Variant report

Variant	nsv1055825
Chromosome Location	chr19:53001299-53037378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:663)
CpG islands
(count:916)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53030319-53030487	K562	blood:	n/a	n/a
2	ARID3A	chr19:53030907-53031004	HepG2	liver:	n/a	n/a
3	ATF1	chr19:53030283-53031114	K562	blood:	n/a	n/a
4	ATF2	chr19:53030186-53030755	GM12878	blood:	n/a	n/a
5	ATF2	chr19:53030243-53030702	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:53030190-53030680	GM12878	blood:	n/a	n/a
7	ATF2	chr19:53030208-53030710	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:53030291-53030590	K562	blood:	n/a	n/a
9	ATF3	chr19:53030298-53030700	K562	blood:	n/a	n/a
10	BACH1	chr19:53030537-53030601	K562	blood:	n/a	n/a
11	BATF	chr19:53004998-53005244	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
12	BATF	chr19:53021956-53022186	GM12878	blood:	n/a	chr19:53022128-53022138 chr19:53022124-53022134
13	BATF	chr19:53030276-53030547	GM12878	blood:	n/a	n/a
14	BATF	chr19:53004948-53005213	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
15	BCL11A	chr19:53028616-53028797	GM12878	blood:	n/a	n/a
16	BCLAF1	chr19:53030266-53030752	GM12878	blood:	n/a	chr19:53030409-53030422
17	BHLHE40	chr19:53030331-53031440	K562	blood:	n/a	n/a
18	BRCA1	chr19:53030788-53031097	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr19:53030524-53030612	GM12878	blood:	n/a	n/a
20	CBX3	chr19:53030053-53031085	K562	blood:	n/a	n/a
21	CBX3	chr19:53030255-53030758	K562	blood:	n/a	n/a
22	CCNT2	chr19:53030418-53030847	K562	blood:	n/a	n/a
23	CEBPB	chr19:53011918-53012150	A549	lung:	n/a	n/a
24	CEBPB	chr19:53030600-53031145	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:53030268-53030737	GM12878	blood:	n/a	n/a
26	CEBPB	chr19:53011938-53012138	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:53023339-53023693	K562	blood:	n/a	chr19:53023522-53023533
28	CEBPB	chr19:53030839-53031138	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:53030801-53031107	K562	blood:	n/a	n/a
30	CEBPB	chr19:53023353-53023673	K562	blood:	n/a	chr19:53023522-53023533
31	CEBPB	chr19:53030405-53030582	K562	blood:	n/a	n/a
32	CEBPB	chr19:53024161-53024462	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:53011963-53012116	K562	blood:	n/a	n/a
34	CEBPB	chr19:53030333-53031155	IMR90	lung:	n/a	n/a
35	CEBPB	chr19:53023382-53023686	HepG2	liver:	n/a	chr19:53023522-53023533
36	CEBPB	chr19:53023422-53023684	H1-hESC	embryonic stem cell:	n/a	chr19:53023522-53023533
37	CEBPD	chr19:53030856-53031116	HepG2	liver:	n/a	n/a
38	CHD1	chr19:53030984-53031204	GM12878	blood:	n/a	n/a
39	CHD2	chr19:53030349-53030741	K562	blood:	n/a	n/a
40	CHD2	chr19:53031443-53031545	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr19:53030912-53031013	HepG2	liver:	n/a	n/a
42	CHD2	chr19:53030964-53031146	K562	blood:	n/a	n/a
43	CHD2	chr19:53030358-53031168	Hela-S3	cervix:	n/a	chr19:53030873-53030883 chr19:53030825-53030835
44	CREB1	chr19:53030240-53031223	GM12878	blood:	n/a	n/a
45	CTCF	chr19:53030400-53030550	GM12871	blood:	n/a	chr19:53030482-53030491
46	CTCF	chr19:53030362-53030601	NHEK	skin:	n/a	chr19:53030482-53030491
47	CTCF	chr19:53030460-53030610	A549	lung:	n/a	chr19:53030482-53030491
48	CTCF	chr19:53030401-53030565	HepG2	liver:	n/a	chr19:53030482-53030491
49	CTCF	chr19:53030460-53030610	HVMF	connective:	n/a	chr19:53030482-53030491
50	CTCF	chr19:53030420-53030570	GM12873	blood:	n/a	chr19:53030482-53030491

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53018151-53018201	HRCEpiC	kidney:	n/a
2	chr19:53018151-53018201	HRCEpiC	kidney:	n/a
3	chr19:53030996-53031046	NHBE	bronchial:	n/a
4	chr19:53030489-53030539	Jurkat	blood:	n/a
5	chr19:53030774-53030824	CMK	blood:	n/a
6	chr19:53030774-53030824	HRE	kidney:	n/a
7	chr19:53031511-53031561	SK-N-SH	brain:	n/a
8	chr19:53018151-53018201	HCT-116	colon:	n/a
9	chr19:53031511-53031561	SAEC	small airway:	n/a
10	chr19:53031333-53031383	BJ	skin:	n/a
11	chr19:53030958-53031008	Hela-S3	cervix:	n/a
12	chr19:53034554-53034604	SK-N-SH	brain:	n/a
13	chr19:53030605-53030655	GM12878	blood:	n/a
14	chr19:53030774-53030824	HUVEC	blood vessel:	n/a
15	chr19:53030996-53031046	MCF-7	breast:	n/a
16	chr19:53028694-53028744	HRE	kidney:	n/a
17	chr19:53030489-53030539	HRPEpiC	eye:	n/a
18	chr19:53030489-53030539	Hela-S3	cervix:	n/a
19	chr19:53018151-53018201	Jurkat	blood:	n/a
20	chr19:53031333-53031383	T-47D	breast:	n/a
21	chr19:53018151-53018201	NH-A	brain:	n/a
22	chr19:53030711-53030761	PANC-1	pancreas:	n/a
23	chr19:53030705-53030755	SKMC	muscle:	n/a
24	chr19:53030736-53030786	H1-hESC	embryonic stem cell:	embryo
25	chr19:53030489-53030539	HEK293	kidney:	embryo
26	chr19:53030705-53030755	HepG2	liver:	n/a
27	chr19:53018151-53018201	HCPEpiC	choroid plexus:	n/a
28	chr19:53030736-53030786	ProgFib	skin:	n/a
29	chr19:53030736-53030786	PANC-1	pancreas:	n/a
30	chr19:53030489-53030539	BJ	skin:	n/a
31	chr19:53030958-53031008	HEEpiC	esophagus:	n/a
32	chr19:53030705-53030755	HNPCEpiC	eye:	n/a
33	chr19:53030774-53030824	HEK293	kidney:	embryo
34	chr19:53030605-53030655	RPTEC	kidney:	n/a
35	chr19:53030705-53030755	HEEpiC	esophagus:	n/a
36	chr19:53030780-53030830	AG04449	skin:	fetal
37	chr19:53018151-53018201	HCF	heart:	n/a
38	chr19:53030958-53031008	MCF-7	breast:	n/a
39	chr19:53030605-53030655	HMEC	breast:	n/a
40	chr19:53030705-53030755	ECC-1	luminal epithelium:	n/a
41	chr19:53030774-53030824	Caco-2	colon:	n/a
42	chr19:53031138-53031188	HRCEpiC	kidney:	n/a
43	chr19:53030996-53031046	HL-60	blood:	n/a
44	chr19:53030996-53031046	HRE	kidney:	n/a
45	chr19:53030705-53030755	LNCaP	prostate:	n/a
46	chr19:53030711-53030761	NB4	blood:	n/a
47	chr19:53030711-53030761	AoSMC	blood vessel:	n/a
48	chr19:53030705-53030755	AG04449	skin:	fetal
49	chr19:53034554-53034604	T-47D	breast:	n/a
50	chr19:53030489-53030539	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53029450..53032188-chr19:53072538..53074123,2	K562	blood:
2	chr19:53024234..53025826-chr19:53029049..53030597,2	MCF-7	breast:
3	chr19:53029459..53032258-chr19:53036873..53039549,6	MCF-7	breast:
4	chr19:53031656..53034156-chr19:53037494..53039065,2	MCF-7	breast:
5	chr19:53024234..53025826-chr19:53029049..53030597,2	MCF-7	breast:
6	chr19:53029127..53032188-chr19:53072538..53075129,3	K562	blood:
7	chr19:53025941..53027882-chr19:53028687..53031111,3	MCF-7	breast:
8	chr19:53029459..53032258-chr19:53036873..53039549,6	MCF-7	breast:

(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
ENSG00000269349	CpG island
ZNF808	CpG island
ENSG00000198482	chromatin interactions
ENSG00000167562	chromatin interactions

Extended variants
information (count: 1884 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1884 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs329929	chr19:53001299-53001300	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566045972	chr19:53001337-53001338	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs151096853	chr19:53001361-53001362	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs112714996	chr19:53001374-53001375	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs141081860	chr19:53001449-53001450	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544133016	chr19:53001461-53001462	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs329930	chr19:53001469-53001470	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs574305216	chr19:53001535-53001536	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111425521	chr19:53001558-53001559	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7256777	chr19:53001566-53001567	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552563333	chr19:53001567-53001568	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11672692	chr19:53001573-53001574	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7257031	chr19:53001578-53001579	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555206512	chr19:53001583-53001584	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7257676	chr19:53001584-53001585	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs58765518	chr19:53001600-53001601	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10421111	chr19:53001632-53001633	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530674585	chr19:53001645-53001646	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370982521	chr19:53001646-53001647	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548882378	chr19:53001649-53001650	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192748059	chr19:53001660-53001661	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10422356	chr19:53001670-53001671	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs143932082	chr19:53001701-53001702	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566083941	chr19:53001708-53001709	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551152142	chr19:53001709-53001710	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4802964	chr19:53001717-53001718	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs329931	chr19:53001723-53001724	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs537709605	chr19:53001765-53001766	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556120911	chr19:53001766-53001767	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183487828	chr19:53001786-53001787	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189348169	chr19:53001839-53001840	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192490934	chr19:53001861-53001862	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141764932	chr19:53001927-53001928	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545096835	chr19:53001933-53001934	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374359332	chr19:53001938-53001939	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75867716	chr19:53001952-53001953	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs398041063	chr19:53001954-53001955	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs398059827	chr19:53001955-53001956	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530462380	chr19:53001956-53001957	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562912709	chr19:53002011-53002012	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574917183	chr19:53002027-53002028	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542492011	chr19:53002031-53002032	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548852742	chr19:53002032-53002033	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139664200	chr19:53002033-53002034	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566101671	chr19:53002050-53002051	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184485864	chr19:53002095-53002096	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143153070	chr19:53002109-53002110	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs386810485	chr19:53002143-53002144	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74839640	chr19:53002144-53002145	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551872300	chr19:53002145-53002146	Weak transcription ZNF genes & repeats Strong transcription Enhancers	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52996200-53002200	Weak transcription	Aorta	Aorta
2	chr19:52996800-53001800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr19:52997000-53008200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr19:52997200-53002000	Weak transcription	Pancreas	Pancrea
5	chr19:52997200-53002200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr19:52997400-53002600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr19:52997600-53009800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr19:52997800-53005400	Weak transcription	Dnd41	blood
9	chr19:52999200-53002400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr19:52999400-53002600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
11	chr19:52999600-53005200	Weak transcription	Fetal Brain Female	brain
12	chr19:53000600-53006000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr19:53000800-53002200	Weak transcription	Ovary	ovary
14	chr19:53000800-53005800	Weak transcription	Brain Anterior Caudate	brain
15	chr19:53001000-53006000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr19:53001400-53002800	Enhancers	Placenta	Placenta
17	chr19:53001600-53002000	ZNF genes & repeats	Brain Germinal Matrix	brain
18	chr19:53002000-53002600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
19	chr19:53002000-53002800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr19:53002000-53002800	ZNF genes & repeats	Left Ventricle	heart
21	chr19:53002000-53002800	ZNF genes & repeats	Pancreas	Pancrea
22	chr19:53002000-53003000	ZNF genes & repeats	Adipose Nuclei	Adipose
23	chr19:53002000-53003000	Strong transcription	Brain Germinal Matrix	brain
24	chr19:53002000-53005400	Weak transcription	Fetal Muscle Leg	muscle
25	chr19:53002200-53002400	ZNF genes & repeats	Aorta	Aorta
26	chr19:53002200-53002600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:53002200-53002800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr19:53002200-53002800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
29	chr19:53002200-53003400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
30	chr19:53002200-53014200	ZNF genes & repeats	Ovary	ovary
31	chr19:53002400-53005200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr19:53002600-53002800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:53002600-53002800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr19:53002600-53002800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr19:53002600-53002800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
36	chr19:53002600-53002800	ZNF genes & repeats	Fetal Stomach	stomach
37	chr19:53002600-53002800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
38	chr19:53002600-53004800	Weak transcription	Right Ventricle	heart
39	chr19:53002600-53021400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:53002800-53003000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:53002800-53003800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr19:53002800-53004400	Weak transcription	Fetal Stomach	stomach
43	chr19:53002800-53004800	Weak transcription	Left Ventricle	heart
44	chr19:53002800-53005200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr19:53002800-53005200	Weak transcription	Stomach Smooth Muscle	stomach
46	chr19:53002800-53006200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr19:53002800-53010600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr19:53003000-53004200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr19:53003000-53014800	Weak transcription	Brain Germinal Matrix	brain
50	chr19:53003200-53009600	Weak transcription	Brain Cingulate Gyrus	brain

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