Variant report

Variant	nsv1064196
Chromosome Location	chr19:28315113-28554522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:976)
CpG islands
(count:367)
Chromatin interactive
region (count:19)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:28508411-28508510	K562	blood:	n/a	n/a
2	ATF1	chr19:28339161-28339543	K562	blood:	n/a	n/a
3	BACH1	chr19:28315056-28315377	H1-hESC	embryonic stem cell:	n/a	chr19:28315233-28315247
4	BACH1	chr19:28466591-28466642	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:28315054-28315423	K562	blood:	n/a	chr19:28315233-28315247
6	BATF	chr19:28453293-28453547	GM12878	blood:	n/a	chr19:28453431-28453442 chr19:28453416-28453425
7	BCL3	chr19:28525929-28526130	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:28484544-28484743	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:28331210-28331428	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:28464926-28465289	GM12878	blood:	n/a	n/a
11	BHLHE40	chr19:28331408-28331601	K562	blood:	n/a	n/a
12	BHLHE40	chr19:28501657-28501858	K562	blood:	n/a	n/a
13	BRCA1	chr19:28321368-28321405	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr19:28330124-28330322	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr19:28375451-28375743	A549	lung:	n/a	n/a
16	CEBPB	chr19:28321916-28322067	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr19:28531517-28531724	A549	lung:	n/a	chr19:28531625-28531636 chr19:28531625-28531636
18	CEBPB	chr19:28510387-28510609	A549	lung:	n/a	n/a
19	CEBPB	chr19:28337973-28338214	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:28490646-28490735	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:28321784-28322155	K562	blood:	n/a	n/a
22	CEBPB	chr19:28530474-28530807	MCF-7	breast:	n/a	n/a
23	CEBPB	chr19:28409910-28410170	HepG2	liver:	n/a	chr19:28410026-28410037 chr19:28410025-28410038
24	CEBPB	chr19:28512031-28512307	A549	lung:	n/a	n/a
25	CEBPB	chr19:28540734-28541094	K562	blood:	n/a	chr19:28540900-28540911
26	CEBPB	chr19:28329508-28329962	HepG2	liver:	n/a	chr19:28329780-28329791
27	CEBPB	chr19:28512130-28512202	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr19:28421407-28421661	A549	lung:	n/a	n/a
29	CEBPB	chr19:28378818-28378941	HepG2	liver:	n/a	n/a
30	CEBPB	chr19:28512136-28512257	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:28323919-28324162	A549	lung:	n/a	chr19:28324037-28324054
32	CEBPB	chr19:28461957-28462469	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr19:28490679-28490748	A549	lung:	n/a	n/a
34	CEBPZ	chr19:28316284-28316369	HepG2	liver:	n/a	n/a
35	CEBPZ	chr19:28339532-28339541	HepG2	liver:	n/a	n/a
36	CHD2	chr19:28330243-28330279	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr19:28499598-28499916	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr19:28457400-28457550	GM12866	blood:	n/a	n/a
39	CTCF	chr19:28331280-28331430	GM12878	blood:	n/a	n/a
40	CTCF	chr19:28457242-28457575	HepG2	liver:	n/a	n/a
41	CTCF	chr19:28400467-28400746	K562	blood:	n/a	chr19:28400700-28400709 chr19:28400566-28400582 chr19:28400565-28400583 chr19:28400583-28400596 chr19:28400662-28400675
42	CTCF	chr19:28457380-28457530	HEK293	kidney:	n/a	n/a
43	CTCF	chr19:28331360-28331510	Caco-2	colon:	n/a	n/a
44	CTCF	chr19:28331300-28331450	NHEK	skin:	n/a	n/a
45	CTCF	chr19:28386520-28386670	A549	lung:	n/a	n/a
46	CTCF	chr19:28321240-28321390	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr19:28503380-28503530	GM12873	blood:	n/a	n/a
48	CTCF	chr19:28464980-28465130	HepG2	liver:	n/a	n/a
49	CTCF	chr19:28457358-28457534	A549	lung:	n/a	n/a
50	CTCF	chr19:28461940-28462090	HRE	kidney:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:28403514-28403564	PFSK-1	brain:	n/a
2	chr19:28403514-28403564	PFSK-1	brain:	n/a
3	chr19:28400281-28400331	AG09319	gingival:	n/a
4	chr19:28399736-28399786	HCM	heart:	n/a
5	chr19:28400281-28400331	SK-N-MC	brain:	n/a
6	chr19:28400822-28400872	SKMC	muscle:	n/a
7	chr19:28399736-28399786	HAEpiC	amniotic membrane:	n/a
8	chr19:28400281-28400331	K562	blood:	n/a
9	chr19:28403514-28403564	SAEC	small airway:	n/a
10	chr19:28403514-28403564	AG09309	skin:	n/a
11	chr19:28401100-28401150	MCF10A-Er-Src	breast:	n/a
12	chr19:28399736-28399786	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:28403514-28403564	IMR90	lung:	fetal
14	chr19:28403514-28403564	ovcar-3	ovarian:	n/a
15	chr19:28400822-28400872	AG04449	skin:	fetal
16	chr19:28401100-28401150	NH-A	brain:	n/a
17	chr19:28401100-28401150	BE2_C	brain:	n/a
18	chr19:28403514-28403564	Jurkat	blood:	n/a
19	chr19:28401100-28401150	SAEC	small airway:	n/a
20	chr19:28399736-28399786	HIPEpiC	eye:	n/a
21	chr19:28399736-28399786	SK-N-SH	brain:	n/a
22	chr19:28399736-28399786	K562	blood:	n/a
23	chr19:28397061-28397111	NB4	blood:	n/a
24	chr19:28400822-28400872	IMR90	lung:	fetal
25	chr19:28400281-28400331	AoSMC	blood vessel:	n/a
26	chr19:28400822-28400872	AG04450	lung:	fetal
27	chr19:28399736-28399786	GM12891	blood:	n/a
28	chr19:28397061-28397111	Caco-2	colon:	n/a
29	chr19:28399736-28399786	ProgFib	skin:	n/a
30	chr19:28399736-28399786	AG04449	skin:	fetal
31	chr19:28400281-28400331	SK-N-SH	brain:	n/a
32	chr19:28399736-28399786	PrEC	prostate:	n/a
33	chr19:28401100-28401150	LNCaP	prostate:	n/a
34	chr19:28400822-28400872	LNCaP	prostate:	n/a
35	chr19:28401100-28401150	IMR90	lung:	fetal
36	chr19:28397061-28397111	HPAEpiC	pulmonary alveolar:	n/a
37	chr19:28399736-28399786	SKMC	muscle:	n/a
38	chr19:28400822-28400872	HRPEpiC	eye:	n/a
39	chr19:28399736-28399786	MCF-7	breast:	n/a
40	chr19:28399736-28399786	HRCEpiC	kidney:	n/a
41	chr19:28401100-28401150	U87	brain:	n/a
42	chr19:28399736-28399786	A549	lung:	n/a
43	chr19:28400281-28400331	GM12892	blood:	n/a
44	chr19:28403514-28403564	MCF-7	breast:	n/a
45	chr19:28400281-28400331	HCF	heart:	n/a
46	chr19:28401100-28401150	HPAEpiC	pulmonary alveolar:	n/a
47	chr19:28400281-28400331	ProgFib	skin:	n/a
48	chr19:28403514-28403564	H1-hESC	embryonic stem cell:	embryo
49	chr19:28403514-28403564	BE2_C	brain:	n/a
50	chr19:28400822-28400872	SAEC	small airway:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:28398796..28401321-chr19:28401925..28404487,2	K562	blood:
2	chr19:28503418..28504150-chr19:28707502..28708498,2	MCF-7	breast:
3	chr19:28502331..28503989-chr19:28509235..28511001,2	MCF-7	breast:
4	chr19:28331441..28333608-chr19:28335036..28336613,2	K562	blood:
5	chr19:28360092..28362208-chr19:28365123..28367340,2	K562	blood:
6	chr19:28464703..28465634-chr19:28707512..28708625,5	MCF-7	breast:
7	chr19:28539840..28540682-chr5:3520532..3521075,2	MCF-7	breast:
8	chr19:28464493..28465594-chr19:28815026..28816551,6	MCF-7	breast:
9	chr19:28456998..28457870-chr2:21351809..21352309,2	MCF-7	breast:
10	chr19:28360092..28362208-chr19:28365123..28367340,2	K562	blood:
11	chr19:28331279..28332941-chr19:28335036..28337118,2	K562	blood:
12	chr19:28331279..28332941-chr19:28335036..28337118,2	K562	blood:
13	chr19:28395608..28398274-chr19:28399828..28402146,2	K562	blood:
14	chr14:105940951..105942780-chr19:28339771..28341271,2	MCF-7	breast:
15	chr14:105940702..105944648-chr19:28339771..28342771,5	MCF-7	breast:
16	chr19:28502331..28503989-chr19:28509235..28511001,2	MCF-7	breast:
17	chr19:28395608..28398274-chr19:28399828..28402146,2	K562	blood:
18	chr19:28331441..28333608-chr19:28335036..28336613,2	K562	blood:
19	chr19:28464838..28465364-chr19:28707556..28708271,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VSTM2B-9	chr19:28393503-28393602	NONHSAT064022
2	lnc-VSTM2B-9	chr19:28447110-28447494	NONHSAT064022
3	lnc-UQCRFS1-6	chr19:28380013-28380130	ENSG00000266977.1
4	lnc-UQCRFS1-6	chr19:28380013-28380105	XLOC_013284
5	lnc-UQCRFS1-18	chr19:28473940-28474240	NONHSAT064026
6	lnc-UQCRFS1-6	chr19:28340562-28340977	XLOC_013284
7	lnc-UQCRFS1-5	chr19:28480019-28480183	XLOC_013285
8	lnc-UQCRFS1-5	chr19:28477699-28477915	XLOC_013285
9	lnc-UQCRFS1-6	chr19:28340638-28340977	ENSG00000266977.1
10	lnc-UQCRFS1-5	chr19:28491139-28491243	XLOC_013285
11	lnc-UQCRFS1-5	chr19:28491139-28491271	XLOC_013285
12	lnc-UQCRFS1-5	chr19:28479862-28480740	XLOC_013285

No data

Variant related genes	Relation type
ENSG00000267623	TF binding region
ENSG00000267768	TF binding region
ENSG00000267509	TF binding region
ENSG00000267630	TF binding region
ENSG00000266977	TF binding region
ENSG00000267389	TF binding region
ENSG00000266906	TF binding region
ENSG00000267623	CpG island
ENSG00000267768	CpG island
ENSG00000267509	CpG island
ENSG00000267630	CpG island
ENSG00000266977	CpG island
ENSG00000267389	CpG island
ENSG00000266906	CpG island
ENSG00000182809	chromatin interactions
ENSG00000267768	chromatin interactions
SRP72	miRNA target sites
SRPK1	miRNA target sites

Extended variants
information (count: 5464 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:5464 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75576925	chr19:28315128-28315129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74567892	chr19:28315130-28315131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573275620	chr19:28315136-28315137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78461105	chr19:28315142-28315143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75976144	chr19:28315146-28315147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74663736	chr19:28315148-28315149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79550492	chr19:28315156-28315157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534456570	chr19:28315162-28315163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540503224	chr19:28315163-28315164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558905407	chr19:28315167-28315168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78344418	chr19:28315168-28315169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78010979	chr19:28315182-28315183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375765303	chr19:28315199-28315200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77934532	chr19:28315204-28315205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76791704	chr19:28315205-28315206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75307589	chr19:28315218-28315219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78093463	chr19:28315221-28315222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79565131	chr19:28315222-28315223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74631523	chr19:28315227-28315228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200077823	chr19:28315228-28315229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79058033	chr19:28315233-28315234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76599224	chr19:28315263-28315264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74540810	chr19:28315266-28315267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74404590	chr19:28315267-28315268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77989621	chr19:28315269-28315270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77886115	chr19:28315270-28315271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73531192	chr19:28315284-28315285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs8112091	chr19:28315297-28315298	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs73033876	chr19:28315310-28315311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75472538	chr19:28315313-28315314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs8112106	chr19:28315314-28315315	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs574343129	chr19:28315320-28315321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79543597	chr19:28315341-28315342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73033878	chr19:28315353-28315354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555866565	chr19:28315365-28315366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4804947	chr19:28315384-28315385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs562933236	chr19:28315390-28315391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541463667	chr19:28315407-28315408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560051856	chr19:28315420-28315421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572256493	chr19:28315421-28315422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546052855	chr19:28315496-28315497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs80339366	chr19:28315506-28315507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76031733	chr19:28315521-28315522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73033883	chr19:28315541-28315542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371527252	chr19:28315546-28315547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375615404	chr19:28315555-28315556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369713375	chr19:28315572-28315573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562596771	chr19:28315591-28315592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373526393	chr19:28315607-28315608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377488992	chr19:28315608-28315609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Myelofibrosis	22110671	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	19287141	CNVD
Lung cancer	18438408	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Astrocytoma	17387387	CNVD
renal disease	20603712	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:28314000-28315400	Enhancers	Dnd41	blood
2	chr19:28314200-28319200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr19:28315000-28315200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr19:28315000-28315400	Enhancers	A549	lung
5	chr19:28318400-28319600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr19:28318600-28319200	ZNF genes & repeats	Aorta	Aorta
7	chr19:28319200-28320000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr19:28320000-28320200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr19:28321800-28322200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr19:28323800-28324000	Enhancers	Right Atrium	heart
11	chr19:28323800-28324400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr19:28323800-28324600	Enhancers	NHEK	skin
13	chr19:28329000-28329600	Enhancers	Dnd41	blood
14	chr19:28329400-28332200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr19:28329600-28330400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr19:28329600-28331200	Weak transcription	Dnd41	blood
17	chr19:28331200-28331600	Enhancers	Dnd41	blood
18	chr19:28339000-28344000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:28339200-28340200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr19:28339400-28340000	ZNF genes & repeats	HepG2	liver
21	chr19:28341400-28342800	ZNF genes & repeats	Colonic Mucosa	Colon
22	chr19:28341400-28342800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
23	chr19:28341800-28342800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:28342000-28343000	ZNF genes & repeats	Gastric	stomach
25	chr19:28342000-28343000	ZNF genes & repeats	Dnd41	blood
26	chr19:28342200-28342800	ZNF genes & repeats	Spleen	Spleen
27	chr19:28342200-28343000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
28	chr19:28342400-28343000	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr19:28344000-28344400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr19:28349400-28352600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr19:28350000-28353200	ZNF genes & repeats	Adipose Nuclei	Adipose
32	chr19:28350200-28353200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
33	chr19:28356800-28357800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr19:28358600-28359600	Enhancers	HSMMtube	muscle
35	chr19:28363200-28363800	ZNF genes & repeats	Pancreas	Pancrea
36	chr19:28367600-28368600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr19:28368000-28373800	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr19:28374600-28376200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr19:28375600-28377000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr19:28376200-28376400	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr19:28376400-28376800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr19:28377600-28378000	Enhancers	HSMMtube	muscle
43	chr19:28378600-28378800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
44	chr19:28378600-28379400	Active TSS	Fetal Heart	heart
45	chr19:28378800-28379200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr19:28379400-28379800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr19:28379400-28381000	Weak transcription	Fetal Heart	heart
48	chr19:28380200-28389200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr19:28381000-28381400	Active TSS	Fetal Heart	heart
50	chr19:28384800-28385600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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