Variant report

Variant	nsv981552
Chromosome Location	chr7:97500692-97502806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:586)
CpG islands
(count:795)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97501595-97501997	K562	blood:	n/a	n/a
2	ATF1	chr7:97501385-97502089	K562	blood:	n/a	n/a
3	ATF2	chr7:97501053-97501801	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:97501307-97501988	GM12878	blood:	n/a	n/a
5	ATF2	chr7:97501494-97501853	GM12878	blood:	n/a	n/a
6	ATF2	chr7:97501083-97501640	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:97501358-97501908	K562	blood:	n/a	n/a
8	ATF3	chr7:97501468-97502016	K562	blood:	n/a	n/a
9	ATF3	chr7:97501531-97502009	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:97501697-97501706	K562	blood:	n/a	n/a
11	BCLAF1	chr7:97501337-97502147	K562	blood:	n/a	chr7:97501839-97501848 chr7:97501820-97501833 chr7:97501812-97501825 chr7:97501859-97501868
12	BCLAF1	chr7:97501213-97501994	GM12878	blood:	n/a	chr7:97501839-97501848 chr7:97501820-97501833 chr7:97501812-97501825 chr7:97501859-97501868
13	BHLHE40	chr7:97502687-97502693	K562	blood:	n/a	n/a
14	BHLHE40	chr7:97501428-97502013	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:97501511-97501874	A549	lung:	n/a	n/a
16	BHLHE40	chr7:97501010-97502256	K562	blood:	n/a	chr7:97501392-97501408
17	BHLHE40	chr7:97501183-97502011	GM12878	blood:	n/a	chr7:97501392-97501408
18	BRCA1	chr7:97501313-97502078	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:97501125-97501542	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr7:97501055-97502127	K562	blood:	n/a	n/a
21	CCNT2	chr7:97500981-97501998	K562	blood:	n/a	chr7:97501816-97501825
22	CEBPB	chr7:97501264-97501909	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr7:97501584-97501948	A549	lung:	n/a	n/a
24	CEBPB	chr7:97501347-97501985	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:97501334-97502046	K562	blood:	n/a	n/a
26	CEBPB	chr7:97501462-97502030	MCF-7	breast:	n/a	n/a
27	CEBPB	chr7:97501424-97502056	A549	lung:	n/a	n/a
28	CEBPB	chr7:97501472-97501994	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:97501630-97501934	K562	blood:	n/a	n/a
30	CEBPB	chr7:97501612-97501889	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:97501614-97501887	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:97501587-97501937	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr7:97501323-97502050	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:97501434-97501965	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:97501239-97502054	MCF-7	breast:	n/a	n/a
36	CEBPB	chr7:97501282-97502047	K562	blood:	n/a	n/a
37	CEBPB	chr7:97501472-97501972	A549	lung:	n/a	n/a
38	CEBPB	chr7:97501573-97501958	HepG2	liver:	n/a	n/a
39	CEBPD	chr7:97501420-97501937	HepG2	liver:	n/a	n/a
40	CEBPD	chr7:97501683-97501922	HepG2	liver:	n/a	n/a
41	CHD1	chr7:97501334-97501745	GM12878	blood:	n/a	chr7:97501623-97501633
42	CHD1	chr7:97501324-97501624	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr7:97501141-97502047	H1-hESC	embryonic stem cell:	n/a	chr7:97501623-97501633
44	CHD2	chr7:97501113-97501913	K562	blood:	n/a	chr7:97501623-97501633
45	CHD2	chr7:97501243-97501965	GM12878	blood:	n/a	chr7:97501623-97501633
46	CHD2	chr7:97501343-97502032	HepG2	liver:	n/a	chr7:97501623-97501633
47	CHD2	chr7:97501212-97502059	Hela-S3	cervix:	n/a	chr7:97501623-97501633
48	CREB1	chr7:97501006-97502037	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr7:97501078-97502095	HepG2	liver:	n/a	n/a
50	CREB1	chr7:97501207-97502061	H1-hESC	embryonic stem cell:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97501417-97501467	NHDF-neo	bronchial:	n/a
2	chr7:97501874-97501924	AG04449	skin:	fetal
3	chr7:97501417-97501467	NHDF-neo	bronchial:	n/a
4	chr7:97501874-97501924	AG04449	skin:	fetal
5	chr7:97502140-97502190	HCPEpiC	choroid plexus:	n/a
6	chr7:97501730-97501780	AG04449	skin:	fetal
7	chr7:97501874-97501924	GM12891	blood:	n/a
8	chr7:97501417-97501467	ECC-1	luminal epithelium:	n/a
9	chr7:97501010-97501060	K562	blood:	n/a
10	chr7:97501736-97501786	U87	brain:	n/a
11	chr7:97501918-97501968	HIPEpiC	eye:	n/a
12	chr7:97501010-97501060	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:97501946-97501996	LNCaP	prostate:	n/a
14	chr7:97502140-97502190	H1-hESC	embryonic stem cell:	embryo
15	chr7:97501010-97501060	Caco-2	colon:	n/a
16	chr7:97501010-97501060	NHDF-neo	bronchial:	n/a
17	chr7:97501417-97501467	K562	blood:	n/a
18	chr7:97502140-97502190	NH-A	brain:	n/a
19	chr7:97501874-97501924	Jurkat	blood:	n/a
20	chr7:97502140-97502190	SK-N-SH	brain:	n/a
21	chr7:97501874-97501924	NHBE	bronchial:	n/a
22	chr7:97502647-97502697	RPTEC	kidney:	n/a
23	chr7:97501488-97501538	HEK293	kidney:	embryo
24	chr7:97501484-97501534	HRE	kidney:	n/a
25	chr7:97501908-97501958	HL-60	blood:	n/a
26	chr7:97501901-97501951	NB4	blood:	n/a
27	chr7:97501946-97501996	HCF	heart:	n/a
28	chr7:97502647-97502697	SKMC	muscle:	n/a
29	chr7:97501736-97501786	GM12878	blood:	n/a
30	chr7:97501736-97501786	HIPEpiC	eye:	n/a
31	chr7:97501946-97501996	PANC-1	pancreas:	n/a
32	chr7:97501010-97501060	NT2-D1	testis:	n/a
33	chr7:97501874-97501924	GM19239	blood:	n/a
34	chr7:97501488-97501538	Caco-2	colon:	n/a
35	chr7:97501908-97501958	SK-N-SH	brain:	n/a
36	chr7:97501946-97501996	BE2_C	brain:	n/a
37	chr7:97501417-97501467	HIPEpiC	eye:	n/a
38	chr7:97501908-97501958	PrEC	prostate:	n/a
39	chr7:97501736-97501786	ECC-1	luminal epithelium:	n/a
40	chr7:97502647-97502697	HCM	heart:	n/a
41	chr7:97501908-97501958	HEEpiC	esophagus:	n/a
42	chr7:97501010-97501060	SKMC	muscle:	n/a
43	chr7:97502140-97502190	AG04450	lung:	fetal
44	chr7:97502647-97502697	GM12892	blood:	n/a
45	chr7:97501918-97501968	SK-N-MC	brain:	n/a
46	chr7:97501908-97501958	GM12878	blood:	n/a
47	chr7:97501736-97501786	HUVEC	blood vessel:	n/a
48	chr7:97501488-97501538	HL-60	blood:	n/a
49	chr7:97501730-97501780	HRCEpiC	kidney:	n/a
50	chr7:97502647-97502697	IMR90	lung:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97499263..97501796-chr7:97600194..97603082,4	K562	blood:
2	chr7:97499263..97502446-chr7:97599755..97603082,5	K562	blood:
3	chr7:97498933..97501538-chr7:115850035..115852126,2	K562	blood:
4	chr7:97496316..97498581-chr7:97499278..97501918,3	MCF-7	breast:
5	chr7:97501305..97502999-chr7:98028998..98030520,2	K562	blood:
6	chr7:97499747..97502097-chr7:97599134..97602634,6	MCF-7	breast:
7	chr7:97499971..97501829-chr7:97601279..97602819,2	MCF-7	breast:

No data

Variant related genes	Relation type
ASNS	TF binding region
ASNS	CpG island
ENSG00000135269	chromatin interactions
ENSG00000006453	chromatin interactions
ENSG00000243554	chromatin interactions
ENSG00000070669	chromatin interactions

Extended variants
information (count: 71 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539296220	chr7:97500747-97500748	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs560637870	chr7:97500793-97500794	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs148480761	chr7:97500794-97500795	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs201755027	chr7:97500813-97500814	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs200115272	chr7:97500814-97500815	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs56364360	chr7:97500815-97500816	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs537944264	chr7:97500816-97500817	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs397933214	chr7:97500826-97500827	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs543298358	chr7:97500882-97500883	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs201825430	chr7:97500889-97500890	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs139859219	chr7:97500905-97500906	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs532072757	chr7:97500906-97500907	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs550291709	chr7:97500947-97500948	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs568863098	chr7:97500952-97500953	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs189474472	chr7:97501003-97501004	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs551177279	chr7:97501005-97501006	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs532836274	chr7:97501036-97501037	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs551076262	chr7:97501058-97501059	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs549685310	chr7:97501080-97501081	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs561501827	chr7:97501122-97501123	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs373156541	chr7:97501149-97501150	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs143412578	chr7:97501157-97501158	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs34050735	chr7:97501160-97501161	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575899108	chr7:97501185-97501186	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs538172007	chr7:97501197-97501198	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs556258402	chr7:97501254-97501255	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs146237419	chr7:97501293-97501294	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs34856818	chr7:97501294-97501295	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs58521276	chr7:97501325-97501326	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs397955501	chr7:97501333-97501334	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs181795423	chr7:97501354-97501355	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs554311983	chr7:97501409-97501410	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs572619653	chr7:97501428-97501429	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs543234898	chr7:97501445-97501446	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs561563965	chr7:97501470-97501471	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs531889222	chr7:97501493-97501494	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs369471147	chr7:97501512-97501513	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs544116496	chr7:97501515-97501516	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs7800135	chr7:97501547-97501548	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs17169208	chr7:97501558-97501559	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573294042	chr7:97501617-97501618	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs3832526	chr7:97501622-97501623	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs148365232	chr7:97501626-97501627	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs57336898	chr7:97501639-97501640	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs11767463	chr7:97501640-97501641	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs17169211	chr7:97501653-97501654	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548887797	chr7:97501678-97501679	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11554430	chr7:97501710-97501711	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs139434751	chr7:97501728-97501729	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs537718545	chr7:97501734-97501735	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
T-cell lymphomas	22341440	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97479000-97501000	Weak transcription	Fetal Intestine Large	intestine
2	chr7:97479200-97500800	Weak transcription	Right Ventricle	heart
3	chr7:97479400-97501000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:97479400-97501000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr7:97479600-97501000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:97481400-97501000	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr7:97481800-97500800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:97481800-97501000	Weak transcription	Fetal Intestine Small	intestine
9	chr7:97481800-97501000	Weak transcription	Gastric	stomach
10	chr7:97481800-97501000	Weak transcription	Pancreas	Pancrea
11	chr7:97481800-97501000	Weak transcription	Spleen	Spleen
12	chr7:97482800-97500800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:97483600-97500800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr7:97483800-97500800	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:97484200-97501000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr7:97484600-97501000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:97486200-97500800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr7:97486200-97501000	Weak transcription	Fetal Lung	lung
19	chr7:97486600-97501000	Weak transcription	Small Intestine	intestine
20	chr7:97487200-97500800	Weak transcription	Fetal Muscle Leg	muscle
21	chr7:97487800-97500800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:97487800-97500800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr7:97487800-97500800	Weak transcription	Adipose Nuclei	Adipose
24	chr7:97487800-97500800	Weak transcription	Duodenum Mucosa	Duodenum
25	chr7:97487800-97500800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr7:97487800-97500800	Weak transcription	Fetal Stomach	stomach
27	chr7:97487800-97501000	Weak transcription	Aorta	Aorta
28	chr7:97487800-97501000	Weak transcription	Brain Substantia Nigra	brain
29	chr7:97487800-97501000	Weak transcription	Ovary	ovary
30	chr7:97488000-97500800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:97489800-97500800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr7:97493000-97500800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:97493000-97501000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr7:97493200-97501000	Weak transcription	Esophagus	oesophagus
35	chr7:97494600-97501000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr7:97496200-97501000	Weak transcription	Lung	lung
37	chr7:97496400-97501000	Weak transcription	Left Ventricle	heart
38	chr7:97496600-97500800	Weak transcription	Brain Germinal Matrix	brain
39	chr7:97496600-97501000	Weak transcription	Fetal Kidney	kidney
40	chr7:97498400-97500800	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr7:97499000-97501000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr7:97499000-97501000	Weak transcription	Fetal Heart	heart
43	chr7:97499400-97500800	Enhancers	Brain Hippocampus Middle	brain
44	chr7:97499600-97500800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:97499800-97500800	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr7:97500000-97501000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr7:97500000-97502200	Active TSS	H1 Cell Line	embryonic stem cell
48	chr7:97500000-97502400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:97500200-97500800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:97500200-97501000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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