Variant report

Variant	nsv580356
Chromosome Location	chr19:56723492-56762780
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	ARID3A	chr19:56760286-56760731	K562	blood:	n/a	n/a
2	ATF1	chr19:56732773-56733067	K562	blood:	n/a	n/a
3	ATF1	chr19:56760362-56760671	K562	blood:	n/a	n/a
4	BATF	chr19:56745875-56746197	GM12878	blood:	n/a	n/a
5	BHLHE40	chr19:56760454-56760539	K562	blood:	n/a	n/a
6	BRCA1	chr19:56745473-56745601	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr19:56760428-56760663	K562	blood:	n/a	n/a
8	CEBPB	chr19:56744025-56744198	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr19:56732791-56733124	H1-hESC	embryonic stem cell:	n/a	chr19:56732934-56732945
10	CEBPB	chr19:56760233-56760622	K562	blood:	n/a	chr19:56760446-56760457
11	CEBPB	chr19:56732731-56733102	K562	blood:	n/a	chr19:56732934-56732945
12	CEBPB	chr19:56732645-56733248	Hela-S3	cervix:	n/a	chr19:56732934-56732945
13	CEBPB	chr19:56736715-56737020	A549	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
14	CEBPB	chr19:56741673-56741957	K562	blood:	n/a	chr19:56741810-56741821
15	CEBPB	chr19:56741714-56741974	IMR90	lung:	n/a	chr19:56741810-56741821
16	CEBPB	chr19:56732726-56733084	MCF-7	breast:	n/a	chr19:56732934-56732945
17	CEBPB	chr19:56736697-56737012	IMR90	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
18	CEBPB	chr19:56741719-56741891	K562	blood:	n/a	chr19:56741810-56741821
19	CEBPB	chr19:56736739-56736963	HepG2	liver:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
20	CEBPB	chr19:56732730-56733098	A549	lung:	n/a	chr19:56732934-56732945
21	CEBPB	chr19:56744051-56744221	K562	blood:	n/a	n/a
22	CEBPB	chr19:56732803-56733050	K562	blood:	n/a	chr19:56732934-56732945
23	CEBPB	chr19:56741741-56741909	H1-hESC	embryonic stem cell:	n/a	chr19:56741810-56741821
24	CEBPB	chr19:56732796-56733078	A549	lung:	n/a	chr19:56732934-56732945
25	CEBPB	chr19:56732764-56733076	HepG2	liver:	n/a	chr19:56732934-56732945
26	CEBPB	chr19:56741646-56741970	HepG2	liver:	n/a	chr19:56741810-56741821
27	CEBPB	chr19:56760261-56760657	K562	blood:	n/a	chr19:56760446-56760457
28	CEBPB	chr19:56736713-56736976	K562	blood:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
29	CEBPB	chr19:56741649-56741971	A549	lung:	n/a	chr19:56741810-56741821
30	CEBPB	chr19:56732747-56733109	K562	blood:	n/a	chr19:56732934-56732945
31	CEBPB	chr19:56732773-56733100	IMR90	lung:	n/a	chr19:56732934-56732945
32	CEBPB	chr19:56736709-56737013	Hela-S3	cervix:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
33	CEBPD	chr19:56760163-56760766	K562	blood:	n/a	n/a
34	CEBPD	chr19:56760271-56760770	K562	blood:	n/a	n/a
35	CEBPD	chr19:56732776-56733035	K562	blood:	n/a	n/a
36	CTCF	chr19:56732940-56733090	GM12864	blood:	n/a	n/a
37	CTCF	chr19:56732982-56733177	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr19:56733009-56733202	LNCaP	prostate:	n/a	n/a
39	CTCF	chr19:56757316-56757402	GM12878	blood:	n/a	n/a
40	CTCF	chr19:56732999-56733153	MCF-7	breast:	n/a	n/a
41	CTCF	chr19:56733017-56733158	Lung_OC	lung:	n/a	n/a
42	CTCF	chr19:56732970-56733163	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr19:56732987-56733179	HepG2	liver:	n/a	n/a
44	CTCF	chr19:56732960-56733110	HCT-116	colon:	n/a	n/a
45	CTCF	chr19:56732980-56733130	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:56734348-56734591	K562	blood:	n/a	n/a
47	CTCF	chr19:56757060-56757210	A549	lung:	n/a	n/a
48	CTCF	chr19:56734500-56734650	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr19:56734360-56734510	GM12875	blood:	n/a	n/a
50	CTCF	chr19:56734420-56734570	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56741019-56741069	SK-N-MC	brain:	n/a
2	chr19:56741019-56741069	SK-N-MC	brain:	n/a
3	chr19:56739749-56739799	U87	brain:	n/a
4	chr19:56739573-56739623	MCF10A-Er-Src	breast:	n/a
5	chr19:56739749-56739799	NH-A	brain:	n/a
6	chr19:56739782-56739832	GM12878	blood:	n/a
7	chr19:56726303-56726353	AG09319	gingival:	n/a
8	chr19:56739782-56739832	IMR90	lung:	fetal
9	chr19:56740672-56740722	AG10803	skin:	n/a
10	chr19:56730494-56730544	HCPEpiC	choroid plexus:	n/a
11	chr19:56739573-56739623	IMR90	lung:	fetal
12	chr19:56728589-56728639	GM06990	blood:	n/a
13	chr19:56741019-56741069	Hepatocyte	liver:	n/a
14	chr19:56739868-56739918	HUVEC	blood vessel:	n/a
15	chr19:56741019-56741069	A549	lung:	n/a
16	chr19:56733045-56733095	HUVEC	blood vessel:	n/a
17	chr19:56739868-56739918	MCF10A-Er-Src	breast:	n/a
18	chr19:56728422-56728472	Jurkat	blood:	n/a
19	chr19:56739788-56739838	SK-N-SH	brain:	n/a
20	chr19:56742355-56742405	PrEC	prostate:	n/a
21	chr19:56742355-56742405	GM06990	blood:	n/a
22	chr19:56739788-56739838	GM12892	blood:	n/a
23	chr19:56732932-56732982	SAEC	small airway:	n/a
24	chr19:56728589-56728639	A549	lung:	n/a
25	chr19:56728422-56728472	NHBE	bronchial:	n/a
26	chr19:56739788-56739838	NHBE	bronchial:	n/a
27	chr19:56741019-56741069	BE2_C	brain:	n/a
28	chr19:56739741-56739791	HL-60	blood:	n/a
29	chr19:56728589-56728639	HL-60	blood:	n/a
30	chr19:56728422-56728472	NHDF-neo	bronchial:	n/a
31	chr19:56739573-56739623	HEEpiC	esophagus:	n/a
32	chr19:56732932-56732982	AG09319	gingival:	n/a
33	chr19:56739788-56739838	HepG2	liver:	n/a
34	chr19:56739788-56739838	HCT-116	colon:	n/a
35	chr19:56739788-56739838	PANC-1	pancreas:	n/a
36	chr19:56728589-56728639	NT2-D1	testis:	n/a
37	chr19:56739868-56739918	SK-N-SH	brain:	n/a
38	chr19:56739782-56739832	PANC-1	pancreas:	n/a
39	chr19:56738933-56738983	U87	brain:	n/a
40	chr19:56739749-56739799	ProgFib	skin:	n/a
41	chr19:56740672-56740722	SK-N-MC	brain:	n/a
42	chr19:56739782-56739832	HNPCEpiC	eye:	n/a
43	chr19:56732932-56732982	AG10803	skin:	n/a
44	chr19:56730494-56730544	AG09319	gingival:	n/a
45	chr19:56741019-56741069	HRE	kidney:	n/a
46	chr19:56733045-56733095	PANC-1	pancreas:	n/a
47	chr19:56741019-56741069	HepG2	liver:	n/a
48	chr19:56739868-56739918	HPAEpiC	pulmonary alveolar:	n/a
49	chr19:56738933-56738983	GM06990	blood:	n/a
50	chr19:56726303-56726353	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
2	chr19:56760039..56762057-chr19:56831322..56833020,2	K562	blood:
3	chr19:56153237..56155682-chr19:56762217..56764183,2	K562	blood:
4	chr19:56587934..56588448-chr19:56732565..56733070,2	MCF-7	breast:
5	chr19:56731454..56732253-chr19:56820726..56821606,2	MCF-7	breast:
6	chr19:56631229..56633438-chr19:56759454..56761104,2	K562	blood:
7	chr19:56750344..56752392-chr19:56783866..56786080,2	K562	blood:

Variant related genes	Relation type
ZSCAN5D	TF binding region
ENSG00000242411	TF binding region
ZSCAN5A	TF binding region
ZSCAN5D	CpG island
ENSG00000242411	CpG island
ZSCAN5A	CpG island
ENSG00000171425	chromatin interactions
ENSG00000213015	chromatin interactions
ENSG00000142409	chromatin interactions
ENSG00000267710	chromatin interactions

Extended variants
information (count: 2206 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2206 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375941974	chr19:56723600-56723601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142181101	chr19:56723613-56723614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573835503	chr19:56723625-56723626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542569019	chr19:56723643-56723644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386811184	chr19:56723651-56723652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1865103	chr19:56723652-56723653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs190443869	chr19:56723728-56723729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547816616	chr19:56723797-56723798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533705840	chr19:56723808-56723809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73067823	chr19:56723826-56723827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs62122461	chr19:56723829-56723830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530670355	chr19:56723839-56723840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550547797	chr19:56723908-56723909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117892455	chr19:56723920-56723921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530384041	chr19:56723955-56723956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546998366	chr19:56723962-56723963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567180178	chr19:56723984-56723985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538838890	chr19:56723995-56723996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182082657	chr19:56724007-56724008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146321500	chr19:56724010-56724011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369725475	chr19:56724068-56724069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139635090	chr19:56724104-56724105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185218878	chr19:56724113-56724114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574758708	chr19:56724143-56724144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189647901	chr19:56724144-56724145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552972221	chr19:56724166-56724167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573126024	chr19:56724207-56724208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549951881	chr19:56724229-56724230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149549924	chr19:56724234-56724235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565076526	chr19:56724265-56724266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181278580	chr19:56724355-56724356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185362183	chr19:56724356-56724357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560910180	chr19:56724391-56724392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529634098	chr19:56724410-56724411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112091593	chr19:56724417-56724418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191658144	chr19:56724429-56724430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144239936	chr19:56724457-56724458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10853884	chr19:56724562-56724563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs10853885	chr19:56724592-56724593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs183505477	chr19:56724594-56724595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148728578	chr19:56724626-56724627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548299414	chr19:56724662-56724663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568570104	chr19:56724682-56724683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533925179	chr19:56724684-56724685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188798940	chr19:56724709-56724710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573006406	chr19:56724715-56724716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538943460	chr19:56724718-56724719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs66694252	chr19:56724737-56724738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs398059861	chr19:56724742-56724743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558750674	chr19:56724749-56724750	Weak transcription	n/a	n/a	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:354 , 50 per page) page: 1 2 3 4 5 6 7 8

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

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