blood:	n/a	chr19:43656521-43656532

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43697480-43697530	MCF10A-Er-Src	breast:	n/a
2	chr19:43691930-43691980	T-47D	breast:	n/a
3	chr19:43697480-43697530	MCF10A-Er-Src	breast:	n/a
4	chr19:43691930-43691980	T-47D	breast:	n/a
5	chr19:43711249-43711299	HNPCEpiC	eye:	n/a
6	chr19:43691930-43691980	AG04449	skin:	fetal
7	chr19:43774893-43774943	GM12891	blood:	n/a
8	chr19:43680072-43680122	SK-N-SH_RA	brain:	n/a
9	chr19:43680072-43680122	Jurkat	blood:	n/a
10	chr19:43697480-43697530	HUVEC	blood vessel:	n/a
11	chr19:43769725-43769775	GM06990	blood:	n/a
12	chr19:43697480-43697530	RPTEC	kidney:	n/a
13	chr19:43709654-43709704	CMK	blood:	n/a
14	chr19:43690622-43690672	AG10803	skin:	n/a
15	chr19:43774893-43774943	GM06990	blood:	n/a
16	chr19:43709360-43709410	HMEC	breast:	n/a
17	chr19:43773649-43773699	SAEC	small airway:	n/a
18	chr19:43709754-43709804	NH-A	brain:	n/a
19	chr19:43709832-43709882	GM06990	blood:	n/a
20	chr19:43691878-43691928	NH-A	brain:	n/a
21	chr19:43691930-43691980	BE2_C	brain:	n/a
22	chr19:43709754-43709804	SKMC	muscle:	n/a
23	chr19:43673501-43673551	U87	brain:	n/a
24	chr19:43690996-43691046	PrEC	prostate:	n/a
25	chr19:43673501-43673551	AG09309	skin:	n/a
26	chr19:43774921-43774971	BJ	skin:	n/a
27	chr19:43683698-43683748	IMR90	lung:	fetal
28	chr19:43769725-43769775	GM12891	blood:	n/a
29	chr19:43774982-43775032	PFSK-1	brain:	n/a
30	chr19:43673501-43673551	HRCEpiC	kidney:	n/a
31	chr19:43774820-43774870	AG04449	skin:	fetal
32	chr19:43673501-43673551	HEK293	kidney:	embryo
33	chr19:43709754-43709804	AoSMC	blood vessel:	n/a
34	chr19:43690622-43690672	HCT-116	colon:	n/a
35	chr19:43691878-43691928	MCF10A-Er-Src	breast:	n/a
36	chr19:43691930-43691980	AG09319	gingival:	n/a
37	chr19:43773649-43773699	AG09309	skin:	n/a
38	chr19:43774893-43774943	HNPCEpiC	eye:	n/a
39	chr19:43774921-43774971	SKMC	muscle:	n/a
40	chr19:43673501-43673551	HCF	heart:	n/a
41	chr19:43697480-43697530	MCF-7	breast:	n/a
42	chr19:43680072-43680122	HRPEpiC	eye:	n/a
43	chr19:43680072-43680122	SAEC	small airway:	n/a
44	chr19:43773649-43773699	ECC-1	luminal epithelium:	n/a
45	chr19:43709654-43709704	RPTEC	kidney:	n/a
46	chr19:43769725-43769775	RPTEC	kidney:	n/a
47	chr19:43774921-43774971	HMEC	breast:	n/a
48	chr19:43673501-43673551	HCT-116	colon:	n/a
49	chr19:43709832-43709882	PrEC	prostate:	n/a
50	chr19:43680072-43680122	HMEC	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
2	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
3	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
4	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
5	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
6	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
7	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
8	chr19:43820533..43821452-chr19:44166758..44167329,2	K562	blood:
9	chr1:117602243..117602763-chr19:43822533..43823090,2	Hela-S3	cervix:
10	chr19:43835562..43838441-chr19:43843809..43845441,2	MCF-7	breast:
11	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
12	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
13	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
14	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
15	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
16	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
17	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
2	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
3	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
4	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
5	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
6	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
7	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
8	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
9	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
10	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
11	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
12	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
13	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
14	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
15	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
16	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
17	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
18	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
19	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
20	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
21	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
22	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
23	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
24	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
25	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
26	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
27	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
28	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
29	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
30	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
31	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
32	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
33	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
34	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+
35	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
36	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594

No data

Variant related genes	Relation type
ENSG00000231412	TF binding region
PSG5	TF binding region
CEACAMP4	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	TF binding region
CEACAMP11	TF binding region
ENSG00000227606	TF binding region
ENSG00000231412	CpG island
PSG5	CpG island
CEACAMP4	CpG island
CEACAMP10	CpG island
PSG9	CpG island
PSG4	CpG island
CEACAMP11	CpG island
ENSG00000227606	CpG island
ENSG00000243137	chromatin interactions
ENSG00000231412	chromatin interactions

Extended variants
information (count: 8928 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8928 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8111681	chr19:43654209-43654210	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114489222	chr19:43654218-43654219	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs10423513	chr19:43654239-43654240	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558194550	chr19:43654250-43654251	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs192474854	chr19:43654258-43654259	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs534135511	chr19:43654308-43654309	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs8111985	chr19:43654310-43654311	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs150084094	chr19:43654340-43654341	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs570218327	chr19:43654350-43654351	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376919841	chr19:43654389-43654390	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs531036710	chr19:43654410-43654411	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs185798690	chr19:43654419-43654420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563062704	chr19:43654423-43654424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138343702	chr19:43654436-43654437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377268380	chr19:43654460-43654461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545282473	chr19:43654508-43654509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563794688	chr19:43654518-43654519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532911063	chr19:43654530-43654531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189062849	chr19:43654546-43654547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62112078	chr19:43654548-43654549	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs559753769	chr19:43654550-43654551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201994530	chr19:43654561-43654562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555640082	chr19:43654564-43654565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180939068	chr19:43654574-43654575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549229266	chr19:43654576-43654577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569071007	chr19:43654584-43654585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186164552	chr19:43654587-43654588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551603572	chr19:43654595-43654596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377758518	chr19:43654605-43654606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571765707	chr19:43654630-43654631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534330991	chr19:43654642-43654643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188528764	chr19:43654653-43654654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574217152	chr19:43654679-43654680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1985996	chr19:43654680-43654681	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs62112079	chr19:43654690-43654691	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs556776884	chr19:43654691-43654692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2354272	chr19:43654706-43654707	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs370524712	chr19:43654809-43654810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545581599	chr19:43654813-43654814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181322343	chr19:43654815-43654816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34017108	chr19:43654822-43654823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577305785	chr19:43654834-43654835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201828951	chr19:43654837-43654838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371855344	chr19:43654838-43654839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539965174	chr19:43654875-43654876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534970984	chr19:43654910-43654911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112904504	chr19:43654917-43654918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545388301	chr19:43654925-43654926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548708794	chr19:43654935-43654936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146336721	chr19:43654978-43654979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43650800-43654600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr19:43650800-43655400	Enhancers	NHEK	skin
3	chr19:43651400-43654400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:43651600-43654400	Enhancers	HMEC	breast
5	chr19:43652200-43655200	Weak transcription	Esophagus	oesophagus
6	chr19:43652600-43654400	Enhancers	NHLF	lung
7	chr19:43653200-43656400	Weak transcription	Osteobl	bone
8	chr19:43653600-43654400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr19:43654000-43655000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr19:43654200-43654400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr19:43654200-43654400	Enhancers	NHDF-Ad	bronchial
12	chr19:43654400-43656000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:43654400-43668200	Weak transcription	NHDF-Ad	bronchial
14	chr19:43654600-43655000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:43655000-43655400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr19:43655000-43655600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr19:43655200-43655600	Enhancers	Esophagus	oesophagus
18	chr19:43655400-43655600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:43655600-43656600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr19:43655600-43656800	Weak transcription	Esophagus	oesophagus
21	chr19:43655600-43665200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr19:43656000-43657000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr19:43656400-43656800	Enhancers	Osteobl	bone
24	chr19:43656600-43657000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr19:43657000-43657200	Enhancers	Esophagus	oesophagus
26	chr19:43662600-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr19:43662800-43663200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr19:43662800-43663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr19:43662800-43663400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr19:43662800-43663600	Enhancers	A549	lung
31	chr19:43663000-43663600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:43663000-43663600	Enhancers	NHEK	skin
33	chr19:43663200-43663400	Enhancers	HSMMtube	muscle
34	chr19:43663200-43663600	Enhancers	HMEC	breast
35	chr19:43663600-43666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr19:43663600-43666000	Weak transcription	HMEC	breast
37	chr19:43663600-43666000	Weak transcription	NHEK	skin
38	chr19:43663600-43668200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr19:43664000-43666200	Weak transcription	HSMMtube	muscle
40	chr19:43665200-43666000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr19:43665600-43666200	Enhancers	Placenta	Placenta
42	chr19:43666000-43666400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr19:43666000-43666800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr19:43666000-43667200	Enhancers	HMEC	breast
45	chr19:43666000-43668600	Enhancers	NHEK	skin
46	chr19:43666200-43666400	Enhancers	HSMMtube	muscle
47	chr19:43666200-43668200	Weak transcription	Placenta	Placenta
48	chr19:43666400-43666600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr19:43666400-43667800	Enhancers	A549	lung
50	chr19:43666400-43668200	Weak transcription	HSMMtube	muscle

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