Variant report

Variant	nsv1034883
Chromosome Location	chr7:5651680-5696147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:749)
CpG islands
(count:490)
Chromatin interactive
region (count:57)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:749 , 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	chr7:5665292-5665987	K562	blood:	n/a	n/a
2	ATF1	chr7:5682942-5683270	K562	blood:	n/a	n/a
3	ATF2	chr7:5665729-5666050	GM12878	blood:	n/a	n/a
4	ATF2	chr7:5678598-5679031	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:5665653-5665935	GM12878	blood:	n/a	n/a
6	ATF2	chr7:5678607-5679025	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:5665601-5666014	K562	blood:	n/a	n/a
8	BACH1	chr7:5676117-5676335	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:5676571-5677031	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr7:5672002-5672209	GM12878	blood:	n/a	chr7:5672043-5672051
11	BHLHE40	chr7:5674039-5674295	K562	blood:	n/a	n/a
12	BHLHE40	chr7:5676823-5676825	K562	blood:	n/a	n/a
13	BRCA1	chr7:5676870-5676882	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr7:5666948-5667041	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:5674119-5674151	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:5670326-5670631	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:5686749-5686834	K562	blood:	n/a	n/a
18	CEBPB	chr7:5686533-5686958	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:5686432-5687056	MCF-7	breast:	n/a	n/a
20	CEBPB	chr7:5658357-5658513	HepG2	liver:	n/a	chr7:5658413-5658430 chr7:5658414-5658427
21	CEBPB	chr7:5658377-5658506	Hela-S3	cervix:	n/a	chr7:5658413-5658430 chr7:5658414-5658427
22	CEBPB	chr7:5658350-5658555	K562	blood:	n/a	chr7:5658413-5658430 chr7:5658414-5658427
23	CEBPB	chr7:5665599-5665974	IMR90	lung:	n/a	n/a
24	CHD2	chr7:5674031-5674228	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:5665820-5665970	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr7:5674080-5674230	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr7:5668740-5668890	HMEC	breast:	n/a	n/a
28	CTCF	chr7:5665840-5665990	HRE	kidney:	n/a	n/a
29	CTCF	chr7:5676700-5676850	AG04449	skin:	n/a	n/a
30	CTCF	chr7:5676520-5676670	AG10803	skin:	n/a	n/a
31	CTCF	chr7:5665760-5665910	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr7:5665740-5665890	NHLF	lung:	n/a	n/a
33	CTCF	chr7:5667600-5667750	BE2_C	brain:	n/a	n/a
34	CTCF	chr7:5665740-5665890	BJ	skin:	n/a	n/a
35	CTCF	chr7:5665780-5665930	AG04450	lung:	n/a	n/a
36	CTCF	chr7:5668776-5668791	Medullo	brain:	n/a	n/a
37	CTCF	chr7:5665740-5665890	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr7:5665700-5665850	HEK293	kidney:	n/a	n/a
39	CTCF	chr7:5676480-5676630	AG10803	skin:	n/a	n/a
40	CTCF	chr7:5669700-5669850	AG09309	skin:	n/a	n/a
41	CTCF	chr7:5668800-5668950	GM12873	blood:	n/a	n/a
42	CTCF	chr7:5668600-5668750	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:5668714-5668789	GM10266	blood:	n/a	n/a
44	CTCF	chr7:5676380-5676530	AG09319	gingival:	n/a	n/a
45	CTCF	chr7:5668740-5668890	HEK293	kidney:	n/a	n/a
46	CTCF	chr7:5665760-5665910	AG09309	skin:	n/a	n/a
47	CTCF	chr7:5665800-5665950	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr7:5686520-5686670	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr7:5668720-5668870	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:5665720-5665870	HCPEpiC	choroid plexus:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5692709-5692759	HL-60	blood:	n/a
2	chr7:5675839-5675889	HEK293	kidney:	embryo
3	chr7:5692709-5692759	HL-60	blood:	n/a
4	chr7:5675839-5675889	HEK293	kidney:	embryo
5	chr7:5666097-5666147	PFSK-1	brain:	n/a
6	chr7:5675839-5675889	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:5666097-5666147	HIPEpiC	eye:	n/a
8	chr7:5682666-5682716	HCM	heart:	n/a
9	chr7:5693657-5693707	HCM	heart:	n/a
10	chr7:5666097-5666147	AG09319	gingival:	n/a
11	chr7:5661076-5661126	RPTEC	kidney:	n/a
12	chr7:5675839-5675889	SK-N-MC	brain:	n/a
13	chr7:5692709-5692759	BE2_C	brain:	n/a
14	chr7:5666097-5666147	HCM	heart:	n/a
15	chr7:5692709-5692759	HMEC	breast:	n/a
16	chr7:5665002-5665052	Caco-2	colon:	n/a
17	chr7:5678706-5678756	PrEC	prostate:	n/a
18	chr7:5675839-5675889	HRCEpiC	kidney:	n/a
19	chr7:5682666-5682716	GM12878	blood:	n/a
20	chr7:5675839-5675889	ECC-1	luminal epithelium:	n/a
21	chr7:5665002-5665052	AG04449	skin:	fetal
22	chr7:5665002-5665052	Hela-S3	cervix:	n/a
23	chr7:5661076-5661126	ECC-1	luminal epithelium:	n/a
24	chr7:5692709-5692759	SK-N-MC	brain:	n/a
25	chr7:5661076-5661126	Hela-S3	cervix:	n/a
26	chr7:5692709-5692759	AG09309	skin:	n/a
27	chr7:5678706-5678756	NB4	blood:	n/a
28	chr7:5661076-5661126	NT2-D1	testis:	n/a
29	chr7:5678706-5678756	AG04450	lung:	fetal
30	chr7:5666097-5666147	HMEC	breast:	n/a
31	chr7:5665002-5665052	MCF10A-Er-Src	breast:	n/a
32	chr7:5675839-5675889	HAEpiC	amniotic membrane:	n/a
33	chr7:5682666-5682716	MCF-7	breast:	n/a
34	chr7:5678706-5678756	PFSK-1	brain:	n/a
35	chr7:5692709-5692759	PANC-1	pancreas:	n/a
36	chr7:5678706-5678756	GM12892	blood:	n/a
37	chr7:5666097-5666147	K562	blood:	n/a
38	chr7:5692709-5692759	T-47D	breast:	n/a
39	chr7:5682666-5682716	HUVEC	blood vessel:	n/a
40	chr7:5693657-5693707	AG10803	skin:	n/a
41	chr7:5675839-5675889	PANC-1	pancreas:	n/a
42	chr7:5666097-5666147	HCPEpiC	choroid plexus:	n/a
43	chr7:5692709-5692759	A549	lung:	n/a
44	chr7:5675839-5675889	NH-A	brain:	n/a
45	chr7:5665002-5665052	AG09319	gingival:	n/a
46	chr7:5675839-5675889	AG10803	skin:	n/a
47	chr7:5693657-5693707	HCPEpiC	choroid plexus:	n/a
48	chr7:5675839-5675889	K562	blood:	n/a
49	chr7:5675839-5675889	HRE	kidney:	n/a
50	chr7:5682666-5682716	HCF	heart:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:5665100..5667122-chr7:5668120..5670662,2	K562	blood:
2	chr7:5663444..5665689-chr7:5666174..5668112,2	K562	blood:
3	chr7:5682005..5684572-chr7:5690822..5692705,2	MCF-7	breast:
4	chr7:5661872..5664251-chr7:5664462..5667384,2	MCF-7	breast:
5	chr7:5680737..5684059-chr7:5686375..5688909,3	MCF-7	breast:
6	chr7:5663656..5665421-chr7:5667676..5669592,2	K562	blood:
7	chr7:5668456..5670547-chr7:5682209..5684790,2	MCF-7	breast:
8	chr7:5632288..5633893-chr7:5656907..5659694,2	MCF-7	breast:
9	chr7:5661872..5664251-chr7:5664462..5667384,2	MCF-7	breast:
10	chr7:5663444..5665689-chr7:5666174..5668112,2	K562	blood:
11	chr7:5652003..5655064-chr7:5663036..5666683,3	MCF-7	breast:
12	chr7:5687349..5689496-chr7:5690114..5692941,3	K562	blood:
13	chr7:5694848..5697610-chr7:5699899..5703275,3	K562	blood:
14	chr7:5663656..5665421-chr7:5667676..5669592,2	K562	blood:
15	chr7:5680737..5684059-chr7:5686375..5688909,3	MCF-7	breast:
16	chr7:5568731..5570253-chr7:5686699..5689101,2	K562	blood:
17	chr7:5687349..5689496-chr7:5690114..5692941,3	K562	blood:
18	chr7:5680983..5682807-chr7:5686516..5688646,2	K562	blood:
19	chr7:5535386..5537242-chr7:5691957..5693613,2	K562	blood:
20	chr7:5665100..5667122-chr7:5668120..5670662,2	K562	blood:
21	chr7:5630929..5633904-chr7:5652494..5654224,2	MCF-7	breast:
22	chr7:5691115..5694271-chr7:5695445..5698769,3	MCF-7	breast:
23	chr7:5601679..5603584-chr7:5667818..5670569,2	MCF-7	breast:
24	chr7:5663770..5665768-chr7:5672068..5673942,2	K562	blood:
25	chr7:5674219..5675152-chr7:5743782..5744684,2	MCF-7	breast:
26	chr7:5680983..5682807-chr7:5686516..5688646,2	K562	blood:
27	chr7:5696126..5698767-chr7:5718167..5720079,2	MCF-7	breast:
28	chr7:5650427..5652222-chr7:5660370..5662038,2	MCF-7	breast:
29	chr7:5630981..5635374-chr7:5673788..5678514,7	K562	blood:
30	chr7:5569849..5571699-chr7:5681727..5683302,2	K562	blood:
31	chr7:5663770..5665922-chr7:5672442..5674114,2	K562	blood:
32	chr7:5661377..5664356-chr7:5673284..5675740,2	MCF-7	breast:
33	chr7:5567941..5570780-chr7:5655569..5657922,2	K562	blood:
34	chr7:5670921..5673137-chr7:5680977..5682945,2	K562	blood:
35	chr7:5670921..5673137-chr7:5680977..5682945,2	K562	blood:
36	chr7:5633680..5635202-chr7:5695155..5698148,2	K562	blood:
37	chr7:5663770..5665768-chr7:5672068..5673942,2	K562	blood:
38	chr7:5570060..5572775-chr7:5691678..5693767,2	MCF-7	breast:
39	chr7:5602390..5604842-chr7:5680680..5682890,2	MCF-7	breast:
40	chr7:5652719..5654979-chr7:5720841..5722728,2	MCF-7	breast:
41	chr7:5631718..5635207-chr7:5679773..5683291,5	MCF-7	breast:
42	chr7:5691115..5694271-chr7:5695445..5698769,3	MCF-7	breast:
43	chr7:5682005..5684572-chr7:5690822..5692705,2	MCF-7	breast:
44	chr7:5650427..5652222-chr7:5660370..5662038,2	MCF-7	breast:
45	chr7:5668201..5671136-chr7:5696894..5699870,2	K562	blood:
46	chr7:5661377..5664356-chr7:5673284..5675740,2	MCF-7	breast:
47	chr7:5673316..5675722-chr7:5676107..5679530,3	K562	blood:
48	chr7:5642213..5645034-chr7:5659207..5661191,2	MCF-7	breast:
49	chr7:5673316..5675722-chr7:5676107..5679530,3	K562	blood:
50	chr7:5659044..5660899-chr7:5710392..5712990,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF216-1	chr7:5655582-5656062	XLOC_006348
2	lnc-RNF216-1	chr7:5653430-5653583	XLOC_006348

No data

Variant related genes	Relation type
RNF216	TF binding region
RNF216	CpG island
ENSG00000075624	chromatin interactions
ENSG00000207973	chromatin interactions
ENSG00000075618	chromatin interactions

Extended variants
information (count: 2267 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2267 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559346169	chr7:5651745-5651746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529791667	chr7:5651765-5651766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188189396	chr7:5651772-5651773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571935606	chr7:5651782-5651783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559743906	chr7:5651819-5651820	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527276873	chr7:5651839-5651840	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11971291	chr7:5651861-5651862	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs570625123	chr7:5651876-5651877	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12530901	chr7:5651913-5651914	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139716997	chr7:5651954-5651955	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549667667	chr7:5652023-5652024	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182508653	chr7:5652086-5652087	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368361289	chr7:5652092-5652093	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551009466	chr7:5652113-5652114	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551785100	chr7:5652118-5652119	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75670303	chr7:5652154-5652155	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572490274	chr7:5652157-5652158	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374614200	chr7:5652174-5652175	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539816379	chr7:5652255-5652256	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558493874	chr7:5652262-5652263	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576620229	chr7:5652274-5652275	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569331781	chr7:5652299-5652300	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs60073378	chr7:5652312-5652313	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114842454	chr7:5652314-5652315	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371874544	chr7:5652323-5652324	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201885736	chr7:5652354-5652355	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368723506	chr7:5652359-5652360	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541558328	chr7:5652362-5652363	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75604637	chr7:5652371-5652372	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527310492	chr7:5652405-5652406	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545345238	chr7:5652406-5652407	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536745026	chr7:5652418-5652419	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531545657	chr7:5652419-5652420	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187235473	chr7:5652424-5652425	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555144728	chr7:5652467-5652468	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568199830	chr7:5652494-5652495	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529068171	chr7:5652539-5652540	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs192164212	chr7:5652568-5652569	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566134278	chr7:5652623-5652624	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs539852594	chr7:5652640-5652641	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557907321	chr7:5652648-5652649	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570029826	chr7:5652698-5652699	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537372293	chr7:5652706-5652707	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149795304	chr7:5652761-5652762	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs574167228	chr7:5652789-5652790	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145778168	chr7:5652826-5652827	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148449418	chr7:5652831-5652832	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs377295807	chr7:5652880-5652881	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139405927	chr7:5652881-5652882	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531477338	chr7:5652885-5652886	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	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
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2218 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5636200-5662000	Weak transcription	Fetal Kidney	kidney
2	chr7:5636600-5661400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:5636800-5661200	Weak transcription	Colon Smooth Muscle	Colon
4	chr7:5638400-5659000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:5638800-5661200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:5638800-5671000	Weak transcription	Right Atrium	heart
7	chr7:5639000-5655200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr7:5639000-5661200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:5641600-5659000	Weak transcription	Thymus	Thymus
10	chr7:5642200-5653400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr7:5642800-5664800	Weak transcription	Hela-S3	cervix
12	chr7:5643600-5660000	Weak transcription	Colonic Mucosa	Colon
13	chr7:5643800-5653200	Weak transcription	HSMMtube	muscle
14	chr7:5643800-5660400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr7:5643800-5661200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:5644000-5659200	Weak transcription	Pancreas	Pancrea
17	chr7:5645000-5655200	Weak transcription	Gastric	stomach
18	chr7:5645000-5661200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:5645000-5661400	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr7:5645000-5662000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:5645000-5662200	Weak transcription	GM12878-XiMat	blood
22	chr7:5645200-5652400	Weak transcription	Brain Substantia Nigra	brain
23	chr7:5645200-5659000	Weak transcription	Aorta	Aorta
24	chr7:5645400-5658600	Weak transcription	Fetal Intestine Large	intestine
25	chr7:5645400-5661000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:5645600-5658400	Weak transcription	Osteobl	bone
27	chr7:5645600-5662000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr7:5645800-5661200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr7:5646800-5659400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr7:5647000-5661600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr7:5647200-5654600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr7:5647200-5659000	Weak transcription	HSMM	muscle
33	chr7:5647200-5661600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr7:5647200-5663000	Weak transcription	NH-A	brain
35	chr7:5647400-5653800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr7:5647400-5659000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr7:5647400-5659200	Weak transcription	Brain Angular Gyrus	brain
38	chr7:5647400-5660000	Weak transcription	Ovary	ovary
39	chr7:5647400-5662200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:5647600-5673200	Weak transcription	Fetal Brain Male	brain
41	chr7:5647800-5655200	Weak transcription	Brain Anterior Caudate	brain
42	chr7:5647800-5659000	Weak transcription	Brain Hippocampus Middle	brain
43	chr7:5647800-5661200	Weak transcription	NHDF-Ad	bronchial
44	chr7:5648000-5659000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr7:5648200-5655400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr7:5648200-5659000	Weak transcription	Right Ventricle	heart
47	chr7:5648400-5653400	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:5648400-5654000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:5648400-5655000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:5648400-5655000	Weak transcription	Brain Germinal Matrix	brain

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