Variant report

Variant	nsv830997
Chromosome Location	chr7:49970866-50136498
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	ATF2	chr7:50132096-50132517	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:50132116-50132482	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:50132077-50132532	GM12878	blood:	n/a	n/a
4	ATF2	chr7:50132134-50132712	GM12878	blood:	n/a	n/a
5	BACH1	chr7:50132228-50132460	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:50109241-50109490	GM12878	blood:	n/a	n/a
7	BATF	chr7:50095738-50096022	GM12878	blood:	n/a	n/a
8	BATF	chr7:50095721-50096024	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:50095744-50096030	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:50108699-50108959	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr7:50132671-50133087	GM12878	blood:	n/a	chr7:50132911-50132920 chr7:50132858-50132867
12	BCLAF1	chr7:50132613-50133116	GM12878	blood:	n/a	chr7:50132911-50132920 chr7:50132858-50132867
13	BHLHE40	chr7:50109143-50109472	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:50109240-50109553	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:50132129-50132627	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:50026408-50026538	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr7:50132130-50132330	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr7:50108871-50109076	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr7:50112750-50112962	K562	blood:	n/a	n/a
20	CBX3	chr7:50112675-50113043	HCT-116	colon:	n/a	n/a
21	CBX3	chr7:50112692-50112992	K562	blood:	n/a	n/a
22	CCNT2	chr7:50132516-50132849	K562	blood:	n/a	n/a
23	CEBPB	chr7:50120232-50120515	A549	lung:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
24	CEBPB	chr7:50018505-50018705	HepG2	liver:	n/a	chr7:50018636-50018647
25	CEBPB	chr7:50013664-50013954	A549	lung:	n/a	chr7:50013814-50013825
26	CEBPB	chr7:50132187-50132489	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:50099216-50099263	HepG2	liver:	n/a	chr7:50099242-50099253
28	CEBPB	chr7:50109388-50109601	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:50120314-50120495	MCF-7	breast:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
30	CEBPB	chr7:50013644-50013995	IMR90	lung:	n/a	chr7:50013814-50013825
31	CEBPB	chr7:50132186-50132450	MCF-7	breast:	n/a	n/a
32	CEBPB	chr7:50120265-50120552	A549	lung:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
33	CEBPB	chr7:50120256-50120566	K562	blood:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
34	CEBPB	chr7:50013696-50013962	K562	blood:	n/a	chr7:50013814-50013825
35	CEBPB	chr7:50099108-50099372	IMR90	lung:	n/a	chr7:50099242-50099253
36	CEBPB	chr7:50128623-50128751	HepG2	liver:	n/a	chr7:50128682-50128693
37	CEBPB	chr7:50120306-50120582	MCF-7	breast:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
38	CEBPB	chr7:50120262-50120564	IMR90	lung:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
39	CEBPB	chr7:50102631-50102785	K562	blood:	n/a	n/a
40	CEBPB	chr7:50108729-50109601	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:50128605-50128805	A549	lung:	n/a	chr7:50128682-50128693
42	CEBPB	chr7:49977309-49977509	A549	lung:	n/a	n/a
43	CEBPB	chr7:50013652-50013985	HepG2	liver:	n/a	chr7:50013814-50013825
44	CEBPB	chr7:50025619-50025716	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:50127936-50127982	A549	lung:	n/a	n/a
46	CEBPB	chr7:50120298-50120462	HepG2	liver:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
47	CEBPB	chr7:50120230-50120597	HepG2	liver:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
48	CEBPD	chr7:50102608-50102885	K562	blood:	n/a	n/a
49	CHD1	chr7:50132232-50132445	GM12878	blood:	n/a	n/a
50	CHD2	chr7:50132231-50132693	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50078531-50078581	A549	lung:	n/a
2	chr7:50133100-50133150	PrEC	prostate:	n/a
3	chr7:50132977-50133027	NHBE	bronchial:	n/a
4	chr7:50133131-50133181	SK-N-SH_RA	brain:	n/a
5	chr7:50109467-50109517	Caco-2	colon:	n/a
6	chr7:50133024-50133074	HCM	heart:	n/a
7	chr7:50133000-50133050	GM12891	blood:	n/a
8	chr7:50133131-50133181	HL-60	blood:	n/a
9	chr7:50133100-50133150	IMR90	lung:	fetal
10	chr7:50132764-50132814	Jurkat	blood:	n/a
11	chr7:50133100-50133150	GM12891	blood:	n/a
12	chr7:50132975-50133025	ECC-1	luminal epithelium:	n/a
13	chr7:50132977-50133027	Caco-2	colon:	n/a
14	chr7:50133212-50133262	HIPEpiC	eye:	n/a
15	chr7:50132573-50132623	HRPEpiC	eye:	n/a
16	chr7:50133131-50133181	LNCaP	prostate:	n/a
17	chr7:50133100-50133150	HRCEpiC	kidney:	n/a
18	chr7:50132975-50133025	SK-N-SH	brain:	n/a
19	chr7:50132573-50132623	HL-60	blood:	n/a
20	chr7:50108936-50108986	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:50108936-50108986	HEK293	kidney:	embryo
22	chr7:50133212-50133262	Hela-S3	cervix:	n/a
23	chr7:50132764-50132814	MCF10A-Er-Src	breast:	n/a
24	chr7:50136102-50136152	SK-N-MC	brain:	n/a
25	chr7:50133212-50133262	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:50133212-50133262	SAEC	small airway:	n/a
27	chr7:50133212-50133262	NHDF-neo	bronchial:	n/a
28	chr7:50133131-50133181	GM12891	blood:	n/a
29	chr7:50109467-50109517	ovcar-3	ovarian:	n/a
30	chr7:50133024-50133074	HEEpiC	esophagus:	n/a
31	chr7:50132764-50132814	HNPCEpiC	eye:	n/a
32	chr7:50133100-50133150	K562	blood:	n/a
33	chr7:50133000-50133050	CMK	blood:	n/a
34	chr7:50133100-50133150	AG10803	skin:	n/a
35	chr7:50133100-50133150	HUVEC	blood vessel:	n/a
36	chr7:50132975-50133025	Jurkat	blood:	n/a
37	chr7:50132541-50132591	NB4	blood:	n/a
38	chr7:50132975-50133025	RPTEC	kidney:	n/a
39	chr7:50078531-50078581	NHDF-neo	bronchial:	n/a
40	chr7:50133100-50133150	AG04450	lung:	fetal
41	chr7:50132764-50132814	HCT-116	colon:	n/a
42	chr7:50109467-50109517	MCF10A-Er-Src	breast:	n/a
43	chr7:50132975-50133025	CMK	blood:	n/a
44	chr7:50133024-50133074	NT2-D1	testis:	n/a
45	chr7:50133131-50133181	HRCEpiC	kidney:	n/a
46	chr7:50132903-50132953	NT2-D1	testis:	n/a
47	chr7:50132975-50133025	AG04449	skin:	fetal
48	chr7:50133212-50133262	PANC-1	pancreas:	n/a
49	chr7:50132541-50132591	HEEpiC	esophagus:	n/a
50	chr7:50132653-50132703	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:50131802..50132527-chr7:50485456..50486116,2	K562	blood:
2	chr7:49996794..49999462-chr7:50000917..50002730,2	K562	blood:
3	chr7:49996794..49999462-chr7:50000917..50002730,2	K562	blood:
4	chr7:50092847..50095845-chr7:50097746..50099637,2	K562	blood:
5	chr7:50131789..50132494-chr7:50485491..50486334,3	MCF-7	breast:
6	chr1:106845778..106848096-chr7:50126573..50128895,2	MCF-7	breast:
7	chr7:49983927..49986729-chr7:49988242..49990694,2	K562	blood:
8	chr7:50092847..50095845-chr7:50097746..50099637,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZPBP-5	chr7:49975347-49975757	NONHSAT120544
2	lnc-C7orf72-1	chr7:50133411-50133755	NONHSAT120545
3	lnc-C7orf72-1	chr7:50132920-50133326	NONHSAT120545

Variant related genes	Relation type
ENSG00000223893	TF binding region
ZPBP	TF binding region
C7orf72	TF binding region
ENSG00000223893	CpG island
ZPBP	CpG island
C7orf72	CpG island
ENSG00000223893	chromatin interactions

Extended variants
information (count: 1882 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:1882 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184122506	chr7:49970870-49970871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564418230	chr7:49970885-49970886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533128855	chr7:49970893-49970894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546835836	chr7:49970898-49970899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560265794	chr7:49970924-49970925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569487502	chr7:49970937-49970938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529031050	chr7:49970966-49970967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143409420	chr7:49970993-49970994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568806096	chr7:49970995-49970996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539653302	chr7:49971017-49971018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116894238	chr7:49971026-49971027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2365784	chr7:49971044-49971045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs534105307	chr7:49971045-49971046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553980204	chr7:49971071-49971072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200960750	chr7:49971075-49971076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201455312	chr7:49971086-49971087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13238712	chr7:49971101-49971102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13221141	chr7:49971108-49971109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556623523	chr7:49971119-49971120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568192368	chr7:49971148-49971149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369795703	chr7:49971150-49971151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576320081	chr7:49971152-49971153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2886462	chr7:49971195-49971196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149877066	chr7:49971236-49971237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544854125	chr7:49971239-49971240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540410158	chr7:49971241-49971242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6963633	chr7:49971273-49971274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528993642	chr7:49971286-49971287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs57404971	chr7:49971306-49971307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115145859	chr7:49971337-49971338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80206086	chr7:49971357-49971358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374130682	chr7:49971358-49971359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531174545	chr7:49971383-49971384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77708887	chr7:49971395-49971396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551384856	chr7:49971438-49971439	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201550989	chr7:49971442-49971443	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571593023	chr7:49971444-49971445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528019751	chr7:49971475-49971476	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573011856	chr7:49971482-49971483	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547583835	chr7:49971525-49971526	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149035412	chr7:49971555-49971556	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540131099	chr7:49971600-49971601	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367803881	chr7:49971637-49971638	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35600904	chr7:49971658-49971659	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs2086697	chr7:49971659-49971660	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563062771	chr7:49971664-49971665	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556350388	chr7:49971678-49971679	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375381633	chr7:49971700-49971701	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538632129	chr7:49971734-49971735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559023373	chr7:49971751-49971752	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Acute myeloid leukemia	17237825	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
Acute lymphoblastic leukemia	18768390	CNVD
Multiple myeloma	16616336	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:49968800-49972600	Weak transcription	Fetal Heart	heart
2	chr7:49971400-49972600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:49972400-49972800	Weak transcription	Ovary	ovary
4	chr7:49975000-49975200	Weak transcription	Ovary	ovary
5	chr7:49996600-49997000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:50004400-50004600	Active TSS	Ovary	ovary
7	chr7:50014400-50015000	Enhancers	Left Ventricle	heart
8	chr7:50020200-50020400	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:50028800-50044400	Weak transcription	Ovary	ovary
10	chr7:50055400-50056000	Active TSS	Fetal Heart	heart
11	chr7:50062400-50062800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:50070000-50070800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:50072000-50072400	Enhancers	Ovary	ovary
14	chr7:50072400-50077000	Weak transcription	Ovary	ovary
15	chr7:50075800-50076000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:50076000-50077000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:50077000-50077400	Enhancers	Ovary	ovary
18	chr7:50077000-50077600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:50077000-50077800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:50077000-50077800	Enhancers	Fetal Kidney	kidney
21	chr7:50077600-50077800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:50080000-50080400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr7:50080000-50081200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:50080200-50081000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr7:50087000-50087800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:50095000-50095600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr7:50096000-50096400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr7:50101000-50103400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:50103400-50106800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr7:50105000-50107400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr7:50106400-50106600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:50106600-50106800	Enhancers	Fetal Intestine Large	intestine
33	chr7:50106600-50107600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:50106800-50107400	Weak transcription	Fetal Intestine Large	intestine
35	chr7:50106800-50108400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr7:50107000-50107200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:50107000-50108000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr7:50107000-50108000	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr7:50107200-50107400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr7:50107200-50107400	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr7:50107200-50107800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:50107200-50107800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr7:50107200-50107800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:50107200-50107800	Active TSS	Stomach Smooth Muscle	stomach
45	chr7:50107200-50108000	Enhancers	Primary T cells from cord blood	blood
46	chr7:50107200-50108000	Enhancers	Primary T cells fromperipheralblood	blood
47	chr7:50107200-50108000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr7:50107200-50108000	Enhancers	Fetal Kidney	kidney
49	chr7:50107200-50108200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:50107200-50108200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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