Variant report

Variant	nsv544090
Chromosome Location	chr19:56384193-56538729
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	chr19:56404597-56404754	GM12878	blood:	n/a	n/a
2	BCL11A	chr19:56404601-56404738	GM12878	blood:	n/a	n/a
3	BCL11A	chr19:56404582-56404766	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:56538297-56538378	K562	blood:	n/a	n/a
5	CBX3	chr19:56485399-56485613	K562	blood:	n/a	n/a
6	CEBPB	chr19:56502244-56502561	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr19:56527867-56528017	K562	blood:	n/a	chr19:56527886-56527897
8	CEBPB	chr19:56385000-56385192	K562	blood:	n/a	n/a
9	CEBPB	chr19:56413999-56414214	HepG2	liver:	n/a	chr19:56414104-56414121 chr19:56414107-56414118 chr19:56414109-56414120 chr19:56414107-56414120 chr19:56414107-56414120
10	CEBPB	chr19:56448063-56448170	A549	lung:	n/a	n/a
11	CEBPB	chr19:56480616-56480742	HepG2	liver:	n/a	chr19:56480657-56480668
12	CEBPB	chr19:56527760-56528021	HepG2	liver:	n/a	chr19:56527886-56527897 chr19:56527850-56527861
13	CEBPB	chr19:56406673-56406772	HepG2	liver:	n/a	chr19:56406697-56406708
14	CEBPB	chr19:56492421-56492621	HepG2	liver:	n/a	chr19:56492531-56492542
15	CEBPB	chr19:56448047-56448229	IMR90	lung:	n/a	n/a
16	CEBPB	chr19:56448024-56448130	K562	blood:	n/a	n/a
17	CEBPB	chr19:56469909-56469933	HepG2	liver:	n/a	n/a
18	CEBPB	chr19:56448058-56448093	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr19:56527810-56527996	A549	lung:	n/a	chr19:56527886-56527897 chr19:56527850-56527861
20	CEBPB	chr19:56527761-56527969	Hela-S3	cervix:	n/a	chr19:56527886-56527897 chr19:56527850-56527861
21	CEBPB	chr19:56413977-56414273	K562	blood:	n/a	chr19:56414104-56414121 chr19:56414107-56414118 chr19:56414109-56414120 chr19:56414107-56414120 chr19:56414107-56414120
22	CEBPB	chr19:56469812-56470113	MCF-7	breast:	n/a	n/a
23	CEBPB	chr19:56384985-56385182	HepG2	liver:	n/a	n/a
24	CREB1	chr19:56410261-56410516	A549	lung:	n/a	n/a
25	CTCF	chr19:56425200-56425350	GM12870	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
26	CTCF	chr19:56425127-56425357	A549	lung:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
27	CTCF	chr19:56457260-56457410	A549	lung:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
28	CTCF	chr19:56478113-56478180	LNCaP	prostate:	n/a	n/a
29	CTCF	chr19:56457276-56457465	H1-hESC	embryonic stem cell:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
30	CTCF	chr19:56457334-56457416	Lung_OC	lung:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
31	CTCF	chr19:56454320-56454470	HCT-116	colon:	n/a	n/a
32	CTCF	chr19:56425200-56425350	HMEC	breast:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
33	CTCF	chr19:56457280-56457430	K562	blood:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
34	CTCF	chr19:56455760-56455910	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:56457300-56457450	SK-N-SH_RA	brain:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
36	CTCF	chr19:56457280-56457430	GM12870	blood:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
37	CTCF	chr19:56425134-56425349	Medullo	brain:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
38	CTCF	chr19:56425160-56425310	HFF-Myc	foreskin:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
39	CTCF	chr19:56425140-56425290	GM12871	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
40	CTCF	chr19:56457260-56457410	GM06990	blood:	n/a	chr19:56457358-56457376 chr19:56457360-56457373 chr19:56457359-56457375
41	CTCF	chr19:56457200-56457350	GM12868	blood:	n/a	n/a
42	CTCF	chr19:56425180-56425330	MCF-7	breast:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
43	CTCF	chr19:56478088-56478203	K562	blood:	n/a	n/a
44	CTCF	chr19:56425103-56425484	K562	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
45	CTCF	chr19:56477980-56478266	K562	blood:	n/a	n/a
46	CTCF	chr19:56404614-56404713	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr19:56454413-56454468	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:56425141-56425358	MCF-7	breast:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
49	CTCF	chr19:56425166-56425324	SK-N-SH_RA	brain:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
50	CTCF	chr19:56425420-56425570	GM12867	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56393163-56393213	HRPEpiC	eye:	n/a
2	chr19:56393163-56393213	HRPEpiC	eye:	n/a
3	chr19:56444163-56444213	HCF	heart:	n/a
4	chr19:56443419-56443469	ProgFib	skin:	n/a
5	chr19:56466500-56466550	GM12878	blood:	n/a
6	chr19:56459234-56459284	IMR90	lung:	fetal
7	chr19:56459108-56459158	GM19239	blood:	n/a
8	chr19:56511149-56511199	H1-hESC	embryonic stem cell:	embryo
9	chr19:56499348-56499398	HepG2	liver:	n/a
10	chr19:56510200-56510250	PrEC	prostate:	n/a
11	chr19:56511149-56511199	SKMC	muscle:	n/a
12	chr19:56499348-56499398	HEK293	kidney:	embryo
13	chr19:56466500-56466550	ovcar-3	ovarian:	n/a
14	chr19:56510200-56510250	H1-hESC	embryonic stem cell:	embryo
15	chr19:56459103-56459153	K562	blood:	n/a
16	chr19:56510892-56510942	AG09309	skin:	n/a
17	chr19:56459137-56459187	H1-hESC	embryonic stem cell:	embryo
18	chr19:56510965-56511015	Caco-2	colon:	n/a
19	chr19:56459103-56459153	BJ	skin:	n/a
20	chr19:56499348-56499398	AG09309	skin:	n/a
21	chr19:56510892-56510942	HEK293	kidney:	embryo
22	chr19:56511149-56511199	Caco-2	colon:	n/a
23	chr19:56511149-56511199	HPAEpiC	pulmonary alveolar:	n/a
24	chr19:56459137-56459187	PrEC	prostate:	n/a
25	chr19:56459234-56459284	NH-A	brain:	n/a
26	chr19:56459108-56459158	NB4	blood:	n/a
27	chr19:56393163-56393213	HCF	heart:	n/a
28	chr19:56458926-56458976	IMR90	lung:	fetal
29	chr19:56443419-56443469	AoSMC	blood vessel:	n/a
30	chr19:56510200-56510250	HRE	kidney:	n/a
31	chr19:56443419-56443469	HL-60	blood:	n/a
32	chr19:56444163-56444213	NH-A	brain:	n/a
33	chr19:56458926-56458976	RPTEC	kidney:	n/a
34	chr19:56510965-56511015	RPTEC	kidney:	n/a
35	chr19:56510200-56510250	PFSK-1	brain:	n/a
36	chr19:56443824-56443874	Hela-S3	cervix:	n/a
37	chr19:56459103-56459153	HMEC	breast:	n/a
38	chr19:56459103-56459153	AG09309	skin:	n/a
39	chr19:56510200-56510250	SKMC	muscle:	n/a
40	chr19:56499348-56499398	NH-A	brain:	n/a
41	chr19:56459137-56459187	PANC-1	pancreas:	n/a
42	chr19:56444551-56444601	T-47D	breast:	n/a
43	chr19:56458926-56458976	AG10803	skin:	n/a
44	chr19:56459103-56459153	GM12891	blood:	n/a
45	chr19:56444551-56444601	AG04449	skin:	fetal
46	chr19:56510833-56510883	A549	lung:	n/a
47	chr19:56444163-56444213	AG09319	gingival:	n/a
48	chr19:56444163-56444213	AoSMC	blood vessel:	n/a
49	chr19:56499348-56499398	GM12891	blood:	n/a
50	chr19:56459234-56459284	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56439351..56441429-chr19:56446067..56448328,2	MCF-7	breast:
2	chr19:56538350..56540357-chr19:56542809..56545691,2	K562	blood:
3	chr19:56464807..56467455-chr19:56469685..56471686,2	K562	blood:
4	chr19:56538480..56540946-chr19:56548359..56549987,2	K562	blood:
5	chr19:56430402..56432379-chr19:56447676..56449907,2	K562	blood:
6	chr19:56532441..56535023-chr19:56626628..56629336,2	K562	blood:
7	chr19:56439351..56441429-chr19:56446067..56448328,2	MCF-7	breast:
8	chr19:56464653..56466307-chr19:56469683..56471185,2	K562	blood:
9	chr19:56437345..56439386-chr19:56452694..56454259,2	K562	blood:
10	chr19:56537372..56539980-chr19:56548359..56550687,2	K562	blood:
11	chr19:56424869..56425718-chr19:56582163..56583125,2	MCF-7	breast:
12	chr19:56437345..56439386-chr19:56452694..56454259,2	K562	blood:
13	chr19:56454965..56456732-chr19:56458857..56460406,2	MCF-7	breast:
14	chr19:56430402..56432379-chr19:56447676..56449907,2	K562	blood:
15	chr19:56464807..56467455-chr19:56469685..56471686,2	K562	blood:
16	chr19:56464653..56466307-chr19:56469683..56471185,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLRP4-1	chr19:56400283-56401109	XLOC_013162
2	lnc-ZNF787-1	chr19:56535081-56535219	ucscGeneNc_uc002pwe_1
3	lnc-NLRP4-1	chr19:56399226-56399347	XLOC_013162
4	lnc-ZNF787-1	chr19:56532996-56533274	ucscGeneNc_uc002pwe_1
5	lnc-ZNF787-1	chr19:56526602-56527706	ucscGeneNc_uc002pwe_1
6	lnc-ZNF787-1	chr19:56528857-56529011	ucscGeneNc_uc002pwe_1
7	lnc-ZNF787-1	chr19:56533954-56534208	ucscGeneNc_uc002pwe_1
8	lnc-ZNF787-1	chr19:56532304-56532600	ucscGeneNc_uc002pwe_1
9	lnc-ZNF787-1	chr19:56529257-56529370	ucscGeneNc_uc002pwe_1

Variant related genes	Relation type
NLRP8	TF binding region
NLRP13	TF binding region
NLRP5	TF binding region
NLRP8	CpG island
NLRP13	CpG island
NLRP5	CpG island
ENSG00000179709	chromatin interactions

Extended variants
information (count: 1144 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1144 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143002824	chr19:56399239-56399240	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs576443475	chr19:56399258-56399259	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs6509968	chr19:56399296-56399297	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs575434347	chr19:56399313-56399314	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs185786469	chr19:56399317-56399318	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs546872771	chr19:56399324-56399325	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs560190915	chr19:56399325-56399326	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs548915193	chr19:56400295-56400296	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs73624525	chr19:56400303-56400304	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs377274342	chr19:56400354-56400355	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs386811131	chr19:56400359-56400360	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs370864980	chr19:56400364-56400365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs540470165	chr19:56400384-56400385	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs149376875	chr19:56400396-56400397	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs537459462	chr19:56400410-56400411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs34713675	chr19:56400414-56400415	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs113694848	chr19:56400440-56400441	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs76841359	chr19:56400463-56400464	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs182635553	chr19:56400561-56400562	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs541931530	chr19:56400562-56400563	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs114757536	chr19:56400573-56400574	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs546190765	chr19:56400605-56400606	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs527361883	chr19:56400614-56400615	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs547631007	chr19:56400662-56400663	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs144755628	chr19:56400688-56400689	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs186839987	chr19:56400711-56400712	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs566175448	chr19:56400723-56400724	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs367814543	chr19:56400741-56400742	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs533684707	chr19:56400759-56400760	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs35739050	chr19:56400764-56400765	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs550157601	chr19:56400770-56400771	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs191677199	chr19:56400790-56400791	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs75490920	chr19:56400919-56400920	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs549345704	chr19:56400939-56400940	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs184272762	chr19:56400945-56400946	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs535122571	chr19:56400990-56400991	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs554052801	chr19:56400999-56401000	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs541683612	chr19:56401073-56401074	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs143748466	chr19:56401077-56401078	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs538334883	chr19:56401101-56401102	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs35549335	chr19:56401102-56401103	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs397948175	chr19:56401108-56401109	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs200544198	chr19:56401109-56401110	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs376030098	chr19:56412407-56412408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561381201	chr19:56412413-56412414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191815935	chr19:56412427-56412428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114189584	chr19:56412453-56412454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530274578	chr19:56412501-56412502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs302833	chr19:56412546-56412547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184426120	chr19:56412598-56412599	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56412400-56413200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr19:56419000-56419400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:56421400-56421600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
4	chr19:56423600-56424600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:56442400-56443000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:56463600-56464400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr19:56468000-56468200	Bivalent Enhancer	HepG2	liver
8	chr19:56482000-56482400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr19:56485200-56486600	Enhancers	Brain Hippocampus Middle	brain
10	chr19:56486200-56487000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr19:56486400-56486800	Flanking Active TSS	Brain Anterior Caudate	brain
12	chr19:56495800-56496400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr19:56496000-56496200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr19:56496200-56497600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr19:56496400-56497600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr19:56497600-56498000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
17	chr19:56497600-56498200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr19:56497600-56498200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:56497800-56498200	ZNF genes & repeats	Pancreas	Pancrea
20	chr19:56502400-56502800	Enhancers	Hela-S3	cervix
21	chr19:56504600-56504800	Active TSS	HSMM	muscle
22	chr19:56504600-56504800	Weak transcription	HSMMtube	muscle
23	chr19:56504600-56505000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr19:56504600-56505000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:56504600-56505000	ZNF genes & repeats	NHEK	skin
26	chr19:56504800-56505000	Enhancers	HSMMtube	muscle
27	chr19:56504800-56505200	Flanking Active TSS	HSMM	muscle
28	chr19:56504800-56505600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
29	chr19:56504800-56505600	Active TSS	GM12878-XiMat	blood
30	chr19:56505000-56505800	Weak transcription	HSMMtube	muscle
31	chr19:56519000-56519400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr19:56521200-56521600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr19:56521400-56521600	Bivalent/Poised TSS	Hela-S3	cervix
34	chr19:56538000-56540200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:56538200-56538800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr19:56538400-56538600	Bivalent/Poised TSS	Hela-S3	cervix
37	chr19:56538600-56539200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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