Variant report

Variant	nsv830998
Chromosome Location	chr7:50103183-50156564
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	chr7:50132077-50132532	GM12878	blood:	n/a	n/a
3	ATF2	chr7:50132134-50132712	GM12878	blood:	n/a	n/a
4	ATF2	chr7:50132116-50132482	H1-hESC	embryonic stem cell:	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	BCL11A	chr7:50108699-50108959	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr7:50132671-50133087	GM12878	blood:	n/a	chr7:50132911-50132920 chr7:50132858-50132867
9	BCLAF1	chr7:50132613-50133116	GM12878	blood:	n/a	chr7:50132911-50132920 chr7:50132858-50132867
10	BHLHE40	chr7:50109240-50109553	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:50109143-50109472	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:50132129-50132627	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:50132130-50132330	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr7:50108871-50109076	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr7:50112692-50112992	K562	blood:	n/a	n/a
16	CBX3	chr7:50112750-50112962	K562	blood:	n/a	n/a
17	CBX3	chr7:50112675-50113043	HCT-116	colon:	n/a	n/a
18	CCNT2	chr7:50132516-50132849	K562	blood:	n/a	n/a
19	CEBPB	chr7:50132186-50132450	MCF-7	breast:	n/a	n/a
20	CEBPB	chr7:50120230-50120597	HepG2	liver:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
21	CEBPB	chr7:50120298-50120462	HepG2	liver:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
22	CEBPB	chr7:50149449-50149518	K562	blood:	n/a	n/a
23	CEBPB	chr7:50108729-50109601	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:50120306-50120582	MCF-7	breast:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
25	CEBPB	chr7:50120265-50120552	A549	lung:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
26	CEBPB	chr7:50128605-50128805	A549	lung:	n/a	chr7:50128682-50128693
27	CEBPB	chr7:50109388-50109601	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:50120256-50120566	K562	blood:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
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	chr7:50128623-50128751	HepG2	liver:	n/a	chr7:50128682-50128693
31	CEBPB	chr7:50120232-50120515	A549	lung:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
32	CEBPB	chr7:50120262-50120564	IMR90	lung:	n/a	chr7:50120409-50120418 chr7:50120407-50120418 chr7:50120409-50120418 chr7:50120409-50120418 chr7:50120409-50120418
33	CEBPB	chr7:50132187-50132489	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:50127936-50127982	A549	lung:	n/a	n/a
35	CHD1	chr7:50132232-50132445	GM12878	blood:	n/a	n/a
36	CHD2	chr7:50132231-50132693	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr7:50108655-50109046	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr7:50108928-50109092	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr7:50132150-50132600	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:50132199-50132408	ProgFib	skin:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
41	CTCF	chr7:50132144-50132371	GM13977	blood:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
42	CTCF	chr7:50132180-50132330	GM12878	blood:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
43	CTCF	chr7:50107760-50107910	HepG2	liver:	n/a	n/a
44	CTCF	chr7:50107760-50107910	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:50132180-50132330	MCF-7	breast:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
46	CTCF	chr7:50152020-50152170	GM12878	blood:	n/a	n/a
47	CTCF	chr7:50132172-50132358	HepG2	liver:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
48	CTCF	chr7:50132134-50132423	A549	lung:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
49	CTCF	chr7:50132160-50132310	GM12870	blood:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278
50	CTCF	chr7:50132141-50132400	Kidney_OC	kidney:	n/a	chr7:50132255-50132273 chr7:50132256-50132272 chr7:50132257-50132278

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50133000-50133050	GM06990	blood:	n/a
2	chr7:50132975-50133025	A549	lung:	n/a
3	chr7:50133131-50133181	NHDF-neo	bronchial:	n/a
4	chr7:50133024-50133074	HIPEpiC	eye:	n/a
5	chr7:50133212-50133262	HMEC	breast:	n/a
6	chr7:50133100-50133150	SK-N-SH	brain:	n/a
7	chr7:50132573-50132623	H1-hESC	embryonic stem cell:	embryo
8	chr7:50132977-50133027	AG10803	skin:	n/a
9	chr7:50133024-50133074	SK-N-SH	brain:	n/a
10	chr7:50133024-50133074	NHBE	bronchial:	n/a
11	chr7:50132653-50132703	SAEC	small airway:	n/a
12	chr7:50132903-50132953	Hela-S3	cervix:	n/a
13	chr7:50132653-50132703	H1-hESC	embryonic stem cell:	embryo
14	chr7:50133100-50133150	SK-N-SH_RA	brain:	n/a
15	chr7:50108936-50108986	MCF10A-Er-Src	breast:	n/a
16	chr7:50133000-50133050	SK-N-SH	brain:	n/a
17	chr7:50132653-50132703	HCM	heart:	n/a
18	chr7:50132653-50132703	NT2-D1	testis:	n/a
19	chr7:50132573-50132623	AG09309	skin:	n/a
20	chr7:50132977-50133027	Caco-2	colon:	n/a
21	chr7:50133212-50133262	A549	lung:	n/a
22	chr7:50133100-50133150	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:50132653-50132703	HRE	kidney:	n/a
24	chr7:50133000-50133050	GM12892	blood:	n/a
25	chr7:50132975-50133025	ECC-1	luminal epithelium:	n/a
26	chr7:50133131-50133181	HIPEpiC	eye:	n/a
27	chr7:50133212-50133262	AG04449	skin:	fetal
28	chr7:50132903-50132953	HRCEpiC	kidney:	n/a
29	chr7:50132975-50133025	HL-60	blood:	n/a
30	chr7:50132977-50133027	MCF-7	breast:	n/a
31	chr7:50132764-50132814	SK-N-MC	brain:	n/a
32	chr7:50132903-50132953	Hepatocyte	liver:	n/a
33	chr7:50133024-50133074	Jurkat	blood:	n/a
34	chr7:50132573-50132623	PrEC	prostate:	n/a
35	chr7:50133024-50133074	AoSMC	blood vessel:	n/a
36	chr7:50132903-50132953	ProgFib	skin:	n/a
37	chr7:50133212-50133262	SK-N-SH_RA	brain:	n/a
38	chr7:50132977-50133027	Hela-S3	cervix:	n/a
39	chr7:50132975-50133025	RPTEC	kidney:	n/a
40	chr7:50132764-50132814	AG09319	gingival:	n/a
41	chr7:50133131-50133181	MCF10A-Er-Src	breast:	n/a
42	chr7:50132903-50132953	HAEpiC	amniotic membrane:	n/a
43	chr7:50108936-50108986	HAEpiC	amniotic membrane:	n/a
44	chr7:50109467-50109517	MCF10A-Er-Src	breast:	n/a
45	chr7:50132764-50132814	HNPCEpiC	eye:	n/a
46	chr7:50132975-50133025	NHBE	bronchial:	n/a
47	chr7:50133131-50133181	RPTEC	kidney:	n/a
48	chr7:50133212-50133262	K562	blood:	n/a
49	chr7:50133024-50133074	GM12891	blood:	n/a
50	chr7:50132975-50133025	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:50153723..50156265-chr7:50158354..50160442,2	K562	blood:
2	chr1:106845778..106848096-chr7:50126573..50128895,2	MCF-7	breast:
3	chr7:50131789..50132494-chr7:50485491..50486334,3	MCF-7	breast:
4	chr7:50131802..50132527-chr7:50485456..50486116,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf72-1	chr7:50132920-50133326	NONHSAT120545
2	lnc-C7orf72-1	chr7:50133411-50133755	NONHSAT120545

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

Extended variants
information (count: 592 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548614886	chr7:50103195-50103196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536443368	chr7:50103206-50103207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181556419	chr7:50103265-50103266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531981919	chr7:50103296-50103297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552836932	chr7:50103328-50103329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566200498	chr7:50103443-50103444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554510448	chr7:50103485-50103486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535320760	chr7:50103494-50103495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575916868	chr7:50103524-50103525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529407675	chr7:50103549-50103550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536978428	chr7:50103577-50103578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117177000	chr7:50103590-50103591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568650646	chr7:50103605-50103606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148945151	chr7:50103623-50103624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557457118	chr7:50103629-50103630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576449261	chr7:50103646-50103647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545833393	chr7:50103772-50103773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375309741	chr7:50103805-50103806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572295651	chr7:50103823-50103824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143719414	chr7:50103915-50103916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560782909	chr7:50103930-50103931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529802208	chr7:50103956-50103957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540731400	chr7:50103966-50103967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559399824	chr7:50104014-50104015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543133987	chr7:50104016-50104017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563188273	chr7:50104045-50104046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532140771	chr7:50104062-50104063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113600528	chr7:50104110-50104111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112953073	chr7:50104138-50104139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565668937	chr7:50104157-50104158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148079907	chr7:50104158-50104159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185230465	chr7:50104181-50104182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188468411	chr7:50104236-50104237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376239772	chr7:50104267-50104268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574492090	chr7:50104268-50104269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557431962	chr7:50104277-50104278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181903837	chr7:50104288-50104289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112937752	chr7:50104351-50104352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553119644	chr7:50104368-50104369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573174858	chr7:50104380-50104381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534619352	chr7:50104394-50104395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192379387	chr7:50104404-50104405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574293329	chr7:50104461-50104462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543170978	chr7:50104491-50104492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28852506	chr7:50104503-50104504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561498092	chr7:50104529-50104530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576914180	chr7:50104636-50104637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545863497	chr7:50104657-50104658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140952638	chr7:50104659-50104660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570480607	chr7:50104689-50104690	Weak transcription	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
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
Burkitt''s lymphoma	20823134	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50101000-50103400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr7:50103400-50106800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:50105000-50107400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:50106400-50106600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:50106600-50106800	Enhancers	Fetal Intestine Large	intestine
6	chr7:50106600-50107600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:50106800-50107400	Weak transcription	Fetal Intestine Large	intestine
8	chr7:50106800-50108400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:50107000-50107200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:50107000-50108000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:50107000-50108000	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr7:50107200-50107400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr7:50107200-50107400	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr7:50107200-50107800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:50107200-50107800	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr7:50107200-50107800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:50107200-50107800	Active TSS	Stomach Smooth Muscle	stomach
18	chr7:50107200-50108000	Enhancers	Primary T cells from cord blood	blood
19	chr7:50107200-50108000	Enhancers	Primary T cells fromperipheralblood	blood
20	chr7:50107200-50108000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:50107200-50108000	Enhancers	Fetal Kidney	kidney
22	chr7:50107200-50108200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:50107200-50108200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:50107200-50108200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:50107200-50108200	Enhancers	Aorta	Aorta
26	chr7:50107200-50108200	Enhancers	Fetal Stomach	stomach
27	chr7:50107200-50108400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr7:50107200-50108400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:50107200-50108400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:50107200-50108400	Enhancers	Fetal Intestine Small	intestine
31	chr7:50107200-50108400	Enhancers	Fetal Thymus	thymus
32	chr7:50107200-50108400	Enhancers	Small Intestine	intestine
33	chr7:50107200-50108600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:50107400-50107600	Enhancers	Brain Cingulate Gyrus	brain
35	chr7:50107400-50107600	Enhancers	GM12878-XiMat	blood
36	chr7:50107400-50107800	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr7:50107400-50107800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:50107400-50107800	Enhancers	Brain Angular Gyrus	brain
39	chr7:50107400-50107800	Enhancers	Colon Smooth Muscle	Colon
40	chr7:50107400-50107800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr7:50107400-50107800	Enhancers	Thymus	Thymus
42	chr7:50107400-50108000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr7:50107400-50108000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr7:50107400-50108000	Enhancers	HMEC	breast
45	chr7:50107400-50108400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr7:50107400-50108400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr7:50107400-50108400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:50107400-50108400	Enhancers	Primary B cells from peripheral blood	blood
49	chr7:50107400-50108400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr7:50107400-50108400	Enhancers	Dnd41	blood

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