Variant report

Variant	nsv963042
Chromosome Location	chr19:37271305-37296858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:734)
Chromatin interactive
region (count:7)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:37288313-37288853	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr19:37288266-37288826	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr19:37288349-37288854	GM12878	blood:	n/a	n/a
4	ATF2	chr19:37288150-37288903	GM12878	blood:	n/a	n/a
5	BACH1	chr19:37288340-37288738	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr19:37288254-37288650	GM12878	blood:	n/a	n/a
7	BRCA1	chr19:37288525-37288715	GM12878	blood:	n/a	n/a
8	BRCA1	chr19:37288417-37288862	H1-hESC	embryonic stem cell:	n/a	chr19:37288775-37288782
9	CEBPB	chr19:37271230-37271418	K562	blood:	n/a	chr19:37271385-37271396
10	CEBPB	chr19:37271315-37271481	A549	lung:	n/a	chr19:37271385-37271396
11	CEBPB	chr19:37271236-37271482	HepG2	liver:	n/a	chr19:37271385-37271396
12	CHD1	chr19:37288164-37288986	IMR90	lung:	n/a	n/a
13	CHD2	chr19:37288075-37288870	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr19:37288663-37288729	HepG2	liver:	n/a	n/a
15	CHD2	chr19:37288175-37288844	GM12878	blood:	n/a	n/a
16	CREB1	chr19:37288163-37288610	A549	lung:	n/a	n/a
17	CREB1	chr19:37288144-37288878	GM12878	blood:	n/a	n/a
18	CREB1	chr19:37288155-37288743	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr19:37282880-37283030	GM12871	blood:	n/a	n/a
20	CTCF	chr19:37288280-37288430	AG09319	gingival:	n/a	n/a
21	CTCF	chr19:37282857-37282978	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:37282800-37282950	HMF	breast:	n/a	n/a
23	CTCF	chr19:37282880-37283030	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr19:37282840-37282990	RPTEC	kidney:	n/a	n/a
25	CTCF	chr19:37282904-37282945	ProgFib	skin:	n/a	n/a
26	CTCF	chr19:37282867-37282991	NHEK	skin:	n/a	n/a
27	CTCF	chr19:37282900-37283050	GM06990	blood:	n/a	n/a
28	CTCF	chr19:37282860-37283010	SAEC	small airway:	n/a	n/a
29	CTCF	chr19:37288424-37288502	LNCaP	prostate:	n/a	n/a
30	CTCF	chr19:37292335-37292349	GM20000	blood:	n/a	n/a
31	CTCF	chr19:37282870-37282949	GM19239	blood:	n/a	n/a
32	CTCF	chr19:37282860-37283010	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr19:37282792-37282976	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr19:37282920-37283070	AG09319	gingival:	n/a	n/a
35	CTCF	chr19:37282840-37282990	GM12874	blood:	n/a	n/a
36	CTCF	chr19:37282896-37282938	GM20000	blood:	n/a	n/a
37	CTCF	chr19:37282900-37283050	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr19:37282825-37282841	Lung_OC	lung:	n/a	n/a
39	CTCF	chr19:37282860-37283010	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr19:37288306-37288609	GM12878	blood:	n/a	n/a
41	CTCF	chr19:37288416-37288450	GM10248	blood:	n/a	n/a
42	CTCF	chr19:37282880-37283030	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr19:37282860-37283010	BE2_C	brain:	n/a	n/a
44	CTCF	chr19:37282980-37283130	RPTEC	kidney:	n/a	n/a
45	CTCF	chr19:37282860-37283010	GM06990	blood:	n/a	n/a
46	CTCF	chr19:37282869-37282943	GM10248	blood:	n/a	n/a
47	CTCF	chr19:37282900-37283050	HCFaa	heart:	n/a	n/a
48	CTCF	chr19:37282868-37282969	LNCaP	prostate:	n/a	n/a
49	CTCF	chr19:37288437-37288451	GM19240	blood:	n/a	n/a
50	CTCF	chr19:37282820-37282970	GM12867	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:37288793-37288843	Jurkat	blood:	n/a
2	chr19:37288705-37288755	HEEpiC	esophagus:	n/a
3	chr19:37288793-37288843	Jurkat	blood:	n/a
4	chr19:37288705-37288755	HEEpiC	esophagus:	n/a
5	chr19:37291668-37291718	AG09309	skin:	n/a
6	chr19:37288450-37288500	U87	brain:	n/a
7	chr19:37282653-37282703	MCF-7	breast:	n/a
8	chr19:37282502-37282552	PFSK-1	brain:	n/a
9	chr19:37282653-37282703	CMK	blood:	n/a
10	chr19:37288291-37288341	H1-hESC	embryonic stem cell:	embryo
11	chr19:37288509-37288559	BJ	skin:	n/a
12	chr19:37288509-37288559	GM19239	blood:	n/a
13	chr19:37291668-37291718	Jurkat	blood:	n/a
14	chr19:37288450-37288500	GM12892	blood:	n/a
15	chr19:37286158-37286208	AG04450	lung:	fetal
16	chr19:37288705-37288755	HRE	kidney:	n/a
17	chr19:37282556-37282606	LNCaP	prostate:	n/a
18	chr19:37288509-37288559	SK-N-SH_RA	brain:	n/a
19	chr19:37288705-37288755	BE2_C	brain:	n/a
20	chr19:37288343-37288393	HRE	kidney:	n/a
21	chr19:37288509-37288559	AG09319	gingival:	n/a
22	chr19:37282502-37282552	NT2-D1	testis:	n/a
23	chr19:37291668-37291718	K562	blood:	n/a
24	chr19:37282653-37282703	HRPEpiC	eye:	n/a
25	chr19:37288509-37288559	HRE	kidney:	n/a
26	chr19:37282653-37282703	NHDF-neo	bronchial:	n/a
27	chr19:37288509-37288559	ProgFib	skin:	n/a
28	chr19:37288291-37288341	PrEC	prostate:	n/a
29	chr19:37282502-37282552	Jurkat	blood:	n/a
30	chr19:37282556-37282606	CMK	blood:	n/a
31	chr19:37288343-37288393	Hepatocyte	liver:	n/a
32	chr19:37282653-37282703	A549	lung:	n/a
33	chr19:37288291-37288341	PFSK-1	brain:	n/a
34	chr19:37288343-37288393	GM06990	blood:	n/a
35	chr19:37288509-37288559	U87	brain:	n/a
36	chr19:37288509-37288559	AG04449	skin:	fetal
37	chr19:37288450-37288500	K562	blood:	n/a
38	chr19:37288291-37288341	NHDF-neo	bronchial:	n/a
39	chr19:37288793-37288843	AG09319	gingival:	n/a
40	chr19:37282931-37282981	NHDF-neo	bronchial:	n/a
41	chr19:37282556-37282606	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:37288343-37288393	AG10803	skin:	n/a
43	chr19:37288509-37288559	HNPCEpiC	eye:	n/a
44	chr19:37288343-37288393	GM12891	blood:	n/a
45	chr19:37282556-37282606	GM12891	blood:	n/a
46	chr19:37288343-37288393	ProgFib	skin:	n/a
47	chr19:37288343-37288393	LNCaP	prostate:	n/a
48	chr19:37282556-37282606	Hepatocyte	liver:	n/a
49	chr19:37282502-37282552	RPTEC	kidney:	n/a
50	chr19:37288343-37288393	AG04449	skin:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:37290133..37291956-chr19:37293759..37296212,2	MCF-7	breast:
2	chr19:37288230..37290127-chr19:37296601..37299448,2	MCF-7	breast:
3	chr19:37270866..37273787-chr19:37294233..37296102,2	MCF-7	breast:
4	chr19:37273460..37274086-chr5:138634312..138635067,2	MCF-7	breast:
5	chr19:37287538..37289947-chr19:37340425..37342708,2	MCF-7	breast:
6	chr19:37290133..37291956-chr19:37293759..37296212,2	MCF-7	breast:
7	chr19:37270866..37273787-chr19:37294233..37296102,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF345-1	chr19:37292105-37292142	NONHSAT066049
2	lnc-ZNF345-1	chr19:37292778-37292835	ENSG00000267254.1
3	lnc-ZNF345-1	chr19:37288452-37288713	NONHSAT066049
4	lnc-ZNF345-1	chr19:37288465-37288713	NONHSAT066050
5	lnc-ZNF345-1	chr19:37292778-37292835	NONHSAT066050
6	lnc-ZNF345-1	chr19:37288465-37288713	ENSG00000247207
7	lnc-ZNF345-1	chr19:37292111-37292142	ENSG00000267254.1
8	lnc-ZNF345-1	chr19:37292778-37292835	ENSG00000247207
9	lnc-ZNF345-1	chr19:37292778-37292835	NONHSAT066049

No data

Variant related genes	Relation type
ENSG00000267353	TF binding region
ENSG00000267254	TF binding region
ENSG00000267353	CpG island
ENSG00000267254	CpG island
ENSG00000251247	chromatin interactions
ENSG00000267254	chromatin interactions
ENSG00000197863	chromatin interactions
CDKN1B	miRNA target sites
FAM47B	miRNA target sites

Extended variants
information (count: 940 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570206238	chr19:37271353-37271354	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs372473623	chr19:37271358-37271359	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534424556	chr19:37271360-37271361	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs546235721	chr19:37271387-37271388	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs536009808	chr19:37271445-37271446	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs180759330	chr19:37271457-37271458	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs371673550	chr19:37271460-37271461	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs35425873	chr19:37271461-37271462	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs142174533	chr19:37271484-37271485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202044228	chr19:37271520-37271521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535350854	chr19:37271524-37271525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560622073	chr19:37271531-37271532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368741544	chr19:37271532-37271533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186558194	chr19:37271537-37271538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78261766	chr19:37271544-37271545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574097557	chr19:37271589-37271590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62112557	chr19:37271641-37271642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34514177	chr19:37271645-37271646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578056617	chr19:37271657-37271658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183026510	chr19:37271680-37271681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1148400	chr19:37271685-37271686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs540752767	chr19:37271716-37271717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552044066	chr19:37271743-37271744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555441685	chr19:37271770-37271771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368627262	chr19:37271818-37271819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544309820	chr19:37271850-37271851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564203468	chr19:37271878-37271879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575660486	chr19:37271879-37271880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563195827	chr19:37271902-37271903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533488042	chr19:37271914-37271915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560630875	chr19:37271917-37271918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140408447	chr19:37271952-37271953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371872452	chr19:37272026-37272027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560320081	chr19:37272123-37272124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559190063	chr19:37272242-37272243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573724673	chr19:37272282-37272283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546688165	chr19:37272283-37272284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185784309	chr19:37272353-37272354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528857039	chr19:37272363-37272364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550350902	chr19:37272466-37272467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569162136	chr19:37272470-37272471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372348746	chr19:37272512-37272513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567930962	chr19:37272513-37272514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377600264	chr19:37272532-37272533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539753695	chr19:37272546-37272547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117526669	chr19:37272547-37272548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566688732	chr19:37272610-37272611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191024403	chr19:37272667-37272668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183337444	chr19:37272697-37272698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528140287	chr19:37272721-37272722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	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

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37264600-37274800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:37267200-37271600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:37267400-37282400	Weak transcription	Ovary	ovary
4	chr19:37267600-37271400	Weak transcription	Right Ventricle	heart
5	chr19:37267600-37271600	Weak transcription	Placenta	Placenta
6	chr19:37267600-37275000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr19:37267600-37282000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:37273000-37273400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr19:37275000-37275200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
10	chr19:37276000-37280600	ZNF genes & repeats	Liver	Liver
11	chr19:37277600-37278000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:37278000-37280000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr19:37280000-37281000	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr19:37281800-37282000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr19:37281800-37282000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr19:37281800-37282200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr19:37281800-37282200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:37281800-37282600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:37281800-37283000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
20	chr19:37281800-37283200	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr19:37281800-37283200	Enhancers	Placenta	Placenta
22	chr19:37282000-37282200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr19:37282000-37282200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr19:37282000-37282400	Enhancers	Fetal Heart	heart
25	chr19:37282000-37282600	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr19:37282000-37282600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr19:37282000-37282600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr19:37282000-37282600	Enhancers	Brain Cingulate Gyrus	brain
29	chr19:37282000-37283000	Active TSS	Primary T cells from cord blood	blood
30	chr19:37282000-37283000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
31	chr19:37282000-37283200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr19:37282000-37283200	Active TSS	Brain Anterior Caudate	brain
33	chr19:37282000-37283400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr19:37282000-37283400	Active TSS	Brain Substantia Nigra	brain
35	chr19:37282200-37282400	Enhancers	Fetal Lung	lung
36	chr19:37282200-37282600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
37	chr19:37282200-37282600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr19:37282200-37282600	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr19:37282200-37282800	Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr19:37282200-37282800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:37282200-37283000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr19:37282200-37283000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:37282200-37283000	ZNF genes & repeats	Brain Germinal Matrix	brain
44	chr19:37282200-37283000	Active TSS	Colon Smooth Muscle	Colon
45	chr19:37282200-37283200	Active TSS	Right Ventricle	heart
46	chr19:37282200-37283200	Active TSS	Osteobl	bone
47	chr19:37282400-37282600	Enhancers	Fetal Muscle Trunk	muscle
48	chr19:37282400-37282600	Flanking Active TSS	Left Ventricle	heart
49	chr19:37282400-37282600	Active TSS	Placenta Amnion	Placenta Amnion
50	chr19:37282400-37282800	Active TSS	H9 Cell Line	embryonic stem cell

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