Variant report

Variant	nsv523863
Chromosome Location	chr1:216517635-216629416
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:216576495-216576502	K562	blood:	n/a	n/a
2	BACH1	chr1:216541739-216541938	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:216562063-216562257	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:216614865-216614936	GM12878	blood:	n/a	n/a
5	BRCA1	chr1:216539982-216540123	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:216585550-216585595	HepG2	liver:	n/a	chr1:216585552-216585563
7	CEBPB	chr1:216581632-216581861	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:216532397-216532549	K562	blood:	n/a	n/a
9	CEBPB	chr1:216559391-216559578	IMR90	lung:	n/a	chr1:216559492-216559501 chr1:216559492-216559503
10	CEBPB	chr1:216541536-216541777	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:216541515-216541757	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:216567764-216567829	IMR90	lung:	n/a	n/a
13	CTCF	chr1:216568980-216569130	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:216552524-216552550	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:216619129-216619194	GM10248	blood:	n/a	n/a
16	CTCF	chr1:216578396-216578435	ProgFib	skin:	n/a	n/a
17	CTCF	chr1:216547243-216547277	GM10266	blood:	n/a	n/a
18	CTCF	chr1:216578343-216578353	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:216626360-216626403	LNCaP	prostate:	n/a	n/a
20	CTCF	chr1:216552340-216552490	GM12864	blood:	n/a	n/a
21	CTCF	chr1:216578185-216578278	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:216578290-216578382	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:216578259-216578371	MCF-7	breast:	n/a	n/a
24	E2F4	chr1:216621297-216621490	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr1:216534794-216535246	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr1:216599439-216599866	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr1:216574432-216574821	MCF10A-Er-Src	breast:	n/a	n/a
28	EBF1	chr1:216590819-216590964	GM12878	blood:	n/a	n/a
29	EBF1	chr1:216589845-216590238	GM12878	blood:	n/a	chr1:216590028-216590038 chr1:216590026-216590039 chr1:216590028-216590037 chr1:216590026-216590037
30	EBF1	chr1:216589906-216590152	GM12878	blood:	n/a	chr1:216590028-216590038 chr1:216590026-216590039 chr1:216590028-216590037 chr1:216590026-216590037
31	EBF1	chr1:216592233-216592435	GM12878	blood:	n/a	n/a
32	EP300	chr1:216564231-216564746	SK-N-SH_RA	brain:	n/a	chr1:216564371-216564385
33	EP300	chr1:216626797-216627754	SK-N-SH	brain:	n/a	chr1:216627588-216627602
34	EP300	chr1:216564240-216564752	SK-N-SH_RA	brain:	n/a	chr1:216564371-216564385
35	EP300	chr1:216621461-216621998	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr1:216620990-216622527	SK-N-SH	brain:	n/a	n/a
37	EP300	chr1:216536551-216536605	GM12878	blood:	n/a	n/a
38	EP300	chr1:216627050-216627490	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr1:216621363-216622012	SK-N-SH	brain:	n/a	n/a
40	EP300	chr1:216621454-216621998	SK-N-SH_RA	brain:	n/a	n/a
41	FOS	chr1:216629118-216629183	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:216621234-216621576	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr1:216621232-216621586	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr1:216621234-216621533	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:216621217-216621577	MCF10A-Er-Src	breast:	n/a	n/a
46	FOXA1	chr1:216596579-216596729	T-47D	breast:	n/a	n/a
47	GATA2	chr1:216627150-216627557	SH-SY5Y	brain:	n/a	n/a
48	GATA2	chr1:216621399-216622048	SH-SY5Y	brain:	n/a	chr1:216621720-216621733 chr1:216621660-216621667 chr1:216621660-216621667 chr1:216621653-216621674 chr1:216621660-216621667
49	GATA3	chr1:216588113-216588126	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr1:216627048-216627559	SH-SY5Y	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:216596639-216596689	HRPEpiC	eye:	n/a
2	chr1:216596639-216596689	GM19239	blood:	n/a
3	chr1:216596808-216596858	NB4	blood:	n/a
4	chr1:216596639-216596689	RPTEC	kidney:	n/a
5	chr1:216596808-216596858	AG04450	lung:	fetal
6	chr1:216596808-216596858	NHDF-neo	bronchial:	n/a
7	chr1:216596808-216596858	HIPEpiC	eye:	n/a
8	chr1:216596639-216596689	SKMC	muscle:	n/a
9	chr1:216561886-216561936	SK-N-MC	brain:	n/a
10	chr1:216596639-216596689	BJ	skin:	n/a
11	chr1:216596808-216596858	ProgFib	skin:	n/a
12	chr1:216596639-216596689	GM12878	blood:	n/a
13	chr1:216596639-216596689	MCF-7	breast:	n/a
14	chr1:216561886-216561936	AoSMC	blood vessel:	n/a
15	chr1:216596639-216596689	AoSMC	blood vessel:	n/a
16	chr1:216561886-216561936	AG09319	gingival:	n/a
17	chr1:216596808-216596858	HCF	heart:	n/a
18	chr1:216596639-216596689	U87	brain:	n/a
19	chr1:216596639-216596689	GM06990	blood:	n/a
20	chr1:216596808-216596858	AG10803	skin:	n/a
21	chr1:216561886-216561936	HNPCEpiC	eye:	n/a
22	chr1:216561886-216561936	PANC-1	pancreas:	n/a
23	chr1:216596639-216596689	NHDF-neo	bronchial:	n/a
24	chr1:216596808-216596858	Hepatocyte	liver:	n/a
25	chr1:216596808-216596858	K562	blood:	n/a
26	chr1:216596808-216596858	SKMC	muscle:	n/a
27	chr1:216561886-216561936	HCM	heart:	n/a
28	chr1:216561886-216561936	AG10803	skin:	n/a
29	chr1:216561886-216561936	HCPEpiC	choroid plexus:	n/a
30	chr1:216596639-216596689	AG04449	skin:	fetal
31	chr1:216561886-216561936	NT2-D1	testis:	n/a
32	chr1:216596639-216596689	T-47D	breast:	n/a
33	chr1:216596808-216596858	A549	lung:	n/a
34	chr1:216561886-216561936	HIPEpiC	eye:	n/a
35	chr1:216561886-216561936	GM19239	blood:	n/a
36	chr1:216596808-216596858	ECC-1	luminal epithelium:	n/a
37	chr1:216596639-216596689	HNPCEpiC	eye:	n/a
38	chr1:216561886-216561936	IMR90	lung:	fetal
39	chr1:216561886-216561936	K562	blood:	n/a
40	chr1:216596808-216596858	BE2_C	brain:	n/a
41	chr1:216596808-216596858	SK-N-SH	brain:	n/a
42	chr1:216561886-216561936	GM06990	blood:	n/a
43	chr1:216561886-216561936	Jurkat	blood:	n/a
44	chr1:216596639-216596689	Caco-2	colon:	n/a
45	chr1:216561886-216561936	BJ	skin:	n/a
46	chr1:216596639-216596689	NHBE	bronchial:	n/a
47	chr1:216596639-216596689	GM12891	blood:	n/a
48	chr1:216596639-216596689	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:216561886-216561936	NHBE	bronchial:	n/a
50	chr1:216596808-216596858	HRPEpiC	eye:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:216593418..216595910-chr1:216597223..216598829,2	K562	blood:
2	chr1:216527475..216530440-chr1:216773266..216776037,2	MCF-7	breast:
3	chr1:216593418..216595910-chr1:216597223..216598829,2	K562	blood:
4	chr1:216547713..216550366-chr1:216550786..216552777,2	MCF-7	breast:
5	chr1:216538707..216540842-chr1:216542556..216544209,2	MCF-7	breast:
6	chr1:216538113..216539944-chr1:216540242..216541940,2	K562	blood:
7	chr1:216622981..216624507-chr1:216637851..216639964,2	MCF-7	breast:
8	chr1:216538707..216540842-chr1:216542556..216544209,2	MCF-7	breast:
9	chr1:216538113..216539944-chr1:216540242..216541940,2	K562	blood:
10	chr1:149856682..149858557-chr1:216537512..216539336,2	MCF-7	breast:
11	chr1:216547713..216550366-chr1:216550786..216552777,2	MCF-7	breast:

No data

Variant related genes	Relation type
USH2A	TF binding region
USH2A	CpG island
ENSG00000184260	chromatin interactions
ENSG00000184678	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1747 , 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	rs545274422	chr1:216518212-216518213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565533027	chr1:216518247-216518248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575863439	chr1:216518248-216518249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530743712	chr1:216518255-216518256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544945108	chr1:216518271-216518272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368620513	chr1:216518311-216518312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76687424	chr1:216518328-216518329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564373418	chr1:216518334-216518335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530071187	chr1:216518335-216518336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76520255	chr1:216518344-216518345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560430201	chr1:216518349-216518350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553550441	chr1:216518353-216518354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528246473	chr1:216518378-216518379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551300229	chr1:216518411-216518412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372327711	chr1:216518416-216518417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571488471	chr1:216518422-216518423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146862226	chr1:216518429-216518430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371280456	chr1:216518517-216518518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537319844	chr1:216518575-216518576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192042658	chr1:216518602-216518603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79581915	chr1:216518609-216518610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6660228	chr1:216518658-216518659	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs552985816	chr1:216518672-216518673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566484872	chr1:216518692-216518693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571863372	chr1:216518694-216518695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572861925	chr1:216518717-216518718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6668781	chr1:216518768-216518769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs144871645	chr1:216518834-216518835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575461750	chr1:216518852-216518853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544489853	chr1:216518884-216518885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528991842	chr1:216518919-216518920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377596195	chr1:216518927-216518928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554885352	chr1:216518934-216518935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145789230	chr1:216518940-216518941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540273759	chr1:216518945-216518946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184187783	chr1:216518995-216518996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187421053	chr1:216519034-216519035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549025395	chr1:216519069-216519070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191549000	chr1:216519095-216519096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564914450	chr1:216519096-216519097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184872065	chr1:216519176-216519177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542424564	chr1:216519215-216519216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6671672	chr1:216519283-216519284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs189371278	chr1:216519342-216519343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529672545	chr1:216519351-216519352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181020405	chr1:216519360-216519361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12085974	chr1:216519361-216519362	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs549870135	chr1:216519374-216519375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373129715	chr1:216519388-216519389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538335145	chr1:216519406-216519407	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	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
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
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216518200-216520000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:216519800-216520200	Enhancers	Fetal Muscle Leg	muscle
3	chr1:216535000-216535200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:216557200-216565000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:216558400-216558800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:216558600-216559200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:216558800-216560400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:216560400-216561000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:216560400-216565400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:216560600-216560800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr1:216560600-216563200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr1:216560600-216563800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:216560800-216561000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
14	chr1:216560800-216561400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr1:216560800-216562600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:216560800-216563800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:216561000-216561600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
18	chr1:216561000-216562600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:216561200-216562200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr1:216561200-216562400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:216561400-216562000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr1:216561400-216562400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr1:216561400-216562800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:216561600-216562000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr1:216561600-216562600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:216562000-216562200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr1:216562000-216563000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:216562200-216562400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
29	chr1:216562400-216563800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr1:216562600-216565000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:216562800-216563200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:216563000-216563400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr1:216563200-216563600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
34	chr1:216563200-216563600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:216563400-216563800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr1:216563800-216564600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:216563800-216566200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:216565000-216565400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:216565400-216566200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:216566200-216566600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:216566400-216566600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:216566400-216566600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:216566600-216567600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:216567600-216567800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:216583200-216585800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:216590000-216590600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:216590600-216595400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:216593400-216596000	Enhancers	Liver	Liver
49	chr1:216593800-216594200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:216595400-216596200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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