Variant report

Variant	nsv543951
Chromosome Location	chr19:22229835-22408495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:1226)
Chromatin interactive
region (count:3)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:22317299-22317405	K562	blood:	n/a	n/a
2	ATF1	chr19:22235032-22235378	K562	blood:	n/a	n/a
3	BACH1	chr19:22276070-22276088	K562	blood:	n/a	n/a
4	BCLAF1	chr19:22327265-22327471	GM12878	blood:	n/a	n/a
5	CBX3	chr19:22234952-22235406	K562	blood:	n/a	n/a
6	CBX3	chr19:22327195-22327536	K562	blood:	n/a	n/a
7	CBX3	chr19:22327284-22327512	HCT-116	colon:	n/a	n/a
8	CBX3	chr19:22327182-22327501	K562	blood:	n/a	n/a
9	CEBPB	chr19:22316342-22316684	A549	lung:	n/a	n/a
10	CEBPB	chr19:22231337-22231754	A549	lung:	n/a	n/a
11	CEBPB	chr19:22268451-22268763	K562	blood:	n/a	n/a
12	CEBPB	chr19:22258511-22258573	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:22235002-22235306	K562	blood:	n/a	n/a
14	CEBPB	chr19:22268494-22268820	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:22353367-22353394	HepG2	liver:	n/a	chr19:22353370-22353381
16	CEBPB	chr19:22268460-22268665	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr19:22229978-22231113	A549	lung:	n/a	n/a
18	CEBPB	chr19:22320453-22320571	A549	lung:	n/a	n/a
19	CEBPB	chr19:22318107-22318751	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:22316363-22316659	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:22268542-22268703	A549	lung:	n/a	n/a
22	CEBPB	chr19:22317520-22317702	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:22377473-22377491	A549	lung:	n/a	n/a
24	CEBPB	chr19:22232727-22233148	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:22318406-22318779	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:22268516-22268793	IMR90	lung:	n/a	n/a
27	CEBPB	chr19:22232756-22233017	A549	lung:	n/a	n/a
28	CEBPB	chr19:22372087-22372275	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:22320441-22320600	HepG2	liver:	n/a	n/a
30	CEBPB	chr19:22231099-22231711	K562	blood:	n/a	n/a
31	CEBPB	chr19:22229982-22231755	HepG2	liver:	n/a	n/a
32	CEBPZ	chr19:22327227-22327553	HepG2	liver:	n/a	n/a
33	CHD2	chr19:22383513-22383543	K562	blood:	n/a	n/a
34	CHD2	chr19:22235124-22235488	K562	blood:	n/a	chr19:22235183-22235193
35	CTCF	chr19:22347623-22347657	GM10248	blood:	n/a	n/a
36	CTCF	chr19:22353464-22353507	Lung_OC	lung:	n/a	n/a
37	CTCF	chr19:22390521-22390585	GM10266	blood:	n/a	n/a
38	CTCF	chr19:22366565-22366635	LNCaP	prostate:	n/a	n/a
39	CTCF	chr19:22386300-22386323	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr19:22397320-22397470	NB4	blood:	n/a	n/a
41	CTCF	chr19:22322395-22322424	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr19:22350251-22350267	GM13976	blood:	n/a	n/a
43	CTCF	chr19:22342028-22342100	LNCaP	prostate:	n/a	n/a
44	CTCF	chr19:22294750-22294821	GM13976	blood:	n/a	n/a
45	CTCF	chr19:22354495-22354502	Medullo	brain:	n/a	n/a
46	CTCF	chr19:22306343-22306483	K562	blood:	n/a	n/a
47	CTCF	chr19:22375499-22375569	Lung_OC	lung:	n/a	n/a
48	CTCF	chr19:22385905-22385977	GM10266	blood:	n/a	n/a
49	CTCF	chr19:22323184-22323240	ProgFib	skin:	n/a	n/a
50	CTCF	chr19:22295793-22295878	GM20000	blood:	n/a	n/a

(count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:22235409-22235459	PrEC	prostate:	n/a
2	chr19:22235199-22235249	AG04449	skin:	fetal
3	chr19:22235409-22235459	SK-N-SH	brain:	n/a
4	chr19:22235454-22235504	SK-N-MC	brain:	n/a
5	chr19:22320975-22321025	CMK	blood:	n/a
6	chr19:22321700-22321750	A549	lung:	n/a
7	chr19:22235409-22235459	PrEC	prostate:	n/a
8	chr19:22235199-22235249	AG04449	skin:	fetal
9	chr19:22235409-22235459	SK-N-SH	brain:	n/a
10	chr19:22235454-22235504	SK-N-MC	brain:	n/a
11	chr19:22320975-22321025	CMK	blood:	n/a
12	chr19:22321700-22321750	A549	lung:	n/a
13	chr19:22320869-22320919	U87	brain:	n/a
14	chr19:22235454-22235504	SK-N-SH_RA	brain:	n/a
15	chr19:22234992-22235042	Hepatocyte	liver:	n/a
16	chr19:22235272-22235322	HCF	heart:	n/a
17	chr19:22234992-22235042	IMR90	lung:	fetal
18	chr19:22318466-22318516	IMR90	lung:	fetal
19	chr19:22235281-22235331	NHDF-neo	bronchial:	n/a
20	chr19:22319196-22319246	HNPCEpiC	eye:	n/a
21	chr19:22235409-22235459	GM06990	blood:	n/a
22	chr19:22234992-22235042	HAEpiC	amniotic membrane:	n/a
23	chr19:22233809-22233859	HAEpiC	amniotic membrane:	n/a
24	chr19:22320744-22320794	H1-hESC	embryonic stem cell:	embryo
25	chr19:22235022-22235072	AG09309	skin:	n/a
26	chr19:22320744-22320794	LNCaP	prostate:	n/a
27	chr19:22321700-22321750	GM19239	blood:	n/a
28	chr19:22234992-22235042	K562	blood:	n/a
29	chr19:22320869-22320919	GM06990	blood:	n/a
30	chr19:22319196-22319246	Jurkat	blood:	n/a
31	chr19:22235256-22235306	Hepatocyte	liver:	n/a
32	chr19:22235272-22235322	CMK	blood:	n/a
33	chr19:22235409-22235459	ProgFib	skin:	n/a
34	chr19:22235199-22235249	K562	blood:	n/a
35	chr19:22234992-22235042	AG04449	skin:	fetal
36	chr19:22319196-22319246	ECC-1	luminal epithelium:	n/a
37	chr19:22235850-22235900	ProgFib	skin:	n/a
38	chr19:22235454-22235504	HUVEC	blood vessel:	n/a
39	chr19:22234992-22235042	AoSMC	blood vessel:	n/a
40	chr19:22235022-22235072	ProgFib	skin:	n/a
41	chr19:22321700-22321750	HepG2	liver:	n/a
42	chr19:22235144-22235194	HRPEpiC	eye:	n/a
43	chr19:22320869-22320919	ECC-1	luminal epithelium:	n/a
44	chr19:22320869-22320919	NT2-D1	testis:	n/a
45	chr19:22320869-22320919	IMR90	lung:	fetal
46	chr19:22235144-22235194	NT2-D1	testis:	n/a
47	chr19:22235454-22235504	Jurkat	blood:	n/a
48	chr19:22235454-22235504	NHBE	bronchial:	n/a
49	chr19:22235454-22235504	NB4	blood:	n/a
50	chr19:22320975-22321025	RPTEC	kidney:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:22236195..22238676-chr19:22281763..22284450,2	K562	blood:
2	chr19:22236195..22238676-chr19:22281763..22284450,2	K562	blood:
3	chr19:22234996..22236729-chr19:22244257..22246826,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF676-3	chr19:22312574-22313120	NONHSAT063766
2	lnc-ZNF729-5	chr19:22386687-22386805	NONHSAT063769
3	lnc-ZNF208-2	chr19:22232617-22232807	ENSG00000269199.1
4	lnc-ZNF729-5	chr19:22385930-22386384	NONHSAT063769
5	lnc-ZNF208-3	chr19:22248630-22249200	NONHSAT063765
6	lnc-ZNF676-3	chr19:22312079-22312249	NONHSAT063766
7	lnc-ZNF729-7	chr19:22235326-22235437	NONHSAT063763
8	lnc-ZNF676-3	chr19:22311429-22311769	NONHSAT063766
9	lnc-ZNF676-2	chr19:22357568-22357993	NONHSAT063768
10	lnc-ZNF729-7	chr19:22246881-22247134	NONHSAT063763
11	lnc-ZNF676-3	chr19:22314709-22314736	NONHSAT063766
12	lnc-ZNF729-7	chr19:22243310-22243430	NONHSAT063763

No data

Variant related genes	Relation type
VN1R85P	TF binding region
ZNF257	TF binding region
ENSG00000268116	TF binding region
ENSG00000268079	TF binding region
PCGF7P	TF binding region
ZNF676	TF binding region
ENSG00000269575	TF binding region
ZNF92P2	TF binding region
ENSG00000269199	TF binding region
ENSG00000269742	TF binding region
VN1R85P	CpG island
ZNF257	CpG island
ENSG00000268116	CpG island
ENSG00000268079	CpG island
PCGF7P	CpG island
ZNF676	CpG island
ENSG00000269575	CpG island
ZNF92P2	CpG island
ENSG00000269199	CpG island
ENSG00000269742	CpG island
ENSG00000197134	chromatin interactions

Extended variants
information (count: 4604 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:4604 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146027114	chr19:22230310-22230311	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs139573177	chr19:22230313-22230314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs34878133	chr19:22230331-22230332	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
4	rs112963647	chr19:22230334-22230335	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs115375842	chr19:22230349-22230350	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs571999892	chr19:22230370-22230371	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs539323349	chr19:22230388-22230389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs394457	chr19:22230428-22230429	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs149706612	chr19:22230450-22230451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536599137	chr19:22230455-22230456	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550885274	chr19:22230471-22230472	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555451014	chr19:22230481-22230482	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs570544069	chr19:22230521-22230522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs573370363	chr19:22230557-22230558	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs192460144	chr19:22230583-22230584	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs552732778	chr19:22230614-22230615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs114900691	chr19:22230664-22230665	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs78993648	chr19:22230665-22230666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs386807887	chr19:22230669-22230670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs409835	chr19:22230671-22230672	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs542620128	chr19:22230674-22230675	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs74768977	chr19:22230734-22230735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs528575748	chr19:22230735-22230736	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs417628	chr19:22230794-22230795	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs114336280	chr19:22230853-22230854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs374764246	chr19:22230855-22230856	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs532741771	chr19:22230879-22230880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs369814455	chr19:22230900-22230901	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs551262204	chr19:22230915-22230916	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs145523617	chr19:22230935-22230936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs422344	chr19:22230956-22230957	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs554917702	chr19:22230978-22230979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs10419969	chr19:22231026-22231027	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534403528	chr19:22231059-22231060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs552793422	chr19:22231088-22231089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs557233968	chr19:22231099-22231100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs543744434	chr19:22231101-22231102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs411020	chr19:22231102-22231103	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs408687	chr19:22231123-22231124	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs184378414	chr19:22231155-22231156	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575419617	chr19:22231159-22231160	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs543034726	chr19:22231166-22231167	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs147126632	chr19:22231175-22231176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs77317433	chr19:22231178-22231179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs538622773	chr19:22231186-22231187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs189674962	chr19:22231196-22231197	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573417407	chr19:22231215-22231216	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs557897498	chr19:22231221-22231222	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs559450460	chr19:22231238-22231239	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs528211858	chr19:22231250-22231251	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:22231200-22231400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
2	chr19:22234200-22234800	Enhancers	Primary hematopoietic stem cells	blood
3	chr19:22234200-22236600	Active TSS	K562	blood
4	chr19:22234400-22235000	Enhancers	Primary B cells from peripheral blood	blood
5	chr19:22234400-22235200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
6	chr19:22234600-22234800	Enhancers	Primary T cells fromperipheralblood	blood
7	chr19:22234600-22234800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr19:22234600-22234800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr19:22234600-22234800	Enhancers	Fetal Muscle Trunk	muscle
10	chr19:22234600-22235000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr19:22234600-22235000	Enhancers	Colon Smooth Muscle	Colon
12	chr19:22234600-22235200	Active TSS	Monocytes-CD14+_RO01746	blood
13	chr19:22234600-22235600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:22234600-22235800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr19:22234600-22236000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr19:22234600-22236200	Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr19:22234600-22236200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr19:22234800-22235000	Enhancers	Primary B cells from cord blood	blood
19	chr19:22234800-22235000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr19:22234800-22235000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr19:22234800-22235000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
22	chr19:22234800-22235000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
23	chr19:22234800-22235200	Flanking Active TSS	Primary hematopoietic stem cells	blood
24	chr19:22234800-22235200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr19:22234800-22235200	Flanking Active TSS	Fetal Muscle Trunk	muscle
26	chr19:22234800-22235400	Active TSS	Adipose Nuclei	Adipose
27	chr19:22234800-22235400	ZNF genes & repeats	Fetal Brain Female	brain
28	chr19:22234800-22235400	Active TSS	Placenta	Placenta
29	chr19:22234800-22235800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr19:22234800-22235800	Active TSS	Primary T helper naive cells from peripheral blood	blood
31	chr19:22234800-22235800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr19:22234800-22235800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr19:22234800-22235800	Active TSS	Brain Substantia Nigra	brain
34	chr19:22234800-22235800	Active TSS	Psoas Muscle	Psoas
35	chr19:22234800-22235800	Active TSS	Rectal Smooth Muscle	rectum
36	chr19:22234800-22235800	Active TSS	HUVEC	blood vessel
37	chr19:22234800-22235800	Active TSS	Osteobl	bone
38	chr19:22234800-22236000	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr19:22234800-22236000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr19:22234800-22236000	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr19:22234800-22236000	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr19:22234800-22236000	Active TSS	Fetal Intestine Large	intestine
43	chr19:22234800-22236000	Active TSS	Fetal Intestine Small	intestine
44	chr19:22234800-22236000	Active TSS	Fetal Kidney	kidney
45	chr19:22234800-22236000	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr19:22234800-22236000	ZNF genes & repeats	Fetal Stomach	stomach
47	chr19:22234800-22236000	Active TSS	Left Ventricle	heart
48	chr19:22234800-22236000	Active TSS	Pancreas	Pancrea
49	chr19:22234800-22236000	Active TSS	Stomach Smooth Muscle	stomach
50	chr19:22234800-22236000	Active TSS	Thymus	Thymus

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