Variant report

Variant	nsv1062563
Chromosome Location	chr19:41976648-42007875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:62)
Chromatin interactive
region (count:4)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41985894-41986022	K562	blood:	n/a	n/a
2	ATF1	chr19:41985515-41985820	K562	blood:	n/a	n/a
3	ATF3	chr19:42007044-42007229	K562	blood:	n/a	n/a
4	BACH1	chr19:41985825-41985834	K562	blood:	n/a	n/a
5	BATF	chr19:42007315-42007464	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:41986254-41986585	K562	blood:	n/a	n/a
7	BHLHE40	chr19:42007430-42007554	K562	blood:	n/a	n/a
8	BHLHE40	chr19:41985631-41985823	K562	blood:	n/a	n/a
9	CBX3	chr19:42007176-42007860	HCT-116	colon:	n/a	n/a
10	CBX3	chr19:41985547-41986099	K562	blood:	n/a	n/a
11	CEBPB	chr19:41992947-41993198	A549	lung:	n/a	chr19:41993068-41993079
12	CEBPB	chr19:41992465-41992478	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr19:41992260-41992553	A549	lung:	n/a	n/a
14	CEBPB	chr19:41992919-41993068	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:41992890-41993261	HepG2	liver:	n/a	chr19:41993068-41993079
16	CEBPB	chr19:41992986-41993092	IMR90	lung:	n/a	chr19:41993068-41993079
17	CEBPB	chr19:41992290-41992562	HepG2	liver:	n/a	n/a
18	CTCF	chr19:41990980-41991130	A549	lung:	n/a	n/a
19	CTCF	chr19:41992387-41992397	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr19:41984420-41984570	A549	lung:	n/a	n/a
21	CTCF	chr19:41982813-41982850	ProgFib	skin:	n/a	n/a
22	CTCF	chr19:41984280-41984430	HEK293	kidney:	n/a	n/a
23	CTCF	chr19:41984380-41984530	GM06990	blood:	n/a	n/a
24	CTCF	chr19:41982900-41983050	GM12869	blood:	n/a	n/a
25	CTCF	chr19:41984200-41984350	A549	lung:	n/a	chr19:41984245-41984254 chr19:41984245-41984258
26	CUX1	chr19:42007456-42007659	K562	blood:	n/a	n/a
27	E2F4	chr19:42007189-42007607	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F6	chr19:42006624-42008253	A549	lung:	n/a	n/a
29	E2F6	chr19:41985892-41986040	K562	blood:	n/a	n/a
30	E2F6	chr19:41986291-41986500	K562	blood:	n/a	n/a
31	E2F6	chr19:42007283-42007624	K562	blood:	n/a	n/a
32	E2F6	chr19:42006864-42008112	A549	lung:	n/a	n/a
33	E2F6	chr19:41986216-41986489	K562	blood:	n/a	n/a
34	E2F6	chr19:42007078-42007279	K562	blood:	n/a	n/a
35	EP300	chr19:42007327-42007661	K562	blood:	n/a	n/a
36	EP300	chr19:41985848-41986019	K562	blood:	n/a	n/a
37	FOS	chr19:42007323-42007645	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
38	FOS	chr19:42007322-42007647	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
39	FOS	chr19:41984858-41986274	HUVEC	blood vessel:	n/a	chr19:41985971-41985982 chr19:41985559-41985568
40	FOS	chr19:41985798-41986124	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
41	FOS	chr19:42007316-42007659	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
42	FOS	chr19:41985870-41986108	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
43	FOS	chr19:42007303-42007652	MCF10A-Er-Src	breast:	n/a	chr19:42007464-42007475
44	FOS	chr19:41985833-41986024	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
45	FOS	chr19:42007233-42007722	HUVEC	blood vessel:	n/a	chr19:42007464-42007475
46	FOS	chr19:42007874-42008336	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr19:41985864-41986064	MCF10A-Er-Src	breast:	n/a	chr19:41985971-41985982
48	FOSL1	chr19:42007174-42007932	HCT-116	colon:	n/a	n/a
49	FOSL1	chr19:42007197-42007840	HCT-116	colon:	n/a	n/a
50	FOSL2	chr19:42007295-42007758	HepG2	liver:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42007378-42007428	HEK293	kidney:	embryo
2	chr19:42007378-42007428	HEK293	kidney:	embryo
3	chr19:42007378-42007428	SK-N-MC	brain:	n/a
4	chr19:42007378-42007428	SK-N-SH_RA	brain:	n/a
5	chr19:42007378-42007428	GM12892	blood:	n/a
6	chr19:42007378-42007428	U87	brain:	n/a
7	chr19:42007378-42007428	HIPEpiC	eye:	n/a
8	chr19:42007378-42007428	ProgFib	skin:	n/a
9	chr19:42007378-42007428	H1-hESC	embryonic stem cell:	embryo
10	chr19:42007378-42007428	CMK	blood:	n/a
11	chr19:42007378-42007428	LNCaP	prostate:	n/a
12	chr19:42007378-42007428	GM06990	blood:	n/a
13	chr19:42007378-42007428	GM19239	blood:	n/a
14	chr19:42007378-42007428	SK-N-SH	brain:	n/a
15	chr19:42007378-42007428	AoSMC	blood vessel:	n/a
16	chr19:42007378-42007428	AG09309	skin:	n/a
17	chr19:42007378-42007428	AG04450	lung:	fetal
18	chr19:42007378-42007428	SKMC	muscle:	n/a
19	chr19:42007378-42007428	HCT-116	colon:	n/a
20	chr19:42007378-42007428	Caco-2	colon:	n/a
21	chr19:42007378-42007428	K562	blood:	n/a
22	chr19:42007378-42007428	HNPCEpiC	eye:	n/a
23	chr19:42007378-42007428	Hela-S3	cervix:	n/a
24	chr19:42007378-42007428	AG10803	skin:	n/a
25	chr19:42007378-42007428	PrEC	prostate:	n/a
26	chr19:42007378-42007428	BJ	skin:	n/a
27	chr19:42007378-42007428	PFSK-1	brain:	n/a
28	chr19:42007378-42007428	PANC-1	pancreas:	n/a
29	chr19:42007378-42007428	NHBE	bronchial:	n/a
30	chr19:42007378-42007428	HPAEpiC	pulmonary alveolar:	n/a
31	chr19:42007378-42007428	HEEpiC	esophagus:	n/a
32	chr19:42007378-42007428	A549	lung:	n/a
33	chr19:42007378-42007428	HMEC	breast:	n/a
34	chr19:42007378-42007428	HUVEC	blood vessel:	n/a
35	chr19:42007378-42007428	HL-60	blood:	n/a
36	chr19:42007378-42007428	HRPEpiC	eye:	n/a
37	chr19:42007378-42007428	RPTEC	kidney:	n/a
38	chr19:42007378-42007428	GM12891	blood:	n/a
39	chr19:42007378-42007428	HCM	heart:	n/a
40	chr19:42007378-42007428	AG04449	skin:	fetal
41	chr19:42007378-42007428	BE2_C	brain:	n/a
42	chr19:42007378-42007428	T-47D	breast:	n/a
43	chr19:42007378-42007428	ovcar-3	ovarian:	n/a
44	chr19:42007378-42007428	HepG2	liver:	n/a
45	chr19:42007378-42007428	HRCEpiC	kidney:	n/a
46	chr19:42007378-42007428	NHDF-neo	bronchial:	n/a
47	chr19:42007378-42007428	MCF10A-Er-Src	breast:	n/a
48	chr19:42007378-42007428	SAEC	small airway:	n/a
49	chr19:42007378-42007428	NT2-D1	testis:	n/a
50	chr19:42007378-42007428	AG09319	gingival:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41979781..41981328-chr19:41984407..41987088,2	K562	blood:
2	chr19:41945911..41947481-chr19:41988789..41990689,2	K562	blood:
3	chr19:41944280..41946189-chr19:42004239..42006678,2	K562	blood:
4	chr19:41944061..41946977-chr19:42000429..42002001,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5SL-1	chr19:41984989-41985192	NONHSAT066451
2	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000249527
3	lnc-ATP5SL-1	chr19:41980371-41980444	ENSG00000267107.2
4	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000249527
5	lnc-ATP5SL-1	chr19:42006494-42006545	NONHSAT066458
6	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000249527
7	lnc-ATP5SL-1	chr19:41984989-41985049	ENSG00000267107.2
8	lnc-ATP5SL-1	chr19:42006494-42006539	ENSG00000267107.2
9	lnc-ATP5SL-1	chr19:42006494-42006554	NONHSAT066453
10	lnc-ATP5SL-1	chr19:42001210-42001335	ENSG00000267107.2
11	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000249527
12	lnc-ATP5SL-1	chr19:41984989-41985192	NONHSAT066453
13	lnc-ATP5SL-1	chr19:42000448-42001335	ENSG00000267107.2
14	lnc-ATP5SL-1	chr19:42006494-42006559	ENSG00000249527
15	lnc-ATP5SL-1	chr19:42001210-42001335	NONHSAT066451
16	lnc-ATP5SL-1	chr19:41985040-41985192	NONHSAT066459
17	lnc-ATP5SL-1	chr19:42006494-42006538	NONHSAT066457
18	lnc-ATP5SL-1	chr19:41984451-41985192	NONHSAT066457
19	lnc-ATP5SL-1	chr19:41984451-41985192	NONHSAT066458
20	lnc-ATP5SL-1	chr19:41984989-41985049	ENSG00000267107.2
21	lnc-ATP5SL-1	chr19:42000448-42001335	ENSG00000249527
22	lnc-ATP5SL-1	chr19:42006494-42006554	ENSG00000267107.2
23	lnc-ATP5SL-1	chr19:42006494-42006540	NONHSAT066451
24	lnc-ATP5SL-1	chr19:41984989-41985051	ENSG00000267107.2
25	lnc-ATP5SL-1	chr19:41984989-41985192	ENSG00000267107.2
26	lnc-ATP5SL-1	chr19:42001210-42001335	NONHSAT066458
27	lnc-ATP5SL-1	chr19:42001210-42001338	NONHSAT066459

No data

Variant related genes	Relation type
ENSG00000267107	TF binding region
ENSG00000268034	TF binding region
ENSG00000267107	CpG island
ENSG00000268034	CpG island
ENSG00000267107	chromatin interactions
ENSG00000105341	chromatin interactions
TMED7	miRNA target sites
CNN3	miRNA target sites
PRSS21	miRNA target sites
CHST11	miRNA target sites
SPTBN1	miRNA target sites
EZH2	miRNA target sites

Extended variants
information (count: 1283 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587710132	chr19:41976660-41976661	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs8110081	chr19:41976754-41976755	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs57463906	chr19:41976769-41976770	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs75968818	chr19:41976809-41976810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587598143	chr19:41976950-41976951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375037608	chr19:41976960-41976961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587709549	chr19:41976962-41976963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185127442	chr19:41976982-41976983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191121769	chr19:41977029-41977030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587768304	chr19:41977053-41977054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587623463	chr19:41977089-41977090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587680843	chr19:41977135-41977136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587718357	chr19:41977148-41977149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587760168	chr19:41977177-41977178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372964864	chr19:41977184-41977185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587696463	chr19:41977196-41977197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375998740	chr19:41977207-41977208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587627976	chr19:41977227-41977228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147335304	chr19:41977232-41977233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587769146	chr19:41977259-41977260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116995921	chr19:41977278-41977279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72480754	chr19:41977292-41977293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs373188312	chr19:41977295-41977296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139239819	chr19:41977340-41977341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149390954	chr19:41977351-41977352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377278694	chr19:41977365-41977366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587605707	chr19:41977370-41977371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376684808	chr19:41977410-41977411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79262657	chr19:41977449-41977450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375449126	chr19:41977598-41977599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367884465	chr19:41977614-41977615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587734115	chr19:41977618-41977619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4803472	chr19:41977654-41977655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs374693339	chr19:41977698-41977699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587729146	chr19:41977715-41977716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184038106	chr19:41977716-41977717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368002704	chr19:41977718-41977719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587689834	chr19:41977727-41977728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34975929	chr19:41977825-41977826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587744950	chr19:41977853-41977854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587620240	chr19:41977901-41977902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367996160	chr19:41977932-41977933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587754753	chr19:41977933-41977934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187280937	chr19:41977948-41977949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60118562	chr19:41977963-41977964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs148524986	chr19:41977997-41977998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142881274	chr19:41978008-41978009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587725384	chr19:41978018-41978019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587773708	chr19:41978081-41978082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587660196	chr19:41978087-41978088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	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
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41968400-41982200	Weak transcription	HUVEC	blood vessel
2	chr19:41976600-41976800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
3	chr19:41976600-41976800	Enhancers	Spleen	Spleen
4	chr19:41976800-41978800	Weak transcription	Spleen	Spleen
5	chr19:41978800-41979600	Enhancers	Spleen	Spleen
6	chr19:41979600-41982200	Weak transcription	Spleen	Spleen
7	chr19:41982200-41982400	Enhancers	Spleen	Spleen
8	chr19:41982200-41982800	Enhancers	GM12878-XiMat	blood
9	chr19:41982200-41983200	Enhancers	Primary B cells from peripheral blood	blood
10	chr19:41982200-41983400	Enhancers	HUVEC	blood vessel
11	chr19:41982400-41982800	Weak transcription	Spleen	Spleen
12	chr19:41982400-41983800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr19:41982800-41983000	Enhancers	Left Ventricle	heart
14	chr19:41982800-41983000	Enhancers	Right Atrium	heart
15	chr19:41982800-41983000	Enhancers	Spleen	Spleen
16	chr19:41982800-41983000	Flanking Active TSS	GM12878-XiMat	blood
17	chr19:41982800-41983600	Enhancers	Lung	lung
18	chr19:41983000-41983600	Genic enhancers	Left Ventricle	heart
19	chr19:41983000-41984000	Weak transcription	Right Atrium	heart
20	chr19:41983000-41986400	Weak transcription	Spleen	Spleen
21	chr19:41983400-41984000	Enhancers	Fetal Muscle Leg	muscle
22	chr19:41983400-41986400	Flanking Active TSS	HUVEC	blood vessel
23	chr19:41983600-41984200	Enhancers	Left Ventricle	heart
24	chr19:41983600-41985200	Active TSS	Lung	lung
25	chr19:41983800-41984600	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
26	chr19:41983800-41985000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr19:41984000-41984200	Bivalent Enhancer	Adipose Nuclei	Adipose
28	chr19:41984000-41984200	Weak transcription	Fetal Muscle Leg	muscle
29	chr19:41984000-41984200	Enhancers	Right Atrium	heart
30	chr19:41984200-41984400	Bivalent/Poised TSS	Fetal Stomach	stomach
31	chr19:41984200-41984400	Flanking Active TSS	Left Ventricle	heart
32	chr19:41984200-41984800	Bivalent/Poised TSS	Right Ventricle	heart
33	chr19:41984200-41985000	Active TSS	Fetal Muscle Leg	muscle
34	chr19:41984200-41985600	Active TSS	Right Atrium	heart
35	chr19:41984200-41986400	Active TSS	Ovary	ovary
36	chr19:41984400-41984600	Active TSS	Adipose Nuclei	Adipose
37	chr19:41984400-41984800	Active TSS	Left Ventricle	heart
38	chr19:41984400-41985000	Active TSS	Fetal Stomach	stomach
39	chr19:41984400-41985000	Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr19:41984600-41985000	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr19:41984600-41985200	Active TSS	Fetal Muscle Trunk	muscle
42	chr19:41984800-41985000	Flanking Active TSS	Left Ventricle	heart
43	chr19:41984800-41985000	Flanking Active TSS	Right Ventricle	heart
44	chr19:41985000-41985400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr19:41985000-41986200	Weak transcription	Left Ventricle	heart
46	chr19:41985000-41986600	Enhancers	Adipose Nuclei	Adipose
47	chr19:41985000-41986600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr19:41985200-41985600	Weak transcription	Fetal Muscle Trunk	muscle
49	chr19:41985200-41986800	Weak transcription	Lung	lung
50	chr19:41985400-41986000	Enhancers	Fetal Heart	heart

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