Variant report

Variant	nsv433032
Chromosome Location	chr7:13792450-13911001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:617)
CpG islands
(count:369)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13889765-13890070	K562	blood:	n/a	n/a
2	ATF1	chr7:13900658-13900844	K562	blood:	n/a	n/a
3	ATF1	chr7:13816892-13817175	K562	blood:	n/a	n/a
4	ATF1	chr7:13820392-13820480	K562	blood:	n/a	n/a
5	ATF1	chr7:13889729-13890161	K562	blood:	n/a	n/a
6	ATF1	chr7:13862322-13862554	K562	blood:	n/a	n/a
7	ATF3	chr7:13889705-13890029	K562	blood:	n/a	n/a
8	BACH1	chr7:13873923-13874075	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:13840793-13840928	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:13889847-13890003	H1-hESC	embryonic stem cell:	n/a	chr7:13889889-13889903
11	BHLHE40	chr7:13810071-13810219	K562	blood:	n/a	n/a
12	BHLHE40	chr7:13889782-13890158	K562	blood:	n/a	n/a
13	CBX3	chr7:13889637-13890195	K562	blood:	n/a	n/a
14	CBX3	chr7:13889630-13890509	HCT-116	colon:	n/a	n/a
15	CBX3	chr7:13889571-13890520	HCT-116	colon:	n/a	n/a
16	CBX3	chr7:13889755-13890146	K562	blood:	n/a	n/a
17	CCNT2	chr7:13889753-13890143	K562	blood:	n/a	n/a
18	CCNT2	chr7:13827899-13828078	K562	blood:	n/a	n/a
19	CEBPB	chr7:13889794-13890080	K562	blood:	n/a	n/a
20	CEBPB	chr7:13866409-13866610	HepG2	liver:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
21	CEBPB	chr7:13869718-13870004	HepG2	liver:	n/a	chr7:13869838-13869849
22	CEBPB	chr7:13794404-13794643	A549	lung:	n/a	chr7:13794489-13794500
23	CEBPB	chr7:13816926-13817206	A549	lung:	n/a	chr7:13817068-13817079
24	CEBPB	chr7:13816925-13817118	K562	blood:	n/a	chr7:13817068-13817079
25	CEBPB	chr7:13900159-13900379	HepG2	liver:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
26	CEBPB	chr7:13903039-13903324	K562	blood:	n/a	n/a
27	CEBPB	chr7:13816932-13817219	IMR90	lung:	n/a	chr7:13817068-13817079
28	CEBPB	chr7:13886123-13886339	K562	blood:	n/a	n/a
29	CEBPB	chr7:13880948-13881315	HepG2	liver:	n/a	chr7:13881124-13881135
30	CEBPB	chr7:13900136-13900404	K562	blood:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
31	CEBPB	chr7:13824938-13825130	K562	blood:	n/a	n/a
32	CEBPB	chr7:13900168-13900410	H1-hESC	embryonic stem cell:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
33	CEBPB	chr7:13816979-13817229	K562	blood:	n/a	chr7:13817068-13817079
34	CEBPB	chr7:13840380-13841070	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:13886050-13886429	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:13900625-13900913	A549	lung:	n/a	n/a
37	CEBPB	chr7:13824851-13825044	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr7:13886138-13886375	A549	lung:	n/a	n/a
39	CEBPB	chr7:13886140-13886336	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:13866280-13866761	IMR90	lung:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
41	CEBPB	chr7:13886155-13886335	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:13816905-13817249	K562	blood:	n/a	chr7:13817068-13817079
43	CEBPB	chr7:13880963-13881277	IMR90	lung:	n/a	chr7:13881124-13881135
44	CEBPB	chr7:13880992-13881274	H1-hESC	embryonic stem cell:	n/a	chr7:13881124-13881135
45	CEBPB	chr7:13869641-13870504	IMR90	lung:	n/a	chr7:13869838-13869849
46	CEBPB	chr7:13881008-13881269	K562	blood:	n/a	chr7:13881124-13881135
47	CEBPB	chr7:13880970-13881205	A549	lung:	n/a	chr7:13881124-13881135
48	CEBPB	chr7:13869719-13869926	K562	blood:	n/a	chr7:13869838-13869849
49	CEBPB	chr7:13873289-13873292	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:13899934-13900452	IMR90	lung:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13812692-13812742	NT2-D1	testis:	n/a
2	chr7:13842752-13842802	SK-N-MC	brain:	n/a
3	chr7:13889871-13889921	NH-A	brain:	n/a
4	chr7:13812692-13812742	NT2-D1	testis:	n/a
5	chr7:13842752-13842802	SK-N-MC	brain:	n/a
6	chr7:13889871-13889921	NH-A	brain:	n/a
7	chr7:13821699-13821749	GM19239	blood:	n/a
8	chr7:13821699-13821749	AoSMC	blood vessel:	n/a
9	chr7:13821699-13821749	BJ	skin:	n/a
10	chr7:13837775-13837825	NHDF-neo	bronchial:	n/a
11	chr7:13837775-13837825	PANC-1	pancreas:	n/a
12	chr7:13805304-13805354	MCF-7	breast:	n/a
13	chr7:13842752-13842802	Jurkat	blood:	n/a
14	chr7:13842752-13842802	HCM	heart:	n/a
15	chr7:13805304-13805354	GM12892	blood:	n/a
16	chr7:13842752-13842802	LNCaP	prostate:	n/a
17	chr7:13842752-13842802	U87	brain:	n/a
18	chr7:13812692-13812742	Hepatocyte	liver:	n/a
19	chr7:13889871-13889921	AoSMC	blood vessel:	n/a
20	chr7:13889871-13889921	HepG2	liver:	n/a
21	chr7:13889871-13889921	A549	lung:	n/a
22	chr7:13812692-13812742	AG09309	skin:	n/a
23	chr7:13821699-13821749	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:13837775-13837825	HCPEpiC	choroid plexus:	n/a
25	chr7:13837775-13837825	IMR90	lung:	fetal
26	chr7:13805304-13805354	HUVEC	blood vessel:	n/a
27	chr7:13805304-13805354	BJ	skin:	n/a
28	chr7:13821699-13821749	CMK	blood:	n/a
29	chr7:13842752-13842802	HEEpiC	esophagus:	n/a
30	chr7:13812692-13812742	NHDF-neo	bronchial:	n/a
31	chr7:13821699-13821749	H1-hESC	embryonic stem cell:	embryo
32	chr7:13805304-13805354	SK-N-MC	brain:	n/a
33	chr7:13805304-13805354	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:13842752-13842802	HEK293	kidney:	embryo
35	chr7:13842752-13842802	Hepatocyte	liver:	n/a
36	chr7:13821699-13821749	MCF-7	breast:	n/a
37	chr7:13889871-13889921	ProgFib	skin:	n/a
38	chr7:13812692-13812742	SK-N-SH	brain:	n/a
39	chr7:13812692-13812742	NH-A	brain:	n/a
40	chr7:13812692-13812742	ovcar-3	ovarian:	n/a
41	chr7:13889871-13889921	HCM	heart:	n/a
42	chr7:13889871-13889921	PFSK-1	brain:	n/a
43	chr7:13821699-13821749	HRCEpiC	kidney:	n/a
44	chr7:13842752-13842802	AG10803	skin:	n/a
45	chr7:13821699-13821749	GM06990	blood:	n/a
46	chr7:13821699-13821749	BE2_C	brain:	n/a
47	chr7:13821699-13821749	HRPEpiC	eye:	n/a
48	chr7:13842752-13842802	HepG2	liver:	n/a
49	chr7:13821699-13821749	K562	blood:	n/a
50	chr7:13889871-13889921	GM06990	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:13888923..13892464-chr7:13896702..13899775,3	K562	blood:
2	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
3	chr7:13888536..13892464-chr7:13896702..13899784,3	K562	blood:
4	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
5	chr17:57922547..57924821-chr7:13833856..13835517,2	MCF-7	breast:
6	chr7:13859282..13862271-chr7:13864269..13866964,2	K562	blood:
7	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
8	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
9	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
10	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
11	chr7:13898559..13901034-chr7:13906643..13908176,2	K562	blood:
12	chr7:13882109..13884330-chr7:14031307..14033942,2	K562	blood:
13	chr7:13894294..13896373-chr7:13930641..13933578,2	K562	blood:
14	chr7:13859282..13862271-chr7:13864269..13866964,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETV1-1	chr7:13893980-13894247	XLOC_006359
2	lnc-ETV1-3	chr7:13865085-13865175	NONHSAT119257
3	lnc-ETV1-3	chr7:13860505-13860772	NONHSAT119257
4	lnc-ETV1-1	chr7:13898560-13898650	XLOC_006359

No data

Variant related genes	Relation type
ENSG00000224330	TF binding region
ENSG00000213875	TF binding region
ENSG00000224330	CpG island
ENSG00000213875	CpG island
ENSG00000224330	chromatin interactions

Extended variants
information (count: 4569 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4569 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6949771	chr7:13792450-13792451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184721975	chr7:13792459-13792460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150679488	chr7:13792466-13792467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537536823	chr7:13792468-13792469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575109100	chr7:13792496-13792497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10271427	chr7:13792525-13792526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557222979	chr7:13792544-13792545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574060233	chr7:13792562-13792563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542691655	chr7:13792585-13792586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559714407	chr7:13792589-13792590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112752245	chr7:13792643-13792644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528467094	chr7:13792676-13792677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189652138	chr7:13792730-13792731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10228470	chr7:13792790-13792791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113974945	chr7:13792793-13792794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551150726	chr7:13792805-13792806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567276815	chr7:13792808-13792809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529778393	chr7:13792815-13792816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546342198	chr7:13792853-13792854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146413492	chr7:13792882-13792883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192243811	chr7:13792891-13792892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114063348	chr7:13792918-13792919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568810857	chr7:13792926-13792927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139825774	chr7:13792957-13792958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7784179	chr7:13793002-13793003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs11761371	chr7:13793009-13793010	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536774749	chr7:13793037-13793038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553616009	chr7:13793080-13793081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143193091	chr7:13793082-13793083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573283725	chr7:13793089-13793090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78545795	chr7:13793128-13793129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145503198	chr7:13793130-13793131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148860380	chr7:13793154-13793155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544512720	chr7:13793175-13793176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185835923	chr7:13793195-13793196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74324395	chr7:13793204-13793205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55861363	chr7:13793229-13793230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543077795	chr7:13793256-13793257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116429596	chr7:13793324-13793325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532028557	chr7:13793326-13793327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189386584	chr7:13793369-13793370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568848316	chr7:13793375-13793376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538159239	chr7:13793396-13793397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143548359	chr7:13793417-13793418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181794910	chr7:13793456-13793457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576526131	chr7:13793504-13793505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185884834	chr7:13793555-13793556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541934480	chr7:13793561-13793562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74528417	chr7:13793568-13793569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77646841	chr7:13793573-13793574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
High-grade prostatic intraepithelial neoplasia	16573809	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
Medulloblastoma	17653508	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
Renal cell carcinoma	18194544	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13791000-13797400	Weak transcription	Fetal Lung	lung
2	chr7:13797400-13798200	Enhancers	Fetal Lung	lung
3	chr7:13797800-13798400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:13799400-13799600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:13799600-13812200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:13803800-13812200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:13804800-13805200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:13805200-13805600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr7:13805200-13805600	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr7:13805600-13812400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr7:13808400-13820200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:13809800-13810200	Enhancers	NHEK	skin
13	chr7:13809800-13810400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr7:13809800-13810600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:13810000-13810400	Enhancers	NHDF-Ad	bronchial
16	chr7:13810000-13810600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:13810000-13810600	Enhancers	HSMM	muscle
18	chr7:13810400-13810800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr7:13810400-13814400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr7:13810600-13818600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:13810800-13818400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr7:13812000-13812800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:13812000-13813200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:13812200-13812400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr7:13812200-13812600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr7:13812200-13813000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:13812400-13813000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr7:13813200-13813400	Enhancers	Osteobl	bone
29	chr7:13813200-13824200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:13813600-13818200	Weak transcription	Osteobl	bone
31	chr7:13814200-13815400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr7:13814400-13814800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr7:13814800-13818200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr7:13818200-13819600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr7:13818200-13819800	Enhancers	Osteobl	bone
36	chr7:13818400-13818600	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:13818400-13819600	Enhancers	NHEK	skin
38	chr7:13818600-13818800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:13818600-13818800	Enhancers	Lung	lung
40	chr7:13818600-13819000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:13818600-13819000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr7:13818600-13819000	Enhancers	HUVEC	blood vessel
43	chr7:13818600-13819200	Enhancers	HSMM	muscle
44	chr7:13818600-13819400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:13818600-13819600	Enhancers	HMEC	breast
46	chr7:13818600-13819600	Enhancers	NH-A	brain
47	chr7:13818800-13819200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:13818800-13819200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:13818800-13824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:13819000-13819600	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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