Variant report

Variant	nsv912511
Chromosome Location	chr19:56521022-56578238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:440)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:56566201-56566376	HepG2	liver:	n/a	n/a
2	BACH1	chr19:56577776-56578366	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr19:56575914-56576204	GM12878	blood:	n/a	chr19:56576070-56576081
4	BATF	chr19:56575864-56576257	GM12878	blood:	n/a	chr19:56576070-56576081
5	BHLHE40	chr19:56577811-56578091	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:56538297-56538378	K562	blood:	n/a	n/a
7	BRCA1	chr19:56539774-56539788	GM12878	blood:	n/a	n/a
8	BRCA1	chr19:56577788-56578046	HepG2	liver:	n/a	n/a
9	CEBPB	chr19:56527761-56527969	Hela-S3	cervix:	n/a	chr19:56527886-56527897 chr19:56527850-56527861
10	CEBPB	chr19:56570277-56570497	HepG2	liver:	n/a	chr19:56570428-56570439
11	CEBPB	chr19:56527867-56528017	K562	blood:	n/a	chr19:56527886-56527897
12	CEBPB	chr19:56553668-56553883	K562	blood:	n/a	n/a
13	CEBPB	chr19:56527810-56527996	A549	lung:	n/a	chr19:56527886-56527897 chr19:56527850-56527861
14	CEBPB	chr19:56566152-56566419	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:56539910-56540217	Hela-S3	cervix:	n/a	chr19:56540063-56540074
16	CEBPB	chr19:56553721-56553786	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:56570308-56570575	A549	lung:	n/a	chr19:56570428-56570439
18	CEBPB	chr19:56539955-56540110	HepG2	liver:	n/a	chr19:56540063-56540074
19	CEBPB	chr19:56527760-56528021	HepG2	liver:	n/a	chr19:56527886-56527897 chr19:56527850-56527861
20	CHD1	chr19:56577872-56578186	GM12878	blood:	n/a	n/a
21	CHD2	chr19:56577817-56578101	GM12878	blood:	n/a	n/a
22	CTCF	chr19:56577880-56578030	HVMF	connective:	n/a	chr19:56577956-56577974
23	CTCF	chr19:56553680-56553830	GM12871	blood:	n/a	n/a
24	CTCF	chr19:56577880-56578030	K562	blood:	n/a	chr19:56577956-56577974
25	CTCF	chr19:56577860-56578010	NHEK	skin:	n/a	chr19:56577956-56577974
26	CTCF	chr19:56577880-56578030	Hela-S3	cervix:	n/a	chr19:56577956-56577974
27	CTCF	chr19:56577880-56578030	HBMEC	blood vessel:	n/a	chr19:56577956-56577974
28	CTCF	chr19:56577796-56578112	MCF-7	breast:	n/a	chr19:56577956-56577974
29	CTCF	chr19:56577860-56578010	GM12868	blood:	n/a	chr19:56577956-56577974
30	CTCF	chr19:56578164-56578307	GM19240	blood:	n/a	n/a
31	CTCF	chr19:56577539-56578344	A549	lung:	n/a	chr19:56577956-56577974
32	CTCF	chr19:56578223-56578333	GM19239	blood:	n/a	n/a
33	CTCF	chr19:56577880-56578030	GM12873	blood:	n/a	chr19:56577956-56577974
34	CTCF	chr19:56577757-56578133	A549	lung:	n/a	chr19:56577956-56577974
35	CTCF	chr19:56577779-56578087	T-47D	breast:	n/a	chr19:56577956-56577974
36	CTCF	chr19:56578234-56578304	NHEK	skin:	n/a	n/a
37	CTCF	chr19:56577815-56578109	Kidney_OC	kidney:	n/a	chr19:56577956-56577974
38	CTCF	chr19:56577657-56578361	HCT-116	colon:	n/a	chr19:56577956-56577974
39	CTCF	chr19:56577560-56577710	GM12867	blood:	n/a	n/a
40	CTCF	chr19:56577880-56578030	GM12870	blood:	n/a	chr19:56577956-56577974
41	CTCF	chr19:56577842-56578066	ECC-1	luminal epithelium:	n/a	chr19:56577956-56577974
42	CTCF	chr19:56578108-56578109	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr19:56577774-56578146	MCF-7	breast:	n/a	chr19:56577956-56577974
44	CTCF	chr19:56578189-56578295	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr19:56577300-56577450	WI-38	lung:	n/a	n/a
46	CTCF	chr19:56577860-56578010	GM12864	blood:	n/a	chr19:56577956-56577974
47	CTCF	chr19:56577900-56578050	HCM	heart:	n/a	chr19:56577956-56577974
48	CTCF	chr19:56577880-56578030	NHLF	lung:	n/a	chr19:56577956-56577974
49	CTCF	chr19:56577778-56578126	ECC-1	luminal epithelium:	n/a	chr19:56577956-56577974
50	CTCF	chr19:56577880-56578030	HRPEpiC	eye:	n/a	chr19:56577956-56577974

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56572945-56572995	HRCEpiC	kidney:	n/a
2	chr19:56572945-56572995	Hela-S3	cervix:	n/a
3	chr19:56572945-56572995	HNPCEpiC	eye:	n/a
4	chr19:56572945-56572995	IMR90	lung:	fetal
5	chr19:56572945-56572995	NB4	blood:	n/a
6	chr19:56572945-56572995	HEK293	kidney:	embryo
7	chr19:56572945-56572995	GM12891	blood:	n/a
8	chr19:56572945-56572995	GM12878	blood:	n/a
9	chr19:56572945-56572995	HPAEpiC	pulmonary alveolar:	n/a
10	chr19:56572945-56572995	SK-N-MC	brain:	n/a
11	chr19:56572945-56572995	NT2-D1	testis:	n/a
12	chr19:56572945-56572995	NH-A	brain:	n/a
13	chr19:56572945-56572995	GM19239	blood:	n/a
14	chr19:56572945-56572995	HEEpiC	esophagus:	n/a
15	chr19:56572945-56572995	Jurkat	blood:	n/a
16	chr19:56572945-56572995	K562	blood:	n/a
17	chr19:56572945-56572995	ProgFib	skin:	n/a
18	chr19:56572945-56572995	ECC-1	luminal epithelium:	n/a
19	chr19:56572945-56572995	HCT-116	colon:	n/a
20	chr19:56572945-56572995	SKMC	muscle:	n/a
21	chr19:56572945-56572995	SAEC	small airway:	n/a
22	chr19:56572945-56572995	HIPEpiC	eye:	n/a
23	chr19:56572945-56572995	HMEC	breast:	n/a
24	chr19:56572945-56572995	SK-N-SH_RA	brain:	n/a
25	chr19:56572945-56572995	Caco-2	colon:	n/a
26	chr19:56572945-56572995	HAEpiC	amniotic membrane:	n/a
27	chr19:56572945-56572995	NHDF-neo	bronchial:	n/a
28	chr19:56572945-56572995	GM12892	blood:	n/a
29	chr19:56572945-56572995	HepG2	liver:	n/a
30	chr19:56572945-56572995	NHBE	bronchial:	n/a
31	chr19:56572945-56572995	BJ	skin:	n/a
32	chr19:56572945-56572995	HCM	heart:	n/a
33	chr19:56572945-56572995	AG09319	gingival:	n/a
34	chr19:56572945-56572995	PrEC	prostate:	n/a
35	chr19:56572945-56572995	HCF	heart:	n/a
36	chr19:56572945-56572995	BE2_C	brain:	n/a
37	chr19:56572945-56572995	PFSK-1	brain:	n/a
38	chr19:56572945-56572995	CMK	blood:	n/a
39	chr19:56572945-56572995	Hepatocyte	liver:	n/a
40	chr19:56572945-56572995	HUVEC	blood vessel:	n/a
41	chr19:56572945-56572995	GM06990	blood:	n/a
42	chr19:56572945-56572995	T-47D	breast:	n/a
43	chr19:56572945-56572995	AG04450	lung:	fetal
44	chr19:56572945-56572995	MCF-7	breast:	n/a
45	chr19:56572945-56572995	AG10803	skin:	n/a
46	chr19:56572945-56572995	HL-60	blood:	n/a
47	chr19:56572945-56572995	RPTEC	kidney:	n/a
48	chr19:56572945-56572995	AoSMC	blood vessel:	n/a
49	chr19:56572945-56572995	HRPEpiC	eye:	n/a
50	chr19:56572945-56572995	H1-hESC	embryonic stem cell:	embryo

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56538350..56540357-chr19:56542809..56545691,2	K562	blood:
2	chr19:56538480..56540946-chr19:56548359..56549987,2	K562	blood:
3	chr19:56538350..56540357-chr19:56542809..56545691,2	K562	blood:
4	chr19:56571281..56574036-chr19:56575798..56577749,2	K562	blood:
5	chr19:56532441..56535023-chr19:56626628..56629336,2	K562	blood:
6	chr19:56571281..56574036-chr19:56575798..56577749,2	K562	blood:
7	chr19:56537372..56539980-chr19:56548359..56550687,2	K562	blood:
8	chr19:56538480..56540946-chr19:56548359..56549987,2	K562	blood:
9	chr19:56569842..56570489-chr19:56587473..56588459,2	MCF-7	breast:
10	chr19:56537372..56539980-chr19:56548359..56550687,2	K562	blood:
11	chr19:56574744..56577085-chr19:56619874..56622339,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLRP5-1	chr19:56578050-56578341	ENSG00000248386
2	lnc-ZNF787-1	chr19:56528857-56529011	ucscGeneNc_uc002pwe_1
3	lnc-ZNF787-1	chr19:56535081-56535219	ucscGeneNc_uc002pwe_1
4	lnc-ZNF787-1	chr19:56532996-56533274	ucscGeneNc_uc002pwe_1
5	lnc-ZNF787-1	chr19:56532304-56532600	ucscGeneNc_uc002pwe_1
6	lnc-ZNF787-1	chr19:56529257-56529370	ucscGeneNc_uc002pwe_1
7	lnc-NLRP5-1	chr19:56578050-56578341	ENSG00000267522.1
8	lnc-ZNF787-1	chr19:56533954-56534208	ucscGeneNc_uc002pwe_1
9	lnc-ZNF787-1	chr19:56526602-56527706	ucscGeneNc_uc002pwe_1

No data

Variant related genes	Relation type
ENSG00000267522	TF binding region
ENSG00000267522	CpG island
E2F6	miRNA target sites

Extended variants
information (count: 759 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531545631	chr19:56521205-56521206	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs143618499	chr19:56521228-56521229	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs561555831	chr19:56521237-56521238	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs16986875	chr19:56521252-56521253	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs137876684	chr19:56521294-56521295	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs564190502	chr19:56521295-56521296	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs533010887	chr19:56521315-56521316	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs141738994	chr19:56521316-56521317	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs144633181	chr19:56521356-56521357	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs16986877	chr19:56521381-56521382	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs138588606	chr19:56521396-56521397	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs549631928	chr19:56521397-56521398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs141679000	chr19:56521398-56521399	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs146177437	chr19:56521457-56521458	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs192361641	chr19:56521507-56521508	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs577721268	chr19:56521510-56521511	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs628370	chr19:56521536-56521537	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs77176989	chr19:56521544-56521545	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs576161714	chr19:56521545-56521546	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs541791139	chr19:56521549-56521550	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549059351	chr19:56521556-56521557	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs573610442	chr19:56521560-56521561	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs553700221	chr19:56521561-56521562	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs138329805	chr19:56521562-56521563	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs180766483	chr19:56521565-56521566	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs572217672	chr19:56521581-56521582	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537189323	chr19:56526602-56526603	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs139766628	chr19:56526604-56526605	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs149807560	chr19:56526640-56526641	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs191932602	chr19:56526655-56526656	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs184234168	chr19:56526657-56526658	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs187767033	chr19:56526688-56526689	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs545377511	chr19:56526709-56526710	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs566710041	chr19:56526712-56526713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs565323614	chr19:56526717-56526718	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs530820320	chr19:56526735-56526736	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs4801661	chr19:56526837-56526838	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561389284	chr19:56526860-56526861	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs201847565	chr19:56526868-56526869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs530183081	chr19:56526873-56526874	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs549232182	chr19:56526885-56526886	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs565857455	chr19:56526891-56526892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs371387952	chr19:56526906-56526907	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs376373493	chr19:56526908-56526909	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs144665185	chr19:56526911-56526912	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs4801662	chr19:56526913-56526914	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542949933	chr19:56526917-56526918	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs191125296	chr19:56526920-56526921	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs536644764	chr19:56526921-56526922	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs139535867	chr19:56526951-56526952	Inactive region	lncRNA	n/a	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
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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56521200-56521600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr19:56521400-56521600	Bivalent/Poised TSS	Hela-S3	cervix
3	chr19:56538000-56540200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:56538200-56538800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:56538400-56538600	Bivalent/Poised TSS	Hela-S3	cervix
6	chr19:56538600-56539200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:56548400-56550600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:56548400-56550800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr19:56549000-56550600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:56549400-56550200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr19:56566000-56566400	Enhancers	HepG2	liver
12	chr19:56574600-56575000	Bivalent Enhancer	HepG2	liver
13	chr19:56575000-56577800	Weak transcription	Pancreas	Pancrea
14	chr19:56575600-56577600	Weak transcription	HUVEC	blood vessel
15	chr19:56576000-56577800	Enhancers	K562	blood
16	chr19:56576600-56576800	Enhancers	NH-A	brain
17	chr19:56576800-56577800	Weak transcription	NH-A	brain
18	chr19:56577200-56577400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:56577200-56577400	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr19:56577200-56577600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr19:56577400-56577600	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr19:56577400-56577600	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr19:56577400-56577800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr19:56577400-56578800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr19:56577600-56577800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
26	chr19:56577600-56577800	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
27	chr19:56577600-56577800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
28	chr19:56577600-56577800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr19:56577600-56577800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr19:56577600-56577800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr19:56577600-56577800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
32	chr19:56577600-56577800	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
33	chr19:56577600-56577800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
34	chr19:56577600-56577800	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr19:56577600-56577800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr19:56577600-56577800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr19:56577600-56577800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr19:56577600-56577800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr19:56577600-56577800	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
40	chr19:56577600-56577800	Bivalent Enhancer	Adipose Nuclei	Adipose
41	chr19:56577600-56577800	Enhancers	Brain Cingulate Gyrus	brain
42	chr19:56577600-56577800	Flanking Active TSS	Brain Germinal Matrix	brain
43	chr19:56577600-56577800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
44	chr19:56577600-56577800	Bivalent Enhancer	Fetal Brain Male	brain
45	chr19:56577600-56577800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
46	chr19:56577600-56577800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
47	chr19:56577600-56577800	Bivalent Enhancer	Dnd41	blood
48	chr19:56577600-56577800	Enhancers	GM12878-XiMat	blood
49	chr19:56577600-56577800	Flanking Bivalent TSS/Enh	Hela-S3	cervix
50	chr19:56577600-56578000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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