Variant report

Variant	nsv1019688
Chromosome Location	chr9:27234184-27356374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1134)
CpG islands
(count:550)
Chromatin interactive
region (count:21)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1134 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:27276433-27276779	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:27261532-27261892	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:27276480-27276766	K562	blood:	n/a	n/a
4	ATF2	chr9:27353230-27353657	GM12878	blood:	n/a	n/a
5	ATF2	chr9:27353339-27353693	GM12878	blood:	n/a	n/a
6	ATF2	chr9:27352330-27352860	GM12878	blood:	n/a	n/a
7	ATF2	chr9:27352454-27352815	GM12878	blood:	n/a	n/a
8	ATF3	chr9:27303237-27303477	K562	blood:	n/a	n/a
9	BACH1	chr9:27354759-27354804	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:27303314-27303568	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:27308693-27309302	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:27303260-27303653	K562	blood:	n/a	n/a
13	BATF	chr9:27352461-27352773	GM12878	blood:	n/a	n/a
14	BATF	chr9:27353336-27353679	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:27353335-27353638	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:27353306-27353704	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:27352393-27352840	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
18	BCL11A	chr9:27352443-27352727	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
19	BCLAF1	chr9:27352397-27352746	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
20	BCLAF1	chr9:27353329-27353747	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:27352426-27352853	GM12878	blood:	n/a	chr9:27352615-27352624 chr9:27352578-27352587
22	BHLHE40	chr9:27281155-27281334	K562	blood:	n/a	n/a
23	BHLHE40	chr9:27303181-27303595	K562	blood:	n/a	n/a
24	BHLHE40	chr9:27261364-27261936	HepG2	liver:	n/a	n/a
25	BHLHE40	chr9:27333307-27333503	K562	blood:	n/a	n/a
26	BHLHE40	chr9:27352412-27353761	GM12878	blood:	n/a	n/a
27	BRCA1	chr9:27261881-27262104	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr9:27333193-27333639	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr9:27303220-27303571	K562	blood:	n/a	n/a
30	CEBPB	chr9:27248839-27249287	IMR90	lung:	n/a	chr9:27249140-27249151 chr9:27248881-27248898
31	CEBPB	chr9:27258776-27259077	A549	lung:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
32	CEBPB	chr9:27316969-27317234	HepG2	liver:	n/a	chr9:27317119-27317130
33	CEBPB	chr9:27333228-27333580	H1-hESC	embryonic stem cell:	n/a	chr9:27333339-27333347
34	CEBPB	chr9:27316982-27317252	Hela-S3	cervix:	n/a	chr9:27317119-27317130
35	CEBPB	chr9:27248999-27249274	HepG2	liver:	n/a	chr9:27249140-27249151
36	CEBPB	chr9:27333222-27333556	HepG2	liver:	n/a	chr9:27333339-27333347
37	CEBPB	chr9:27261315-27261855	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:27258771-27259071	K562	blood:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
39	CEBPB	chr9:27261286-27261670	MCF-7	breast:	n/a	n/a
40	CEBPB	chr9:27333188-27333603	Hela-S3	cervix:	n/a	chr9:27333339-27333347
41	CEBPB	chr9:27248970-27249261	A549	lung:	n/a	chr9:27249140-27249151
42	CEBPB	chr9:27333282-27333519	K562	blood:	n/a	chr9:27333339-27333347
43	CEBPB	chr9:27303105-27303500	K562	blood:	n/a	n/a
44	CEBPB	chr9:27333147-27333559	A549	lung:	n/a	chr9:27333339-27333347
45	CEBPB	chr9:27341228-27341562	H1-hESC	embryonic stem cell:	n/a	chr9:27341393-27341406
46	CEBPB	chr9:27261315-27262115	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr9:27258775-27259094	HepG2	liver:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
48	CEBPB	chr9:27272984-27273198	A549	lung:	n/a	chr9:27273158-27273171
49	CEBPB	chr9:27238842-27239132	HepG2	liver:	n/a	chr9:27238966-27238975
50	CHD1	chr9:27333921-27334049	H1-hESC	embryonic stem cell:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:27297089-27297139	HCT-116	colon:	n/a
2	chr9:27297089-27297139	HCT-116	colon:	n/a
3	chr9:27292606-27292656	AG04450	lung:	fetal
4	chr9:27342183-27342233	BE2_C	brain:	n/a
5	chr9:27297089-27297139	A549	lung:	n/a
6	chr9:27342183-27342233	PANC-1	pancreas:	n/a
7	chr9:27282776-27282826	HCT-116	colon:	n/a
8	chr9:27292606-27292656	A549	lung:	n/a
9	chr9:27297089-27297139	HNPCEpiC	eye:	n/a
10	chr9:27297335-27297385	GM12878	blood:	n/a
11	chr9:27248473-27248523	MCF-7	breast:	n/a
12	chr9:27282580-27282630	HL-60	blood:	n/a
13	chr9:27327953-27328003	HCF	heart:	n/a
14	chr9:27292606-27292656	Caco-2	colon:	n/a
15	chr9:27327953-27328003	T-47D	breast:	n/a
16	chr9:27282580-27282630	A549	lung:	n/a
17	chr9:27282776-27282826	SK-N-MC	brain:	n/a
18	chr9:27333402-27333452	U87	brain:	n/a
19	chr9:27342183-27342233	HCM	heart:	n/a
20	chr9:27297335-27297385	HepG2	liver:	n/a
21	chr9:27342183-27342233	MCF10A-Er-Src	breast:	n/a
22	chr9:27282580-27282630	K562	blood:	n/a
23	chr9:27297089-27297139	SAEC	small airway:	n/a
24	chr9:27292606-27292656	RPTEC	kidney:	n/a
25	chr9:27282580-27282630	HMEC	breast:	n/a
26	chr9:27282580-27282630	HIPEpiC	eye:	n/a
27	chr9:27297089-27297139	HepG2	liver:	n/a
28	chr9:27297335-27297385	HIPEpiC	eye:	n/a
29	chr9:27292606-27292656	ECC-1	luminal epithelium:	n/a
30	chr9:27297335-27297385	BJ	skin:	n/a
31	chr9:27333402-27333452	HAEpiC	amniotic membrane:	n/a
32	chr9:27282776-27282826	HAEpiC	amniotic membrane:	n/a
33	chr9:27292606-27292656	PFSK-1	brain:	n/a
34	chr9:27282776-27282826	HMEC	breast:	n/a
35	chr9:27282580-27282630	HUVEC	blood vessel:	n/a
36	chr9:27333402-27333452	HCM	heart:	n/a
37	chr9:27292606-27292656	GM19239	blood:	n/a
38	chr9:27282776-27282826	GM19239	blood:	n/a
39	chr9:27292606-27292656	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:27248473-27248523	AG04449	skin:	fetal
41	chr9:27333402-27333452	AG04449	skin:	fetal
42	chr9:27248473-27248523	PANC-1	pancreas:	n/a
43	chr9:27297335-27297385	PrEC	prostate:	n/a
44	chr9:27282776-27282826	GM12878	blood:	n/a
45	chr9:27327953-27328003	U87	brain:	n/a
46	chr9:27282776-27282826	NHBE	bronchial:	n/a
47	chr9:27292606-27292656	NHDF-neo	bronchial:	n/a
48	chr9:27248473-27248523	Hepatocyte	liver:	n/a
49	chr9:27297335-27297385	HUVEC	blood vessel:	n/a
50	chr9:27297335-27297385	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:27300012..27302683-chr9:27305254..27307396,2	K562	blood:
2	chr1:146644212..146644715-chr9:27340015..27340515,2	MCF-7	breast:
3	chr9:27329438..27331174-chr9:27537261..27539824,2	K562	blood:
4	chr9:27280860..27282970-chr9:27289180..27290823,2	K562	blood:
5	chr9:27328788..27330536-chr9:27524466..27526577,2	K562	blood:
6	chr9:27332939..27333807-chr9:27547988..27549046,3	K562	blood:
7	chr9:27033503..27034503-chr9:27276144..27277065,4	K562	blood:
8	chr9:27332980..27333834-chr9:27547941..27548663,3	MCF-7	breast:
9	chr9:27328991..27331118-chr9:27335749..27338717,2	K562	blood:
10	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
11	chr9:27332966..27333852-chr9:27535507..27536468,2	K562	blood:
12	chr9:27328991..27331118-chr9:27335749..27338717,2	K562	blood:
13	chr9:27247560..27248337-chr9:27547652..27548456,2	MCF-7	breast:
14	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
15	chr9:27333009..27333876-chr9:27535565..27536408,4	MCF-7	breast:
16	chr9:27247423..27248703-chr9:27275999..27276820,3	MCF-7	breast:
17	chr9:27300012..27302683-chr9:27305254..27307396,2	K562	blood:
18	chr9:27033902..27034442-chr9:27247489..27248319,2	MCF-7	breast:
19	chr9:27332963..27333812-chr9:27529343..27530314,6	MCF-7	breast:
20	chr9:27247423..27248703-chr9:27275999..27276820,3	MCF-7	breast:
21	chr9:27033540..27034483-chr9:27275947..27276717,3	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf11-1	chr9:27235682-27235760	NONHSAT130610
2	lnc-C9orf11-1	chr9:27270426-27270613	l_3745_NR_026687
3	lnc-C9orf11-1	chr9:27253207-27253263	NONHSAT130610
4	lnc-C9orf11-1	chr9:27248410-27248517	NONHSAT130610
5	lnc-C9orf11-1	chr9:27253207-27253263	l_3745_NR_026687
6	lnc-C9orf11-1	chr9:27270426-27270613	NONHSAT130610
7	lnc-C9orf11-1	chr9:27237388-27237508	l_3745_NR_026687
8	lnc-C9orf11-1	chr9:27252710-27252801	NONHSAT130610
9	lnc-C9orf11-1	chr9:27237388-27237508	NONHSAT130610
10	lnc-C9orf11-1	chr9:27258419-27258515	l_3745_NR_026687
11	lnc-C9orf11-1	chr9:27258419-27258515	NONHSAT130610
12	lnc-TEK-2	chr9:27245986-27246282	XLOC_007307
13	lnc-C9orf11-1	chr9:27268359-27268726	l_3745_NR_026687
14	lnc-C9orf11-1	chr9:27267549-27267774	NONHSAT130610
15	lnc-MOB3B-1	chr9:27292411-27292485	NONHSAT130613
16	lnc-C9orf11-1	chr9:27261925-27262086	l_3745_NR_026687
17	lnc-C9orf11-1	chr9:27267549-27267774	l_3745_NR_026687
18	lnc-C9orf11-1	chr9:27248410-27248517	l_3745_NR_026687
19	lnc-C9orf11-1	chr9:27266962-27267108	l_3745_NR_026687
20	lnc-C9orf11-1	chr9:27251828-27252034	NONHSAT130610
21	lnc-C9orf11-1	chr9:27266962-27267108	NONHSAT130610
22	lnc-C9orf11-1	chr9:27248693-27248766	NONHSAT130610
23	lnc-C9orf11-1	chr9:27264088-27264284	l_3745_NR_026687
24	lnc-C9orf11-1	chr9:27235684-27235760	l_3745_NR_026687
25	lnc-C9orf11-1	chr9:27272328-27272791	l_3745_NR_026687
26	lnc-TEK-2	chr9:27245472-27245673	XLOC_007307
27	lnc-C9orf11-1	chr9:27261925-27262086	NONHSAT130610
28	lnc-C9orf11-1	chr9:27270766-27270922	NONHSAT130610
29	lnc-C9orf11-1	chr9:27251828-27252034	l_3745_NR_026687
30	lnc-C9orf11-1	chr9:27265780-27265948	l_3745_NR_026687
31	lnc-MOB3B-1	chr9:27296611-27296738	NONHSAT130613
32	lnc-MOB3B-1	chr9:27294314-27294493	NONHSAT130613
33	lnc-C9orf11-1	chr9:27252710-27252801	l_3745_NR_026687
34	lnc-C9orf11-1	chr9:27248693-27248766	l_3745_NR_026687
35	lnc-C9orf11-1	chr9:27264088-27264284	NONHSAT130610
36	lnc-C9orf11-1	chr9:27272328-27272791	NONHSAT130610
37	lnc-C9orf11-1	chr9:27265780-27265948	NONHSAT130610
38	lnc-C9orf11-1	chr9:27268359-27268726	NONHSAT130610
39	lnc-C9orf11-1	chr9:27270766-27270922	l_3745_NR_026687

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MOBKL2B	hsa-miR-181a-5p	chr9:27329179-27329173
2	MOBKL2B	hsa-miR-98-5p	chr9:27328932-27328925

Variant related genes	Relation type
LINC00032	TF binding region
EQTN	TF binding region
LINC00032	CpG island
EQTN	CpG island
ENSG00000237188	chromatin interactions
ENSG00000231459	chromatin interactions
ENSG00000120162	chromatin interactions
ATP6V1B2	miRNA target sites

Extended variants
information (count: 3776 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:3776 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576126241	chr9:27235690-27235691	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs12341363	chr9:27235707-27235708	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs372259306	chr9:27235710-27235711	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557139335	chr9:27235728-27235729	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs200537554	chr9:27235734-27235735	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs538864358	chr9:27235756-27235757	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs2208634	chr9:27237399-27237400	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549268882	chr9:27237400-27237401	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs142593490	chr9:27237415-27237416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556857103	chr9:27237434-27237435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs574891706	chr9:27237442-27237443	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs542282647	chr9:27237484-27237485	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs560485969	chr9:27237494-27237495	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs376568044	chr9:27245512-27245513	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs570365264	chr9:27245532-27245533	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs528344920	chr9:27245541-27245542	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs546220804	chr9:27245548-27245549	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs570884299	chr9:27245555-27245556	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs538353200	chr9:27245566-27245567	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs369612363	chr9:27245585-27245586	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs568853094	chr9:27245595-27245596	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs373302727	chr9:27245605-27245606	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs375158738	chr9:27245634-27245635	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs554845063	chr9:27245635-27245636	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs573613526	chr9:27245642-27245643	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs144539229	chr9:27245653-27245654	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs368546740	chr9:27246018-27246019	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs74685567	chr9:27246019-27246020	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs78873333	chr9:27246026-27246027	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs539393411	chr9:27246040-27246041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs187106372	chr9:27246042-27246043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs577601377	chr9:27246045-27246046	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs17834925	chr9:27246055-27246056	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1885382	chr9:27246116-27246117	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs574907806	chr9:27246117-27246118	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs541922054	chr9:27246135-27246136	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs199873969	chr9:27246149-27246150	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs1885381	chr9:27246151-27246152	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs57082575	chr9:27246160-27246161	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs367979816	chr9:27246170-27246171	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs572664709	chr9:27246245-27246246	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs542515470	chr9:27247600-27247601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568238136	chr9:27247608-27247609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535710105	chr9:27247665-27247666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535245685	chr9:27247670-27247671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12238077	chr9:27247792-27247793	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116017306	chr9:27247797-27247798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs151013929	chr9:27247813-27247814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377341821	chr9:27247822-27247823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545807886	chr9:27247834-27247835	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Epilepsy	22083797	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1302 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27247600-27248200	Enhancers	Stomach Mucosa	stomach
2	chr9:27247600-27248600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:27247600-27249400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:27247800-27248600	Enhancers	Placenta	Placenta
5	chr9:27247800-27249000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:27247800-27249200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:27247800-27249200	Enhancers	NHEK	skin
8	chr9:27247800-27249400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:27247800-27249400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:27247800-27249400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:27247800-27249400	Enhancers	Osteobl	bone
12	chr9:27248000-27248800	Enhancers	Hela-S3	cervix
13	chr9:27248200-27249400	Enhancers	HSMM	muscle
14	chr9:27248400-27249200	Enhancers	Placenta Amnion	Placenta Amnion
15	chr9:27249000-27249200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:27259400-27259600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr9:27260200-27260600	Enhancers	Lung	lung
18	chr9:27260600-27262200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr9:27260800-27262400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:27261000-27262000	Enhancers	HepG2	liver
21	chr9:27261000-27262200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:27261000-27262200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr9:27261200-27261400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:27261200-27261400	Enhancers	Placenta	Placenta
25	chr9:27261200-27261800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:27261200-27262200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr9:27261200-27262200	Enhancers	Hela-S3	cervix
28	chr9:27261400-27261800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:27261400-27262200	Enhancers	Gastric	stomach
30	chr9:27261600-27261800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:27261600-27261800	Enhancers	Stomach Mucosa	stomach
32	chr9:27261600-27262000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr9:27261600-27262200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr9:27261800-27262200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:27261800-27262200	Enhancers	NHEK	skin
36	chr9:27262000-27262200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:27262000-27262200	Enhancers	Placenta	Placenta
38	chr9:27262200-27262400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr9:27266800-27267000	Enhancers	Pancreas	Pancrea
40	chr9:27269600-27270400	Enhancers	Stomach Mucosa	stomach
41	chr9:27270000-27270400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:27270400-27272800	Weak transcription	Stomach Mucosa	stomach
43	chr9:27272600-27273000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr9:27272600-27273000	Enhancers	Fetal Intestine Large	intestine
45	chr9:27272600-27274600	Enhancers	Fetal Intestine Small	intestine
46	chr9:27272800-27273600	Enhancers	Stomach Mucosa	stomach
47	chr9:27273000-27276000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr9:27273000-27278200	Weak transcription	Fetal Intestine Large	intestine
49	chr9:27273600-27276200	Weak transcription	Stomach Mucosa	stomach
50	chr9:27274600-27276000	Weak transcription	Fetal Intestine Small	intestine

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