Variant report

Variant	esv2761127
Chromosome Location	chr7:15051210-15152813
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	chr7:15055726-15056046	HepG2	liver:	n/a	n/a
2	BACH1	chr7:15051037-15051612	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:15052301-15052317	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:15136729-15136926	K562	blood:	n/a	n/a
5	BHLHE40	chr7:15055727-15055963	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:15055872-15056060	K562	blood:	n/a	n/a
7	CEBPB	chr7:15107136-15107410	Hela-S3	cervix:	n/a	chr7:15107268-15107279
8	CEBPB	chr7:15107146-15107394	A549	lung:	n/a	chr7:15107268-15107279
9	CEBPB	chr7:15107141-15107395	HepG2	liver:	n/a	chr7:15107268-15107279
10	CEBPB	chr7:15107126-15107433	IMR90	lung:	n/a	chr7:15107268-15107279
11	CEBPB	chr7:15077096-15077349	HepG2	liver:	n/a	chr7:15077196-15077207
12	CEBPB	chr7:15126055-15126326	IMR90	lung:	n/a	chr7:15126178-15126189
13	CEBPB	chr7:15080351-15081311	Hela-S3	cervix:	n/a	chr7:15081129-15081142
14	CEBPB	chr7:15056178-15057050	HCT-116	colon:	n/a	chr7:15056927-15056938
15	CEBPB	chr7:15126040-15126347	Hela-S3	cervix:	n/a	chr7:15126178-15126189
16	CEBPB	chr7:15126038-15126244	HepG2	liver:	n/a	chr7:15126178-15126189
17	CTCF	chr7:15055820-15055970	SAEC	small airway:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
18	CTCF	chr7:15055820-15055970	AG04449	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
19	CTCF	chr7:15055860-15056010	HCM	heart:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
20	CTCF	chr7:15055820-15055970	AG09309	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
21	CTCF	chr7:15093689-15093709	LNCaP	prostate:	n/a	n/a
22	CTCF	chr7:15055780-15055930	GM12873	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
23	CTCF	chr7:15055840-15055990	GM12867	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
24	CTCF	chr7:15055840-15055990	SK-N-SH_RA	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
25	CTCF	chr7:15055160-15055310	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr7:15055790-15056016	K562	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
27	CTCF	chr7:15055840-15055990	GM12878	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
28	CTCF	chr7:15055820-15055970	GM12865	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
29	CTCF	chr7:15055806-15055992	GM13976	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
30	CTCF	chr7:15055821-15056001	GM20000	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
31	CTCF	chr7:15055420-15055570	AG04449	skin:	n/a	n/a
32	CTCF	chr7:15055420-15055570	GM12875	blood:	n/a	n/a
33	CTCF	chr7:15055800-15055950	GM12878	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
34	CTCF	chr7:15055280-15055430	HFF	foreskin:	n/a	n/a
35	CTCF	chr7:15055713-15055996	ECC-1	luminal epithelium:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
36	CTCF	chr7:15055678-15056168	GM12878	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
37	CTCF	chr7:15055820-15055970	HRPEpiC	eye:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
38	CTCF	chr7:15055776-15056017	Gliobla	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
39	CTCF	chr7:15055780-15055930	MCF-7	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
40	CTCF	chr7:15055671-15055998	H1-hESC	embryonic stem cell:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
41	CTCF	chr7:15055900-15056050	HMEC	breast:	n/a	n/a
42	CTCF	chr7:15055097-15056226	SK-N-SH	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
43	CTCF	chr7:15055840-15055990	K562	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
44	CTCF	chr7:15055440-15055590	GM12872	blood:	n/a	n/a
45	CTCF	chr7:15055726-15056073	K562	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
46	CTCF	chr7:15055802-15055962	A549	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
47	CTCF	chr7:15055740-15055890	HEK293	kidney:	n/a	n/a
48	CTCF	chr7:15055786-15056162	HCT-116	colon:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
49	CTCF	chr7:15055780-15055930	NHEK	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
50	CTCF	chr7:15055840-15055990	WERI-Rb-1	eye:	n/a	chr7:15055896-15055905 chr7:15055892-15055905

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15055459-15055509	Hepatocyte	liver:	n/a
2	chr7:15055459-15055509	IMR90	lung:	fetal
3	chr7:15055459-15055509	SAEC	small airway:	n/a
4	chr7:15055459-15055509	GM06990	blood:	n/a
5	chr7:15055459-15055509	U87	brain:	n/a
6	chr7:15055459-15055509	K562	blood:	n/a
7	chr7:15055459-15055509	AG04449	skin:	fetal
8	chr7:15055459-15055509	LNCaP	prostate:	n/a
9	chr7:15055459-15055509	MCF-7	breast:	n/a
10	chr7:15055459-15055509	NT2-D1	testis:	n/a
11	chr7:15055459-15055509	GM12892	blood:	n/a
12	chr7:15055459-15055509	HCPEpiC	choroid plexus:	n/a
13	chr7:15055459-15055509	SK-N-MC	brain:	n/a
14	chr7:15055459-15055509	PANC-1	pancreas:	n/a
15	chr7:15055459-15055509	ProgFib	skin:	n/a
16	chr7:15055459-15055509	HRCEpiC	kidney:	n/a
17	chr7:15055459-15055509	ovcar-3	ovarian:	n/a
18	chr7:15055459-15055509	HCT-116	colon:	n/a
19	chr7:15055459-15055509	NHBE	bronchial:	n/a
20	chr7:15055459-15055509	T-47D	breast:	n/a
21	chr7:15055459-15055509	NH-A	brain:	n/a
22	chr7:15055459-15055509	HCM	heart:	n/a
23	chr7:15055459-15055509	GM19239	blood:	n/a
24	chr7:15055459-15055509	HepG2	liver:	n/a
25	chr7:15055459-15055509	CMK	blood:	n/a
26	chr7:15055459-15055509	HEEpiC	esophagus:	n/a
27	chr7:15055459-15055509	HNPCEpiC	eye:	n/a
28	chr7:15055459-15055509	Jurkat	blood:	n/a
29	chr7:15055459-15055509	AG09319	gingival:	n/a
30	chr7:15055459-15055509	HRE	kidney:	n/a
31	chr7:15055459-15055509	Caco-2	colon:	n/a
32	chr7:15055459-15055509	AG04450	lung:	fetal
33	chr7:15055459-15055509	SK-N-SH	brain:	n/a
34	chr7:15055459-15055509	AG09309	skin:	n/a
35	chr7:15055459-15055509	Hela-S3	cervix:	n/a
36	chr7:15055459-15055509	ECC-1	luminal epithelium:	n/a
37	chr7:15055459-15055509	AG10803	skin:	n/a
38	chr7:15055459-15055509	HMEC	breast:	n/a
39	chr7:15055459-15055509	MCF10A-Er-Src	breast:	n/a
40	chr7:15055459-15055509	H1-hESC	embryonic stem cell:	embryo
41	chr7:15055459-15055509	GM12891	blood:	n/a
42	chr7:15055459-15055509	SKMC	muscle:	n/a
43	chr7:15055459-15055509	HUVEC	blood vessel:	n/a
44	chr7:15055459-15055509	PrEC	prostate:	n/a
45	chr7:15055459-15055509	NB4	blood:	n/a
46	chr7:15055459-15055509	BE2_C	brain:	n/a
47	chr7:15055459-15055509	HL-60	blood:	n/a
48	chr7:15055459-15055509	HAEpiC	amniotic membrane:	n/a
49	chr7:15055459-15055509	HEK293	kidney:	embryo
50	chr7:15055459-15055509	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
2	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
3	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:
4	chr7:15148394..15150106-chr7:15160727..15163235,2	K562	blood:
5	chr6:10529800..10530510-chr7:15146578..15147089,2	MCF-7	breast:
6	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
7	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
8	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:
9	chr7:13317591..13319993-chr7:15056107..15057980,2	K562	blood:
10	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-9	chr7:15074455-15074801	NONHSAT119273
2	lnc-AC006035.2-9	chr7:15072357-15072662	NONHSAT119273
3	lnc-AC006035.2-4	chr7:15105832-15106137	XLOC_005990
4	lnc-AC006035.2-4	chr7:15107930-15108276	XLOC_005990

Variant related genes	Relation type
ENSG00000227489	TF binding region
ENSG00000227489	CpG island
ENSG00000111846	chromatin interactions

Extended variants
information (count: 3031 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3031 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6949740	chr7:15051210-15051211	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551385058	chr7:15051225-15051226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527934441	chr7:15051228-15051229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10950547	chr7:15051233-15051234	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs200930499	chr7:15051266-15051267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77362795	chr7:15051269-15051270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs386710642	chr7:15051272-15051273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565103413	chr7:15051278-15051279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6949910	chr7:15051281-15051282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367700176	chr7:15051287-15051288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190260864	chr7:15051292-15051293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6967637	chr7:15051310-15051311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553167032	chr7:15051390-15051391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62448617	chr7:15051399-15051400	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs538689345	chr7:15051408-15051409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558593658	chr7:15051426-15051427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377347363	chr7:15051437-15051438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575170886	chr7:15051448-15051449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544191473	chr7:15051487-15051488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563854788	chr7:15051491-15051492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193240678	chr7:15051497-15051498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542829445	chr7:15051536-15051537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6954315	chr7:15051539-15051540	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs112425669	chr7:15051547-15051548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149814658	chr7:15051570-15051571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113169623	chr7:15051577-15051578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530859817	chr7:15051583-15051584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550934170	chr7:15051603-15051604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567462798	chr7:15051628-15051629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188277407	chr7:15051636-15051637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6972333	chr7:15051643-15051644	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs113563087	chr7:15051654-15051655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535592553	chr7:15051662-15051663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566628868	chr7:15051709-15051710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538825636	chr7:15051718-15051719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6954633	chr7:15051746-15051747	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6972083	chr7:15051754-15051755	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs386710643	chr7:15051788-15051789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6972516	chr7:15051789-15051790	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs574017817	chr7:15051811-15051812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578015350	chr7:15051831-15051832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577254968	chr7:15051834-15051835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553162070	chr7:15051838-15051839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6972667	chr7:15051868-15051869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181046757	chr7:15051910-15051911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6972293	chr7:15051923-15051924	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141830271	chr7:15051924-15051925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114699548	chr7:15051927-15051928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35752980	chr7:15051933-15051934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376499574	chr7:15051936-15051937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15047600-15055000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:15049600-15055000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:15050600-15051600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:15050800-15051800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr7:15050800-15052000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr7:15051000-15051400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:15051000-15051800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:15051200-15051600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:15051200-15051600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr7:15051200-15052800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:15051200-15054800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:15051400-15051600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:15051600-15052200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr7:15051600-15052200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr7:15051600-15054400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:15051600-15054800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:15051600-15054800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:15051600-15055000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr7:15051800-15052200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:15051800-15055000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr7:15051800-15055000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:15052000-15052200	Enhancers	Right Ventricle	heart
23	chr7:15052000-15055000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr7:15052200-15052400	Enhancers	Left Ventricle	heart
25	chr7:15052200-15054200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr7:15052200-15055000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr7:15052200-15055200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:15052200-15055200	Weak transcription	Right Ventricle	heart
29	chr7:15052800-15055000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:15054000-15054200	Enhancers	Psoas Muscle	Psoas
31	chr7:15054200-15054400	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr7:15054400-15054800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr7:15054400-15055000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:15054800-15055000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:15054800-15055000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:15054800-15055000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:15054800-15055200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr7:15055000-15055200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
39	chr7:15055000-15055200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:15055000-15055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:15055000-15055200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
42	chr7:15055000-15055200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr7:15055000-15055200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr7:15055000-15055200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr7:15055000-15055200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:15055000-15055200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:15055000-15055200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:15055000-15055200	Enhancers	Liver	Liver
49	chr7:15055000-15055200	Enhancers	Brain Germinal Matrix	brain
50	chr7:15055000-15055200	Enhancers	Brain Hippocampus Middle	brain

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