Variant report

Variant	nsv1026333
Chromosome Location	chr7:145094377-145283848
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:310)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:145129000-145129298	GM12878	blood:	n/a	n/a
2	BATF	chr7:145129012-145129289	GM12878	blood:	n/a	n/a
3	BHLHE40	chr7:145129000-145129258	GM12878	blood:	n/a	n/a
4	CCNT2	chr7:145241737-145241738	K562	blood:	n/a	n/a
5	CCNT2	chr7:145244891-145245039	K562	blood:	n/a	n/a
6	CEBPB	chr7:145179121-145179439	A549	lung:	n/a	chr7:145179284-145179295
7	CEBPB	chr7:145174454-145174620	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:145179121-145179428	H1-hESC	embryonic stem cell:	n/a	chr7:145179284-145179295
9	CEBPB	chr7:145171454-145171719	A549	lung:	n/a	chr7:145171593-145171604
10	CEBPB	chr7:145250185-145250422	HepG2	liver:	n/a	chr7:145250266-145250277
11	CEBPB	chr7:145247653-145247998	IMR90	lung:	n/a	chr7:145247820-145247831
12	CEBPB	chr7:145171541-145171740	H1-hESC	embryonic stem cell:	n/a	chr7:145171593-145171604
13	CEBPB	chr7:145179116-145179479	HepG2	liver:	n/a	chr7:145179284-145179295
14	CEBPB	chr7:145250158-145250333	K562	blood:	n/a	chr7:145250266-145250277
15	CEBPB	chr7:145247687-145247945	H1-hESC	embryonic stem cell:	n/a	chr7:145247820-145247831
16	CEBPB	chr7:145250186-145250314	H1-hESC	embryonic stem cell:	n/a	chr7:145250266-145250277
17	CEBPB	chr7:145238511-145238707	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:145179174-145179396	K562	blood:	n/a	chr7:145179284-145179295
19	CEBPB	chr7:145171430-145171764	IMR90	lung:	n/a	chr7:145171593-145171604
20	CEBPB	chr7:145247685-145248017	A549	lung:	n/a	chr7:145247820-145247831
21	CEBPB	chr7:145214338-145214495	A549	lung:	n/a	chr7:145214401-145214412 chr7:145214403-145214412
22	CEBPB	chr7:145179108-145179479	IMR90	lung:	n/a	chr7:145179284-145179295
23	CEBPB	chr7:145247654-145247961	HepG2	liver:	n/a	chr7:145247820-145247831
24	CEBPB	chr7:145214381-145214581	HepG2	liver:	n/a	chr7:145214401-145214412 chr7:145214403-145214412
25	CEBPB	chr7:145247694-145247989	K562	blood:	n/a	chr7:145247820-145247831
26	CEBPB	chr7:145250135-145250421	IMR90	lung:	n/a	chr7:145250266-145250277
27	CEBPB	chr7:145171461-145171748	HepG2	liver:	n/a	chr7:145171593-145171604
28	CEBPB	chr7:145250130-145250405	A549	lung:	n/a	chr7:145250266-145250277
29	CEBPB	chr7:145171469-145171729	K562	blood:	n/a	chr7:145171593-145171604
30	CTCF	chr7:145096000-145096150	HCPEpiC	choroid plexus:	n/a	chr7:145096105-145096118
31	CTCF	chr7:145096340-145096490	A549	lung:	n/a	n/a
32	CTCF	chr7:145129780-145129930	GM12864	blood:	n/a	n/a
33	CTCF	chr7:145146487-145146718	T-47D	breast:	n/a	n/a
34	CTCF	chr7:145095980-145096130	HBMEC	blood vessel:	n/a	chr7:145096105-145096118
35	CTCF	chr7:145096040-145096190	HPF	lung:	n/a	chr7:145096105-145096118
36	CTCF	chr7:145112929-145113000	GM10248	blood:	n/a	n/a
37	CTCF	chr7:145096000-145096150	HPF	lung:	n/a	chr7:145096105-145096118
38	CTCF	chr7:145254980-145255130	GM06990	blood:	n/a	n/a
39	CTCF	chr7:145146540-145146690	HMF	breast:	n/a	n/a
40	CTCF	chr7:145146580-145146730	HMF	breast:	n/a	n/a
41	CTCF	chr7:145096020-145096170	HCFaa	heart:	n/a	chr7:145096105-145096118
42	CTCF	chr7:145146520-145146670	HEK293	kidney:	n/a	n/a
43	CTCF	chr7:145144760-145144910	HRE	kidney:	n/a	n/a
44	CTCF	chr7:145146512-145146774	GM12878	blood:	n/a	n/a
45	CTCF	chr7:145163140-145163290	AG10803	skin:	n/a	n/a
46	CTCF	chr7:145135518-145135540	Lung_OC	lung:	n/a	n/a
47	CTCF	chr7:145146592-145146704	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:145282196-145282253	GM20000	blood:	n/a	n/a
49	CTCF	chr7:145096020-145096170	HCPEpiC	choroid plexus:	n/a	chr7:145096105-145096118
50	CTCF	chr7:145146500-145146650	HPF	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145150123-145150173	GM12878	blood:	n/a
2	chr7:145280278-145280328	Hepatocyte	liver:	n/a
3	chr7:145280278-145280328	RPTEC	kidney:	n/a
4	chr7:145280278-145280328	HMEC	breast:	n/a
5	chr7:145280278-145280328	AG04450	lung:	fetal
6	chr7:145280278-145280328	Caco-2	colon:	n/a
7	chr7:145150123-145150173	AoSMC	blood vessel:	n/a
8	chr7:145150123-145150173	HCF	heart:	n/a
9	chr7:145150123-145150173	HCPEpiC	choroid plexus:	n/a
10	chr7:145280278-145280328	SK-N-MC	brain:	n/a
11	chr7:145280278-145280328	SAEC	small airway:	n/a
12	chr7:145280278-145280328	MCF10A-Er-Src	breast:	n/a
13	chr7:145280278-145280328	AG04449	skin:	fetal
14	chr7:145150123-145150173	SKMC	muscle:	n/a
15	chr7:145280278-145280328	HL-60	blood:	n/a
16	chr7:145150123-145150173	RPTEC	kidney:	n/a
17	chr7:145280278-145280328	GM12892	blood:	n/a
18	chr7:145280278-145280328	GM12878	blood:	n/a
19	chr7:145280278-145280328	PFSK-1	brain:	n/a
20	chr7:145280278-145280328	PrEC	prostate:	n/a
21	chr7:145150123-145150173	GM19239	blood:	n/a
22	chr7:145150123-145150173	HIPEpiC	eye:	n/a
23	chr7:145280278-145280328	HUVEC	blood vessel:	n/a
24	chr7:145150123-145150173	GM12891	blood:	n/a
25	chr7:145280278-145280328	HCF	heart:	n/a
26	chr7:145280278-145280328	A549	lung:	n/a
27	chr7:145280278-145280328	AG09319	gingival:	n/a
28	chr7:145150123-145150173	Hela-S3	cervix:	n/a
29	chr7:145280278-145280328	HIPEpiC	eye:	n/a
30	chr7:145280278-145280328	K562	blood:	n/a
31	chr7:145150123-145150173	AG04449	skin:	fetal
32	chr7:145150123-145150173	HCM	heart:	n/a
33	chr7:145280278-145280328	HCT-116	colon:	n/a
34	chr7:145150123-145150173	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:145280278-145280328	Jurkat	blood:	n/a
36	chr7:145280278-145280328	SK-N-SH_RA	brain:	n/a
37	chr7:145150123-145150173	HNPCEpiC	eye:	n/a
38	chr7:145150123-145150173	IMR90	lung:	fetal
39	chr7:145280278-145280328	Hela-S3	cervix:	n/a
40	chr7:145150123-145150173	HMEC	breast:	n/a
41	chr7:145150123-145150173	AG04450	lung:	fetal
42	chr7:145280278-145280328	NH-A	brain:	n/a
43	chr7:145150123-145150173	GM06990	blood:	n/a
44	chr7:145150123-145150173	GM12892	blood:	n/a
45	chr7:145280278-145280328	HRE	kidney:	n/a
46	chr7:145150123-145150173	LNCaP	prostate:	n/a
47	chr7:145280278-145280328	ProgFib	skin:	n/a
48	chr7:145150123-145150173	BE2_C	brain:	n/a
49	chr7:145150123-145150173	AG09309	skin:	n/a
50	chr7:145150123-145150173	AG09319	gingival:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:145219074..145221037-chr7:145221655..145223287,2	K562	blood:
2	chr7:145238372..145239192-chrX:32945954..32946528,2	MCF-7	breast:
3	chr7:145092217..145095000-chr7:145095944..145098182,2	K562	blood:
4	chr7:145158763..145160358-chr7:145164525..145166463,2	K562	blood:
5	chr7:145151878..145154218-chr7:145156730..145158665,2	K562	blood:
6	chr7:145158763..145160358-chr7:145164525..145166463,2	K562	blood:
7	chr7:145132695..145134284-chr7:145149181..145151050,2	K562	blood:
8	chr7:145117531..145119456-chr7:145131833..145134247,2	K562	blood:
9	chr7:145148269..145150358-chr7:145165598..145168422,2	K562	blood:
10	chr7:145207787..145209952-chr7:145212993..145214952,2	K562	blood:
11	chr7:145161705..145165268-chr7:145166298..145169955,3	K562	blood:
12	chr7:145092217..145095000-chr7:145095944..145098182,2	K562	blood:
13	chr7:145152342..145154668-chr7:145163522..145165930,2	K562	blood:
14	chr12:54363693..54365297-chr7:145185991..145188976,2	MCF-7	breast:
15	chr7:145161705..145165268-chr7:145166298..145169955,3	K562	blood:
16	chr7:145164333..145166039-chr7:145187783..145190029,2	K562	blood:
17	chr7:145117531..145119456-chr7:145131833..145134247,2	K562	blood:
18	chr7:145164333..145166039-chr7:145187783..145190029,2	K562	blood:
19	chr7:145148269..145150358-chr7:145165598..145168422,2	K562	blood:
20	chr7:145132695..145134284-chr7:145149181..145151050,2	K562	blood:
21	chr7:145151878..145154218-chr7:145156730..145158665,2	K562	blood:
22	chr7:145219074..145221037-chr7:145221655..145223287,2	K562	blood:
23	chr7:145207787..145209952-chr7:145212993..145214952,2	K562	blood:
24	chr7:145152342..145154668-chr7:145163522..145165930,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP2-6	chr7:145243099-145243518	expReg_chr7_11777_+
2	lnc-CNTNAP2-7	chr7:145177093-145178871	expReg_chr7_11752_+

No data

Variant related genes	Relation type
ENSG00000231839	TF binding region
ENSG00000231839	CpG island

Extended variants
information (count: 1038 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs850344	chr7:145094377-145094378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545935245	chr7:145094400-145094401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566672451	chr7:145094426-145094427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534099884	chr7:145094433-145094434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192480168	chr7:145094454-145094455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570447967	chr7:145094469-145094470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536040505	chr7:145094487-145094488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537469468	chr7:145094518-145094519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76667494	chr7:145094538-145094539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564007560	chr7:145094550-145094551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574232661	chr7:145094553-145094554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11448077	chr7:145094562-145094563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75587102	chr7:145094577-145094578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138850875	chr7:145094610-145094611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554746090	chr7:145094632-145094633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111762579	chr7:145094648-145094649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184741414	chr7:145094655-145094656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113404032	chr7:145094660-145094661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188477578	chr7:145094662-145094663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544316664	chr7:145094704-145094705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562863817	chr7:145094705-145094706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113531828	chr7:145094759-145094760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548658633	chr7:145094761-145094762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147044163	chr7:145094767-145094768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527465272	chr7:145094770-145094771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138530952	chr7:145094774-145094775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570687048	chr7:145094797-145094798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538132704	chr7:145094803-145094804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144059744	chr7:145094826-145094827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74579162	chr7:145094842-145094843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535185522	chr7:145094887-145094888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13225537	chr7:145094899-145094900	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs573407809	chr7:145094926-145094927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534158404	chr7:145094931-145094932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559094052	chr7:145094939-145094940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577509688	chr7:145095022-145095023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538168797	chr7:145095030-145095031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544888945	chr7:145095099-145095100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7791756	chr7:145095124-145095125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574848770	chr7:145095129-145095130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529551684	chr7:145095161-145095162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs578078813	chr7:145095201-145095202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192948347	chr7:145095253-145095254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560594551	chr7:145095288-145095289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201218043	chr7:145095292-145095293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116359839	chr7:145095301-145095302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369501523	chr7:145095306-145095307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551191600	chr7:145095324-145095325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569435207	chr7:145095330-145095331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184751170	chr7:145095341-145095342	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145093000-145094600	Weak transcription	Fetal Lung	lung
2	chr7:145094600-145096400	Enhancers	Fetal Lung	lung
3	chr7:145095000-145096600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:145095000-145096800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:145095800-145096200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:145105600-145108600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:145106000-145106600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:145106800-145107400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:145107400-145108000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr7:145108000-145108200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:145108000-145108400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:145108000-145108400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:145108000-145108600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr7:145118400-145119000	Active TSS	Fetal Heart	heart
15	chr7:145126200-145126600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:145126200-145126800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:145130000-145131200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:145130200-145130400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr7:145131200-145133600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:145143400-145143800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr7:145160000-145160400	Enhancers	Pancreas	Pancrea
22	chr7:145160400-145166400	Weak transcription	Pancreas	Pancrea
23	chr7:145166400-145166800	ZNF genes & repeats	Pancreas	Pancrea
24	chr7:145168400-145169000	Enhancers	Fetal Kidney	kidney
25	chr7:145169000-145171000	Weak transcription	Fetal Kidney	kidney
26	chr7:145170800-145171200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr7:145171000-145171200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:145171000-145171800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:145171000-145171800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr7:145171000-145171800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr7:145171000-145171800	Enhancers	Fetal Kidney	kidney
32	chr7:145171200-145171800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:145171200-145172000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:145171400-145172000	Enhancers	Fetal Lung	lung
35	chr7:145171800-145172000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr7:145175800-145176000	Enhancers	Gastric	stomach
37	chr7:145194800-145195400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:145194800-145195400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:145216600-145218400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr7:145217000-145217600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:145255000-145255200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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