Variant report

Variant	nsv961238
Chromosome Location	chr19:53144650-53221094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1193)
CpG islands
(count:733)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53191096-53191296	K562	blood:	n/a	n/a
2	ARID3A	chr19:53199511-53199604	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:53193667-53194024	K562	blood:	n/a	n/a
4	ARID3A	chr19:53168737-53169156	K562	blood:	n/a	n/a
5	ARID3A	chr19:53193641-53193781	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:53192381-53192469	K562	blood:	n/a	n/a
7	ARID3A	chr19:53161930-53162203	HepG2	liver:	n/a	n/a
8	ARID3A	chr19:53192180-53192511	HepG2	liver:	n/a	n/a
9	ARID3A	chr19:53195806-53196040	K562	blood:	n/a	n/a
10	ATF1	chr19:53168873-53169110	K562	blood:	n/a	n/a
11	ATF1	chr19:53193490-53194355	K562	blood:	n/a	n/a
12	ATF1	chr19:53219224-53219418	K562	blood:	n/a	n/a
13	ATF1	chr19:53150020-53150354	K562	blood:	n/a	n/a
14	ATF3	chr19:53168777-53169106	K562	blood:	n/a	n/a
15	ATF3	chr19:53194034-53194304	K562	blood:	n/a	n/a
16	BACH1	chr19:53193336-53193863	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr19:53218901-53219394	GM12878	blood:	n/a	chr19:53219199-53219209 chr19:53219203-53219213
18	BATF	chr19:53173308-53173530	GM12878	blood:	n/a	chr19:53173435-53173446 chr19:53173379-53173390
19	BATF	chr19:53218901-53219396	GM12878	blood:	n/a	chr19:53219199-53219209 chr19:53219203-53219213
20	BCL11A	chr19:53197538-53197794	GM12878	blood:	n/a	n/a
21	BCL11A	chr19:53173321-53173566	GM12878	blood:	n/a	n/a
22	BCL11A	chr19:53219022-53219347	GM12878	blood:	n/a	chr19:53219201-53219210
23	BCL11A	chr19:53194989-53195320	GM12878	blood:	n/a	n/a
24	BCL11A	chr19:53194937-53195373	GM12878	blood:	n/a	n/a
25	BCL11A	chr19:53219085-53219334	GM12878	blood:	n/a	chr19:53219201-53219210
26	BCL3	chr19:53173304-53173745	GM12878	blood:	n/a	n/a
27	BCL3	chr19:53173348-53173599	GM12878	blood:	n/a	n/a
28	BCL3	chr19:53168692-53169149	GM12878	blood:	n/a	n/a
29	BCLAF1	chr19:53193362-53193867	GM12878	blood:	n/a	chr19:53193813-53193826
30	BHLHE40	chr19:53195726-53196072	K562	blood:	n/a	n/a
31	BHLHE40	chr19:53193162-53194353	K562	blood:	n/a	chr19:53193865-53193881
32	BHLHE40	chr19:53195775-53196073	GM12878	blood:	n/a	n/a
33	BHLHE40	chr19:53194652-53194696	K562	blood:	n/a	n/a
34	BHLHE40	chr19:53194976-53195415	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:53193397-53194098	GM12878	blood:	n/a	chr19:53193865-53193881
36	BRCA1	chr19:53193363-53193993	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr19:53219929-53220101	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr19:53149990-53150565	HCT-116	colon:	n/a	n/a
39	CBX3	chr19:53150055-53150488	HCT-116	colon:	n/a	n/a
40	CBX3	chr19:53150111-53150413	K562	blood:	n/a	n/a
41	CBX3	chr19:53208757-53209318	K562	blood:	n/a	n/a
42	CBX3	chr19:53168708-53169191	K562	blood:	n/a	n/a
43	CBX3	chr19:53173195-53173904	HCT-116	colon:	n/a	n/a
44	CBX3	chr19:53193513-53194817	K562	blood:	n/a	n/a
45	CBX3	chr19:53197400-53197751	K562	blood:	n/a	n/a
46	CBX3	chr19:53150016-53150408	K562	blood:	n/a	n/a
47	CBX3	chr19:53195364-53196189	K562	blood:	n/a	n/a
48	CCNT2	chr19:53195781-53196100	K562	blood:	n/a	n/a
49	CCNT2	chr19:53193165-53194338	K562	blood:	n/a	chr19:53193869-53193878
50	CEBPB	chr19:53212122-53212441	A549	lung:	n/a	chr19:53212306-53212319 chr19:53212308-53212319 chr19:53212308-53212317 chr19:53212308-53212317 chr19:53212308-53212317 chr19:53212308-53212317

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53189507-53189557	Jurkat	blood:	n/a
2	chr19:53189507-53189557	Jurkat	blood:	n/a
3	chr19:53193944-53193994	HepG2	liver:	n/a
4	chr19:53194124-53194174	NHDF-neo	bronchial:	n/a
5	chr19:53189507-53189557	GM12878	blood:	n/a
6	chr19:53193466-53193516	HRCEpiC	kidney:	n/a
7	chr19:53193944-53193994	AG09319	gingival:	n/a
8	chr19:53189507-53189557	U87	brain:	n/a
9	chr19:53193302-53193352	ECC-1	luminal epithelium:	n/a
10	chr19:53193912-53193962	HEEpiC	esophagus:	n/a
11	chr19:53194124-53194174	SK-N-SH_RA	brain:	n/a
12	chr19:53193302-53193352	GM12891	blood:	n/a
13	chr19:53193466-53193516	HCT-116	colon:	n/a
14	chr19:53193302-53193352	HRE	kidney:	n/a
15	chr19:53189507-53189557	GM06990	blood:	n/a
16	chr19:53194695-53194745	HMEC	breast:	n/a
17	chr19:53207899-53207949	SK-N-SH	brain:	n/a
18	chr19:53193466-53193516	PANC-1	pancreas:	n/a
19	chr19:53192577-53192627	SK-N-SH	brain:	n/a
20	chr19:53193302-53193352	HNPCEpiC	eye:	n/a
21	chr19:53197405-53197455	LNCaP	prostate:	n/a
22	chr19:53192577-53192627	HEK293	kidney:	embryo
23	chr19:53194699-53194749	HUVEC	blood vessel:	n/a
24	chr19:53193302-53193352	CMK	blood:	n/a
25	chr19:53197405-53197455	A549	lung:	n/a
26	chr19:53193912-53193962	SAEC	small airway:	n/a
27	chr19:53192577-53192627	GM19239	blood:	n/a
28	chr19:53207899-53207949	SAEC	small airway:	n/a
29	chr19:53192577-53192627	ProgFib	skin:	n/a
30	chr19:53189507-53189557	MCF-7	breast:	n/a
31	chr19:53193912-53193962	Hepatocyte	liver:	n/a
32	chr19:53189507-53189557	SKMC	muscle:	n/a
33	chr19:53193912-53193962	PANC-1	pancreas:	n/a
34	chr19:53193938-53193988	HAEpiC	amniotic membrane:	n/a
35	chr19:53192577-53192627	AoSMC	blood vessel:	n/a
36	chr19:53194124-53194174	MCF10A-Er-Src	breast:	n/a
37	chr19:53193912-53193962	HRE	kidney:	n/a
38	chr19:53193912-53193962	Caco-2	colon:	n/a
39	chr19:53194124-53194174	BJ	skin:	n/a
40	chr19:53189507-53189557	PrEC	prostate:	n/a
41	chr19:53192577-53192627	BE2_C	brain:	n/a
42	chr19:53193938-53193988	A549	lung:	n/a
43	chr19:53194124-53194174	AG04450	lung:	fetal
44	chr19:53193302-53193352	PANC-1	pancreas:	n/a
45	chr19:53194124-53194174	ovcar-3	ovarian:	n/a
46	chr19:53194695-53194745	AG09319	gingival:	n/a
47	chr19:53193466-53193516	MCF10A-Er-Src	breast:	n/a
48	chr19:53193912-53193962	NH-A	brain:	n/a
49	chr19:53189507-53189557	HEK293	kidney:	embryo
50	chr19:53193944-53193994	GM19239	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53167030..53169267-chr19:53236508..53239018,2	K562	blood:
2	chr19:53177587..53179889-chr19:53180855..53183073,2	K562	blood:
3	chr19:53181410..53183710-chr19:53186655..53189133,2	MCF-7	breast:
4	chr19:53138548..53141148-chr19:53148838..53150932,2	K562	blood:
5	chr19:53188791..53192135-chr19:53192312..53195847,5	K562	blood:
6	chr19:53193334..53193838-chr19:53445297..53445972,2	Hela-S3	cervix:
7	chr19:53149533..53152778-chr19:53154420..53157722,3	K562	blood:
8	chr19:53185339..53188409-chr19:53192365..53195013,3	K562	blood:
9	chr19:53199473..53201886-chr19:53208932..53211700,2	K562	blood:
10	chr19:53170186..53171994-chr19:53174375..53177795,3	K562	blood:
11	chr19:53148354..53151033-chr19:53154176..53155920,2	K562	blood:
12	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
13	chr19:53170186..53171994-chr19:53174375..53177795,3	K562	blood:
14	chr19:53178289..53180774-chr19:53181913..53184015,2	K562	blood:
15	chr19:53185339..53187127-chr19:53191376..53195013,3	K562	blood:
16	chr19:53161300..53164636-chr19:53165227..53168992,3	K562	blood:
17	chr19:53141360..53143345-chr19:53143350..53145363,3	K562	blood:
18	chr19:53181410..53183710-chr19:53186655..53189133,2	MCF-7	breast:
19	chr19:53215678..53217452-chr19:53219568..53222029,2	K562	blood:
20	chr19:53191910..53193662-chr19:53562323..53563875,2	K562	blood:
21	chr19:53177587..53179889-chr19:53180855..53183073,2	K562	blood:
22	chr19:53139623..53144311-chr19:53192220..53194807,4	MCF-7	breast:
23	chr19:53178289..53180774-chr19:53181913..53184015,2	K562	blood:
24	chr19:53169045..53171439-chr19:53172531..53174974,2	K562	blood:
25	chr19:53215678..53217452-chr19:53219568..53222029,2	K562	blood:
26	chr19:53148354..53151033-chr19:53154176..53155920,2	K562	blood:
27	chr19:53199473..53201886-chr19:53208932..53211700,2	K562	blood:
28	chr19:53143960..53145524-chr19:53164055..53166816,2	K562	blood:
29	chr19:53169045..53171439-chr19:53172531..53174974,2	K562	blood:
30	chr19:53109653..53111853-chr19:53175457..53178162,2	K562	blood:
31	chr19:53193667..53194241-chr2:61403847..61404574,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF611-1	chr19:53153690-53156537	ENSG00000269825.1
2	lnc-ZNF83-3	chr19:53211674-53212084	NONHSAT067577
3	lnc-ZNF83-3	chr19:53211457-53211582	NONHSAT067577

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF611	hsa-miR-155-5p	chr19:53207486-53207509

Variant related genes	Relation type
ZNF611	TF binding region
ENSG00000269825	TF binding region
ZNF83	TF binding region
ZNF611	CpG island
ENSG00000269825	CpG island
ZNF83	CpG island
ENSG00000198538	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000173209	chromatin interactions
ENSG00000269825	chromatin interactions
ENSG00000213020	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000213801	chromatin interactions

Extended variants
information (count: 3794 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3794 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16984039	chr19:53144653-53144654	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559336490	chr19:53144690-53144691	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149464780	chr19:53144781-53144782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs329954	chr19:53144803-53144804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs376174788	chr19:53144811-53144812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs329953	chr19:53144820-53144821	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs537745867	chr19:53144824-53144825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182560713	chr19:53144873-53144874	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs567821300	chr19:53144882-53144883	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534727113	chr19:53144895-53144896	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs529495803	chr19:53144986-53144987	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577794052	chr19:53144988-53144989	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576510937	chr19:53144990-53144991	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs116188840	chr19:53145048-53145049	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371253454	chr19:53145054-53145055	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575493695	chr19:53145056-53145057	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs542858576	chr19:53145061-53145062	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143943638	chr19:53145209-53145210	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs117117275	chr19:53145222-53145223	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs58494832	chr19:53145230-53145231	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs543273501	chr19:53145246-53145247	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs115599543	chr19:53145275-53145276	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10406117	chr19:53145297-53145298	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533242968	chr19:53145304-53145305	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs189231800	chr19:53145320-53145321	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs563653480	chr19:53145353-53145354	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371847478	chr19:53145392-53145393	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs531120269	chr19:53145396-53145397	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531474290	chr19:53145398-53145399	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190841615	chr19:53145418-53145419	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs329952	chr19:53145451-53145452	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs148642071	chr19:53145478-53145479	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571404800	chr19:53145494-53145495	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535171334	chr19:53145564-53145565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs369187897	chr19:53145565-53145566	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs182990190	chr19:53145636-53145637	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs201187697	chr19:53145645-53145646	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs556683735	chr19:53145662-53145663	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs142114010	chr19:53145669-53145670	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs367811022	chr19:53145678-53145679	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536171613	chr19:53145711-53145712	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs554414794	chr19:53145713-53145714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs146367297	chr19:53145740-53145741	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs139727545	chr19:53145741-53145742	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs144505190	chr19:53145749-53145750	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577719168	chr19:53145777-53145778	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs79668442	chr19:53145812-53145813	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs369768814	chr19:53145823-53145824	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs187458675	chr19:53145824-53145825	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs374303312	chr19:53145835-53145836	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Adrenocortical carcinoma	18281524	CNVD

Chromatin state (count:2555 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53141800-53160000	Weak transcription	Hela-S3	cervix
2	chr19:53142200-53147200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:53142200-53147400	Weak transcription	Ovary	ovary
4	chr19:53142200-53147800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:53142200-53149200	Weak transcription	Pancreas	Pancrea
6	chr19:53142200-53149600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:53142200-53149600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr19:53142200-53151200	Weak transcription	Aorta	Aorta
9	chr19:53142200-53151800	Weak transcription	NHDF-Ad	bronchial
10	chr19:53142200-53155800	Weak transcription	Brain Anterior Caudate	brain
11	chr19:53142400-53145000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr19:53142400-53148000	Weak transcription	Fetal Stomach	stomach
13	chr19:53142400-53149400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr19:53142400-53149800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr19:53142400-53150200	Weak transcription	NH-A	brain
16	chr19:53142400-53150600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr19:53142400-53151000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:53142400-53151000	Weak transcription	HSMM	muscle
19	chr19:53142400-53151000	Weak transcription	Osteobl	bone
20	chr19:53142400-53151200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr19:53142400-53151200	Weak transcription	HSMMtube	muscle
22	chr19:53142400-53152000	Weak transcription	Stomach Smooth Muscle	stomach
23	chr19:53142400-53154000	Weak transcription	Brain Angular Gyrus	brain
24	chr19:53142400-53154000	Weak transcription	Brain Hippocampus Middle	brain
25	chr19:53142400-53154200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr19:53142400-53156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr19:53142400-53156400	Weak transcription	Brain Substantia Nigra	brain
28	chr19:53142600-53146800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr19:53142600-53147200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr19:53142600-53147200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr19:53142600-53148800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr19:53142600-53149200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr19:53142600-53149200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr19:53142600-53149400	Weak transcription	Fetal Muscle Leg	muscle
35	chr19:53142600-53149600	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr19:53142600-53149600	Weak transcription	Brain Germinal Matrix	brain
37	chr19:53142600-53149600	Weak transcription	Fetal Lung	lung
38	chr19:53142600-53150000	Weak transcription	Dnd41	blood
39	chr19:53142600-53150200	Weak transcription	Left Ventricle	heart
40	chr19:53142600-53150600	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr19:53142600-53152600	Weak transcription	Fetal Brain Female	brain
42	chr19:53142600-53156400	Weak transcription	Fetal Brain Male	brain
43	chr19:53142800-53149600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr19:53143000-53154200	Weak transcription	Primary T cells from cord blood	blood
45	chr19:53143000-53154400	Weak transcription	Colon Smooth Muscle	Colon
46	chr19:53144200-53144800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr19:53144200-53150000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr19:53144200-53155800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr19:53144400-53145000	Enhancers	Placenta	Placenta
50	chr19:53144600-53145000	Weak transcription	Lung	lung

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