Variant report

Variant	nsv1056633
Chromosome Location	chr19:43789914-43856672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:876)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
4	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
5	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
6	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
7	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
8	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
10	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
13	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
16	CEBPB	chr19:43848766-43848967	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
19	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
21	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:43848801-43848963	K562	blood:	n/a	n/a
25	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43848780-43848968	A549	lung:	n/a	n/a
28	CEBPB	chr19:43848755-43848998	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
30	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
32	CEBPD	chr19:43818150-43818430	K562	blood:	n/a	n/a
33	CHD2	chr19:43833232-43833538	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr19:43820019-43820330	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr19:43820875-43821218	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr19:43790318-43790669	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr19:43820096-43820344	K562	blood:	n/a	n/a
38	CTCF	chr19:43837360-43837510	HRE	kidney:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
39	CTCF	chr19:43820837-43821244	K562	blood:	n/a	n/a
40	CTCF	chr19:43837380-43837530	HBMEC	blood vessel:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
41	CTCF	chr19:43837340-43837490	GM12871	blood:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
42	CTCF	chr19:43837380-43837530	HMF	breast:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
43	CTCF	chr19:43847800-43847950	SAEC	small airway:	n/a	n/a
44	CTCF	chr19:43820860-43821010	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr19:43809925-43810048	Pancreas_OC	pancreas:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
46	CTCF	chr19:43837314-43837609	H1-hESC	embryonic stem cell:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837597-43837605 chr19:43837439-43837457
47	CTCF	chr19:43795428-43795526	HepG2	liver:	n/a	n/a
48	CTCF	chr19:43837380-43837530	Hela-S3	cervix:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
49	CTCF	chr19:43793144-43793368	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr19:43820920-43821070	GM06990	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43856594-43856644	PANC-1	pancreas:	n/a
2	chr19:43856594-43856644	ProgFib	skin:	n/a
3	chr19:43856594-43856644	PFSK-1	brain:	n/a
4	chr19:43851787-43851837	GM12878	blood:	n/a
5	chr19:43856594-43856644	Jurkat	blood:	n/a
6	chr19:43851787-43851837	HPAEpiC	pulmonary alveolar:	n/a
7	chr19:43856594-43856644	HCPEpiC	choroid plexus:	n/a
8	chr19:43851787-43851837	HAEpiC	amniotic membrane:	n/a
9	chr19:43851787-43851837	AG10803	skin:	n/a
10	chr19:43851787-43851837	HUVEC	blood vessel:	n/a
11	chr19:43856594-43856644	RPTEC	kidney:	n/a
12	chr19:43851787-43851837	BE2_C	brain:	n/a
13	chr19:43851787-43851837	SK-N-MC	brain:	n/a
14	chr19:43851787-43851837	U87	brain:	n/a
15	chr19:43856594-43856644	T-47D	breast:	n/a
16	chr19:43856594-43856644	HRPEpiC	eye:	n/a
17	chr19:43856594-43856644	SK-N-SH	brain:	n/a
18	chr19:43851787-43851837	T-47D	breast:	n/a
19	chr19:43851787-43851837	H1-hESC	embryonic stem cell:	embryo
20	chr19:43851787-43851837	AG04449	skin:	fetal
21	chr19:43856594-43856644	PrEC	prostate:	n/a
22	chr19:43856594-43856644	HL-60	blood:	n/a
23	chr19:43856594-43856644	NT2-D1	testis:	n/a
24	chr19:43856594-43856644	NHDF-neo	bronchial:	n/a
25	chr19:43851787-43851837	GM19239	blood:	n/a
26	chr19:43856594-43856644	AG09309	skin:	n/a
27	chr19:43856594-43856644	SK-N-MC	brain:	n/a
28	chr19:43856594-43856644	Caco-2	colon:	n/a
29	chr19:43851787-43851837	SK-N-SH_RA	brain:	n/a
30	chr19:43851787-43851837	IMR90	lung:	fetal
31	chr19:43851787-43851837	NHBE	bronchial:	n/a
32	chr19:43856594-43856644	HMEC	breast:	n/a
33	chr19:43856594-43856644	HAEpiC	amniotic membrane:	n/a
34	chr19:43856594-43856644	HepG2	liver:	n/a
35	chr19:43856594-43856644	NB4	blood:	n/a
36	chr19:43851787-43851837	GM12891	blood:	n/a
37	chr19:43856594-43856644	SK-N-SH_RA	brain:	n/a
38	chr19:43851787-43851837	HRPEpiC	eye:	n/a
39	chr19:43856594-43856644	CMK	blood:	n/a
40	chr19:43851787-43851837	Hela-S3	cervix:	n/a
41	chr19:43856594-43856644	H1-hESC	embryonic stem cell:	embryo
42	chr19:43856594-43856644	MCF-7	breast:	n/a
43	chr19:43851787-43851837	SKMC	muscle:	n/a
44	chr19:43851787-43851837	SK-N-SH	brain:	n/a
45	chr19:43851787-43851837	NHDF-neo	bronchial:	n/a
46	chr19:43851787-43851837	AoSMC	blood vessel:	n/a
47	chr19:43851787-43851837	K562	blood:	n/a
48	chr19:43856594-43856644	IMR90	lung:	fetal
49	chr19:43856594-43856644	HRE	kidney:	n/a
50	chr19:43851787-43851837	AG09309	skin:	n/a

(count:15 , 50 per page) page: 1

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

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD177-2	chr19:43853208-43853700	NONHSAT066596
2	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
3	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
4	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
5	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
6	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+

No data

Variant related genes	Relation type
CD177	TF binding region
ENSG00000231412	TF binding region
CEACAMP11	TF binding region
CEACAMP4	TF binding region
CD177	CpG island
ENSG00000231412	CpG island
CEACAMP11	CpG island
CEACAMP4	CpG island
ENSG00000231412	chromatin interactions

Extended variants
information (count: 2639 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2639 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10411716	chr19:43789914-43789915	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs149582271	chr19:43789918-43789919	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs117775717	chr19:43789924-43789925	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs569400404	chr19:43789926-43789927	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs147254092	chr19:43789939-43789940	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs34981938	chr19:43789940-43789941	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs7250583	chr19:43789941-43789942	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs534227336	chr19:43789972-43789973	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs369066776	chr19:43789978-43789979	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs4324252	chr19:43789983-43789984	Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs4324253	chr19:43790005-43790006	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs556317893	chr19:43790008-43790009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4324254	chr19:43790012-43790013	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
14	rs4533395	chr19:43790016-43790017	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs188674195	chr19:43790027-43790028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7250735	chr19:43790041-43790042	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs7250740	chr19:43790047-43790048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560428684	chr19:43790048-43790049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199970631	chr19:43790053-43790054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542863622	chr19:43790054-43790055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562638424	chr19:43790055-43790056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150110209	chr19:43790073-43790074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551803554	chr19:43790075-43790076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571646030	chr19:43790079-43790080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10411968	chr19:43790081-43790082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140236227	chr19:43790088-43790089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145199125	chr19:43790092-43790093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536520778	chr19:43790095-43790096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139023775	chr19:43790109-43790110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34327279	chr19:43790118-43790119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34160223	chr19:43790120-43790121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35260957	chr19:43790123-43790124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557882856	chr19:43790133-43790134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577646737	chr19:43790143-43790144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191824782	chr19:43790169-43790170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149423064	chr19:43790171-43790172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573997943	chr19:43790184-43790185	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs368007803	chr19:43790200-43790201	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566143751	chr19:43790203-43790204	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs148135571	chr19:43790210-43790211	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs539893796	chr19:43790215-43790216	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs183341890	chr19:43790216-43790217	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs117517393	chr19:43790217-43790218	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141911548	chr19:43790230-43790231	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs551475661	chr19:43790244-43790245	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113388008	chr19:43790258-43790259	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
47	rs537073148	chr19:43790276-43790277	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs567289910	chr19:43790277-43790278	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530339050	chr19:43790286-43790287	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs556034357	chr19:43790297-43790298	Flanking Active TSS	TF binding region	1 gene(s)	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:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43789800-43790000	Flanking Active TSS	Hela-S3	cervix
2	chr19:43790000-43790200	Enhancers	Hela-S3	cervix
3	chr19:43790200-43790800	Flanking Active TSS	Hela-S3	cervix
4	chr19:43790400-43790600	Enhancers	Colon Smooth Muscle	Colon
5	chr19:43790800-43791000	Enhancers	Hela-S3	cervix
6	chr19:43791000-43791200	Flanking Active TSS	Hela-S3	cervix
7	chr19:43791200-43792200	Enhancers	Hela-S3	cervix
8	chr19:43794000-43795800	ZNF genes & repeats	Adipose Nuclei	Adipose
9	chr19:43794200-43795400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr19:43794800-43795800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr19:43795000-43795400	Active TSS	Fetal Heart	heart
12	chr19:43795400-43795600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
13	chr19:43803800-43805800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:43804200-43804800	Enhancers	HMEC	breast
15	chr19:43804200-43805600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr19:43804400-43805600	Enhancers	NHEK	skin
17	chr19:43804400-43806000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr19:43804800-43810200	Weak transcription	HMEC	breast
19	chr19:43805600-43809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr19:43805600-43810200	Weak transcription	NHEK	skin
21	chr19:43805800-43810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr19:43806000-43809600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr19:43809600-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr19:43809800-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr19:43809800-43811200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr19:43810000-43811000	Enhancers	NHDF-Ad	bronchial
27	chr19:43810000-43811200	Enhancers	Hela-S3	cervix
28	chr19:43810200-43810400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr19:43810200-43810600	Enhancers	NHEK	skin
30	chr19:43810200-43810800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr19:43810200-43810800	Enhancers	Placenta Amnion	Placenta Amnion
32	chr19:43810200-43810800	Enhancers	HMEC	breast
33	chr19:43810200-43811200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr19:43810400-43810600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr19:43810600-43811400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr19:43810800-43811200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr19:43811000-43812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr19:43811200-43814400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr19:43811200-43815800	Weak transcription	Hela-S3	cervix
40	chr19:43812000-43812800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr19:43814000-43815200	Enhancers	NHEK	skin
42	chr19:43814200-43814800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr19:43814400-43815000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr19:43814600-43815000	Enhancers	HMEC	breast
47	chr19:43815000-43830000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr19:43815800-43816400	Enhancers	Hela-S3	cervix
49	chr19:43816400-43820800	Weak transcription	Hela-S3	cervix
50	chr19:43820600-43820800	Enhancers	H1 Cell Line	embryonic stem cell

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