Variant report

Variant	nsv1063592
Chromosome Location	chr19:39257977-39287265
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	chr19:39271665-39272026	K562	blood:	n/a	n/a
2	ARID3A	chr19:39274947-39275249	HepG2	liver:	n/a	n/a
3	ATF1	chr19:39271683-39272097	K562	blood:	n/a	n/a
4	BACH1	chr19:39260633-39260724	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr19:39260146-39260863	A549	lung:	n/a	chr19:39260547-39260560
6	BCLAF1	chr19:39260404-39260725	GM12878	blood:	n/a	chr19:39260547-39260560
7	BHLHE40	chr19:39260480-39260797	GM12878	blood:	n/a	chr19:39260550-39260566
8	BHLHE40	chr19:39271678-39272003	K562	blood:	n/a	n/a
9	CBX3	chr19:39271625-39272114	K562	blood:	n/a	n/a
10	CBX3	chr19:39260336-39260750	K562	blood:	n/a	n/a
11	CCNT2	chr19:39271734-39272046	K562	blood:	n/a	n/a
12	CEBPB	chr19:39271641-39271999	K562	blood:	n/a	n/a
13	CEBPB	chr19:39274981-39275364	Hela-S3	cervix:	n/a	chr19:39275209-39275220
14	CEBPB	chr19:39275079-39275339	K562	blood:	n/a	chr19:39275209-39275220
15	CEBPB	chr19:39274900-39275470	A549	lung:	n/a	chr19:39275209-39275220
16	CEBPB	chr19:39275046-39275399	A549	lung:	n/a	chr19:39275209-39275220
17	CEBPB	chr19:39276654-39277062	A549	lung:	n/a	chr19:39276929-39276938 chr19:39276927-39276938 chr19:39276929-39276940 chr19:39276927-39276940
18	CEBPB	chr19:39276794-39277112	HepG2	liver:	n/a	chr19:39276929-39276938 chr19:39276927-39276938 chr19:39276929-39276940 chr19:39276927-39276940
19	CEBPB	chr19:39266249-39266305	K562	blood:	n/a	n/a
20	CEBPB	chr19:39276777-39276994	K562	blood:	n/a	chr19:39276929-39276938 chr19:39276927-39276938 chr19:39276929-39276940 chr19:39276927-39276940
21	CEBPB	chr19:39275011-39275358	IMR90	lung:	n/a	chr19:39275209-39275220
22	CEBPB	chr19:39276763-39277079	K562	blood:	n/a	chr19:39276929-39276938 chr19:39276927-39276938 chr19:39276929-39276940 chr19:39276927-39276940
23	CEBPB	chr19:39276783-39277114	A549	lung:	n/a	chr19:39276929-39276938 chr19:39276927-39276938 chr19:39276929-39276940 chr19:39276927-39276940
24	CEBPB	chr19:39275062-39275293	K562	blood:	n/a	chr19:39275209-39275220
25	CEBPB	chr19:39275019-39275352	HepG2	liver:	n/a	chr19:39275209-39275220
26	CEBPB	chr19:39266120-39266376	A549	lung:	n/a	n/a
27	CEBPB	chr19:39275016-39275374	A549	lung:	n/a	chr19:39275209-39275220
28	CEBPB	chr19:39275070-39275223	HepG2	liver:	n/a	chr19:39275209-39275220
29	CEBPB	chr19:39271655-39272036	K562	blood:	n/a	n/a
30	CEBPB	chr19:39276745-39277059	IMR90	lung:	n/a	chr19:39276929-39276938 chr19:39276927-39276938 chr19:39276929-39276940 chr19:39276927-39276940
31	CEBPD	chr19:39274902-39275295	K562	blood:	n/a	chr19:39275209-39275220
32	CEBPD	chr19:39271556-39272117	K562	blood:	n/a	n/a
33	CHD1	chr19:39283726-39283828	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:39260543-39260598	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr19:39283347-39283518	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr19:39260295-39260842	A549	lung:	n/a	n/a
37	CTCF	chr19:39283300-39283450	HFF	foreskin:	n/a	n/a
38	CTCF	chr19:39283300-39283450	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr19:39283320-39283470	HRE	kidney:	n/a	n/a
40	CTCF	chr19:39260388-39260722	Spleen_OC	spleen:	n/a	chr19:39260556-39260565
41	CTCF	chr19:39260762-39260833	GM13977	blood:	n/a	n/a
42	CTCF	chr19:39260398-39260863	GM19239	blood:	n/a	chr19:39260556-39260565
43	CTCF	chr19:39260500-39260650	GM12865	blood:	n/a	chr19:39260556-39260565
44	CTCF	chr19:39283316-39283529	GM19239	blood:	n/a	n/a
45	CTCF	chr19:39260480-39260630	HMF	breast:	n/a	chr19:39260556-39260565
46	CTCF	chr19:39260411-39260841	GM12878	blood:	n/a	chr19:39260556-39260565
47	CTCF	chr19:39283380-39283530	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr19:39283300-39283450	HPF	lung:	n/a	n/a
49	CTCF	chr19:39260315-39260791	H1-hESC	embryonic stem cell:	n/a	chr19:39260556-39260565
50	CTCF	chr19:39260425-39260675	A549	lung:	n/a	chr19:39260556-39260565

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39260304-39260354	Hepatocyte	liver:	n/a
2	chr19:39278997-39279047	HRPEpiC	eye:	n/a
3	chr19:39264720-39264770	Hela-S3	cervix:	n/a
4	chr19:39279703-39279753	MCF-7	breast:	n/a
5	chr19:39260304-39260354	Hepatocyte	liver:	n/a
6	chr19:39278997-39279047	HRPEpiC	eye:	n/a
7	chr19:39264720-39264770	Hela-S3	cervix:	n/a
8	chr19:39279703-39279753	MCF-7	breast:	n/a
9	chr19:39264646-39264696	HepG2	liver:	n/a
10	chr19:39282077-39282127	HNPCEpiC	eye:	n/a
11	chr19:39279324-39279374	AG09309	skin:	n/a
12	chr19:39265241-39265291	GM19239	blood:	n/a
13	chr19:39282077-39282127	HEEpiC	esophagus:	n/a
14	chr19:39286793-39286843	AG04450	lung:	fetal
15	chr19:39260304-39260354	PFSK-1	brain:	n/a
16	chr19:39261921-39261971	PANC-1	pancreas:	n/a
17	chr19:39260304-39260354	T-47D	breast:	n/a
18	chr19:39260954-39261004	HRE	kidney:	n/a
19	chr19:39283540-39283590	HEK293	kidney:	embryo
20	chr19:39286793-39286843	AG09309	skin:	n/a
21	chr19:39260954-39261004	NHBE	bronchial:	n/a
22	chr19:39262936-39262986	HCT-116	colon:	n/a
23	chr19:39265241-39265291	HL-60	blood:	n/a
24	chr19:39279324-39279374	HUVEC	blood vessel:	n/a
25	chr19:39264646-39264696	NHBE	bronchial:	n/a
26	chr19:39264720-39264770	AG04449	skin:	fetal
27	chr19:39278997-39279047	HEK293	kidney:	embryo
28	chr19:39279703-39279753	HUVEC	blood vessel:	n/a
29	chr19:39261921-39261971	HL-60	blood:	n/a
30	chr19:39261921-39261971	ProgFib	skin:	n/a
31	chr19:39278997-39279047	HL-60	blood:	n/a
32	chr19:39281374-39281424	IMR90	lung:	fetal
33	chr19:39265056-39265106	AG10803	skin:	n/a
34	chr19:39286793-39286843	HCPEpiC	choroid plexus:	n/a
35	chr19:39265241-39265291	GM06990	blood:	n/a
36	chr19:39264720-39264770	HMEC	breast:	n/a
37	chr19:39279324-39279374	HRE	kidney:	n/a
38	chr19:39279324-39279374	HRCEpiC	kidney:	n/a
39	chr19:39260304-39260354	GM19239	blood:	n/a
40	chr19:39265241-39265291	HCM	heart:	n/a
41	chr19:39283334-39283384	GM12891	blood:	n/a
42	chr19:39286793-39286843	HNPCEpiC	eye:	n/a
43	chr19:39264646-39264696	SK-N-MC	brain:	n/a
44	chr19:39282077-39282127	HCM	heart:	n/a
45	chr19:39286793-39286843	HRE	kidney:	n/a
46	chr19:39278997-39279047	SAEC	small airway:	n/a
47	chr19:39279266-39279316	H1-hESC	embryonic stem cell:	embryo
48	chr19:39286793-39286843	HRCEpiC	kidney:	n/a
49	chr19:39260460-39260510	NHBE	bronchial:	n/a
50	chr19:39265241-39265291	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:39266403..39269301-chr19:39271888..39274043,2	K562	blood:
2	chr19:39263336..39266472-chr19:39281321..39283014,3	K562	blood:
3	chr19:39260065..39260751-chr19:39420671..39421390,2	MCF-7	breast:
4	chr19:39278557..39281313-chr19:39305805..39307829,2	MCF-7	breast:
5	chr19:39277481..39279141-chr19:39336896..39339737,2	K562	blood:
6	chr19:39268163..39272229-chr19:39339868..39344081,3	K562	blood:
7	chr19:39269835..39272730-chr19:39322585..39324827,2	K562	blood:
8	chr19:39266403..39269301-chr19:39271888..39274043,2	K562	blood:
9	chr19:39264503..39266421-chr19:39288858..39290428,2	MCF-7	breast:
10	chr19:39260117..39262134-chr19:39341376..39343069,2	K562	blood:
11	chr19:39275124..39276670-chr19:39905372..39907606,2	K562	blood:
12	chr19:39269322..39272229-chr19:39339868..39342618,2	K562	blood:

Variant related genes	Relation type
LGALS7B	TF binding region
CAPN12	TF binding region
LGALS7	TF binding region
LGALS7B	CpG island
CAPN12	CpG island
LGALS7	CpG island
ENSG00000205076	chromatin interactions
ENSG00000104835	chromatin interactions
ENSG00000104824	chromatin interactions
ENSG00000104823	chromatin interactions
ENSG00000128626	chromatin interactions
ENSG00000090924	chromatin interactions

Extended variants
information (count: 1127 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1127 , 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	rs7248248	chr19:39257977-39257978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7248584	chr19:39258110-39258111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs142074950	chr19:39258111-39258112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184328502	chr19:39258127-39258128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547692235	chr19:39258132-39258133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189225457	chr19:39258139-39258140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547614219	chr19:39258160-39258161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565833988	chr19:39258210-39258211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565959915	chr19:39258227-39258228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146336888	chr19:39258252-39258253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539680687	chr19:39258290-39258291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386809119	chr19:39258296-39258297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7248831	chr19:39258298-39258299	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs537068851	chr19:39258302-39258303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561654040	chr19:39258330-39258331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370761883	chr19:39258340-39258341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180988405	chr19:39258362-39258363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs578024296	chr19:39258435-39258436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545200345	chr19:39258436-39258437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184833183	chr19:39258439-39258440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374592975	chr19:39258447-39258448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116169984	chr19:39258468-39258469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs8104072	chr19:39258541-39258542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs560841867	chr19:39258651-39258652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189649034	chr19:39258686-39258687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78713751	chr19:39258701-39258702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543086180	chr19:39258708-39258709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7249248	chr19:39258709-39258710	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs565217803	chr19:39258710-39258711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59162025	chr19:39258721-39258722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532716317	chr19:39258734-39258735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547578058	chr19:39258786-39258787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565897233	chr19:39258848-39258849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186795519	chr19:39258854-39258855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374661816	chr19:39258911-39258912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548633390	chr19:39258944-39258945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555537658	chr19:39258960-39258961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570066715	chr19:39258968-39258969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537435222	chr19:39258971-39258972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs36085229	chr19:39258972-39258973	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs199659877	chr19:39258992-39258993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200788789	chr19:39259003-39259004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202073593	chr19:39259014-39259015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571561202	chr19:39259032-39259033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142219550	chr19:39259044-39259045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199885364	chr19:39259048-39259049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554117531	chr19:39259068-39259069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2368521	chr19:39259100-39259101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs555484319	chr19:39259138-39259139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559646633	chr19:39259155-39259156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39246400-39270800	Weak transcription	K562	blood
2	chr19:39251600-39259800	Weak transcription	NHEK	skin
3	chr19:39254200-39265400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr19:39255600-39259400	Weak transcription	Fetal Intestine Small	intestine
5	chr19:39255800-39260200	Weak transcription	Fetal Intestine Large	intestine
6	chr19:39256400-39260200	Weak transcription	A549	lung
7	chr19:39259400-39260000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:39259400-39260000	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr19:39259400-39260200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr19:39259600-39259800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:39259800-39260000	Enhancers	GM12878-XiMat	blood
12	chr19:39259800-39260000	Enhancers	NHEK	skin
13	chr19:39259800-39260200	Enhancers	Primary B cells from peripheral blood	blood
14	chr19:39259800-39260200	Enhancers	Primary hematopoietic stem cells	blood
15	chr19:39259800-39260200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr19:39259800-39260200	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr19:39259800-39260200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:39259800-39260400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr19:39259800-39260600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr19:39259800-39261000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr19:39259800-39261000	Enhancers	Placenta Amnion	Placenta Amnion
22	chr19:39260000-39260200	Enhancers	H9 Cell Line	embryonic stem cell
23	chr19:39260000-39260200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr19:39260000-39260200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr19:39260000-39260200	Enhancers	Primary B cells from cord blood	blood
26	chr19:39260000-39260200	Enhancers	Primary T cells fromperipheralblood	blood
27	chr19:39260000-39260200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr19:39260000-39260200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr19:39260000-39260200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr19:39260000-39260200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr19:39260000-39260200	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr19:39260000-39260200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr19:39260000-39260200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr19:39260000-39260200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:39260000-39260200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr19:39260000-39260200	Enhancers	Colonic Mucosa	Colon
37	chr19:39260000-39260200	Enhancers	Fetal Intestine Small	intestine
38	chr19:39260000-39260200	Enhancers	Fetal Muscle Trunk	muscle
39	chr19:39260000-39260200	Enhancers	Fetal Muscle Leg	muscle
40	chr19:39260000-39260200	Enhancers	Fetal Thymus	thymus
41	chr19:39260000-39260200	Enhancers	Left Ventricle	heart
42	chr19:39260000-39260200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr19:39260000-39260200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr19:39260000-39260200	Enhancers	Thymus	Thymus
45	chr19:39260000-39260200	Enhancers	HUVEC	blood vessel
46	chr19:39260000-39260200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr19:39260000-39260400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr19:39260000-39260400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr19:39260000-39260400	Enhancers	Esophagus	oesophagus
50	chr19:39260000-39260400	Flanking Active TSS	GM12878-XiMat	blood

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