Variant report

Variant	nsv470789
Chromosome Location	chr1:242741023-242859680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:389)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:242749196-242749772	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:242765415-242765554	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:242802067-242802078	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:242848092-242848258	K562	blood:	n/a	n/a
5	BCL11A	chr1:242749309-242749565	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
7	BCL3	chr1:242843343-242843676	GM12878	blood:	n/a	n/a
8	BRCA1	chr1:242749358-242749729	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr1:242798548-242798608	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:242815292-242815888	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:242766610-242766982	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:242774611-242774728	A549	lung:	n/a	n/a
13	CEBPB	chr1:242749263-242749763	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:242791286-242791544	HepG2	liver:	n/a	chr1:242791427-242791436 chr1:242791479-242791490 chr1:242791479-242791492 chr1:242791425-242791436 chr1:242791480-242791491 chr1:242791479-242791492 chr1:242791479-242791490
15	CEBPB	chr1:242774541-242774804	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:242815630-242815862	A549	lung:	n/a	n/a
17	CEBPB	chr1:242766634-242766975	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:242798128-242798506	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:242742398-242742616	HepG2	liver:	n/a	chr1:242742505-242742516
20	CEBPB	chr1:242774529-242774815	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:242766628-242766982	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:242766651-242766980	A549	lung:	n/a	n/a
23	CHD1	chr1:242748570-242748576	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:242749188-242749790	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:242815200-242815350	HepG2	liver:	n/a	n/a
26	CTCF	chr1:242804200-242804350	HRE	kidney:	n/a	n/a
27	CTCF	chr1:242815240-242815390	GM06990	blood:	n/a	n/a
28	CTCF	chr1:242815220-242815370	GM12874	blood:	n/a	n/a
29	CTCF	chr1:242815200-242815350	GM12878	blood:	n/a	n/a
30	CTCF	chr1:242815200-242815350	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr1:242815220-242815370	HMEC	breast:	n/a	n/a
32	CTCF	chr1:242804360-242804510	HMEC	breast:	n/a	chr1:242804410-242804428 chr1:242804405-242804426
33	CTCF	chr1:242815220-242815370	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr1:242815200-242815350	GM12864	blood:	n/a	n/a
35	CTCF	chr1:242785240-242785390	HL-60	blood:	n/a	n/a
36	CTCF	chr1:242815220-242815370	GM12873	blood:	n/a	n/a
37	CTCF	chr1:242815220-242815370	HCT-116	colon:	n/a	n/a
38	CTCF	chr1:242853840-242853990	HMEC	breast:	n/a	n/a
39	CTCF	chr1:242815179-242815417	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr1:242815156-242815374	A549	lung:	n/a	n/a
41	CTCF	chr1:242815240-242815390	GM12801	blood:	n/a	n/a
42	CTCF	chr1:242815400-242815550	GM12870	blood:	n/a	n/a
43	CTCF	chr1:242853880-242854030	HMEC	breast:	n/a	n/a
44	CTCF	chr1:242815200-242815350	RPTEC	kidney:	n/a	n/a
45	CTCF	chr1:242815210-242815371	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:242815160-242815310	GM12873	blood:	n/a	n/a
47	CTCF	chr1:242815200-242815350	A549	lung:	n/a	n/a
48	CTCF	chr1:242815160-242815310	HEK293	kidney:	n/a	n/a
49	CTCF	chr1:242815260-242815410	HMEC	breast:	n/a	n/a
50	CTCF	chr1:242815200-242815350	GM12874	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242767942-242767992	ovcar-3	ovarian:	n/a
2	chr1:242749065-242749115	HEK293	kidney:	embryo
3	chr1:242749065-242749115	AoSMC	blood vessel:	n/a
4	chr1:242767942-242767992	GM19239	blood:	n/a
5	chr1:242767942-242767992	T-47D	breast:	n/a
6	chr1:242767727-242767777	SAEC	small airway:	n/a
7	chr1:242767942-242767992	HEK293	kidney:	embryo
8	chr1:242749065-242749115	K562	blood:	n/a
9	chr1:242749065-242749115	NH-A	brain:	n/a
10	chr1:242749065-242749115	NT2-D1	testis:	n/a
11	chr1:242767727-242767777	NHBE	bronchial:	n/a
12	chr1:242749065-242749115	MCF10A-Er-Src	breast:	n/a
13	chr1:242767727-242767777	U87	brain:	n/a
14	chr1:242749065-242749115	LNCaP	prostate:	n/a
15	chr1:242749065-242749115	ProgFib	skin:	n/a
16	chr1:242767942-242767992	SK-N-SH	brain:	n/a
17	chr1:242767942-242767992	Hepatocyte	liver:	n/a
18	chr1:242749065-242749115	A549	lung:	n/a
19	chr1:242767942-242767992	HCT-116	colon:	n/a
20	chr1:242749065-242749115	HAEpiC	amniotic membrane:	n/a
21	chr1:242749065-242749115	ovcar-3	ovarian:	n/a
22	chr1:242767942-242767992	HL-60	blood:	n/a
23	chr1:242767727-242767777	HEEpiC	esophagus:	n/a
24	chr1:242767727-242767777	SKMC	muscle:	n/a
25	chr1:242767727-242767777	NT2-D1	testis:	n/a
26	chr1:242767727-242767777	HRCEpiC	kidney:	n/a
27	chr1:242767942-242767992	Caco-2	colon:	n/a
28	chr1:242767727-242767777	PrEC	prostate:	n/a
29	chr1:242767942-242767992	U87	brain:	n/a
30	chr1:242767942-242767992	AG09309	skin:	n/a
31	chr1:242767727-242767777	HCT-116	colon:	n/a
32	chr1:242767942-242767992	SAEC	small airway:	n/a
33	chr1:242749065-242749115	Caco-2	colon:	n/a
34	chr1:242767942-242767992	HCM	heart:	n/a
35	chr1:242767727-242767777	GM06990	blood:	n/a
36	chr1:242749065-242749115	GM06990	blood:	n/a
37	chr1:242767727-242767777	HRPEpiC	eye:	n/a
38	chr1:242767942-242767992	HCF	heart:	n/a
39	chr1:242749065-242749115	GM12891	blood:	n/a
40	chr1:242749065-242749115	NHBE	bronchial:	n/a
41	chr1:242767942-242767992	SKMC	muscle:	n/a
42	chr1:242767942-242767992	PANC-1	pancreas:	n/a
43	chr1:242767942-242767992	Hela-S3	cervix:	n/a
44	chr1:242749065-242749115	MCF-7	breast:	n/a
45	chr1:242767727-242767777	RPTEC	kidney:	n/a
46	chr1:242749065-242749115	H1-hESC	embryonic stem cell:	embryo
47	chr1:242767942-242767992	ProgFib	skin:	n/a
48	chr1:242767942-242767992	HRCEpiC	kidney:	n/a
49	chr1:242767942-242767992	SK-N-SH_RA	brain:	n/a
50	chr1:242749065-242749115	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:242725284..242727359-chr1:242740097..242742633,2	K562	blood:
2	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SDCCAG8-4	chr1:242834442-242834878	NONHSAT010573

No data

Variant related genes	Relation type
ENSG00000270859	TF binding region
ENSG00000270859	CpG island

Extended variants
information (count: 4152 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4152 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1938341	chr1:242741023-242741024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140369051	chr1:242741204-242741205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77658213	chr1:242741257-242741258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530006620	chr1:242741271-242741272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181123027	chr1:242741279-242741280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186409377	chr1:242741318-242741319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111875659	chr1:242741322-242741323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143637419	chr1:242741323-242741324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532026305	chr1:242741356-242741357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191734166	chr1:242741411-242741412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568838861	chr1:242741512-242741513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572397928	chr1:242741520-242741521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557317129	chr1:242741529-242741530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568328554	chr1:242741562-242741563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534178780	chr1:242741643-242741644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79979620	chr1:242741660-242741661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577132449	chr1:242741665-242741666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183563482	chr1:242741672-242741673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75998225	chr1:242741679-242741680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73138205	chr1:242741722-242741723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs545440534	chr1:242741756-242741757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542381183	chr1:242741760-242741761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35411787	chr1:242741783-242741784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561024374	chr1:242741836-242741837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574687366	chr1:242741837-242741838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564087884	chr1:242741899-242741900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140515086	chr1:242742022-242742023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187338726	chr1:242742028-242742029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532467052	chr1:242742039-242742040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531341774	chr1:242742115-242742116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549813752	chr1:242742146-242742147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562547908	chr1:242742185-242742186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531267680	chr1:242742189-242742190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191062876	chr1:242742242-242742243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150423361	chr1:242742243-242742244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527892577	chr1:242742254-242742255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575586284	chr1:242742296-242742297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571033587	chr1:242742305-242742306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544224488	chr1:242742308-242742309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138194890	chr1:242742413-242742414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142552262	chr1:242742443-242742444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10926776	chr1:242742468-242742469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs146679627	chr1:242742486-242742487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555914092	chr1:242742498-242742499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35392777	chr1:242742549-242742550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139353158	chr1:242742550-242742551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143314663	chr1:242742587-242742588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540032839	chr1:242742588-242742589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529050203	chr1:242742599-242742600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1938340	chr1:242742737-242742738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:93)

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
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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242734000-242747800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:242742600-242742800	Enhancers	A549	lung
3	chr1:242742800-242743200	Flanking Active TSS	A549	lung
4	chr1:242743200-242743600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:242743200-242744200	Enhancers	A549	lung
6	chr1:242744200-242746000	Weak transcription	A549	lung
7	chr1:242745800-242747200	Enhancers	HepG2	liver
8	chr1:242746000-242746200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:242746000-242746400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:242746000-242747000	Enhancers	A549	lung
11	chr1:242746200-242746400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:242746400-242747800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:242746600-242748800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:242747800-242748000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:242747800-242748000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr1:242747800-242748000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:242747800-242748000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:242748000-242748600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:242748000-242749600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:242748400-242750000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:242748400-242750200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:242748600-242749000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:242748600-242750000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:242748800-242749000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:242748800-242749000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr1:242748800-242749600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:242748800-242749800	Enhancers	Brain Germinal Matrix	brain
28	chr1:242748800-242750200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr1:242748800-242750200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:242748800-242750200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:242748800-242750600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr1:242749000-242749200	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr1:242749000-242750600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:242749000-242750800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:242749200-242749400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr1:242749200-242749800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:242749200-242750200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:242749200-242750600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr1:242749400-242749800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr1:242749600-242750200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:242749600-242750200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:242749600-242750200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr1:242749800-242750000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr1:242750200-242753000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:242750600-242751000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:242755600-242756200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:242756800-242757000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:242757000-242757200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:242757200-242757400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:242757400-242762000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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