Variant report

Variant	nsv947475
Chromosome Location	chr1:242119659-242136347
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	chr1:242135954-242136215	HepG2	liver:	n/a	n/a
2	ATF1	chr1:242130694-242130726	K562	blood:	n/a	n/a
3	ATF1	chr1:242128209-242128497	K562	blood:	n/a	n/a
4	ATF3	chr1:242136065-242136245	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr1:242136045-242136302	K562	blood:	n/a	n/a
6	BHLHE40	chr1:242121224-242121872	K562	blood:	n/a	n/a
7	CBX3	chr1:242121536-242121885	K562	blood:	n/a	n/a
8	CEBPB	chr1:242127874-242128487	Hela-S3	cervix:	n/a	chr1:242128050-242128061
9	CEBPB	chr1:242135790-242136340	HepG2	liver:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
10	CEBPB	chr1:242127958-242128206	H1-hESC	embryonic stem cell:	n/a	chr1:242128050-242128061
11	CEBPB	chr1:242135926-242136336	H1-hESC	embryonic stem cell:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
12	CEBPB	chr1:242127883-242128178	K562	blood:	n/a	chr1:242128050-242128061
13	CEBPB	chr1:242135831-242136336	A549	lung:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
14	CEBPB	chr1:242120460-242120534	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:242135805-242136343	HepG2	liver:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
16	CEBPB	chr1:242127950-242128236	HepG2	liver:	n/a	chr1:242128050-242128061
17	CEBPB	chr1:242131600-242131768	A549	lung:	n/a	n/a
18	CEBPB	chr1:242135784-242136341	K562	blood:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
19	CEBPB	chr1:242135942-242136282	Hela-S3	cervix:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
20	CEBPB	chr1:242125193-242125314	K562	blood:	n/a	n/a
21	CEBPB	chr1:242135979-242136319	K562	blood:	n/a	chr1:242136167-242136178
22	CEBPB	chr1:242127931-242128152	K562	blood:	n/a	chr1:242128050-242128061
23	CEBPB	chr1:242127899-242128239	MCF-7	breast:	n/a	chr1:242128050-242128061
24	CEBPB	chr1:242127958-242128195	A549	lung:	n/a	chr1:242128050-242128061
25	CEBPB	chr1:242135874-242136183	IMR90	lung:	n/a	chr1:242136167-242136178 chr1:242135952-242135961 chr1:242135950-242135963
26	CEBPB	chr1:242127849-242128342	K562	blood:	n/a	chr1:242128050-242128061
27	CHD2	chr1:242121333-242121484	K562	blood:	n/a	n/a
28	CTCF	chr1:242125740-242125890	GM12871	blood:	n/a	n/a
29	CTCF	chr1:242121670-242121781	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:242121595-242121848	K562	blood:	n/a	n/a
31	CTCF	chr1:242121097-242121461	K562	blood:	n/a	n/a
32	CTCF	chr1:242121169-242121394	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:242121620-242121770	K562	blood:	n/a	n/a
34	CTCF	chr1:242121135-242121935	K562	blood:	n/a	n/a
35	CTCF	chr1:242121173-242121385	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:242121005-242122050	K562	blood:	n/a	n/a
37	CTCF	chr1:242121680-242121830	HVMF	connective:	n/a	n/a
38	CTCF	chr1:242121128-242121439	K562	blood:	n/a	n/a
39	CTCF	chr1:242121201-242121328	K562	blood:	n/a	n/a
40	CTCF	chr1:242121199-242121360	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:242121252-242121294	A549	lung:	n/a	n/a
42	CTCF	chr1:242121213-242121332	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:242121151-242121405	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:242121214-242121347	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:242121490-242121935	K562	blood:	n/a	n/a
46	CTCF	chr1:242121160-242121310	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:242132924-242132955	LNCaP	prostate:	n/a	n/a
48	CTCF	chr1:242121620-242121770	HVMF	connective:	n/a	n/a
49	CTCF	chr1:242121200-242121350	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:242121701-242121743	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242121827-242121877	HUVEC	blood vessel:	n/a
2	chr1:242121230-242121280	NH-A	brain:	n/a
3	chr1:242121827-242121877	AG09319	gingival:	n/a
4	chr1:242120638-242120688	HCT-116	colon:	n/a
5	chr1:242121827-242121877	HEEpiC	esophagus:	n/a
6	chr1:242121230-242121280	K562	blood:	n/a
7	chr1:242120907-242120957	H1-hESC	embryonic stem cell:	embryo
8	chr1:242121230-242121280	A549	lung:	n/a
9	chr1:242121827-242121877	SK-N-SH	brain:	n/a
10	chr1:242121230-242121280	NHBE	bronchial:	n/a
11	chr1:242122063-242122113	AG09309	skin:	n/a
12	chr1:242121526-242121576	GM12891	blood:	n/a
13	chr1:242121526-242121576	HCF	heart:	n/a
14	chr1:242121827-242121877	Jurkat	blood:	n/a
15	chr1:242120638-242120688	NT2-D1	testis:	n/a
16	chr1:242121526-242121576	Caco-2	colon:	n/a
17	chr1:242121827-242121877	PrEC	prostate:	n/a
18	chr1:242121526-242121576	HRPEpiC	eye:	n/a
19	chr1:242121827-242121877	HL-60	blood:	n/a
20	chr1:242121230-242121280	HL-60	blood:	n/a
21	chr1:242120638-242120688	SK-N-SH_RA	brain:	n/a
22	chr1:242120638-242120688	AG04449	skin:	fetal
23	chr1:242121827-242121877	NHDF-neo	bronchial:	n/a
24	chr1:242121230-242121280	AG09309	skin:	n/a
25	chr1:242121827-242121877	HNPCEpiC	eye:	n/a
26	chr1:242120638-242120688	T-47D	breast:	n/a
27	chr1:242121230-242121280	PrEC	prostate:	n/a
28	chr1:242120907-242120957	Hela-S3	cervix:	n/a
29	chr1:242120638-242120688	NH-A	brain:	n/a
30	chr1:242122063-242122113	HIPEpiC	eye:	n/a
31	chr1:242122063-242122113	Hepatocyte	liver:	n/a
32	chr1:242121526-242121576	HCT-116	colon:	n/a
33	chr1:242121526-242121576	SK-N-SH_RA	brain:	n/a
34	chr1:242120907-242120957	GM12891	blood:	n/a
35	chr1:242120638-242120688	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:242121230-242121280	HEEpiC	esophagus:	n/a
37	chr1:242121230-242121280	SAEC	small airway:	n/a
38	chr1:242120907-242120957	HL-60	blood:	n/a
39	chr1:242121230-242121280	IMR90	lung:	fetal
40	chr1:242121230-242121280	MCF-7	breast:	n/a
41	chr1:242121526-242121576	AG10803	skin:	n/a
42	chr1:242122063-242122113	HRCEpiC	kidney:	n/a
43	chr1:242121526-242121576	HUVEC	blood vessel:	n/a
44	chr1:242120907-242120957	PrEC	prostate:	n/a
45	chr1:242120907-242120957	SK-N-SH_RA	brain:	n/a
46	chr1:242122063-242122113	GM12878	blood:	n/a
47	chr1:242122063-242122113	GM06990	blood:	n/a
48	chr1:242120638-242120688	H1-hESC	embryonic stem cell:	embryo
49	chr1:242121526-242121576	CMK	blood:	n/a
50	chr1:242122063-242122113	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:242121060..242121703-chr1:242148791..242149743,4	MCF-7	breast:
2	chr1:242120814..242121654-chr1:242161517..242162480,3	MCF-7	breast:
3	chr1:242130029..242131689-chr1:242138065..242140950,2	K562	blood:

Variant related genes	Relation type
BECN1P1	TF binding region
BECN1P1	CpG island
ENSG00000197769	chromatin interactions

Extended variants
information (count: 736 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560566043	chr1:242119668-242119669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544394065	chr1:242119671-242119672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561067384	chr1:242119686-242119687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560468387	chr1:242119809-242119810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572659640	chr1:242119851-242119852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547154910	chr1:242119866-242119867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566748957	chr1:242119888-242119889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182750510	chr1:242119922-242119923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552576375	chr1:242119937-242119938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60298418	chr1:242119986-242119987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs75722249	chr1:242120018-242120019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370535937	chr1:242120022-242120023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72757280	chr1:242120050-242120051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149937162	chr1:242120056-242120057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568357329	chr1:242120058-242120059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144976993	chr1:242120106-242120107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553063288	chr1:242120125-242120126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28405571	chr1:242120151-242120152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs71648675	chr1:242120215-242120216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558290149	chr1:242120220-242120221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575563488	chr1:242120263-242120264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531263740	chr1:242120273-242120274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531327274	chr1:242120294-242120295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188546363	chr1:242120302-242120303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374670596	chr1:242120307-242120308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373279435	chr1:242120308-242120309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs36083518	chr1:242120310-242120311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs71570924	chr1:242120342-242120343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200773000	chr1:242120344-242120345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201823920	chr1:242120346-242120347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71174876	chr1:242120353-242120354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370023334	chr1:242120354-242120355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112072278	chr1:242120385-242120386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146756231	chr1:242120388-242120389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552514090	chr1:242120399-242120400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562544506	chr1:242120400-242120401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565575660	chr1:242120413-242120414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192191863	chr1:242120429-242120430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370650757	chr1:242120461-242120462	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs75369772	chr1:242120476-242120477	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs534160809	chr1:242120495-242120496	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs142638838	chr1:242120547-242120548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547688864	chr1:242120551-242120552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34735536	chr1:242120552-242120553	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs538359780	chr1:242120594-242120595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144949764	chr1:242120602-242120603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34652934	chr1:242120607-242120608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570539969	chr1:242120625-242120626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538133200	chr1:242120634-242120635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558559153	chr1:242120638-242120639	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
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
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242114000-242121200	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:242121000-242121200	Weak transcription	Right Atrium	heart
3	chr1:242121200-242121400	ZNF genes & repeats	Right Atrium	heart
4	chr1:242121200-242121400	Flanking Bivalent TSS/Enh	K562	blood
5	chr1:242121200-242122200	Enhancers	Fetal Muscle Leg	muscle
6	chr1:242121400-242121600	Bivalent Enhancer	K562	blood
7	chr1:242121400-242121800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:242121400-242161800	Weak transcription	Right Atrium	heart
9	chr1:242121600-242122000	Enhancers	Fetal Muscle Trunk	muscle
10	chr1:242121800-242126800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:242127000-242127200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:242127200-242127800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:242127800-242128400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:242128000-242128400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:242128000-242128600	Enhancers	HUVEC	blood vessel
16	chr1:242128400-242135800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:242129800-242141600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:242131400-242132800	Enhancers	Fetal Lung	lung
19	chr1:242132800-242133600	Weak transcription	Fetal Lung	lung
20	chr1:242133200-242133800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:242133600-242133800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:242133600-242133800	Enhancers	Fetal Lung	lung
23	chr1:242133600-242133800	Enhancers	HSMMtube	muscle
24	chr1:242133800-242135000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:242133800-242136000	Weak transcription	Fetal Lung	lung
26	chr1:242134400-242135800	Weak transcription	HSMMtube	muscle
27	chr1:242134800-242138000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:242135000-242137600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:242135800-242136200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:242135800-242136400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:242135800-242136400	Enhancers	Fetal Muscle Leg	muscle
32	chr1:242135800-242136400	Enhancers	HSMMtube	muscle
33	chr1:242135800-242136800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr1:242135800-242136800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr1:242135800-242136800	Enhancers	HSMM	muscle
36	chr1:242135800-242137000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:242135800-242137000	Enhancers	NH-A	brain
38	chr1:242135800-242137200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:242135800-242137600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:242135800-242137600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr1:242136000-242136200	Enhancers	Fetal Lung	lung
42	chr1:242136000-242136400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr1:242136000-242136400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr1:242136000-242136400	Enhancers	Fetal Brain Male	brain
45	chr1:242136000-242136400	Enhancers	Fetal Muscle Trunk	muscle
46	chr1:242136000-242136400	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:242136000-242136400	Enhancers	NHDF-Ad	bronchial
48	chr1:242136000-242136400	Enhancers	Osteobl	bone
49	chr1:242136000-242136600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr1:242136000-242136600	Enhancers	Brain Germinal Matrix	brain

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