Variant report

Variant	esv1801415
Chromosome Location	chr7:80130554-80149152
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	chr7:80144844-80144963	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:80144664-80145063	MCF-7	breast:	n/a	chr7:80144903-80144914
3	CEBPB	chr7:80142279-80142318	IMR90	lung:	n/a	chr7:80142287-80142298 chr7:80142287-80142296 chr7:80142285-80142298
4	CEBPB	chr7:80144819-80145031	HepG2	liver:	n/a	chr7:80144903-80144914
5	CEBPB	chr7:80145307-80145525	HepG2	liver:	n/a	chr7:80145428-80145440 chr7:80145440-80145451
6	CEBPB	chr7:80144661-80145105	MCF-7	breast:	n/a	chr7:80144903-80144914
7	CEBPB	chr7:80148305-80148467	Hela-S3	cervix:	n/a	chr7:80148367-80148380 chr7:80148367-80148380 chr7:80148369-80148380 chr7:80148369-80148380 chr7:80148367-80148380
8	CEBPB	chr7:80135250-80135976	MCF-7	breast:	n/a	chr7:80135843-80135854
9	CEBPB	chr7:80144060-80144307	HepG2	liver:	n/a	chr7:80144169-80144180
10	CEBPB	chr7:80144067-80144301	IMR90	lung:	n/a	chr7:80144169-80144180
11	CTCF	chr7:80146935-80147045	HepG2	liver:	n/a	n/a
12	CTCF	chr7:80146935-80147013	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:80146860-80147010	HRE	kidney:	n/a	n/a
14	CTCF	chr7:80146953-80147125	GM12878	blood:	n/a	n/a
15	CTCF	chr7:80146960-80147110	HRE	kidney:	n/a	n/a
16	CTCF	chr7:80133369-80133438	Lung_OC	lung:	n/a	n/a
17	CTCF	chr7:80146840-80146990	SAEC	small airway:	n/a	n/a
18	CTCF	chr7:80146860-80147010	HMF	breast:	n/a	n/a
19	CTCF	chr7:80146911-80147043	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:80146945-80147034	NHEK	skin:	n/a	n/a
21	CTCF	chr7:80146900-80147050	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr7:80147766-80147836	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr7:80146891-80147056	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:80146880-80147030	AG09319	gingival:	n/a	n/a
25	CTCF	chr7:80146908-80147049	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:80146307-80146352	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr7:80146800-80146950	BE2_C	brain:	n/a	n/a
28	CTCF	chr7:80146940-80147090	RPTEC	kidney:	n/a	n/a
29	CTCF	chr7:80146900-80147050	RPTEC	kidney:	n/a	n/a
30	CTCF	chr7:80146941-80147027	LNCaP	prostate:	n/a	n/a
31	CTCF	chr7:80146858-80147043	HepG2	liver:	n/a	n/a
32	CTCF	chr7:80146904-80147064	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:80146920-80147070	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr7:80146920-80147070	HRPEpiC	eye:	n/a	n/a
35	E2F4	chr7:80138764-80138896	MCF10A-Er-Src	breast:	n/a	n/a
36	EP300	chr7:80137795-80138026	Hela-S3	cervix:	n/a	chr7:80137917-80137926 chr7:80137916-80137925
37	EP300	chr7:80144225-80145145	T-47D	breast:	n/a	n/a
38	EP300	chr7:80135173-80136058	T-47D	breast:	n/a	n/a
39	EP300	chr7:80135429-80135890	T-47D	breast:	n/a	n/a
40	ESR1	chr7:80135332-80135853	T-47D	breast:	n/a	n/a
41	ESR1	chr7:80135335-80135814	T-47D	breast:	n/a	n/a
42	ESR1	chr7:80135329-80135859	T-47D	breast:	n/a	n/a
43	FOS	chr7:80137633-80138214	HUVEC	blood vessel:	n/a	chr7:80137915-80137927 chr7:80137917-80137926 chr7:80137918-80137925 chr7:80137916-80137926 chr7:80137915-80137926 chr7:80137916-80137925 chr7:80137917-80137925
44	FOS	chr7:80137861-80138016	MCF10A-Er-Src	breast:	n/a	chr7:80137915-80137927 chr7:80137917-80137926 chr7:80137918-80137925 chr7:80137916-80137926 chr7:80137915-80137926 chr7:80137916-80137925 chr7:80137917-80137925
45	FOS	chr7:80137782-80138046	MCF10A-Er-Src	breast:	n/a	chr7:80137915-80137927 chr7:80137917-80137926 chr7:80137918-80137925 chr7:80137916-80137926 chr7:80137915-80137926 chr7:80137916-80137925 chr7:80137917-80137925
46	FOS	chr7:80137864-80138064	MCF10A-Er-Src	breast:	n/a	chr7:80137915-80137927 chr7:80137917-80137926 chr7:80137918-80137925 chr7:80137916-80137926 chr7:80137915-80137926 chr7:80137916-80137925 chr7:80137917-80137925
47	FOS	chr7:80137802-80138013	MCF10A-Er-Src	breast:	n/a	chr7:80137915-80137927 chr7:80137917-80137926 chr7:80137918-80137925 chr7:80137916-80137926 chr7:80137915-80137926 chr7:80137916-80137925 chr7:80137917-80137925
48	FOSL2	chr7:80137615-80138233	SK-N-SH	brain:	n/a	chr7:80137915-80137927 chr7:80137917-80137926 chr7:80137918-80137925 chr7:80137916-80137926 chr7:80137916-80137925 chr7:80137623-80137635 chr7:80137917-80137925
49	FOXA1	chr7:80144655-80144996	T-47D	breast:	n/a	n/a
50	FOXA1	chr7:80135398-80135997	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80142060-80142110	HL-60	blood:	n/a
2	chr7:80142634-80142684	HepG2	liver:	n/a
3	chr7:80142634-80142684	NHDF-neo	bronchial:	n/a
4	chr7:80142634-80142684	MCF10A-Er-Src	breast:	n/a
5	chr7:80142634-80142684	LNCaP	prostate:	n/a
6	chr7:80142060-80142110	RPTEC	kidney:	n/a
7	chr7:80142060-80142110	NT2-D1	testis:	n/a
8	chr7:80142634-80142684	AG04450	lung:	fetal
9	chr7:80142060-80142110	HepG2	liver:	n/a
10	chr7:80142060-80142110	AG09309	skin:	n/a
11	chr7:80142634-80142684	A549	lung:	n/a
12	chr7:80142634-80142684	NHBE	bronchial:	n/a
13	chr7:80142060-80142110	BE2_C	brain:	n/a
14	chr7:80142060-80142110	NH-A	brain:	n/a
15	chr7:80142060-80142110	HRCEpiC	kidney:	n/a
16	chr7:80142060-80142110	HMEC	breast:	n/a
17	chr7:80142060-80142110	NB4	blood:	n/a
18	chr7:80142634-80142684	Caco-2	colon:	n/a
19	chr7:80142060-80142110	Hela-S3	cervix:	n/a
20	chr7:80142634-80142684	H1-hESC	embryonic stem cell:	embryo
21	chr7:80142634-80142684	HCPEpiC	choroid plexus:	n/a
22	chr7:80142634-80142684	HNPCEpiC	eye:	n/a
23	chr7:80142060-80142110	PANC-1	pancreas:	n/a
24	chr7:80142060-80142110	GM12891	blood:	n/a
25	chr7:80142634-80142684	BE2_C	brain:	n/a
26	chr7:80142060-80142110	Caco-2	colon:	n/a
27	chr7:80142634-80142684	NH-A	brain:	n/a
28	chr7:80142634-80142684	IMR90	lung:	fetal
29	chr7:80142060-80142110	A549	lung:	n/a
30	chr7:80142634-80142684	T-47D	breast:	n/a
31	chr7:80142060-80142110	GM12878	blood:	n/a
32	chr7:80142634-80142684	PFSK-1	brain:	n/a
33	chr7:80142634-80142684	AG10803	skin:	n/a
34	chr7:80142634-80142684	ovcar-3	ovarian:	n/a
35	chr7:80142634-80142684	HEK293	kidney:	embryo
36	chr7:80142634-80142684	SAEC	small airway:	n/a
37	chr7:80142060-80142110	AG09319	gingival:	n/a
38	chr7:80142060-80142110	IMR90	lung:	fetal
39	chr7:80142634-80142684	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:80142634-80142684	HCT-116	colon:	n/a
41	chr7:80142634-80142684	AG04449	skin:	fetal
42	chr7:80142060-80142110	NHDF-neo	bronchial:	n/a
43	chr7:80142060-80142110	AG10803	skin:	n/a
44	chr7:80142060-80142110	U87	brain:	n/a
45	chr7:80142060-80142110	SK-N-SH_RA	brain:	n/a
46	chr7:80142634-80142684	GM12892	blood:	n/a
47	chr7:80142634-80142684	NT2-D1	testis:	n/a
48	chr7:80142060-80142110	GM12892	blood:	n/a
49	chr7:80142060-80142110	HCPEpiC	choroid plexus:	n/a
50	chr7:80142634-80142684	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:80139898..80142086-chr7:80143666..80145731,2	MCF-7	breast:
2	chr7:80125854..80128249-chr7:80143744..80146199,2	MCF-7	breast:
3	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
4	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:

Variant related genes	Relation type
GNAT3	TF binding region
GNAT3	CpG island
ENSG00000214415	chromatin interactions

Extended variants
information (count: 702 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530102621	chr7:80130559-80130560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543519722	chr7:80130569-80130570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200198758	chr7:80130669-80130670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563495111	chr7:80130746-80130747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532564983	chr7:80130885-80130886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552537215	chr7:80130929-80130930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568877167	chr7:80130942-80130943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114295875	chr7:80130946-80130947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548133711	chr7:80130979-80130980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568070719	chr7:80131042-80131043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146702459	chr7:80131049-80131050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574341150	chr7:80131108-80131109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536852369	chr7:80131140-80131141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570599296	chr7:80131156-80131157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539624844	chr7:80131226-80131227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552923167	chr7:80131351-80131352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556796933	chr7:80131355-80131356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116112051	chr7:80131373-80131374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371404679	chr7:80131380-80131381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554911643	chr7:80131382-80131383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374033505	chr7:80131408-80131409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574496747	chr7:80131467-80131468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367879507	chr7:80131490-80131491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576744984	chr7:80131504-80131505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182181623	chr7:80131520-80131521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185080790	chr7:80131539-80131540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574209146	chr7:80131550-80131551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148842567	chr7:80131575-80131576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375374700	chr7:80131577-80131578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190767854	chr7:80131578-80131579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576959707	chr7:80131615-80131616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546349137	chr7:80131641-80131642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559711776	chr7:80131711-80131712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369988211	chr7:80131755-80131756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181816893	chr7:80131763-80131764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185329313	chr7:80131771-80131772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147361704	chr7:80131775-80131776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548603737	chr7:80131790-80131791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559327309	chr7:80131807-80131808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10258421	chr7:80131842-80131843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553550579	chr7:80131856-80131857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10258426	chr7:80131858-80131859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546116601	chr7:80131871-80131872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550627794	chr7:80131891-80131892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189691352	chr7:80131924-80131925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561463170	chr7:80131934-80131935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539183198	chr7:80131938-80131939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546741021	chr7:80131958-80131959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530268301	chr7:80132014-80132015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562587200	chr7:80132023-80132024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80126000-80130600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:80129200-80147800	Weak transcription	Left Ventricle	heart
3	chr7:80130000-80137000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr7:80130600-80136800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:80136600-80138600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:80136800-80137000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:80137000-80138200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr7:80137200-80138200	Enhancers	HUVEC	blood vessel
9	chr7:80137200-80138600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:80137400-80138200	Enhancers	NHLF	lung
11	chr7:80137600-80138200	Enhancers	Hela-S3	cervix
12	chr7:80138000-80138400	Enhancers	Ovary	ovary
13	chr7:80138200-80140600	Weak transcription	NHLF	lung
14	chr7:80139400-80139600	Enhancers	Aorta	Aorta
15	chr7:80141000-80142200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:80142200-80142800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr7:80143800-80144800	Enhancers	Fetal Lung	lung
18	chr7:80144400-80146000	Weak transcription	Fetal Intestine Large	intestine
19	chr7:80144400-80147000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:80144400-80147200	Enhancers	Adipose Nuclei	Adipose
21	chr7:80144600-80145000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:80144800-80146800	Weak transcription	Fetal Lung	lung
23	chr7:80145000-80146400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:80145200-80145400	Enhancers	Small Intestine	intestine
25	chr7:80145400-80146400	Weak transcription	Small Intestine	intestine
26	chr7:80146000-80146800	Enhancers	Duodenum Mucosa	Duodenum
27	chr7:80146000-80147000	Enhancers	Fetal Intestine Large	intestine
28	chr7:80146000-80147200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr7:80146000-80147200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr7:80146200-80146400	Enhancers	HSMMtube	muscle
31	chr7:80146200-80147000	Enhancers	Fetal Intestine Small	intestine
32	chr7:80146200-80147000	Enhancers	NHDF-Ad	bronchial
33	chr7:80146200-80147200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr7:80146400-80147000	Enhancers	Fetal Heart	heart
35	chr7:80146400-80147000	Enhancers	Small Intestine	intestine
36	chr7:80146400-80147000	Enhancers	Stomach Mucosa	stomach
37	chr7:80146400-80147000	Enhancers	Spleen	Spleen
38	chr7:80146400-80147200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:80146800-80147000	Enhancers	Placenta	Placenta
40	chr7:80146800-80147400	Enhancers	Fetal Lung	lung
41	chr7:80146800-80149000	Weak transcription	Duodenum Mucosa	Duodenum
42	chr7:80147000-80147600	Weak transcription	Placenta	Placenta
43	chr7:80147000-80151200	Weak transcription	Fetal Intestine Small	intestine
44	chr7:80147000-80151400	Weak transcription	Stomach Mucosa	stomach
45	chr7:80147200-80153000	Weak transcription	Adipose Nuclei	Adipose
46	chr7:80147600-80148400	Enhancers	Placenta	Placenta
47	chr7:80147800-80148000	Enhancers	Left Ventricle	heart
48	chr7:80148000-80151000	Weak transcription	Left Ventricle	heart
49	chr7:80148400-80148800	Weak transcription	Placenta	Placenta
50	chr7:80148800-80150000	Enhancers	Placenta	Placenta

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