Variant report

Variant	nsv831001
Chromosome Location	chr7:53003534-53152783
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	BACH1	chr7:53118189-53118465	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr7:53053123-53053374	K562	blood:	n/a	n/a
3	CEBPB	chr7:53125637-53125841	HepG2	liver:	n/a	chr7:53125694-53125707
4	CEBPB	chr7:53030413-53030728	A549	lung:	n/a	n/a
5	CEBPB	chr7:53030455-53030731	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr7:53020732-53021027	HepG2	liver:	n/a	chr7:53020864-53020875
7	CEBPB	chr7:53020728-53020955	A549	lung:	n/a	chr7:53020864-53020875
8	CEBPB	chr7:53049612-53049915	HepG2	liver:	n/a	chr7:53049739-53049752 chr7:53049740-53049751 chr7:53049785-53049796
9	CEBPB	chr7:53119101-53119192	K562	blood:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
10	CEBPB	chr7:53030460-53030730	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:53030356-53030814	MCF-7	breast:	n/a	n/a
12	CEBPB	chr7:53020727-53021059	IMR90	lung:	n/a	chr7:53020864-53020875
13	CEBPB	chr7:53118954-53119310	HepG2	liver:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
14	CEBPB	chr7:53101896-53102047	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:53117015-53117347	HepG2	liver:	n/a	chr7:53117164-53117177 chr7:53117164-53117177 chr7:53117164-53117177 chr7:53117164-53117175
16	CEBPB	chr7:53118946-53119288	H1-hESC	embryonic stem cell:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
17	CEBPB	chr7:53125684-53125704	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:53030481-53030703	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:53118958-53119292	IMR90	lung:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
20	CEBPB	chr7:53119013-53119280	A549	lung:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
21	CEBPB	chr7:53049704-53049817	K562	blood:	n/a	chr7:53049739-53049752 chr7:53049740-53049751 chr7:53049785-53049796
22	CTCF	chr7:53066550-53066577	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:53066526-53066644	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:53066557-53066587	Gliobla	brain:	n/a	n/a
25	CTCF	chr7:53066360-53066510	BE2_C	brain:	n/a	n/a
26	CTCF	chr7:53076894-53076954	GM10266	blood:	n/a	n/a
27	CTCF	chr7:53114918-53114945	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr7:53066504-53066534	GM20000	blood:	n/a	n/a
29	CTCF	chr7:53069141-53069216	GM10248	blood:	n/a	n/a
30	CTCF	chr7:53049460-53049610	GM12878	blood:	n/a	n/a
31	CTCF	chr7:53066380-53066530	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr7:53066460-53066610	RPTEC	kidney:	n/a	n/a
33	E2F4	chr7:53137208-53137409	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F6	chr7:53103207-53103394	K562	blood:	n/a	n/a
35	EBF1	chr7:53023106-53023217	GM12878	blood:	n/a	n/a
36	FOS	chr7:53023943-53024513	HUVEC	blood vessel:	n/a	n/a
37	FOS	chr7:53012688-53012888	MCF10A-Er-Src	breast:	n/a	chr7:53012827-53012834 chr7:53012825-53012836 chr7:53012827-53012836
38	FOS	chr7:53088570-53088594	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr7:53138581-53138948	HUVEC	blood vessel:	n/a	chr7:53138779-53138788 chr7:53138773-53138783 chr7:53138772-53138783 chr7:53138768-53138777 chr7:53138773-53138783
40	FOS	chr7:53012432-53013018	HUVEC	blood vessel:	n/a	chr7:53012827-53012834 chr7:53012825-53012836 chr7:53012827-53012836
41	FOSL2	chr7:53012626-53013046	MCF-7	breast:	n/a	chr7:53012827-53012834 chr7:53012827-53012836
42	FOXA1	chr7:53080828-53081117	T-47D	breast:	n/a	n/a
43	FOXA1	chr7:53080829-53081072	T-47D	breast:	n/a	n/a
44	FOXA1	chr7:53111539-53111786	HepG2	liver:	n/a	n/a
45	FOXA2	chr7:53099343-53099706	A549	lung:	n/a	n/a
46	FOXA2	chr7:53099262-53099883	A549	lung:	n/a	n/a
47	GABPA	chr7:53041785-53041837	GM12878	blood:	n/a	n/a
48	GATA2	chr7:53023237-53023856	SH-SY5Y	brain:	n/a	n/a
49	GATA2	chr7:53023054-53024549	HUVEC	blood vessel:	n/a	n/a
50	GATA2	chr7:53026876-53027506	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:53103287-53103337	SK-N-SH_RA	brain:	n/a
2	chr7:53103287-53103337	SK-N-SH_RA	brain:	n/a
3	chr7:53103214-53103264	LNCaP	prostate:	n/a
4	chr7:53103285-53103335	AoSMC	blood vessel:	n/a
5	chr7:53106426-53106476	IMR90	lung:	fetal
6	chr7:53103576-53103626	Hepatocyte	liver:	n/a
7	chr7:53103285-53103335	BE2_C	brain:	n/a
8	chr7:53103310-53103360	AoSMC	blood vessel:	n/a
9	chr7:53103576-53103626	HEEpiC	esophagus:	n/a
10	chr7:53103310-53103360	HEEpiC	esophagus:	n/a
11	chr7:53104336-53104386	MCF-7	breast:	n/a
12	chr7:53103576-53103626	BJ	skin:	n/a
13	chr7:53104001-53104051	SAEC	small airway:	n/a
14	chr7:53103789-53103839	AG04449	skin:	fetal
15	chr7:53099739-53099789	HIPEpiC	eye:	n/a
16	chr7:53102694-53102744	HNPCEpiC	eye:	n/a
17	chr7:53102721-53102771	HUVEC	blood vessel:	n/a
18	chr7:53103576-53103626	A549	lung:	n/a
19	chr7:53104001-53104051	PFSK-1	brain:	n/a
20	chr7:53104001-53104051	NHDF-neo	bronchial:	n/a
21	chr7:53103310-53103360	HCM	heart:	n/a
22	chr7:53106426-53106476	HCF	heart:	n/a
23	chr7:53104001-53104051	SK-N-SH	brain:	n/a
24	chr7:53103214-53103264	HMEC	breast:	n/a
25	chr7:53099739-53099789	SAEC	small airway:	n/a
26	chr7:53103287-53103337	HRPEpiC	eye:	n/a
27	chr7:53104001-53104051	HAEpiC	amniotic membrane:	n/a
28	chr7:53102721-53102771	SAEC	small airway:	n/a
29	chr7:53103285-53103335	Caco-2	colon:	n/a
30	chr7:53103287-53103337	PANC-1	pancreas:	n/a
31	chr7:53106426-53106476	HEK293	kidney:	embryo
32	chr7:53103576-53103626	GM06990	blood:	n/a
33	chr7:53103287-53103337	NHDF-neo	bronchial:	n/a
34	chr7:53103214-53103264	HNPCEpiC	eye:	n/a
35	chr7:53103789-53103839	BJ	skin:	n/a
36	chr7:53102694-53102744	IMR90	lung:	fetal
37	chr7:53103789-53103839	HRCEpiC	kidney:	n/a
38	chr7:53103310-53103360	H1-hESC	embryonic stem cell:	embryo
39	chr7:53104001-53104051	GM19239	blood:	n/a
40	chr7:53103312-53103362	AG04449	skin:	fetal
41	chr7:53104336-53104386	Caco-2	colon:	n/a
42	chr7:53103285-53103335	HCT-116	colon:	n/a
43	chr7:53103789-53103839	GM06990	blood:	n/a
44	chr7:53103789-53103839	MCF-7	breast:	n/a
45	chr7:53103576-53103626	MCF10A-Er-Src	breast:	n/a
46	chr7:53102694-53102744	PFSK-1	brain:	n/a
47	chr7:53103576-53103626	HIPEpiC	eye:	n/a
48	chr7:53103576-53103626	GM12878	blood:	n/a
49	chr7:53103789-53103839	Hepatocyte	liver:	n/a
50	chr7:53102694-53102744	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:53099169..53101604-chr7:53102398..53104340,2	MCF-7	breast:
2	chr1:108671845..108673381-chr7:53151723..53153225,2	MCF-7	breast:
3	chr7:53072533..53075522-chr7:54813629..54815998,2	MCF-7	breast:
4	chr7:53104943..53106770-chr7:53108333..53110312,2	K562	blood:
5	chr19:12903724..12904375-chr7:53082834..53083354,3	Hela-S3	cervix:
6	chr7:53104943..53106770-chr7:53108333..53110312,2	K562	blood:

Variant related genes	Relation type
ENSG00000223970	TF binding region
POM121L12	TF binding region
ENSG00000223970	CpG island
POM121L12	CpG island
ENSG00000221900	chromatin interactions

Extended variants
information (count: 3923 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:3923 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73115305	chr7:53003557-53003558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12718726	chr7:53003564-53003565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs148414069	chr7:53003581-53003582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386713307	chr7:53003596-53003597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11972554	chr7:53003599-53003600	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73351186	chr7:53003634-53003635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79502402	chr7:53003645-53003646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56119115	chr7:53003675-53003676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144039639	chr7:53003678-53003679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185213834	chr7:53003690-53003691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78232124	chr7:53003730-53003731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145977106	chr7:53003760-53003761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569178946	chr7:53003797-53003798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533802110	chr7:53003817-53003818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111763400	chr7:53003827-53003828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190848653	chr7:53003839-53003840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577653680	chr7:53003864-53003865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143391151	chr7:53003966-53003967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151214514	chr7:53003977-53003978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573596075	chr7:53003983-53003984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140394451	chr7:53004002-53004003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562016605	chr7:53004091-53004092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183117996	chr7:53004143-53004144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544383625	chr7:53004162-53004163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564366756	chr7:53004208-53004209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117413741	chr7:53004228-53004229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1919940	chr7:53004261-53004262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs1113062	chr7:53004266-53004267	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551539193	chr7:53004295-53004296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146767520	chr7:53004315-53004316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149972569	chr7:53004333-53004334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12535207	chr7:53004346-53004347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555013587	chr7:53004353-53004354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538178582	chr7:53004406-53004407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371123515	chr7:53004410-53004411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551581268	chr7:53004474-53004475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571399844	chr7:53004475-53004476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375087431	chr7:53004482-53004483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368329998	chr7:53004509-53004510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12537571	chr7:53004524-53004525	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs371637022	chr7:53004672-53004673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12668082	chr7:53004708-53004709	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1689292	chr7:53004725-53004726	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535811500	chr7:53004727-53004728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534670200	chr7:53004733-53004734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555774623	chr7:53004747-53004748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs367998410	chr7:53004761-53004762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145185491	chr7:53004795-53004796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373993186	chr7:53004863-53004864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544550966	chr7:53004879-53004880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
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
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53002600-53004600	Weak transcription	Aorta	Aorta
2	chr7:53004600-53004800	Enhancers	Aorta	Aorta
3	chr7:53004800-53005200	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr7:53004800-53005800	Weak transcription	Aorta	Aorta
5	chr7:53006200-53006800	Enhancers	Placenta	Placenta
6	chr7:53006200-53007800	Enhancers	Placenta Amnion	Placenta Amnion
7	chr7:53006400-53006600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:53006400-53006600	Enhancers	Fetal Muscle Leg	muscle
9	chr7:53006600-53007600	Weak transcription	Fetal Muscle Leg	muscle
10	chr7:53006800-53007200	Weak transcription	Placenta	Placenta
11	chr7:53007200-53007400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:53007200-53007400	Enhancers	Placenta	Placenta
13	chr7:53007400-53008400	Weak transcription	Placenta	Placenta
14	chr7:53007600-53008600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr7:53007600-53009000	Enhancers	Fetal Muscle Leg	muscle
16	chr7:53007800-53009000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr7:53008400-53008600	Enhancers	Aorta	Aorta
18	chr7:53008400-53008800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:53008400-53009000	Enhancers	Placenta	Placenta
20	chr7:53008600-53009200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr7:53008800-53010400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:53009000-53009400	Enhancers	Placenta Amnion	Placenta Amnion
23	chr7:53010400-53010600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:53012200-53013200	Enhancers	HUVEC	blood vessel
25	chr7:53015800-53017200	Enhancers	Fetal Heart	heart
26	chr7:53015800-53018400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:53016000-53017000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:53016000-53017000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr7:53016000-53017000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr7:53016000-53017000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr7:53016000-53017200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr7:53016000-53017400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:53016200-53016800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:53016200-53017200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:53016600-53017200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr7:53016600-53017200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:53016600-53017400	Enhancers	Placenta	Placenta
38	chr7:53016800-53017400	Enhancers	Ovary	ovary
39	chr7:53016800-53023400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:53017200-53023400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:53017200-53026200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:53017200-53026800	Weak transcription	Fetal Heart	heart
43	chr7:53018400-53023400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:53022600-53024000	Enhancers	HUVEC	blood vessel
45	chr7:53022600-53025200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:53023000-53023600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:53023000-53025000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr7:53023000-53031000	Enhancers	Placenta	Placenta
49	chr7:53023200-53023400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:53023200-53024000	Enhancers	Ovary	ovary

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