Variant report

Variant	nsv1058567
Chromosome Location	chr19:52992455-53021505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr19:53004998-53005244	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
2	BATF	chr19:53004948-53005213	GM12878	blood:	n/a	chr19:53005032-53005042 chr19:53005035-53005046 chr19:53005036-53005046
3	BRCA1	chr19:52996530-52996612	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr19:53011918-53012150	A549	lung:	n/a	n/a
5	CEBPB	chr19:53011938-53012138	IMR90	lung:	n/a	n/a
6	CEBPB	chr19:53011963-53012116	K562	blood:	n/a	n/a
7	CEBPB	chr19:52993321-52993417	HepG2	liver:	n/a	chr19:52993340-52993349 chr19:52993338-52993351 chr19:52993338-52993349 chr19:52993340-52993349 chr19:52993339-52993350 chr19:52993340-52993349 chr19:52993340-52993349
8	CEBPB	chr19:52996555-52996636	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr19:52995873-52996149	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr19:52996409-52996675	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr19:52996480-52996630	HUVEC	blood vessel:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
12	CTCF	chr19:52996371-52996622	K562	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
13	CTCF	chr19:52996372-52996793	K562	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
14	CTCF	chr19:53019560-53019710	K562	blood:	n/a	n/a
15	CTCF	chr19:52996380-52996530	HMEC	breast:	n/a	chr19:52996521-52996529
16	CTCF	chr19:53007913-53008059	GM20000	blood:	n/a	n/a
17	CTCF	chr19:53014326-53014380	GM10248	blood:	n/a	n/a
18	CTCF	chr19:52996400-52996645	K562	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
19	CTCF	chr19:52996460-52996610	WERI-Rb-1	eye:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
20	CTCF	chr19:52996349-52996758	H1-hESC	embryonic stem cell:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
21	CTCF	chr19:52996487-52996602	NHEK	skin:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
22	CTCF	chr19:52996532-52996550	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr19:52996454-52996618	K562	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
24	CTCF	chr19:52996440-52996590	HBMEC	blood vessel:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
25	CTCF	chr19:52996523-52996549	GM12878	blood:	n/a	n/a
26	CTCF	chr19:53019584-53019702	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr19:52996373-52996665	K562	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
28	CTCF	chr19:53006699-53006731	GM13976	blood:	n/a	n/a
29	CTCF	chr19:52996462-52996601	Kidney_OC	kidney:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
30	CTCF	chr19:52996500-52996564	Lung_OC	lung:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
31	CTCF	chr19:53019500-53019701	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr19:52996513-52996581	GM19238	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
33	CTCF	chr19:52996477-52996564	Spleen_OC	spleen:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
34	CTCF	chr19:52995784-52996132	H1-hESC	embryonic stem cell:	n/a	chr19:52995951-52995964 chr19:52996074-52996084 chr19:52995949-52995967
35	CTCF	chr19:52996420-52996570	K562	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
36	CTCF	chr19:52996447-52996640	Fibrobl	skin:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
37	CTCF	chr19:52996414-52996639	H1-hESC	embryonic stem cell:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
38	CTCF	chr19:52995952-52995983	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr19:53010275-53010313	Lung_OC	lung:	n/a	n/a
40	CTCF	chr19:52996361-52996748	H1-hESC	embryonic stem cell:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
41	CTCF	chr19:52996387-52996660	GM12878	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
42	CTCF	chr19:52996440-52996583	Pancreas_OC	pancreas:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
43	CTCF	chr19:52995876-52996084	H1-hESC	embryonic stem cell:	n/a	chr19:52995951-52995964 chr19:52996074-52996084 chr19:52995949-52995967
44	CTCF	chr19:52996332-52996662	T-47D	breast:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
45	CTCF	chr19:52996420-52996570	GM12868	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
46	CTCF	chr19:52996400-52996550	GM12866	blood:	n/a	chr19:52996521-52996529 chr19:52996520-52996541
47	E2F6	chr19:52995871-52996112	K562	blood:	n/a	chr19:52996018-52996026 chr19:52996019-52996026 chr19:52996018-52996026
48	E2F6	chr19:52996303-52996712	K562	blood:	n/a	chr19:52996383-52996395 chr19:52996425-52996437
49	E2F6	chr19:52995692-52996831	H1-hESC	embryonic stem cell:	n/a	chr19:52996018-52996026 chr19:52996383-52996395 chr19:52996425-52996437 chr19:52996019-52996026 chr19:52996018-52996026
50	E2F6	chr19:52995781-52996847	H1-hESC	embryonic stem cell:	n/a	chr19:52996018-52996026 chr19:52996383-52996395 chr19:52996425-52996437 chr19:52996019-52996026 chr19:52996018-52996026

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53018151-53018201	SK-N-SH	brain:	n/a
2	chr19:53018151-53018201	SK-N-SH	brain:	n/a
3	chr19:52992415-52992465	GM12892	blood:	n/a
4	chr19:52999520-52999570	NHBE	bronchial:	n/a
5	chr19:52999520-52999570	NH-A	brain:	n/a
6	chr19:52996352-52996402	HL-60	blood:	n/a
7	chr19:53018151-53018201	T-47D	breast:	n/a
8	chr19:52996617-52996667	SK-N-SH_RA	brain:	n/a
9	chr19:52996083-52996133	Hela-S3	cervix:	n/a
10	chr19:53018151-53018201	MCF10A-Er-Src	breast:	n/a
11	chr19:52996083-52996133	NHDF-neo	bronchial:	n/a
12	chr19:52995647-52995697	ovcar-3	ovarian:	n/a
13	chr19:52996548-52996598	HCT-116	colon:	n/a
14	chr19:52996548-52996598	HEK293	kidney:	embryo
15	chr19:52996083-52996133	SAEC	small airway:	n/a
16	chr19:52996617-52996667	GM06990	blood:	n/a
17	chr19:52995647-52995697	SK-N-SH	brain:	n/a
18	chr19:52996352-52996402	RPTEC	kidney:	n/a
19	chr19:52996352-52996402	SK-N-MC	brain:	n/a
20	chr19:52995647-52995697	AG10803	skin:	n/a
21	chr19:52995647-52995697	ECC-1	luminal epithelium:	n/a
22	chr19:52996352-52996402	ECC-1	luminal epithelium:	n/a
23	chr19:52996083-52996133	HCPEpiC	choroid plexus:	n/a
24	chr19:52996548-52996598	U87	brain:	n/a
25	chr19:52996548-52996598	AG09309	skin:	n/a
26	chr19:52996617-52996667	H1-hESC	embryonic stem cell:	embryo
27	chr19:52999520-52999570	HCF	heart:	n/a
28	chr19:52996352-52996402	HCF	heart:	n/a
29	chr19:53018151-53018201	MCF-7	breast:	n/a
30	chr19:52995647-52995697	AG04449	skin:	fetal
31	chr19:52996083-52996133	HEEpiC	esophagus:	n/a
32	chr19:53018151-53018201	HCPEpiC	choroid plexus:	n/a
33	chr19:52995647-52995697	NT2-D1	testis:	n/a
34	chr19:52996548-52996598	Hepatocyte	liver:	n/a
35	chr19:52996548-52996598	HEEpiC	esophagus:	n/a
36	chr19:52996352-52996402	PANC-1	pancreas:	n/a
37	chr19:52996548-52996598	PrEC	prostate:	n/a
38	chr19:52996352-52996402	ovcar-3	ovarian:	n/a
39	chr19:53018151-53018201	HEEpiC	esophagus:	n/a
40	chr19:52995647-52995697	U87	brain:	n/a
41	chr19:53018151-53018201	PANC-1	pancreas:	n/a
42	chr19:52992415-52992465	HMEC	breast:	n/a
43	chr19:52999520-52999570	Hela-S3	cervix:	n/a
44	chr19:53018151-53018201	CMK	blood:	n/a
45	chr19:52999520-52999570	HRPEpiC	eye:	n/a
46	chr19:52996617-52996667	GM12891	blood:	n/a
47	chr19:52995647-52995697	GM06990	blood:	n/a
48	chr19:53018151-53018201	AG04449	skin:	fetal
49	chr19:52996548-52996598	NH-A	brain:	n/a
50	chr19:52996617-52996667	CMK	blood:	n/a

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

Variant related genes	Relation type
ENSG00000269349	TF binding region
ZNF578	TF binding region
ENSG00000269349	CpG island
ZNF578	CpG island

Extended variants
information (count: 1617 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1617 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200949342	chr19:52992506-52992507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562236177	chr19:52992509-52992510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs199685640	chr19:52992510-52992511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60115889	chr19:52992514-52992515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368184267	chr19:52992580-52992581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77093835	chr19:52992589-52992590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373634858	chr19:52992613-52992614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559948416	chr19:52992630-52992631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376617806	chr19:52992656-52992657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551475384	chr19:52992671-52992672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113399839	chr19:52992696-52992697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563403056	chr19:52992705-52992706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530407145	chr19:52992706-52992707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145813659	chr19:52992709-52992710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567443782	chr19:52992776-52992777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534869701	chr19:52992795-52992796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111229762	chr19:52992816-52992817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539270039	chr19:52992837-52992838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10412040	chr19:52992897-52992898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538469584	chr19:52992924-52992925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532140264	chr19:52992925-52992926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77795941	chr19:52992936-52992937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs193207846	chr19:52992952-52992953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576521707	chr19:52992958-52992959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537046329	chr19:52992963-52992964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62119308	chr19:52992982-52992983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150872580	chr19:52992987-52992988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74182409	chr19:52993009-52993010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79895840	chr19:52993010-52993011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56104361	chr19:52993017-52993018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560109486	chr19:52993037-52993038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578199357	chr19:52993049-52993050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144396550	chr19:52993069-52993070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563230350	chr19:52993092-52993093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530680066	chr19:52993117-52993118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185359247	chr19:52993126-52993127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140000651	chr19:52993138-52993139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188616929	chr19:52993145-52993146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10413273	chr19:52993161-52993162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369461984	chr19:52993253-52993254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546461994	chr19:52993264-52993265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571236577	chr19:52993318-52993319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538430994	chr19:52993332-52993333	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs550407352	chr19:52993348-52993349	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568960533	chr19:52993358-52993359	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs373201912	chr19:52993393-52993394	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs374240970	chr19:52993407-52993408	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537510737	chr19:52993423-52993424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555594713	chr19:52993449-52993450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573948184	chr19:52993464-52993465	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
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

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr19:52992200-52992600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:52992600-52995400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:52993000-52995400	Weak transcription	Left Ventricle	heart
6	chr19:52993000-52995600	Weak transcription	Brain Germinal Matrix	brain
7	chr19:52994200-52997200	ZNF genes & repeats	Ovary	ovary
8	chr19:52994600-52994800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr19:52994600-52994800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
10	chr19:52994600-52996400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
11	chr19:52994600-52999400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr19:52994800-52995400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr19:52994800-52995800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr19:52994800-52996600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr19:52994800-52997000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
16	chr19:52994800-52997200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr19:52994800-52997600	ZNF genes & repeats	Fetal Stomach	stomach
18	chr19:52995000-52995600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr19:52995200-52995400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr19:52995200-52995400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr19:52995200-52995400	Enhancers	Dnd41	blood
22	chr19:52995200-52997200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
23	chr19:52995400-52995600	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr19:52995400-52995800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
25	chr19:52995400-52995800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr19:52995400-52995800	Flanking Active TSS	Dnd41	blood
27	chr19:52995400-52996000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:52995400-52996800	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr19:52995400-52996800	ZNF genes & repeats	Left Ventricle	heart
30	chr19:52995400-52997000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
31	chr19:52995400-52997200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr19:52995400-52997200	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr19:52995400-52997200	ZNF genes & repeats	Adipose Nuclei	Adipose
34	chr19:52995400-52997400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr19:52995600-52995800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr19:52995600-52995800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:52995600-52995800	ZNF genes & repeats	Brain Hippocampus Middle	brain
38	chr19:52995600-52995800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr19:52995600-52995800	Enhancers	Fetal Muscle Leg	muscle
40	chr19:52995600-52995800	ZNF genes & repeats	Right Ventricle	heart
41	chr19:52995600-52996000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr19:52995600-52996000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr19:52995600-52996400	Active TSS	Primary T cells from cord blood	blood
44	chr19:52995600-52996400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
45	chr19:52995600-52996600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr19:52995600-52996600	ZNF genes & repeats	Brain Germinal Matrix	brain
47	chr19:52995600-52997000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr19:52995600-52997000	ZNF genes & repeats	Esophagus	oesophagus
49	chr19:52995600-52997200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr19:52995600-52997200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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