Variant report

Variant	nsv1034510
Chromosome Location	chr7:146719973-146848581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 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	BACH1	chr7:146796893-146796911	K562	blood:	n/a	n/a
2	BACH1	chr7:146842403-146842603	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:146793808-146794055	GM12878	blood:	n/a	n/a
4	CEBPB	chr7:146769663-146769977	K562	blood:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
5	CEBPB	chr7:146846864-146846986	A549	lung:	n/a	chr7:146846897-146846908
6	CEBPB	chr7:146843108-146843141	K562	blood:	n/a	chr7:146843117-146843130 chr7:146843117-146843128
7	CEBPB	chr7:146830735-146831054	HepG2	liver:	n/a	chr7:146830912-146830923 chr7:146830910-146830927
8	CEBPB	chr7:146769719-146769861	H1-hESC	embryonic stem cell:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
9	CEBPB	chr7:146769619-146769984	HepG2	liver:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
10	CEBPB	chr7:146793958-146794294	HepG2	liver:	n/a	chr7:146794140-146794153 chr7:146794140-146794151
11	CEBPB	chr7:146846869-146846957	HepG2	liver:	n/a	chr7:146846897-146846908
12	CEBPB	chr7:146832319-146832519	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:146738575-146738797	HepG2	liver:	n/a	chr7:146738715-146738732 chr7:146738754-146738767
14	CEBPB	chr7:146769642-146769942	IMR90	lung:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
15	CEBPB	chr7:146846845-146846953	K562	blood:	n/a	chr7:146846897-146846908
16	CEBPB	chr7:146842223-146842579	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:146769642-146769941	A549	lung:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
18	CEBPB	chr7:146794034-146794272	A549	lung:	n/a	chr7:146794140-146794153 chr7:146794140-146794151
19	CEBPZ	chr7:146762179-146762302	HepG2	liver:	n/a	n/a
20	CTBP2	chr7:146842373-146842945	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:146776280-146776430	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr7:146734047-146734118	Medullo	brain:	n/a	n/a
23	CTCF	chr7:146776292-146776414	LNCaP	prostate:	n/a	n/a
24	CTCF	chr7:146733960-146734110	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr7:146776258-146776530	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:146776339-146776472	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:146776300-146776454	Gliobla	brain:	n/a	n/a
28	CTCF	chr7:146733716-146733792	GM20000	blood:	n/a	n/a
29	CTCF	chr7:146811544-146811602	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr7:146788649-146788763	GM10248	blood:	n/a	n/a
31	CTCF	chr7:146776261-146776450	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:146776311-146776454	Fibrobl	skin:	n/a	n/a
33	CTCF	chr7:146810574-146810594	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr7:146737360-146737510	HCFaa	heart:	n/a	n/a
35	CTCF	chr7:146734040-146734190	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:146776360-146776510	GM12869	blood:	n/a	n/a
37	CTCF	chr7:146776268-146776411	Medullo	brain:	n/a	n/a
38	CTCF	chr7:146776340-146776490	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr7:146733980-146734130	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr7:146737380-146737530	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr7:146776280-146776430	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:146830939-146831032	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:146737380-146737530	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr7:146776240-146776390	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:146778616-146778673	Fibrobl	skin:	n/a	n/a
46	CTCF	chr7:146737340-146737490	HEK293	kidney:	n/a	n/a
47	CTCF	chr7:146776200-146776350	NB4	blood:	n/a	n/a
48	CTCF	chr7:146776318-146776419	ProgFib	skin:	n/a	n/a
49	CTCF	chr7:146778633-146778742	GM20000	blood:	n/a	n/a
50	CTCF	chr7:146734040-146734190	HCFaa	heart:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146820536-146820586	HEEpiC	esophagus:	n/a
2	chr7:146820536-146820586	HEEpiC	esophagus:	n/a
3	chr7:146820536-146820586	Hepatocyte	liver:	n/a
4	chr7:146842348-146842398	Caco-2	colon:	n/a
5	chr7:146820536-146820586	HRPEpiC	eye:	n/a
6	chr7:146820536-146820586	CMK	blood:	n/a
7	chr7:146820536-146820586	GM12892	blood:	n/a
8	chr7:146842348-146842398	NT2-D1	testis:	n/a
9	chr7:146820536-146820586	HCM	heart:	n/a
10	chr7:146820536-146820586	T-47D	breast:	n/a
11	chr7:146842348-146842398	HCF	heart:	n/a
12	chr7:146842348-146842398	Hela-S3	cervix:	n/a
13	chr7:146842348-146842398	PFSK-1	brain:	n/a
14	chr7:146842348-146842398	ProgFib	skin:	n/a
15	chr7:146820536-146820586	AG04449	skin:	fetal
16	chr7:146842348-146842398	HMEC	breast:	n/a
17	chr7:146820536-146820586	GM06990	blood:	n/a
18	chr7:146842348-146842398	HEEpiC	esophagus:	n/a
19	chr7:146820536-146820586	ovcar-3	ovarian:	n/a
20	chr7:146842348-146842398	H1-hESC	embryonic stem cell:	embryo
21	chr7:146842348-146842398	GM12892	blood:	n/a
22	chr7:146842348-146842398	HAEpiC	amniotic membrane:	n/a
23	chr7:146842348-146842398	HUVEC	blood vessel:	n/a
24	chr7:146842348-146842398	U87	brain:	n/a
25	chr7:146820536-146820586	GM19239	blood:	n/a
26	chr7:146820536-146820586	HepG2	liver:	n/a
27	chr7:146820536-146820586	BJ	skin:	n/a
28	chr7:146820536-146820586	Caco-2	colon:	n/a
29	chr7:146820536-146820586	HMEC	breast:	n/a
30	chr7:146820536-146820586	LNCaP	prostate:	n/a
31	chr7:146842348-146842398	AG04450	lung:	fetal
32	chr7:146820536-146820586	NHDF-neo	bronchial:	n/a
33	chr7:146842348-146842398	GM12878	blood:	n/a
34	chr7:146820536-146820586	HUVEC	blood vessel:	n/a
35	chr7:146820536-146820586	PANC-1	pancreas:	n/a
36	chr7:146820536-146820586	SAEC	small airway:	n/a
37	chr7:146842348-146842398	HRPEpiC	eye:	n/a
38	chr7:146842348-146842398	HepG2	liver:	n/a
39	chr7:146842348-146842398	BE2_C	brain:	n/a
40	chr7:146820536-146820586	AG09319	gingival:	n/a
41	chr7:146820536-146820586	NB4	blood:	n/a
42	chr7:146842348-146842398	HRCEpiC	kidney:	n/a
43	chr7:146842348-146842398	IMR90	lung:	fetal
44	chr7:146820536-146820586	K562	blood:	n/a
45	chr7:146842348-146842398	HEK293	kidney:	embryo
46	chr7:146820536-146820586	HRCEpiC	kidney:	n/a
47	chr7:146842348-146842398	MCF-7	breast:	n/a
48	chr7:146842348-146842398	Hepatocyte	liver:	n/a
49	chr7:146820536-146820586	SK-N-MC	brain:	n/a
50	chr7:146820536-146820586	Hela-S3	cervix:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
2	chr7:146771218..146771738-chrX:153626554..153627086,2	Hela-S3	cervix:
3	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
4	chr7:146814469..146816823-chr7:146819196..146821242,2	K562	blood:
5	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
6	chr7:146826412..146830203-chr7:146830446..146834436,3	K562	blood:
7	chr7:146826412..146830203-chr7:146830446..146834436,3	K562	blood:
8	chr7:146761282..146763181-chr7:146763573..146765951,2	K562	blood:
9	chr7:146761282..146763181-chr7:146763573..146765951,2	K562	blood:
10	chr7:146814469..146816823-chr7:146819196..146821242,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EZH2-4	chr7:146794524-146794701	ENSG00000236795.1
2	lnc-C7orf33-8	chr7:146843434-146843848	NONHSAT123953
3	lnc-EZH2-4	chr7:146779632-146780313	ENSG00000236795.1
4	lnc-EZH2-4	chr7:146782785-146782914	ENSG00000236795.1
5	lnc-EZH2-4	chr7:146778026-146779180	ENSG00000236795.1

No data

Variant related genes	Relation type
ENSG00000236795	TF binding region
DUTP3	TF binding region
ENSG00000236795	CpG island
DUTP3	CpG island
ENSG00000147403	chromatin interactions

Extended variants
information (count: 2458 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2458 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554363384	chr7:146720011-146720012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574605963	chr7:146720035-146720036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75198391	chr7:146720049-146720050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76314732	chr7:146720053-146720054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576751581	chr7:146720067-146720068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200263536	chr7:146720097-146720098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545645909	chr7:146720129-146720130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185637541	chr7:146720169-146720170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531589997	chr7:146720253-146720254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373773258	chr7:146720266-146720267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376757386	chr7:146720317-146720318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568926380	chr7:146720341-146720342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527750532	chr7:146720348-146720349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375879759	chr7:146720416-146720417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539727027	chr7:146720491-146720492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547694936	chr7:146720522-146720523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190495467	chr7:146720551-146720552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540144185	chr7:146720578-146720579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75235771	chr7:146720611-146720612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62483988	chr7:146720635-146720636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537420458	chr7:146720681-146720682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs56397784	chr7:146720691-146720692	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs574465752	chr7:146720706-146720707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2109305	chr7:146720738-146720739	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553556674	chr7:146720766-146720767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112346580	chr7:146720787-146720788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545733616	chr7:146720804-146720805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562441587	chr7:146720851-146720852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576061046	chr7:146720886-146720887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541873018	chr7:146720953-146720954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544294807	chr7:146721029-146721030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143386547	chr7:146721042-146721043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs118145830	chr7:146721052-146721053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74901004	chr7:146721059-146721060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564707639	chr7:146721093-146721094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147136898	chr7:146721203-146721204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373770644	chr7:146721216-146721217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139648250	chr7:146721258-146721259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570349991	chr7:146721261-146721262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536113724	chr7:146721295-146721296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149744686	chr7:146721306-146721307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568005424	chr7:146721307-146721308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533659476	chr7:146721318-146721319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113963943	chr7:146721358-146721359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144570059	chr7:146721372-146721373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181751128	chr7:146721385-146721386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555632122	chr7:146722202-146722203	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs62483991	chr7:146722234-146722235	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs78889580	chr7:146722235-146722236	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs373026647	chr7:146722269-146722270	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146719200-146721000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:146719200-146721400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr7:146722200-146722400	Active TSS	HSMM	muscle
4	chr7:146722400-146722600	Flanking Active TSS	HSMM	muscle
5	chr7:146730800-146731600	Enhancers	Fetal Lung	lung
6	chr7:146731000-146731600	Enhancers	Ovary	ovary
7	chr7:146741800-146742800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:146742800-146744600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:146744800-146745000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:146746800-146747000	Enhancers	Fetal Kidney	kidney
11	chr7:146749000-146750400	Enhancers	Fetal Lung	lung
12	chr7:146749400-146749600	Enhancers	Fetal Kidney	kidney
13	chr7:146749600-146750200	Weak transcription	Fetal Kidney	kidney
14	chr7:146750200-146750400	Enhancers	Fetal Kidney	kidney
15	chr7:146750400-146753400	Weak transcription	Fetal Lung	lung
16	chr7:146751000-146751400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:146751000-146751400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:146751000-146751400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:146752600-146752800	Enhancers	Gastric	stomach
20	chr7:146753400-146753600	Enhancers	Fetal Lung	lung
21	chr7:146753600-146754200	Weak transcription	Fetal Lung	lung
22	chr7:146754200-146755200	Enhancers	Fetal Lung	lung
23	chr7:146754600-146755000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:146756800-146757800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:146757000-146757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:146757800-146758200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr7:146758200-146758400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr7:146758400-146760200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr7:146759600-146760200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr7:146760200-146760400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr7:146765800-146766200	Enhancers	Fetal Heart	heart
32	chr7:146767000-146767400	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:146767400-146768000	Enhancers	Fetal Lung	lung
34	chr7:146767400-146768800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr7:146767800-146769600	Enhancers	Fetal Kidney	kidney
36	chr7:146768800-146769000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:146768800-146769400	Enhancers	Duodenum Mucosa	Duodenum
38	chr7:146769000-146769200	Enhancers	Pancreas	Pancrea
39	chr7:146769200-146780200	Weak transcription	Pancreas	Pancrea
40	chr7:146769600-146777200	Weak transcription	Fetal Kidney	kidney
41	chr7:146774800-146775600	Enhancers	Fetal Heart	heart
42	chr7:146775200-146776400	Enhancers	Fetal Brain Male	brain
43	chr7:146775600-146775800	Enhancers	Fetal Brain Female	brain
44	chr7:146775800-146778200	Weak transcription	Fetal Brain Female	brain
45	chr7:146776400-146777200	Weak transcription	Fetal Brain Male	brain
46	chr7:146777000-146777200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:146777200-146777400	Enhancers	Fetal Kidney	kidney
48	chr7:146777200-146778800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr7:146777200-146780400	Enhancers	Fetal Brain Male	brain
50	chr7:146778200-146779400	Enhancers	Fetal Brain Female	brain

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