Variant report

Variant	nsv608927
Chromosome Location	chr7:145803095-145882001
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	chr7:145878136-145878188	K562	blood:	n/a	n/a
2	BACH1	chr7:145812851-145813178	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:145813392-145814179	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:145842137-145842377	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:145845611-145845615	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:145824603-145824809	K562	blood:	n/a	chr7:145824732-145824741 chr7:145824733-145824742 chr7:145824732-145824741
7	BHLHE40	chr7:145812888-145813075	K562	blood:	n/a	n/a
8	CBX3	chr7:145812824-145813236	K562	blood:	n/a	n/a
9	CBX3	chr7:145812871-145813165	K562	blood:	n/a	n/a
10	CCNT2	chr7:145813815-145814042	K562	blood:	n/a	n/a
11	CCNT2	chr7:145808087-145808172	K562	blood:	n/a	n/a
12	CCNT2	chr7:145838134-145838337	K562	blood:	n/a	n/a
13	CCNT2	chr7:145813050-145813510	K562	blood:	n/a	n/a
14	CEBPB	chr7:145872821-145873202	MCF-7	breast:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
15	CEBPB	chr7:145881435-145881595	A549	lung:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
16	CEBPB	chr7:145872838-145873169	A549	lung:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
17	CEBPB	chr7:145838886-145839016	A549	lung:	n/a	chr7:145838922-145838931 chr7:145838921-145838932 chr7:145838920-145838931
18	CEBPB	chr7:145816237-145816462	HepG2	liver:	n/a	chr7:145816401-145816412
19	CEBPB	chr7:145847394-145847598	HepG2	liver:	n/a	chr7:145847573-145847590 chr7:145847576-145847589
20	CEBPB	chr7:145881370-145881627	HepG2	liver:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
21	CEBPB	chr7:145872819-145873166	HepG2	liver:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
22	CEBPB	chr7:145881325-145881626	IMR90	lung:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
23	CEBPB	chr7:145838848-145839167	HepG2	liver:	n/a	chr7:145838922-145838931 chr7:145838921-145838932 chr7:145838920-145838931
24	CEBPB	chr7:145818808-145819059	K562	blood:	n/a	chr7:145818945-145818958
25	CEBPB	chr7:145850014-145850299	HepG2	liver:	n/a	chr7:145850146-145850157
26	CEBPB	chr7:145850024-145850278	A549	lung:	n/a	chr7:145850146-145850157
27	CEBPB	chr7:145881484-145881582	H1-hESC	embryonic stem cell:	n/a	chr7:145881497-145881508 chr7:145881496-145881507 chr7:145881498-145881507
28	CEBPB	chr7:145872800-145873072	H1-hESC	embryonic stem cell:	n/a	chr7:145872971-145872982 chr7:145872971-145872984 chr7:145873001-145873012
29	CHD1	chr7:145812804-145813353	H1-hESC	embryonic stem cell:	n/a	chr7:145813043-145813053
30	CHD2	chr7:145813014-145813128	K562	blood:	n/a	chr7:145813043-145813053
31	CHD2	chr7:145812779-145814147	H1-hESC	embryonic stem cell:	n/a	chr7:145813043-145813053
32	CHD2	chr7:145825258-145825274	GM12878	blood:	n/a	n/a
33	CTBP2	chr7:145812742-145814278	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:145828960-145829110	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr7:145816200-145816350	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr7:145872980-145873130	HPF	lung:	n/a	n/a
37	CTCF	chr7:145828920-145829070	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr7:145824210-145824531	K562	blood:	n/a	n/a
39	CTCF	chr7:145826449-145826649	Medullo	brain:	n/a	n/a
40	CTCF	chr7:145812900-145813050	HAc	cerebellar:	n/a	n/a
41	CTCF	chr7:145812880-145813030	AG09319	gingival:	n/a	n/a
42	CTCF	chr7:145873020-145873170	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr7:145813920-145814070	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr7:145869380-145869530	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:145867222-145867267	GM13976	blood:	n/a	n/a
46	CTCF	chr7:145872920-145873070	HEK293	kidney:	n/a	n/a
47	CTCF	chr7:145869380-145869530	Caco-2	colon:	n/a	n/a
48	CTCF	chr7:145869370-145869549	GM12878	blood:	n/a	n/a
49	CTCF	chr7:145824348-145824444	K562	blood:	n/a	n/a
50	CTCF	chr7:145812880-145813030	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145813008-145813058	HAEpiC	amniotic membrane:	n/a
2	chr7:145813008-145813058	HAEpiC	amniotic membrane:	n/a
3	chr7:145812842-145812892	GM12892	blood:	n/a
4	chr7:145813432-145813482	HAEpiC	amniotic membrane:	n/a
5	chr7:145813413-145813463	HRCEpiC	kidney:	n/a
6	chr7:145812871-145812921	AG04449	skin:	fetal
7	chr7:145813432-145813482	AG10803	skin:	n/a
8	chr7:145814306-145814356	SK-N-SH_RA	brain:	n/a
9	chr7:145813915-145813965	HMEC	breast:	n/a
10	chr7:145813066-145813116	HCF	heart:	n/a
11	chr7:145812871-145812921	RPTEC	kidney:	n/a
12	chr7:145813031-145813081	HUVEC	blood vessel:	n/a
13	chr7:145812871-145812921	HUVEC	blood vessel:	n/a
14	chr7:145814152-145814202	HRPEpiC	eye:	n/a
15	chr7:145813066-145813116	AG09319	gingival:	n/a
16	chr7:145813437-145813487	HRCEpiC	kidney:	n/a
17	chr7:145813066-145813116	PFSK-1	brain:	n/a
18	chr7:145813008-145813058	PANC-1	pancreas:	n/a
19	chr7:145814152-145814202	HEK293	kidney:	embryo
20	chr7:145813432-145813482	BE2_C	brain:	n/a
21	chr7:145813008-145813058	HIPEpiC	eye:	n/a
22	chr7:145813437-145813487	HEK293	kidney:	embryo
23	chr7:145813432-145813482	RPTEC	kidney:	n/a
24	chr7:145813494-145813544	GM12878	blood:	n/a
25	chr7:145814003-145814053	HRE	kidney:	n/a
26	chr7:145813946-145813996	PrEC	prostate:	n/a
27	chr7:145813494-145813544	HNPCEpiC	eye:	n/a
28	chr7:145813946-145813996	NB4	blood:	n/a
29	chr7:145813413-145813463	T-47D	breast:	n/a
30	chr7:145812842-145812892	HAEpiC	amniotic membrane:	n/a
31	chr7:145813417-145813467	HCPEpiC	choroid plexus:	n/a
32	chr7:145814152-145814202	IMR90	lung:	fetal
33	chr7:145813437-145813487	GM19239	blood:	n/a
34	chr7:145813417-145813467	HAEpiC	amniotic membrane:	n/a
35	chr7:145814306-145814356	A549	lung:	n/a
36	chr7:145813432-145813482	Hepatocyte	liver:	n/a
37	chr7:145813946-145813996	ovcar-3	ovarian:	n/a
38	chr7:145813066-145813116	MCF-7	breast:	n/a
39	chr7:145813031-145813081	ProgFib	skin:	n/a
40	chr7:145813417-145813467	GM12878	blood:	n/a
41	chr7:145813432-145813482	BJ	skin:	n/a
42	chr7:145813031-145813081	CMK	blood:	n/a
43	chr7:145813915-145813965	ovcar-3	ovarian:	n/a
44	chr7:145813946-145813996	HRE	kidney:	n/a
45	chr7:145814152-145814202	GM12892	blood:	n/a
46	chr7:145813031-145813081	AG04449	skin:	fetal
47	chr7:145813915-145813965	NHBE	bronchial:	n/a
48	chr7:145813031-145813081	A549	lung:	n/a
49	chr7:145812871-145812921	NB4	blood:	n/a
50	chr7:145812842-145812892	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:118909733..118910708-chr7:145816212..145816735,2	MCF-7	breast:
2	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
3	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
4	chr7:145800703..145803223-chr7:145808125..145812343,3	K562	blood:
5	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:
6	chr7:145806708..145809039-chr7:145812340..145814652,2	K562	blood:
7	chr7:145794339..145796121-chr7:145802069..145803645,2	K562	blood:
8	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
9	chr7:145816235..145818075-chr7:145818635..145820633,2	K562	blood:
10	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
11	chr7:145800703..145803223-chr7:145808125..145812343,3	K562	blood:
12	chr7:145816235..145818075-chr7:145818635..145820633,2	K562	blood:
13	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:
14	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
15	chr7:145782508..145785032-chr7:145801785..145804184,2	K562	blood:

Variant related genes	Relation type
CNTNAP2	TF binding region
CNTNAP2	CpG island
ENSG00000174469	chromatin interactions

Extended variants
information (count: 1191 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1191 , 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	rs567160949	chr7:145806711-145806712	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs34365721	chr7:145806761-145806762	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1526075	chr7:145806780-145806781	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs56844364	chr7:145806799-145806800	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35451295	chr7:145806817-145806818	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs73452010	chr7:145806865-145806866	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544290154	chr7:145806882-145806883	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531026459	chr7:145806966-145806967	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549587274	chr7:145806977-145806978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370141634	chr7:145806988-145806989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115848301	chr7:145806998-145806999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190633176	chr7:145807014-145807015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138047481	chr7:145807028-145807029	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374476407	chr7:145807029-145807030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571313067	chr7:145807043-145807044	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538621831	chr7:145807099-145807100	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556854217	chr7:145807106-145807107	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182466649	chr7:145807107-145807108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114323934	chr7:145807168-145807169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554797863	chr7:145807187-145807188	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145308274	chr7:145807225-145807226	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540337745	chr7:145807232-145807233	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538886755	chr7:145807294-145807295	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555986343	chr7:145807356-145807357	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs578099547	chr7:145807370-145807371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs144988426	chr7:145807406-145807407	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs553492314	chr7:145807412-145807413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562328235	chr7:145807427-145807428	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2692359	chr7:145807447-145807448	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs187846549	chr7:145807461-145807462	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191163471	chr7:145807482-145807483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182950225	chr7:145807502-145807503	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187414778	chr7:145807643-145807644	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571374192	chr7:145807685-145807686	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532457644	chr7:145807693-145807694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35065825	chr7:145807774-145807775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550983108	chr7:145807779-145807780	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149094499	chr7:145807786-145807787	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117505769	chr7:145807861-145807862	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7791053	chr7:145807864-145807865	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143283601	chr7:145807876-145807877	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs151286074	chr7:145807900-145807901	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558699855	chr7:145807919-145807920	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs544838411	chr7:145807946-145807947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116244502	chr7:145807965-145807966	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs193169189	chr7:145808004-145808005	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560698721	chr7:145808013-145808014	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527977224	chr7:145808027-145808028	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543383618	chr7:145808071-145808072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs117104902	chr7:145808083-145808084	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145812000-145812600	Enhancers	Brain Germinal Matrix	brain
2	chr7:145812000-145813600	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr7:145812200-145812600	Enhancers	Fetal Brain Male	brain
4	chr7:145812200-145813600	Active TSS	Brain Anterior Caudate	brain
5	chr7:145812200-145815200	Active TSS	Brain Angular Gyrus	brain
6	chr7:145812400-145812600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:145812400-145812600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr7:145812400-145812600	Enhancers	Fetal Lung	lung
9	chr7:145812400-145812800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:145812400-145813600	Active TSS	Brain Hippocampus Middle	brain
11	chr7:145812400-145815200	Active TSS	Fetal Brain Female	brain
12	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
13	chr7:145812600-145812800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:145812600-145812800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
16	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
17	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
18	chr7:145812600-145812800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:145812600-145812800	Enhancers	Primary hematopoietic stem cells	blood
20	chr7:145812600-145812800	Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr7:145812600-145812800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr7:145812600-145812800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:145812600-145812800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:145812600-145812800	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr7:145812600-145812800	Flanking Active TSS	Brain Substantia Nigra	brain
27	chr7:145812600-145812800	Enhancers	Fetal Heart	heart
28	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
29	chr7:145812600-145812800	Enhancers	Fetal Muscle Trunk	muscle
30	chr7:145812600-145812800	Enhancers	Fetal Muscle Leg	muscle
31	chr7:145812600-145812800	Active TSS	Fetal Stomach	stomach
32	chr7:145812600-145812800	Enhancers	Ovary	ovary
33	chr7:145812600-145812800	Enhancers	Pancreas	Pancrea
34	chr7:145812600-145813000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:145812600-145813000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:145812600-145813000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:145812600-145813000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:145812600-145813000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:145812600-145813000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr7:145812600-145813000	Flanking Active TSS	Fetal Lung	lung
41	chr7:145812600-145813000	Bivalent Enhancer	Fetal Thymus	thymus
42	chr7:145812600-145813400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:145812600-145813400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:145812600-145813400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:145812600-145813800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr7:145812600-145814000	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr7:145812600-145814000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:145812600-145814000	Active TSS	Brain Cingulate Gyrus	brain
49	chr7:145812600-145814000	Active TSS	Fetal Brain Male	brain
50	chr7:145812600-145814200	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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