Variant report

Variant	nsv516511
Chromosome Location	chr7:12439672-12479584
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:917)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12445132-12445205	K562	blood:	n/a	n/a
2	ARID3A	chr7:12441428-12441976	K562	blood:	n/a	n/a
3	ARID3A	chr7:12443002-12443779	K562	blood:	n/a	n/a
4	ARID3A	chr7:12473648-12473985	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:12442512-12442624	K562	blood:	n/a	n/a
6	ARID3A	chr7:12473668-12473988	K562	blood:	n/a	n/a
7	ATF1	chr7:12441677-12441884	K562	blood:	n/a	n/a
8	ATF1	chr7:12442940-12444036	K562	blood:	n/a	n/a
9	ATF2	chr7:12463290-12464092	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:12463437-12464243	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:12443361-12443704	K562	blood:	n/a	n/a
12	BACH1	chr7:12443045-12443428	K562	blood:	n/a	n/a
13	BACH1	chr7:12443123-12443675	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr7:12463938-12464115	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr7:12463807-12464153	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCLAF1	chr7:12442724-12444060	K562	blood:	n/a	chr7:12443627-12443636 chr7:12443692-12443705
17	BCLAF1	chr7:12443085-12443960	K562	blood:	n/a	chr7:12443627-12443636 chr7:12443692-12443705
18	BHLHE40	chr7:12441675-12441916	K562	blood:	n/a	n/a
19	BHLHE40	chr7:12444086-12444098	K562	blood:	n/a	n/a
20	BHLHE40	chr7:12442950-12443807	K562	blood:	n/a	n/a
21	BRCA1	chr7:12443076-12443269	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr7:12442888-12444084	K562	blood:	n/a	n/a
23	CBX3	chr7:12442863-12443396	K562	blood:	n/a	n/a
24	CCNT2	chr7:12442982-12443788	K562	blood:	n/a	n/a
25	CEBPB	chr7:12463181-12463787	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr7:12475774-12475947	A549	lung:	n/a	chr7:12475916-12475927 chr7:12475916-12475927 chr7:12475914-12475927
27	CEBPB	chr7:12463151-12463582	A549	lung:	n/a	n/a
28	CEBPB	chr7:12462151-12462633	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:12463057-12463705	A549	lung:	n/a	n/a
30	CEBPB	chr7:12443052-12443399	K562	blood:	n/a	n/a
31	CEBPB	chr7:12463261-12463571	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr7:12463214-12463587	A549	lung:	n/a	n/a
33	CEBPB	chr7:12461559-12461648	K562	blood:	n/a	n/a
34	CEBPB	chr7:12463242-12463599	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:12443418-12444101	K562	blood:	n/a	n/a
36	CEBPB	chr7:12463228-12463549	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:12443480-12443656	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:12443413-12444076	K562	blood:	n/a	n/a
39	CEBPB	chr7:12463236-12464248	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPD	chr7:12442836-12443948	K562	blood:	n/a	n/a
41	CHD1	chr7:12463436-12464416	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr7:12442741-12443325	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr7:12463175-12464241	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr7:12442748-12442931	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr7:12443230-12443898	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr7:12443076-12443682	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr7:12442991-12443949	K562	blood:	n/a	n/a
48	CREB1	chr7:12443080-12443849	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr7:12443010-12443910	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr7:12442783-12444210	K562	blood:	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	chr7:12444095-12444145	HRE	kidney:	n/a
2	chr7:12443146-12443196	ECC-1	luminal epithelium:	n/a
3	chr7:12444095-12444145	HRE	kidney:	n/a
4	chr7:12443146-12443196	ECC-1	luminal epithelium:	n/a
5	chr7:12443478-12443528	HCT-116	colon:	n/a
6	chr7:12443880-12443930	GM12892	blood:	n/a
7	chr7:12443191-12443241	NB4	blood:	n/a
8	chr7:12443926-12443976	AG04450	lung:	fetal
9	chr7:12443542-12443592	HIPEpiC	eye:	n/a
10	chr7:12444013-12444063	HUVEC	blood vessel:	n/a
11	chr7:12443529-12443579	Jurkat	blood:	n/a
12	chr7:12462597-12462647	SK-N-SH	brain:	n/a
13	chr7:12462597-12462647	ProgFib	skin:	n/a
14	chr7:12444095-12444145	SK-N-MC	brain:	n/a
15	chr7:12462597-12462647	BE2_C	brain:	n/a
16	chr7:12443478-12443528	SKMC	muscle:	n/a
17	chr7:12444115-12444165	Jurkat	blood:	n/a
18	chr7:12443146-12443196	Hepatocyte	liver:	n/a
19	chr7:12443926-12443976	HepG2	liver:	n/a
20	chr7:12443529-12443579	AG09309	skin:	n/a
21	chr7:12462597-12462647	SAEC	small airway:	n/a
22	chr7:12443529-12443579	SK-N-SH	brain:	n/a
23	chr7:12443886-12443936	Hepatocyte	liver:	n/a
24	chr7:12443880-12443930	U87	brain:	n/a
25	chr7:12443880-12443930	AG04449	skin:	fetal
26	chr7:12443542-12443592	NT2-D1	testis:	n/a
27	chr7:12443146-12443196	HMEC	breast:	n/a
28	chr7:12446327-12446377	GM19239	blood:	n/a
29	chr7:12443191-12443241	NHDF-neo	bronchial:	n/a
30	chr7:12443926-12443976	HCPEpiC	choroid plexus:	n/a
31	chr7:12443542-12443592	HepG2	liver:	n/a
32	chr7:12443146-12443196	GM12891	blood:	n/a
33	chr7:12443886-12443936	HRCEpiC	kidney:	n/a
34	chr7:12444115-12444165	HCT-116	colon:	n/a
35	chr7:12443191-12443241	HCM	heart:	n/a
36	chr7:12443478-12443528	MCF10A-Er-Src	breast:	n/a
37	chr7:12444095-12444145	SKMC	muscle:	n/a
38	chr7:12443704-12443754	HEK293	kidney:	embryo
39	chr7:12443529-12443579	AG09319	gingival:	n/a
40	chr7:12443146-12443196	HIPEpiC	eye:	n/a
41	chr7:12446327-12446377	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:12443880-12443930	AG09319	gingival:	n/a
43	chr7:12443191-12443241	K562	blood:	n/a
44	chr7:12444290-12444340	Jurkat	blood:	n/a
45	chr7:12462597-12462647	HRE	kidney:	n/a
46	chr7:12443191-12443241	ovcar-3	ovarian:	n/a
47	chr7:12443191-12443241	MCF-7	breast:	n/a
48	chr7:12444290-12444340	NH-A	brain:	n/a
49	chr7:12443478-12443528	Caco-2	colon:	n/a
50	chr7:12443529-12443579	HAEpiC	amniotic membrane:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
2	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
3	chr7:12476531..12477332-chr7:12536046..12536815,3	MCF-7	breast:
4	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
5	chr20:40278409..40280542-chr7:12478341..12480011,2	MCF-7	breast:
6	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
7	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
8	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:
9	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
10	chr7:12443122..12444791-chr7:12465079..12466887,2	K562	blood:
11	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
12	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
13	chr7:12441796..12443703-chr7:12463390..12465045,2	MCF-7	breast:
14	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
15	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
16	chr7:12441879..12443410-chr7:12725306..12727318,2	K562	blood:
17	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
18	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
19	chr7:12421246..12422799-chr7:12438154..12440817,2	K562	blood:
20	chr7:12479476..12481083-chr7:12493598..12496034,2	K562	blood:
21	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
22	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
23	chr7:12441983..12444239-chr7:12724759..12726454,2	K562	blood:
24	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
25	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
26	chr20:47537945..47538638-chr7:12442691..12443569,2	Hela-S3	cervix:
27	chr7:12473109..12473862-chr7:12558519..12559485,2	K562	blood:

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000122644	chromatin interactions
ENSG00000226690	chromatin interactions
ENSG00000146530	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000271253	chromatin interactions

Extended variants
information (count: 1677 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1677 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1595802	chr7:12439672-12439673	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73054745	chr7:12439680-12439681	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs860221	chr7:12439686-12439687	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs6966791	chr7:12439714-12439715	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs548481491	chr7:12439736-12439737	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150644730	chr7:12439757-12439758	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79521877	chr7:12439798-12439799	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1595800	chr7:12439816-12439817	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs573369438	chr7:12439883-12439884	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545574724	chr7:12439885-12439886	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571017655	chr7:12439923-12439924	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571197164	chr7:12439924-12439925	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531019788	chr7:12439940-12439941	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139758990	chr7:12439973-12439974	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186604324	chr7:12439982-12439983	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191463724	chr7:12440026-12440027	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs557006155	chr7:12440030-12440031	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs847994	chr7:12440040-12440041	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143026738	chr7:12440084-12440085	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs551156121	chr7:12440123-12440124	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs571049985	chr7:12440126-12440127	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs536727895	chr7:12440148-12440149	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11981363	chr7:12440251-12440252	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs567166588	chr7:12440271-12440272	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs147455840	chr7:12440272-12440273	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs111254313	chr7:12440290-12440291	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs542803753	chr7:12440306-12440307	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552704062	chr7:12440315-12440316	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs139462462	chr7:12440316-12440317	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs139805903	chr7:12440325-12440326	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs545660370	chr7:12440326-12440327	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559182193	chr7:12440333-12440334	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs535331414	chr7:12440383-12440384	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145303796	chr7:12440387-12440388	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs544736732	chr7:12440427-12440428	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs112792950	chr7:12440478-12440479	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs111747713	chr7:12440482-12440483	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs147629688	chr7:12440492-12440493	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148670698	chr7:12440531-12440532	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs76206668	chr7:12440542-12440543	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs111825888	chr7:12440569-12440570	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs59739486	chr7:12440578-12440579	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571130911	chr7:12440587-12440588	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs564966416	chr7:12440589-12440590	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs118030912	chr7:12440615-12440616	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185455304	chr7:12440703-12440704	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12673085	chr7:12440776-12440777	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs371347797	chr7:12440785-12440786	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561428358	chr7:12440787-12440788	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552926662	chr7:12440829-12440830	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Autism	22495309	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:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12433400-12441200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:12438600-12441000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:12438600-12441200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:12438600-12442000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:12438800-12445400	Active TSS	K562	blood
6	chr7:12439000-12439800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr7:12439000-12440600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:12439000-12441000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:12439000-12441400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr7:12439000-12441600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:12439400-12440800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:12439600-12440000	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr7:12439600-12444400	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr7:12439800-12440600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:12440000-12440800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:12440600-12441000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr7:12440600-12443400	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr7:12440800-12441000	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr7:12440800-12441000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr7:12441000-12441200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr7:12441000-12441200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:12441000-12441200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr7:12441000-12441800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr7:12441000-12442400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:12441200-12441400	Flanking Active TSS	H9 Cell Line	embryonic stem cell
26	chr7:12441200-12441400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr7:12441200-12441400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr7:12441200-12441600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr7:12441200-12442600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr7:12441200-12443600	Active TSS	H1 Cell Line	embryonic stem cell
31	chr7:12441400-12441600	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr7:12441400-12441600	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr7:12441400-12441600	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr7:12441400-12443200	Active TSS	Right Atrium	heart
35	chr7:12441400-12443800	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr7:12441400-12443800	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr7:12441400-12444200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr7:12441400-12444200	Active TSS	H9 Cell Line	embryonic stem cell
39	chr7:12441600-12441800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr7:12441600-12441800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr7:12441600-12441800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:12441600-12442600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr7:12441600-12443800	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr7:12441800-12442200	Enhancers	Primary hematopoietic stem cells	blood
45	chr7:12441800-12442400	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr7:12441800-12442400	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr7:12441800-12442400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:12441800-12443800	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr7:12442000-12442400	Enhancers	A549	lung
50	chr7:12442000-12444200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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