Variant report

Variant	nsv887697
Chromosome Location	chr7:13841798-13899446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:334)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:334 , 50 per page) page: 1 2 3 4 5 6 7

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	chr7:13862322-13862554	K562	blood:	n/a	n/a
3	ATF1	chr7:13889729-13890161	K562	blood:	n/a	n/a
4	ATF3	chr7:13889705-13890029	K562	blood:	n/a	n/a
5	BACH1	chr7:13873923-13874075	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:13889847-13890003	H1-hESC	embryonic stem cell:	n/a	chr7:13889889-13889903
7	BHLHE40	chr7:13889782-13890158	K562	blood:	n/a	n/a
8	CBX3	chr7:13889630-13890509	HCT-116	colon:	n/a	n/a
9	CBX3	chr7:13889571-13890520	HCT-116	colon:	n/a	n/a
10	CBX3	chr7:13889637-13890195	K562	blood:	n/a	n/a
11	CBX3	chr7:13889755-13890146	K562	blood:	n/a	n/a
12	CCNT2	chr7:13889753-13890143	K562	blood:	n/a	n/a
13	CEBPB	chr7:13889742-13890398	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:13880963-13881277	IMR90	lung:	n/a	chr7:13881124-13881135
15	CEBPB	chr7:13886140-13886336	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:13880970-13881205	A549	lung:	n/a	chr7:13881124-13881135
17	CEBPB	chr7:13873289-13873292	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:13866409-13866610	HepG2	liver:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
19	CEBPB	chr7:13869741-13869988	A549	lung:	n/a	chr7:13869838-13869849
20	CEBPB	chr7:13886138-13886375	A549	lung:	n/a	n/a
21	CEBPB	chr7:13891431-13891773	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:13869719-13869926	K562	blood:	n/a	chr7:13869838-13869849
23	CEBPB	chr7:13886123-13886339	K562	blood:	n/a	n/a
24	CEBPB	chr7:13869718-13870004	HepG2	liver:	n/a	chr7:13869838-13869849
25	CEBPB	chr7:13871986-13872328	K562	blood:	n/a	chr7:13872154-13872167 chr7:13872154-13872167 chr7:13872156-13872167
26	CEBPB	chr7:13871988-13872319	IMR90	lung:	n/a	chr7:13872154-13872167 chr7:13872154-13872167 chr7:13872156-13872167
27	CEBPB	chr7:13880992-13881274	H1-hESC	embryonic stem cell:	n/a	chr7:13881124-13881135
28	CEBPB	chr7:13866317-13866517	K562	blood:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
29	CEBPB	chr7:13886155-13886335	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:13869641-13870504	IMR90	lung:	n/a	chr7:13869838-13869849
31	CEBPB	chr7:13889794-13890080	K562	blood:	n/a	n/a
32	CEBPB	chr7:13886050-13886429	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:13881008-13881269	K562	blood:	n/a	chr7:13881124-13881135
34	CEBPB	chr7:13880948-13881315	HepG2	liver:	n/a	chr7:13881124-13881135
35	CEBPB	chr7:13867368-13867612	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:13866280-13866761	IMR90	lung:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
37	CHD2	chr7:13873933-13874094	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr7:13873279-13873288	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:13845800-13845950	HVMF	connective:	n/a	n/a
40	CTCF	chr7:13845943-13846097	K562	blood:	n/a	n/a
41	CTCF	chr7:13845820-13845970	Caco-2	colon:	n/a	n/a
42	CTCF	chr7:13845940-13846090	HepG2	liver:	n/a	n/a
43	CTCF	chr7:13888618-13888716	Lung_OC	lung:	n/a	n/a
44	CTCF	chr7:13845838-13846239	K562	blood:	n/a	n/a
45	CTCF	chr7:13845950-13846071	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:13845933-13846083	K562	blood:	n/a	n/a
47	CTCF	chr7:13845920-13846070	K562	blood:	n/a	n/a
48	CTCF	chr7:13858494-13858501	Medullo	brain:	n/a	n/a
49	CTCF	chr7:13889820-13890234	K562	blood:	n/a	chr7:13889868-13889886 chr7:13889863-13889884
50	CTCF	chr7:13877865-13877940	Lung_OC	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13889871-13889921	NHDF-neo	bronchial:	n/a
2	chr7:13889871-13889921	T-47D	breast:	n/a
3	chr7:13889871-13889921	A549	lung:	n/a
4	chr7:13842752-13842802	HepG2	liver:	n/a
5	chr7:13889871-13889921	SKMC	muscle:	n/a
6	chr7:13889871-13889921	HIPEpiC	eye:	n/a
7	chr7:13842752-13842802	HAEpiC	amniotic membrane:	n/a
8	chr7:13842752-13842802	GM19239	blood:	n/a
9	chr7:13842752-13842802	BE2_C	brain:	n/a
10	chr7:13842752-13842802	GM12891	blood:	n/a
11	chr7:13842752-13842802	HCM	heart:	n/a
12	chr7:13842752-13842802	GM06990	blood:	n/a
13	chr7:13889871-13889921	PFSK-1	brain:	n/a
14	chr7:13889871-13889921	HEEpiC	esophagus:	n/a
15	chr7:13889871-13889921	SAEC	small airway:	n/a
16	chr7:13889871-13889921	NT2-D1	testis:	n/a
17	chr7:13842752-13842802	U87	brain:	n/a
18	chr7:13889871-13889921	AG10803	skin:	n/a
19	chr7:13889871-13889921	SK-N-SH_RA	brain:	n/a
20	chr7:13842752-13842802	NHBE	bronchial:	n/a
21	chr7:13889871-13889921	PrEC	prostate:	n/a
22	chr7:13889871-13889921	HEK293	kidney:	embryo
23	chr7:13842752-13842802	MCF10A-Er-Src	breast:	n/a
24	chr7:13842752-13842802	HEEpiC	esophagus:	n/a
25	chr7:13842752-13842802	PANC-1	pancreas:	n/a
26	chr7:13842752-13842802	HRCEpiC	kidney:	n/a
27	chr7:13842752-13842802	SAEC	small airway:	n/a
28	chr7:13889871-13889921	NH-A	brain:	n/a
29	chr7:13842752-13842802	ProgFib	skin:	n/a
30	chr7:13842752-13842802	Hepatocyte	liver:	n/a
31	chr7:13842752-13842802	K562	blood:	n/a
32	chr7:13842752-13842802	HMEC	breast:	n/a
33	chr7:13889871-13889921	U87	brain:	n/a
34	chr7:13842752-13842802	RPTEC	kidney:	n/a
35	chr7:13842752-13842802	SK-N-SH	brain:	n/a
36	chr7:13889871-13889921	LNCaP	prostate:	n/a
37	chr7:13889871-13889921	GM12891	blood:	n/a
38	chr7:13842752-13842802	ECC-1	luminal epithelium:	n/a
39	chr7:13889871-13889921	AG09319	gingival:	n/a
40	chr7:13842752-13842802	AG09319	gingival:	n/a
41	chr7:13889871-13889921	Jurkat	blood:	n/a
42	chr7:13889871-13889921	HAEpiC	amniotic membrane:	n/a
43	chr7:13889871-13889921	NHBE	bronchial:	n/a
44	chr7:13889871-13889921	GM12878	blood:	n/a
45	chr7:13889871-13889921	HCM	heart:	n/a
46	chr7:13842752-13842802	NT2-D1	testis:	n/a
47	chr7:13889871-13889921	IMR90	lung:	fetal
48	chr7:13889871-13889921	HUVEC	blood vessel:	n/a
49	chr7:13842752-13842802	HCT-116	colon:	n/a
50	chr7:13889871-13889921	NB4	blood:	n/a

(count:12 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 2081 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10256467	chr7:13841798-13841799	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140151134	chr7:13841807-13841808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145681680	chr7:13841816-13841817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147752182	chr7:13841825-13841826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547866263	chr7:13841826-13841827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537467806	chr7:13841841-13841842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376635298	chr7:13841845-13841846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574022172	chr7:13841870-13841871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374047396	chr7:13841879-13841880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553188670	chr7:13841898-13841899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140075727	chr7:13841914-13841915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545223166	chr7:13841922-13841923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73269525	chr7:13841932-13841933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191034485	chr7:13841934-13841935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369802556	chr7:13841945-13841946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372664147	chr7:13841959-13841960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544224346	chr7:13841970-13841971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144946435	chr7:13841980-13841981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530060111	chr7:13841991-13841992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149060852	chr7:13842009-13842010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566727920	chr7:13842038-13842039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144736916	chr7:13842098-13842099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532358827	chr7:13842099-13842100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182932290	chr7:13842132-13842133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549574747	chr7:13842149-13842150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185766943	chr7:13842153-13842154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192327495	chr7:13842176-13842177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537127368	chr7:13842182-13842183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561172122	chr7:13842197-13842198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113022095	chr7:13842216-13842217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528938144	chr7:13842227-13842228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183830925	chr7:13842239-13842240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10227855	chr7:13842265-13842266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553253780	chr7:13842280-13842281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543650515	chr7:13842281-13842282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138688484	chr7:13842331-13842332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187673183	chr7:13842350-13842351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575347513	chr7:13842368-13842369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557132127	chr7:13842385-13842386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544317275	chr7:13842456-13842457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7458687	chr7:13842479-13842480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112957569	chr7:13842499-13842500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62452173	chr7:13842501-13842502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560925967	chr7:13842510-13842511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574489000	chr7:13842566-13842567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116239032	chr7:13842589-13842590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560413972	chr7:13842609-13842610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532288804	chr7:13842616-13842617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541236444	chr7:13842619-13842620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552375226	chr7:13842659-13842660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13837600-13845000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:13840200-13843000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr7:13840400-13841800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:13840600-13843400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:13840600-13844200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr7:13840800-13843000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:13841000-13842800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:13841000-13845000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr7:13841200-13841800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr7:13841600-13845000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:13841600-13845200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:13841800-13844800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:13841800-13845600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr7:13842400-13843000	Enhancers	K562	blood
15	chr7:13842800-13843000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:13842800-13843000	Enhancers	HMEC	breast
17	chr7:13842800-13843200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:13842800-13843800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:13843000-13843600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:13843000-13843800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:13843000-13845000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr7:13843000-13845000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr7:13843400-13844600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:13843600-13843800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:13843800-13845800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:13843800-13845800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:13843800-13845800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:13844200-13844400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr7:13844200-13846400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:13844400-13846600	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr7:13844600-13845000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:13844800-13846400	Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr7:13845000-13846400	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr7:13845000-13846400	Active TSS	H1 Cell Line	embryonic stem cell
35	chr7:13845000-13846400	Active TSS	H9 Cell Line	embryonic stem cell
36	chr7:13845000-13846400	Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr7:13845000-13846400	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr7:13845000-13846400	Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr7:13845200-13846200	Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr7:13845600-13846200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:13845600-13846400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr7:13845800-13846200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:13845800-13846400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:13845800-13846400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:13845800-13846400	Active TSS	Placenta	Placenta
46	chr7:13860400-13860800	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr7:13860800-13861000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr7:13860800-13861200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:13860800-13861200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:13860800-13861200	Enhancers	Fetal Lung	lung

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