Variant report

Variant	nsv1066717
Chromosome Location	chr19:52993620-53041995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1002)
CpG islands
(count:1652)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1002 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53030907-53031004	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:53030319-53030487	K562	blood:	n/a	n/a
3	ATF1	chr19:53030283-53031114	K562	blood:	n/a	n/a
4	ATF2	chr19:53030208-53030710	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:53039130-53039581	GM12878	blood:	n/a	n/a
6	ATF2	chr19:53030243-53030702	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr19:53039109-53039574	GM12878	blood:	n/a	n/a
8	ATF2	chr19:53030186-53030755	GM12878	blood:	n/a	n/a
9	ATF2	chr19:53030190-53030680	GM12878	blood:	n/a	n/a
10	ATF3	chr19:53030291-53030590	K562	blood:	n/a	n/a
11	ATF3	chr19:53030298-53030700	K562	blood:	n/a	n/a
12	BACH1	chr19:53030537-53030601	K562	blood:	n/a	n/a
13	BACH1	chr19:53039301-53039394	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr19:53030276-53030547	GM12878	blood:	n/a	n/a
15	BATF	chr19:53004948-53005213	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
16	BATF	chr19:53004998-53005244	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
17	BATF	chr19:53021956-53022186	GM12878	blood:	n/a	chr19:53022128-53022138 chr19:53022124-53022134
18	BCL11A	chr19:53028616-53028797	GM12878	blood:	n/a	n/a
19	BCLAF1	chr19:53039125-53039440	GM12878	blood:	n/a	n/a
20	BCLAF1	chr19:53030266-53030752	GM12878	blood:	n/a	chr19:53030409-53030422
21	BHLHE40	chr19:53039187-53039663	GM12878	blood:	n/a	n/a
22	BHLHE40	chr19:53030331-53031440	K562	blood:	n/a	n/a
23	BRCA1	chr19:52996530-52996612	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr19:53030524-53030612	GM12878	blood:	n/a	n/a
25	BRCA1	chr19:53039272-53039472	GM12878	blood:	n/a	n/a
26	BRCA1	chr19:53030788-53031097	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr19:53030053-53031085	K562	blood:	n/a	n/a
28	CBX3	chr19:53030255-53030758	K562	blood:	n/a	n/a
29	CCNT2	chr19:53030418-53030847	K562	blood:	n/a	n/a
30	CEBPB	chr19:53011938-53012138	IMR90	lung:	n/a	n/a
31	CEBPB	chr19:53011963-53012116	K562	blood:	n/a	n/a
32	CEBPB	chr19:53024161-53024462	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:53011918-53012150	A549	lung:	n/a	n/a
34	CEBPB	chr19:53023339-53023693	K562	blood:	n/a	chr19:53023522-53023533
35	CEBPB	chr19:53030600-53031145	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:53030801-53031107	K562	blood:	n/a	n/a
37	CEBPB	chr19:53023382-53023686	HepG2	liver:	n/a	chr19:53023522-53023533
38	CEBPB	chr19:53030333-53031155	IMR90	lung:	n/a	n/a
39	CEBPB	chr19:53030268-53030737	GM12878	blood:	n/a	n/a
40	CEBPB	chr19:53030405-53030582	K562	blood:	n/a	n/a
41	CEBPB	chr19:53023422-53023684	H1-hESC	embryonic stem cell:	n/a	chr19:53023522-53023533
42	CEBPB	chr19:53023353-53023673	K562	blood:	n/a	chr19:53023522-53023533
43	CEBPB	chr19:52996555-52996636	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr19:53030839-53031138	HepG2	liver:	n/a	n/a
45	CEBPD	chr19:53030856-53031116	HepG2	liver:	n/a	n/a
46	CHD1	chr19:53039390-53039441	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr19:53030984-53031204	GM12878	blood:	n/a	n/a
48	CHD1	chr19:53038918-53038933	GM12878	blood:	n/a	n/a
49	CHD1	chr19:53039185-53039651	GM12878	blood:	n/a	n/a
50	CHD2	chr19:53039031-53039447	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53030489-53030539	GM19239	blood:	n/a
2	chr19:53031333-53031383	Hepatocyte	liver:	n/a
3	chr19:53039444-53039494	PFSK-1	brain:	n/a
4	chr19:53030711-53030761	HepG2	liver:	n/a
5	chr19:53030705-53030755	HMEC	breast:	n/a
6	chr19:53030489-53030539	GM19239	blood:	n/a
7	chr19:53031333-53031383	Hepatocyte	liver:	n/a
8	chr19:53039444-53039494	PFSK-1	brain:	n/a
9	chr19:53030711-53030761	HepG2	liver:	n/a
10	chr19:53030705-53030755	HMEC	breast:	n/a
11	chr19:53030780-53030830	T-47D	breast:	n/a
12	chr19:53030711-53030761	SK-N-MC	brain:	n/a
13	chr19:52999520-52999570	CMK	blood:	n/a
14	chr19:53030489-53030539	SK-N-SH	brain:	n/a
15	chr19:52996352-52996402	GM12878	blood:	n/a
16	chr19:53030958-53031008	U87	brain:	n/a
17	chr19:53039145-53039195	RPTEC	kidney:	n/a
18	chr19:53030958-53031008	Jurkat	blood:	n/a
19	chr19:53030736-53030786	MCF-7	breast:	n/a
20	chr19:53030489-53030539	HEK293	kidney:	embryo
21	chr19:53031511-53031561	HMEC	breast:	n/a
22	chr19:52996352-52996402	HAEpiC	amniotic membrane:	n/a
23	chr19:53030705-53030755	AG09319	gingival:	n/a
24	chr19:53030711-53030761	Hela-S3	cervix:	n/a
25	chr19:52996617-52996667	HRPEpiC	eye:	n/a
26	chr19:52999520-52999570	SK-N-SH	brain:	n/a
27	chr19:53030774-53030824	H1-hESC	embryonic stem cell:	embryo
28	chr19:53030605-53030655	BE2_C	brain:	n/a
29	chr19:53030996-53031046	HCM	heart:	n/a
30	chr19:53039534-53039584	LNCaP	prostate:	n/a
31	chr19:53038972-53039022	NHBE	bronchial:	n/a
32	chr19:52996548-52996598	HUVEC	blood vessel:	n/a
33	chr19:53030605-53030655	Jurkat	blood:	n/a
34	chr19:52996548-52996598	GM12891	blood:	n/a
35	chr19:52995647-52995697	Hela-S3	cervix:	n/a
36	chr19:53039534-53039584	NHBE	bronchial:	n/a
37	chr19:53039534-53039584	HCF	heart:	n/a
38	chr19:53018151-53018201	HCPEpiC	choroid plexus:	n/a
39	chr19:53030736-53030786	NT2-D1	testis:	n/a
40	chr19:53028694-53028744	SKMC	muscle:	n/a
41	chr19:53039145-53039195	LNCaP	prostate:	n/a
42	chr19:53028694-53028744	RPTEC	kidney:	n/a
43	chr19:53030705-53030755	A549	lung:	n/a
44	chr19:53028694-53028744	SK-N-SH	brain:	n/a
45	chr19:53039145-53039195	T-47D	breast:	n/a
46	chr19:53034554-53034604	AG10803	skin:	n/a
47	chr19:53030996-53031046	BJ	skin:	n/a
48	chr19:53031138-53031188	K562	blood:	n/a
49	chr19:53031511-53031561	Hepatocyte	liver:	n/a
50	chr19:53040230-53040280	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53025941..53027882-chr19:53028687..53031111,3	MCF-7	breast:
2	chr19:53039240..53039740-chr19:53289638..53290383,2	NB4	blood:
3	chr19:53039880..53042500-chr19:53052327..53054340,2	MCF-7	breast:
4	chr19:53039676..53041332-chr19:53072309..53073853,2	MCF-7	breast:
5	chr19:53029459..53032258-chr19:53036873..53039549,6	MCF-7	breast:
6	chr19:53024234..53025826-chr19:53029049..53030597,2	MCF-7	breast:
7	chr19:53029459..53032258-chr19:53036873..53039549,6	MCF-7	breast:
8	chr19:53031656..53034156-chr19:53037494..53039065,2	MCF-7	breast:
9	chr19:53024234..53025826-chr19:53029049..53030597,2	MCF-7	breast:
10	chr19:53029450..53032188-chr19:53072538..53074123,2	K562	blood:
11	chr19:53031656..53034156-chr19:53037494..53039065,2	MCF-7	breast:
12	chr19:53029127..53032188-chr19:53072538..53075129,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF83-7	chr19:53015428-53015595	ENSG00000269349.1
2	lnc-ZNF83-7	chr19:53014535-53015246	ENSG00000269349.1

No data

Variant related genes	Relation type
ENSG00000269349	TF binding region
ZNF808	TF binding region
ZNF578	TF binding region
ENSG00000269349	CpG island
ZNF808	CpG island
ZNF578	CpG island
ENSG00000189190	chromatin interactions
ENSG00000167562	chromatin interactions
ENSG00000198482	chromatin interactions

Extended variants
information (count: 2614 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2614 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1673917	chr19:52993620-52993621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577515736	chr19:52993622-52993623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143586977	chr19:52993633-52993634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534200668	chr19:52993656-52993657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1673918	chr19:52993662-52993663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs377299696	chr19:52993704-52993705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563861232	chr19:52993767-52993768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139597097	chr19:52993797-52993798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200619554	chr19:52993891-52993892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60946234	chr19:52993892-52993893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560842027	chr19:52993893-52993894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200893705	chr19:52993908-52993909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528056156	chr19:52993913-52993914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111793631	chr19:52993930-52993931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564835155	chr19:52993951-52993952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532226946	chr19:52993970-52993971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550469303	chr19:52993976-52993977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34932752	chr19:52994015-52994016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568998776	chr19:52994039-52994040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35369831	chr19:52994040-52994041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529868193	chr19:52994047-52994048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151186398	chr19:52994058-52994059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567685421	chr19:52994090-52994091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535004123	chr19:52994102-52994103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77558777	chr19:52994115-52994116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571674036	chr19:52994145-52994146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191888945	chr19:52994149-52994150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs207477256	chr19:52994187-52994188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575767163	chr19:52994216-52994217	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs542881739	chr19:52994300-52994301	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs554634252	chr19:52994314-52994315	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs572642470	chr19:52994356-52994357	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs368155911	chr19:52994364-52994365	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs564746979	chr19:52994481-52994482	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs576219975	chr19:52994484-52994485	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs543739012	chr19:52994491-52994492	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs201667472	chr19:52994492-52994493	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs564499549	chr19:52994496-52994497	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs199923627	chr19:52994498-52994499	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112121975	chr19:52994499-52994500	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs77721359	chr19:52994503-52994504	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs544466224	chr19:52994514-52994515	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs61191258	chr19:52994576-52994577	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs545777600	chr19:52994618-52994619	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529881301	chr19:52994631-52994632	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs529269718	chr19:52994666-52994667	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs4802963	chr19:52994667-52994668	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs374931289	chr19:52994683-52994684	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs2633512	chr19:52994706-52994707	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs184080108	chr19:52994760-52994761	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Adrenocortical carcinoma	18281524	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1582 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52990400-52994800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr19:52990800-52994600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr19:52992600-52995400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:52993000-52995400	Weak transcription	Left Ventricle	heart
5	chr19:52993000-52995600	Weak transcription	Brain Germinal Matrix	brain
6	chr19:52994200-52997200	ZNF genes & repeats	Ovary	ovary
7	chr19:52994600-52994800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr19:52994600-52994800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
9	chr19:52994600-52996400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr19:52994600-52999400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr19:52994800-52995400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr19:52994800-52995800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr19:52994800-52996600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr19:52994800-52997000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
15	chr19:52994800-52997200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:52994800-52997600	ZNF genes & repeats	Fetal Stomach	stomach
17	chr19:52995000-52995600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr19:52995200-52995400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr19:52995200-52995400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr19:52995200-52995400	Enhancers	Dnd41	blood
21	chr19:52995200-52997200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
22	chr19:52995400-52995600	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr19:52995400-52995800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
24	chr19:52995400-52995800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr19:52995400-52995800	Flanking Active TSS	Dnd41	blood
26	chr19:52995400-52996000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:52995400-52996800	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr19:52995400-52996800	ZNF genes & repeats	Left Ventricle	heart
29	chr19:52995400-52997000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
30	chr19:52995400-52997200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr19:52995400-52997200	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr19:52995400-52997200	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr19:52995400-52997400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr19:52995600-52995800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr19:52995600-52995800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:52995600-52995800	ZNF genes & repeats	Brain Hippocampus Middle	brain
37	chr19:52995600-52995800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr19:52995600-52995800	Enhancers	Fetal Muscle Leg	muscle
39	chr19:52995600-52995800	ZNF genes & repeats	Right Ventricle	heart
40	chr19:52995600-52996000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr19:52995600-52996000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr19:52995600-52996400	Active TSS	Primary T cells from cord blood	blood
43	chr19:52995600-52996400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
44	chr19:52995600-52996600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:52995600-52996600	ZNF genes & repeats	Brain Germinal Matrix	brain
46	chr19:52995600-52997000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr19:52995600-52997000	ZNF genes & repeats	Esophagus	oesophagus
48	chr19:52995600-52997200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
49	chr19:52995600-52997200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
50	chr19:52995600-52997200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin

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