Variant report

Variant	nsv871288
Chromosome Location	chr1:47363893-47507808
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	chr1:47456846-47457081	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:47407911-47408095	HepG2	liver:	n/a	n/a
3	ATF1	chr1:47376935-47376945	K562	blood:	n/a	n/a
4	BACH1	chr1:47489244-47489445	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:47390862-47391006	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:47449788-47450018	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:47413385-47413596	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:47506533-47506550	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:47489311-47489598	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr1:47373174-47373415	K562	blood:	n/a	n/a
11	CEBPB	chr1:47426647-47426872	HepG2	liver:	n/a	chr1:47426704-47426715 chr1:47426706-47426717 chr1:47426706-47426715
12	CEBPB	chr1:47496150-47496401	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:47426686-47426777	K562	blood:	n/a	chr1:47426704-47426715 chr1:47426706-47426717 chr1:47426706-47426715
14	CEBPB	chr1:47498947-47499243	K562	blood:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
15	CEBPB	chr1:47498941-47499139	H1-hESC	embryonic stem cell:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
16	CEBPB	chr1:47424621-47424813	HepG2	liver:	n/a	chr1:47424681-47424692
17	CEBPB	chr1:47485419-47485541	K562	blood:	n/a	chr1:47485446-47485457
18	CEBPB	chr1:47407842-47408063	HepG2	liver:	n/a	chr1:47407954-47407963 chr1:47407954-47407965
19	CEBPB	chr1:47457992-47458199	A549	lung:	n/a	chr1:47458064-47458075
20	CEBPB	chr1:47462538-47463107	A549	lung:	n/a	n/a
21	CEBPB	chr1:47498924-47499142	MCF-7	breast:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
22	CEBPB	chr1:47498905-47499216	HepG2	liver:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
23	CEBPB	chr1:47478872-47479484	Hela-S3	cervix:	n/a	chr1:47478883-47478894
24	CEBPB	chr1:47469301-47469803	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr1:47498926-47499218	A549	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
26	CEBPB	chr1:47407765-47408138	HepG2	liver:	n/a	chr1:47407954-47407963 chr1:47407954-47407965
27	CEBPB	chr1:47498927-47499225	IMR90	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
28	CEBPB	chr1:47457975-47458107	K562	blood:	n/a	chr1:47458064-47458075
29	CEBPB	chr1:47458008-47458201	HepG2	liver:	n/a	chr1:47458064-47458075
30	CEBPB	chr1:47400611-47400768	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:47424651-47424710	H1-hESC	embryonic stem cell:	n/a	chr1:47424681-47424692
32	CEBPB	chr1:47485351-47485535	HepG2	liver:	n/a	chr1:47485446-47485457
33	CEBPB	chr1:47492324-47492550	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:47462344-47463113	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:47462780-47463046	K562	blood:	n/a	n/a
36	CEBPB	chr1:47369289-47369609	MCF-7	breast:	n/a	n/a
37	CEBPB	chr1:47462783-47463088	HepG2	liver:	n/a	n/a
38	CHD1	chr1:47449455-47449653	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr1:47449063-47449366	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:47489249-47489669	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr1:47435000-47435193	K562	blood:	n/a	chr1:47435074-47435095 chr1:47435079-47435097 chr1:47435084-47435092
42	CTCF	chr1:47435020-47435170	Caco-2	colon:	n/a	chr1:47435074-47435095 chr1:47435079-47435097 chr1:47435084-47435092
43	CTCF	chr1:47400660-47400810	Caco-2	colon:	n/a	n/a
44	CTCF	chr1:47456809-47457019	Pancreas_OC	pancreas:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
45	CTCF	chr1:47434940-47435090	GM12869	blood:	n/a	n/a
46	CTCF	chr1:47457060-47457210	HCT-116	colon:	n/a	n/a
47	CTCF	chr1:47434938-47435204	H1-hESC	embryonic stem cell:	n/a	chr1:47435074-47435095 chr1:47435079-47435097 chr1:47435084-47435092
48	CTCF	chr1:47468000-47468150	GM12871	blood:	n/a	chr1:47468065-47468083 chr1:47468060-47468081 chr1:47468070-47468078
49	CTCF	chr1:47456745-47457058	GM12878	blood:	n/a	chr1:47456901-47456919 chr1:47456896-47456917 chr1:47456902-47456918
50	CTCF	chr1:47434980-47435130	Caco-2	colon:	n/a	chr1:47435074-47435095 chr1:47435079-47435097 chr1:47435084-47435092

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47406950-47407000	Hela-S3	cervix:	n/a
2	chr1:47488111-47488161	GM12892	blood:	n/a
3	chr1:47406950-47407000	Hela-S3	cervix:	n/a
4	chr1:47488111-47488161	GM12892	blood:	n/a
5	chr1:47366730-47366780	NB4	blood:	n/a
6	chr1:47493419-47493469	HCM	heart:	n/a
7	chr1:47469065-47469115	SAEC	small airway:	n/a
8	chr1:47469065-47469115	HMEC	breast:	n/a
9	chr1:47400701-47400751	AG04450	lung:	fetal
10	chr1:47489539-47489589	H1-hESC	embryonic stem cell:	embryo
11	chr1:47486850-47486900	GM19239	blood:	n/a
12	chr1:47489543-47489593	ProgFib	skin:	n/a
13	chr1:47366366-47366416	NH-A	brain:	n/a
14	chr1:47489776-47489826	SK-N-SH_RA	brain:	n/a
15	chr1:47366730-47366780	HCM	heart:	n/a
16	chr1:47493419-47493469	AG04449	skin:	fetal
17	chr1:47488111-47488161	ovcar-3	ovarian:	n/a
18	chr1:47366730-47366780	HUVEC	blood vessel:	n/a
19	chr1:47366730-47366780	GM12892	blood:	n/a
20	chr1:47489413-47489463	RPTEC	kidney:	n/a
21	chr1:47449205-47449255	PFSK-1	brain:	n/a
22	chr1:47366366-47366416	GM12891	blood:	n/a
23	chr1:47407043-47407093	AG04449	skin:	fetal
24	chr1:47400701-47400751	HEK293	kidney:	embryo
25	chr1:47488111-47488161	Caco-2	colon:	n/a
26	chr1:47489543-47489593	AG09319	gingival:	n/a
27	chr1:47400701-47400751	PANC-1	pancreas:	n/a
28	chr1:47449205-47449255	RPTEC	kidney:	n/a
29	chr1:47489282-47489332	HL-60	blood:	n/a
30	chr1:47488111-47488161	A549	lung:	n/a
31	chr1:47489539-47489589	NB4	blood:	n/a
32	chr1:47489776-47489826	NHDF-neo	bronchial:	n/a
33	chr1:47469065-47469115	ProgFib	skin:	n/a
34	chr1:47493419-47493469	AG09319	gingival:	n/a
35	chr1:47366366-47366416	AG09319	gingival:	n/a
36	chr1:47489413-47489463	HCT-116	colon:	n/a
37	chr1:47488111-47488161	HepG2	liver:	n/a
38	chr1:47488757-47488807	HL-60	blood:	n/a
39	chr1:47406950-47407000	ECC-1	luminal epithelium:	n/a
40	chr1:47365990-47366040	AG09309	skin:	n/a
41	chr1:47488256-47488306	AG10803	skin:	n/a
42	chr1:47488757-47488807	U87	brain:	n/a
43	chr1:47493419-47493469	HCPEpiC	choroid plexus:	n/a
44	chr1:47407043-47407093	GM12878	blood:	n/a
45	chr1:47488934-47488984	IMR90	lung:	fetal
46	chr1:47488111-47488161	HCPEpiC	choroid plexus:	n/a
47	chr1:47407158-47407208	ECC-1	luminal epithelium:	n/a
48	chr1:47488934-47488984	MCF10A-Er-Src	breast:	n/a
49	chr1:47493419-47493469	ovcar-3	ovarian:	n/a
50	chr1:47365990-47366040	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:47481637..47484566-chr1:47494285..47496054,2	K562	blood:
2	chr1:47497049..47498622-chr1:47515812..47517726,2	MCF-7	breast:
3	chr1:47481637..47484566-chr1:47494285..47496054,2	K562	blood:
4	chr1:47457191..47460016-chr1:47461610..47463680,2	K562	blood:
5	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:
6	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:
7	chr1:47500877..47503360-chr1:47503581..47505847,2	K562	blood:
8	chr1:47462174..47464956-chr1:47466807..47468355,2	K562	blood:
9	chr1:47457191..47460016-chr1:47461610..47463680,2	K562	blood:
10	chr1:47462174..47464956-chr1:47466807..47468355,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP4X1-1	chr1:47417509-47417697	NONHSAT003043
2	lnc-CYP4A11-1	chr1:47417449-47417530	NONHSAT003042
3	lnc-CYP4A11-1	chr1:47416428-47416708	NONHSAT003042
4	lnc-CYP4X1-1	chr1:47418127-47418416	NONHSAT003043
5	lnc-CYP4A11-2	chr1:47468777-47469021	expReg_chr1_7623_-

Variant related genes	Relation type
CYP4A11	TF binding region
CYP4A26P	TF binding region
CYP4X1	TF binding region
CYP4A44P	TF binding region
CYP4A27P	TF binding region
CYP4Z2P	TF binding region
CYP4A43P	TF binding region
CYP4A11	CpG island
CYP4A26P	CpG island
CYP4X1	CpG island
CYP4A44P	CpG island
CYP4A27P	CpG island
CYP4Z2P	CpG island
CYP4A43P	CpG island
ENSG00000186377	chromatin interactions

Extended variants
information (count: 4073 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4073 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114524706	chr1:47366143-47366144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs543760123	chr1:47366149-47366150	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561957269	chr1:47366150-47366151	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs569591491	chr1:47366175-47366176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs115668566	chr1:47366190-47366191	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531790040	chr1:47366206-47366207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188316197	chr1:47366293-47366294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147397275	chr1:47366320-47366321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551981126	chr1:47366322-47366323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181144478	chr1:47366367-47366368	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs548543508	chr1:47366388-47366389	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs185589989	chr1:47366392-47366393	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs549715675	chr1:47366483-47366484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139251260	chr1:47366731-47366732	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs189639159	chr1:47366766-47366767	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs562043763	chr1:47366767-47366768	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs574119518	chr1:47366768-47366769	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs565598611	chr1:47367011-47367012	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370407753	chr1:47367024-47367025	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557907949	chr1:47367033-47367034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs202074235	chr1:47367037-47367038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576187680	chr1:47367050-47367051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs537541042	chr1:47367076-47367077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs145200670	chr1:47367077-47367078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs574077294	chr1:47367078-47367079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs541387582	chr1:47367081-47367082	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185243568	chr1:47367085-47367086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs111948226	chr1:47367110-47367111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs189952427	chr1:47367112-47367113	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563883689	chr1:47367127-47367128	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531046800	chr1:47367178-47367179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs10736429	chr1:47367216-47367217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs375297748	chr1:47367217-47367218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs556091319	chr1:47367261-47367262	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs188563883	chr1:47367602-47367603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148179876	chr1:47367691-47367692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61784272	chr1:47367706-47367707	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577674031	chr1:47368232-47368233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544635574	chr1:47368235-47368236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563308467	chr1:47368246-47368247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374910370	chr1:47368294-47368295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77946043	chr1:47368385-47368386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543442701	chr1:47368412-47368413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549323960	chr1:47368416-47368417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150075348	chr1:47368536-47368537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528333732	chr1:47368569-47368570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7415933	chr1:47368587-47368588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183642850	chr1:47368604-47368605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138394823	chr1:47368729-47368730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142732006	chr1:47368732-47368733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Squamous cell cancer	19001599	CNVD

Chromatin state (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47367600-47367800	Enhancers	Stomach Mucosa	stomach
2	chr1:47368200-47369200	Weak transcription	Stomach Mucosa	stomach
3	chr1:47368800-47369200	Enhancers	Fetal Kidney	kidney
4	chr1:47369200-47369800	Enhancers	Stomach Mucosa	stomach
5	chr1:47369400-47369600	Enhancers	Liver	Liver
6	chr1:47369400-47369800	Enhancers	Pancreas	Pancrea
7	chr1:47371400-47372400	Enhancers	Liver	Liver
8	chr1:47373800-47374400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:47374400-47376600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:47376600-47377000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:47391000-47391400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:47391000-47391600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:47391400-47393000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:47391600-47393800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:47393000-47393200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:47393200-47400400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:47393800-47394400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:47394600-47396200	Weak transcription	Liver	Liver
19	chr1:47396200-47400600	Strong transcription	Liver	Liver
20	chr1:47400400-47400600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:47400400-47400800	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr1:47400600-47401600	Weak transcription	Liver	Liver
23	chr1:47400800-47402600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr1:47401600-47403800	Genic enhancers	Liver	Liver
25	chr1:47402600-47404000	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr1:47402600-47404000	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr1:47402800-47403200	Enhancers	Pancreas	Pancrea
28	chr1:47403200-47406000	Weak transcription	Pancreas	Pancrea
29	chr1:47403800-47404400	Transcr. at gene 5' and 3'	Liver	Liver
30	chr1:47404000-47406000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr1:47404000-47406400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr1:47404400-47404600	Active TSS	Liver	Liver
33	chr1:47404600-47405800	Flanking Active TSS	Liver	Liver
34	chr1:47405200-47406200	Enhancers	Duodenum Mucosa	Duodenum
35	chr1:47405400-47406800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:47405800-47407800	Enhancers	Fetal Intestine Small	intestine
37	chr1:47405800-47408000	Enhancers	Fetal Intestine Large	intestine
38	chr1:47405800-47408200	Active TSS	Liver	Liver
39	chr1:47406000-47406200	Enhancers	Fetal Kidney	kidney
40	chr1:47406000-47407400	Enhancers	Pancreas	Pancrea
41	chr1:47406000-47407400	Enhancers	Stomach Mucosa	stomach
42	chr1:47406200-47406400	Flanking Active TSS	Fetal Kidney	kidney
43	chr1:47406200-47406400	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr1:47406200-47406800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr1:47406200-47406800	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr1:47406200-47407200	Enhancers	Gastric	stomach
47	chr1:47406200-47408600	Enhancers	HepG2	liver
48	chr1:47406400-47406600	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr1:47406400-47406800	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr1:47406400-47407000	Active TSS	Fetal Kidney	kidney

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