Variant report

Variant	nsv548475
Chromosome Location	chr1:188735336-188870483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:520)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:188818322-188818328	K562	blood:	n/a	n/a
2	BRCA1	chr1:188857430-188857935	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr1:188751264-188751748	HCT-116	colon:	n/a	n/a
4	CEBPB	chr1:188861237-188861445	H1-hESC	embryonic stem cell:	n/a	chr1:188861298-188861309
5	CEBPB	chr1:188749833-188750148	A549	lung:	n/a	chr1:188750018-188750031 chr1:188749997-188750008 chr1:188749997-188750010
6	CEBPB	chr1:188861165-188861434	K562	blood:	n/a	chr1:188861298-188861309
7	CEBPB	chr1:188749632-188750193	HepG2	liver:	n/a	chr1:188750018-188750031 chr1:188749997-188750008 chr1:188749997-188750010
8	CEBPB	chr1:188743018-188743248	A549	lung:	n/a	chr1:188743109-188743120
9	CEBPB	chr1:188854862-188855129	HepG2	liver:	n/a	chr1:188854961-188854974 chr1:188854963-188854974 chr1:188854961-188854972 chr1:188854961-188854974
10	CEBPB	chr1:188795984-188796250	A549	lung:	n/a	chr1:188796129-188796140
11	CEBPB	chr1:188794707-188794885	A549	lung:	n/a	chr1:188794818-188794829
12	CEBPB	chr1:188794647-188794936	Hela-S3	cervix:	n/a	chr1:188794818-188794829
13	CEBPB	chr1:188795978-188796298	K562	blood:	n/a	chr1:188796129-188796140
14	CEBPB	chr1:188795959-188796302	IMR90	lung:	n/a	chr1:188796129-188796140
15	CEBPB	chr1:188738874-188739447	MCF-7	breast:	n/a	n/a
16	CEBPB	chr1:188794594-188795042	A549	lung:	n/a	chr1:188794818-188794829
17	CEBPB	chr1:188861137-188861478	HepG2	liver:	n/a	chr1:188861298-188861309
18	CEBPB	chr1:188738866-188739491	MCF-7	breast:	n/a	n/a
19	CEBPB	chr1:188794656-188794952	HepG2	liver:	n/a	chr1:188794818-188794829
20	CEBPB	chr1:188857286-188858045	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:188845139-188845339	HepG2	liver:	n/a	chr1:188845215-188845226 chr1:188845214-188845227
22	CEBPB	chr1:188795967-188796275	HepG2	liver:	n/a	chr1:188796129-188796140
23	CEBPB	chr1:188861120-188861477	IMR90	lung:	n/a	chr1:188861298-188861309
24	CEBPB	chr1:188861151-188861446	A549	lung:	n/a	chr1:188861298-188861309
25	CEBPB	chr1:188794566-188795108	MCF-7	breast:	n/a	chr1:188794818-188794829
26	CEBPB	chr1:188794612-188794962	MCF-7	breast:	n/a	chr1:188794818-188794829
27	CEBPB	chr1:188861142-188861475	Hela-S3	cervix:	n/a	chr1:188861298-188861309
28	CEBPB	chr1:188857462-188857804	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:188742969-188743293	HepG2	liver:	n/a	chr1:188743109-188743120
30	CEBPB	chr1:188833745-188833994	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:188739051-188739257	HepG2	liver:	n/a	n/a
32	CHD2	chr1:188857543-188857987	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:188751473-188751615	LNCaP	prostate:	n/a	n/a
34	CTCF	chr1:188751440-188751590	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr1:188751331-188751744	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:188751204-188751928	SK-N-SH	brain:	n/a	n/a
37	CTCF	chr1:188751451-188751632	GM12891	blood:	n/a	n/a
38	CTCF	chr1:188751299-188751757	T-47D	breast:	n/a	n/a
39	CTCF	chr1:188751480-188751630	GM12874	blood:	n/a	n/a
40	CTCF	chr1:188751418-188751662	GM19238	blood:	n/a	n/a
41	CTCF	chr1:188751480-188751630	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr1:188751439-188751660	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:188751456-188751629	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:188751460-188751610	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr1:188751420-188751570	HMF	breast:	n/a	n/a
46	CTCF	chr1:188751388-188751691	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:188751440-188751590	WI-38	lung:	n/a	n/a
48	CTCF	chr1:188751460-188751610	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr1:188751431-188751687	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr1:188751540-188751690	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:188826889-188826939	HepG2	liver:	n/a
2	chr1:188826889-188826939	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:188826889-188826939	NT2-D1	testis:	n/a
4	chr1:188826823-188826873	AG09309	skin:	n/a
5	chr1:188826823-188826873	HMEC	breast:	n/a
6	chr1:188826823-188826873	HRPEpiC	eye:	n/a
7	chr1:188826889-188826939	BJ	skin:	n/a
8	chr1:188826823-188826873	H1-hESC	embryonic stem cell:	embryo
9	chr1:188826823-188826873	ECC-1	luminal epithelium:	n/a
10	chr1:188826889-188826939	NH-A	brain:	n/a
11	chr1:188826823-188826873	NT2-D1	testis:	n/a
12	chr1:188826889-188826939	HAEpiC	amniotic membrane:	n/a
13	chr1:188826823-188826873	HUVEC	blood vessel:	n/a
14	chr1:188826889-188826939	PrEC	prostate:	n/a
15	chr1:188826823-188826873	T-47D	breast:	n/a
16	chr1:188826823-188826873	SKMC	muscle:	n/a
17	chr1:188826823-188826873	HAEpiC	amniotic membrane:	n/a
18	chr1:188826823-188826873	Hela-S3	cervix:	n/a
19	chr1:188826823-188826873	PFSK-1	brain:	n/a
20	chr1:188826889-188826939	Hepatocyte	liver:	n/a
21	chr1:188826889-188826939	SK-N-SH	brain:	n/a
22	chr1:188826889-188826939	MCF-7	breast:	n/a
23	chr1:188826823-188826873	NH-A	brain:	n/a
24	chr1:188826889-188826939	GM12891	blood:	n/a
25	chr1:188826823-188826873	HRE	kidney:	n/a
26	chr1:188826889-188826939	BE2_C	brain:	n/a
27	chr1:188826823-188826873	Caco-2	colon:	n/a
28	chr1:188826889-188826939	HL-60	blood:	n/a
29	chr1:188826889-188826939	AG04449	skin:	fetal
30	chr1:188826823-188826873	ovcar-3	ovarian:	n/a
31	chr1:188826823-188826873	MCF-7	breast:	n/a
32	chr1:188826823-188826873	PANC-1	pancreas:	n/a
33	chr1:188826823-188826873	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:188826823-188826873	MCF10A-Er-Src	breast:	n/a
35	chr1:188826823-188826873	HIPEpiC	eye:	n/a
36	chr1:188826823-188826873	BE2_C	brain:	n/a
37	chr1:188826823-188826873	K562	blood:	n/a
38	chr1:188826889-188826939	K562	blood:	n/a
39	chr1:188826889-188826939	LNCaP	prostate:	n/a
40	chr1:188826889-188826939	HMEC	breast:	n/a
41	chr1:188826823-188826873	CMK	blood:	n/a
42	chr1:188826823-188826873	NHDF-neo	bronchial:	n/a
43	chr1:188826823-188826873	HL-60	blood:	n/a
44	chr1:188826823-188826873	SK-N-SH_RA	brain:	n/a
45	chr1:188826889-188826939	HIPEpiC	eye:	n/a
46	chr1:188826889-188826939	PFSK-1	brain:	n/a
47	chr1:188826823-188826873	BJ	skin:	n/a
48	chr1:188826889-188826939	HCF	heart:	n/a
49	chr1:188826889-188826939	PANC-1	pancreas:	n/a
50	chr1:188826823-188826873	GM06990	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:188866159..188868933-chr1:188870871..188872423,2	MCF-7	breast:
2	chr1:188846061..188848491-chr1:188851171..188853585,2	MCF-7	breast:
3	chr1:188846061..188848491-chr1:188851171..188853585,2	MCF-7	breast:
4	chr1:188789143..188792283-chr1:188793641..188795538,3	K562	blood:
5	chr1:188401580..188402198-chr1:188862429..188863519,3	MCF-7	breast:
6	chr1:188753407..188755924-chr1:188760366..188763242,2	K562	blood:
7	chr1:188746632..188749210-chr1:189368064..189370522,2	K562	blood:
8	chr1:188789143..188792283-chr1:188793641..188795538,3	K562	blood:
9	chr1:188751121..188751789-chr1:188907053..188907934,3	MCF-7	breast:
10	chr1:188636854..188637418-chr1:188751018..188751851,2	MCF-7	breast:
11	chr1:188733061..188735226-chr1:188736574..188738238,2	K562	blood:
12	chr1:188751072..188751772-chr1:189118548..189119200,2	MCF-7	breast:
13	chr1:188773169..188775117-chr1:188777054..188779991,2	K562	blood:
14	chr1:188773169..188775117-chr1:188777054..188779991,2	K562	blood:
15	chr1:188788862..188791265-chr1:188817309..188819818,2	MCF-7	breast:
16	chr1:188762438..188765055-chr1:189455240..189458166,2	MCF-7	breast:
17	chr1:188753407..188755924-chr1:188760366..188763242,2	K562	blood:
18	chr1:188788862..188791265-chr1:188817309..188819818,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-2	chr1:188856372-188856565	XLOC_001129
2	lnc-FAM5C-2	chr1:188838608-188838879	XLOC_001129
3	lnc-PLA2G4A-17	chr1:188860643-188860786	refGeneNc_416_NR_033922

No data

Variant related genes	Relation type
ENSG00000238054	TF binding region
LINC01035	TF binding region
ENSG00000238054	CpG island
LINC01035	CpG island
KIAA0494	miRNA target sites

Extended variants
information (count: 1158 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10754227	chr1:188735336-188735337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147573432	chr1:188735370-188735371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367767722	chr1:188735378-188735379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547504600	chr1:188735428-188735429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140294395	chr1:188735450-188735451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533465549	chr1:188735468-188735469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550012658	chr1:188735489-188735490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371367249	chr1:188735514-188735515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149701606	chr1:188735566-188735567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4317809	chr1:188735606-188735607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528276530	chr1:188735621-188735622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35079767	chr1:188735637-188735638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs4319333	chr1:188735807-188735808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs145494127	chr1:188735829-188735830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553819860	chr1:188735837-188735838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576881128	chr1:188735896-188735897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189194026	chr1:188735908-188735909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10801622	chr1:188735933-188735934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528725235	chr1:188735972-188735973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576279772	chr1:188735986-188735987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114577910	chr1:188736014-188736015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs193238086	chr1:188736081-188736082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35125239	chr1:188736143-188736144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560935750	chr1:188736148-188736149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148986604	chr1:188736165-188736166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541097626	chr1:188736177-188736178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71681567	chr1:188736184-188736185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551505090	chr1:188736187-188736188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs398103475	chr1:188736188-188736189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564141267	chr1:188736321-188736322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185669983	chr1:188736333-188736334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568270522	chr1:188736389-188736390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549753028	chr1:188736420-188736421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377141388	chr1:188736424-188736425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143738489	chr1:188736463-188736464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189415290	chr1:188736529-188736530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6670462	chr1:188736617-188736618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs180890568	chr1:188736630-188736631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547469475	chr1:188736670-188736671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146637744	chr1:188736682-188736683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539483519	chr1:188736711-188736712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141465635	chr1:188736734-188736735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569882322	chr1:188736760-188736761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535726565	chr1:188736770-188736771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568941099	chr1:188736786-188736787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185518836	chr1:188736801-188736802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572157727	chr1:188736803-188736804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541134522	chr1:188736806-188736807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557867953	chr1:188736825-188736826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34983043	chr1:188736852-188736853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	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
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:188734800-188738200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:188738000-188738400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr1:188738000-188738800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:188738000-188739000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:188738200-188738400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:188738200-188738400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:188738200-188738800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:188738200-188739200	Enhancers	Placenta	Placenta
9	chr1:188742000-188742200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:188742200-188745000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:188744600-188745000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:188745000-188745400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:188749000-188749400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:188751400-188751600	Enhancers	Aorta	Aorta
15	chr1:188769000-188769600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:188769000-188769800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:188791000-188791400	Active TSS	Fetal Muscle Leg	muscle
18	chr1:188791200-188792000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:188791200-188792200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:188791400-188791600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr1:188791400-188791800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:188791400-188791800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:188791400-188791800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:188791400-188791800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:188791400-188792000	Enhancers	Fetal Muscle Leg	muscle
26	chr1:188791600-188792000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:188791800-188793200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:188793200-188793600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:188793400-188793800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:188812200-188812600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:188812200-188813000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr1:188812400-188813000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:188812800-188813000	Enhancers	Pancreas	Pancrea
34	chr1:188813000-188815600	Weak transcription	Pancreas	Pancrea
35	chr1:188815600-188816000	ZNF genes & repeats	Pancreas	Pancrea
36	chr1:188815800-188816000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:188819600-188820400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:188820400-188821400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr1:188820600-188820800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:188823800-188824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr1:188823800-188824600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr1:188824200-188824600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr1:188826600-188826800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:188826600-188827000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:188826600-188827200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:188826800-188827000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:188827000-188827200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:188835000-188835400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:188846600-188847200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:188846600-188847600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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