Variant report

Variant	nsv464376
Chromosome Location	chr7:12429488-12526282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1283)
CpG islands
(count:1101)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12513875-12513883	K562	blood:	n/a	n/a
2	ARID3A	chr7:12445132-12445205	K562	blood:	n/a	n/a
3	ARID3A	chr7:12443002-12443779	K562	blood:	n/a	n/a
4	ARID3A	chr7:12441428-12441976	K562	blood:	n/a	n/a
5	ARID3A	chr7:12498199-12498492	K562	blood:	n/a	n/a
6	ARID3A	chr7:12473668-12473988	K562	blood:	n/a	n/a
7	ARID3A	chr7:12442512-12442624	K562	blood:	n/a	n/a
8	ARID3A	chr7:12498256-12498470	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:12514982-12515589	K562	blood:	n/a	n/a
10	ARID3A	chr7:12473648-12473985	HepG2	liver:	n/a	n/a
11	ATF1	chr7:12442940-12444036	K562	blood:	n/a	n/a
12	ATF1	chr7:12514936-12515269	K562	blood:	n/a	n/a
13	ATF1	chr7:12437894-12438340	K562	blood:	n/a	n/a
14	ATF1	chr7:12484873-12485016	K562	blood:	n/a	n/a
15	ATF1	chr7:12441677-12441884	K562	blood:	n/a	n/a
16	ATF2	chr7:12463290-12464092	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:12463437-12464243	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr7:12443361-12443704	K562	blood:	n/a	n/a
19	BACH1	chr7:12514877-12514883	K562	blood:	n/a	n/a
20	BACH1	chr7:12443123-12443675	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:12443045-12443428	K562	blood:	n/a	n/a
22	BCL11A	chr7:12463807-12464153	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr7:12524666-12525474	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:12463938-12464115	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCLAF1	chr7:12442724-12444060	K562	blood:	n/a	chr7:12443627-12443636 chr7:12443692-12443705
26	BCLAF1	chr7:12443085-12443960	K562	blood:	n/a	chr7:12443627-12443636 chr7:12443692-12443705
27	BHLHE40	chr7:12444086-12444098	K562	blood:	n/a	n/a
28	BHLHE40	chr7:12521491-12521740	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:12442950-12443807	K562	blood:	n/a	n/a
30	BHLHE40	chr7:12441675-12441916	K562	blood:	n/a	n/a
31	BHLHE40	chr7:12431674-12431880	K562	blood:	n/a	n/a
32	BHLHE40	chr7:12514983-12515167	K562	blood:	n/a	n/a
33	BRCA1	chr7:12443076-12443269	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr7:12437595-12438594	K562	blood:	n/a	n/a
35	CBX3	chr7:12442863-12443396	K562	blood:	n/a	n/a
36	CBX3	chr7:12437315-12438267	K562	blood:	n/a	n/a
37	CBX3	chr7:12442888-12444084	K562	blood:	n/a	n/a
38	CCNT2	chr7:12442982-12443788	K562	blood:	n/a	n/a
39	CCNT2	chr7:12432707-12432774	K562	blood:	n/a	n/a
40	CCNT2	chr7:12430237-12430378	K562	blood:	n/a	n/a
41	CEBPB	chr7:12514937-12515253	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:12463242-12463599	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:12463181-12463787	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:12435069-12435310	K562	blood:	n/a	chr7:12435202-12435215 chr7:12435203-12435214 chr7:12435204-12435213 chr7:12435202-12435215 chr7:12435202-12435213
45	CEBPB	chr7:12521403-12521540	H1-hESC	embryonic stem cell:	n/a	chr7:12521454-12521465
46	CEBPB	chr7:12521423-12521514	HepG2	liver:	n/a	chr7:12521454-12521465
47	CEBPB	chr7:12430682-12430949	K562	blood:	n/a	chr7:12430766-12430775 chr7:12430766-12430775 chr7:12430765-12430776
48	CEBPB	chr7:12514983-12515227	A549	lung:	n/a	n/a
49	CEBPB	chr7:12430777-12430888	A549	lung:	n/a	n/a
50	CEBPB	chr7:12437901-12438111	K562	blood:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12510665-12510715	Hela-S3	cervix:	n/a
2	chr7:12444115-12444165	NH-A	brain:	n/a
3	chr7:12446327-12446377	MCF-7	breast:	n/a
4	chr7:12510665-12510715	Hela-S3	cervix:	n/a
5	chr7:12444115-12444165	NH-A	brain:	n/a
6	chr7:12446327-12446377	MCF-7	breast:	n/a
7	chr7:12462597-12462647	MCF-7	breast:	n/a
8	chr7:12443146-12443196	GM12891	blood:	n/a
9	chr7:12510863-12510913	GM12892	blood:	n/a
10	chr7:12443704-12443754	RPTEC	kidney:	n/a
11	chr7:12444290-12444340	LNCaP	prostate:	n/a
12	chr7:12443542-12443592	K562	blood:	n/a
13	chr7:12443478-12443528	SK-N-MC	brain:	n/a
14	chr7:12443146-12443196	HAEpiC	amniotic membrane:	n/a
15	chr7:12443478-12443528	Hepatocyte	liver:	n/a
16	chr7:12446327-12446377	SKMC	muscle:	n/a
17	chr7:12443880-12443930	GM12878	blood:	n/a
18	chr7:12443529-12443579	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:12443926-12443976	ECC-1	luminal epithelium:	n/a
20	chr7:12462597-12462647	HCF	heart:	n/a
21	chr7:12446327-12446377	HRPEpiC	eye:	n/a
22	chr7:12443886-12443936	LNCaP	prostate:	n/a
23	chr7:12444115-12444165	HMEC	breast:	n/a
24	chr7:12443704-12443754	U87	brain:	n/a
25	chr7:12443478-12443528	U87	brain:	n/a
26	chr7:12444290-12444340	HNPCEpiC	eye:	n/a
27	chr7:12443146-12443196	AoSMC	blood vessel:	n/a
28	chr7:12443926-12443976	AG09309	skin:	n/a
29	chr7:12443880-12443930	A549	lung:	n/a
30	chr7:12510863-12510913	GM12891	blood:	n/a
31	chr7:12443880-12443930	ovcar-3	ovarian:	n/a
32	chr7:12443146-12443196	HCT-116	colon:	n/a
33	chr7:12462597-12462647	LNCaP	prostate:	n/a
34	chr7:12443704-12443754	SK-N-SH_RA	brain:	n/a
35	chr7:12443704-12443754	GM12891	blood:	n/a
36	chr7:12443704-12443754	MCF10A-Er-Src	breast:	n/a
37	chr7:12443529-12443579	AG04450	lung:	fetal
38	chr7:12443529-12443579	HIPEpiC	eye:	n/a
39	chr7:12443529-12443579	HepG2	liver:	n/a
40	chr7:12444013-12444063	SK-N-SH	brain:	n/a
41	chr7:12443886-12443936	T-47D	breast:	n/a
42	chr7:12462597-12462647	A549	lung:	n/a
43	chr7:12443880-12443930	AG09319	gingival:	n/a
44	chr7:12443191-12443241	Jurkat	blood:	n/a
45	chr7:12443886-12443936	NHBE	bronchial:	n/a
46	chr7:12443704-12443754	GM06990	blood:	n/a
47	chr7:12444013-12444063	GM19239	blood:	n/a
48	chr7:12444115-12444165	SK-N-SH	brain:	n/a
49	chr7:12444115-12444165	SAEC	small airway:	n/a
50	chr7:12510772-12510822	MCF10A-Er-Src	breast:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:12496465..12498567-chr7:12529648..12531435,2	K562	blood:
2	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
3	chr7:12497870..12498820-chr7:12528972..12530631,10	MCF-7	breast:
4	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:
5	chr7:12473109..12473862-chr7:12558519..12559485,2	K562	blood:
6	chr7:12497882..12499037-chr7:12533987..12535337,10	MCF-7	breast:
7	chr20:40278409..40280542-chr7:12478341..12480011,2	MCF-7	breast:
8	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
9	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
10	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
11	chr7:12497885..12498702-chr7:12558562..12559343,2	MCF-7	breast:
12	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
13	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
14	chr7:12479476..12481083-chr7:12493598..12496034,2	K562	blood:
15	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
16	chr7:12442216..12444802-chr7:12483847..12486014,2	K562	blood:
17	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
18	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
19	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
20	chr7:11466869..11467685-chr7:12498254..12498786,2	MCF-7	breast:
21	chr7:12480338..12484247-chr7:12487058..12490542,4	K562	blood:
22	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:
23	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
24	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
25	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
26	chr7:12497991..12498705-chr7:12529442..12530188,2	MCF-7	breast:
27	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
28	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
29	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
30	chr7:12498003..12498630-chr7:12536129..12537096,2	K562	blood:
31	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
32	chr7:12479476..12481083-chr7:12493598..12496034,2	K562	blood:
33	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
34	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
35	chr7:12497831..12498808-chr7:12529325..12530426,5	K562	blood:
36	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
37	chr7:12497629..12498696-chr7:12535919..12536815,4	MCF-7	breast:
38	chr7:12441983..12444239-chr7:12724759..12726454,2	K562	blood:
39	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
40	chr7:12488598..12490554-chr7:12506071..12508415,2	K562	blood:
41	chr7:12480338..12484247-chr7:12487058..12490542,4	K562	blood:
42	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
43	chr7:12441879..12443410-chr7:12725306..12727318,2	K562	blood:
44	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
45	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
46	chr7:12497632..12498790-chr7:12662958..12664405,3	K562	blood:
47	chr20:47537945..47538638-chr7:12442691..12443569,2	Hela-S3	cervix:
48	chr7:12441796..12443703-chr7:12463390..12465045,2	MCF-7	breast:
49	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
50	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:

No data

Variant related genes	Relation type
VWDE	TF binding region
TAS2R2P	TF binding region
ENSG00000236048	TF binding region
VWDE	CpG island
TAS2R2P	CpG island
ENSG00000236048	CpG island
ENSG00000226690	chromatin interactions
ENSG00000122644	chromatin interactions
ENSG00000146530	chromatin interactions
ENSG00000271253	chromatin interactions
ENSG00000203523	chromatin interactions
ENSG00000124198	chromatin interactions

Extended variants
information (count: 3838 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3838 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs848013	chr7:12429488-12429489	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566854725	chr7:12429517-12429518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541922342	chr7:12429523-12429524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534942181	chr7:12429563-12429564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112802513	chr7:12429587-12429588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571413417	chr7:12429652-12429653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537257459	chr7:12429663-12429664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556875991	chr7:12429669-12429670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188894263	chr7:12429682-12429683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573443880	chr7:12429713-12429714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543137574	chr7:12429743-12429744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562327978	chr7:12429746-12429747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193226807	chr7:12429787-12429788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552040450	chr7:12429790-12429791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200320227	chr7:12429791-12429792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs848012	chr7:12429801-12429802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572527538	chr7:12429807-12429808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544645568	chr7:12429814-12429815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17165982	chr7:12429850-12429851	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs531065230	chr7:12429898-12429899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532023248	chr7:12429899-12429900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544835849	chr7:12429942-12429943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183493313	chr7:12429947-12429948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17540141	chr7:12429996-12429997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562308210	chr7:12430001-12430002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547091566	chr7:12430026-12430027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566940165	chr7:12430074-12430075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187379698	chr7:12430186-12430187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367678978	chr7:12430212-12430213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548480963	chr7:12430226-12430227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552244721	chr7:12430229-12430230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191791417	chr7:12430287-12430288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs702473	chr7:12430319-12430320	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374855343	chr7:12430337-12430338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184335541	chr7:12430419-12430420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2356173	chr7:12430438-12430439	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs543434999	chr7:12430440-12430441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140097513	chr7:12430493-12430494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188631514	chr7:12430531-12430532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372339181	chr7:12430560-12430561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538631055	chr7:12430564-12430565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111649832	chr7:12430580-12430581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561350058	chr7:12430594-12430595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1470101	chr7:12430615-12430616	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs191554972	chr7:12430640-12430641	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575106326	chr7:12430740-12430741	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146802637	chr7:12430757-12430758	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140532738	chr7:12430770-12430771	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs848011	chr7:12430812-12430813	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs848010	chr7:12430854-12430855	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12368200-12433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:12419200-12432800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:12420400-12437600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:12424200-12434800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:12424600-12436200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr7:12425400-12431000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:12426000-12430800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr7:12426800-12431200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:12427600-12431400	Strong transcription	K562	blood
10	chr7:12428600-12433800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:12428800-12431200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:12428800-12431200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:12428800-12436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:12428800-12437000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:12428800-12437400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:12429200-12430600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:12429400-12430800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:12430600-12431200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:12430800-12431000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr7:12430800-12431800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:12431000-12431400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr7:12431000-12431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:12431200-12431600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:12431200-12431600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:12431200-12431800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:12431400-12431600	Genic enhancers	K562	blood
27	chr7:12431400-12432200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr7:12431600-12431800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr7:12431600-12432000	Transcr. at gene 5' and 3'	K562	blood
30	chr7:12431600-12436800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr7:12431800-12433200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr7:12431800-12434800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:12431800-12437200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:12432000-12436400	Genic enhancers	K562	blood
35	chr7:12432200-12437200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr7:12432800-12433400	Enhancers	H9 Cell Line	embryonic stem cell
37	chr7:12433200-12433400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:12433200-12434000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:12433400-12441200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr7:12433800-12434000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:12434000-12434400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr7:12434000-12437600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr7:12434400-12435200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:12434800-12435000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:12434800-12435000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:12435000-12437600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:12436400-12436800	Weak transcription	K562	blood
48	chr7:12436800-12438800	ZNF genes & repeats	K562	blood
49	chr7:12436800-12439000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:12437000-12437400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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