Variant report

Variant	nsv526966
Chromosome Location	chr19:43806995-43870887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:883)
CpG islands
(count:549)
Chromatin interactive
region (count:15)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:883 , 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	chr19:43822401-43822627	K562	blood:	n/a	n/a
3	BACH1	chr19:43822387-43822697	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr19:43818405-43818585	GM12878	blood:	n/a	n/a
5	BHLHE40	chr19:43820640-43821187	K562	blood:	n/a	n/a
6	BHLHE40	chr19:43809984-43810194	K562	blood:	n/a	chr19:43810115-43810131
7	BHLHE40	chr19:43858417-43858453	K562	blood:	n/a	n/a
8	BRCA1	chr19:43819994-43820173	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr19:43820772-43821192	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr19:43809902-43809911	HepG2	liver:	n/a	n/a
11	CEBPB	chr19:43846103-43846304	IMR90	lung:	n/a	n/a
12	CEBPB	chr19:43820878-43821315	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr19:43848766-43848967	HepG2	liver:	n/a	n/a
14	CEBPB	chr19:43818219-43818490	K562	blood:	n/a	n/a
15	CEBPB	chr19:43846212-43846413	A549	lung:	n/a	n/a
16	CEBPB	chr19:43846192-43846480	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:43820866-43821143	K562	blood:	n/a	n/a
18	CEBPB	chr19:43834287-43834297	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:43846182-43846350	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr19:43848780-43848968	A549	lung:	n/a	n/a
21	CEBPB	chr19:43839594-43839725	Hela-S3	cervix:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
22	CEBPB	chr19:43810985-43811120	HepG2	liver:	n/a	chr19:43811035-43811046
23	CEBPB	chr19:43848755-43848998	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:43834192-43834392	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:43829661-43830104	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:43822954-43823273	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:43833226-43833597	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43848801-43848963	K562	blood:	n/a	n/a
29	CEBPB	chr19:43839550-43839831	HepG2	liver:	n/a	chr19:43839700-43839711 chr19:43839656-43839667
30	CEBPB	chr19:43830957-43831314	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr19:43818150-43818430	K562	blood:	n/a	n/a
32	CHD2	chr19:43833232-43833538	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr19:43820875-43821218	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:43820096-43820344	K562	blood:	n/a	n/a
35	CHD2	chr19:43820019-43820330	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr19:43858370-43858769	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr19:43858009-43858828	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr19:43837304-43837602	Gliobla	brain:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
39	CTCF	chr19:43837360-43837510	HCPEpiC	choroid plexus:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
40	CTCF	chr19:43820921-43821159	HepG2	liver:	n/a	n/a
41	CTCF	chr19:43809780-43809930	GM12873	blood:	n/a	n/a
42	CTCF	chr19:43820918-43821148	LNCaP	prostate:	n/a	n/a
43	CTCF	chr19:43837380-43837530	A549	lung:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
44	CTCF	chr19:43809940-43810090	AG09309	skin:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
45	CTCF	chr19:43809980-43810130	GM12873	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011
46	CTCF	chr19:43851874-43851920	LNCaP	prostate:	n/a	n/a
47	CTCF	chr19:43809935-43810080	Lung_OC	lung:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
48	CTCF	chr19:43837380-43837530	HRPEpiC	eye:	n/a	chr19:43837442-43837452 chr19:43837445-43837454 chr19:43837439-43837457
49	CTCF	chr19:43820980-43821130	HMF	breast:	n/a	n/a
50	CTCF	chr19:43862280-43862352	GM13976	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43866487-43866537	LNCaP	prostate:	n/a
2	chr19:43857874-43857924	NT2-D1	testis:	n/a
3	chr19:43856594-43856644	AoSMC	blood vessel:	n/a
4	chr19:43857861-43857911	HRCEpiC	kidney:	n/a
5	chr19:43866487-43866537	HEK293	kidney:	embryo
6	chr19:43851787-43851837	AG09319	gingival:	n/a
7	chr19:43857874-43857924	GM12878	blood:	n/a
8	chr19:43856594-43856644	U87	brain:	n/a
9	chr19:43856594-43856644	BJ	skin:	n/a
10	chr19:43857717-43857767	HNPCEpiC	eye:	n/a
11	chr19:43866487-43866537	Caco-2	colon:	n/a
12	chr19:43866487-43866537	A549	lung:	n/a
13	chr19:43857874-43857924	PrEC	prostate:	n/a
14	chr19:43851787-43851837	H1-hESC	embryonic stem cell:	embryo
15	chr19:43857861-43857911	CMK	blood:	n/a
16	chr19:43858174-43858224	HCM	heart:	n/a
17	chr19:43856746-43856796	GM12878	blood:	n/a
18	chr19:43851787-43851837	HUVEC	blood vessel:	n/a
19	chr19:43858174-43858224	IMR90	lung:	fetal
20	chr19:43857717-43857767	GM12892	blood:	n/a
21	chr19:43857074-43857124	HRPEpiC	eye:	n/a
22	chr19:43856594-43856644	IMR90	lung:	fetal
23	chr19:43866487-43866537	ProgFib	skin:	n/a
24	chr19:43858174-43858224	NH-A	brain:	n/a
25	chr19:43857074-43857124	AoSMC	blood vessel:	n/a
26	chr19:43857874-43857924	HRCEpiC	kidney:	n/a
27	chr19:43856746-43856796	BJ	skin:	n/a
28	chr19:43857074-43857124	GM12891	blood:	n/a
29	chr19:43857874-43857924	ECC-1	luminal epithelium:	n/a
30	chr19:43857861-43857911	Jurkat	blood:	n/a
31	chr19:43857074-43857124	SKMC	muscle:	n/a
32	chr19:43858174-43858224	HUVEC	blood vessel:	n/a
33	chr19:43851787-43851837	Hela-S3	cervix:	n/a
34	chr19:43856746-43856796	CMK	blood:	n/a
35	chr19:43851787-43851837	HCF	heart:	n/a
36	chr19:43857861-43857911	SK-N-MC	brain:	n/a
37	chr19:43856594-43856644	SK-N-MC	brain:	n/a
38	chr19:43866487-43866537	PFSK-1	brain:	n/a
39	chr19:43857874-43857924	T-47D	breast:	n/a
40	chr19:43858174-43858224	HRPEpiC	eye:	n/a
41	chr19:43856746-43856796	HL-60	blood:	n/a
42	chr19:43857717-43857767	HCT-116	colon:	n/a
43	chr19:43866487-43866537	HepG2	liver:	n/a
44	chr19:43858174-43858224	K562	blood:	n/a
45	chr19:43856746-43856796	MCF-7	breast:	n/a
46	chr19:43857717-43857767	GM12891	blood:	n/a
47	chr19:43856746-43856796	ovcar-3	ovarian:	n/a
48	chr19:43857861-43857911	HCPEpiC	choroid plexus:	n/a
49	chr19:43856746-43856796	GM19239	blood:	n/a
50	chr19:43858174-43858224	GM12878	blood:	n/a

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

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

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

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

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
ENSG00000231412	chromatin interactions
ENSG00000124466	chromatin interactions

Extended variants
information (count: 2805 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2805 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2240616	chr19:43806995-43806996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189037070	chr19:43806996-43806997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181751986	chr19:43807014-43807015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529478367	chr19:43807028-43807029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373051927	chr19:43807040-43807041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549138275	chr19:43807054-43807055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567817460	chr19:43807064-43807065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536792452	chr19:43807083-43807084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556637117	chr19:43807121-43807122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570380872	chr19:43807122-43807123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140935535	chr19:43807142-43807143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs8102132	chr19:43807152-43807153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149759688	chr19:43807156-43807157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs5009916	chr19:43807182-43807183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs187130378	chr19:43807215-43807216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372618320	chr19:43807236-43807237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544762078	chr19:43807250-43807251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564578999	chr19:43807273-43807274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533202976	chr19:43807320-43807321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145634301	chr19:43807322-43807323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192355860	chr19:43807323-43807324	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs531267067	chr19:43807330-43807331	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs549173375	chr19:43807385-43807386	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs569157127	chr19:43807440-43807441	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs531768706	chr19:43807557-43807558	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs77773594	chr19:43807619-43807620	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs2215124	chr19:43807640-43807641	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs533223666	chr19:43807678-43807679	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs180757307	chr19:43807697-43807698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116422929	chr19:43807713-43807714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535790344	chr19:43807746-43807747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555695384	chr19:43807758-43807759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575536632	chr19:43807767-43807768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201491187	chr19:43807798-43807799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548380521	chr19:43807803-43807804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557984190	chr19:43807804-43807805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71169222	chr19:43807848-43807849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10579028	chr19:43807850-43807851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs56727073	chr19:43807852-43807853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56758183	chr19:43807858-43807859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146074148	chr19:43807880-43807881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578024689	chr19:43807968-43807969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138096510	chr19:43807980-43807981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186089648	chr19:43808085-43808086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529240054	chr19:43808088-43808089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62113681	chr19:43808093-43808094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs62113682	chr19:43808118-43808119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs62113683	chr19:43808139-43808140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76975065	chr19:43808151-43808152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140017447	chr19:43808154-43808155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43804800-43810200	Weak transcription	HMEC	breast
2	chr19:43805600-43809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr19:43805600-43810200	Weak transcription	NHEK	skin
4	chr19:43805800-43810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr19:43806000-43809600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr19:43809600-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr19:43809800-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr19:43809800-43811200	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr19:43810000-43811000	Enhancers	NHDF-Ad	bronchial
10	chr19:43810000-43811200	Enhancers	Hela-S3	cervix
11	chr19:43810200-43810400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr19:43810200-43810600	Enhancers	NHEK	skin
13	chr19:43810200-43810800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr19:43810200-43810800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr19:43810200-43810800	Enhancers	HMEC	breast
16	chr19:43810200-43811200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr19:43810400-43810600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr19:43810600-43811400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr19:43810800-43811200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr19:43811000-43812000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:43811200-43814400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr19:43811200-43815800	Weak transcription	Hela-S3	cervix
23	chr19:43812000-43812800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr19:43814000-43815200	Enhancers	NHEK	skin
25	chr19:43814200-43814800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:43814200-43815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr19:43814400-43815000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr19:43814600-43815000	Enhancers	HMEC	breast
30	chr19:43815000-43830000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr19:43815800-43816400	Enhancers	Hela-S3	cervix
32	chr19:43816400-43820800	Weak transcription	Hela-S3	cervix
33	chr19:43820600-43820800	Enhancers	H1 Cell Line	embryonic stem cell
34	chr19:43820600-43820800	Bivalent Enhancer	K562	blood
35	chr19:43820600-43821000	Enhancers	HMEC	breast
36	chr19:43820600-43823200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr19:43820800-43821000	Flanking Bivalent TSS/Enh	K562	blood
38	chr19:43820800-43821200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
39	chr19:43820800-43821400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr19:43820800-43823000	Enhancers	Hela-S3	cervix
41	chr19:43821000-43821200	ZNF genes & repeats	Right Atrium	heart
42	chr19:43821000-43821200	Active TSS	K562	blood
43	chr19:43821000-43822400	Weak transcription	HMEC	breast
44	chr19:43821200-43837800	Weak transcription	Right Atrium	heart
45	chr19:43821600-43830000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr19:43822400-43822600	Enhancers	HMEC	breast
47	chr19:43822400-43822800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:43822800-43823200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr19:43822800-43833600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:43823000-43824000	Flanking Active TSS	Hela-S3	cervix

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