Variant report

Variant	nsv579836
Chromosome Location	chr19:43774853-43845593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1249)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
6	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
7	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
9	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
10	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
12	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	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	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
16	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
23	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
27	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
28	CEBPB	chr19:43820866-43821143	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	chr19:43820875-43821218	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr19:43820019-43820330	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr19:43790318-43790669	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr19:43833232-43833538	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr19:43820096-43820344	K562	blood:	n/a	n/a
36	CTCF	chr19:43820424-43821417	A549	lung:	n/a	n/a
37	CTCF	chr19:43779220-43779370	BE2_C	brain:	n/a	n/a
38	CTCF	chr19:43775321-43775551	Fibrobl	skin:	n/a	chr19:43775423-43775439 chr19:43775417-43775438 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437
39	CTCF	chr19:43775157-43775621	A549	lung:	n/a	chr19:43775423-43775439 chr19:43775417-43775438 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437
40	CTCF	chr19:43778978-43779189	Fibrobl	skin:	n/a	n/a
41	CTCF	chr19:43809980-43810130	NB4	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011
42	CTCF	chr19:43775260-43775410	HFF	foreskin:	n/a	n/a
43	CTCF	chr19:43775600-43775750	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr19:43778960-43779110	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr19:43820895-43821184	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr19:43837300-43837450	HCM	heart:	n/a	n/a
47	CTCF	chr19:43779220-43779370	GM12873	blood:	n/a	n/a
48	CTCF	chr19:43837360-43837510	Caco-2	colon:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
49	CTCF	chr19:43775480-43775630	HFF	foreskin:	n/a	n/a
50	CTCF	chr19:43775324-43775551	ProgFib	skin:	n/a	chr19:43775423-43775439 chr19:43775417-43775438 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43774982-43775032	H1-hESC	embryonic stem cell:	embryo
2	chr19:43774820-43774870	PrEC	prostate:	n/a
3	chr19:43774982-43775032	A549	lung:	n/a
4	chr19:43774982-43775032	HIPEpiC	eye:	n/a
5	chr19:43774921-43774971	A549	lung:	n/a
6	chr19:43774893-43774943	NH-A	brain:	n/a
7	chr19:43774921-43774971	PFSK-1	brain:	n/a
8	chr19:43774893-43774943	HCPEpiC	choroid plexus:	n/a
9	chr19:43774982-43775032	HNPCEpiC	eye:	n/a
10	chr19:43774982-43775032	SKMC	muscle:	n/a
11	chr19:43774921-43774971	GM19239	blood:	n/a
12	chr19:43774982-43775032	HCM	heart:	n/a
13	chr19:43774893-43774943	SK-N-MC	brain:	n/a
14	chr19:43774982-43775032	GM19239	blood:	n/a
15	chr19:43774820-43774870	SK-N-MC	brain:	n/a
16	chr19:43774982-43775032	ECC-1	luminal epithelium:	n/a
17	chr19:43774921-43774971	ProgFib	skin:	n/a
18	chr19:43774982-43775032	Caco-2	colon:	n/a
19	chr19:43774982-43775032	CMK	blood:	n/a
20	chr19:43774982-43775032	HEEpiC	esophagus:	n/a
21	chr19:43774893-43774943	MCF10A-Er-Src	breast:	n/a
22	chr19:43774921-43774971	H1-hESC	embryonic stem cell:	embryo
23	chr19:43774982-43775032	PrEC	prostate:	n/a
24	chr19:43774893-43774943	NHDF-neo	bronchial:	n/a
25	chr19:43774893-43774943	ECC-1	luminal epithelium:	n/a
26	chr19:43774893-43774943	HepG2	liver:	n/a
27	chr19:43774982-43775032	HUVEC	blood vessel:	n/a
28	chr19:43774921-43774971	HNPCEpiC	eye:	n/a
29	chr19:43774820-43774870	NT2-D1	testis:	n/a
30	chr19:43774921-43774971	PrEC	prostate:	n/a
31	chr19:43774982-43775032	HCF	heart:	n/a
32	chr19:43774921-43774971	AoSMC	blood vessel:	n/a
33	chr19:43774820-43774870	HAEpiC	amniotic membrane:	n/a
34	chr19:43774820-43774870	HRE	kidney:	n/a
35	chr19:43774982-43775032	BE2_C	brain:	n/a
36	chr19:43774982-43775032	AG09319	gingival:	n/a
37	chr19:43774982-43775032	SK-N-MC	brain:	n/a
38	chr19:43774982-43775032	HL-60	blood:	n/a
39	chr19:43774921-43774971	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:43774893-43774943	AG09309	skin:	n/a
41	chr19:43774820-43774870	HepG2	liver:	n/a
42	chr19:43774820-43774870	PANC-1	pancreas:	n/a
43	chr19:43774820-43774870	AG09309	skin:	n/a
44	chr19:43774893-43774943	HRCEpiC	kidney:	n/a
45	chr19:43774893-43774943	HAEpiC	amniotic membrane:	n/a
46	chr19:43774982-43775032	SK-N-SH	brain:	n/a
47	chr19:43774982-43775032	GM12892	blood:	n/a
48	chr19:43774921-43774971	CMK	blood:	n/a
49	chr19:43774893-43774943	NHBE	bronchial:	n/a
50	chr19:43774820-43774870	HIPEpiC	eye:	n/a

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

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

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

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

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: 2783 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2783 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11672322	chr19:43774853-43774854	ZNF genes & repeats Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541341879	chr19:43774868-43774869	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs150020799	chr19:43774875-43774876	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112124885	chr19:43774882-43774883	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs376910856	chr19:43774901-43774902	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs550212012	chr19:43774905-43774906	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs562199162	chr19:43774908-43774909	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs531304186	chr19:43774909-43774910	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs77933005	chr19:43774931-43774932	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs115870832	chr19:43774932-43774933	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs534120431	chr19:43774935-43774936	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs115552582	chr19:43774947-43774948	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs572602740	chr19:43774963-43774964	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs536410649	chr19:43774982-43774983	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs556697468	chr19:43774993-43774994	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs576655861	chr19:43775005-43775006	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs539119378	chr19:43775010-43775011	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs184014657	chr19:43775018-43775019	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs10417387	chr19:43775026-43775027	ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs185657146	chr19:43775039-43775040	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs558247281	chr19:43775073-43775074	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541728807	chr19:43775076-43775077	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561384516	chr19:43775077-43775078	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs148732079	chr19:43775092-43775093	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs77047027	chr19:43775096-43775097	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558405258	chr19:43775098-43775099	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576342070	chr19:43775106-43775107	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs563527929	chr19:43775121-43775122	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531336299	chr19:43775125-43775126	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs551165800	chr19:43775150-43775151	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs142276118	chr19:43775156-43775157	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs10417630	chr19:43775158-43775159	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs547677921	chr19:43775180-43775181	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567520923	chr19:43775238-43775239	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs536547300	chr19:43775276-43775277	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs543438134	chr19:43775279-43775280	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs562437773	chr19:43775292-43775293	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs114583823	chr19:43775303-43775304	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs376877573	chr19:43775311-43775312	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs574429057	chr19:43775323-43775324	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs541728446	chr19:43775325-43775326	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs558749649	chr19:43775328-43775329	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs572415955	chr19:43775340-43775341	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs12975725	chr19:43775372-43775373	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs140823281	chr19:43775373-43775374	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs574837449	chr19:43775378-43775379	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543689363	chr19:43775380-43775381	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs557158343	chr19:43775388-43775389	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576994379	chr19:43775425-43775426	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs527505434	chr19:43775426-43775427	Weak transcription	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:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43772000-43778800	Weak transcription	NHDF-Ad	bronchial
2	chr19:43772200-43785200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:43773200-43775000	ZNF genes & repeats	Placenta	Placenta
4	chr19:43774400-43784800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr19:43774800-43775400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr19:43778600-43779000	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr19:43778800-43779000	Enhancers	NHDF-Ad	bronchial
8	chr19:43788800-43789800	Enhancers	Hela-S3	cervix
9	chr19:43789800-43790000	Flanking Active TSS	Hela-S3	cervix
10	chr19:43790000-43790200	Enhancers	Hela-S3	cervix
11	chr19:43790200-43790800	Flanking Active TSS	Hela-S3	cervix
12	chr19:43790400-43790600	Enhancers	Colon Smooth Muscle	Colon
13	chr19:43790800-43791000	Enhancers	Hela-S3	cervix
14	chr19:43791000-43791200	Flanking Active TSS	Hela-S3	cervix
15	chr19:43791200-43792200	Enhancers	Hela-S3	cervix
16	chr19:43794000-43795800	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr19:43794200-43795400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr19:43794800-43795800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr19:43795000-43795400	Active TSS	Fetal Heart	heart
20	chr19:43795400-43795600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
21	chr19:43803800-43805800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr19:43804200-43804800	Enhancers	HMEC	breast
23	chr19:43804200-43805600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr19:43804400-43805600	Enhancers	NHEK	skin
25	chr19:43804400-43806000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:43804800-43810200	Weak transcription	HMEC	breast
27	chr19:43805600-43809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr19:43805600-43810200	Weak transcription	NHEK	skin
29	chr19:43805800-43810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr19:43806000-43809600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr19:43809600-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr19:43809800-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr19:43809800-43811200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr19:43810000-43811000	Enhancers	NHDF-Ad	bronchial
35	chr19:43810000-43811200	Enhancers	Hela-S3	cervix
36	chr19:43810200-43810400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr19:43810200-43810600	Enhancers	NHEK	skin
38	chr19:43810200-43810800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr19:43810200-43810800	Enhancers	Placenta Amnion	Placenta Amnion
40	chr19:43810200-43810800	Enhancers	HMEC	breast
41	chr19:43810200-43811200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr19:43810400-43810600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:43810600-43811400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr19:43810800-43811200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr19:43811000-43812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:43811200-43814400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:43811200-43815800	Weak transcription	Hela-S3	cervix
48	chr19:43812000-43812800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr19:43814000-43815200	Enhancers	NHEK	skin
50	chr19:43814200-43814800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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