Variant report

Variant	nsv818475
Chromosome Location	chr7:6187783-6212656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:6201433-6201909	GM12878	blood:	n/a	n/a
2	BACH1	chr7:6199913-6200132	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:6204016-6204358	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr7:6200018-6200134	K562	blood:	n/a	n/a
5	CCNT2	chr7:6194167-6194449	K562	blood:	n/a	n/a
6	CEBPB	chr7:6200710-6200995	HepG2	liver:	n/a	chr7:6200829-6200840
7	CEBPB	chr7:6200666-6201009	IMR90	lung:	n/a	chr7:6200829-6200840
8	CHD2	chr7:6198047-6198084	K562	blood:	n/a	n/a
9	CHD2	chr7:6204212-6204322	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr7:6196841-6196885	HepG2	liver:	n/a	n/a
11	CHD2	chr7:6211312-6211829	H1-hESC	embryonic stem cell:	n/a	chr7:6211548-6211558
12	CTCF	chr7:6204140-6204290	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr7:6206240-6206390	BE2_C	brain:	n/a	n/a
14	CTCF	chr7:6204180-6204330	HRE	kidney:	n/a	n/a
15	CTCF	chr7:6204180-6204330	HCFaa	heart:	n/a	n/a
16	CTCF	chr7:6204160-6204310	HCM	heart:	n/a	n/a
17	CTCF	chr7:6204160-6204310	HRE	kidney:	n/a	n/a
18	CTCF	chr7:6199880-6200030	HCFaa	heart:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
19	CTCF	chr7:6199840-6199990	GM06990	blood:	n/a	n/a
20	CTCF	chr7:6199900-6200050	NHDF-neo	bronchial:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
21	CTCF	chr7:6199713-6200422	IMR90	lung:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
22	CTCF	chr7:6199900-6200050	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
23	CTCF	chr7:6200140-6200290	AG10803	skin:	n/a	n/a
24	CTCF	chr7:6204113-6204348	A549	lung:	n/a	n/a
25	CTCF	chr7:6204200-6204350	AG09309	skin:	n/a	n/a
26	CTCF	chr7:6199851-6200131	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
27	CTCF	chr7:6199838-6200139	MCF-7	breast:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
28	CTCF	chr7:6199673-6200334	HCT-116	colon:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
29	CTCF	chr7:6199880-6200030	AoAF	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
30	CTCF	chr7:6199908-6200053	Kidney_OC	kidney:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
31	CTCF	chr7:6199860-6200010	HRE	kidney:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
32	CTCF	chr7:6204200-6204350	AG09319	gingival:	n/a	n/a
33	CTCF	chr7:6204140-6204290	K562	blood:	n/a	n/a
34	CTCF	chr7:6199840-6199990	GM12872	blood:	n/a	n/a
35	CTCF	chr7:6204220-6204370	GM12864	blood:	n/a	n/a
36	CTCF	chr7:6199839-6200216	K562	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
37	CTCF	chr7:6199880-6200030	HFF	foreskin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
38	CTCF	chr7:6199900-6200050	BE2_C	brain:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
39	CTCF	chr7:6204040-6204190	HCM	heart:	n/a	n/a
40	CTCF	chr7:6204140-6204290	HPF	lung:	n/a	n/a
41	CTCF	chr7:6204182-6204304	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:6199880-6200030	HRE	kidney:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
43	CTCF	chr7:6204180-6204330	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr7:6205560-6205710	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:6199898-6200077	GM10266	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
46	CTCF	chr7:6199940-6200090	GM12875	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
47	CTCF	chr7:6199880-6200030	AG09309	skin:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
48	CTCF	chr7:6199920-6200070	HBMEC	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
49	CTCF	chr7:6199940-6200090	HPAF	blood vessel:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998
50	CTCF	chr7:6199880-6200030	K562	blood:	n/a	chr7:6199983-6199999 chr7:6199985-6199998 chr7:6199982-6200000 chr7:6199985-6199998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6189770-6189820	BE2_C	brain:	n/a
2	chr7:6209226-6209276	AG09319	gingival:	n/a
3	chr7:6198846-6198896	A549	lung:	n/a
4	chr7:6210236-6210286	RPTEC	kidney:	n/a
5	chr7:6203156-6203206	H1-hESC	embryonic stem cell:	embryo
6	chr7:6189539-6189589	A549	lung:	n/a
7	chr7:6197678-6197728	SAEC	small airway:	n/a
8	chr7:6198604-6198654	GM12878	blood:	n/a
9	chr7:6203156-6203206	ovcar-3	ovarian:	n/a
10	chr7:6198004-6198054	HEEpiC	esophagus:	n/a
11	chr7:6189770-6189820	BE2_C	brain:	n/a
12	chr7:6209226-6209276	AG09319	gingival:	n/a
13	chr7:6198846-6198896	A549	lung:	n/a
14	chr7:6210236-6210286	RPTEC	kidney:	n/a
15	chr7:6203156-6203206	H1-hESC	embryonic stem cell:	embryo
16	chr7:6189539-6189589	A549	lung:	n/a
17	chr7:6197678-6197728	SAEC	small airway:	n/a
18	chr7:6198604-6198654	GM12878	blood:	n/a
19	chr7:6203156-6203206	ovcar-3	ovarian:	n/a
20	chr7:6198004-6198054	HEEpiC	esophagus:	n/a
21	chr7:6203267-6203317	NT2-D1	testis:	n/a
22	chr7:6198496-6198546	AG04449	skin:	fetal
23	chr7:6209931-6209981	GM06990	blood:	n/a
24	chr7:6198496-6198546	HEK293	kidney:	embryo
25	chr7:6197678-6197728	ProgFib	skin:	n/a
26	chr7:6189539-6189589	CMK	blood:	n/a
27	chr7:6212576-6212626	ProgFib	skin:	n/a
28	chr7:6205417-6205467	HCM	heart:	n/a
29	chr7:6193974-6194024	NH-A	brain:	n/a
30	chr7:6198604-6198654	HCF	heart:	n/a
31	chr7:6204269-6204319	NT2-D1	testis:	n/a
32	chr7:6191921-6191971	MCF10A-Er-Src	breast:	n/a
33	chr7:6204269-6204319	PFSK-1	brain:	n/a
34	chr7:6200116-6200166	LNCaP	prostate:	n/a
35	chr7:6198703-6198753	GM12891	blood:	n/a
36	chr7:6204521-6204571	MCF-7	breast:	n/a
37	chr7:6200886-6200936	HCT-116	colon:	n/a
38	chr7:6188871-6188921	HUVEC	blood vessel:	n/a
39	chr7:6188804-6188854	ProgFib	skin:	n/a
40	chr7:6199980-6200030	H1-hESC	embryonic stem cell:	embryo
41	chr7:6208213-6208263	HepG2	liver:	n/a
42	chr7:6191780-6191830	ECC-1	luminal epithelium:	n/a
43	chr7:6210667-6210717	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:6205492-6205542	HRPEpiC	eye:	n/a
45	chr7:6197678-6197728	AG09309	skin:	n/a
46	chr7:6198496-6198546	AG10803	skin:	n/a
47	chr7:6209326-6209376	PrEC	prostate:	n/a
48	chr7:6208213-6208263	NHDF-neo	bronchial:	n/a
49	chr7:6205492-6205542	T-47D	breast:	n/a
50	chr7:6204774-6204824	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
2	chr7:6199558..6200447-chr7:6362313..6363284,3	MCF-7	breast:
3	chr7:6195312..6197722-chr7:6310990..6313470,2	K562	blood:
4	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
5	chr7:6204442..6207336-chr7:6209471..6212385,2	MCF-7	breast:
6	chr7:6197102..6199080-chr7:6201748..6203601,2	K562	blood:
7	chr7:6199867..6200929-chr7:6475011..6475738,3	MCF-7	breast:
8	chr7:6197102..6199080-chr7:6201748..6203601,2	K562	blood:
9	chr7:6194450..6196699-chr7:6202081..6204089,2	MCF-7	breast:
10	chr7:6047355..6050049-chr7:6209625..6211423,2	MCF-7	breast:
11	chr7:6064779..6066813-chr7:6192306..6194117,2	MCF-7	breast:
12	chr7:6203849..6207393-chr7:6209598..6212801,3	K562	blood:
13	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
14	chr7:6202248..6204197-chr7:6205375..6207619,2	K562	blood:
15	chr7:6195894..6198040-chr7:6361741..6363493,2	MCF-7	breast:
16	chr7:6206063..6207710-chr7:6310368..6312250,2	MCF-7	breast:
17	chr7:6196482..6198122-chr7:6199857..6201667,2	K562	blood:
18	chr7:6194593..6196125-chr7:6200629..6202167,2	K562	blood:
19	chr7:6142710..6146060-chr7:6197801..6200881,4	MCF-7	breast:
20	chr7:6186873..6189164-chr7:6206563..6209171,2	K562	blood:
21	chr7:6186873..6189164-chr7:6206563..6209171,2	K562	blood:
22	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
23	chr7:6208105..6209788-chr7:6212799..6214937,2	K562	blood:
24	chr7:6202248..6204197-chr7:6205375..6207619,2	K562	blood:
25	chr7:6173956..6175782-chr7:6186484..6188682,2	MCF-7	breast:
26	chr7:6176618..6179246-chr7:6186332..6188449,2	MCF-7	breast:
27	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
28	chr7:6189338..6192083-chr7:6192220..6194410,2	K562	blood:
29	chr7:6196482..6198122-chr7:6199857..6201667,2	K562	blood:
30	chr7:6198597..6201773-chr7:6386005..6390187,3	MCF-7	breast:
31	chr7:6200618..6201665-chr7:6361362..6362302,3	K562	blood:
32	chr7:6189338..6192083-chr7:6192220..6194410,2	K562	blood:
33	chr7:6204362..6204955-chr7:51756969..51757469,2	Hela-S3	cervix:
34	chr7:6183038..6185913-chr7:6186874..6189877,3	K562	blood:
35	chr7:6203205..6205349-chr7:6208114..6211098,2	K562	blood:
36	chr7:6177505..6181688-chr7:6185145..6188693,4	MCF-7	breast:
37	chr7:6199039..6200525-chr7:6362284..6363316,17	MCF-7	breast:
38	chr7:6205893..6207874-chr7:6209038..6211442,3	K562	blood:
39	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:
40	chr7:6185367..6187227-chr7:6188994..6190699,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2AK1-3	chr7:6212362-6212706	NONHSAT118988
2	lnc-EIF2AK1-3	chr7:6210757-6210945	NONHSAT118988

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP42	hsa-miR-320a	chr7:6200204-6200226
2	USP42	hsa-miR-103a-3p	chr7:6200427-6200450
3	USP42	hsa-miR-16-5p	chr7:6200429-6200451
4	USP42	hsa-miR-16-5p	chr7:6199383-6199389
5	USP42	hsa-miR-103a-3p	chr7:6199382-6199388
6	CYTH3	hsa-miR-320a	chr7:6202808-6202802

Variant related genes	Relation type
CYTH3	TF binding region
CYTH3	CpG island
ENSG00000106305	chromatin interactions
ENSG00000238534	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000178397	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000086232	chromatin interactions

Extended variants
information (count: 1424 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556718	chr7:6187783-6187784	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562864890	chr7:6187793-6187794	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530138731	chr7:6187798-6187799	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542295195	chr7:6187848-6187849	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560578067	chr7:6187873-6187874	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574615486	chr7:6187900-6187901	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528284724	chr7:6187920-6187921	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546820144	chr7:6187926-6187927	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11543636	chr7:6187934-6187935	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532473144	chr7:6187941-6187942	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550616901	chr7:6187959-6187960	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530212786	chr7:6187990-6187991	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139616246	chr7:6188012-6188013	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149516361	chr7:6188022-6188023	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367753920	chr7:6188053-6188054	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554206555	chr7:6188054-6188055	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566274212	chr7:6188055-6188056	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78352443	chr7:6188078-6188079	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182711617	chr7:6188123-6188124	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187030669	chr7:6188127-6188128	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77870088	chr7:6188132-6188133	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544860221	chr7:6188133-6188134	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556898051	chr7:6188188-6188189	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34870794	chr7:6188223-6188224	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554172616	chr7:6188255-6188256	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190856671	chr7:6188261-6188262	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560565291	chr7:6188266-6188267	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527814862	chr7:6188276-6188277	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11535148	chr7:6188322-6188323	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs10243841	chr7:6188330-6188331	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs116350406	chr7:6188339-6188340	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575290136	chr7:6188388-6188389	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148697880	chr7:6188418-6188419	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546271997	chr7:6188425-6188426	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142059017	chr7:6188442-6188443	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7780867	chr7:6188466-6188467	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146677533	chr7:6188471-6188472	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533849236	chr7:6188474-6188475	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182733871	chr7:6188488-6188489	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531521127	chr7:6188574-6188575	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543632406	chr7:6188596-6188597	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139103105	chr7:6188626-6188627	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144016118	chr7:6188642-6188643	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556885858	chr7:6188643-6188644	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188906525	chr7:6188661-6188662	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146459333	chr7:6188724-6188725	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116833979	chr7:6188762-6188763	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116454726	chr7:6188799-6188800	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564428940	chr7:6188847-6188848	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576931069	chr7:6188860-6188861	Strong transcription Weak transcription Genic enhancers	n/a	n/a	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
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
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6146800-6218200	Weak transcription	Stomach Mucosa	stomach
2	chr7:6157400-6188400	Weak transcription	Psoas Muscle	Psoas
3	chr7:6157400-6189400	Weak transcription	Fetal Heart	heart
4	chr7:6160600-6201800	Strong transcription	Fetal Thymus	thymus
5	chr7:6161400-6199600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:6161400-6202200	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr7:6161600-6192000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:6164000-6192400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:6164200-6199400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr7:6167400-6205600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:6172800-6202600	Strong transcription	Dnd41	blood
12	chr7:6173200-6192600	Strong transcription	Fetal Muscle Trunk	muscle
13	chr7:6173200-6204800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:6173800-6192200	Strong transcription	Primary B cells from cord blood	blood
15	chr7:6173800-6205000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:6174000-6193400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr7:6174200-6204800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:6174400-6190800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:6174400-6200600	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr7:6174600-6202200	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:6174800-6200000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:6175200-6199200	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:6175400-6193200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:6175400-6204200	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:6175600-6198800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:6175800-6193600	Strong transcription	Fetal Intestine Large	intestine
27	chr7:6176000-6198200	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr7:6177000-6199400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:6177600-6199600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:6177600-6202400	Strong transcription	Primary B cells from peripheral blood	blood
31	chr7:6178000-6190200	Strong transcription	Hela-S3	cervix
32	chr7:6178000-6197800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:6178000-6198800	Strong transcription	Fetal Muscle Leg	muscle
34	chr7:6178200-6192600	Strong transcription	HepG2	liver
35	chr7:6178200-6194800	Strong transcription	Colonic Mucosa	Colon
36	chr7:6178200-6199200	Strong transcription	Brain Germinal Matrix	brain
37	chr7:6178200-6201800	Strong transcription	Liver	Liver
38	chr7:6178200-6204600	Strong transcription	Thymus	Thymus
39	chr7:6178400-6198800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:6178600-6192200	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr7:6178600-6192600	Strong transcription	NH-A	brain
42	chr7:6178600-6192800	Strong transcription	Fetal Lung	lung
43	chr7:6178600-6196800	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr7:6178600-6198400	Strong transcription	Fetal Brain Female	brain
45	chr7:6178600-6199200	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr7:6178600-6199800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr7:6178800-6198600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:6180200-6204800	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr7:6181200-6199200	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr7:6181200-6199600	Strong transcription	Primary T cells from cord blood	blood

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