Variant report

Variant	nsv470299
Chromosome Location	chr7:71740458-71815170
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	ATF1	chr7:71748535-71748603	K562	blood:	n/a	n/a
2	BACH1	chr7:71801868-71802965	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:71800945-71801571	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:71799942-71799978	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr7:71814539-71814706	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr7:71752628-71752861	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:71757503-71757552	HepG2	liver:	n/a	n/a
8	CHD1	chr7:71800735-71800917	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr7:71802439-71802627	H1-hESC	embryonic stem cell:	n/a	chr7:71802464-71802474
10	CHD1	chr7:71801446-71801578	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr7:71800728-71800940	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr7:71800362-71800483	K562	blood:	n/a	n/a
13	CTBP2	chr7:71801632-71802487	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr7:71800558-71801338	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:71799180-71799330	GM12864	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
16	CTCF	chr7:71757239-71757361	HepG2	liver:	n/a	n/a
17	CTCF	chr7:71799160-71799310	AG10803	skin:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
18	CTCF	chr7:71799180-71799330	GM12872	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
19	CTCF	chr7:71799180-71799330	HEK293	kidney:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
20	CTCF	chr7:71799140-71799290	GM12878	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
21	CTCF	chr7:71743564-71743842	K562	blood:	n/a	n/a
22	CTCF	chr7:71799120-71799379	K562	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
23	CTCF	chr7:71799120-71799270	HMF	breast:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
24	CTCF	chr7:71799200-71799350	WERI-Rb-1	eye:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
25	CTCF	chr7:71799198-71799290	GM13977	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
26	CTCF	chr7:71801104-71801215	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:71799174-71799342	MCF-7	breast:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
28	CTCF	chr7:71743660-71743810	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr7:71799269-71799287	LNCaP	prostate:	n/a	n/a
30	CTCF	chr7:71780518-71780619	GM10248	blood:	n/a	n/a
31	CTCF	chr7:71757129-71757479	K562	blood:	n/a	n/a
32	CTCF	chr7:71743620-71743770	K562	blood:	n/a	n/a
33	CTCF	chr7:71799131-71799350	HepG2	liver:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
34	CTCF	chr7:71799140-71799290	HMF	breast:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
35	CTCF	chr7:71799856-71799964	H1-hESC	embryonic stem cell:	n/a	chr7:71799908-71799917
36	CTCF	chr7:71757020-71757472	K562	blood:	n/a	n/a
37	CTCF	chr7:71743653-71743785	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:71757278-71757315	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:71799240-71799267	Lung_OC	lung:	n/a	n/a
40	CTCF	chr7:71799180-71799330	BE2_C	brain:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
41	CTCF	chr7:71743651-71743794	K562	blood:	n/a	n/a
42	CTCF	chr7:71799180-71799330	GM12873	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
43	CTCF	chr7:71800560-71800710	HepG2	liver:	n/a	n/a
44	CTCF	chr7:71799140-71799290	GM12864	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
45	CTCF	chr7:71809065-71809124	LNCaP	prostate:	n/a	n/a
46	CTCF	chr7:71798880-71799030	GM12865	blood:	n/a	chr7:71798916-71798924
47	CTCF	chr7:71757188-71757402	HepG2	liver:	n/a	n/a
48	CTCF	chr7:71799140-71799290	AG04449	skin:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
49	CTCF	chr7:71812459-71812496	ProgFib	skin:	n/a	n/a
50	CTCF	chr7:71799054-71799444	K562	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71802184-71802234	GM19239	blood:	n/a
2	chr7:71799982-71800032	HAEpiC	amniotic membrane:	n/a
3	chr7:71747028-71747078	PFSK-1	brain:	n/a
4	chr7:71798428-71798478	AG09309	skin:	n/a
5	chr7:71802184-71802234	Jurkat	blood:	n/a
6	chr7:71799982-71800032	ECC-1	luminal epithelium:	n/a
7	chr7:71806067-71806117	Hela-S3	cervix:	n/a
8	chr7:71802184-71802234	NHDF-neo	bronchial:	n/a
9	chr7:71803433-71803483	Hela-S3	cervix:	n/a
10	chr7:71802574-71802624	ProgFib	skin:	n/a
11	chr7:71747632-71747682	HNPCEpiC	eye:	n/a
12	chr7:71799982-71800032	BJ	skin:	n/a
13	chr7:71747028-71747078	HEK293	kidney:	embryo
14	chr7:71744787-71744837	ProgFib	skin:	n/a
15	chr7:71800412-71800462	GM12878	blood:	n/a
16	chr7:71799220-71799270	HMEC	breast:	n/a
17	chr7:71744787-71744837	AG09319	gingival:	n/a
18	chr7:71799982-71800032	HCF	heart:	n/a
19	chr7:71800412-71800462	HAEpiC	amniotic membrane:	n/a
20	chr7:71801793-71801843	AG09319	gingival:	n/a
21	chr7:71806067-71806117	AG04449	skin:	fetal
22	chr7:71747028-71747078	AoSMC	blood vessel:	n/a
23	chr7:71803433-71803483	SAEC	small airway:	n/a
24	chr7:71802184-71802234	Caco-2	colon:	n/a
25	chr7:71803433-71803483	HEEpiC	esophagus:	n/a
26	chr7:71801793-71801843	NT2-D1	testis:	n/a
27	chr7:71800987-71801037	HIPEpiC	eye:	n/a
28	chr7:71744787-71744837	PANC-1	pancreas:	n/a
29	chr7:71800987-71801037	MCF-7	breast:	n/a
30	chr7:71744787-71744837	SAEC	small airway:	n/a
31	chr7:71799982-71800032	HRCEpiC	kidney:	n/a
32	chr7:71806067-71806117	ProgFib	skin:	n/a
33	chr7:71747632-71747682	HRE	kidney:	n/a
34	chr7:71744787-71744837	BE2_C	brain:	n/a
35	chr7:71802184-71802234	NHBE	bronchial:	n/a
36	chr7:71800412-71800462	NHDF-neo	bronchial:	n/a
37	chr7:71799220-71799270	GM19239	blood:	n/a
38	chr7:71803123-71803173	GM12878	blood:	n/a
39	chr7:71799982-71800032	GM19239	blood:	n/a
40	chr7:71799982-71800032	HEEpiC	esophagus:	n/a
41	chr7:71803433-71803483	IMR90	lung:	fetal
42	chr7:71799177-71799227	BJ	skin:	n/a
43	chr7:71802184-71802234	SK-N-SH_RA	brain:	n/a
44	chr7:71799177-71799227	AG10803	skin:	n/a
45	chr7:71803433-71803483	HRE	kidney:	n/a
46	chr7:71802574-71802624	HMEC	breast:	n/a
47	chr7:71799982-71800032	HMEC	breast:	n/a
48	chr7:71801535-71801585	HEEpiC	esophagus:	n/a
49	chr7:71800412-71800462	LNCaP	prostate:	n/a
50	chr7:71800412-71800462	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:71806092..71808807-chr7:71850228..71852499,2	K562	blood:
2	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
3	chr7:71804343..71806702-chr7:71808239..71810092,2	K562	blood:
4	chr7:71800589..71802149-chr7:71805434..71807505,2	K562	blood:
5	chr7:71789897..71791400-chr7:71794472..71797210,2	K562	blood:
6	chr7:71804343..71806702-chr7:71808239..71810092,2	K562	blood:
7	chr7:71810202..71812135-chr7:71814451..71816672,2	K562	blood:
8	chr7:71789897..71791400-chr7:71794472..71797210,2	K562	blood:
9	chr7:71743468..71744150-chr7:71798805..71799347,2	MCF-7	breast:
10	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
11	chr7:71390296..71390850-chr7:71798734..71799708,2	K562	blood:
12	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
13	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
14	chr7:71810202..71812135-chr7:71814451..71816672,2	K562	blood:
15	chr7:71390493..71391255-chr7:71799190..71800147,2	MCF-7	breast:
16	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:

Variant related genes	Relation type
CALN1	TF binding region
CALN1	CpG island
ENSG00000183166	chromatin interactions

Extended variants
information (count: 3595 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:3595 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1468163	chr7:71740458-71740459	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140357509	chr7:71740488-71740489	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375728635	chr7:71740536-71740537	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75099598	chr7:71740537-71740538	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574774630	chr7:71740541-71740542	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192647902	chr7:71740571-71740572	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550717392	chr7:71740578-71740579	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530978016	chr7:71740623-71740624	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552746871	chr7:71740630-71740631	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564376976	chr7:71740707-71740708	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528633700	chr7:71740714-71740715	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143589632	chr7:71740732-71740733	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76744781	chr7:71740744-71740745	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199520384	chr7:71740752-71740753	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571944838	chr7:71740815-71740816	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539632558	chr7:71740831-71740832	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374453194	chr7:71740867-71740868	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536531106	chr7:71740900-71740901	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1914385	chr7:71740914-71740915	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs573006044	chr7:71740920-71740921	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569983322	chr7:71740944-71740945	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536806706	chr7:71740953-71740954	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550955918	chr7:71741002-71741003	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558761515	chr7:71741007-71741008	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370921391	chr7:71741034-71741035	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534747532	chr7:71741046-71741047	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552527747	chr7:71741057-71741058	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574065690	chr7:71741066-71741067	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541439442	chr7:71741094-71741095	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538982369	chr7:71741164-71741165	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547706880	chr7:71741168-71741169	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575896489	chr7:71741169-71741170	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35526560	chr7:71741232-71741233	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185206455	chr7:71741272-71741273	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs528563472	chr7:71741299-71741300	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs190166915	chr7:71741302-71741303	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs78979408	chr7:71741304-71741305	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs529273126	chr7:71741358-71741359	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs376564209	chr7:71741373-71741374	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112590710	chr7:71741403-71741404	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551007134	chr7:71741412-71741413	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1914384	chr7:71741443-71741444	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs148065075	chr7:71741444-71741445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77227555	chr7:71741511-71741512	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570652827	chr7:71741549-71741550	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534537104	chr7:71741561-71741562	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75057903	chr7:71741570-71741571	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567823523	chr7:71741590-71741591	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530705494	chr7:71741615-71741616	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79972219	chr7:71741618-71741619	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21990379	CNVD
Williams Syndrome	16773131	CNVD
Breast cancer	16417655	CNVD
Rheumatoid arthritis	21728841	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Williams Syndrome	16617304	CNVD
Williams Syndrome	20206275	CNVD
Williams Syndrome	16199537	CNVD
Williams Syndrome	18923514	CNVD
Williams Syndrome	20970697	CNVD
Williams-beuren syndrome	20926892	CNVD
Williams-beuren syndrome	21808859	CNVD
periventricular nodular heterotopia	20648244	CNVD
Williams Syndrome	20425783	CNVD
Williams-beuren syndrome	22226172	CNVD
Williams-beuren syndrome	18923513	CNVD
Williams-beuren syndrome	17565757	CNVD
Williams-beuren syndrome	18787571	CNVD
Williams Syndrome	22241247	CNVD
Autism	21686962	CNVD
Autism	20970697	CNVD
Epilepsy	22118685	CNVD
Epilepsy	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21686962	CNVD
Schizophrenia	22118685	CNVD
Williams-beuren syndrome	18337728	CNVD
language delay	21686962	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
Mental retardation	16773131	CNVD
Colorectal cancer	19455253	CNVD
Williams-beuren syndrome	16971481	CNVD
Idiopathic infantile hypercalcaemia	20466674	CNVD
Williams Syndrome	18308711	CNVD
Williams Syndrome	19255058	CNVD
Williams Syndrome	18924169	CNVD
Williams Syndrome	21939500	CNVD
Williams Syndrome	20425784	CNVD
Williams Syndrome	22241097	CNVD
Williams Syndrome	19176822	CNVD
Williams Syndrome	17505701	CNVD
Supravalvular aortic stenosis	19844261	CNVD
Williams Syndrome	16760918	CNVD
Williams-beuren syndrome	18452001	CNVD
Williams-beuren syndrome	19880526	CNVD
Autism	17666889	CNVD
speech delay	17666889	CNVD
Metanephric adenoma	20802469	CNVD

Chromatin state (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71732600-71760600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:71732800-71758000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:71733000-71741800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:71733600-71744000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:71734200-71741400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr7:71734800-71744200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:71736800-71741200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:71737800-71741200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr7:71739200-71740800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:71739800-71741200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:71740200-71741000	Genic enhancers	Fetal Thymus	thymus
12	chr7:71740200-71741200	Weak transcription	Thymus	Thymus
13	chr7:71740400-71741800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:71740400-71743200	Weak transcription	Brain Anterior Caudate	brain
15	chr7:71740800-71742600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
16	chr7:71741000-71742800	ZNF genes & repeats	Fetal Thymus	thymus
17	chr7:71741200-71742800	ZNF genes & repeats	Thymus	Thymus
18	chr7:71741200-71743200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:71741200-71743400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
20	chr7:71741200-71743400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:71741400-71742000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr7:71741800-71742000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr7:71741800-71742600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:71742000-71743600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr7:71742600-71743600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:71742600-71744600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:71742800-71743000	Strong transcription	Fetal Thymus	thymus
28	chr7:71742800-71743000	Weak transcription	Thymus	Thymus
29	chr7:71743000-71745000	Genic enhancers	Fetal Thymus	thymus
30	chr7:71743000-71745800	Genic enhancers	Thymus	Thymus
31	chr7:71743200-71744400	Enhancers	Brain Anterior Caudate	brain
32	chr7:71743200-71744800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:71743400-71744600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:71743400-71747400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr7:71743600-71743800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:71743600-71743800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
37	chr7:71743800-71744400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:71743800-71748200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:71744000-71744800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:71744200-71744600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:71744200-71744800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr7:71744400-71744600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr7:71744400-71744800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr7:71744600-71745000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:71744600-71747400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:71744800-71745400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:71745000-71747200	Enhancers	Fetal Thymus	thymus
48	chr7:71745000-71747400	Enhancers	Dnd41	blood
49	chr7:71745400-71747200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:71745800-71746000	Enhancers	Thymus	Thymus

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