Variant report

Variant	nsv1004995
Chromosome Location	chr1:191749623-191884147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:0)
Chromatin interactive
region (count:35)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:191812278-191812435	K562	blood:	n/a	n/a
2	ARID3A	chr1:191845875-191846144	K562	blood:	n/a	n/a
3	ARID3A	chr1:191791882-191792051	K562	blood:	n/a	n/a
4	ARID3A	chr1:191857246-191857609	K562	blood:	n/a	n/a
5	ARID3A	chr1:191792309-191793479	K562	blood:	n/a	n/a
6	ARID3A	chr1:191857928-191858619	K562	blood:	n/a	n/a
7	ATF1	chr1:191845848-191846111	K562	blood:	n/a	n/a
8	ATF1	chr1:191792801-191793314	K562	blood:	n/a	n/a
9	ATF1	chr1:191791954-191792148	K562	blood:	n/a	n/a
10	ATF1	chr1:191858055-191858697	K562	blood:	n/a	n/a
11	ATF1	chr1:191821456-191821889	K562	blood:	n/a	n/a
12	ATF2	chr1:191838896-191839199	GM12878	blood:	n/a	n/a
13	ATF3	chr1:191820973-191821210	K562	blood:	n/a	n/a
14	ATF3	chr1:191858154-191858679	K562	blood:	n/a	n/a
15	BATF	chr1:191838976-191839163	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:191858061-191858651	K562	blood:	n/a	n/a
17	BHLHE40	chr1:191857301-191857435	K562	blood:	n/a	n/a
18	BHLHE40	chr1:191853684-191853687	K562	blood:	n/a	n/a
19	BHLHE40	chr1:191792761-191793301	K562	blood:	n/a	n/a
20	CBX3	chr1:191782745-191783119	K562	blood:	n/a	n/a
21	CBX3	chr1:191858024-191858814	K562	blood:	n/a	n/a
22	CBX3	chr1:191792445-191793273	K562	blood:	n/a	n/a
23	CBX3	chr1:191861885-191862176	K562	blood:	n/a	n/a
24	CBX3	chr1:191782674-191783126	K562	blood:	n/a	n/a
25	CBX3	chr1:191877847-191878202	K562	blood:	n/a	n/a
26	CBX3	chr1:191861784-191862212	K562	blood:	n/a	n/a
27	CCNT2	chr1:191858179-191858676	K562	blood:	n/a	n/a
28	CCNT2	chr1:191792545-191793400	K562	blood:	n/a	n/a
29	CEBPB	chr1:191864221-191864551	IMR90	lung:	n/a	chr1:191864384-191864395
30	CEBPB	chr1:191830317-191830421	K562	blood:	n/a	n/a
31	CEBPB	chr1:191792624-191793308	K562	blood:	n/a	chr1:191792783-191792795
32	CEBPB	chr1:191774586-191774668	HepG2	liver:	n/a	chr1:191774601-191774612 chr1:191774600-191774613 chr1:191774600-191774611
33	CEBPB	chr1:191770811-191771077	K562	blood:	n/a	chr1:191770924-191770935 chr1:191770926-191770937 chr1:191770926-191770935
34	CEBPB	chr1:191782787-191783000	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:191805286-191805538	A549	lung:	n/a	n/a
36	CEBPB	chr1:191845843-191846117	K562	blood:	n/a	n/a
37	CEBPB	chr1:191770776-191771068	IMR90	lung:	n/a	chr1:191770924-191770935 chr1:191770926-191770937 chr1:191770926-191770935
38	CEBPB	chr1:191770782-191771024	A549	lung:	n/a	chr1:191770924-191770935 chr1:191770926-191770937 chr1:191770926-191770935
39	CEBPB	chr1:191834669-191835023	IMR90	lung:	n/a	chr1:191834839-191834850
40	CEBPB	chr1:191845874-191846144	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:191864209-191864553	K562	blood:	n/a	chr1:191864384-191864395
42	CEBPB	chr1:191770749-191771091	HepG2	liver:	n/a	chr1:191770924-191770935 chr1:191770926-191770937 chr1:191770926-191770935
43	CEBPB	chr1:191864254-191864514	A549	lung:	n/a	chr1:191864384-191864395
44	CEBPB	chr1:191834813-191834972	H1-hESC	embryonic stem cell:	n/a	chr1:191834839-191834850
45	CEBPB	chr1:191834701-191834983	HepG2	liver:	n/a	chr1:191834839-191834850
46	CEBPB	chr1:191791786-191791887	K562	blood:	n/a	n/a
47	CEBPB	chr1:191857259-191857476	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:191858083-191858671	K562	blood:	n/a	n/a
49	CEBPB	chr1:191774590-191774666	K562	blood:	n/a	chr1:191774601-191774612 chr1:191774600-191774613 chr1:191774600-191774611
50	CEBPB	chr1:191858098-191858539	K562	blood:	n/a	n/a

No data

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:191773972..191778173-chr1:191779534..191782112,5	K562	blood:
2	chr1:191864173..191866057-chr1:191874341..191876184,2	K562	blood:
3	chr1:191858381..191859932-chr1:191864838..191867185,2	K562	blood:
4	chr1:191836436..191839226-chr1:191842786..191844832,2	K562	blood:
5	chr1:191854730..191856594-chr1:191856723..191859160,2	K562	blood:
6	chr1:191864173..191866057-chr1:191874341..191876184,2	K562	blood:
7	chr1:191764970..191767101-chr1:192222254..192224537,2	K562	blood:
8	chr1:190926824..190927388-chr1:191800448..191800967,2	MCF-7	breast:
9	chr1:191850241..191852634-chr1:191855846..191858464,3	K562	blood:
10	chr1:191747805..191749831-chr1:191750174..191752382,2	MCF-7	breast:
11	chr1:191777063..191778903-chr1:191781034..191782929,2	K562	blood:
12	chr1:191807170..191809175-chr1:191810201..191811757,2	K562	blood:
13	chr1:191844983..191847069-chr1:191850769..191852531,2	K562	blood:
14	chr1:191777063..191778903-chr1:191781034..191782929,2	K562	blood:
15	chr1:191788611..191790988-chr1:191796591..191799173,2	MCF-7	breast:
16	chr1:191773972..191778173-chr1:191779534..191782112,5	K562	blood:
17	chr1:191815192..191816719-chr1:191819191..191822159,2	K562	blood:
18	chr1:191807170..191809175-chr1:191810201..191811757,2	K562	blood:
19	chr1:191788611..191790988-chr1:191796591..191799173,2	MCF-7	breast:
20	chr1:191802155..191804937-chr1:191853608..191855643,2	K562	blood:
21	chr1:191849617..191851741-chr1:191856964..191859134,3	K562	blood:
22	chr1:191747805..191749831-chr1:191750174..191752382,2	MCF-7	breast:
23	chr1:191784628..191787361-chr1:191791989..191794077,2	K562	blood:
24	chr1:191850241..191852634-chr1:191855846..191858464,3	K562	blood:
25	chr1:191754947..191757355-chr1:191758290..191760631,2	MCF-7	breast:
26	chr1:191841073..191843437-chr1:191843646..191846298,2	K562	blood:
27	chr1:191858381..191861097-chr1:191864368..191867185,2	K562	blood:
28	chr1:191711996..191714385-chr1:191821887..191824152,2	K562	blood:
29	chr1:191802155..191804937-chr1:191853608..191855643,2	K562	blood:
30	chr1:191815192..191816719-chr1:191819191..191822159,2	K562	blood:
31	chr1:191854730..191856594-chr1:191856723..191859160,2	K562	blood:
32	chr1:191849617..191851741-chr1:191856964..191859134,3	K562	blood:
33	chr1:191784628..191787361-chr1:191791989..191794077,2	K562	blood:
34	chr1:191844983..191847069-chr1:191850769..191852531,2	K562	blood:
35	chr1:191754947..191757355-chr1:191758290..191760631,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-1	chr1:191844625-191844830	ENSG00000228215.2
2	lnc-UCHL5-3	chr1:191827893-191828310	XLOC_001132
3	lnc-RGS18-1	chr1:191844625-191844830	XLOC_000507
4	lnc-UCHL5-3	chr1:191859195-191859359	XLOC_001132
5	lnc-UCHL5-3	chr1:191827837-191828310	XLOC_001132
6	lnc-UCHL5-3	chr1:191835950-191836090	XLOC_001132

No data

Variant related genes	Relation type
ENSG00000228215	TF binding region
ENSG00000223344	TF binding region
ENSG00000228215	chromatin interactions
ENSG00000223344	chromatin interactions
PLAG1	miRNA target sites
CCNT2	miRNA target sites

Extended variants
information (count: 1749 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1749 , 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	rs183547049	chr1:191750809-191750810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142431676	chr1:191750845-191750846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114621785	chr1:191750897-191750898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111624974	chr1:191750953-191750954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559108760	chr1:191750969-191750970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568830715	chr1:191751001-191751002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117180031	chr1:191751111-191751112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374454297	chr1:191751172-191751173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574120786	chr1:191751186-191751187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540131367	chr1:191751210-191751211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368882389	chr1:191751236-191751237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371294114	chr1:191751253-191751254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12030813	chr1:191751272-191751273	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577073636	chr1:191751286-191751287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116917764	chr1:191751313-191751314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144720551	chr1:191751325-191751326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138523920	chr1:191751360-191751361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78218393	chr1:191755208-191755209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs833987	chr1:191755233-191755234	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs576424158	chr1:191755242-191755243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569787331	chr1:191755323-191755324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535569512	chr1:191755324-191755325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549343622	chr1:191755335-191755336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183748767	chr1:191755345-191755346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535322925	chr1:191755359-191755360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558206305	chr1:191755370-191755371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372027831	chr1:191755380-191755381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112250969	chr1:191755448-191755449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578202670	chr1:191755495-191755496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188074851	chr1:191755543-191755544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140064530	chr1:191755592-191755593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180747665	chr1:191755615-191755616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150293405	chr1:191755623-191755624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386637990	chr1:191755663-191755664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1415136	chr1:191755666-191755667	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs544999668	chr1:191755768-191755769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7514425	chr1:191755799-191755800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs375143682	chr1:191755849-191755850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs833986	chr1:191755912-191755913	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs543968830	chr1:191755914-191755915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530782267	chr1:191756014-191756015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs137936011	chr1:191756034-191756035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570790526	chr1:191756066-191756067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149639784	chr1:191756115-191756116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186441728	chr1:191756116-191756117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566055979	chr1:191756117-191756118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537620451	chr1:191756184-191756185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559011913	chr1:191756264-191756265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542833895	chr1:191756350-191756351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189656117	chr1:191756372-191756373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191750800-191751200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:191751000-191751400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:191755200-191755400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr1:191755400-191757600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr1:191756800-191757000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr1:191757000-191758000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:191757400-191758200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:191757600-191758400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:191757600-191758400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr1:191757600-191758400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr1:191757600-191758800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr1:191757800-191758400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:191758000-191758400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr1:191758000-191758400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr1:191758000-191758600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:191782800-191784200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr1:191791600-191791800	Enhancers	K562	blood
18	chr1:191791600-191792400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:191791600-191792600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:191791800-191793000	Flanking Active TSS	K562	blood
21	chr1:191791800-191793600	Enhancers	Primary hematopoietic stem cells	blood
22	chr1:191791800-191793600	Enhancers	Dnd41	blood
23	chr1:191792200-191793000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:191792200-191793600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr1:191792200-191793600	Enhancers	HUVEC	blood vessel
26	chr1:191792400-191792800	Enhancers	Fetal Brain Male	brain
27	chr1:191792400-191793200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:191792400-191793400	Enhancers	Fetal Lung	lung
29	chr1:191792600-191793000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:191792600-191793200	Enhancers	Fetal Heart	heart
31	chr1:191792800-191793200	Enhancers	Brain Hippocampus Middle	brain
32	chr1:191792800-191793200	Enhancers	Fetal Stomach	stomach
33	chr1:191792800-191793400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr1:191792800-191793400	Active TSS	Fetal Brain Male	brain
35	chr1:191793000-191793200	Enhancers	K562	blood
36	chr1:191793000-191793400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:191793000-191793600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:191793200-191793400	Flanking Active TSS	K562	blood
39	chr1:191793200-191793600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:191798000-191798600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:191808600-191809000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:191808800-191809000	Enhancers	NH-A	brain
43	chr1:191808800-191810000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:191809000-191809400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:191809000-191809400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr1:191809000-191809400	Enhancers	Fetal Heart	heart
47	chr1:191809000-191809400	Flanking Active TSS	NH-A	brain
48	chr1:191809000-191809800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr1:191809200-191809600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:191809200-191809800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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