Variant report

Variant	nsv887639
Chromosome Location	chr7:12448482-12488535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:517)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12473668-12473988	K562	blood:	n/a	n/a
2	ARID3A	chr7:12473648-12473985	HepG2	liver:	n/a	n/a
3	ATF1	chr7:12484873-12485016	K562	blood:	n/a	n/a
4	ATF2	chr7:12463437-12464243	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:12463290-12464092	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr7:12463807-12464153	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr7:12463938-12464115	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:12463057-12463705	A549	lung:	n/a	n/a
9	CEBPB	chr7:12462151-12462633	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:12463261-12463571	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr7:12463151-12463582	A549	lung:	n/a	n/a
12	CEBPB	chr7:12463242-12463599	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:12475774-12475947	A549	lung:	n/a	chr7:12475916-12475927 chr7:12475916-12475927 chr7:12475914-12475927
14	CEBPB	chr7:12463181-12463787	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:12484968-12485143	K562	blood:	n/a	chr7:12485017-12485034 chr7:12485020-12485033 chr7:12485020-12485033 chr7:12485022-12485033 chr7:12485022-12485033
16	CEBPB	chr7:12482363-12482524	K562	blood:	n/a	n/a
17	CEBPB	chr7:12463228-12463549	MCF-7	breast:	n/a	n/a
18	CEBPB	chr7:12463214-12463587	A549	lung:	n/a	n/a
19	CEBPB	chr7:12461559-12461648	K562	blood:	n/a	n/a
20	CEBPB	chr7:12463236-12464248	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr7:12463436-12464416	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:12463175-12464241	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr7:12473880-12474030	RPTEC	kidney:	n/a	n/a
24	CTCF	chr7:12473840-12473990	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr7:12476860-12477010	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:12473740-12473890	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:12476920-12477070	A549	lung:	n/a	n/a
28	CTCF	chr7:12473796-12473977	A549	lung:	n/a	n/a
29	CTCF	chr7:12476910-12477025	GM10266	blood:	n/a	n/a
30	CTCF	chr7:12476840-12476990	RPTEC	kidney:	n/a	n/a
31	CTCF	chr7:12473780-12473930	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr7:12476924-12477031	GM12878	blood:	n/a	n/a
33	CTCF	chr7:12476861-12477001	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:12473740-12473890	GM12801	blood:	n/a	n/a
35	CTCF	chr7:12473680-12473830	GM12871	blood:	n/a	n/a
36	CTCF	chr7:12476889-12477045	ProgFib	skin:	n/a	n/a
37	CTCF	chr7:12473200-12473350	GM12873	blood:	n/a	n/a
38	CTCF	chr7:12473721-12473969	Medullo	brain:	n/a	n/a
39	CTCF	chr7:12473780-12473930	GM12865	blood:	n/a	n/a
40	CTCF	chr7:12473380-12473530	AG09319	gingival:	n/a	n/a
41	CTCF	chr7:12476880-12477030	GM12865	blood:	n/a	n/a
42	CTCF	chr7:12476960-12477110	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr7:12476900-12477050	RPTEC	kidney:	n/a	n/a
44	CTCF	chr7:12476900-12477050	AG04450	lung:	n/a	n/a
45	CTCF	chr7:12473780-12473930	HMF	breast:	n/a	n/a
46	CTCF	chr7:12476847-12477053	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:12473785-12473910	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr7:12476899-12477047	NHEK	skin:	n/a	n/a
49	CTCF	chr7:12476840-12476990	GM12866	blood:	n/a	n/a
50	CTCF	chr7:12476940-12477090	AG04450	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12462597-12462647	GM12891	blood:	n/a
2	chr7:12462597-12462647	HIPEpiC	eye:	n/a
3	chr7:12462597-12462647	PANC-1	pancreas:	n/a
4	chr7:12462597-12462647	Jurkat	blood:	n/a
5	chr7:12462597-12462647	LNCaP	prostate:	n/a
6	chr7:12462597-12462647	AG10803	skin:	n/a
7	chr7:12462597-12462647	NHBE	bronchial:	n/a
8	chr7:12462597-12462647	BJ	skin:	n/a
9	chr7:12462597-12462647	U87	brain:	n/a
10	chr7:12462597-12462647	HCF	heart:	n/a
11	chr7:12462597-12462647	HepG2	liver:	n/a
12	chr7:12462597-12462647	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:12462597-12462647	NHDF-neo	bronchial:	n/a
14	chr7:12462597-12462647	Caco-2	colon:	n/a
15	chr7:12462597-12462647	HMEC	breast:	n/a
16	chr7:12462597-12462647	ovcar-3	ovarian:	n/a
17	chr7:12462597-12462647	MCF-7	breast:	n/a
18	chr7:12462597-12462647	PFSK-1	brain:	n/a
19	chr7:12462597-12462647	HCT-116	colon:	n/a
20	chr7:12462597-12462647	HCPEpiC	choroid plexus:	n/a
21	chr7:12462597-12462647	BE2_C	brain:	n/a
22	chr7:12462597-12462647	GM19239	blood:	n/a
23	chr7:12462597-12462647	HEK293	kidney:	embryo
24	chr7:12462597-12462647	GM12878	blood:	n/a
25	chr7:12462597-12462647	GM12892	blood:	n/a
26	chr7:12462597-12462647	HL-60	blood:	n/a
27	chr7:12462597-12462647	PrEC	prostate:	n/a
28	chr7:12462597-12462647	K562	blood:	n/a
29	chr7:12462597-12462647	HCM	heart:	n/a
30	chr7:12462597-12462647	HRCEpiC	kidney:	n/a
31	chr7:12462597-12462647	H1-hESC	embryonic stem cell:	embryo
32	chr7:12462597-12462647	HNPCEpiC	eye:	n/a
33	chr7:12462597-12462647	CMK	blood:	n/a
34	chr7:12462597-12462647	A549	lung:	n/a
35	chr7:12462597-12462647	HRE	kidney:	n/a
36	chr7:12462597-12462647	AG09309	skin:	n/a
37	chr7:12462597-12462647	Hepatocyte	liver:	n/a
38	chr7:12462597-12462647	ProgFib	skin:	n/a
39	chr7:12462597-12462647	AoSMC	blood vessel:	n/a
40	chr7:12462597-12462647	HEEpiC	esophagus:	n/a
41	chr7:12462597-12462647	NB4	blood:	n/a
42	chr7:12462597-12462647	SK-N-MC	brain:	n/a
43	chr7:12462597-12462647	HRPEpiC	eye:	n/a
44	chr7:12462597-12462647	Hela-S3	cervix:	n/a
45	chr7:12462597-12462647	RPTEC	kidney:	n/a
46	chr7:12462597-12462647	IMR90	lung:	fetal
47	chr7:12462597-12462647	SKMC	muscle:	n/a
48	chr7:12462597-12462647	MCF10A-Er-Src	breast:	n/a
49	chr7:12462597-12462647	ECC-1	luminal epithelium:	n/a
50	chr7:12462597-12462647	NH-A	brain:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
2	chr7:12479476..12481083-chr7:12493598..12496034,2	K562	blood:
3	chr7:12443122..12444791-chr7:12465079..12466887,2	K562	blood:
4	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
5	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
6	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
7	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
8	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
9	chr7:12473109..12473862-chr7:12558519..12559485,2	K562	blood:
10	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
11	chr7:12442216..12444802-chr7:12483847..12486014,2	K562	blood:
12	chr7:12476531..12477332-chr7:12536046..12536815,3	MCF-7	breast:
13	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
14	chr7:12441796..12443703-chr7:12463390..12465045,2	MCF-7	breast:
15	chr20:40278409..40280542-chr7:12478341..12480011,2	MCF-7	breast:
16	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
17	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
18	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
19	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
20	chr7:12480338..12484247-chr7:12487058..12490542,4	K562	blood:
21	chr7:12480338..12484247-chr7:12487058..12490542,4	K562	blood:
22	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
23	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
24	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
25	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000226690	chromatin interactions
ENSG00000146530	chromatin interactions

Extended variants
information (count: 1729 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1729 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10254572	chr7:12448482-12448483	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138727205	chr7:12448555-12448556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528904371	chr7:12448578-12448579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149342914	chr7:12448584-12448585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539173648	chr7:12448594-12448595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117697092	chr7:12448601-12448602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116484989	chr7:12448609-12448610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541419006	chr7:12448622-12448623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183219910	chr7:12448641-12448642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572386797	chr7:12448662-12448663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570832777	chr7:12448699-12448700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77276366	chr7:12448723-12448724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76637559	chr7:12448724-12448725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74476970	chr7:12448725-12448726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188220907	chr7:12448734-12448735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539952121	chr7:12448767-12448768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs5882359	chr7:12448768-12448769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564548852	chr7:12448774-12448775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533538589	chr7:12448775-12448776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1020153	chr7:12448784-12448785	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs563757316	chr7:12448809-12448810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1020152	chr7:12448822-12448823	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs549390021	chr7:12448835-12448836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568399013	chr7:12448847-12448848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138113125	chr7:12448849-12448850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375765730	chr7:12448863-12448864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547679711	chr7:12448911-12448912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570562834	chr7:12448915-12448916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539572379	chr7:12448927-12448928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35998202	chr7:12448943-12448944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551441777	chr7:12448952-12448953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556031280	chr7:12448953-12448954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571369556	chr7:12448985-12448986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs67015252	chr7:12449011-12449012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10255444	chr7:12449038-12449039	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192453344	chr7:12449090-12449091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62448597	chr7:12449110-12449111	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs571675838	chr7:12449139-12449140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184366979	chr7:12449150-12449151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142590976	chr7:12449171-12449172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578114247	chr7:12449183-12449184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543994371	chr7:12449192-12449193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375200714	chr7:12449209-12449210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187842498	chr7:12449221-12449222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543072389	chr7:12449222-12449223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145998787	chr7:12449230-12449231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192350071	chr7:12449242-12449243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547717259	chr7:12449260-12449261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570721853	chr7:12449316-12449317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533017921	chr7:12449324-12449325	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	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
Glioblastoma multiforme	17002787	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12444600-12448800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:12444600-12448800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:12445600-12448800	Weak transcription	K562	blood
4	chr7:12448400-12449200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr7:12448400-12449400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:12448600-12449400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr7:12448600-12449400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:12448600-12449400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr7:12448800-12449200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:12448800-12449400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr7:12448800-12449400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:12448800-12449400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:12448800-12449400	Enhancers	K562	blood
14	chr7:12449200-12449400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr7:12449400-12452800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr7:12449400-12453000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr7:12449400-12453000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:12452800-12453400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:12453000-12453400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:12453000-12453400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:12453000-12453400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:12453000-12453400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:12453000-12453400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr7:12453400-12461600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr7:12458000-12458400	Enhancers	HUVEC	blood vessel
26	chr7:12458200-12458800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:12458400-12461800	Weak transcription	HUVEC	blood vessel
28	chr7:12458800-12462400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:12458800-12463200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr7:12461000-12461800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:12461000-12462600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:12461000-12463400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:12461200-12463400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:12461400-12461600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr7:12461400-12461600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr7:12461400-12462800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:12461400-12463400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:12461400-12463400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:12461400-12463800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:12461600-12462200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:12461600-12462200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:12461600-12462600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr7:12461600-12463000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:12461600-12463200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:12461600-12463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:12461600-12464000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:12461600-12464200	Enhancers	HMEC	breast
48	chr7:12461800-12462200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:12461800-12462400	Enhancers	A549	lung
50	chr7:12461800-12464000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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