Variant report

Variant	nsv887704
Chromosome Location	chr7:13997159-14029739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:730)
CpG islands
(count:917)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:14028304-14029468	K562	blood:	n/a	n/a
2	ARID3A	chr7:14025489-14026374	K562	blood:	n/a	n/a
3	ARID3A	chr7:14019807-14021691	K562	blood:	n/a	chr7:14020786-14020802 chr7:14020787-14020803
4	ARID3A	chr7:14022012-14023126	K562	blood:	n/a	n/a
5	ARID3A	chr7:14027058-14028051	K562	blood:	n/a	n/a
6	ARID3A	chr7:14023492-14023912	K562	blood:	n/a	n/a
7	ARID3A	chr7:14024325-14025263	K562	blood:	n/a	n/a
8	ATF1	chr7:14028906-14031452	K562	blood:	n/a	n/a
9	ATF1	chr7:14027157-14027465	K562	blood:	n/a	n/a
10	ATF1	chr7:14020698-14021136	K562	blood:	n/a	n/a
11	ATF1	chr7:14019904-14020081	K562	blood:	n/a	n/a
12	ATF1	chr7:14022540-14022952	K562	blood:	n/a	n/a
13	ATF1	chr7:14027694-14028014	K562	blood:	n/a	n/a
14	ATF3	chr7:14020590-14021036	K562	blood:	n/a	n/a
15	ATF3	chr7:14020788-14020993	K562	blood:	n/a	n/a
16	ATF3	chr7:14022508-14022915	K562	blood:	n/a	n/a
17	BACH1	chr7:14029018-14029030	K562	blood:	n/a	n/a
18	BACH1	chr7:14020708-14021014	H1-hESC	embryonic stem cell:	n/a	chr7:14020850-14020864
19	BCLAF1	chr7:14020709-14021202	K562	blood:	n/a	chr7:14020853-14020862 chr7:14020852-14020861
20	BHLHE40	chr7:14020621-14021121	K562	blood:	n/a	n/a
21	BHLHE40	chr7:14027538-14032370	K562	blood:	n/a	n/a
22	BRCA1	chr7:14029444-14029472	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr7:14020686-14021294	HCT-116	colon:	n/a	n/a
24	CCNT2	chr7:14019439-14019595	K562	blood:	n/a	n/a
25	CCNT2	chr7:14027613-14027934	K562	blood:	n/a	n/a
26	CCNT2	chr7:14028784-14029584	K562	blood:	n/a	n/a
27	CCNT2	chr7:14020845-14021045	K562	blood:	n/a	n/a
28	CCNT2	chr7:14022390-14022906	K562	blood:	n/a	n/a
29	CCNT2	chr7:14025553-14025753	K562	blood:	n/a	n/a
30	CEBPB	chr7:14029083-14029645	A549	lung:	n/a	n/a
31	CEBPB	chr7:14024790-14024990	A549	lung:	n/a	chr7:14024803-14024814 chr7:14024883-14024894
32	CEBPB	chr7:14019756-14020094	K562	blood:	n/a	chr7:14019938-14019949
33	CEBPB	chr7:14029209-14029715	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:14022307-14022889	K562	blood:	n/a	n/a
35	CEBPB	chr7:14022555-14022766	K562	blood:	n/a	n/a
36	CEBPB	chr7:14029243-14029604	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:14029191-14029540	A549	lung:	n/a	n/a
38	CEBPB	chr7:14029280-14029555	K562	blood:	n/a	n/a
39	CEBPB	chr7:14020519-14021361	HCT-116	colon:	n/a	n/a
40	CEBPB	chr7:14029025-14029606	K562	blood:	n/a	n/a
41	CEBPB	chr7:14019316-14020073	IMR90	lung:	n/a	chr7:14019938-14019949
42	CEBPB	chr7:14020713-14021145	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:14018578-14018927	K562	blood:	n/a	n/a
44	CEBPB	chr7:14028902-14029684	K562	blood:	n/a	n/a
45	CEBPB	chr7:14020633-14021062	K562	blood:	n/a	n/a
46	CEBPB	chr7:14026370-14026599	K562	blood:	n/a	n/a
47	CEBPB	chr7:14025392-14025544	H1-hESC	embryonic stem cell:	n/a	chr7:14025468-14025481
48	CEBPB	chr7:14029282-14029549	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:14020654-14021116	K562	blood:	n/a	n/a
50	CEBPB	chr7:14028888-14029558	H1-hESC	embryonic stem cell:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14028690-14028740	AG04450	lung:	fetal
2	chr7:14029680-14029730	PrEC	prostate:	n/a
3	chr7:14028690-14028740	AG04450	lung:	fetal
4	chr7:14029680-14029730	PrEC	prostate:	n/a
5	chr7:14029360-14029410	AG09319	gingival:	n/a
6	chr7:14025907-14025957	AG04450	lung:	fetal
7	chr7:14028845-14028895	GM06990	blood:	n/a
8	chr7:14028690-14028740	Caco-2	colon:	n/a
9	chr7:14028690-14028740	HepG2	liver:	n/a
10	chr7:14029514-14029564	A549	lung:	n/a
11	chr7:14029701-14029751	T-47D	breast:	n/a
12	chr7:14029360-14029410	HRPEpiC	eye:	n/a
13	chr7:14028845-14028895	GM12892	blood:	n/a
14	chr7:14029592-14029642	NH-A	brain:	n/a
15	chr7:14029057-14029107	MCF10A-Er-Src	breast:	n/a
16	chr7:14029085-14029135	AG09319	gingival:	n/a
17	chr7:14029360-14029410	GM12878	blood:	n/a
18	chr7:14029057-14029107	HNPCEpiC	eye:	n/a
19	chr7:14029657-14029707	HMEC	breast:	n/a
20	chr7:14029701-14029751	NHBE	bronchial:	n/a
21	chr7:14028954-14029004	BJ	skin:	n/a
22	chr7:14029514-14029564	PrEC	prostate:	n/a
23	chr7:14028690-14028740	BE2_C	brain:	n/a
24	chr7:14029015-14029065	ECC-1	luminal epithelium:	n/a
25	chr7:14029680-14029730	U87	brain:	n/a
26	chr7:14028690-14028740	PrEC	prostate:	n/a
27	chr7:14029421-14029471	SK-N-MC	brain:	n/a
28	chr7:14028690-14028740	K562	blood:	n/a
29	chr7:14029057-14029107	BJ	skin:	n/a
30	chr7:14025907-14025957	AG04449	skin:	fetal
31	chr7:14029701-14029751	AG04450	lung:	fetal
32	chr7:14028954-14029004	SAEC	small airway:	n/a
33	chr7:14029680-14029730	GM12878	blood:	n/a
34	chr7:14028690-14028740	ECC-1	luminal epithelium:	n/a
35	chr7:14029360-14029410	Hepatocyte	liver:	n/a
36	chr7:14029285-14029335	HMEC	breast:	n/a
37	chr7:14029057-14029107	NH-A	brain:	n/a
38	chr7:14029701-14029751	HepG2	liver:	n/a
39	chr7:14029592-14029642	CMK	blood:	n/a
40	chr7:14028845-14028895	GM12878	blood:	n/a
41	chr7:14029421-14029471	HEEpiC	esophagus:	n/a
42	chr7:14029701-14029751	CMK	blood:	n/a
43	chr7:14029592-14029642	GM12892	blood:	n/a
44	chr7:14028690-14028740	HCPEpiC	choroid plexus:	n/a
45	chr7:14029592-14029642	GM06990	blood:	n/a
46	chr7:14029057-14029107	H1-hESC	embryonic stem cell:	embryo
47	chr7:14029514-14029564	SK-N-SH_RA	brain:	n/a
48	chr7:14029701-14029751	ovcar-3	ovarian:	n/a
49	chr7:14028690-14028740	HAEpiC	amniotic membrane:	n/a
50	chr7:14029592-14029642	NT2-D1	testis:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:14008374..14010454-chr7:14010741..14014267,3	K562	blood:
2	chr7:14007347..14010372-chr7:14013891..14016149,3	K562	blood:
3	chr7:13996982..13998734-chr7:14003556..14005276,2	K562	blood:
4	chr7:13989697..13992273-chr7:13998903..14000492,2	K562	blood:
5	chr7:13985844..13987492-chr7:14019235..14021498,3	K562	blood:
6	chr7:13996982..14001014-chr7:14002058..14006442,5	K562	blood:
7	chr7:13997095..13998598-chr7:14011763..14014097,2	K562	blood:
8	chr7:13972971..13975876-chr7:14017215..14019067,2	K562	blood:
9	chr7:13989697..13991875-chr7:13998508..14000403,2	K562	blood:
10	chr7:13994487..13997447-chr7:13998861..14001557,3	K562	blood:
11	chr7:13999444..14001578-chr7:14011983..14013986,2	K562	blood:
12	chr7:13991446..13994404-chr7:14016165..14019066,2	K562	blood:
13	chr7:13997566..14001513-chr7:14018273..14020813,4	K562	blood:
14	chr7:14006832..14009874-chr7:14010267..14013655,4	K562	blood:
15	chr7:14016754..14019512-chr7:14048392..14050407,2	K562	blood:
16	chr7:13999444..14001578-chr7:14011983..14013986,2	K562	blood:
17	chr7:13998712..14001529-chr7:14011348..14014089,2	K562	blood:
18	chr7:14007601..14010058-chr7:14027934..14029828,2	K562	blood:
19	chr7:14006832..14009874-chr7:14010267..14013655,4	K562	blood:
20	chr7:14006642..14008318-chr7:14033077..14034662,2	K562	blood:
21	chr7:13997007..14000342-chr7:14017723..14020427,3	K562	blood:
22	chr7:14007347..14010372-chr7:14013891..14016149,3	K562	blood:
23	chr7:14006507..14011484-chr7:14016197..14021172,5	K562	blood:
24	chr7:14006507..14011484-chr7:14016197..14021172,5	K562	blood:
25	chr7:14014823..14017219-chr7:14018906..14020830,2	MCF-7	breast:
26	chr7:14011992..14014933-chr7:14015921..14017592,2	K562	blood:
27	chr7:13980622..13983188-chr7:14022030..14023536,2	K562	blood:
28	chr7:14000124..14001645-chr7:14029158..14031129,2	K562	blood:
29	chr7:13996982..13998734-chr7:14003556..14005276,2	K562	blood:
30	chr7:13997566..14001513-chr7:14018273..14020813,4	K562	blood:
31	chr7:13996982..14001014-chr7:14002058..14006442,5	K562	blood:
32	chr7:13998712..14001529-chr7:14011348..14014089,2	K562	blood:
33	chr7:13993113..13994903-chr7:14003071..14005104,2	K562	blood:
34	chr7:14027263..14030675-chr7:14047798..14051480,3	K562	blood:
35	chr7:13964325..13967217-chr7:14020611..14022495,2	K562	blood:
36	chr7:14008558..14010409-chr7:14028328..14031106,2	K562	blood:
37	chr7:13997007..14000342-chr7:14017723..14020427,3	K562	blood:
38	chr7:13997095..13998598-chr7:14011763..14014097,2	K562	blood:
39	chr7:14014823..14017219-chr7:14018906..14020830,2	MCF-7	breast:
40	chr7:13994487..13997447-chr7:13998861..14001557,3	K562	blood:
41	chr7:14008374..14010454-chr7:14010741..14014267,3	K562	blood:
42	chr7:14011992..14014933-chr7:14015921..14017592,2	K562	blood:

No data

Variant related genes	Relation type
ETV1	TF binding region
ETV1	CpG island
ENSG00000252374	chromatin interactions
ENSG00000006468	chromatin interactions

Extended variants
information (count: 1396 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3779118	chr7:13997159-13997160	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77605777	chr7:13997164-13997165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190024850	chr7:13997168-13997169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532652501	chr7:13997191-13997192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140442933	chr7:13997289-13997290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs118168433	chr7:13997290-13997291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575956458	chr7:13997381-13997382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537708445	chr7:13997432-13997433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149993085	chr7:13997446-13997447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3837100	chr7:13997478-13997479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397841222	chr7:13997481-13997482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568411406	chr7:13997499-13997500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147688409	chr7:13997539-13997540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113046254	chr7:13997544-13997545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12699568	chr7:13997573-13997574	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs74984495	chr7:13997645-13997646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142400955	chr7:13997667-13997668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146579240	chr7:13997719-13997720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546172497	chr7:13997720-13997721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561221713	chr7:13997779-13997780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572271462	chr7:13997785-13997786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574825326	chr7:13997797-13997798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540198214	chr7:13997825-13997826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560133776	chr7:13997835-13997836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139338754	chr7:13997845-13997846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532452860	chr7:13997867-13997868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117660440	chr7:13997897-13997898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112649568	chr7:13997931-13997932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531529539	chr7:13997965-13997966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548434065	chr7:13997966-13997967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568346158	chr7:13997986-13997987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181236962	chr7:13998032-13998033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534097961	chr7:13998038-13998039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567757731	chr7:13998040-13998041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17167689	chr7:13998041-13998042	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs183826335	chr7:13998077-13998078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188157785	chr7:13998096-13998097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139200172	chr7:13998150-13998151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180730671	chr7:13998166-13998167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186343306	chr7:13998170-13998171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574762378	chr7:13998182-13998183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113900020	chr7:13998237-13998238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560072977	chr7:13998242-13998243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113441260	chr7:13998282-13998283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545923306	chr7:13998309-13998310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111315745	chr7:13998340-13998341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370356981	chr7:13998352-13998353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548371131	chr7:13998368-13998369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369958002	chr7:13998395-13998396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535358402	chr7:13998396-13998397	Weak transcription Strong 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
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
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	18628472	CNVD

Chromatin state (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13975600-14003600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:13975600-14003600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:13975600-14013800	Weak transcription	Left Ventricle	heart
4	chr7:13978800-14004600	Weak transcription	Fetal Lung	lung
5	chr7:13979200-13998000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:13985800-14004600	Weak transcription	NHLF	lung
7	chr7:13988000-14012800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:13988200-14010400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:13989000-14019400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:13989400-14003600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr7:13990000-14003400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr7:13990000-14003600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:13990200-13997200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:13990400-13997800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:13990800-14014000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:13990800-14014400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr7:13995200-13997200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr7:13996000-13997200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:13996400-14011000	Weak transcription	Fetal Heart	heart
20	chr7:13997000-13997800	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:13997000-13998200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:13997000-13998600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:13997000-13999000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:13997200-13997600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:13997200-13998000	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr7:13997200-14000000	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr7:13997600-14003600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:13997800-13998400	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr7:13997800-14003400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:13998000-13998600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr7:13998000-14003400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr7:13998200-14009800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:13998400-14003400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr7:13998600-14003400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr7:13998600-14014000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:13999000-14009000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:14000000-14008000	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr7:14002400-14019600	Weak transcription	K562	blood
39	chr7:14003400-14003600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:14003400-14004000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr7:14003400-14004000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr7:14003400-14004200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:14003400-14004200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:14003600-14004000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr7:14003600-14004000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr7:14003600-14004000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:14003600-14004000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:14003600-14004200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr7:14003600-14004800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:14003600-14006000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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