Variant report

Variant	nsv1011086
Chromosome Location	chr1:47259078-47305191
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	ATF1	chr1:47298656-47298680	K562	blood:	n/a	n/a
2	CEBPB	chr1:47272508-47272610	K562	blood:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
3	CEBPB	chr1:47272373-47272770	ECC-1	luminal epithelium:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
4	CEBPB	chr1:47275993-47276259	HepG2	liver:	n/a	chr1:47276116-47276125 chr1:47276116-47276125 chr1:47276114-47276125 chr1:47276116-47276125 chr1:47276114-47276127 chr1:47276116-47276127 chr1:47276116-47276125
5	CEBPB	chr1:47272398-47272736	Hela-S3	cervix:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
6	CEBPB	chr1:47275958-47276196	IMR90	lung:	n/a	chr1:47276116-47276125 chr1:47276116-47276125 chr1:47276114-47276125 chr1:47276116-47276125 chr1:47276114-47276127 chr1:47276116-47276127 chr1:47276116-47276125
7	CEBPB	chr1:47272435-47272799	MCF-7	breast:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
8	CEBPB	chr1:47272347-47272776	ECC-1	luminal epithelium:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
9	CEBPB	chr1:47275979-47276251	K562	blood:	n/a	chr1:47276116-47276125 chr1:47276116-47276125 chr1:47276114-47276125 chr1:47276116-47276125 chr1:47276114-47276127 chr1:47276116-47276127 chr1:47276116-47276125
10	CEBPB	chr1:47272175-47272836	MCF-7	breast:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
11	CEBPB	chr1:47272476-47272676	H1-hESC	embryonic stem cell:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
12	CEBPB	chr1:47272292-47272727	HepG2	liver:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
13	CEBPB	chr1:47272465-47272698	IMR90	lung:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
14	CTCF	chr1:47301260-47301410	HCT-116	colon:	n/a	n/a
15	CTCF	chr1:47272077-47272151	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr1:47288160-47288310	HEK293	kidney:	n/a	n/a
17	CTCF	chr1:47272840-47272990	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr1:47301240-47301390	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:47301274-47301412	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:47272920-47273070	NHEK	skin:	n/a	n/a
21	CTCF	chr1:47272820-47272970	HepG2	liver:	n/a	n/a
22	CTCF	chr1:47301323-47301325	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:47301220-47301370	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr1:47301292-47301412	HepG2	liver:	n/a	n/a
25	CTCF	chr1:47272820-47272970	Caco-2	colon:	n/a	n/a
26	CTCF	chr1:47301240-47301390	HEK293	kidney:	n/a	n/a
27	CTCF	chr1:47301260-47301410	A549	lung:	n/a	n/a
28	CTCF	chr1:47301280-47301430	HepG2	liver:	n/a	n/a
29	CTCF	chr1:47301253-47301414	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:47288047-47288130	K562	blood:	n/a	n/a
31	CTCF	chr1:47301280-47301430	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:47272920-47273070	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:47272960-47273110	NHEK	skin:	n/a	n/a
34	CTCF	chr1:47301131-47301466	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:47301283-47301414	Gliobla	brain:	n/a	n/a
36	CTCF	chr1:47278520-47278670	GM12872	blood:	n/a	chr1:47278531-47278540
37	CTCF	chr1:47301249-47301462	K562	blood:	n/a	n/a
38	CTCF	chr1:47272919-47272921	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:47301260-47301410	K562	blood:	n/a	n/a
40	CTCF	chr1:47301244-47301437	K562	blood:	n/a	n/a
41	CTCF	chr1:47272860-47272917	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:47272400-47272550	NHEK	skin:	n/a	n/a
43	CTCF	chr1:47301297-47301398	Medullo	brain:	n/a	n/a
44	CTCF	chr1:47272840-47272990	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr1:47288021-47288125	K562	blood:	n/a	n/a
46	CTCF	chr1:47301326-47301394	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:47301140-47301290	HCT-116	colon:	n/a	n/a
48	CTCF	chr1:47272878-47272978	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr1:47286580-47286730	HepG2	liver:	n/a	n/a
50	CTCF	chr1:47288040-47288190	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47279985-47280035	HL-60	blood:	n/a
2	chr1:47279985-47280035	HCF	heart:	n/a
3	chr1:47279985-47280035	ProgFib	skin:	n/a
4	chr1:47264866-47264916	Hela-S3	cervix:	n/a
5	chr1:47263236-47263286	GM12892	blood:	n/a
6	chr1:47264601-47264651	HNPCEpiC	eye:	n/a
7	chr1:47279985-47280035	HCT-116	colon:	n/a
8	chr1:47279985-47280035	SK-N-MC	brain:	n/a
9	chr1:47264866-47264916	MCF10A-Er-Src	breast:	n/a
10	chr1:47279985-47280035	HIPEpiC	eye:	n/a
11	chr1:47284627-47284677	SK-N-MC	brain:	n/a
12	chr1:47264866-47264916	AG04450	lung:	fetal
13	chr1:47264866-47264916	AG04449	skin:	fetal
14	chr1:47263713-47263763	SAEC	small airway:	n/a
15	chr1:47279985-47280035	HEEpiC	esophagus:	n/a
16	chr1:47263236-47263286	HRPEpiC	eye:	n/a
17	chr1:47263236-47263286	AG09319	gingival:	n/a
18	chr1:47264601-47264651	H1-hESC	embryonic stem cell:	embryo
19	chr1:47264601-47264651	A549	lung:	n/a
20	chr1:47263236-47263286	GM12878	blood:	n/a
21	chr1:47264866-47264916	HCM	heart:	n/a
22	chr1:47284627-47284677	GM12891	blood:	n/a
23	chr1:47264866-47264916	SKMC	muscle:	n/a
24	chr1:47263713-47263763	Jurkat	blood:	n/a
25	chr1:47284627-47284677	GM06990	blood:	n/a
26	chr1:47279985-47280035	HCPEpiC	choroid plexus:	n/a
27	chr1:47264866-47264916	K562	blood:	n/a
28	chr1:47284627-47284677	SKMC	muscle:	n/a
29	chr1:47284627-47284677	NB4	blood:	n/a
30	chr1:47263713-47263763	IMR90	lung:	fetal
31	chr1:47263236-47263286	HIPEpiC	eye:	n/a
32	chr1:47263713-47263763	SK-N-SH	brain:	n/a
33	chr1:47284627-47284677	HCT-116	colon:	n/a
34	chr1:47279985-47280035	HAEpiC	amniotic membrane:	n/a
35	chr1:47263713-47263763	K562	blood:	n/a
36	chr1:47263713-47263763	HMEC	breast:	n/a
37	chr1:47279985-47280035	AG09319	gingival:	n/a
38	chr1:47264601-47264651	HepG2	liver:	n/a
39	chr1:47284627-47284677	GM12878	blood:	n/a
40	chr1:47284627-47284677	NH-A	brain:	n/a
41	chr1:47264601-47264651	SK-N-SH_RA	brain:	n/a
42	chr1:47284627-47284677	HMEC	breast:	n/a
43	chr1:47284627-47284677	SK-N-SH	brain:	n/a
44	chr1:47263713-47263763	MCF-7	breast:	n/a
45	chr1:47263236-47263286	SAEC	small airway:	n/a
46	chr1:47264866-47264916	HEEpiC	esophagus:	n/a
47	chr1:47264601-47264651	NH-A	brain:	n/a
48	chr1:47279985-47280035	MCF10A-Er-Src	breast:	n/a
49	chr1:47264601-47264651	GM19239	blood:	n/a
50	chr1:47264601-47264651	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:47272192..47274421-chr1:47282299..47283950,2	K562	blood:
2	chr1:47263957..47267463-chr1:47271063..47272982,3	MCF-7	breast:
3	chr1:47263957..47267463-chr1:47271063..47272982,3	MCF-7	breast:
4	chr1:47266762..47268483-chr1:47274674..47276282,2	MCF-7	breast:
5	chr1:47221048..47223209-chr1:47267479..47269912,2	MCF-7	breast:
6	chr1:47282268..47284457-chr1:47286910..47288924,2	K562	blood:
7	chr1:47270918..47272980-chr1:47278589..47280565,2	K562	blood:
8	chr1:47275758..47278616-chr1:47280662..47283634,2	K562	blood:
9	chr1:47250372..47251921-chr1:47261970..47263587,2	K562	blood:
10	chr1:47272192..47274421-chr1:47282299..47283950,2	K562	blood:
11	chr1:47263919..47266818-chr1:47267658..47269946,3	MCF-7	breast:
12	chr1:47264251..47266259-chr1:47267707..47269923,2	K562	blood:
13	chr1:47275758..47278616-chr1:47280662..47283634,2	K562	blood:
14	chr1:47274872..47277380-chr1:47277423..47279681,2	K562	blood:
15	chr1:47266762..47268483-chr1:47274674..47276282,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATPAF1-AS1-2	chr1:47276480-47276522	NONHSAT003037

Variant related genes	Relation type
CYP4B1	TF binding region
CYP4B1	CpG island
ENSG00000142973	chromatin interactions

Extended variants
information (count: 1951 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1951 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567712504	chr1:47259082-47259083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76542135	chr1:47259114-47259115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558351631	chr1:47259124-47259125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576733573	chr1:47259136-47259137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs863915	chr1:47259138-47259139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs562610341	chr1:47259139-47259140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149680381	chr1:47259149-47259150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565718951	chr1:47259201-47259202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145522764	chr1:47259213-47259214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148866924	chr1:47259222-47259223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527614538	chr1:47259226-47259227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552068077	chr1:47259299-47259300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570265974	chr1:47259312-47259313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531412519	chr1:47259313-47259314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs864489	chr1:47259357-47259358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568586771	chr1:47259378-47259379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535462891	chr1:47259386-47259387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552656197	chr1:47259418-47259419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566097365	chr1:47259434-47259435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569319466	chr1:47259454-47259455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540111933	chr1:47259464-47259465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558490454	chr1:47259491-47259492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576667823	chr1:47259496-47259497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs837406	chr1:47259497-47259498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182376850	chr1:47259515-47259516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187377830	chr1:47259532-47259533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79685448	chr1:47259536-47259537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560059855	chr1:47259562-47259563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113189123	chr1:47259584-47259585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571729258	chr1:47259591-47259592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7543829	chr1:47259611-47259612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564081922	chr1:47259709-47259710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28417546	chr1:47259722-47259723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531400180	chr1:47259773-47259774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148075195	chr1:47259844-47259845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562028575	chr1:47259869-47259870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529356323	chr1:47259880-47259881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200614320	chr1:47259913-47259914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374397722	chr1:47259916-47259917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371640682	chr1:47259987-47259988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180941912	chr1:47260018-47260019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201180494	chr1:47260028-47260029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201797707	chr1:47260034-47260035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566034254	chr1:47260037-47260038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539848611	chr1:47260040-47260041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141852884	chr1:47260055-47260056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570406275	chr1:47260062-47260063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368455214	chr1:47260063-47260064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185162327	chr1:47260067-47260068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369113386	chr1:47260108-47260109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47256600-47263400	Weak transcription	Lung	lung
2	chr1:47263400-47263600	Enhancers	Gastric	stomach
3	chr1:47263400-47263600	Enhancers	Lung	lung
4	chr1:47263400-47264000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:47263600-47264600	Enhancers	Esophagus	oesophagus
6	chr1:47263600-47264600	Weak transcription	Gastric	stomach
7	chr1:47263600-47264600	Weak transcription	Lung	lung
8	chr1:47263600-47264800	Enhancers	Duodenum Mucosa	Duodenum
9	chr1:47263600-47264800	Enhancers	NHEK	skin
10	chr1:47263600-47265400	Enhancers	Fetal Intestine Small	intestine
11	chr1:47263800-47264400	Enhancers	Adipose Nuclei	Adipose
12	chr1:47263800-47264600	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr1:47264000-47265200	Enhancers	Stomach Mucosa	stomach
14	chr1:47264200-47264400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:47264200-47265200	Enhancers	Right Atrium	heart
16	chr1:47264400-47265200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:47264400-47265800	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr1:47264600-47264800	Flanking Active TSS	Esophagus	oesophagus
19	chr1:47264600-47264800	Enhancers	Fetal Muscle Leg	muscle
20	chr1:47264600-47264800	Enhancers	Lung	lung
21	chr1:47264600-47264800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
22	chr1:47264600-47265000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
23	chr1:47264600-47265600	Enhancers	Gastric	stomach
24	chr1:47264600-47265600	Bivalent/Poised TSS	Psoas Muscle	Psoas
25	chr1:47264600-47269200	Active TSS	Left Ventricle	heart
26	chr1:47264800-47265000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:47264800-47265000	Flanking Active TSS	Duodenum Mucosa	Duodenum
28	chr1:47264800-47265200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr1:47264800-47265200	Flanking Active TSS	Lung	lung
30	chr1:47264800-47265600	Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr1:47264800-47265800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
32	chr1:47264800-47266800	Active TSS	Esophagus	oesophagus
33	chr1:47265000-47265400	Active TSS	Duodenum Mucosa	Duodenum
34	chr1:47265000-47265600	Active TSS	Colon Smooth Muscle	Colon
35	chr1:47265000-47265600	Enhancers	Pancreas	Pancrea
36	chr1:47265000-47265600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
37	chr1:47265000-47265600	Active TSS	Spleen	Spleen
38	chr1:47265200-47265600	Flanking Active TSS	Right Atrium	heart
39	chr1:47265200-47265800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:47265200-47267200	Active TSS	Lung	lung
41	chr1:47265200-47267400	Weak transcription	Stomach Mucosa	stomach
42	chr1:47265400-47268600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr1:47265400-47271400	Weak transcription	Fetal Intestine Small	intestine
44	chr1:47265600-47265800	Active TSS	Right Atrium	heart
45	chr1:47265600-47266400	Weak transcription	Colon Smooth Muscle	Colon
46	chr1:47265600-47268800	Active TSS	Psoas Muscle	Psoas
47	chr1:47265600-47271800	Weak transcription	Spleen	Spleen
48	chr1:47265600-47279200	Weak transcription	Gastric	stomach
49	chr1:47265800-47266400	Active TSS	Adipose Nuclei	Adipose
50	chr1:47265800-47269800	Weak transcription	Right Atrium	heart

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