Variant report

Variant	nsv579843
Chromosome Location	chr19:43794586-43870887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:925)
CpG islands
(count:551)
Chromatin interactive
region (count:16)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr19:43820857-43821149	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:43822401-43822627	K562	blood:	n/a	n/a
4	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
5	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:43858417-43858453	K562	blood:	n/a	n/a
7	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
8	BHLHE40	chr19:43820640-43821187	K562	blood:	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	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
14	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr19:43848766-43848967	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
18	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
19	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
20	CEBPB	chr19:43848801-43848963	K562	blood:	n/a	n/a
21	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
24	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
26	CEBPB	chr19:43848755-43848998	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43848780-43848968	A549	lung:	n/a	n/a
28	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
30	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
32	CEBPD	chr19:43818150-43818430	K562	blood:	n/a	n/a
33	CHD2	chr19:43820019-43820330	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:43858370-43858769	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr19:43820096-43820344	K562	blood:	n/a	n/a
36	CHD2	chr19:43820875-43821218	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr19:43833232-43833538	Hela-S3	cervix:	n/a	n/a
38	CTBP2	chr19:43858009-43858828	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr19:43870880-43871030	GM12864	blood:	n/a	n/a
40	CTCF	chr19:43837340-43837490	BE2_C	brain:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
41	CTCF	chr19:43837560-43837710	GM12878	blood:	n/a	chr19:43837597-43837605 chr19:43837672-43837680
42	CTCF	chr19:43837360-43837510	GM12864	blood:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
43	CTCF	chr19:43820960-43821110	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr19:43809680-43809830	GM12864	blood:	n/a	n/a
45	CTCF	chr19:43837340-43837490	NHEK	skin:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
46	CTCF	chr19:43860783-43860835	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr19:43837273-43837573	H1-hESC	embryonic stem cell:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
48	CTCF	chr19:43809934-43810053	GM12878	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
49	CTCF	chr19:43821000-43821150	SAEC	small airway:	n/a	n/a
50	CTCF	chr19:43837420-43837570	GM12868	blood:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43856746-43856796	Hepatocyte	liver:	n/a
2	chr19:43858174-43858224	T-47D	breast:	n/a
3	chr19:43856746-43856796	Hepatocyte	liver:	n/a
4	chr19:43858174-43858224	T-47D	breast:	n/a
5	chr19:43857874-43857924	ProgFib	skin:	n/a
6	chr19:43866487-43866537	GM19239	blood:	n/a
7	chr19:43866487-43866537	PANC-1	pancreas:	n/a
8	chr19:43851787-43851837	Caco-2	colon:	n/a
9	chr19:43858174-43858224	AG10803	skin:	n/a
10	chr19:43857874-43857924	BJ	skin:	n/a
11	chr19:43851787-43851837	LNCaP	prostate:	n/a
12	chr19:43857717-43857767	HCT-116	colon:	n/a
13	chr19:43857861-43857911	HEEpiC	esophagus:	n/a
14	chr19:43856746-43856796	AG09309	skin:	n/a
15	chr19:43851787-43851837	RPTEC	kidney:	n/a
16	chr19:43857717-43857767	Jurkat	blood:	n/a
17	chr19:43857861-43857911	Hela-S3	cervix:	n/a
18	chr19:43857717-43857767	Hepatocyte	liver:	n/a
19	chr19:43851787-43851837	HCPEpiC	choroid plexus:	n/a
20	chr19:43857717-43857767	SK-N-MC	brain:	n/a
21	chr19:43857717-43857767	RPTEC	kidney:	n/a
22	chr19:43857717-43857767	Hela-S3	cervix:	n/a
23	chr19:43857074-43857124	SK-N-SH_RA	brain:	n/a
24	chr19:43857074-43857124	CMK	blood:	n/a
25	chr19:43857874-43857924	GM19239	blood:	n/a
26	chr19:43851787-43851837	H1-hESC	embryonic stem cell:	embryo
27	chr19:43866487-43866537	HRPEpiC	eye:	n/a
28	chr19:43851787-43851837	HCM	heart:	n/a
29	chr19:43856594-43856644	HMEC	breast:	n/a
30	chr19:43857074-43857124	HPAEpiC	pulmonary alveolar:	n/a
31	chr19:43856594-43856644	HCM	heart:	n/a
32	chr19:43858174-43858224	Caco-2	colon:	n/a
33	chr19:43856594-43856644	HepG2	liver:	n/a
34	chr19:43857861-43857911	A549	lung:	n/a
35	chr19:43856594-43856644	HCT-116	colon:	n/a
36	chr19:43856746-43856796	HL-60	blood:	n/a
37	chr19:43857717-43857767	SAEC	small airway:	n/a
38	chr19:43857861-43857911	HL-60	blood:	n/a
39	chr19:43866487-43866537	AoSMC	blood vessel:	n/a
40	chr19:43856746-43856796	NHBE	bronchial:	n/a
41	chr19:43857861-43857911	HRE	kidney:	n/a
42	chr19:43866487-43866537	GM12892	blood:	n/a
43	chr19:43858174-43858224	NHBE	bronchial:	n/a
44	chr19:43851787-43851837	GM06990	blood:	n/a
45	chr19:43857717-43857767	H1-hESC	embryonic stem cell:	embryo
46	chr19:43856594-43856644	HAEpiC	amniotic membrane:	n/a
47	chr19:43857074-43857124	U87	brain:	n/a
48	chr19:43857874-43857924	U87	brain:	n/a
49	chr19:43866487-43866537	Hepatocyte	liver:	n/a
50	chr19:43858174-43858224	HCT-116	colon:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
2	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
3	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:
4	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
5	chr19:43820685..43821690-chr19:43929045..43930443,5	MCF-7	breast:
6	chr1:117602243..117602763-chr19:43822533..43823090,2	Hela-S3	cervix:
7	chr19:43820533..43821452-chr19:44166758..44167329,2	K562	blood:
8	chr19:43821071..43821590-chr19:43929652..43930334,2	MCF-7	breast:
9	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
10	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
11	chr19:43857729..43859549-chr19:43967499..43969532,2	MCF-7	breast:
12	chr19:43837425..43840449-chr19:43845958..43849291,3	MCF-7	breast:
13	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
14	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
15	chr19:43835562..43838441-chr19:43843809..43845441,2	MCF-7	breast:
16	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD177-2	chr19:43853208-43853700	NONHSAT066596
2	lnc-PSG9-1	chr19:43808621-43808675	NONHSAT066594
3	lnc-AC005392.1-1	chr19:43864837-43864995	ENSG00000272396.1
4	lnc-AC005392.1-2	chr19:43833447-43833660	ENSG00000231412.2
5	lnc-PSG9-1	chr19:43807323-43807688	NONHSAT066594
6	lnc-CD177-3	chr19:43831344-43831587	expReg_chr19_6043_+
7	lnc-AC005392.1-2	chr19:43835496-43835582	ENSG00000231412.2
8	lnc-AC005392.1-1	chr19:43866622-43866779	ENSG00000272396.1

No data

Variant related genes	Relation type
CD177	TF binding region
ENSG00000231412	TF binding region
CEACAMP4	TF binding region
CD177	CpG island
ENSG00000231412	CpG island
CEACAMP4	CpG island
ENSG00000124466	chromatin interactions
ENSG00000231412	chromatin interactions

Extended variants
information (count: 3005 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3005 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4263045	chr19:43794586-43794587	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4263046	chr19:43794618-43794619	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs577241926	chr19:43794625-43794626	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs376585050	chr19:43794634-43794635	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs543780730	chr19:43794655-43794656	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs182783560	chr19:43794669-43794670	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs532807431	chr19:43794682-43794683	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs546103676	chr19:43794692-43794693	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs187404392	chr19:43794712-43794713	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs150536478	chr19:43794722-43794723	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs367844868	chr19:43794742-43794743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs192263402	chr19:43794763-43794764	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs185680499	chr19:43794768-43794769	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs529684934	chr19:43794782-43794783	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs535789001	chr19:43794783-43794784	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs549734139	chr19:43794785-43794786	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs575412292	chr19:43794808-43794809	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs569866086	chr19:43794809-43794810	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs542902173	chr19:43794822-43794823	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs372425694	chr19:43794843-43794844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs567192424	chr19:43794847-43794848	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs73037743	chr19:43794855-43794856	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371258511	chr19:43794917-43794918	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs565494246	chr19:43794918-43794919	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs190504384	chr19:43794927-43794928	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs4377258	chr19:43794929-43794930	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs369742648	chr19:43794946-43794947	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs537860637	chr19:43794947-43794948	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs574578730	chr19:43794993-43794994	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs192672749	chr19:43795006-43795007	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs557696411	chr19:43795059-43795060	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs139493271	chr19:43795073-43795074	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546436971	chr19:43795100-43795101	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs560080305	chr19:43795154-43795155	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs369682357	chr19:43795168-43795169	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs542419836	chr19:43795171-43795172	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184418957	chr19:43795180-43795181	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs565243998	chr19:43795183-43795184	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188576654	chr19:43795190-43795191	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs549532752	chr19:43795204-43795205	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs112040941	chr19:43795205-43795206	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532582663	chr19:43795211-43795212	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs552091853	chr19:43795218-43795219	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs540701273	chr19:43795222-43795223	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs534545186	chr19:43795224-43795225	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs373690598	chr19:43795243-43795244	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs114297729	chr19:43795245-43795246	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs572984699	chr19:43795269-43795270	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs114639576	chr19:43795280-43795281	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs537506676	chr19:43795288-43795289	ZNF genes & repeats 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:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43794000-43795800	ZNF genes & repeats	Adipose Nuclei	Adipose
2	chr19:43794200-43795400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr19:43794800-43795800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:43795000-43795400	Active TSS	Fetal Heart	heart
5	chr19:43795400-43795600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
6	chr19:43803800-43805800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr19:43804200-43804800	Enhancers	HMEC	breast
8	chr19:43804200-43805600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr19:43804400-43805600	Enhancers	NHEK	skin
10	chr19:43804400-43806000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:43804800-43810200	Weak transcription	HMEC	breast
12	chr19:43805600-43809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr19:43805600-43810200	Weak transcription	NHEK	skin
14	chr19:43805800-43810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:43806000-43809600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr19:43809600-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr19:43809800-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:43809800-43811200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr19:43810000-43811000	Enhancers	NHDF-Ad	bronchial
20	chr19:43810000-43811200	Enhancers	Hela-S3	cervix
21	chr19:43810200-43810400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:43810200-43810600	Enhancers	NHEK	skin
23	chr19:43810200-43810800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr19:43810200-43810800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr19:43810200-43810800	Enhancers	HMEC	breast
26	chr19:43810200-43811200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr19:43810400-43810600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr19:43810600-43811400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr19:43810800-43811200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:43811000-43812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr19:43811200-43814400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr19:43811200-43815800	Weak transcription	Hela-S3	cervix
33	chr19:43812000-43812800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr19:43814000-43815200	Enhancers	NHEK	skin
35	chr19:43814200-43814800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:43814400-43815000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr19:43814600-43815000	Enhancers	HMEC	breast
40	chr19:43815000-43830000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:43815800-43816400	Enhancers	Hela-S3	cervix
42	chr19:43816400-43820800	Weak transcription	Hela-S3	cervix
43	chr19:43820600-43820800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr19:43820600-43820800	Bivalent Enhancer	K562	blood
45	chr19:43820600-43821000	Enhancers	HMEC	breast
46	chr19:43820600-43823200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr19:43820800-43821000	Flanking Bivalent TSS/Enh	K562	blood
48	chr19:43820800-43821200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr19:43820800-43821400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr19:43820800-43823000	Enhancers	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links