Variant report

Variant	nsv946310
Chromosome Location	chr1:147390598-147399371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:147391111-147391487	K562	blood:	n/a	n/a
2	BACH1	chr1:147397017-147397245	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:147397066-147397248	K562	blood:	n/a	n/a
4	BHLHE40	chr1:147397076-147397078	K562	blood:	n/a	n/a
5	BRCA1	chr1:147391493-147391618	GM12878	blood:	n/a	n/a
6	CEBPD	chr1:147399350-147399851	K562	blood:	n/a	n/a
7	CEBPZ	chr1:147393964-147394348	HepG2	liver:	n/a	n/a
8	CTCF	chr1:147399322-147399347	Lung_OC	lung:	n/a	n/a
9	CTCF	chr1:147394424-147394494	ProgFib	skin:	n/a	n/a
10	CUX1	chr1:147391211-147391425	GM12878	blood:	n/a	n/a
11	GATA1	chr1:147399154-147399750	PBDE	blood:	n/a	n/a
12	GATA3	chr1:147391057-147391252	SH-SY5Y	brain:	n/a	n/a
13	IKZF1	chr1:147390890-147391234	GM12878	blood:	n/a	n/a
14	IRF1	chr1:147390907-147391182	K562	blood:	n/a	n/a
15	IRF3	chr1:147391391-147391580	GM12878	blood:	n/a	chr1:147391560-147391574 chr1:147391415-147391425
16	JUN	chr1:147396808-147397287	K562	blood:	n/a	chr1:147397142-147397154 chr1:147397143-147397153 chr1:147397144-147397152 chr1:147397143-147397153
17	JUN	chr1:147390767-147391609	K562	blood:	n/a	n/a
18	JUND	chr1:147393583-147393634	H1-hESC	embryonic stem cell:	n/a	n/a
19	JUND	chr1:147397017-147397264	K562	blood:	n/a	chr1:147397142-147397154 chr1:147397143-147397153 chr1:147397144-147397152 chr1:147397143-147397153
20	JUND	chr1:147397046-147397229	H1-hESC	embryonic stem cell:	n/a	chr1:147397142-147397154 chr1:147397143-147397153 chr1:147397144-147397152 chr1:147397143-147397153
21	MAFF	chr1:147391062-147391324	K562	blood:	n/a	n/a
22	MAFF	chr1:147397049-147397221	K562	blood:	n/a	n/a
23	MAFK	chr1:147391040-147391299	HepG2	liver:	n/a	n/a
24	MAFK	chr1:147390988-147391308	HepG2	liver:	n/a	n/a
25	MAFK	chr1:147396986-147397280	K562	blood:	n/a	chr1:147397142-147397151
26	MAZ	chr1:147397105-147397232	K562	blood:	n/a	n/a
27	MAZ	chr1:147391455-147391508	GM12878	blood:	n/a	n/a
28	MXI1	chr1:147390810-147390816	GM12878	blood:	n/a	n/a
29	NFE2	chr1:147394165-147394170	GM12878	blood:	n/a	n/a
30	NR2F2	chr1:147399186-147399928	K562	blood:	n/a	n/a
31	POLR2A	chr1:147398704-147399042	HepG2	liver:	n/a	n/a
32	POLR2A	chr1:147399311-147401304	K562	blood:	n/a	n/a
33	POLR2A	chr1:147399106-147399291	K562	blood:	n/a	n/a
34	RCOR1	chr1:147397025-147397184	K562	blood:	n/a	n/a
35	SMC3	chr1:147391456-147391563	GM12878	blood:	n/a	n/a
36	STAT5A	chr1:147399173-147399885	K562	blood:	n/a	n/a
37	TEAD4	chr1:147399366-147399714	K562	blood:	n/a	n/a
38	TRIM28	chr1:147399244-147399896	K562	blood:	n/a	n/a
39	UBTF	chr1:147394251-147394476	K562	blood:	n/a	n/a
40	ZNF143	chr1:147390992-147390998	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:147396752-147396802	HMEC	breast:	n/a
2	chr1:147396752-147396802	HUVEC	blood vessel:	n/a
3	chr1:147396752-147396802	NT2-D1	testis:	n/a
4	chr1:147396752-147396802	H1-hESC	embryonic stem cell:	embryo
5	chr1:147396752-147396802	Caco-2	colon:	n/a
6	chr1:147396752-147396802	GM19239	blood:	n/a
7	chr1:147396752-147396802	Hepatocyte	liver:	n/a
8	chr1:147396752-147396802	PrEC	prostate:	n/a
9	chr1:147396752-147396802	MCF-7	breast:	n/a
10	chr1:147396752-147396802	K562	blood:	n/a
11	chr1:147396752-147396802	NHDF-neo	bronchial:	n/a
12	chr1:147396752-147396802	IMR90	lung:	fetal
13	chr1:147396752-147396802	HEK293	kidney:	embryo
14	chr1:147396752-147396802	HAEpiC	amniotic membrane:	n/a
15	chr1:147396752-147396802	HCT-116	colon:	n/a
16	chr1:147396752-147396802	HNPCEpiC	eye:	n/a
17	chr1:147396752-147396802	AoSMC	blood vessel:	n/a
18	chr1:147396752-147396802	SK-N-MC	brain:	n/a
19	chr1:147396752-147396802	NH-A	brain:	n/a
20	chr1:147396752-147396802	AG09309	skin:	n/a
21	chr1:147396752-147396802	ovcar-3	ovarian:	n/a
22	chr1:147396752-147396802	HRPEpiC	eye:	n/a
23	chr1:147396752-147396802	PANC-1	pancreas:	n/a
24	chr1:147396752-147396802	PFSK-1	brain:	n/a
25	chr1:147396752-147396802	SAEC	small airway:	n/a
26	chr1:147396752-147396802	ECC-1	luminal epithelium:	n/a
27	chr1:147396752-147396802	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:147396752-147396802	SK-N-SH_RA	brain:	n/a
29	chr1:147396752-147396802	Jurkat	blood:	n/a
30	chr1:147396752-147396802	HRE	kidney:	n/a
31	chr1:147396752-147396802	SK-N-SH	brain:	n/a
32	chr1:147396752-147396802	GM12878	blood:	n/a
33	chr1:147396752-147396802	HepG2	liver:	n/a
34	chr1:147396752-147396802	HL-60	blood:	n/a
35	chr1:147396752-147396802	GM12892	blood:	n/a
36	chr1:147396752-147396802	U87	brain:	n/a
37	chr1:147396752-147396802	Hela-S3	cervix:	n/a
38	chr1:147396752-147396802	AG09319	gingival:	n/a
39	chr1:147396752-147396802	T-47D	breast:	n/a
40	chr1:147396752-147396802	ProgFib	skin:	n/a
41	chr1:147396752-147396802	AG04450	lung:	fetal
42	chr1:147396752-147396802	A549	lung:	n/a
43	chr1:147396752-147396802	HIPEpiC	eye:	n/a
44	chr1:147396752-147396802	HRCEpiC	kidney:	n/a
45	chr1:147396752-147396802	AG10803	skin:	n/a
46	chr1:147396752-147396802	BJ	skin:	n/a
47	chr1:147396752-147396802	AG04449	skin:	fetal
48	chr1:147396752-147396802	GM12891	blood:	n/a
49	chr1:147396752-147396802	GM06990	blood:	n/a
50	chr1:147396752-147396802	MCF10A-Er-Src	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:147384361..147386129-chr1:147392472..147394344,2	MCF-7	breast:
2	chr1:145829205..145830837-chr1:147397586..147399180,2	MCF-7	breast:
3	chr1:147393808..147395971-chr1:147400048..147401997,2	K562	blood:
4	chr1:147393891..147395662-chr1:147399091..147400658,2	MCF-7	breast:
5	chr1:147383934..147385482-chr1:147388298..147390717,2	K562	blood:
6	chr1:147383526..147385434-chr1:147389217..147390933,2	K562	blood:
7	chr1:147377360..147379404-chr1:147393843..147396481,2	MCF-7	breast:
8	chr1:147381518..147385211-chr1:147394468..147398390,4	MCF-7	breast:
9	chr1:145832905..145834476-chr1:147394324..147396015,2	MCF-7	breast:

No data

Variant related genes	Relation type
GPR89B	TF binding region
GPR89B	CpG island
ENSG00000188092	chromatin interactions

Extended variants
information (count: 498 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72702377	chr1:147390621-147390622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143628764	chr1:147390654-147390655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74123757	chr1:147390664-147390665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72702378	chr1:147390683-147390684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80222463	chr1:147390698-147390699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72702379	chr1:147390701-147390702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587721551	chr1:147390743-147390744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587772592	chr1:147390747-147390748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs67578473	chr1:147390750-147390751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367974882	chr1:147390758-147390759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370149475	chr1:147390762-147390763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149163442	chr1:147390772-147390773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs386368272	chr1:147390775-147390776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113961442	chr1:147390783-147390784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587728708	chr1:147390784-147390785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139768463	chr1:147390792-147390793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78676090	chr1:147390793-147390794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587647407	chr1:147390795-147390796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs5025853	chr1:147390827-147390828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79188086	chr1:147390828-147390829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141918645	chr1:147390832-147390833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369313037	chr1:147390833-147390834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112166455	chr1:147390849-147390850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs386635286	chr1:147390883-147390884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs5025851	chr1:147390884-147390885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5025850	chr1:147390890-147390891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs5025849	chr1:147390891-147390892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587708892	chr1:147390929-147390930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs5025848	chr1:147390938-147390939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587748821	chr1:147390976-147390977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587652399	chr1:147390987-147390988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77617167	chr1:147391018-147391019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587708026	chr1:147391019-147391020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72998940	chr1:147391031-147391032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587606555	chr1:147391042-147391043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74123759	chr1:147391067-147391068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587661007	chr1:147391073-147391074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74123760	chr1:147391074-147391075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587716458	chr1:147391076-147391077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35340224	chr1:147391096-147391097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72998941	chr1:147391108-147391109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72702380	chr1:147391148-147391149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78717632	chr1:147391161-147391162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79652292	chr1:147391163-147391164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78190395	chr1:147391182-147391183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs67275355	chr1:147391197-147391198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587626248	chr1:147391198-147391199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587674457	chr1:147391225-147391226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28480577	chr1:147391260-147391261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587626821	chr1:147391271-147391272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:148)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	20369283	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
Melanoma	21430779	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Neuroblastoma	19536264	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147390000-147391200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:147390000-147400400	Weak transcription	HSMM	muscle
3	chr1:147391200-147391600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:147391400-147391600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:147391400-147391800	Enhancers	Fetal Heart	heart
6	chr1:147391600-147392200	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr1:147391800-147392000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:147392000-147392200	Enhancers	GM12878-XiMat	blood
9	chr1:147392000-147392400	Enhancers	HSMMtube	muscle
10	chr1:147392000-147392400	Enhancers	Osteobl	bone
11	chr1:147392000-147393400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:147392200-147392400	Enhancers	NHLF	lung
13	chr1:147393400-147393800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:147393800-147394000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:147394000-147394200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:147394200-147394400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:147394200-147394600	Enhancers	K562	blood
18	chr1:147394400-147394600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:147394600-147396800	Weak transcription	K562	blood
20	chr1:147395200-147400400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr1:147396600-147400400	Weak transcription	Thymus	Thymus
22	chr1:147396800-147397000	Enhancers	Fetal Muscle Leg	muscle
23	chr1:147396800-147397200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:147396800-147397200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:147396800-147397200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:147396800-147397200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:147396800-147397200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:147396800-147397200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:147396800-147397200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:147396800-147397200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:147396800-147397200	Enhancers	K562	blood
32	chr1:147397000-147397200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:147397000-147398000	Weak transcription	Fetal Muscle Leg	muscle
34	chr1:147397200-147398600	Weak transcription	K562	blood
35	chr1:147397200-147400400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:147397200-147400400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr1:147397200-147400400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:147397200-147400400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr1:147397200-147400400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr1:147397200-147400400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr1:147397200-147400400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:147397200-147400600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr1:147398000-147398800	Enhancers	Fetal Muscle Leg	muscle
44	chr1:147398600-147399400	Enhancers	K562	blood
45	chr1:147398800-147400400	Weak transcription	Fetal Muscle Leg	muscle

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