Variant report

Variant	nsv1020988
Chromosome Location	chr7:7348251-7497484
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1271)
CpG islands
(count:183)
Chromatin interactive
region (count:81)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1271 , 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	chr7:7464097-7464338	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:7478472-7478836	HepG2	liver:	n/a	n/a
3	ATF1	chr7:7491171-7491232	K562	blood:	n/a	n/a
4	ATF1	chr7:7376740-7376811	K562	blood:	n/a	n/a
5	ATF1	chr7:7369805-7369903	K562	blood:	n/a	n/a
6	ATF1	chr7:7464065-7464481	K562	blood:	n/a	n/a
7	ATF2	chr7:7392145-7392924	H1-hESC	embryonic stem cell:	n/a	chr7:7392484-7392495
8	ATF2	chr7:7361332-7361786	GM12878	blood:	n/a	n/a
9	ATF3	chr7:7478333-7478974	A549	lung:	n/a	n/a
10	BACH1	chr7:7392453-7392825	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:7458714-7458862	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr7:7361281-7361798	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:7363058-7363128	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:7362908-7363336	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:7364477-7364520	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:7440697-7440745	A549	lung:	n/a	n/a
17	BRCA1	chr7:7464042-7464369	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr7:7464181-7464259	HepG2	liver:	n/a	n/a
19	BRCA1	chr7:7478442-7478892	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr7:7455775-7456204	HCT-116	colon:	n/a	n/a
21	CBX3	chr7:7488708-7488988	K562	blood:	n/a	n/a
22	CBX3	chr7:7478342-7479021	HCT-116	colon:	n/a	n/a
23	CBX3	chr7:7487828-7488056	K562	blood:	n/a	n/a
24	CBX3	chr7:7478353-7479081	HCT-116	colon:	n/a	n/a
25	CEBPB	chr7:7348920-7349120	A549	lung:	n/a	n/a
26	CEBPB	chr7:7372008-7372244	A549	lung:	n/a	chr7:7372136-7372147
27	CEBPB	chr7:7384237-7384548	ECC-1	luminal epithelium:	n/a	chr7:7384390-7384401
28	CEBPB	chr7:7384237-7384566	A549	lung:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
29	CEBPB	chr7:7348903-7349190	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:7384206-7384599	H1-hESC	embryonic stem cell:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
31	CEBPB	chr7:7478008-7479033	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:7408372-7408658	HepG2	liver:	n/a	chr7:7408500-7408511
33	CEBPB	chr7:7384222-7384581	HepG2	liver:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
34	CEBPB	chr7:7464846-7465009	K562	blood:	n/a	n/a
35	CEBPB	chr7:7441816-7441970	HepG2	liver:	n/a	chr7:7441922-7441935 chr7:7441844-7441855
36	CEBPB	chr7:7447928-7448459	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:7478474-7478949	A549	lung:	n/a	n/a
38	CEBPB	chr7:7420648-7420932	HepG2	liver:	n/a	chr7:7420765-7420776 chr7:7420763-7420774 chr7:7420765-7420774
39	CEBPB	chr7:7420648-7420885	IMR90	lung:	n/a	chr7:7420765-7420776 chr7:7420763-7420774 chr7:7420765-7420774
40	CEBPB	chr7:7384246-7384564	Hela-S3	cervix:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
41	CEBPB	chr7:7478454-7479012	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:7462392-7462592	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:7372046-7372298	HepG2	liver:	n/a	chr7:7372136-7372147
44	CEBPB	chr7:7358269-7358363	K562	blood:	n/a	n/a
45	CEBPB	chr7:7348950-7349150	K562	blood:	n/a	n/a
46	CEBPB	chr7:7408469-7408594	K562	blood:	n/a	chr7:7408500-7408511
47	CEBPB	chr7:7408401-7408642	IMR90	lung:	n/a	chr7:7408500-7408511
48	CEBPB	chr7:7384218-7384568	K562	blood:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
49	CEBPB	chr7:7361292-7361745	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr7:7420673-7420920	A549	lung:	n/a	chr7:7420765-7420776 chr7:7420763-7420774 chr7:7420765-7420774

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7474236-7474286	HRCEpiC	kidney:	n/a
2	chr7:7474236-7474286	GM06990	blood:	n/a
3	chr7:7474236-7474286	AG04449	skin:	fetal
4	chr7:7392557-7392607	HCT-116	colon:	n/a
5	chr7:7474236-7474286	MCF-7	breast:	n/a
6	chr7:7478820-7478870	K562	blood:	n/a
7	chr7:7392557-7392607	AoSMC	blood vessel:	n/a
8	chr7:7392557-7392607	HEEpiC	esophagus:	n/a
9	chr7:7474236-7474286	HNPCEpiC	eye:	n/a
10	chr7:7392557-7392607	PANC-1	pancreas:	n/a
11	chr7:7474236-7474286	SK-N-MC	brain:	n/a
12	chr7:7392557-7392607	HIPEpiC	eye:	n/a
13	chr7:7474236-7474286	H1-hESC	embryonic stem cell:	embryo
14	chr7:7392557-7392607	HRPEpiC	eye:	n/a
15	chr7:7478820-7478870	A549	lung:	n/a
16	chr7:7392557-7392607	U87	brain:	n/a
17	chr7:7478820-7478870	BE2_C	brain:	n/a
18	chr7:7392557-7392607	ovcar-3	ovarian:	n/a
19	chr7:7392557-7392607	HAEpiC	amniotic membrane:	n/a
20	chr7:7478820-7478870	Caco-2	colon:	n/a
21	chr7:7392557-7392607	A549	lung:	n/a
22	chr7:7474236-7474286	GM19239	blood:	n/a
23	chr7:7478820-7478870	Hepatocyte	liver:	n/a
24	chr7:7474236-7474286	K562	blood:	n/a
25	chr7:7392557-7392607	ECC-1	luminal epithelium:	n/a
26	chr7:7474236-7474286	AG04450	lung:	fetal
27	chr7:7474236-7474286	IMR90	lung:	fetal
28	chr7:7478820-7478870	NT2-D1	testis:	n/a
29	chr7:7392557-7392607	MCF-7	breast:	n/a
30	chr7:7474236-7474286	AoSMC	blood vessel:	n/a
31	chr7:7392557-7392607	H1-hESC	embryonic stem cell:	embryo
32	chr7:7478820-7478870	Jurkat	blood:	n/a
33	chr7:7392557-7392607	Caco-2	colon:	n/a
34	chr7:7474236-7474286	NHBE	bronchial:	n/a
35	chr7:7392557-7392607	PFSK-1	brain:	n/a
36	chr7:7392557-7392607	Jurkat	blood:	n/a
37	chr7:7474236-7474286	HL-60	blood:	n/a
38	chr7:7478820-7478870	AG09309	skin:	n/a
39	chr7:7392557-7392607	NT2-D1	testis:	n/a
40	chr7:7478820-7478870	AG04449	skin:	fetal
41	chr7:7474236-7474286	BE2_C	brain:	n/a
42	chr7:7474236-7474286	BJ	skin:	n/a
43	chr7:7478820-7478870	Hela-S3	cervix:	n/a
44	chr7:7474236-7474286	NT2-D1	testis:	n/a
45	chr7:7478820-7478870	GM12878	blood:	n/a
46	chr7:7392557-7392607	NB4	blood:	n/a
47	chr7:7474236-7474286	ProgFib	skin:	n/a
48	chr7:7478820-7478870	SK-N-SH_RA	brain:	n/a
49	chr7:7392557-7392607	AG09319	gingival:	n/a
50	chr7:7392557-7392607	ProgFib	skin:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:7395478..7398428-chr7:7405476..7407279,2	K562	blood:
2	chr7:7394187..7395000-chr7:7458752..7459656,4	MCF-7	breast:
3	chr7:7408553..7410116-chr7:7415727..7417970,2	K562	blood:
4	chr7:7492127..7496167-chr7:7498814..7501004,3	K562	blood:
5	chr7:7381460..7384866-chr7:7386223..7388631,3	K562	blood:
6	chr7:7357978..7359775-chr7:7359913..7361736,2	MCF-7	breast:
7	chr7:7473373..7475762-chr7:7594753..7597282,2	MCF-7	breast:
8	chr7:7456758..7459628-chr7:7464929..7467571,2	K562	blood:
9	chr7:7381460..7384866-chr7:7386223..7388631,3	K562	blood:
10	chr7:7467878..7469732-chr7:7578364..7581316,2	K562	blood:
11	chr7:7456425..7458799-chr7:7459595..7461119,2	K562	blood:
12	chr7:7361062..7361815-chr7:7394117..7394640,2	MCF-7	breast:
13	chr7:7342819..7345113-chr7:7345346..7349373,3	K562	blood:
14	chr7:7347784..7350780-chr7:7350970..7352634,2	K562	blood:
15	chr7:7445984..7447777-chr7:7451084..7453972,2	K562	blood:
16	chr7:7463700..7464480-chr7:7580427..7581567,10	MCF-7	breast:
17	chr7:7456758..7459628-chr7:7464929..7467571,2	K562	blood:
18	chr7:7457672..7460558-chr7:7460578..7462678,3	MCF-7	breast:
19	chr7:7395478..7398428-chr7:7405476..7407279,2	K562	blood:
20	chr7:7381460..7385807-chr7:7386068..7388631,3	K562	blood:
21	chr7:7463581..7464271-chr7:8335248..8335877,2	K562	blood:
22	chr7:7142761..7143623-chr7:7463315..7464213,2	MCF-7	breast:
23	chr7:7220227..7222107-chr7:7381152..7382805,2	MCF-7	breast:
24	chr7:7391197..7393340-chr7:7455899..7457673,2	MCF-7	breast:
25	chr7:7387784..7390020-chr7:7393795..7395424,3	K562	blood:
26	chr7:7361584..7363113-chr7:7367144..7369907,2	MCF-7	breast:
27	chr20:52681572..52682154-chr7:7496312..7497133,2	MCF-7	breast:
28	chr20:52218363..52218883-chr7:7436125..7436645,2	MCF-7	breast:
29	chr7:7486591..7488164-chr7:7496470..7498337,2	K562	blood:
30	chr7:7484454..7487980-chr7:7492862..7495926,3	MCF-7	breast:
31	chr7:7393627..7396092-chr7:7403638..7406248,2	MCF-7	breast:
32	chr7:7348114..7350291-chr7:7350684..7352673,2	MCF-7	breast:
33	chr7:7457858..7459653-chr7:7472855..7475146,2	K562	blood:
34	chr7:7355886..7358804-chr7:8301834..8303624,2	K562	blood:
35	chr7:7360934..7361969-chr7:7458890..7459963,5	MCF-7	breast:
36	chr7:7408553..7410116-chr7:7415727..7417970,2	K562	blood:
37	chr7:7392567..7394806-chr7:7395645..7397946,2	K562	blood:
38	chr7:7361052..7361969-chr7:7458671..7459963,8	MCF-7	breast:
39	chr7:7391197..7393340-chr7:7455899..7457673,2	MCF-7	breast:
40	chr7:7393627..7396092-chr7:7403638..7406248,2	MCF-7	breast:
41	chr7:7385330..7388046-chr7:7388768..7391419,2	K562	blood:
42	chr7:7357978..7359775-chr7:7359913..7361736,2	MCF-7	breast:
43	chr7:7347784..7350780-chr7:7350970..7352634,2	K562	blood:
44	chr7:7464180..7464696-chr7:7579103..7579829,2	MCF-7	breast:
45	chr7:7361031..7361660-chr7:7458707..7459324,2	MCF-7	breast:
46	chr7:7361584..7363113-chr7:7367144..7369907,2	MCF-7	breast:
47	chr7:7342773..7344566-chr7:7352462..7355167,2	K562	blood:
48	chr7:7361209..7361979-chr7:7394117..7394769,3	MCF-7	breast:
49	chr7:7457858..7459653-chr7:7472855..7475146,2	K562	blood:
50	chr7:7361031..7361660-chr7:7458707..7459324,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPA3-5	chr7:7459516-7459941	NONHSAT119111
2	lnc-RPA3-5	chr7:7457263-7457558	NONHSAT119111

No data

Variant related genes	Relation type
COL28A1	TF binding region
COL28A1	CpG island
ENSG00000003147	chromatin interactions
ENSG00000135390	chromatin interactions
ENSG00000201218	chromatin interactions
ENSG00000215018	chromatin interactions
ENSG00000164654	chromatin interactions
ENSG00000229970	chromatin interactions
ENSG00000272894	chromatin interactions
ENSG00000244239	chromatin interactions

Extended variants
information (count: 6619 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6619 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549902007	chr7:7348251-7348252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568211536	chr7:7348297-7348298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143286586	chr7:7348305-7348306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553684008	chr7:7348322-7348323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566505520	chr7:7348362-7348363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192621672	chr7:7348443-7348444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183857073	chr7:7348491-7348492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113115592	chr7:7348495-7348496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577225166	chr7:7348502-7348503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544381887	chr7:7348507-7348508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186987943	chr7:7348538-7348539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574971947	chr7:7348560-7348561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542522144	chr7:7348575-7348576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191934412	chr7:7348596-7348597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10486156	chr7:7348633-7348634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs549837395	chr7:7348638-7348639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377174752	chr7:7348641-7348642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545777147	chr7:7348650-7348651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs57245189	chr7:7348713-7348714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184497174	chr7:7348747-7348748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17166299	chr7:7348778-7348779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148247257	chr7:7348783-7348784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13242733	chr7:7348803-7348804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs561897023	chr7:7348814-7348815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530172562	chr7:7348826-7348827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141235821	chr7:7348832-7348833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150380082	chr7:7348856-7348857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190364316	chr7:7348878-7348879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558474889	chr7:7348921-7348922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193053519	chr7:7348922-7348923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138180533	chr7:7348925-7348926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556413634	chr7:7348927-7348928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529205287	chr7:7348930-7348931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542409673	chr7:7348945-7348946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554417994	chr7:7348970-7348971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143709719	chr7:7349000-7349001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147149378	chr7:7349035-7349036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114696680	chr7:7349039-7349040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185565279	chr7:7349043-7349044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543483473	chr7:7349049-7349050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190443982	chr7:7349069-7349070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149284443	chr7:7349081-7349082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528970673	chr7:7349083-7349084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548643860	chr7:7349093-7349094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369517649	chr7:7349105-7349106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180708182	chr7:7349124-7349125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560545090	chr7:7349145-7349146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559123888	chr7:7349173-7349174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2024257	chr7:7349212-7349213	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs551425018	chr7:7349248-7349249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	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
T-cell lymphomas	22341440	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7345800-7348400	Weak transcription	Gastric	stomach
2	chr7:7346000-7360200	Weak transcription	Esophagus	oesophagus
3	chr7:7348400-7348600	Enhancers	Gastric	stomach
4	chr7:7349600-7350200	Enhancers	Stomach Mucosa	stomach
5	chr7:7355400-7356000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:7355600-7356200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:7357800-7358800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:7358000-7358600	Enhancers	K562	blood
9	chr7:7358200-7358800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:7358200-7359800	Enhancers	Placenta	Placenta
11	chr7:7358800-7361000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:7359600-7363200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:7359800-7361000	Weak transcription	Placenta	Placenta
14	chr7:7360200-7361200	Enhancers	Duodenum Mucosa	Duodenum
15	chr7:7360200-7361200	Enhancers	Esophagus	oesophagus
16	chr7:7360200-7364600	Enhancers	Fetal Intestine Large	intestine
17	chr7:7360400-7360600	Enhancers	Fetal Kidney	kidney
18	chr7:7360400-7361200	Enhancers	Spleen	Spleen
19	chr7:7360400-7361600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr7:7360400-7361800	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr7:7360400-7362400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:7360400-7364400	Enhancers	Fetal Intestine Small	intestine
23	chr7:7360600-7363000	Weak transcription	Fetal Kidney	kidney
24	chr7:7360800-7361800	Enhancers	Primary B cells from cord blood	blood
25	chr7:7360800-7362800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:7361000-7361200	Bivalent Enhancer	HepG2	liver
27	chr7:7361000-7361600	Enhancers	Placenta Amnion	Placenta Amnion
28	chr7:7361000-7361600	Enhancers	GM12878-XiMat	blood
29	chr7:7361000-7361800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:7361000-7361800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:7361000-7361800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:7361000-7361800	Enhancers	Fetal Stomach	stomach
33	chr7:7361000-7361800	Enhancers	Psoas Muscle	Psoas
34	chr7:7361000-7362000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr7:7361000-7362200	Enhancers	Placenta	Placenta
36	chr7:7361000-7363000	Enhancers	Stomach Mucosa	stomach
37	chr7:7361000-7363600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:7361000-7363800	Enhancers	Primary B cells from peripheral blood	blood
39	chr7:7361200-7361800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:7361200-7361800	Enhancers	HSMMtube	muscle
41	chr7:7361200-7362200	Enhancers	NHEK	skin
42	chr7:7361200-7363000	Enhancers	HepG2	liver
43	chr7:7361200-7363200	Weak transcription	Esophagus	oesophagus
44	chr7:7361200-7363200	Weak transcription	Spleen	Spleen
45	chr7:7361400-7361600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:7361400-7361800	Enhancers	Hela-S3	cervix
47	chr7:7361600-7361800	Enhancers	Gastric	stomach
48	chr7:7361600-7362000	Flanking Active TSS	GM12878-XiMat	blood
49	chr7:7361600-7362200	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr7:7361600-7366000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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