Variant report

Variant	nsv607460
Chromosome Location	chr7:71713735-71817899
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	ATF2	chr7:71730568-71730921	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:71730494-71730993	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:71800945-71801571	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:71801868-71802965	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:71799942-71799978	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:71730295-71730461	K562	blood:	n/a	n/a
8	BRCA1	chr7:71814539-71814706	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:71723050-71723323	A549	lung:	n/a	chr7:71723174-71723185
10	CEBPB	chr7:71723036-71723330	IMR90	lung:	n/a	chr7:71723174-71723185
11	CEBPB	chr7:71723021-71723355	HepG2	liver:	n/a	chr7:71723174-71723185
12	CEBPB	chr7:71752628-71752861	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:71723120-71723245	K562	blood:	n/a	chr7:71723174-71723185
14	CEBPB	chr7:71757503-71757552	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:71721022-71721087	HepG2	liver:	n/a	chr7:71721064-71721077
16	CEBPB	chr7:71729286-71729372	HepG2	liver:	n/a	chr7:71729324-71729335
17	CHD1	chr7:71800735-71800917	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr7:71802439-71802627	H1-hESC	embryonic stem cell:	n/a	chr7:71802464-71802474
19	CHD1	chr7:71801446-71801578	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr7:71722105-71722245	K562	blood:	n/a	n/a
21	CHD2	chr7:71800362-71800483	K562	blood:	n/a	n/a
22	CHD2	chr7:71800728-71800940	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr7:71800558-71801338	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr7:71801632-71802487	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:71799120-71799379	K562	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
26	CTCF	chr7:71799180-71799330	GM12873	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
27	CTCF	chr7:71757240-71757390	HepG2	liver:	n/a	n/a
28	CTCF	chr7:71799200-71799350	WERI-Rb-1	eye:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
29	CTCF	chr7:71799180-71799330	K562	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
30	CTCF	chr7:71812376-71812555	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:71799140-71799290	GM12873	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
32	CTCF	chr7:71757176-71757389	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:71743660-71743810	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:71799200-71799350	GM12872	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
35	CTCF	chr7:71757220-71757370	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr7:71799171-71799315	HUVEC	blood vessel:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
37	CTCF	chr7:71799178-71799293	Pancreas_OC	pancreas:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
38	CTCF	chr7:71743673-71743779	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:71798986-71799394	H1-hESC	embryonic stem cell:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
40	CTCF	chr7:71780518-71780619	GM10248	blood:	n/a	n/a
41	CTCF	chr7:71812471-71812495	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:71799180-71799330	AG04449	skin:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
43	CTCF	chr7:71799160-71799310	GM12865	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
44	CTCF	chr7:71757201-71757385	K562	blood:	n/a	n/a
45	CTCF	chr7:71799180-71799330	GM12864	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
46	CTCF	chr7:71799160-71799310	AG10803	skin:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
47	CTCF	chr7:71799201-71799325	GM12878	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
48	CTCF	chr7:71799220-71799370	GM06990	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
49	CTCF	chr7:71799180-71799330	BE2_C	brain:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249
50	CTCF	chr7:71799090-71799407	K562	blood:	n/a	chr7:71799227-71799248 chr7:71799232-71799250 chr7:71799233-71799249

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71729065-71729115	HIPEpiC	eye:	n/a
2	chr7:71729065-71729115	HIPEpiC	eye:	n/a
3	chr7:71803433-71803483	U87	brain:	n/a
4	chr7:71747028-71747078	ECC-1	luminal epithelium:	n/a
5	chr7:71798428-71798478	LNCaP	prostate:	n/a
6	chr7:71803123-71803173	HL-60	blood:	n/a
7	chr7:71747632-71747682	AG04449	skin:	fetal
8	chr7:71747028-71747078	AG09309	skin:	n/a
9	chr7:71747028-71747078	HRCEpiC	kidney:	n/a
10	chr7:71799220-71799270	PFSK-1	brain:	n/a
11	chr7:71798428-71798478	K562	blood:	n/a
12	chr7:71802184-71802234	GM06990	blood:	n/a
13	chr7:71803123-71803173	HCM	heart:	n/a
14	chr7:71801535-71801585	GM06990	blood:	n/a
15	chr7:71798428-71798478	BE2_C	brain:	n/a
16	chr7:71800412-71800462	ProgFib	skin:	n/a
17	chr7:71800987-71801037	AG04449	skin:	fetal
18	chr7:71800412-71800462	HEK293	kidney:	embryo
19	chr7:71806067-71806117	HAEpiC	amniotic membrane:	n/a
20	chr7:71803123-71803173	SK-N-SH	brain:	n/a
21	chr7:71802184-71802234	U87	brain:	n/a
22	chr7:71803123-71803173	ProgFib	skin:	n/a
23	chr7:71799177-71799227	Hepatocyte	liver:	n/a
24	chr7:71800987-71801037	SK-N-SH_RA	brain:	n/a
25	chr7:71802574-71802624	HAEpiC	amniotic membrane:	n/a
26	chr7:71729065-71729115	HEK293	kidney:	embryo
27	chr7:71806067-71806117	Hepatocyte	liver:	n/a
28	chr7:71803123-71803173	SK-N-SH_RA	brain:	n/a
29	chr7:71801793-71801843	Hepatocyte	liver:	n/a
30	chr7:71801535-71801585	HCT-116	colon:	n/a
31	chr7:71799220-71799270	MCF10A-Er-Src	breast:	n/a
32	chr7:71747028-71747078	AG04449	skin:	fetal
33	chr7:71747028-71747078	HMEC	breast:	n/a
34	chr7:71806067-71806117	AG10803	skin:	n/a
35	chr7:71806067-71806117	LNCaP	prostate:	n/a
36	chr7:71799982-71800032	HL-60	blood:	n/a
37	chr7:71799220-71799270	IMR90	lung:	fetal
38	chr7:71798428-71798478	Hepatocyte	liver:	n/a
39	chr7:71799220-71799270	NT2-D1	testis:	n/a
40	chr7:71802574-71802624	SK-N-SH	brain:	n/a
41	chr7:71798428-71798478	SAEC	small airway:	n/a
42	chr7:71802574-71802624	A549	lung:	n/a
43	chr7:71802574-71802624	U87	brain:	n/a
44	chr7:71744787-71744837	HCPEpiC	choroid plexus:	n/a
45	chr7:71806067-71806117	MCF-7	breast:	n/a
46	chr7:71799982-71800032	NB4	blood:	n/a
47	chr7:71800412-71800462	GM19239	blood:	n/a
48	chr7:71803123-71803173	AG09309	skin:	n/a
49	chr7:71799177-71799227	AG04450	lung:	fetal
50	chr7:71729065-71729115	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
2	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
3	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:
4	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
5	chr7:71806092..71808807-chr7:71850228..71852499,2	K562	blood:
6	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
7	chr7:71789897..71791400-chr7:71794472..71797210,2	K562	blood:
8	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
9	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
10	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:
11	chr7:71789897..71791400-chr7:71794472..71797210,2	K562	blood:
12	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
13	chr7:71390296..71390850-chr7:71798734..71799708,2	K562	blood:
14	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
15	chr7:71810202..71812135-chr7:71814451..71816672,2	K562	blood:
16	chr7:71810202..71812135-chr7:71814451..71816672,2	K562	blood:
17	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
18	chr7:71390493..71391255-chr7:71799190..71800147,2	MCF-7	breast:
19	chr7:71804343..71806702-chr7:71808239..71810092,2	K562	blood:
20	chr7:71743468..71744150-chr7:71798805..71799347,2	MCF-7	breast:
21	chr7:71804343..71806702-chr7:71808239..71810092,2	K562	blood:
22	chr7:71800589..71802149-chr7:71805434..71807505,2	K562	blood:
23	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:

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

Extended variants
information (count: 4837 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:4837 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs472393	chr7:71713735-71713736	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147021275	chr7:71713736-71713737	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs538182109	chr7:71713750-71713751	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs556508225	chr7:71713758-71713759	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs117943551	chr7:71713766-71713767	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs540738249	chr7:71713799-71713800	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs201168824	chr7:71713805-71713806	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs35949137	chr7:71713806-71713807	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs71531797	chr7:71713816-71713817	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs529863253	chr7:71713826-71713827	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs575573304	chr7:71713828-71713829	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs546129458	chr7:71713884-71713885	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs185780380	chr7:71713902-71713903	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs371304479	chr7:71713921-71713922	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs139021175	chr7:71713946-71713947	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs528334933	chr7:71713985-71713986	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs10234985	chr7:71714000-71714001	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs13244320	chr7:71714028-71714029	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528978351	chr7:71714079-71714080	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs190682299	chr7:71714084-71714085	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs143032587	chr7:71714093-71714094	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs386714593	chr7:71714102-71714103	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs552100745	chr7:71714103-71714104	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs73359147	chr7:71714139-71714140	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147055691	chr7:71714175-71714176	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs555555976	chr7:71714216-71714217	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567718114	chr7:71714240-71714241	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538355005	chr7:71714264-71714265	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534242972	chr7:71714267-71714268	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181159508	chr7:71714313-71714314	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370074487	chr7:71714338-71714339	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577966437	chr7:71714346-71714347	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2677276	chr7:71714392-71714393	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572932098	chr7:71714409-71714410	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540395739	chr7:71714410-71714411	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10238714	chr7:71714436-71714437	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs142587696	chr7:71714454-71714455	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573362156	chr7:71714489-71714490	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138139096	chr7:71714494-71714495	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6974939	chr7:71714521-71714522	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562143901	chr7:71714541-71714542	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373567427	chr7:71714561-71714562	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377444824	chr7:71714562-71714563	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10699280	chr7:71714565-71714566	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532806526	chr7:71714604-71714605	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551773164	chr7:71714607-71714608	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148117682	chr7:71714644-71714645	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377665852	chr7:71714719-71714720	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567865563	chr7:71714753-71714754	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs386714594	chr7:71714836-71714837	Weak transcription ZNF genes & repeats Strong 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:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71688600-71714000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:71709000-71731000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:71712600-71717800	ZNF genes & repeats	Fetal Thymus	thymus
4	chr7:71712800-71717200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:71713600-71714200	Weak transcription	Thymus	Thymus
6	chr7:71714000-71714600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
7	chr7:71714200-71716800	Strong transcription	Thymus	Thymus
8	chr7:71714800-71716800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:71715400-71716400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:71716800-71722000	Weak transcription	Thymus	Thymus
11	chr7:71717200-71719000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:71717800-71722000	Strong transcription	Fetal Thymus	thymus
13	chr7:71718000-71720200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:71719000-71720000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:71720000-71722200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:71720200-71730200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:71721400-71734600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr7:71721600-71722000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr7:71721800-71722000	Enhancers	Adipose Nuclei	Adipose
20	chr7:71721800-71727200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:71722000-71722400	ZNF genes & repeats	Fetal Thymus	thymus
22	chr7:71722000-71722400	Genic enhancers	Thymus	Thymus
23	chr7:71722200-71722600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:71722200-71722800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr7:71722200-71723200	Weak transcription	Adipose Nuclei	Adipose
26	chr7:71722400-71723600	Strong transcription	Fetal Thymus	thymus
27	chr7:71722400-71725000	Weak transcription	Thymus	Thymus
28	chr7:71722600-71723000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:71722800-71735200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:71723000-71729800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:71723200-71723600	Enhancers	Adipose Nuclei	Adipose
32	chr7:71723600-71724800	Weak transcription	Fetal Thymus	thymus
33	chr7:71724800-71726600	Genic enhancers	Fetal Thymus	thymus
34	chr7:71725000-71725400	Genic enhancers	Thymus	Thymus
35	chr7:71725400-71726000	Enhancers	Thymus	Thymus
36	chr7:71726000-71727200	Genic enhancers	Thymus	Thymus
37	chr7:71726600-71729000	Strong transcription	Fetal Thymus	thymus
38	chr7:71727200-71728200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:71727200-71728400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:71727200-71728600	Weak transcription	Thymus	Thymus
41	chr7:71727400-71728200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:71727400-71728400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:71727600-71728200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr7:71727800-71728000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr7:71727800-71728200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:71727800-71728200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr7:71728000-71728200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:71728000-71728200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr7:71728000-71731400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:71728200-71730000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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