Variant report

Variant	nsv608941
Chromosome Location	chr7:146406379-146759900
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	ATF1	chr7:146424454-146424457	K562	blood:	n/a	n/a
2	ATF1	chr7:146554072-146554083	K562	blood:	n/a	n/a
3	ATF2	chr7:146488761-146489246	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:146488664-146489290	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:146469204-146469208	K562	blood:	n/a	n/a
6	BACH1	chr7:146427038-146427199	K562	blood:	n/a	n/a
7	BCL11A	chr7:146488707-146489095	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr7:146488748-146488970	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr7:146437201-146437466	K562	blood:	n/a	n/a
10	CCNT2	chr7:146463543-146463700	K562	blood:	n/a	n/a
11	CCNT2	chr7:146578068-146578178	K562	blood:	n/a	n/a
12	CEBPB	chr7:146582398-146582629	ECC-1	luminal epithelium:	n/a	chr7:146582542-146582553
13	CEBPB	chr7:146550317-146550587	A549	lung:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
14	CEBPB	chr7:146502234-146502442	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:146487590-146487652	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:146702238-146702507	HepG2	liver:	n/a	chr7:146702320-146702331 chr7:146702320-146702333
17	CEBPB	chr7:146547738-146547759	K562	blood:	n/a	n/a
18	CEBPB	chr7:146645855-146646062	A549	lung:	n/a	n/a
19	CEBPB	chr7:146461096-146461208	HepG2	liver:	n/a	chr7:146461132-146461143
20	CEBPB	chr7:146690433-146690694	H1-hESC	embryonic stem cell:	n/a	chr7:146690555-146690566
21	CEBPB	chr7:146471196-146471467	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:146472308-146472591	IMR90	lung:	n/a	chr7:146472465-146472476
23	CEBPB	chr7:146573237-146573380	HepG2	liver:	n/a	chr7:146573302-146573313
24	CEBPB	chr7:146571872-146572192	A549	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
25	CEBPB	chr7:146690401-146690637	IMR90	lung:	n/a	chr7:146690555-146690566
26	CEBPB	chr7:146571842-146572194	H1-hESC	embryonic stem cell:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
27	CEBPB	chr7:146690455-146690710	HepG2	liver:	n/a	chr7:146690555-146690566
28	CEBPB	chr7:146631955-146632230	A549	lung:	n/a	n/a
29	CEBPB	chr7:146650625-146650798	K562	blood:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
30	CEBPB	chr7:146631945-146632234	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:146571860-146572193	HepG2	liver:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
32	CEBPB	chr7:146653225-146653552	A549	lung:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
33	CEBPB	chr7:146487554-146487672	K562	blood:	n/a	n/a
34	CEBPB	chr7:146547720-146547928	HepG2	liver:	n/a	chr7:146547770-146547781
35	CEBPB	chr7:146571827-146572187	K562	blood:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
36	CEBPB	chr7:146738575-146738797	HepG2	liver:	n/a	chr7:146738715-146738732 chr7:146738754-146738767
37	CEBPB	chr7:146650551-146650805	IMR90	lung:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
38	CEBPB	chr7:146471198-146471404	A549	lung:	n/a	n/a
39	CEBPB	chr7:146471161-146471490	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:146690528-146690601	K562	blood:	n/a	chr7:146690555-146690566
41	CEBPB	chr7:146658691-146659162	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr7:146472354-146472570	HepG2	liver:	n/a	chr7:146472465-146472476
43	CEBPB	chr7:146532369-146532435	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:146653286-146653563	HepG2	liver:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
45	CEBPB	chr7:146571852-146572197	IMR90	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
46	CEBPB	chr7:146550344-146550639	HepG2	liver:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
47	CEBPB	chr7:146673718-146673968	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr7:146488619-146489150	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr7:146488554-146489358	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr7:146658679-146659194	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146489513-146489563	SAEC	small airway:	n/a
2	chr7:146489513-146489563	SAEC	small airway:	n/a
3	chr7:146635353-146635403	SKMC	muscle:	n/a
4	chr7:146484609-146484659	HIPEpiC	eye:	n/a
5	chr7:146484504-146484554	RPTEC	kidney:	n/a
6	chr7:146572638-146572688	K562	blood:	n/a
7	chr7:146484609-146484659	Jurkat	blood:	n/a
8	chr7:146484504-146484554	GM12878	blood:	n/a
9	chr7:146603166-146603216	NHDF-neo	bronchial:	n/a
10	chr7:146484609-146484659	HRCEpiC	kidney:	n/a
11	chr7:146484518-146484568	HRE	kidney:	n/a
12	chr7:146489513-146489563	SKMC	muscle:	n/a
13	chr7:146484609-146484659	CMK	blood:	n/a
14	chr7:146484504-146484554	BJ	skin:	n/a
15	chr7:146635353-146635403	BJ	skin:	n/a
16	chr7:146635353-146635403	HRE	kidney:	n/a
17	chr7:146603166-146603216	IMR90	lung:	fetal
18	chr7:146635353-146635403	ProgFib	skin:	n/a
19	chr7:146484504-146484554	HepG2	liver:	n/a
20	chr7:146484518-146484568	HEK293	kidney:	embryo
21	chr7:146484504-146484554	HNPCEpiC	eye:	n/a
22	chr7:146603166-146603216	HCPEpiC	choroid plexus:	n/a
23	chr7:146484518-146484568	NB4	blood:	n/a
24	chr7:146635353-146635403	MCF-7	breast:	n/a
25	chr7:146603166-146603216	SK-N-SH_RA	brain:	n/a
26	chr7:146635353-146635403	BE2_C	brain:	n/a
27	chr7:146603166-146603216	AG04450	lung:	fetal
28	chr7:146484504-146484554	Hela-S3	cervix:	n/a
29	chr7:146484518-146484568	PFSK-1	brain:	n/a
30	chr7:146484504-146484554	GM12891	blood:	n/a
31	chr7:146484518-146484568	GM06990	blood:	n/a
32	chr7:146484518-146484568	PrEC	prostate:	n/a
33	chr7:146484609-146484659	GM06990	blood:	n/a
34	chr7:146572638-146572688	RPTEC	kidney:	n/a
35	chr7:146484609-146484659	HAEpiC	amniotic membrane:	n/a
36	chr7:146635353-146635403	HepG2	liver:	n/a
37	chr7:146484504-146484554	SK-N-SH	brain:	n/a
38	chr7:146484518-146484568	AG04450	lung:	fetal
39	chr7:146484518-146484568	HCT-116	colon:	n/a
40	chr7:146484504-146484554	NT2-D1	testis:	n/a
41	chr7:146484518-146484568	AG10803	skin:	n/a
42	chr7:146484518-146484568	SAEC	small airway:	n/a
43	chr7:146635353-146635403	GM12892	blood:	n/a
44	chr7:146603166-146603216	Hela-S3	cervix:	n/a
45	chr7:146635353-146635403	HRCEpiC	kidney:	n/a
46	chr7:146572638-146572688	HepG2	liver:	n/a
47	chr7:146603166-146603216	Hepatocyte	liver:	n/a
48	chr7:146489513-146489563	IMR90	lung:	fetal
49	chr7:146484609-146484659	AG09309	skin:	n/a
50	chr7:146484504-146484554	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
2	chr7:146486735..146488259-chr7:146492496..146494438,2	K562	blood:
3	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
4	chr11:86510283..86512929-chr7:146532947..146535829,2	MCF-7	breast:
5	chr7:146498401..146500562-chr7:146505202..146506866,2	K562	blood:
6	chr7:146465957..146468048-chr7:146468672..146471163,2	K562	blood:
7	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
8	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
9	chr7:146465957..146468048-chr7:146468672..146471163,2	K562	blood:
10	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
11	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
12	chr7:146500988..146503359-chr7:146527735..146530660,2	K562	blood:
13	chr7:146498401..146500562-chr7:146505202..146506866,2	K562	blood:
14	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
15	chr7:146486735..146488259-chr7:146492496..146494438,2	K562	blood:
16	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
17	chr7:146500988..146503359-chr7:146527735..146530660,2	K562	blood:
18	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
19	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
20	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
21	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
22	chr7:146479043..146481876-chr7:146483638..146485825,2	K562	blood:
23	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
24	chr7:146479043..146481876-chr7:146483638..146485825,2	K562	blood:
25	chr7:146433613..146434480-chr7:146942002..146942841,3	MCF-7	breast:
26	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
27	chr7:146433750..146434499-chr7:147781098..147781819,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221766	TF binding region
ENSG00000221766	CpG island
ENSG00000150687	chromatin interactions

Extended variants
information (count: 5631 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:5631 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2533096	chr7:146406379-146406380	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6951437	chr7:146406407-146406408	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568152055	chr7:146406414-146406415	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs535595084	chr7:146406466-146406467	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs138716858	chr7:146406476-146406477	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142723028	chr7:146406486-146406487	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs556878165	chr7:146406527-146406528	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs565590020	chr7:146406545-146406546	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs6955893	chr7:146406579-146406580	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543044112	chr7:146406581-146406582	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs369545557	chr7:146406593-146406594	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs563029123	chr7:146406608-146406609	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs182193161	chr7:146406621-146406622	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs549157848	chr7:146406653-146406654	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs147346381	chr7:146406680-146406681	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs2533095	chr7:146406691-146406692	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551351492	chr7:146406714-146406715	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs370986591	chr7:146406717-146406718	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs571584796	chr7:146406764-146406765	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs537418981	chr7:146406869-146406870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551027375	chr7:146406871-146406872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567750567	chr7:146406899-146406900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536700779	chr7:146406913-146406914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370365507	chr7:146406947-146406948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553443787	chr7:146407014-146407015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374521447	chr7:146407057-146407058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138225419	chr7:146407069-146407070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539244595	chr7:146407071-146407072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558965616	chr7:146407081-146407082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575568331	chr7:146407134-146407135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543005455	chr7:146407148-146407149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186863627	chr7:146407223-146407224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572907480	chr7:146407249-146407250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199765100	chr7:146407256-146407257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190754636	chr7:146407283-146407284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73168707	chr7:146407311-146407312	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182624247	chr7:146407336-146407337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528244124	chr7:146407346-146407347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545215280	chr7:146407347-146407348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565159807	chr7:146407390-146407391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530864983	chr7:146407403-146407404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187323295	chr7:146407420-146407421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550988618	chr7:146407428-146407429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73740806	chr7:146407447-146407448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530125946	chr7:146407465-146407466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115051054	chr7:146407467-146407468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144058716	chr7:146407478-146407479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79686326	chr7:146407535-146407536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189836658	chr7:146407559-146407560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs67507935	chr7:146407595-146407596	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:100)

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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146406200-146406400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:146406200-146406400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:146406400-146406800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:146406400-146406800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:146406400-146407000	Enhancers	Fetal Lung	lung
6	chr7:146406400-146407400	Enhancers	Primary hematopoietic stem cells	blood
7	chr7:146406400-146407400	Enhancers	Ovary	ovary
8	chr7:146406400-146407600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr7:146406400-146407800	Enhancers	Stomach Mucosa	stomach
10	chr7:146406600-146407400	Enhancers	Pancreas	Pancrea
11	chr7:146406800-146407400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:146406800-146407400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:146407400-146407800	Weak transcription	Ovary	ovary
14	chr7:146407400-146407800	Weak transcription	Pancreas	Pancrea
15	chr7:146407800-146408200	Enhancers	Ovary	ovary
16	chr7:146407800-146408200	Enhancers	Pancreas	Pancrea
17	chr7:146410800-146417400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:146417000-146417800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:146417000-146417800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:146417400-146417600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:146417600-146417800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:146417800-146422600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr7:146422600-146423200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:146425800-146426400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:146425800-146426400	Enhancers	Fetal Heart	heart
26	chr7:146433400-146433600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:146433600-146433800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:146433800-146438600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:146437600-146438200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
30	chr7:146437600-146438200	ZNF genes & repeats	Aorta	Aorta
31	chr7:146438200-146438800	Enhancers	Fetal Brain Male	brain
32	chr7:146438600-146439000	Enhancers	Fetal Brain Female	brain
33	chr7:146438800-146439200	Weak transcription	Fetal Brain Male	brain
34	chr7:146439000-146439200	Weak transcription	Brain Germinal Matrix	brain
35	chr7:146439200-146439600	Enhancers	Fetal Brain Male	brain
36	chr7:146440200-146440600	Enhancers	Brain Germinal Matrix	brain
37	chr7:146440600-146441800	Weak transcription	Brain Germinal Matrix	brain
38	chr7:146441600-146442200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:146442000-146442200	Enhancers	Brain Germinal Matrix	brain
40	chr7:146461000-146461200	Enhancers	Fetal Brain Male	brain
41	chr7:146461000-146462200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr7:146461400-146462600	Weak transcription	Fetal Brain Male	brain
43	chr7:146462600-146463000	Enhancers	Fetal Brain Male	brain
44	chr7:146463000-146465400	Weak transcription	Fetal Brain Male	brain
45	chr7:146465400-146465600	Enhancers	Fetal Brain Female	brain
46	chr7:146465400-146465800	Enhancers	Pancreas	Pancrea
47	chr7:146465400-146466200	Enhancers	Ovary	ovary
48	chr7:146465400-146467000	Enhancers	Fetal Brain Male	brain
49	chr7:146466200-146466400	Enhancers	Fetal Brain Female	brain
50	chr7:146469200-146469400	Enhancers	Primary hematopoietic stem cells	blood

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