Variant report

Variant	nsv1017055
Chromosome Location	chr7:12509227-12553217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:669)
CpG islands
(count:246)
Chromatin interactive
region (count:21)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12536356-12536848	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:12513875-12513883	K562	blood:	n/a	n/a
3	ARID3A	chr7:12529812-12530097	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:12514982-12515589	K562	blood:	n/a	n/a
5	ARID3A	chr7:12533106-12533341	K562	blood:	n/a	n/a
6	ARID3A	chr7:12536532-12536802	K562	blood:	n/a	n/a
7	ATF1	chr7:12514936-12515269	K562	blood:	n/a	n/a
8	ATF1	chr7:12529814-12530077	K562	blood:	n/a	n/a
9	BACH1	chr7:12532972-12533274	K562	blood:	n/a	n/a
10	BACH1	chr7:12514877-12514883	K562	blood:	n/a	n/a
11	BACH1	chr7:12532994-12533280	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr7:12524666-12525474	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:12533085-12533378	K562	blood:	n/a	n/a
14	BHLHE40	chr7:12514983-12515167	K562	blood:	n/a	n/a
15	BHLHE40	chr7:12521491-12521740	GM12878	blood:	n/a	n/a
16	CCNT2	chr7:12533047-12533307	K562	blood:	n/a	n/a
17	CEBPB	chr7:12514893-12515314	K562	blood:	n/a	n/a
18	CEBPB	chr7:12521423-12521514	HepG2	liver:	n/a	chr7:12521454-12521465
19	CEBPB	chr7:12536996-12537150	A549	lung:	n/a	n/a
20	CEBPB	chr7:12514937-12515253	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:12529776-12530104	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:12521403-12521540	H1-hESC	embryonic stem cell:	n/a	chr7:12521454-12521465
23	CEBPB	chr7:12514581-12515394	K562	blood:	n/a	n/a
24	CEBPB	chr7:12519704-12519859	K562	blood:	n/a	n/a
25	CEBPB	chr7:12519662-12519793	A549	lung:	n/a	n/a
26	CEBPB	chr7:12514983-12515227	A549	lung:	n/a	n/a
27	CEBPB	chr7:12529839-12530092	A549	lung:	n/a	n/a
28	CEBPB	chr7:12533125-12533486	K562	blood:	n/a	n/a
29	CEBPB	chr7:12534206-12534533	K562	blood:	n/a	n/a
30	CEBPB	chr7:12514935-12515135	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:12514886-12515412	Hela-S3	cervix:	n/a	n/a
32	CEBPD	chr7:12532996-12533568	K562	blood:	n/a	n/a
33	CHD2	chr7:12534687-12534708	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:12529840-12529990	GM12870	blood:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
35	CTCF	chr7:12534420-12534570	A549	lung:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
36	CTCF	chr7:12536599-12536671	GM13976	blood:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
37	CTCF	chr7:12529723-12530114	MCF-7	breast:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
38	CTCF	chr7:12529840-12529990	GM12864	blood:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
39	CTCF	chr7:12534320-12534470	GM12871	blood:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
40	CTCF	chr7:12534340-12534490	HRPEpiC	eye:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
41	CTCF	chr7:12534449-12534544	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr7:12529600-12529750	HCT-116	colon:	n/a	n/a
43	CTCF	chr7:12534400-12534550	HepG2	liver:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
44	CTCF	chr7:12529880-12530030	AG04450	lung:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
45	CTCF	chr7:12530140-12530290	GM12878	blood:	n/a	n/a
46	CTCF	chr7:12529800-12529950	NHDF-neo	bronchial:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
47	CTCF	chr7:12536520-12536670	GM12872	blood:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
48	CTCF	chr7:12529820-12529970	HAc	cerebellar:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
49	CTCF	chr7:12529847-12530018	MCF-7	breast:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
50	CTCF	chr7:12534360-12534510	K562	blood:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12510665-12510715	HRCEpiC	kidney:	n/a
2	chr7:12537108-12537158	GM06990	blood:	n/a
3	chr7:12510665-12510715	HRCEpiC	kidney:	n/a
4	chr7:12537108-12537158	GM06990	blood:	n/a
5	chr7:12510665-12510715	LNCaP	prostate:	n/a
6	chr7:12537108-12537158	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:12510863-12510913	A549	lung:	n/a
8	chr7:12510772-12510822	HMEC	breast:	n/a
9	chr7:12510772-12510822	NHDF-neo	bronchial:	n/a
10	chr7:12537108-12537158	BE2_C	brain:	n/a
11	chr7:12510665-12510715	BJ	skin:	n/a
12	chr7:12510863-12510913	PANC-1	pancreas:	n/a
13	chr7:12510772-12510822	HCT-116	colon:	n/a
14	chr7:12537108-12537158	HMEC	breast:	n/a
15	chr7:12537108-12537158	NHBE	bronchial:	n/a
16	chr7:12510863-12510913	HL-60	blood:	n/a
17	chr7:12510772-12510822	HepG2	liver:	n/a
18	chr7:12510772-12510822	HIPEpiC	eye:	n/a
19	chr7:12510863-12510913	HCPEpiC	choroid plexus:	n/a
20	chr7:12510665-12510715	AG04450	lung:	fetal
21	chr7:12537108-12537158	PrEC	prostate:	n/a
22	chr7:12510863-12510913	SK-N-MC	brain:	n/a
23	chr7:12537108-12537158	MCF-7	breast:	n/a
24	chr7:12510863-12510913	AG09319	gingival:	n/a
25	chr7:12537108-12537158	LNCaP	prostate:	n/a
26	chr7:12510863-12510913	BJ	skin:	n/a
27	chr7:12510863-12510913	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:12537108-12537158	NH-A	brain:	n/a
29	chr7:12510772-12510822	BJ	skin:	n/a
30	chr7:12537108-12537158	HCM	heart:	n/a
31	chr7:12537108-12537158	PFSK-1	brain:	n/a
32	chr7:12537108-12537158	NHDF-neo	bronchial:	n/a
33	chr7:12510665-12510715	T-47D	breast:	n/a
34	chr7:12510863-12510913	HRCEpiC	kidney:	n/a
35	chr7:12537108-12537158	HEK293	kidney:	embryo
36	chr7:12510772-12510822	SKMC	muscle:	n/a
37	chr7:12510772-12510822	PANC-1	pancreas:	n/a
38	chr7:12510665-12510715	HEEpiC	esophagus:	n/a
39	chr7:12537108-12537158	A549	lung:	n/a
40	chr7:12510665-12510715	HCT-116	colon:	n/a
41	chr7:12537108-12537158	ovcar-3	ovarian:	n/a
42	chr7:12510665-12510715	GM19239	blood:	n/a
43	chr7:12510863-12510913	ECC-1	luminal epithelium:	n/a
44	chr7:12510863-12510913	GM12891	blood:	n/a
45	chr7:12510665-12510715	ovcar-3	ovarian:	n/a
46	chr7:12510772-12510822	HRE	kidney:	n/a
47	chr7:12537108-12537158	AG04449	skin:	fetal
48	chr7:12510863-12510913	MCF10A-Er-Src	breast:	n/a
49	chr7:12510665-12510715	HCPEpiC	choroid plexus:	n/a
50	chr7:12510863-12510913	AG04449	skin:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
2	chr7:12528914..12532541-chr7:12534824..12536655,4	K562	blood:
3	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:
4	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
5	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
6	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
7	chr7:12528914..12532541-chr7:12534824..12536655,4	K562	blood:
8	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
9	chr7:12497870..12498820-chr7:12528972..12530631,10	MCF-7	breast:
10	chr7:12498003..12498630-chr7:12536129..12537096,2	K562	blood:
11	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
12	chr7:12497882..12499037-chr7:12533987..12535337,10	MCF-7	breast:
13	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
14	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
15	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
16	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
17	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
18	chr7:12497831..12498808-chr7:12529325..12530426,5	K562	blood:
19	chr7:12326033..12327864-chr7:12530775..12532531,2	K562	blood:
20	chr7:12497991..12498705-chr7:12529442..12530188,2	MCF-7	breast:
21	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCIN-3	chr7:12546915-12547104	NONHSAT119232
2	lnc-SCIN-3	chr7:12547071-12547552	l_3363_chr7:12529385-12547552_testes
3	lnc-SCIN-3	chr7:12537187-12537243	l_3363_chr7:12529385-12547552_testes
4	lnc-SCIN-3	chr7:12535053-12535266	l_3363_chr7:12529385-12547552_testes
5	lnc-SCIN-4	chr7:12530721-12531630	NONHSAT119228
6	lnc-SCIN-3	chr7:12531971-12532055	l_3363_chr7:12529385-12547552_testes
7	lnc-SCIN-3	chr7:12529386-12529577	l_3363_chr7:12529385-12547552_testes
8	lnc-SCIN-2	chr7:12544025-12544172	ENSG00000226690.2
9	lnc-SCIN-2	chr7:12544050-12544172	ENSG00000226690.2
10	lnc-SCIN-2	chr7:12536055-12536265	ENSG00000226690.2
11	lnc-SCIN-3	chr7:12545633-12545694	NONHSAT119232
12	lnc-SCIN-3	chr7:12546429-12546638	NONHSAT119232

No data

Variant related genes	Relation type
ENSG00000224667	TF binding region
TAS2R2P	TF binding region
ENSG00000226690	TF binding region
ENSG00000236048	TF binding region
ENSG00000224667	CpG island
TAS2R2P	CpG island
ENSG00000226690	CpG island
ENSG00000236048	CpG island
ENSG00000226690	chromatin interactions
ENSG00000203523	chromatin interactions

Extended variants
information (count: 1316 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs847962	chr7:12509227-12509228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570966904	chr7:12509251-12509252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539558972	chr7:12509260-12509261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149341145	chr7:12509318-12509319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7793981	chr7:12509325-12509326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535424044	chr7:12509345-12509346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189708439	chr7:12509365-12509366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574367961	chr7:12509402-12509403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540465310	chr7:12509427-12509428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184219072	chr7:12509433-12509434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564986467	chr7:12509439-12509440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530826970	chr7:12509471-12509472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112923813	chr7:12509482-12509483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576925169	chr7:12509485-12509486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557680133	chr7:12509492-12509493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188718093	chr7:12509528-12509529	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs6945187	chr7:12509538-12509539	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs191997237	chr7:12509555-12509556	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs375964406	chr7:12509564-12509565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143620571	chr7:12509594-12509595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73056724	chr7:12509614-12509615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs548031374	chr7:12509618-12509619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6965273	chr7:12509639-12509640	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs183319551	chr7:12509667-12509668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550022014	chr7:12509673-12509674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569797758	chr7:12509687-12509688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188300856	chr7:12509696-12509697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555335994	chr7:12509735-12509736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568052975	chr7:12509755-12509756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191622790	chr7:12509759-12509760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553983730	chr7:12509781-12509782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs847961	chr7:12509789-12509790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs28427549	chr7:12509795-12509796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545965304	chr7:12509825-12509826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62449482	chr7:12509838-12509839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs184154043	chr7:12509859-12509860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2053383	chr7:12509873-12509874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561678657	chr7:12509904-12509905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550271392	chr7:12509919-12509920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527239026	chr7:12509920-12509921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375371383	chr7:12509938-12509939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564767260	chr7:12509944-12509945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34884308	chr7:12510004-12510005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533394766	chr7:12510013-12510014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549939597	chr7:12510015-12510016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569197508	chr7:12510045-12510046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569861042	chr7:12510058-12510059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529335207	chr7:12510078-12510079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549023992	chr7:12510089-12510090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186944484	chr7:12510135-12510136	Weak transcription	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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12504000-12510600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:12510600-12510800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:12510800-12515000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:12513400-12514000	Enhancers	K562	blood
5	chr7:12513600-12514200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:12513600-12516200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:12514000-12515000	Weak transcription	K562	blood
8	chr7:12514200-12515200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:12514600-12516000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:12515000-12515200	Enhancers	K562	blood
11	chr7:12515000-12515400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr7:12515000-12515600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:12515000-12515600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:12515000-12515600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:12515000-12515600	Enhancers	Fetal Heart	heart
16	chr7:12515000-12515600	Enhancers	Ovary	ovary
17	chr7:12515000-12515600	Enhancers	NH-A	brain
18	chr7:12515000-12515600	Enhancers	Osteobl	bone
19	chr7:12515000-12515800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:12515000-12515800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:12515200-12515400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:12515200-12515600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:12515200-12515600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:12515200-12515600	Enhancers	Hela-S3	cervix
25	chr7:12515200-12515600	Flanking Active TSS	K562	blood
26	chr7:12515200-12515800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr7:12515200-12515800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:12515200-12516000	Enhancers	Fetal Lung	lung
29	chr7:12515400-12515600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:12515400-12515800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:12515400-12515800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:12515400-12516000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:12515600-12516000	Enhancers	K562	blood
34	chr7:12515600-12521000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:12521000-12521400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr7:12521000-12521600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:12521000-12521600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:12521000-12521800	Enhancers	Primary T cells from cord blood	blood
39	chr7:12521000-12522400	Enhancers	GM12878-XiMat	blood
40	chr7:12521200-12521400	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr7:12521400-12521800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr7:12521400-12521800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:12521400-12521800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr7:12521400-12522000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr7:12521400-12522400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:12521600-12521800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:12521600-12522000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr7:12521800-12522000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr7:12521800-12522000	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr7:12521800-12522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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