Variant report

Variant	nsv1027520
Chromosome Location	chr7:14905287-15035993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:401)
CpG islands
(count:123)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:14905831-14905873	K562	blood:	n/a	n/a
2	BACH1	chr7:14942659-14942800	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:15035586-15035785	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:14929044-14929078	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr7:14939548-14939801	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:14911740-14911984	HepG2	liver:	n/a	chr7:14911805-14911818
7	CEBPB	chr7:14938661-14939041	Hela-S3	cervix:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
8	CEBPB	chr7:14938711-14939019	HepG2	liver:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
9	CEBPB	chr7:14949720-14949986	H1-hESC	embryonic stem cell:	n/a	chr7:14949816-14949827
10	CEBPB	chr7:14938665-14939042	IMR90	lung:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
11	CEBPB	chr7:14938713-14938985	H1-hESC	embryonic stem cell:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
12	CEBPB	chr7:14938731-14939006	K562	blood:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
13	CEBPB	chr7:14939715-14939885	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:14915086-14915258	A549	lung:	n/a	n/a
15	CEBPB	chr7:14949737-14949944	HepG2	liver:	n/a	chr7:14949816-14949827
16	CEBPB	chr7:14939681-14940006	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:14938706-14938950	A549	lung:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
18	CEBPB	chr7:14949798-14949837	Hela-S3	cervix:	n/a	chr7:14949816-14949827
19	CEBPB	chr7:14938702-14939000	A549	lung:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
20	CEBPD	chr7:14922292-14922606	K562	blood:	n/a	n/a
21	CTBP2	chr7:14942158-14943272	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:14964080-14964230	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr7:14964140-14964290	HMF	breast:	n/a	n/a
24	CTCF	chr7:14964120-14964270	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr7:14964120-14964270	HPF	lung:	n/a	n/a
26	CTCF	chr7:14926300-14926450	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr7:14964160-14964310	AG10803	skin:	n/a	n/a
28	CTCF	chr7:14998280-14998430	SK-N-SH_RA	brain:	n/a	chr7:14998380-14998398 chr7:14998387-14998395
29	CTCF	chr7:14928800-14928950	AG09319	gingival:	n/a	n/a
30	CTCF	chr7:14928900-14929050	AG09319	gingival:	n/a	n/a
31	CTCF	chr7:14964240-14964390	HMEC	breast:	n/a	n/a
32	CTCF	chr7:14963924-14964343	HCT-116	colon:	n/a	n/a
33	CTCF	chr7:15028840-15028990	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:14943020-14943089	Fibrobl	skin:	n/a	n/a
35	CTCF	chr7:14964520-14964670	AG10803	skin:	n/a	n/a
36	CTCF	chr7:14964108-14964368	IMR90	lung:	n/a	n/a
37	CTCF	chr7:14964141-14964305	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr7:14964140-14964290	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr7:15001180-15001330	GM12866	blood:	n/a	n/a
40	CTCF	chr7:14964160-14964310	BJ	skin:	n/a	n/a
41	CTCF	chr7:14964080-14964230	HCM	heart:	n/a	n/a
42	CTCF	chr7:14964120-14964270	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr7:14928865-14928924	ProgFib	skin:	n/a	n/a
44	CTCF	chr7:15028940-15029090	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:14964280-14964430	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr7:14998320-14998470	HPAF	blood vessel:	n/a	chr7:14998380-14998398 chr7:14998387-14998395
47	CTCF	chr7:14980184-14980214	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr7:14928760-14928910	AG10803	skin:	n/a	n/a
49	CTCF	chr7:14964180-14964330	AG09319	gingival:	n/a	n/a
50	CTCF	chr7:14964120-14964270	AG09309	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14942359-14942409	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:14942359-14942409	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:14942359-14942409	SK-N-MC	brain:	n/a
4	chr7:14942815-14942865	HCM	heart:	n/a
5	chr7:14942815-14942865	IMR90	lung:	fetal
6	chr7:14942815-14942865	ProgFib	skin:	n/a
7	chr7:14942815-14942865	GM12891	blood:	n/a
8	chr7:14942815-14942865	PrEC	prostate:	n/a
9	chr7:14942815-14942865	NHBE	bronchial:	n/a
10	chr7:14942359-14942409	HMEC	breast:	n/a
11	chr7:14942815-14942865	AG04449	skin:	fetal
12	chr7:14942815-14942865	H1-hESC	embryonic stem cell:	embryo
13	chr7:14942815-14942865	SK-N-SH_RA	brain:	n/a
14	chr7:14942359-14942409	HAEpiC	amniotic membrane:	n/a
15	chr7:14942359-14942409	AoSMC	blood vessel:	n/a
16	chr7:14942815-14942865	PFSK-1	brain:	n/a
17	chr7:14942815-14942865	HepG2	liver:	n/a
18	chr7:14942815-14942865	GM12892	blood:	n/a
19	chr7:14942815-14942865	HRCEpiC	kidney:	n/a
20	chr7:14942815-14942865	HEK293	kidney:	embryo
21	chr7:14942359-14942409	HCT-116	colon:	n/a
22	chr7:14942359-14942409	HNPCEpiC	eye:	n/a
23	chr7:14942815-14942865	AoSMC	blood vessel:	n/a
24	chr7:14942815-14942865	CMK	blood:	n/a
25	chr7:14942359-14942409	Hela-S3	cervix:	n/a
26	chr7:14942815-14942865	A549	lung:	n/a
27	chr7:14942359-14942409	NT2-D1	testis:	n/a
28	chr7:14942359-14942409	HL-60	blood:	n/a
29	chr7:14942359-14942409	GM06990	blood:	n/a
30	chr7:14942359-14942409	RPTEC	kidney:	n/a
31	chr7:14942359-14942409	GM12892	blood:	n/a
32	chr7:14942815-14942865	GM06990	blood:	n/a
33	chr7:14942359-14942409	NHBE	bronchial:	n/a
34	chr7:14942359-14942409	HUVEC	blood vessel:	n/a
35	chr7:14942359-14942409	ProgFib	skin:	n/a
36	chr7:14942815-14942865	AG10803	skin:	n/a
37	chr7:14942359-14942409	AG04450	lung:	fetal
38	chr7:14942815-14942865	Caco-2	colon:	n/a
39	chr7:14942359-14942409	AG10803	skin:	n/a
40	chr7:14942815-14942865	AG04450	lung:	fetal
41	chr7:14942815-14942865	K562	blood:	n/a
42	chr7:14942359-14942409	HEK293	kidney:	embryo
43	chr7:14942815-14942865	RPTEC	kidney:	n/a
44	chr7:14942359-14942409	Caco-2	colon:	n/a
45	chr7:14942815-14942865	SK-N-MC	brain:	n/a
46	chr7:14942359-14942409	SK-N-SH_RA	brain:	n/a
47	chr7:14942815-14942865	MCF-7	breast:	n/a
48	chr7:14942815-14942865	HCPEpiC	choroid plexus:	n/a
49	chr7:14942815-14942865	GM12878	blood:	n/a
50	chr7:14942815-14942865	HUVEC	blood vessel:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:14958102..14960838-chr7:14962374..14965166,2	K562	blood:
2	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
3	chr7:15002300..15004911-chr7:15009747..15012507,2	MCF-7	breast:
4	chr7:15002300..15004911-chr7:15009747..15012507,2	MCF-7	breast:
5	chr7:15003480..15005257-chr7:15044429..15047091,2	K562	blood:
6	chr7:14995312..14997683-chr7:15009030..15011950,2	K562	blood:
7	chr7:14958102..14960838-chr7:14962374..14965166,2	K562	blood:
8	chr7:14995312..14997683-chr7:15009030..15011950,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DGKB-1	chr7:15025003-15025699	NONHSAT119271

No data

Variant related genes	Relation type
DGKB	TF binding region
ENSG00000225816	TF binding region
DGKB	CpG island
ENSG00000225816	CpG island

Extended variants
information (count: 2505 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2505 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569946365	chr7:14908223-14908224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6966249	chr7:14908240-14908241	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs367749079	chr7:14908242-14908243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568692323	chr7:14908261-14908262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113881836	chr7:14908367-14908368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535923590	chr7:14908378-14908379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139861684	chr7:14908383-14908384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566058283	chr7:14908391-14908392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7802899	chr7:14908409-14908410	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs75218876	chr7:14908528-14908529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192854506	chr7:14908566-14908567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565726338	chr7:14908580-14908581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184827477	chr7:14908588-14908589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539375246	chr7:14911000-14911001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs170093	chr7:14911020-14911021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146057055	chr7:14911022-14911023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544369677	chr7:14911034-14911035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561391627	chr7:14911100-14911101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369715411	chr7:14911108-14911109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs217558	chr7:14911110-14911111	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs217559	chr7:14911119-14911120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs58737612	chr7:14911124-14911125	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532261652	chr7:14911179-14911180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552083903	chr7:14911180-14911181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190711789	chr7:14911182-14911183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367893030	chr7:14911192-14911193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548094352	chr7:14911229-14911230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111902716	chr7:14911250-14911251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568102529	chr7:14911257-14911258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533673382	chr7:14911298-14911299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547382791	chr7:14911309-14911310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138832143	chr7:14911331-14911332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs61231693	chr7:14911369-14911370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115997759	chr7:14915634-14915635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551892204	chr7:14915660-14915661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117644430	chr7:14915666-14915667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569210647	chr7:14915671-14915672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73287411	chr7:14915702-14915703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574243475	chr7:14915726-14915727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546988561	chr7:14915756-14915757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193262615	chr7:14915793-14915794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10236088	chr7:14915830-14915831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143975574	chr7:14915838-14915839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372175979	chr7:14915840-14915841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537873462	chr7:14915842-14915843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545511214	chr7:14915869-14915870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565340385	chr7:14915911-14915912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575670092	chr7:14915942-14915943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113443721	chr7:14915967-14915968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370594623	chr7:14915977-14915978	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14908200-14908600	Enhancers	Placenta Amnion	Placenta Amnion
2	chr7:14911000-14911400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:14915600-14916000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:14919000-14919800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:14919600-14920000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr7:14921000-14921400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr7:14921000-14921400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:14925600-14928200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:14926200-14927000	Enhancers	Brain Anterior Caudate	brain
10	chr7:14926800-14927200	Enhancers	Brain Cingulate Gyrus	brain
11	chr7:14927000-14928600	Weak transcription	Brain Anterior Caudate	brain
12	chr7:14927800-14929200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:14927800-14929200	Enhancers	Osteobl	bone
14	chr7:14928000-14928400	Enhancers	Colon Smooth Muscle	Colon
15	chr7:14928000-14929200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:14928200-14929000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:14928600-14929000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:14928600-14929000	Enhancers	Brain Anterior Caudate	brain
19	chr7:14928600-14929000	Enhancers	Psoas Muscle	Psoas
20	chr7:14928600-14929200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:14928600-14929200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:14928600-14929200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr7:14928800-14929000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr7:14928800-14929200	Enhancers	Rectal Smooth Muscle	rectum
25	chr7:14929000-14929600	Weak transcription	Brain Anterior Caudate	brain
26	chr7:14929000-14938800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:14929000-14940800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr7:14929200-14930200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:14929200-14935000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr7:14929200-14940800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:14930200-14930400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:14930400-14931000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:14931000-14931200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:14932800-14933000	Enhancers	HUVEC	blood vessel
35	chr7:14933000-14934000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:14933000-14934000	Weak transcription	HUVEC	blood vessel
37	chr7:14934000-14934600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:14934000-14934800	Enhancers	HUVEC	blood vessel
39	chr7:14934600-14935200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr7:14935000-14935800	Enhancers	Rectal Smooth Muscle	rectum
41	chr7:14935200-14940600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:14935800-14938400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr7:14937800-14938400	Active TSS	Brain Anterior Caudate	brain
44	chr7:14938200-14938400	Enhancers	Right Atrium	heart
45	chr7:14938200-14938600	Enhancers	Fetal Lung	lung
46	chr7:14938200-14939200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:14938400-14938600	Enhancers	Rectal Smooth Muscle	rectum
48	chr7:14938400-14938800	Enhancers	Osteobl	bone
49	chr7:14938400-14939200	Weak transcription	Brain Anterior Caudate	brain
50	chr7:14938400-14939400	Enhancers	Colon Smooth Muscle	Colon

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