Variant report

Variant	esv3528005
Chromosome Location	chr19:56712029-56750105
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	ATF1	chr19:56732773-56733067	K562	blood:	n/a	n/a
2	BATF	chr19:56745875-56746197	GM12878	blood:	n/a	n/a
3	BRCA1	chr19:56720561-56720808	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr19:56745473-56745601	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr19:56723261-56723384	K562	blood:	n/a	n/a
6	CEBPB	chr19:56732791-56733124	H1-hESC	embryonic stem cell:	n/a	chr19:56732934-56732945
7	CEBPB	chr19:56736713-56736976	K562	blood:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
8	CEBPB	chr19:56732747-56733109	K562	blood:	n/a	chr19:56732934-56732945
9	CEBPB	chr19:56741719-56741891	K562	blood:	n/a	chr19:56741810-56741821
10	CEBPB	chr19:56720517-56720847	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr19:56741646-56741970	HepG2	liver:	n/a	chr19:56741810-56741821
12	CEBPB	chr19:56716360-56717024	Hela-S3	cervix:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
13	CEBPB	chr19:56732731-56733102	K562	blood:	n/a	chr19:56732934-56732945
14	CEBPB	chr19:56716430-56716674	HepG2	liver:	n/a	chr19:56716533-56716544
15	CEBPB	chr19:56732645-56733248	Hela-S3	cervix:	n/a	chr19:56732934-56732945
16	CEBPB	chr19:56716429-56716798	A549	lung:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
17	CEBPB	chr19:56716455-56716760	IMR90	lung:	n/a	chr19:56716533-56716544
18	CEBPB	chr19:56744051-56744221	K562	blood:	n/a	n/a
19	CEBPB	chr19:56741673-56741957	K562	blood:	n/a	chr19:56741810-56741821
20	CEBPB	chr19:56732764-56733076	HepG2	liver:	n/a	chr19:56732934-56732945
21	CEBPB	chr19:56744025-56744198	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr19:56732730-56733098	A549	lung:	n/a	chr19:56732934-56732945
23	CEBPB	chr19:56732726-56733084	MCF-7	breast:	n/a	chr19:56732934-56732945
24	CEBPB	chr19:56732773-56733100	IMR90	lung:	n/a	chr19:56732934-56732945
25	CEBPB	chr19:56736739-56736963	HepG2	liver:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
26	CEBPB	chr19:56736709-56737013	Hela-S3	cervix:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
27	CEBPB	chr19:56741714-56741974	IMR90	lung:	n/a	chr19:56741810-56741821
28	CEBPB	chr19:56732796-56733078	A549	lung:	n/a	chr19:56732934-56732945
29	CEBPB	chr19:56716510-56716908	K562	blood:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
30	CEBPB	chr19:56732803-56733050	K562	blood:	n/a	chr19:56732934-56732945
31	CEBPB	chr19:56736715-56737020	A549	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
32	CEBPB	chr19:56741741-56741909	H1-hESC	embryonic stem cell:	n/a	chr19:56741810-56741821
33	CEBPB	chr19:56736697-56737012	IMR90	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
34	CEBPB	chr19:56741649-56741971	A549	lung:	n/a	chr19:56741810-56741821
35	CEBPD	chr19:56732776-56733035	K562	blood:	n/a	n/a
36	CHD2	chr19:56720635-56720730	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr19:56720040-56720297	K562	blood:	n/a	n/a
38	CTCF	chr19:56734300-56734450	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr19:56732981-56733171	NHEK	skin:	n/a	n/a
40	CTCF	chr19:56732940-56733090	GM12865	blood:	n/a	n/a
41	CTCF	chr19:56723281-56723310	Gliobla	brain:	n/a	n/a
42	CTCF	chr19:56733180-56733330	MCF-7	breast:	n/a	n/a
43	CTCF	chr19:56719092-56719277	Fibrobl	skin:	n/a	n/a
44	CTCF	chr19:56732940-56733090	Caco-2	colon:	n/a	n/a
45	CTCF	chr19:56732920-56733070	WI-38	lung:	n/a	n/a
46	CTCF	chr19:56732978-56733170	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:56734402-56734595	K562	blood:	n/a	n/a
48	CTCF	chr19:56732940-56733090	NHLF	lung:	n/a	n/a
49	CTCF	chr19:56734373-56734556	K562	blood:	n/a	n/a
50	CTCF	chr19:56717973-56718013	Spleen_OC	spleen:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56739782-56739832	NT2-D1	testis:	n/a
2	chr19:56739782-56739832	NT2-D1	testis:	n/a
3	chr19:56739749-56739799	HAEpiC	amniotic membrane:	n/a
4	chr19:56739573-56739623	GM19239	blood:	n/a
5	chr19:56739573-56739623	HUVEC	blood vessel:	n/a
6	chr19:56741019-56741069	HRPEpiC	eye:	n/a
7	chr19:56741019-56741069	NT2-D1	testis:	n/a
8	chr19:56738933-56738983	LNCaP	prostate:	n/a
9	chr19:56733045-56733095	SK-N-SH	brain:	n/a
10	chr19:56741019-56741069	PFSK-1	brain:	n/a
11	chr19:56739731-56739781	A549	lung:	n/a
12	chr19:56741019-56741069	HCF	heart:	n/a
13	chr19:56732932-56732982	PrEC	prostate:	n/a
14	chr19:56728422-56728472	HEEpiC	esophagus:	n/a
15	chr19:56726303-56726353	NHDF-neo	bronchial:	n/a
16	chr19:56739868-56739918	A549	lung:	n/a
17	chr19:56742355-56742405	NB4	blood:	n/a
18	chr19:56742355-56742405	HRE	kidney:	n/a
19	chr19:56739573-56739623	HepG2	liver:	n/a
20	chr19:56732932-56732982	LNCaP	prostate:	n/a
21	chr19:56728422-56728472	Caco-2	colon:	n/a
22	chr19:56739741-56739791	Jurkat	blood:	n/a
23	chr19:56740672-56740722	GM12891	blood:	n/a
24	chr19:56739573-56739623	AG04450	lung:	fetal
25	chr19:56728589-56728639	HCM	heart:	n/a
26	chr19:56742355-56742405	HIPEpiC	eye:	n/a
27	chr19:56741019-56741069	AG10803	skin:	n/a
28	chr19:56728589-56728639	HIPEpiC	eye:	n/a
29	chr19:56728589-56728639	HEEpiC	esophagus:	n/a
30	chr19:56732932-56732982	GM12878	blood:	n/a
31	chr19:56739731-56739781	SAEC	small airway:	n/a
32	chr19:56739573-56739623	Jurkat	blood:	n/a
33	chr19:56730494-56730544	MCF-7	breast:	n/a
34	chr19:56726303-56726353	GM06990	blood:	n/a
35	chr19:56739868-56739918	HPAEpiC	pulmonary alveolar:	n/a
36	chr19:56741019-56741069	H1-hESC	embryonic stem cell:	embryo
37	chr19:56739868-56739918	GM19239	blood:	n/a
38	chr19:56739731-56739781	HL-60	blood:	n/a
39	chr19:56728589-56728639	U87	brain:	n/a
40	chr19:56730494-56730544	NHDF-neo	bronchial:	n/a
41	chr19:56739573-56739623	NT2-D1	testis:	n/a
42	chr19:56739749-56739799	MCF10A-Er-Src	breast:	n/a
43	chr19:56739782-56739832	AG04449	skin:	fetal
44	chr19:56726303-56726353	AG10803	skin:	n/a
45	chr19:56738933-56738983	BJ	skin:	n/a
46	chr19:56739788-56739838	BJ	skin:	n/a
47	chr19:56733045-56733095	U87	brain:	n/a
48	chr19:56741019-56741069	SK-N-SH_RA	brain:	n/a
49	chr19:56742355-56742405	NH-A	brain:	n/a
50	chr19:56730494-56730544	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56731454..56732253-chr19:56820726..56821606,2	MCF-7	breast:
2	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
3	chr19:56587934..56588448-chr19:56732565..56733070,2	MCF-7	breast:
4	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:

Variant related genes	Relation type
ZSCAN5B	TF binding region
ZSCAN5C	TF binding region
ENSG00000242411	TF binding region
ZSCAN5D	TF binding region
ZSCAN5A	TF binding region
ZSCAN5B	CpG island
ZSCAN5C	CpG island
ENSG00000242411	CpG island
ZSCAN5D	CpG island
ZSCAN5A	CpG island

Extended variants
information (count: 1508 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1508 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542186687	chr19:56712073-56712074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12979377	chr19:56712080-56712081	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562630557	chr19:56712082-56712083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs62120856	chr19:56712092-56712093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs3859418	chr19:56712098-56712099	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542238832	chr19:56712106-56712107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375011077	chr19:56712109-56712110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532355343	chr19:56712148-56712149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552264888	chr19:56712185-56712186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562622550	chr19:56712190-56712191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs367893539	chr19:56712196-56712197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181332884	chr19:56712214-56712215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548152088	chr19:56712229-56712230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs62120857	chr19:56712232-56712233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568012876	chr19:56712237-56712238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186931600	chr19:56712306-56712307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112234511	chr19:56712311-56712312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183507980	chr19:56712320-56712321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62120858	chr19:56712340-56712341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527829169	chr19:56712350-56712351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539667174	chr19:56712376-56712377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541183900	chr19:56712385-56712386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533481730	chr19:56712900-56712901	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs550341273	chr19:56712939-56712940	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs570199876	chr19:56712945-56712946	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs189919154	chr19:56712975-56712976	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs77936413	chr19:56712982-56712983	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs11879559	chr19:56712994-56712995	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
29	rs59644879	chr19:56713022-56713023	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs145964845	chr19:56713053-56713054	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs148643508	chr19:56713072-56713073	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs546157829	chr19:56713075-56713076	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs544796168	chr19:56713121-56713122	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs111591158	chr19:56713135-56713136	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs570676150	chr19:56713161-56713162	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs556278381	chr19:56713175-56713176	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs531068512	chr19:56714450-56714451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550690073	chr19:56714468-56714469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536392714	chr19:56715768-56715769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs546617887	chr19:56715807-56715808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566480732	chr19:56715819-56715820	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs181501166	chr19:56715830-56715831	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186466761	chr19:56715931-56715932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs560068580	chr19:56715965-56715966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs190847411	chr19:56715974-56715975	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566442570	chr19:56716360-56716361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144518410	chr19:56716393-56716394	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs12984780	chr19:56716395-56716396	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535351948	chr19:56716413-56716414	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs117424106	chr19:56716458-56716459	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56710800-56712400	Enhancers	Liver	Liver
2	chr19:56716600-56717200	Bivalent Enhancer	Hela-S3	cervix
3	chr19:56723600-56727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:56724400-56728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:56725000-56725200	Active TSS	A549	lung
6	chr19:56725200-56727400	Weak transcription	A549	lung
7	chr19:56727400-56727600	ZNF genes & repeats	A549	lung
8	chr19:56727400-56727800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:56727400-56728200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr19:56727600-56735800	Weak transcription	A549	lung
11	chr19:56727800-56728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:56727800-56729000	Enhancers	Dnd41	blood
13	chr19:56728000-56728400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr19:56728000-56728400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr19:56728000-56728400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr19:56728000-56728400	Enhancers	Esophagus	oesophagus
19	chr19:56728000-56728800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:56728000-56729400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr19:56728200-56728400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr19:56728200-56728400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr19:56728200-56728400	Enhancers	Primary hematopoietic stem cells	blood
24	chr19:56728200-56728400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr19:56728200-56728400	Enhancers	HMEC	breast
28	chr19:56728200-56728400	Enhancers	HUVEC	blood vessel
29	chr19:56728200-56728600	Bivalent Enhancer	Thymus	Thymus
30	chr19:56728200-56728800	Bivalent Enhancer	Placenta	Placenta
31	chr19:56728200-56728800	Bivalent Enhancer	Fetal Thymus	thymus
32	chr19:56728200-56729200	Active TSS	Rectal Mucosa Donor 31	rectum
33	chr19:56728200-56729400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:56728200-56729400	Enhancers	Fetal Heart	heart
35	chr19:56728400-56728600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
36	chr19:56728400-56728600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr19:56728400-56728600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr19:56728400-56728600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
39	chr19:56728400-56728600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr19:56728400-56728600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr19:56728400-56728600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:56728400-56728600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:56728400-56728600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
44	chr19:56728400-56728600	Bivalent Enhancer	Brain Germinal Matrix	brain
45	chr19:56728400-56728600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
46	chr19:56728400-56728600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
47	chr19:56728400-56728600	Flanking Active TSS	Esophagus	oesophagus
48	chr19:56728400-56728600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr19:56728400-56728600	Bivalent Enhancer	Fetal Brain Female	brain
50	chr19:56728400-56728600	Flanking Active TSS	Fetal Lung	lung

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