Variant report

Variant	nsv436629
Chromosome Location	chr1:149713442-149719709
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr1:149719574-149719759	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr1:149718853-149718928	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr1:149719609-149719643	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr1:149718397-149718703	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr1:149718440-149718636	H1-hESC	embryonic stem cell:	n/a	n/a
6	EBF1	chr1:149713448-149713708	GM12878	blood:	n/a	n/a
7	MXI1	chr1:149718395-149718719	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr1:149713514-149713581	Gliobla	brain:	n/a	n/a
9	POLR2A	chr1:149719274-149719728	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr1:149718672-149718680	MCF-7	breast:	n/a	n/a
11	POLR2A	chr1:149719204-149719732	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr1:149719278-149719803	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr1:149718345-149718893	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr1:149718258-149718957	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr1:149718404-149718668	MCF-7	breast:	n/a	n/a
16	POLR2A	chr1:149718459-149718669	MCF-7	breast:	n/a	n/a
17	POLR2A	chr1:149719562-149719581	MCF-7	breast:	n/a	n/a
18	POLR2A	chr1:149719446-149719670	MCF-7	breast:	n/a	n/a
19	POLR2A	chr1:149718881-149718897	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr1:149718109-149720170	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr1:149719011-149719883	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr1:149718317-149718902	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr1:149719616-149719624	MCF-7	breast:	n/a	n/a
24	POLR2A	chr1:149719538-149719556	MCF-7	breast:	n/a	n/a
25	POLR2A	chr1:149718307-149718873	H1-hESC	embryonic stem cell:	n/a	n/a
26	RAD21	chr1:149718388-149718734	H1-hESC	embryonic stem cell:	n/a	n/a
27	RAD21	chr1:149718314-149718765	H1-hESC	embryonic stem cell:	n/a	n/a
28	RAD21	chr1:149718377-149718699	H1-hESC	embryonic stem cell:	n/a	n/a
29	RFX5	chr1:149718375-149718579	HepG2	liver:	n/a	chr1:149718452-149718461
30	RFX5	chr1:149718322-149718721	H1-hESC	embryonic stem cell:	n/a	chr1:149718452-149718461
31	RXRA	chr1:149718371-149718699	H1-hESC	embryonic stem cell:	n/a	chr1:149718547-149718554 chr1:149718539-149718559
32	SIN3A	chr1:149718443-149718768	H1-hESC	embryonic stem cell:	n/a	n/a
33	TAF1	chr1:149719069-149719973	H1-hESC	embryonic stem cell:	n/a	n/a
34	TAF1	chr1:149718289-149719000	H1-hESC	embryonic stem cell:	n/a	n/a
35	TAF1	chr1:149719161-149719698	H1-hESC	embryonic stem cell:	n/a	n/a
36	TAF1	chr1:149718391-149719017	H1-hESC	embryonic stem cell:	n/a	n/a
37	TBP	chr1:149718512-149718575	H1-hESC	embryonic stem cell:	n/a	n/a
38	TCF12	chr1:149718588-149718858	H1-hESC	embryonic stem cell:	n/a	chr1:149718670-149718677
39	TCF12	chr1:149718664-149718833	H1-hESC	embryonic stem cell:	n/a	chr1:149718670-149718677
40	TEAD4	chr1:149719015-149719604	H1-hESC	embryonic stem cell:	n/a	n/a
41	TEAD4	chr1:149718209-149718799	H1-hESC	embryonic stem cell:	n/a	n/a
42	TEAD4	chr1:149719049-149719597	H1-hESC	embryonic stem cell:	n/a	n/a
43	YY1	chr1:149718375-149718704	H1-hESC	embryonic stem cell:	n/a	n/a
44	YY1	chr1:149718397-149718797	H1-hESC	embryonic stem cell:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:149718671-149718721	GM12891	blood:	n/a
2	chr1:149719461-149719511	ovcar-3	ovarian:	n/a
3	chr1:149719461-149719511	BJ	skin:	n/a
4	chr1:149719461-149719511	GM06990	blood:	n/a
5	chr1:149718651-149718701	NH-A	brain:	n/a
6	chr1:149718651-149718701	SKMC	muscle:	n/a
7	chr1:149719536-149719586	SK-N-SH_RA	brain:	n/a
8	chr1:149719243-149719293	HCT-116	colon:	n/a
9	chr1:149719536-149719586	HNPCEpiC	eye:	n/a
10	chr1:149718651-149718701	GM12891	blood:	n/a
11	chr1:149718671-149718721	Hepatocyte	liver:	n/a
12	chr1:149719536-149719586	NB4	blood:	n/a
13	chr1:149718671-149718721	HCT-116	colon:	n/a
14	chr1:149717620-149717670	AG10803	skin:	n/a
15	chr1:149718671-149718721	HRE	kidney:	n/a
16	chr1:149717620-149717670	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:149719243-149719293	PFSK-1	brain:	n/a
18	chr1:149719461-149719511	HIPEpiC	eye:	n/a
19	chr1:149719461-149719511	Jurkat	blood:	n/a
20	chr1:149718651-149718701	NHBE	bronchial:	n/a
21	chr1:149717620-149717670	HNPCEpiC	eye:	n/a
22	chr1:149718671-149718721	BE2_C	brain:	n/a
23	chr1:149718651-149718701	H1-hESC	embryonic stem cell:	embryo
24	chr1:149717620-149717670	PFSK-1	brain:	n/a
25	chr1:149719243-149719293	CMK	blood:	n/a
26	chr1:149719243-149719293	AG09309	skin:	n/a
27	chr1:149717620-149717670	ECC-1	luminal epithelium:	n/a
28	chr1:149717620-149717670	HL-60	blood:	n/a
29	chr1:149719243-149719293	HMEC	breast:	n/a
30	chr1:149718671-149718721	AoSMC	blood vessel:	n/a
31	chr1:149719243-149719293	ProgFib	skin:	n/a
32	chr1:149719461-149719511	GM12892	blood:	n/a
33	chr1:149718671-149718721	Caco-2	colon:	n/a
34	chr1:149718671-149718721	MCF10A-Er-Src	breast:	n/a
35	chr1:149717620-149717670	H1-hESC	embryonic stem cell:	embryo
36	chr1:149719243-149719293	SAEC	small airway:	n/a
37	chr1:149718651-149718701	HCT-116	colon:	n/a
38	chr1:149718651-149718701	PANC-1	pancreas:	n/a
39	chr1:149719536-149719586	HepG2	liver:	n/a
40	chr1:149719536-149719586	RPTEC	kidney:	n/a
41	chr1:149719536-149719586	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:149719461-149719511	HEEpiC	esophagus:	n/a
43	chr1:149719536-149719586	SAEC	small airway:	n/a
44	chr1:149718651-149718701	IMR90	lung:	fetal
45	chr1:149719243-149719293	NHBE	bronchial:	n/a
46	chr1:149717620-149717670	GM12892	blood:	n/a
47	chr1:149718671-149718721	GM19239	blood:	n/a
48	chr1:149718671-149718721	HAEpiC	amniotic membrane:	n/a
49	chr1:149718651-149718701	NT2-D1	testis:	n/a
50	chr1:149718671-149718721	HEK293	kidney:	embryo

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST2H2BF-3	chr1:149718450-149720133	NONHSAT006245

No data

Variant related genes	Relation type
ENSG00000263825	TF binding region
ENSG00000234232	TF binding region
ENSG00000263825	CpG island
ENSG00000234232	CpG island

Extended variants
information (count: 215 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:215 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587690127	chr1:149713463-149713464	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs587758638	chr1:149713468-149713469	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs147228112	chr1:149713475-149713476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs12085173	chr1:149713476-149713477	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs587635484	chr1:149713611-149713612	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs12085216	chr1:149713621-149713622	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs138363847	chr1:149713624-149713625	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2597722	chr1:149713680-149713681	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs587715161	chr1:149713744-149713745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587769937	chr1:149713750-149713751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374117991	chr1:149713755-149713756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs58017708	chr1:149713760-149713761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150879475	chr1:149713776-149713777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587701631	chr1:149713789-149713790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587763552	chr1:149713798-149713799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144065108	chr1:149713803-149713804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587647553	chr1:149713805-149713806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs59188617	chr1:149713810-149713811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58050775	chr1:149713818-149713819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139128517	chr1:149713884-149713885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200674799	chr1:149713899-149713900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs60560973	chr1:149713928-149713929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140143274	chr1:149714021-149714022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61470894	chr1:149714096-149714097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587710973	chr1:149714104-149714105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58164353	chr1:149714196-149714197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12408651	chr1:149714207-149714208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143884983	chr1:149714222-149714223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587609626	chr1:149714542-149714543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201127283	chr1:149714614-149714615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587665409	chr1:149714638-149714639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375772844	chr1:149714653-149714654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587604984	chr1:149714681-149714682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374983876	chr1:149714696-149714697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6672348	chr1:149714789-149714790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587679563	chr1:149714836-149714837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12089010	chr1:149714840-149714841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200086654	chr1:149714854-149714855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201277693	chr1:149714877-149714878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587730393	chr1:149714907-149714908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587626031	chr1:149714943-149714944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12089065	chr1:149714956-149714957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587737469	chr1:149715026-149715027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587633732	chr1:149715042-149715043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587717544	chr1:149715043-149715044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587772003	chr1:149715045-149715046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587647784	chr1:149715083-149715084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587684172	chr1:149715119-149715120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202036595	chr1:149715252-149715253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61806513	chr1:149715391-149715392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149712400-149718600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:149712600-149718400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:149717400-149718200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr1:149717600-149717800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr1:149718000-149718200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:149718200-149718400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
7	chr1:149718200-149719000	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr1:149718200-149719800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chr1:149718200-149720000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr1:149718200-149720000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr1:149718200-149720200	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr1:149718200-149720200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
13	chr1:149718400-149718600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:149718400-149718600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:149718400-149718600	Active TSS	Primary monocytes fromperipheralblood	blood
16	chr1:149718400-149718600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr1:149718400-149718600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
18	chr1:149718400-149718600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:149718400-149718600	Bivalent/Poised TSS	Adipose Nuclei	Adipose
20	chr1:149718400-149718600	Active TSS	Monocytes-CD14+_RO01746	blood
21	chr1:149718400-149718800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr1:149718400-149718800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
23	chr1:149718400-149718800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:149718400-149718800	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr1:149718400-149719000	Active TSS	Primary hematopoietic stem cells	blood
26	chr1:149718400-149719000	Enhancers	Spleen	Spleen
27	chr1:149718400-149719400	Bivalent Enhancer	Fetal Thymus	thymus
28	chr1:149718400-149719600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:149718400-149719600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:149718400-149719600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr1:149718400-149719800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr1:149718400-149720000	Active TSS	H9 Cell Line	embryonic stem cell
33	chr1:149718400-149720000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr1:149718400-149720000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:149718600-149718800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:149718600-149718800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:149718600-149718800	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:149718600-149718800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:149718600-149718800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr1:149718600-149718800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:149718600-149718800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
42	chr1:149718600-149718800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:149718600-149718800	Bivalent Enhancer	Fetal Brain Male	brain
44	chr1:149718600-149718800	Bivalent Enhancer	Left Ventricle	heart
45	chr1:149718600-149718800	Enhancers	Right Ventricle	heart
46	chr1:149718600-149718800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
47	chr1:149718600-149719000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
48	chr1:149718600-149719000	Bivalent Enhancer	Primary B cells from cord blood	blood
49	chr1:149718600-149719000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr1:149718600-149719000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum

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