Variant report

Variant	nsv1003356
Chromosome Location	chr1:74983681-75024938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:75000150-75000202	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:75018563-75018835	HepG2	liver:	n/a	chr1:75018731-75018744 chr1:75018733-75018744 chr1:75018731-75018744 chr1:75018733-75018742
3	CEBPB	chr1:75007339-75007399	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:75014193-75014388	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:75000289-75000474	IMR90	lung:	n/a	n/a
6	CHD2	chr1:74993857-74993943	HepG2	liver:	n/a	n/a
7	CHD2	chr1:74987849-74988223	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr1:75013247-75013320	Lung_OC	lung:	n/a	n/a
9	CTCF	chr1:75008500-75008650	NHLF	lung:	n/a	n/a
10	CTCF	chr1:75008713-75008800	GM13976	blood:	n/a	n/a
11	CTCF	chr1:75000140-75000290	AG10803	skin:	n/a	n/a
12	EBF1	chr1:74983462-74983698	GM12878	blood:	n/a	chr1:74983586-74983597
13	EBF1	chr1:74983392-74983710	GM12878	blood:	n/a	chr1:74983586-74983597
14	EBF1	chr1:74983367-74983776	GM12878	blood:	n/a	chr1:74983586-74983597
15	EP300	chr1:74996472-74998097	SK-N-SH	brain:	n/a	chr1:74996779-74996793
16	EP300	chr1:75014202-75016247	SK-N-SH	brain:	n/a	chr1:75015651-75015658 chr1:75014515-75014523
17	EP300	chr1:75014957-75015254	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr1:75014954-75015292	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr1:74999840-75000494	SK-N-SH	brain:	n/a	n/a
20	FOSL2	chr1:74984463-74984622	HepG2	liver:	n/a	n/a
21	FOSL2	chr1:74999842-75000313	SK-N-SH	brain:	n/a	n/a
22	GABPA	chr1:75008730-75008820	HepG2	liver:	n/a	n/a
23	GABPA	chr1:74984504-74984588	HepG2	liver:	n/a	n/a
24	GATA2	chr1:75014840-75015594	SH-SY5Y	brain:	n/a	chr1:75015365-75015386
25	GATA3	chr1:75014299-75014404	SH-SY5Y	brain:	n/a	chr1:75014317-75014327
26	GATA3	chr1:75014891-75015612	SK-N-SH	brain:	n/a	chr1:75015365-75015386
27	GATA3	chr1:74999763-75000465	SK-N-SH	brain:	n/a	chr1:75000371-75000382
28	GATA3	chr1:75003667-75003859	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr1:74999845-75000366	SK-N-SH	brain:	n/a	n/a
30	GATA3	chr1:75014875-75015626	SH-SY5Y	brain:	n/a	chr1:75015365-75015386
31	GATA3	chr1:75014952-75015479	SK-N-SH	brain:	n/a	chr1:75015365-75015386
32	GTF2F1	chr1:74987889-74987951	H1-hESC	embryonic stem cell:	n/a	n/a
33	IRF3	chr1:74995141-74995157	GM12878	blood:	n/a	n/a
34	JUN	chr1:75004540-75004744	HepG2	liver:	n/a	chr1:75004673-75004686
35	JUND	chr1:74987839-74988269	H1-hESC	embryonic stem cell:	n/a	n/a
36	JUND	chr1:74999844-75000345	SK-N-SH	brain:	n/a	n/a
37	MAFF	chr1:75018410-75018574	HepG2	liver:	n/a	n/a
38	MAFK	chr1:75017087-75017287	HepG2	liver:	n/a	chr1:75017177-75017188 chr1:75017177-75017188
39	MAFK	chr1:75018333-75018636	HepG2	liver:	n/a	n/a
40	MAFK	chr1:75003426-75003579	HepG2	liver:	n/a	chr1:75003472-75003487
41	MAFK	chr1:75003343-75003644	HepG2	liver:	n/a	chr1:75003472-75003487
42	NANOG	chr1:74989872-74990162	H1-hESC	embryonic stem cell:	n/a	n/a
43	NANOG	chr1:74987840-74988095	H1-hESC	embryonic stem cell:	n/a	n/a
44	NFIC	chr1:74999881-75000486	SK-N-SH	brain:	n/a	n/a
45	PBX3	chr1:74999855-75000352	SK-N-SH	brain:	n/a	n/a
46	PBX3	chr1:74999906-75000365	SK-N-SH	brain:	n/a	n/a
47	PBX3	chr1:74984495-74984590	GM12878	blood:	n/a	n/a
48	POLR2A	chr1:74999967-75000257	SK-N-SH	brain:	n/a	n/a
49	POLR2A	chr1:74986120-74986263	K562	blood:	n/a	n/a
50	POLR2A	chr1:75004168-75005407	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:75009674-75009724	NHBE	bronchial:	n/a
2	chr1:74988194-74988244	AG04449	skin:	fetal
3	chr1:75009674-75009724	ovcar-3	ovarian:	n/a
4	chr1:74988194-74988244	LNCaP	prostate:	n/a
5	chr1:74988194-74988244	CMK	blood:	n/a
6	chr1:75009674-75009724	HepG2	liver:	n/a
7	chr1:74988194-74988244	ovcar-3	ovarian:	n/a
8	chr1:75009674-75009724	AoSMC	blood vessel:	n/a
9	chr1:75009674-75009724	Jurkat	blood:	n/a
10	chr1:75009674-75009724	HAEpiC	amniotic membrane:	n/a
11	chr1:75009674-75009724	HCPEpiC	choroid plexus:	n/a
12	chr1:75009674-75009724	NT2-D1	testis:	n/a
13	chr1:75009674-75009724	MCF-7	breast:	n/a
14	chr1:74988194-74988244	MCF-7	breast:	n/a
15	chr1:74988194-74988244	AoSMC	blood vessel:	n/a
16	chr1:74988194-74988244	HNPCEpiC	eye:	n/a
17	chr1:74988194-74988244	HRCEpiC	kidney:	n/a
18	chr1:74988194-74988244	RPTEC	kidney:	n/a
19	chr1:74988194-74988244	SK-N-SH_RA	brain:	n/a
20	chr1:75009674-75009724	HCT-116	colon:	n/a
21	chr1:75009674-75009724	GM06990	blood:	n/a
22	chr1:74988194-74988244	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:74988194-74988244	GM12892	blood:	n/a
24	chr1:75009674-75009724	HCF	heart:	n/a
25	chr1:74988194-74988244	PFSK-1	brain:	n/a
26	chr1:75009674-75009724	HRPEpiC	eye:	n/a
27	chr1:74988194-74988244	BE2_C	brain:	n/a
28	chr1:75009674-75009724	AG10803	skin:	n/a
29	chr1:75009674-75009724	NH-A	brain:	n/a
30	chr1:74988194-74988244	A549	lung:	n/a
31	chr1:75009674-75009724	MCF10A-Er-Src	breast:	n/a
32	chr1:74988194-74988244	GM19239	blood:	n/a
33	chr1:75009674-75009724	GM19239	blood:	n/a
34	chr1:74988194-74988244	AG09319	gingival:	n/a
35	chr1:75009674-75009724	HIPEpiC	eye:	n/a
36	chr1:75009674-75009724	BE2_C	brain:	n/a
37	chr1:74988194-74988244	AG10803	skin:	n/a
38	chr1:75009674-75009724	SK-N-MC	brain:	n/a
39	chr1:74988194-74988244	AG09309	skin:	n/a
40	chr1:75009674-75009724	NHDF-neo	bronchial:	n/a
41	chr1:74988194-74988244	SAEC	small airway:	n/a
42	chr1:74988194-74988244	HCT-116	colon:	n/a
43	chr1:74988194-74988244	Jurkat	blood:	n/a
44	chr1:75009674-75009724	HUVEC	blood vessel:	n/a
45	chr1:74988194-74988244	HL-60	blood:	n/a
46	chr1:74988194-74988244	PrEC	prostate:	n/a
47	chr1:74988194-74988244	U87	brain:	n/a
48	chr1:74988194-74988244	ProgFib	skin:	n/a
49	chr1:74988194-74988244	BJ	skin:	n/a
50	chr1:75009674-75009724	HRE	kidney:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74990321..74992157-chr1:75009741..75011754,2	K562	blood:
2	chr1:74990321..74992157-chr1:75009741..75011754,2	K562	blood:
3	chr1:75002770..75004477-chr3:136927967..136930965,2	K562	blood:

No data

Variant related genes	Relation type
TNNI3K	TF binding region
TNNI3K	CpG island

Extended variants
information (count: 1735 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17095498	chr1:74983681-74983682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs17095501	chr1:74983721-74983722	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs531783916	chr1:74983741-74983742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183740403	chr1:74983751-74983752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17095502	chr1:74983782-74983783	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539542347	chr1:74983797-74983798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10493544	chr1:74983835-74983836	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144294993	chr1:74983912-74983913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150604107	chr1:74983932-74983933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535267515	chr1:74983937-74983938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139699335	chr1:74984003-74984004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187874499	chr1:74984009-74984010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149843613	chr1:74984126-74984127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373123070	chr1:74984127-74984128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537515405	chr1:74984166-74984167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191820512	chr1:74984199-74984200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17095503	chr1:74984208-74984209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs17095504	chr1:74984220-74984221	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560177379	chr1:74984232-74984233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145879024	chr1:74984251-74984252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545781970	chr1:74984270-74984271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374370433	chr1:74984275-74984276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183589578	chr1:74984318-74984319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141731939	chr1:74984345-74984346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61778068	chr1:74984361-74984362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs562211712	chr1:74984363-74984364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114398114	chr1:74984373-74984374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547774058	chr1:74984379-74984380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565944420	chr1:74984383-74984384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551805752	chr1:74984386-74984387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556335115	chr1:74984389-74984390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537272205	chr1:74984436-74984437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529126349	chr1:74984440-74984441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114661453	chr1:74984441-74984442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567854080	chr1:74984470-74984471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535183986	chr1:74984510-74984511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371941980	chr1:74984528-74984529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374805633	chr1:74984541-74984542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200030502	chr1:74984546-74984547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147780464	chr1:74984555-74984556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141727622	chr1:74984558-74984559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367595807	chr1:74984579-74984580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7535572	chr1:74984583-74984584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562369014	chr1:74984711-74984712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571967104	chr1:74984791-74984792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546044713	chr1:74984814-74984815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545085548	chr1:74984977-74984978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6604868	chr1:74984989-74984990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576301342	chr1:74985029-74985030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560209529	chr1:74985053-74985054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
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
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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:139 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74978800-74989800	Weak transcription	Right Atrium	heart
2	chr1:74979000-74986400	Weak transcription	Left Ventricle	heart
3	chr1:74979000-74986800	Weak transcription	Fetal Heart	heart
4	chr1:74979600-74987800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:74980000-74987800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr1:74983000-74984400	Enhancers	GM12878-XiMat	blood
7	chr1:74983600-74987200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:74986400-74986800	Enhancers	Left Ventricle	heart
9	chr1:74986600-74986800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:74986800-74988200	Enhancers	Fetal Heart	heart
11	chr1:74986800-74989200	Weak transcription	Left Ventricle	heart
12	chr1:74986800-74989600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:74987000-74987600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr1:74987200-74987800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:74987200-74987800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:74987200-74987800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr1:74987200-74989800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr1:74987200-74992400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:74987400-74987600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:74987400-74988400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:74987600-74988000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr1:74987600-74988200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr1:74987600-74988400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:74987600-74988400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:74987600-74988600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr1:74987800-74988000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:74987800-74988200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr1:74987800-74988200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr1:74987800-74988200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:74987800-74988400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:74987800-74988400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr1:74987800-74988600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr1:74987800-74988600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:74987800-74988800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:74987800-74988800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:74987800-74988800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:74987800-74988800	Enhancers	HSMMtube	muscle
38	chr1:74988000-74988400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:74988000-74990400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:74988000-74991800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:74988200-74989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr1:74988200-74989200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr1:74988200-74989200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr1:74988200-74990000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:74988200-74990200	Weak transcription	Fetal Heart	heart
46	chr1:74988400-74989600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:74988400-74991200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:74988400-74992000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:74988600-74990800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr1:74988600-74991200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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