Variant report

Variant	nsv522393
Chromosome Location	chr7:7328775-7427535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:61)
Chromatin interactive
region (count:50)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:7344855-7345031	K562	blood:	n/a	n/a
2	ATF1	chr7:7369805-7369903	K562	blood:	n/a	n/a
3	ATF1	chr7:7376740-7376811	K562	blood:	n/a	n/a
4	ATF2	chr7:7361332-7361786	GM12878	blood:	n/a	n/a
5	ATF2	chr7:7392145-7392924	H1-hESC	embryonic stem cell:	n/a	chr7:7392484-7392495
6	BACH1	chr7:7392453-7392825	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr7:7361281-7361798	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:7363058-7363128	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:7364477-7364520	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:7362908-7363336	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:7332331-7332638	K562	blood:	n/a	n/a
12	CEBPB	chr7:7384237-7384548	ECC-1	luminal epithelium:	n/a	chr7:7384390-7384401
13	CEBPB	chr7:7344742-7345069	K562	blood:	n/a	n/a
14	CEBPB	chr7:7384222-7384581	HepG2	liver:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
15	CEBPB	chr7:7420648-7420885	IMR90	lung:	n/a	chr7:7420765-7420776 chr7:7420763-7420774 chr7:7420765-7420774
16	CEBPB	chr7:7384221-7384573	IMR90	lung:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
17	CEBPB	chr7:7384192-7384697	MCF-7	breast:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
18	CEBPB	chr7:7358269-7358363	K562	blood:	n/a	n/a
19	CEBPB	chr7:7372008-7372244	A549	lung:	n/a	chr7:7372136-7372147
20	CEBPB	chr7:7384224-7384529	K562	blood:	n/a	chr7:7384390-7384401
21	CEBPB	chr7:7384264-7384479	HepG2	liver:	n/a	chr7:7384390-7384401
22	CEBPB	chr7:7384237-7384566	A549	lung:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
23	CEBPB	chr7:7408372-7408658	HepG2	liver:	n/a	chr7:7408500-7408511
24	CEBPB	chr7:7408371-7408642	Hela-S3	cervix:	n/a	chr7:7408500-7408511
25	CEBPB	chr7:7348540-7348748	HepG2	liver:	n/a	chr7:7348617-7348628
26	CEBPB	chr7:7348489-7348683	A549	lung:	n/a	chr7:7348617-7348628
27	CEBPB	chr7:7332352-7332653	K562	blood:	n/a	n/a
28	CEBPB	chr7:7420648-7420932	HepG2	liver:	n/a	chr7:7420765-7420776 chr7:7420763-7420774 chr7:7420765-7420774
29	CEBPB	chr7:7332303-7332671	K562	blood:	n/a	n/a
30	CEBPB	chr7:7384218-7384568	K562	blood:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
31	CEBPB	chr7:7348903-7349190	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:7348920-7349120	A549	lung:	n/a	n/a
33	CEBPB	chr7:7384206-7384599	H1-hESC	embryonic stem cell:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
34	CEBPB	chr7:7384255-7384628	MCF-7	breast:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
35	CEBPB	chr7:7348950-7349150	K562	blood:	n/a	n/a
36	CEBPB	chr7:7372046-7372298	HepG2	liver:	n/a	chr7:7372136-7372147
37	CEBPB	chr7:7408469-7408594	K562	blood:	n/a	chr7:7408500-7408511
38	CEBPB	chr7:7361259-7361741	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr7:7408401-7408642	IMR90	lung:	n/a	chr7:7408500-7408511
40	CEBPB	chr7:7420673-7420920	A549	lung:	n/a	chr7:7420765-7420776 chr7:7420763-7420774 chr7:7420765-7420774
41	CEBPB	chr7:7361292-7361745	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr7:7394140-7394758	MCF-7	breast:	n/a	n/a
43	CEBPB	chr7:7384246-7384564	Hela-S3	cervix:	n/a	chr7:7384538-7384549 chr7:7384390-7384401
44	CEBPB	chr7:7344807-7345062	HepG2	liver:	n/a	n/a
45	CEBPD	chr7:7384300-7384466	HepG2	liver:	n/a	n/a
46	CHD1	chr7:7391305-7391402	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr7:7392600-7392750	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:7370740-7370890	SAEC	small airway:	n/a	chr7:7370847-7370868 chr7:7370845-7370863
49	CTCF	chr7:7392794-7392796	GM10266	blood:	n/a	n/a
50	CTCF	chr7:7392620-7392770	HEK293	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7392557-7392607	MCF-7	breast:	n/a
2	chr7:7392557-7392607	BE2_C	brain:	n/a
3	chr7:7392557-7392607	PANC-1	pancreas:	n/a
4	chr7:7392557-7392607	RPTEC	kidney:	n/a
5	chr7:7392557-7392607	SKMC	muscle:	n/a
6	chr7:7392557-7392607	SK-N-SH_RA	brain:	n/a
7	chr7:7392557-7392607	GM12878	blood:	n/a
8	chr7:7392557-7392607	Jurkat	blood:	n/a
9	chr7:7392557-7392607	T-47D	breast:	n/a
10	chr7:7392557-7392607	Hepatocyte	liver:	n/a
11	chr7:7392557-7392607	SAEC	small airway:	n/a
12	chr7:7392557-7392607	CMK	blood:	n/a
13	chr7:7392557-7392607	H1-hESC	embryonic stem cell:	embryo
14	chr7:7392557-7392607	IMR90	lung:	fetal
15	chr7:7392557-7392607	NHDF-neo	bronchial:	n/a
16	chr7:7392557-7392607	HRCEpiC	kidney:	n/a
17	chr7:7392557-7392607	SK-N-SH	brain:	n/a
18	chr7:7392557-7392607	HCM	heart:	n/a
19	chr7:7392557-7392607	NB4	blood:	n/a
20	chr7:7392557-7392607	HNPCEpiC	eye:	n/a
21	chr7:7392557-7392607	NHBE	bronchial:	n/a
22	chr7:7392557-7392607	NT2-D1	testis:	n/a
23	chr7:7392557-7392607	AG04450	lung:	fetal
24	chr7:7392557-7392607	HRE	kidney:	n/a
25	chr7:7392557-7392607	GM12892	blood:	n/a
26	chr7:7392557-7392607	AG04449	skin:	fetal
27	chr7:7392557-7392607	HMEC	breast:	n/a
28	chr7:7392557-7392607	HRPEpiC	eye:	n/a
29	chr7:7392557-7392607	GM12891	blood:	n/a
30	chr7:7392557-7392607	HL-60	blood:	n/a
31	chr7:7392557-7392607	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:7392557-7392607	AG09309	skin:	n/a
33	chr7:7392557-7392607	HAEpiC	amniotic membrane:	n/a
34	chr7:7392557-7392607	AG10803	skin:	n/a
35	chr7:7392557-7392607	ProgFib	skin:	n/a
36	chr7:7392557-7392607	Caco-2	colon:	n/a
37	chr7:7392557-7392607	HEEpiC	esophagus:	n/a
38	chr7:7392557-7392607	AG09319	gingival:	n/a
39	chr7:7392557-7392607	MCF10A-Er-Src	breast:	n/a
40	chr7:7392557-7392607	U87	brain:	n/a
41	chr7:7392557-7392607	SK-N-MC	brain:	n/a
42	chr7:7392557-7392607	ovcar-3	ovarian:	n/a
43	chr7:7392557-7392607	HUVEC	blood vessel:	n/a
44	chr7:7392557-7392607	GM06990	blood:	n/a
45	chr7:7392557-7392607	PrEC	prostate:	n/a
46	chr7:7392557-7392607	BJ	skin:	n/a
47	chr7:7392557-7392607	GM19239	blood:	n/a
48	chr7:7392557-7392607	HCPEpiC	choroid plexus:	n/a
49	chr7:7392557-7392607	NH-A	brain:	n/a
50	chr7:7392557-7392607	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:7387784..7390020-chr7:7393795..7395424,3	K562	blood:
2	chr7:7361062..7361815-chr7:7394117..7394640,2	MCF-7	breast:
3	chr7:7347784..7350780-chr7:7350970..7352634,2	K562	blood:
4	chr7:7355886..7358804-chr7:8301834..8303624,2	K562	blood:
5	chr7:7391197..7393340-chr7:7455899..7457673,2	MCF-7	breast:
6	chr7:7357978..7359775-chr7:7359913..7361736,2	MCF-7	breast:
7	chr7:7394315..7395000-chr7:7458752..7459656,3	MCF-7	breast:
8	chr7:7360934..7361969-chr7:7458890..7459963,5	MCF-7	breast:
9	chr7:7361209..7361979-chr7:7394117..7394769,3	MCF-7	breast:
10	chr7:7342773..7344566-chr7:7352462..7355167,2	K562	blood:
11	chr7:7342819..7345113-chr7:7345346..7349373,3	K562	blood:
12	chr7:7381460..7384866-chr7:7386223..7388631,3	K562	blood:
13	chr7:7322726..7325575-chr7:7329256..7331422,2	MCF-7	breast:
14	chr7:7361584..7363113-chr7:7367144..7369907,2	MCF-7	breast:
15	chr7:7381460..7384866-chr7:7386223..7388631,3	K562	blood:
16	chr7:7385330..7388046-chr7:7388768..7391419,2	K562	blood:
17	chr7:7381460..7385807-chr7:7386068..7388631,3	K562	blood:
18	chr7:7381460..7385807-chr7:7386068..7388631,3	K562	blood:
19	chr7:7350418..7352862-chr7:7353431..7355937,2	MCF-7	breast:
20	chr7:7395478..7398428-chr7:7405476..7407279,2	K562	blood:
21	chr7:7348114..7350291-chr7:7350684..7352673,2	MCF-7	breast:
22	chr7:7229626..7232056-chr7:7343354..7345777,2	K562	blood:
23	chr7:7348114..7350291-chr7:7350684..7352673,2	MCF-7	breast:
24	chr12:54069652..54070365-chr7:7364476..7364996,2	MCF-7	breast:
25	chr7:7395478..7398428-chr7:7405476..7407279,2	K562	blood:
26	chr7:7318004..7320924-chr7:7330269..7333078,2	K562	blood:
27	chr7:7354935..7358098-chr7:7360992..7363611,4	K562	blood:
28	chr7:7350418..7352862-chr7:7353431..7355937,2	MCF-7	breast:
29	chr7:7408553..7410116-chr7:7415727..7417970,2	K562	blood:
30	chr7:7382930..7384595-chr7:7606937..7608643,2	K562	blood:
31	chr7:7361062..7361815-chr7:7394117..7394640,2	MCF-7	breast:
32	chr7:7347784..7350780-chr7:7350970..7352634,2	K562	blood:
33	chr7:7392567..7394806-chr7:7395645..7397946,2	K562	blood:
34	chr7:7354935..7358098-chr7:7360992..7363611,4	K562	blood:
35	chr7:7361052..7361969-chr7:7458671..7459963,8	MCF-7	breast:
36	chr7:7143123..7143712-chr7:7389680..7390354,2	MCF-7	breast:
37	chr7:7408553..7410116-chr7:7415727..7417970,2	K562	blood:
38	chr7:7361584..7363113-chr7:7367144..7369907,2	MCF-7	breast:
39	chr7:7393627..7396092-chr7:7403638..7406248,2	MCF-7	breast:
40	chr7:7385330..7388046-chr7:7388768..7391419,2	K562	blood:
41	chr7:7393627..7396092-chr7:7403638..7406248,2	MCF-7	breast:
42	chr7:7392567..7394806-chr7:7395645..7397946,2	K562	blood:
43	chr7:7342819..7345113-chr7:7345346..7349373,3	K562	blood:
44	chr7:7394187..7395000-chr7:7458752..7459656,4	MCF-7	breast:
45	chr7:7361031..7361660-chr7:7458707..7459324,2	MCF-7	breast:
46	chr7:7361209..7361979-chr7:7394117..7394769,3	MCF-7	breast:
47	chr7:7342773..7344566-chr7:7352462..7355167,2	K562	blood:
48	chr7:7220227..7222107-chr7:7381152..7382805,2	MCF-7	breast:
49	chr7:7357978..7359775-chr7:7359913..7361736,2	MCF-7	breast:
50	chr7:7387784..7390020-chr7:7393795..7395424,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1GALT1-3	chr7:7333139-7333511	NONHSAT119110

No data

Variant related genes	Relation type
ENSG00000236712	TF binding region
COL28A1	TF binding region
ENSG00000236712	CpG island
COL28A1	CpG island
ENSG00000229970	chromatin interactions
ENSG00000244239	chromatin interactions
ENSG00000003147	chromatin interactions
ENSG00000135390	chromatin interactions
ENSG00000164654	chromatin interactions
ENSG00000215018	chromatin interactions

Extended variants
information (count: 4228 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4228 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386709923	chr7:7328775-7328776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115203095	chr7:7328776-7328777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112550538	chr7:7328784-7328785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181626470	chr7:7328791-7328792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186099618	chr7:7328841-7328842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531615799	chr7:7328865-7328866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549842308	chr7:7328890-7328891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10257131	chr7:7328897-7328898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530087634	chr7:7328901-7328902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548617213	chr7:7328937-7328938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566640054	chr7:7328940-7328941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36066792	chr7:7328947-7328948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191013112	chr7:7328963-7328964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556988489	chr7:7328973-7328974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10238967	chr7:7328997-7328998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148188987	chr7:7329025-7329026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571475638	chr7:7329115-7329116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539063378	chr7:7329125-7329126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557695223	chr7:7329170-7329171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538970661	chr7:7329181-7329182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541466900	chr7:7329234-7329235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572642284	chr7:7329236-7329237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183532572	chr7:7329244-7329245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73676813	chr7:7329252-7329253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185263458	chr7:7329290-7329291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564259789	chr7:7329293-7329294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531448029	chr7:7329303-7329304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543699177	chr7:7329341-7329342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563902749	chr7:7329342-7329343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530070162	chr7:7329374-7329375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548198826	chr7:7329388-7329389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146301294	chr7:7329400-7329401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191150108	chr7:7329429-7329430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560141743	chr7:7329461-7329462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182664187	chr7:7329469-7329470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553178208	chr7:7329470-7329471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552292239	chr7:7329481-7329482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570705380	chr7:7329494-7329495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531152675	chr7:7329507-7329508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141680880	chr7:7329528-7329529	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs7779267	chr7:7329539-7329540	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs6463667	chr7:7329540-7329541	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs553782920	chr7:7329542-7329543	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs534961076	chr7:7329543-7329544	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs539532450	chr7:7329561-7329562	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs547019701	chr7:7329572-7329573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs375315425	chr7:7329575-7329576	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs6463668	chr7:7329583-7329584	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs576139919	chr7:7329591-7329592	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs57433974	chr7:7329593-7329594	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

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

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7320000-7332000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:7322600-7332200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:7329800-7330800	Enhancers	HepG2	liver
4	chr7:7329800-7335000	Enhancers	Liver	Liver
5	chr7:7331400-7332000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:7331400-7332200	Enhancers	K562	blood
7	chr7:7331400-7335200	Enhancers	Fetal Intestine Large	intestine
8	chr7:7331600-7332000	Enhancers	GM12878-XiMat	blood
9	chr7:7331800-7332800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:7332000-7332400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:7332200-7332400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:7332200-7332400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:7332200-7332600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:7332200-7332600	Enhancers	Pancreas	Pancrea
15	chr7:7332200-7333200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:7332200-7333200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:7332200-7333200	Enhancers	Placenta	Placenta
18	chr7:7332400-7333400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr7:7332600-7335000	Enhancers	Fetal Intestine Small	intestine
20	chr7:7332800-7334200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr7:7333200-7333600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:7333400-7333800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:7333400-7334200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:7334400-7335000	Enhancers	HepG2	liver
25	chr7:7335000-7335800	Weak transcription	Fetal Intestine Small	intestine
26	chr7:7335800-7336000	Enhancers	Fetal Intestine Small	intestine
27	chr7:7338000-7338200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:7338200-7341000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:7340200-7340400	Enhancers	Gastric	stomach
30	chr7:7340400-7340600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:7340400-7344400	Weak transcription	Gastric	stomach
32	chr7:7340600-7343000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:7340800-7345000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:7341000-7341800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:7341200-7341400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:7341400-7342600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:7341800-7342000	Enhancers	Fetal Intestine Small	intestine
38	chr7:7341800-7342800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:7341800-7344800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:7342000-7342800	Weak transcription	Fetal Intestine Small	intestine
41	chr7:7342000-7343200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:7342400-7342800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr7:7342400-7343200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:7342600-7343000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr7:7342800-7343400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr7:7342800-7343600	Enhancers	H9 Cell Line	embryonic stem cell
47	chr7:7342800-7345000	Enhancers	Placenta	Placenta
48	chr7:7342800-7346000	Enhancers	Esophagus	oesophagus
49	chr7:7343000-7343400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:7343000-7343400	Enhancers	Duodenum Mucosa	Duodenum

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