Variant report

Variant	nsv511618
Chromosome Location	chr19:43770566-43845593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1256)
CpG islands
(count:307)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
2	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
5	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
6	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
7	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
9	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
10	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
13	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
14	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
15	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
17	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
19	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
22	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
23	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
29	CEBPD	chr19:43818150-43818430	K562	blood:	n/a	n/a
30	CHD1	chr19:43778774-43779172	IMR90	lung:	n/a	n/a
31	CHD2	chr19:43820019-43820330	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr19:43820096-43820344	K562	blood:	n/a	n/a
33	CHD2	chr19:43833232-43833538	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr19:43790318-43790669	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr19:43820875-43821218	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr19:43837360-43837510	GM12866	blood:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
37	CTCF	chr19:43778740-43778890	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr19:43778980-43779130	HFF	foreskin:	n/a	n/a
39	CTCF	chr19:43809940-43810090	AoAF	blood vessel:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
40	CTCF	chr19:43820960-43821110	GM12869	blood:	n/a	n/a
41	CTCF	chr19:43775260-43775410	BJ	skin:	n/a	n/a
42	CTCF	chr19:43820889-43821222	MCF-7	breast:	n/a	n/a
43	CTCF	chr19:43778980-43779130	A549	lung:	n/a	n/a
44	CTCF	chr19:43837320-43837470	HEK293	kidney:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
45	CTCF	chr19:43778983-43779150	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr19:43837328-43837586	MCF-7	breast:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
47	CTCF	chr19:43820980-43821130	AG04449	skin:	n/a	n/a
48	CTCF	chr19:43775385-43775735	HCT-116	colon:	n/a	chr19:43775423-43775439 chr19:43775417-43775438 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437
49	CTCF	chr19:43809880-43810030	HEK293	kidney:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
50	CTCF	chr19:43821020-43821170	AG04450	lung:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774982-43775032	GM19239	blood:	n/a
2	chr19:43774893-43774943	Hepatocyte	liver:	n/a
3	chr19:43774982-43775032	GM19239	blood:	n/a
4	chr19:43774893-43774943	Hepatocyte	liver:	n/a
5	chr19:43774921-43774971	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:43773649-43773699	AG10803	skin:	n/a
7	chr19:43774982-43775032	CMK	blood:	n/a
8	chr19:43774921-43774971	AG09319	gingival:	n/a
9	chr19:43773649-43773699	GM12892	blood:	n/a
10	chr19:43774820-43774870	BE2_C	brain:	n/a
11	chr19:43774893-43774943	HAEpiC	amniotic membrane:	n/a
12	chr19:43774893-43774943	HCM	heart:	n/a
13	chr19:43774893-43774943	HRCEpiC	kidney:	n/a
14	chr19:43773649-43773699	GM12878	blood:	n/a
15	chr19:43774820-43774870	AoSMC	blood vessel:	n/a
16	chr19:43774893-43774943	CMK	blood:	n/a
17	chr19:43774820-43774870	HRPEpiC	eye:	n/a
18	chr19:43773649-43773699	ECC-1	luminal epithelium:	n/a
19	chr19:43774921-43774971	GM12892	blood:	n/a
20	chr19:43774982-43775032	HCF	heart:	n/a
21	chr19:43774820-43774870	HEEpiC	esophagus:	n/a
22	chr19:43774820-43774870	K562	blood:	n/a
23	chr19:43774893-43774943	K562	blood:	n/a
24	chr19:43773649-43773699	NHDF-neo	bronchial:	n/a
25	chr19:43774820-43774870	PFSK-1	brain:	n/a
26	chr19:43774820-43774870	Caco-2	colon:	n/a
27	chr19:43774893-43774943	HUVEC	blood vessel:	n/a
28	chr19:43774921-43774971	HEK293	kidney:	embryo
29	chr19:43774921-43774971	AG04450	lung:	fetal
30	chr19:43774921-43774971	PFSK-1	brain:	n/a
31	chr19:43774820-43774870	HIPEpiC	eye:	n/a
32	chr19:43773649-43773699	AG04449	skin:	fetal
33	chr19:43774921-43774971	SKMC	muscle:	n/a
34	chr19:43774921-43774971	SK-N-MC	brain:	n/a
35	chr19:43774982-43775032	PrEC	prostate:	n/a
36	chr19:43773649-43773699	RPTEC	kidney:	n/a
37	chr19:43774921-43774971	AG10803	skin:	n/a
38	chr19:43773649-43773699	GM12891	blood:	n/a
39	chr19:43774820-43774870	NHBE	bronchial:	n/a
40	chr19:43774820-43774870	SK-N-MC	brain:	n/a
41	chr19:43774820-43774870	HRE	kidney:	n/a
42	chr19:43774820-43774870	AG09319	gingival:	n/a
43	chr19:43773649-43773699	SK-N-MC	brain:	n/a
44	chr19:43774982-43775032	BE2_C	brain:	n/a
45	chr19:43774820-43774870	NT2-D1	testis:	n/a
46	chr19:43774982-43775032	Caco-2	colon:	n/a
47	chr19:43773649-43773699	SKMC	muscle:	n/a
48	chr19:43774921-43774971	HRE	kidney:	n/a
49	chr19:43774921-43774971	NHBE	bronchial:	n/a
50	chr19:43774893-43774943	MCF-7	breast:	n/a

(count:14 , 50 per page) page: 1

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

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+
2	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
3	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
4	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
5	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2

No data

Variant related genes	Relation type
ENSG00000231412	TF binding region
CEACAMP4	TF binding region
PSG9	TF binding region
CEACAMP11	TF binding region
ENSG00000231412	CpG island
CEACAMP4	CpG island
PSG9	CpG island
CEACAMP11	CpG island
ENSG00000231412	chromatin interactions

Extended variants
information (count: 3166 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3166 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6509074	chr19:43770566-43770567	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144277636	chr19:43770591-43770592	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535951961	chr19:43770593-43770594	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147360212	chr19:43770598-43770599	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577058901	chr19:43770607-43770608	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545903487	chr19:43770610-43770611	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377155289	chr19:43770616-43770617	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559423994	chr19:43770631-43770632	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528068382	chr19:43770637-43770638	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542125671	chr19:43770658-43770659	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201680409	chr19:43770669-43770670	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561797636	chr19:43770696-43770697	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199657535	chr19:43770705-43770706	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192942566	chr19:43770737-43770738	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550551216	chr19:43770770-43770771	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535835121	chr19:43770780-43770781	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185059253	chr19:43770788-43770789	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533288542	chr19:43770800-43770801	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546670131	chr19:43770812-43770813	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566549331	chr19:43770821-43770822	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs10426441	chr19:43770842-43770843	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs556035857	chr19:43770863-43770864	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs62115908	chr19:43770868-43770869	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs150037800	chr19:43770885-43770886	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs190246982	chr19:43770888-43770889	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs113154291	chr19:43770923-43770924	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs374217671	chr19:43771007-43771008	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs117806098	chr19:43771044-43771045	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs145308580	chr19:43771052-43771053	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs559001570	chr19:43771067-43771068	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs553073156	chr19:43771074-43771075	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs572810265	chr19:43771114-43771115	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs371134245	chr19:43771171-43771172	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181745885	chr19:43771177-43771178	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs184699431	chr19:43771186-43771187	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577350415	chr19:43771199-43771200	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs544504779	chr19:43771241-43771242	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530756075	chr19:43771244-43771245	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375665285	chr19:43771248-43771249	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs35207205	chr19:43771274-43771275	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189439509	chr19:43771280-43771281	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs546705064	chr19:43771282-43771283	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs34420375	chr19:43771284-43771285	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs115749421	chr19:43771349-43771350	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs529291916	chr19:43771356-43771357	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs12971301	chr19:43771382-43771383	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs180783268	chr19:43771383-43771384	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs538188965	chr19:43771387-43771388	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs542354647	chr19:43771388-43771389	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs145042370	chr19:43771410-43771411	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43767200-43772000	Enhancers	NHDF-Ad	bronchial
2	chr19:43768000-43771600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr19:43768000-43771600	Enhancers	HMEC	breast
4	chr19:43768200-43771200	Enhancers	NH-A	brain
5	chr19:43768200-43771400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:43768200-43771600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr19:43768200-43771600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr19:43768200-43771600	Enhancers	Osteobl	bone
9	chr19:43768200-43772000	Enhancers	Hela-S3	cervix
10	chr19:43768200-43772200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:43768800-43771400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr19:43769000-43771600	Enhancers	NHLF	lung
13	chr19:43769400-43770600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr19:43770000-43770800	Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr19:43770200-43770600	Weak transcription	A549	lung
16	chr19:43770200-43772000	Enhancers	NHEK	skin
17	chr19:43770400-43770800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr19:43770400-43771000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr19:43770400-43773200	Active TSS	Placenta	Placenta
20	chr19:43770600-43771400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:43770600-43771400	Enhancers	A549	lung
22	chr19:43770800-43771000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr19:43770800-43771200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr19:43770800-43772000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:43771000-43771200	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr19:43771000-43771200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr19:43771200-43771600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr19:43771400-43773400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr19:43771600-43772400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr19:43772000-43774800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr19:43772000-43778800	Weak transcription	NHDF-Ad	bronchial
32	chr19:43772200-43785200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr19:43773200-43775000	ZNF genes & repeats	Placenta	Placenta
34	chr19:43773400-43774400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:43774400-43784800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr19:43774800-43775400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr19:43778600-43779000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr19:43778800-43779000	Enhancers	NHDF-Ad	bronchial
39	chr19:43788800-43789800	Enhancers	Hela-S3	cervix
40	chr19:43789800-43790000	Flanking Active TSS	Hela-S3	cervix
41	chr19:43790000-43790200	Enhancers	Hela-S3	cervix
42	chr19:43790200-43790800	Flanking Active TSS	Hela-S3	cervix
43	chr19:43790400-43790600	Enhancers	Colon Smooth Muscle	Colon
44	chr19:43790800-43791000	Enhancers	Hela-S3	cervix
45	chr19:43791000-43791200	Flanking Active TSS	Hela-S3	cervix
46	chr19:43791200-43792200	Enhancers	Hela-S3	cervix
47	chr19:43794000-43795800	ZNF genes & repeats	Adipose Nuclei	Adipose
48	chr19:43794200-43795400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
49	chr19:43794800-43795800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr19:43795000-43795400	Active TSS	Fetal Heart	heart

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