Variant report

Variant	nsv464377
Chromosome Location	chr7:12512802-12564128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:887)
CpG islands
(count:61)
Chromatin interactive
region (count:34)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:887 , 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	chr7:12536532-12536802	K562	blood:	n/a	n/a
2	ARID3A	chr7:12529812-12530097	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:12533106-12533341	K562	blood:	n/a	n/a
4	ARID3A	chr7:12536356-12536848	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:12514982-12515589	K562	blood:	n/a	n/a
6	ARID3A	chr7:12513875-12513883	K562	blood:	n/a	n/a
7	ATF1	chr7:12529814-12530077	K562	blood:	n/a	n/a
8	ATF1	chr7:12514936-12515269	K562	blood:	n/a	n/a
9	BACH1	chr7:12532994-12533280	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:12532972-12533274	K562	blood:	n/a	n/a
11	BACH1	chr7:12514877-12514883	K562	blood:	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	chr7:12521491-12521740	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:12514983-12515167	K562	blood:	n/a	n/a
16	CBX3	chr7:12557129-12557384	K562	blood:	n/a	n/a
17	CBX3	chr7:12557088-12557431	K562	blood:	n/a	n/a
18	CBX3	chr7:12558748-12559243	HCT-116	colon:	n/a	n/a
19	CCNT2	chr7:12533047-12533307	K562	blood:	n/a	n/a
20	CEBPB	chr7:12514983-12515227	A549	lung:	n/a	n/a
21	CEBPB	chr7:12529776-12530104	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:12519662-12519793	A549	lung:	n/a	n/a
23	CEBPB	chr7:12534206-12534533	K562	blood:	n/a	n/a
24	CEBPB	chr7:12514886-12515412	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:12514893-12515314	K562	blood:	n/a	n/a
26	CEBPB	chr7:12514581-12515394	K562	blood:	n/a	n/a
27	CEBPB	chr7:12514935-12515135	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:12533125-12533486	K562	blood:	n/a	n/a
29	CEBPB	chr7:12521403-12521540	H1-hESC	embryonic stem cell:	n/a	chr7:12521454-12521465
30	CEBPB	chr7:12529839-12530092	A549	lung:	n/a	n/a
31	CEBPB	chr7:12514937-12515253	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:12536996-12537150	A549	lung:	n/a	n/a
33	CEBPB	chr7:12519704-12519859	K562	blood:	n/a	n/a
34	CEBPB	chr7:12521423-12521514	HepG2	liver:	n/a	chr7:12521454-12521465
35	CEBPD	chr7:12532996-12533568	K562	blood:	n/a	n/a
36	CHD2	chr7:12534687-12534708	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr7:12536560-12536710	AG10803	skin:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
38	CTCF	chr7:12558671-12558716	Gliobla	brain:	n/a	n/a
39	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
40	CTCF	chr7:12534440-12534590	GM12878	blood:	n/a	n/a
41	CTCF	chr7:12536442-12536820	IMR90	lung:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
42	CTCF	chr7:12534388-12534512	HepG2	liver:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
43	CTCF	chr7:12558880-12559030	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:12558820-12558970	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr7:12529840-12529990	WERI-Rb-1	eye:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
46	CTCF	chr7:12558821-12559163	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:12534440-12534590	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr7:12558920-12559070	AG04450	lung:	n/a	n/a
49	CTCF	chr7:12530600-12530750	HPF	lung:	n/a	n/a
50	CTCF	chr7:12529840-12529990	GM06990	blood:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12537108-12537158	HAEpiC	amniotic membrane:	n/a
2	chr7:12537108-12537158	HCPEpiC	choroid plexus:	n/a
3	chr7:12537108-12537158	SAEC	small airway:	n/a
4	chr7:12537108-12537158	MCF10A-Er-Src	breast:	n/a
5	chr7:12537108-12537158	NB4	blood:	n/a
6	chr7:12537108-12537158	NHDF-neo	bronchial:	n/a
7	chr7:12537108-12537158	K562	blood:	n/a
8	chr7:12537108-12537158	AG10803	skin:	n/a
9	chr7:12537108-12537158	Hela-S3	cervix:	n/a
10	chr7:12537108-12537158	A549	lung:	n/a
11	chr7:12537108-12537158	GM19239	blood:	n/a
12	chr7:12537108-12537158	HEEpiC	esophagus:	n/a
13	chr7:12537108-12537158	BJ	skin:	n/a
14	chr7:12537108-12537158	ECC-1	luminal epithelium:	n/a
15	chr7:12537108-12537158	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:12537108-12537158	BE2_C	brain:	n/a
17	chr7:12537108-12537158	RPTEC	kidney:	n/a
18	chr7:12537108-12537158	CMK	blood:	n/a
19	chr7:12537108-12537158	GM06990	blood:	n/a
20	chr7:12537108-12537158	HEK293	kidney:	embryo
21	chr7:12537108-12537158	H1-hESC	embryonic stem cell:	embryo
22	chr7:12537108-12537158	HCF	heart:	n/a
23	chr7:12537108-12537158	Hepatocyte	liver:	n/a
24	chr7:12537108-12537158	HRCEpiC	kidney:	n/a
25	chr7:12537108-12537158	AG04449	skin:	fetal
26	chr7:12537108-12537158	MCF-7	breast:	n/a
27	chr7:12537108-12537158	NT2-D1	testis:	n/a
28	chr7:12537108-12537158	SKMC	muscle:	n/a
29	chr7:12537108-12537158	HUVEC	blood vessel:	n/a
30	chr7:12537108-12537158	AoSMC	blood vessel:	n/a
31	chr7:12537108-12537158	ProgFib	skin:	n/a
32	chr7:12537108-12537158	PANC-1	pancreas:	n/a
33	chr7:12537108-12537158	HCT-116	colon:	n/a
34	chr7:12537108-12537158	PFSK-1	brain:	n/a
35	chr7:12537108-12537158	T-47D	breast:	n/a
36	chr7:12537108-12537158	HIPEpiC	eye:	n/a
37	chr7:12537108-12537158	HL-60	blood:	n/a
38	chr7:12537108-12537158	HepG2	liver:	n/a
39	chr7:12537108-12537158	SK-N-SH_RA	brain:	n/a
40	chr7:12537108-12537158	LNCaP	prostate:	n/a
41	chr7:12537108-12537158	U87	brain:	n/a
42	chr7:12537108-12537158	HCM	heart:	n/a
43	chr7:12537108-12537158	HRPEpiC	eye:	n/a
44	chr7:12537108-12537158	SK-N-MC	brain:	n/a
45	chr7:12537108-12537158	HMEC	breast:	n/a
46	chr7:12537108-12537158	Caco-2	colon:	n/a
47	chr7:12537108-12537158	AG04450	lung:	fetal
48	chr7:12537108-12537158	GM12878	blood:	n/a
49	chr7:12537108-12537158	Jurkat	blood:	n/a
50	chr7:12537108-12537158	SK-N-SH	brain:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12563798..12566063-chr7:12723431..12726105,2	K562	blood:
2	chr7:12558222..12560896-chr7:12563188..12565683,2	K562	blood:
3	chr7:12563571..12565144-chr7:12668072..12670277,2	K562	blood:
4	chr7:12497870..12498820-chr7:12528972..12530631,10	MCF-7	breast:
5	chr7:12564097..12565730-chr7:12662861..12664188,13	K562	blood:
6	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
7	chr7:12249540..12251997-chr7:12556631..12559101,2	K562	blood:
8	chr7:12558222..12560896-chr7:12563188..12565683,2	K562	blood:
9	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
10	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
11	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:
12	chr7:12557824..12559651-chr7:12562613..12565542,2	K562	blood:
13	chr7:12558622..12559420-chr7:12663224..12663821,2	MCF-7	breast:
14	chr7:12528914..12532541-chr7:12534824..12536655,4	K562	blood:
15	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
16	chr7:12497882..12499037-chr7:12533987..12535337,10	MCF-7	breast:
17	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
18	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
19	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:
20	chr7:12528914..12532541-chr7:12534824..12536655,4	K562	blood:
21	chr7:12473109..12473862-chr7:12558519..12559485,2	K562	blood:
22	chr7:12497831..12498808-chr7:12529325..12530426,5	K562	blood:
23	chr7:12498003..12498630-chr7:12536129..12537096,2	K562	blood:
24	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
25	chr7:12497991..12498705-chr7:12529442..12530188,2	MCF-7	breast:
26	chr7:12564069..12565148-chr7:12663270..12664407,15	MCF-7	breast:
27	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
28	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
29	chr7:12558451..12560515-chr7:12754100..12757020,2	K562	blood:
30	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
31	chr7:12497885..12498702-chr7:12558562..12559343,2	MCF-7	breast:
32	chr7:12326033..12327864-chr7:12530775..12532531,2	K562	blood:
33	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
34	chr7:12557824..12559651-chr7:12562613..12565542,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCIN-2	chr7:12536055-12536265	ENSG00000226690.2
2	lnc-SCIN-3	chr7:12545633-12545694	NONHSAT119232
3	lnc-SCIN-3	chr7:12537187-12537243	l_3363_chr7:12529385-12547552_testes
4	lnc-SCIN-4	chr7:12530721-12531630	NONHSAT119228
5	lnc-SCIN-2	chr7:12544025-12544172	ENSG00000226690.2
6	lnc-SCIN-3	chr7:12547071-12547552	l_3363_chr7:12529385-12547552_testes
7	lnc-SCIN-3	chr7:12531971-12532055	l_3363_chr7:12529385-12547552_testes
8	lnc-SCIN-2	chr7:12544050-12544172	ENSG00000226690.2
9	lnc-SCIN-3	chr7:12546915-12547104	NONHSAT119232
10	lnc-SCIN-3	chr7:12535053-12535266	l_3363_chr7:12529385-12547552_testes
11	lnc-SCIN-3	chr7:12529386-12529577	l_3363_chr7:12529385-12547552_testes
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
ENSG00000224667	CpG island
TAS2R2P	CpG island
ENSG00000226690	CpG island
ENSG00000226690	chromatin interactions
ENSG00000106460	chromatin interactions
ENSG00000203523	chromatin interactions
ENSG00000271253	chromatin interactions

Extended variants
information (count: 1461 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1461 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs847953	chr7:12512802-12512803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73056737	chr7:12512823-12512824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs847952	chr7:12512831-12512832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs538971679	chr7:12512846-12512847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs847951	chr7:12512889-12512890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182411072	chr7:12512919-12512920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1659946	chr7:12512936-12512937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs1659947	chr7:12512939-12512940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs189082230	chr7:12512954-12512955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534240461	chr7:12512968-12512969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553889434	chr7:12512988-12512989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113945364	chr7:12513008-12513009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577125014	chr7:12513009-12513010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374984303	chr7:12513017-12513018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74543330	chr7:12513021-12513022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564804452	chr7:12513040-12513041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563666137	chr7:12513055-12513056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574519784	chr7:12513062-12513063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113648975	chr7:12513088-12513089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575131074	chr7:12513092-12513093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147898915	chr7:12513094-12513095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560697809	chr7:12513125-12513126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529743297	chr7:12513134-12513135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554132145	chr7:12513148-12513149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559895131	chr7:12513154-12513155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs847950	chr7:12513185-12513186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552917610	chr7:12513188-12513189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569553017	chr7:12513211-12513212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs847949	chr7:12513221-12513222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548795168	chr7:12513257-12513258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75990040	chr7:12513341-12513342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534040299	chr7:12513343-12513344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367662266	chr7:12513345-12513346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140460928	chr7:12513349-12513350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548477754	chr7:12513371-12513372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577186373	chr7:12513376-12513377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539432106	chr7:12513391-12513392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558453276	chr7:12513407-12513408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193013843	chr7:12513427-12513428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150402138	chr7:12513451-12513452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549405798	chr7:12513531-12513532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560933788	chr7:12513552-12513553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574526696	chr7:12513580-12513581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6966349	chr7:12513594-12513595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs185685580	chr7:12513627-12513628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6966481	chr7:12513630-12513631	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs6966629	chr7:12513704-12513705	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570186375	chr7:12513732-12513733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138109341	chr7:12513749-12513750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532055243	chr7:12513757-12513758	Weak transcription Enhancers	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:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12510800-12515000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:12513400-12514000	Enhancers	K562	blood
3	chr7:12513600-12514200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:12513600-12516200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:12514000-12515000	Weak transcription	K562	blood
6	chr7:12514200-12515200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:12514600-12516000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:12515000-12515200	Enhancers	K562	blood
9	chr7:12515000-12515400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr7:12515000-12515600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:12515000-12515600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:12515000-12515600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:12515000-12515600	Enhancers	Fetal Heart	heart
14	chr7:12515000-12515600	Enhancers	Ovary	ovary
15	chr7:12515000-12515600	Enhancers	NH-A	brain
16	chr7:12515000-12515600	Enhancers	Osteobl	bone
17	chr7:12515000-12515800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:12515000-12515800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:12515200-12515400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr7:12515200-12515600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr7:12515200-12515600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:12515200-12515600	Enhancers	Hela-S3	cervix
23	chr7:12515200-12515600	Flanking Active TSS	K562	blood
24	chr7:12515200-12515800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr7:12515200-12515800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr7:12515200-12516000	Enhancers	Fetal Lung	lung
27	chr7:12515400-12515600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:12515400-12515800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:12515400-12515800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:12515400-12516000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:12515600-12516000	Enhancers	K562	blood
32	chr7:12515600-12521000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:12521000-12521400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr7:12521000-12521600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:12521000-12521600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:12521000-12521800	Enhancers	Primary T cells from cord blood	blood
37	chr7:12521000-12522400	Enhancers	GM12878-XiMat	blood
38	chr7:12521200-12521400	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:12521400-12521800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr7:12521400-12521800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:12521400-12521800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr7:12521400-12522000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr7:12521400-12522400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr7:12521600-12521800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr7:12521600-12522000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr7:12521800-12522000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:12521800-12522000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr7:12521800-12522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:12522400-12522600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr7:12528000-12528200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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