Variant report

Variant	nsv527462
Chromosome Location	chr7:50933370-50989383
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	BHLHE40	chr7:50982323-50982502	K562	blood:	n/a	n/a
2	BRCA1	chr7:50937070-50937509	Hela-S3	cervix:	n/a	chr7:50937313-50937320
3	BRCA1	chr7:50950912-50950937	Hela-S3	cervix:	n/a	n/a
4	CCNT2	chr7:50982843-50982986	K562	blood:	n/a	n/a
5	CCNT2	chr7:50982164-50982558	K562	blood:	n/a	chr7:50982407-50982427
6	CEBPB	chr7:50936956-50937544	A549	lung:	n/a	chr7:50937277-50937288
7	CEBPB	chr7:50953840-50954092	Hela-S3	cervix:	n/a	chr7:50953969-50953980
8	CEBPB	chr7:50953790-50954134	MCF-7	breast:	n/a	chr7:50953969-50953980
9	CEBPB	chr7:50937059-50937482	Hela-S3	cervix:	n/a	chr7:50937277-50937288
10	CEBPB	chr7:50936967-50937484	A549	lung:	n/a	chr7:50937277-50937288
11	CEBPB	chr7:50953777-50954193	A549	lung:	n/a	chr7:50953969-50953980
12	CEBPB	chr7:50976734-50976791	K562	blood:	n/a	n/a
13	CEBPB	chr7:50937093-50937426	HepG2	liver:	n/a	chr7:50937277-50937288
14	CEBPB	chr7:50983836-50984108	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:50936985-50937523	IMR90	lung:	n/a	chr7:50937277-50937288
16	CEBPB	chr7:50953751-50954092	MCF-7	breast:	n/a	chr7:50953969-50953980
17	CEBPB	chr7:50936931-50937554	HCT-116	colon:	n/a	chr7:50937277-50937288
18	CEBPB	chr7:50987955-50988377	MCF-7	breast:	n/a	chr7:50988157-50988170
19	CEBPB	chr7:50953837-50954107	A549	lung:	n/a	chr7:50953969-50953980
20	CEBPB	chr7:50953849-50954146	HepG2	liver:	n/a	chr7:50953969-50953980
21	CEBPB	chr7:50937064-50937498	A549	lung:	n/a	chr7:50937277-50937288
22	CTCF	chr7:50946122-50946143	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr7:50940320-50940470	HepG2	liver:	n/a	n/a
24	CTCF	chr7:50955389-50955422	LNCaP	prostate:	n/a	n/a
25	CTCF	chr7:50985680-50985830	HepG2	liver:	n/a	n/a
26	CTCF	chr7:50942804-50942910	GM13976	blood:	n/a	n/a
27	CTCF	chr7:50940300-50940450	Caco-2	colon:	n/a	n/a
28	CUX1	chr7:50978102-50978105	K562	blood:	n/a	n/a
29	CUX1	chr7:50980768-50980897	GM12878	blood:	n/a	n/a
30	E2F4	chr7:50937111-50937409	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr7:50960985-50961477	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr7:50940305-50940450	GM12878	blood:	n/a	n/a
33	EGR1	chr7:50988809-50989101	K562	blood:	n/a	chr7:50988986-50989000 chr7:50988988-50988998 chr7:50988988-50988998
34	EGR1	chr7:50988893-50989072	K562	blood:	n/a	chr7:50988986-50989000 chr7:50988988-50988998 chr7:50988988-50988998
35	EGR1	chr7:50988626-50989287	HCT-116	colon:	n/a	chr7:50988986-50989000 chr7:50988988-50988998 chr7:50988988-50988998
36	EGR1	chr7:50988841-50989218	HCT-116	colon:	n/a	chr7:50988986-50989000 chr7:50988988-50988998 chr7:50988988-50988998
37	EGR1	chr7:50988800-50989237	MCF-7	breast:	n/a	chr7:50988986-50989000 chr7:50988988-50988998 chr7:50988988-50988998
38	EGR1	chr7:50988733-50989293	MCF-7	breast:	n/a	chr7:50988986-50989000 chr7:50988988-50988998 chr7:50988988-50988998
39	EP300	chr7:50936853-50937575	A549	lung:	n/a	n/a
40	EP300	chr7:50936962-50937504	A549	lung:	n/a	n/a
41	EP300	chr7:50937067-50937517	Hela-S3	cervix:	n/a	n/a
42	EP300	chr7:50982269-50982575	K562	blood:	n/a	chr7:50982386-50982393
43	EP300	chr7:50976998-50977018	K562	blood:	n/a	n/a
44	FOS	chr7:50988818-50989119	MCF10A-Er-Src	breast:	n/a	chr7:50988960-50988971 chr7:50988965-50988972 chr7:50988962-50988973 chr7:50988963-50988972
45	FOS	chr7:50933203-50933501	MCF10A-Er-Src	breast:	n/a	chr7:50933223-50933232
46	FOS	chr7:50982085-50982433	MCF10A-Er-Src	breast:	n/a	chr7:50982238-50982246 chr7:50982236-50982248
47	FOS	chr7:50988793-50989120	MCF10A-Er-Src	breast:	n/a	chr7:50988960-50988971 chr7:50988965-50988972 chr7:50988962-50988973 chr7:50988963-50988972
48	FOS	chr7:50988828-50989155	MCF10A-Er-Src	breast:	n/a	chr7:50988960-50988971 chr7:50988965-50988972 chr7:50988962-50988973 chr7:50988963-50988972
49	FOS	chr7:50988821-50989119	MCF10A-Er-Src	breast:	n/a	chr7:50988960-50988971 chr7:50988965-50988972 chr7:50988962-50988973 chr7:50988963-50988972
50	FOS	chr7:50937038-50937437	MCF10A-Er-Src	breast:	n/a	chr7:50937142-50937151

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50934682-50934732	Hepatocyte	liver:	n/a
2	chr7:50935286-50935336	Caco-2	colon:	n/a
3	chr7:50935274-50935324	K562	blood:	n/a
4	chr7:50934682-50934732	H1-hESC	embryonic stem cell:	embryo
5	chr7:50935274-50935324	HRCEpiC	kidney:	n/a
6	chr7:50935286-50935336	HIPEpiC	eye:	n/a
7	chr7:50935274-50935324	PANC-1	pancreas:	n/a
8	chr7:50934682-50934732	NT2-D1	testis:	n/a
9	chr7:50934682-50934732	AG09319	gingival:	n/a
10	chr7:50935274-50935324	HL-60	blood:	n/a
11	chr7:50935286-50935336	HepG2	liver:	n/a
12	chr7:50934682-50934732	HepG2	liver:	n/a
13	chr7:50935274-50935324	HRPEpiC	eye:	n/a
14	chr7:50934682-50934732	AG04449	skin:	fetal
15	chr7:50935274-50935324	HCF	heart:	n/a
16	chr7:50934682-50934732	PANC-1	pancreas:	n/a
17	chr7:50935286-50935336	U87	brain:	n/a
18	chr7:50935274-50935324	GM19239	blood:	n/a
19	chr7:50934682-50934732	HUVEC	blood vessel:	n/a
20	chr7:50935274-50935324	Hela-S3	cervix:	n/a
21	chr7:50935274-50935324	NT2-D1	testis:	n/a
22	chr7:50935286-50935336	AG04449	skin:	fetal
23	chr7:50935286-50935336	LNCaP	prostate:	n/a
24	chr7:50935286-50935336	HRCEpiC	kidney:	n/a
25	chr7:50934682-50934732	HCT-116	colon:	n/a
26	chr7:50934682-50934732	SAEC	small airway:	n/a
27	chr7:50935286-50935336	SK-N-SH_RA	brain:	n/a
28	chr7:50935274-50935324	T-47D	breast:	n/a
29	chr7:50935274-50935324	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:50935286-50935336	HL-60	blood:	n/a
31	chr7:50935274-50935324	HEEpiC	esophagus:	n/a
32	chr7:50935274-50935324	HepG2	liver:	n/a
33	chr7:50935274-50935324	Hepatocyte	liver:	n/a
34	chr7:50935286-50935336	H1-hESC	embryonic stem cell:	embryo
35	chr7:50935274-50935324	HIPEpiC	eye:	n/a
36	chr7:50935274-50935324	GM12892	blood:	n/a
37	chr7:50934682-50934732	Caco-2	colon:	n/a
38	chr7:50934682-50934732	HRCEpiC	kidney:	n/a
39	chr7:50934682-50934732	HIPEpiC	eye:	n/a
40	chr7:50934682-50934732	GM12892	blood:	n/a
41	chr7:50935286-50935336	AG09319	gingival:	n/a
42	chr7:50935286-50935336	Hela-S3	cervix:	n/a
43	chr7:50934682-50934732	ECC-1	luminal epithelium:	n/a
44	chr7:50935286-50935336	RPTEC	kidney:	n/a
45	chr7:50935274-50935324	H1-hESC	embryonic stem cell:	embryo
46	chr7:50935286-50935336	IMR90	lung:	fetal
47	chr7:50935274-50935324	BE2_C	brain:	n/a
48	chr7:50935274-50935324	AG09319	gingival:	n/a
49	chr7:50935274-50935324	MCF10A-Er-Src	breast:	n/a
50	chr7:50934682-50934732	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:50979021..50981681-chr7:50988406..50989972,2	K562	blood:
2	chr7:50979021..50981681-chr7:50988406..50989972,2	K562	blood:
3	chr7:50859580..50861266-chr7:50980891..50982813,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IKZF1-2	chr7:50934444-50934467	ENSG00000228204.2

Variant related genes	Relation type
ENSG00000228204	TF binding region
ENSG00000228204	CpG island
ENSG00000106070	chromatin interactions
ITM2B	miRNA target sites

Extended variants
information (count: 1304 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1304 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10264737	chr7:50933370-50933371	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529043143	chr7:50933380-50933381	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs34809728	chr7:50933386-50933387	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549074672	chr7:50933412-50933413	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs569104761	chr7:50933505-50933506	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs538002304	chr7:50933538-50933539	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189138075	chr7:50933586-50933587	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577500766	chr7:50933596-50933597	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs371688597	chr7:50933637-50933638	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571474301	chr7:50933647-50933648	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs539461998	chr7:50933653-50933654	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs553376007	chr7:50933658-50933659	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs10274003	chr7:50933678-50933679	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs181517051	chr7:50933686-50933687	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs555425991	chr7:50933707-50933708	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs145796847	chr7:50933775-50933776	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs544744139	chr7:50933799-50933800	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs564633479	chr7:50933817-50933818	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs578225715	chr7:50933829-50933830	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs540567780	chr7:50933841-50933842	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs148977485	chr7:50933887-50933888	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528878912	chr7:50933976-50933977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549113538	chr7:50934023-50934024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562540705	chr7:50934061-50934062	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs531538290	chr7:50934063-50934064	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs184188491	chr7:50934084-50934085	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs571344676	chr7:50934085-50934086	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs534939283	chr7:50934111-50934112	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs547355679	chr7:50934144-50934145	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs552659639	chr7:50934185-50934186	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs556679623	chr7:50934199-50934200	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs144327080	chr7:50934210-50934211	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs535426191	chr7:50934268-50934269	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs188519530	chr7:50934301-50934302	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568967827	chr7:50934315-50934316	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs537941108	chr7:50934317-50934318	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs558374653	chr7:50934325-50934326	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs145122985	chr7:50934330-50934331	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs578094365	chr7:50934350-50934351	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs540955716	chr7:50934431-50934432	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs75033338	chr7:50934443-50934444	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs529828347	chr7:50934513-50934514	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542600066	chr7:50934560-50934561	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562581353	chr7:50934575-50934576	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377636892	chr7:50934582-50934583	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531475773	chr7:50934591-50934592	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557063920	chr7:50934696-50934697	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181267374	chr7:50934755-50934756	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs544774141	chr7:50934778-50934779	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs565120284	chr7:50934838-50934839	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50926200-50934600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:50926200-50935600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:50927000-50935600	Weak transcription	Pancreas	Pancrea
4	chr7:50930400-50934600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:50932200-50934400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr7:50932400-50933600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:50932400-50935000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr7:50932600-50934200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:50932800-50934000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:50932800-50934200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:50933000-50933400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:50933200-50933400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:50933200-50933400	Bivalent Enhancer	NHEK	skin
14	chr7:50933200-50934200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:50933200-50934200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:50933200-50934200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr7:50933200-50934400	Weak transcription	Left Ventricle	heart
18	chr7:50933200-50936400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:50933400-50936400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:50933400-50936800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:50933600-50933800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:50933600-50937600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:50933600-50937800	Enhancers	Fetal Heart	heart
24	chr7:50933800-50936000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:50934000-50934400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:50934000-50935600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:50934200-50934400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:50934200-50934400	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr7:50934200-50934800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:50934200-50934800	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr7:50934200-50935000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:50934200-50935000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr7:50934200-50935000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr7:50934400-50934600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr7:50934400-50935000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
36	chr7:50934400-50935000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr7:50934400-50935000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr7:50934400-50935200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr7:50934400-50935400	Enhancers	Left Ventricle	heart
40	chr7:50934400-50936200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:50934400-50936400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:50934600-50934800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:50934600-50934800	Enhancers	Rectal Smooth Muscle	rectum
44	chr7:50934600-50934800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr7:50934600-50935000	Enhancers	Right Ventricle	heart
46	chr7:50934600-50935200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:50934600-50936400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr7:50934600-50936400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr7:50934800-50935000	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr7:50934800-50935400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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