Variant report

Variant	nsv888764
Chromosome Location	chr7:97832628-97844578
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	ARID3A	chr7:97841106-97841413	HepG2	liver:	n/a	n/a
2	ATF2	chr7:97832563-97833050	GM12878	blood:	n/a	n/a
3	ATF2	chr7:97832597-97832988	GM12878	blood:	n/a	n/a
4	ATF3	chr7:97841200-97841340	K562	blood:	n/a	n/a
5	BACH1	chr7:97839948-97840290	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:97840715-97840870	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:97832640-97833033	GM12878	blood:	n/a	n/a
8	BATF	chr7:97832660-97833056	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:97832657-97832962	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:97832623-97833012	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:97840950-97841274	K562	blood:	n/a	n/a
12	BHLHE40	chr7:97843618-97843621	K562	blood:	n/a	n/a
13	BHLHE40	chr7:97841083-97841121	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:97840739-97841503	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:97831481-97833086	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:97841048-97841415	HepG2	liver:	n/a	n/a
17	CCNT2	chr7:97840716-97841121	K562	blood:	n/a	n/a
18	CCNT2	chr7:97835012-97835236	K562	blood:	n/a	n/a
19	CCNT2	chr7:97841471-97841671	K562	blood:	n/a	n/a
20	CEBPB	chr7:97841211-97841387	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:97832592-97833125	GM12878	blood:	n/a	chr7:97833057-97833070
22	CHD2	chr7:97831705-97833052	GM12878	blood:	n/a	n/a
23	CHD2	chr7:97844264-97844285	HepG2	liver:	n/a	n/a
24	CHD2	chr7:97840957-97841477	HepG2	liver:	n/a	n/a
25	CHD2	chr7:97839942-97840021	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:97832728-97832926	GM12878	blood:	n/a	chr7:97832803-97832816
27	CTCF	chr7:97841157-97841208	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:97840565-97840717	HepG2	liver:	n/a	chr7:97840589-97840599
29	CTCF	chr7:97833986-97834014	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr7:97832785-97832812	GM12891	blood:	n/a	n/a
31	CTCF	chr7:97841120-97841270	HepG2	liver:	n/a	n/a
32	CTCF	chr7:97841217-97841244	GM12891	blood:	n/a	n/a
33	E2F6	chr7:97840978-97841208	K562	blood:	n/a	n/a
34	EBF1	chr7:97831706-97833032	GM12878	blood:	n/a	chr7:97832025-97832036
35	EBF1	chr7:97832504-97832942	GM12878	blood:	n/a	n/a
36	EGR1	chr7:97840998-97841531	K562	blood:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
37	EGR1	chr7:97840946-97841568	K562	blood:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
38	EGR1	chr7:97840917-97841582	MCF-7	breast:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
39	ELF1	chr7:97831800-97833030	GM12878	blood:	n/a	n/a
40	ELF1	chr7:97832575-97833067	GM12878	blood:	n/a	n/a
41	EP300	chr7:97831609-97833123	GM12878	blood:	n/a	chr7:97833043-97833057
42	EP300	chr7:97840895-97841575	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317
43	EP300	chr7:97840966-97841484	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317
44	FOS	chr7:97841251-97841417	MCF10A-Er-Src	breast:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
45	FOSL1	chr7:97841101-97841449	K562	blood:	n/a	chr7:97841307-97841318 chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
46	FOSL1	chr7:97841064-97841466	K562	blood:	n/a	chr7:97841307-97841318 chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
47	FOSL2	chr7:97841053-97841512	MCF-7	breast:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
48	FOSL2	chr7:97840959-97841573	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
49	FOSL2	chr7:97840900-97841588	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
50	FOXA1	chr7:97841130-97841604	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97844391-97844441	AG09319	gingival:	n/a
2	chr7:97838663-97838713	HRPEpiC	eye:	n/a
3	chr7:97833154-97833204	HEK293	kidney:	embryo
4	chr7:97841998-97842048	HEEpiC	esophagus:	n/a
5	chr7:97844391-97844441	AG09319	gingival:	n/a
6	chr7:97838663-97838713	HRPEpiC	eye:	n/a
7	chr7:97833154-97833204	HEK293	kidney:	embryo
8	chr7:97841998-97842048	HEEpiC	esophagus:	n/a
9	chr7:97841001-97841051	HUVEC	blood vessel:	n/a
10	chr7:97832841-97832891	GM12891	blood:	n/a
11	chr7:97841591-97841641	AG10803	skin:	n/a
12	chr7:97832830-97832880	BE2_C	brain:	n/a
13	chr7:97838663-97838713	H1-hESC	embryonic stem cell:	embryo
14	chr7:97844391-97844441	K562	blood:	n/a
15	chr7:97836563-97836613	HepG2	liver:	n/a
16	chr7:97841334-97841384	HepG2	liver:	n/a
17	chr7:97838659-97838709	HRPEpiC	eye:	n/a
18	chr7:97841001-97841051	K562	blood:	n/a
19	chr7:97841513-97841563	NB4	blood:	n/a
20	chr7:97841447-97841497	HCPEpiC	choroid plexus:	n/a
21	chr7:97844391-97844441	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:97840014-97840064	NB4	blood:	n/a
23	chr7:97841071-97841121	NHDF-neo	bronchial:	n/a
24	chr7:97835192-97835242	HRPEpiC	eye:	n/a
25	chr7:97841864-97841914	T-47D	breast:	n/a
26	chr7:97841071-97841121	K562	blood:	n/a
27	chr7:97834623-97834673	AG10803	skin:	n/a
28	chr7:97836247-97836297	RPTEC	kidney:	n/a
29	chr7:97833388-97833438	MCF-7	breast:	n/a
30	chr7:97842268-97842318	HRCEpiC	kidney:	n/a
31	chr7:97841334-97841384	HCM	heart:	n/a
32	chr7:97834623-97834673	HCM	heart:	n/a
33	chr7:97832841-97832891	NH-A	brain:	n/a
34	chr7:97835841-97835891	HL-60	blood:	n/a
35	chr7:97833388-97833438	HRPEpiC	eye:	n/a
36	chr7:97841071-97841121	Caco-2	colon:	n/a
37	chr7:97837957-97838007	PANC-1	pancreas:	n/a
38	chr7:97834674-97834724	HRCEpiC	kidney:	n/a
39	chr7:97832945-97832995	HRE	kidney:	n/a
40	chr7:97841941-97841991	U87	brain:	n/a
41	chr7:97832830-97832880	HCPEpiC	choroid plexus:	n/a
42	chr7:97837957-97838007	RPTEC	kidney:	n/a
43	chr7:97841941-97841991	Caco-2	colon:	n/a
44	chr7:97841502-97841552	HMEC	breast:	n/a
45	chr7:97841502-97841552	HCPEpiC	choroid plexus:	n/a
46	chr7:97844391-97844441	IMR90	lung:	fetal
47	chr7:97840113-97840163	RPTEC	kidney:	n/a
48	chr7:97835192-97835242	BJ	skin:	n/a
49	chr7:97842268-97842318	PrEC	prostate:	n/a
50	chr7:97839870-97839920	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
2	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
3	chr7:97839660..97842920-chr7:97872632..97874833,3	K562	blood:
4	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
5	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
6	chr7:97826253..97828518-chr7:97833038..97835255,2	K562	blood:
7	chr7:97843965..97846398-chr7:97856911..97858412,2	K562	blood:
8	chr10:8099641..8101523-chr7:97840811..97843007,2	MCF-7	breast:
9	chr7:97831874..97833996-chr7:97840662..97842294,3	K562	blood:
10	chr7:97839794..97841701-chr7:97843448..97845628,2	MCF-7	breast:
11	chr7:97842812..97845120-chr7:97865672..97868033,2	K562	blood:
12	chr7:97815298..97817791-chr7:97831369..97832934,2	MCF-7	breast:
13	chr7:97829526..97831904-chr7:97833458..97836322,3	K562	blood:
14	chr7:97834447..97836459-chr7:97921103..97922884,2	K562	blood:
15	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BHLHA15-1	chr7:97842411-97844754	NONHSAT122177
2	lnc-BHLHA15-1	chr7:97841568-97841603	NONHSAT122177
3	lnc-BHLHA15-1	chr7:97840778-97840810	NONHSAT122177

Variant related genes	Relation type
BHLHA15	TF binding region
BHLHA15	CpG island
ENSG00000205356	chromatin interactions
ENSG00000107485	chromatin interactions
ENSG00000180535	chromatin interactions

Extended variants
information (count: 520 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3807510	chr7:97832628-97832629	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576947936	chr7:97832634-97832635	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541211557	chr7:97832672-97832673	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139891758	chr7:97832722-97832723	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559549459	chr7:97832733-97832734	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs530323517	chr7:97832799-97832800	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542156939	chr7:97832830-97832831	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372766999	chr7:97832841-97832842	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377178552	chr7:97832842-97832843	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201266798	chr7:97832890-97832891	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372562991	chr7:97832906-97832907	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145430337	chr7:97832925-97832926	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs116216163	chr7:97832927-97832928	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376374002	chr7:97832931-97832932	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141328136	chr7:97832935-97832936	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs146973469	chr7:97832936-97832937	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371099644	chr7:97832944-97832945	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200702141	chr7:97832947-97832948	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs45488394	chr7:97832980-97832981	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs188760642	chr7:97832996-97832997	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143044215	chr7:97833008-97833009	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532281800	chr7:97833009-97833010	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199890482	chr7:97833011-97833012	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368346888	chr7:97833025-97833026	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375173332	chr7:97833028-97833029	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568200371	chr7:97833045-97833046	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368109185	chr7:97833069-97833070	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs193041674	chr7:97833084-97833085	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554809949	chr7:97833110-97833111	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143336209	chr7:97833115-97833116	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs537425573	chr7:97833150-97833151	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147523577	chr7:97833154-97833155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576905030	chr7:97833175-97833176	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534836842	chr7:97833180-97833181	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139800123	chr7:97833194-97833195	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs73406037	chr7:97833215-97833216	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs377442488	chr7:97833216-97833217	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377448948	chr7:97833223-97833224	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574649939	chr7:97833360-97833361	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371508931	chr7:97833368-97833369	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535584744	chr7:97833369-97833370	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368696715	chr7:97833370-97833371	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148189559	chr7:97833381-97833382	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542059077	chr7:97833389-97833390	Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141683058	chr7:97833403-97833404	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs202016789	chr7:97833409-97833410	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs200807391	chr7:97833410-97833411	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs200365227	chr7:97833422-97833423	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs145344475	chr7:97833424-97833425	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs137912661	chr7:97833440-97833441	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97765800-97840800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:97782400-97839800	Weak transcription	Fetal Brain Male	brain
3	chr7:97793400-97841000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:97808400-97833600	Weak transcription	Stomach Mucosa	stomach
5	chr7:97808600-97839800	Weak transcription	Right Atrium	heart
6	chr7:97812000-97841000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:97816000-97839200	Weak transcription	Psoas Muscle	Psoas
8	chr7:97816600-97839800	Weak transcription	NH-A	brain
9	chr7:97819200-97834800	Weak transcription	HUVEC	blood vessel
10	chr7:97822400-97841000	Weak transcription	K562	blood
11	chr7:97822800-97837600	Weak transcription	Fetal Kidney	kidney
12	chr7:97823000-97851000	Weak transcription	HSMMtube	muscle
13	chr7:97823600-97833400	Weak transcription	A549	lung
14	chr7:97823800-97834400	Weak transcription	Brain Substantia Nigra	brain
15	chr7:97823800-97840000	Weak transcription	Small Intestine	intestine
16	chr7:97824000-97835600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:97824200-97833200	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:97824200-97833800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:97824200-97834200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:97824400-97834000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:97824400-97834000	Weak transcription	NHLF	lung
22	chr7:97824400-97834600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:97824400-97839800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:97824600-97834000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:97824600-97839800	Weak transcription	Osteobl	bone
26	chr7:97824600-97840800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr7:97824800-97834600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr7:97824800-97834800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:97824800-97835000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:97824800-97839800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:97824800-97839800	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr7:97824800-97840000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:97825000-97833400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr7:97825000-97833600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr7:97825000-97834200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr7:97825000-97835000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr7:97825000-97836000	Weak transcription	Brain Angular Gyrus	brain
38	chr7:97825200-97833600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr7:97825200-97835600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr7:97825200-97851000	Weak transcription	Fetal Lung	lung
41	chr7:97825800-97833600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:97825800-97834000	Weak transcription	Brain Anterior Caudate	brain
43	chr7:97825800-97835200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr7:97826000-97832800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr7:97826000-97832800	Weak transcription	Placenta	Placenta
46	chr7:97826000-97833400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:97826000-97834000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:97826600-97833000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:97826800-97833000	Weak transcription	Ovary	ovary
50	chr7:97826800-97833400	Weak transcription	Pancreas	Pancrea

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