Variant report

Variant	nsv1014507
Chromosome Location	chr1:104307231-104784753
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	chr1:104332136-104332202	HepG2	liver:	n/a	n/a
2	ATF1	chr1:104435470-104435596	K562	blood:	n/a	n/a
3	ATF2	chr1:104480261-104480901	GM12878	blood:	n/a	n/a
4	ATF2	chr1:104480353-104480818	GM12878	blood:	n/a	n/a
5	BACH1	chr1:104612948-104613054	K562	blood:	n/a	n/a
6	BACH1	chr1:104782197-104782240	K562	blood:	n/a	n/a
7	BATF	chr1:104480376-104480887	GM12878	blood:	n/a	n/a
8	BATF	chr1:104480394-104480652	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:104635351-104635616	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr1:104751628-104751863	GM12878	blood:	n/a	n/a
11	BCL3	chr1:104751571-104751823	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:104480577-104480607	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:104519193-104519299	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:104524798-104524808	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:104326501-104326782	GM12878	blood:	n/a	n/a
16	CEBPB	chr1:104753787-104754126	HepG2	liver:	n/a	chr1:104753931-104753942
17	CEBPB	chr1:104432910-104433274	HepG2	liver:	n/a	chr1:104433036-104433047
18	CEBPB	chr1:104518019-104518281	K562	blood:	n/a	chr1:104518118-104518129 chr1:104518117-104518130 chr1:104518119-104518128
19	CEBPB	chr1:104502096-104502455	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr1:104562642-104562864	A549	lung:	n/a	n/a
21	CEBPB	chr1:104528434-104528672	HepG2	liver:	n/a	chr1:104528542-104528553 chr1:104528450-104528461 chr1:104528541-104528554
22	CEBPB	chr1:104522824-104523092	IMR90	lung:	n/a	chr1:104522963-104522972 chr1:104522961-104522974 chr1:104522961-104522972 chr1:104522963-104522974
23	CEBPB	chr1:104388549-104388858	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:104562695-104562839	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:104663908-104664251	HepG2	liver:	n/a	chr1:104664078-104664091 chr1:104664079-104664090 chr1:104664080-104664089 chr1:104664078-104664091 chr1:104664078-104664089
26	CEBPB	chr1:104753894-104754116	K562	blood:	n/a	chr1:104753931-104753942
27	CEBPB	chr1:104509604-104509895	IMR90	lung:	n/a	chr1:104509727-104509738
28	CEBPB	chr1:104562260-104562820	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr1:104502185-104502446	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr1:104663974-104664248	A549	lung:	n/a	chr1:104664078-104664091 chr1:104664079-104664090 chr1:104664080-104664089 chr1:104664078-104664091 chr1:104664078-104664089
31	CEBPB	chr1:104454820-104455067	H1-hESC	embryonic stem cell:	n/a	chr1:104454929-104454940
32	CEBPB	chr1:104509608-104509861	HepG2	liver:	n/a	chr1:104509727-104509738
33	CEBPB	chr1:104607042-104607460	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:104635379-104635659	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:104627016-104627263	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:104654432-104654632	HepG2	liver:	n/a	chr1:104654533-104654544
37	CEBPB	chr1:104663922-104664252	H1-hESC	embryonic stem cell:	n/a	chr1:104664078-104664091 chr1:104664079-104664090 chr1:104664080-104664089 chr1:104664078-104664091 chr1:104664078-104664089
38	CEBPB	chr1:104454794-104455114	HepG2	liver:	n/a	chr1:104454929-104454940
39	CEBPB	chr1:104619494-104619671	IMR90	lung:	n/a	chr1:104619629-104619640
40	CEBPB	chr1:104386981-104387251	HepG2	liver:	n/a	chr1:104387108-104387119
41	CEBPB	chr1:104307250-104307433	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:104753768-104754118	H1-hESC	embryonic stem cell:	n/a	chr1:104753931-104753942
43	CEBPB	chr1:104454800-104455064	IMR90	lung:	n/a	chr1:104454929-104454940
44	CEBPB	chr1:104329336-104329610	HepG2	liver:	n/a	chr1:104329485-104329496 chr1:104329484-104329497
45	CEBPB	chr1:104433013-104433213	A549	lung:	n/a	chr1:104433036-104433047
46	CEBPB	chr1:104663902-104664280	Hela-S3	cervix:	n/a	chr1:104664078-104664091 chr1:104664079-104664090 chr1:104664080-104664089 chr1:104664078-104664091 chr1:104664078-104664089
47	CEBPB	chr1:104522829-104523124	HepG2	liver:	n/a	chr1:104522963-104522972 chr1:104522961-104522974 chr1:104522961-104522972 chr1:104522963-104522974
48	CEBPB	chr1:104432982-104433095	H1-hESC	embryonic stem cell:	n/a	chr1:104433036-104433047
49	CEBPB	chr1:104619489-104619773	HepG2	liver:	n/a	chr1:104619629-104619640
50	CEBPB	chr1:104500309-104500557	HepG2	liver:	n/a	chr1:104500435-104500444 chr1:104500433-104500446 chr1:104500435-104500444 chr1:104500433-104500444 chr1:104500435-104500444 chr1:104500433-104500444 chr1:104500433-104500446 chr1:104500435-104500444 chr1:104500434-104500445

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104615609-104615659	HCPEpiC	choroid plexus:	n/a
2	chr1:104615609-104615659	HCPEpiC	choroid plexus:	n/a
3	chr1:104616267-104616317	BJ	skin:	n/a
4	chr1:104615609-104615659	HRPEpiC	eye:	n/a
5	chr1:104615867-104615917	SKMC	muscle:	n/a
6	chr1:104523359-104523409	CMK	blood:	n/a
7	chr1:104696931-104696981	BJ	skin:	n/a
8	chr1:104635600-104635650	ECC-1	luminal epithelium:	n/a
9	chr1:104615867-104615917	HCPEpiC	choroid plexus:	n/a
10	chr1:104616267-104616317	GM06990	blood:	n/a
11	chr1:104615609-104615659	SK-N-SH_RA	brain:	n/a
12	chr1:104635600-104635650	HCT-116	colon:	n/a
13	chr1:104616267-104616317	HL-60	blood:	n/a
14	chr1:104635600-104635650	HEEpiC	esophagus:	n/a
15	chr1:104523359-104523409	HCT-116	colon:	n/a
16	chr1:104523359-104523409	GM19239	blood:	n/a
17	chr1:104523359-104523409	HAEpiC	amniotic membrane:	n/a
18	chr1:104696931-104696981	NT2-D1	testis:	n/a
19	chr1:104696931-104696981	HepG2	liver:	n/a
20	chr1:104616118-104616168	HEK293	kidney:	embryo
21	chr1:104696931-104696981	GM12878	blood:	n/a
22	chr1:104616118-104616168	AG10803	skin:	n/a
23	chr1:104616267-104616317	SAEC	small airway:	n/a
24	chr1:104635600-104635650	HIPEpiC	eye:	n/a
25	chr1:104696931-104696981	SKMC	muscle:	n/a
26	chr1:104615609-104615659	HEK293	kidney:	embryo
27	chr1:104616267-104616317	PrEC	prostate:	n/a
28	chr1:104523359-104523409	GM12878	blood:	n/a
29	chr1:104615867-104615917	ECC-1	luminal epithelium:	n/a
30	chr1:104616267-104616317	U87	brain:	n/a
31	chr1:104523359-104523409	HUVEC	blood vessel:	n/a
32	chr1:104635600-104635650	H1-hESC	embryonic stem cell:	embryo
33	chr1:104696931-104696981	SAEC	small airway:	n/a
34	chr1:104696931-104696981	LNCaP	prostate:	n/a
35	chr1:104615609-104615659	AG10803	skin:	n/a
36	chr1:104615867-104615917	U87	brain:	n/a
37	chr1:104616267-104616317	AG04449	skin:	fetal
38	chr1:104635600-104635650	SAEC	small airway:	n/a
39	chr1:104615609-104615659	BJ	skin:	n/a
40	chr1:104696931-104696981	NH-A	brain:	n/a
41	chr1:104696931-104696981	SK-N-MC	brain:	n/a
42	chr1:104615867-104615917	NT2-D1	testis:	n/a
43	chr1:104635600-104635650	PFSK-1	brain:	n/a
44	chr1:104616118-104616168	Jurkat	blood:	n/a
45	chr1:104696931-104696981	H1-hESC	embryonic stem cell:	embryo
46	chr1:104616267-104616317	HNPCEpiC	eye:	n/a
47	chr1:104616267-104616317	LNCaP	prostate:	n/a
48	chr1:104615867-104615917	AG04450	lung:	fetal
49	chr1:104615867-104615917	HEK293	kidney:	embryo
50	chr1:104635600-104635650	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:104659954..104662571-chr1:104673545..104675551,2	K562	blood:
2	chr1:104330809..104331725-chr1:104675161..104675727,2	MCF-7	breast:
3	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
4	chr1:104693612..104696464-chr1:104700325..104702158,2	K562	blood:
5	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
6	chr1:104490807..104491700-chr1:104674682..104675320,2	MCF-7	breast:
7	chr1:104330211..104331667-chr1:104674701..104675769,4	MCF-7	breast:
8	chr1:104490807..104491700-chr1:104674682..104675320,2	MCF-7	breast:
9	chr1:104725861..104727973-chr1:104730004..104731951,2	K562	blood:
10	chr1:104659954..104662571-chr1:104673545..104675551,2	K562	blood:
11	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:
12	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
13	chr1:104725861..104727973-chr1:104730004..104731951,2	K562	blood:
14	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
15	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:
16	chr1:104330211..104331667-chr1:104674701..104675769,4	MCF-7	breast:
17	chr1:104330809..104331725-chr1:104675161..104675727,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1C-2	chr1:104668178-104668541	NONHSAT004905
2	lnc-AMY1C-2	chr1:104668179-104668541	XLOC_000326
3	lnc-AMY1C-2	chr1:104672444-104672483	XLOC_000326
4	lnc-AMY1C-3	chr1:104469189-104470428	NONHSAT004901
5	lnc-AMY1C-2	chr1:104672443-104672483	NONHSAT004905

Variant related genes	Relation type
ENSG00000215869	TF binding region
ENSG00000225191	TF binding region
ENSG00000243500	TF binding region
FTLP17	TF binding region
ENSG00000215869	CpG island
ENSG00000225191	CpG island
ENSG00000243500	CpG island
FTLP17	CpG island
ENSG00000228347	chromatin interactions

Extended variants
information (count: 4755 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4755 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138900324	chr1:104316469-104316470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533112650	chr1:104316477-104316478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551624262	chr1:104316483-104316484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569733507	chr1:104316491-104316492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560815518	chr1:104316536-104316537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116238547	chr1:104316550-104316551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548834870	chr1:104316551-104316552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567251832	chr1:104316557-104316558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141458829	chr1:104316587-104316588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553592586	chr1:104316603-104316604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182631409	chr1:104316622-104316623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571614062	chr1:104316641-104316642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538822434	chr1:104316794-104316795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186741465	chr1:104316800-104316801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575457650	chr1:104316827-104316828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543102210	chr1:104316936-104316937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554804265	chr1:104316981-104316982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528356923	chr1:104317013-104317014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573150231	chr1:104317035-104317036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376472228	chr1:104317036-104317037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115471742	chr1:104317042-104317043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376560693	chr1:104317095-104317096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559658343	chr1:104317133-104317134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533280942	chr1:104317155-104317156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562287674	chr1:104317249-104317250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369960498	chr1:104317305-104317306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563450708	chr1:104317333-104317334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571419168	chr1:104317343-104317344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115570472	chr1:104317360-104317361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150778916	chr1:104317372-104317373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138046183	chr1:104317380-104317381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528046166	chr1:104317424-104317425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190687907	chr1:104317455-104317456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532250735	chr1:104317491-104317492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538921155	chr1:104317508-104317509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557277041	chr1:104317537-104317538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149500809	chr1:104317566-104317567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536454973	chr1:104317571-104317572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551009825	chr1:104317577-104317578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554999298	chr1:104317607-104317608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182994355	chr1:104317659-104317660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569252879	chr1:104317757-104317758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554251544	chr1:104317766-104317767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs604575	chr1:104317783-104317784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577338924	chr1:104317794-104317795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147221123	chr1:104317825-104317826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140562589	chr1:104317829-104317830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555016146	chr1:104317838-104317839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530693308	chr1:104317857-104317858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61814742	chr1:104317871-104317872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	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
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	17550852	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104316400-104317800	Enhancers	Fetal Heart	heart
2	chr1:104317800-104322000	Weak transcription	Fetal Heart	heart
3	chr1:104326200-104327000	Enhancers	GM12878-XiMat	blood
4	chr1:104360000-104360400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:104360200-104360600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:104369800-104370200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:104369800-104370200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
8	chr1:104373200-104373600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:104377600-104378400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:104430400-104431200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr1:104430600-104431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr1:104430800-104431200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:104438600-104439200	Enhancers	Fetal Heart	heart
14	chr1:104439200-104441400	Weak transcription	Fetal Heart	heart
15	chr1:104441400-104442000	Enhancers	Fetal Heart	heart
16	chr1:104442000-104442800	Weak transcription	Fetal Heart	heart
17	chr1:104442400-104443000	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr1:104442800-104444200	Enhancers	Fetal Heart	heart
19	chr1:104443000-104444400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr1:104444200-104444600	Flanking Active TSS	Fetal Heart	heart
21	chr1:104444400-104444600	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr1:104444600-104444800	Enhancers	Fetal Heart	heart
23	chr1:104444600-104445000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr1:104445000-104445400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr1:104460000-104460400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:104460000-104460600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:104460000-104460600	Enhancers	Fetal Heart	heart
28	chr1:104460200-104460600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:104474600-104475000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:104474600-104475400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:104477000-104478400	Enhancers	Fetal Heart	heart
32	chr1:104483800-104484800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:104483800-104485800	Enhancers	Fetal Lung	lung
34	chr1:104484000-104484400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:104484200-104485000	Enhancers	Pancreas	Pancrea
36	chr1:104485400-104486000	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr1:104485800-104487400	Weak transcription	Fetal Lung	lung
38	chr1:104487400-104487600	Enhancers	Fetal Lung	lung
39	chr1:104488400-104488600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:104488600-104488800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:104492400-104493000	Enhancers	Fetal Brain Female	brain
42	chr1:104492400-104493000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr1:104502200-104503000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:104502200-104504000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:104503200-104504000	ZNF genes & repeats	Pancreas	Pancrea
46	chr1:104503600-104503800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:104503800-104504000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:104542800-104543400	Enhancers	Fetal Brain Female	brain
49	chr1:104566000-104566600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:104570800-104571400	Active TSS	Fetal Lung	lung

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