Variant report

Variant	esv32764
Chromosome Location	chr7:97601058-97638993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:786)
CpG islands
(count:1344)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97601076-97601213	K562	blood:	n/a	n/a
2	ARID3A	chr7:97601658-97602066	K562	blood:	n/a	n/a
3	ARID3A	chr7:97601580-97601847	HepG2	liver:	n/a	n/a
4	ATF2	chr7:97601461-97601858	GM12878	blood:	n/a	n/a
5	ATF2	chr7:97601391-97601917	GM12878	blood:	n/a	n/a
6	ATF3	chr7:97601422-97601844	A549	lung:	n/a	n/a
7	ATF3	chr7:97601550-97601907	A549	lung:	n/a	n/a
8	BCL11A	chr7:97601613-97601863	GM12878	blood:	n/a	n/a
9	BCL3	chr7:97601393-97601964	A549	lung:	n/a	chr7:97601427-97601436
10	BCL3	chr7:97601401-97601928	A549	lung:	n/a	chr7:97601427-97601436
11	BCLAF1	chr7:97601363-97601966	GM12878	blood:	n/a	chr7:97601427-97601436 chr7:97601390-97601399
12	BCLAF1	chr7:97600750-97601139	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:97600813-97601872	GM12878	blood:	n/a	chr7:97601313-97601329 chr7:97601310-97601326 chr7:97601307-97601323
14	BHLHE40	chr7:97629756-97630082	K562	blood:	n/a	n/a
15	BHLHE40	chr7:97629658-97629874	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:97600834-97602072	K562	blood:	n/a	chr7:97601313-97601329 chr7:97601310-97601326 chr7:97601307-97601323
17	BHLHE40	chr7:97629711-97629997	HepG2	liver:	n/a	n/a
18	BHLHE40	chr7:97600832-97601696	HepG2	liver:	n/a	chr7:97601313-97601329 chr7:97601310-97601326 chr7:97601307-97601323
19	BRCA1	chr7:97601517-97601893	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:97601393-97601718	HepG2	liver:	n/a	n/a
21	CBX3	chr7:97601400-97602281	K562	blood:	n/a	n/a
22	CBX3	chr7:97601511-97601907	K562	blood:	n/a	n/a
23	CCNT2	chr7:97601322-97601833	K562	blood:	n/a	n/a
24	CEBPB	chr7:97601086-97601281	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:97603865-97604223	K562	blood:	n/a	chr7:97604035-97604046
26	CEBPB	chr7:97603852-97604171	HepG2	liver:	n/a	chr7:97604035-97604046
27	CEBPB	chr7:97603855-97604215	IMR90	lung:	n/a	chr7:97604035-97604046
28	CEBPB	chr7:97604577-97604689	HepG2	liver:	n/a	chr7:97604661-97604672
29	CEBPB	chr7:97603862-97604170	A549	lung:	n/a	chr7:97604035-97604046
30	CEBPB	chr7:97609802-97610036	K562	blood:	n/a	n/a
31	CEBPB	chr7:97600980-97601334	K562	blood:	n/a	chr7:97601079-97601090
32	CEBPB	chr7:97600919-97601267	HepG2	liver:	n/a	chr7:97601079-97601090
33	CEBPB	chr7:97601479-97601842	K562	blood:	n/a	n/a
34	CEBPB	chr7:97604017-97604110	H1-hESC	embryonic stem cell:	n/a	chr7:97604035-97604046
35	CEBPB	chr7:97600918-97601256	K562	blood:	n/a	chr7:97601079-97601090
36	CEBPB	chr7:97600819-97601881	Hela-S3	cervix:	n/a	chr7:97601079-97601090
37	CEBPB	chr7:97601415-97601971	GM12878	blood:	n/a	n/a
38	CEBPB	chr7:97609859-97610008	K562	blood:	n/a	n/a
39	CEBPB	chr7:97600947-97601472	IMR90	lung:	n/a	chr7:97601079-97601090
40	CEBPB	chr7:97603931-97604145	Hela-S3	cervix:	n/a	chr7:97604035-97604046
41	CEBPD	chr7:97601455-97601830	HepG2	liver:	n/a	n/a
42	CEBPD	chr7:97601529-97601804	HepG2	liver:	n/a	n/a
43	CHD1	chr7:97601017-97601884	GM12878	blood:	n/a	n/a
44	CHD2	chr7:97601575-97601853	K562	blood:	n/a	n/a
45	CHD2	chr7:97601639-97601846	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr7:97600922-97601946	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr7:97601434-97601859	HepG2	liver:	n/a	n/a
48	CHD2	chr7:97602561-97602976	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr7:97601016-97602094	GM12878	blood:	n/a	n/a
50	CREB1	chr7:97600785-97601924	GM12878	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97601586-97601636	ovcar-3	ovarian:	n/a
2	chr7:97601469-97601519	HRE	kidney:	n/a
3	chr7:97601586-97601636	ovcar-3	ovarian:	n/a
4	chr7:97601469-97601519	HRE	kidney:	n/a
5	chr7:97619372-97619422	NH-A	brain:	n/a
6	chr7:97601680-97601730	HRE	kidney:	n/a
7	chr7:97601708-97601758	ECC-1	luminal epithelium:	n/a
8	chr7:97601644-97601694	HUVEC	blood vessel:	n/a
9	chr7:97602715-97602765	GM06990	blood:	n/a
10	chr7:97619372-97619422	LNCaP	prostate:	n/a
11	chr7:97601677-97601727	NHBE	bronchial:	n/a
12	chr7:97601644-97601694	ECC-1	luminal epithelium:	n/a
13	chr7:97620123-97620173	PFSK-1	brain:	n/a
14	chr7:97602580-97602630	HAEpiC	amniotic membrane:	n/a
15	chr7:97601024-97601074	MCF10A-Er-Src	breast:	n/a
16	chr7:97614123-97614173	T-47D	breast:	n/a
17	chr7:97601903-97601953	ProgFib	skin:	n/a
18	chr7:97620777-97620827	T-47D	breast:	n/a
19	chr7:97620915-97620965	PANC-1	pancreas:	n/a
20	chr7:97601677-97601727	Hepatocyte	liver:	n/a
21	chr7:97602580-97602630	BJ	skin:	n/a
22	chr7:97615658-97615708	Hela-S3	cervix:	n/a
23	chr7:97602715-97602765	NB4	blood:	n/a
24	chr7:97602481-97602531	K562	blood:	n/a
25	chr7:97601708-97601758	Jurkat	blood:	n/a
26	chr7:97601102-97601152	LNCaP	prostate:	n/a
27	chr7:97601102-97601152	HRE	kidney:	n/a
28	chr7:97601586-97601636	H1-hESC	embryonic stem cell:	embryo
29	chr7:97601698-97601748	SK-N-MC	brain:	n/a
30	chr7:97601708-97601758	BE2_C	brain:	n/a
31	chr7:97620777-97620827	HCF	heart:	n/a
32	chr7:97601708-97601758	PFSK-1	brain:	n/a
33	chr7:97601677-97601727	HMEC	breast:	n/a
34	chr7:97614123-97614173	PANC-1	pancreas:	n/a
35	chr7:97620915-97620965	NH-A	brain:	n/a
36	chr7:97615658-97615708	PFSK-1	brain:	n/a
37	chr7:97620777-97620827	NH-A	brain:	n/a
38	chr7:97601698-97601748	PFSK-1	brain:	n/a
39	chr7:97601708-97601758	AG04450	lung:	fetal
40	chr7:97619469-97619519	Caco-2	colon:	n/a
41	chr7:97602701-97602751	Hepatocyte	liver:	n/a
42	chr7:97620915-97620965	BE2_C	brain:	n/a
43	chr7:97601190-97601240	AG10803	skin:	n/a
44	chr7:97601024-97601074	U87	brain:	n/a
45	chr7:97602481-97602531	GM06990	blood:	n/a
46	chr7:97620777-97620827	HCT-116	colon:	n/a
47	chr7:97601677-97601727	HNPCEpiC	eye:	n/a
48	chr7:97615658-97615708	AG10803	skin:	n/a
49	chr7:97602580-97602630	GM06990	blood:	n/a
50	chr7:97602701-97602751	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97595673..97597568-chr7:97600883..97603299,2	K562	blood:
2	chr7:97499971..97501829-chr7:97601279..97602819,2	MCF-7	breast:
3	chr7:97618042..97620323-chr7:97624322..97626052,2	MCF-7	breast:
4	chr7:97600402..97603121-chr7:97603491..97605923,3	MCF-7	breast:
5	chr7:97596068..97599027-chr7:97601330..97603299,2	K562	blood:
6	chr7:97591972..97594579-chr7:97599900..97601644,2	MCF-7	breast:
7	chr7:97499747..97502097-chr7:97599134..97602634,6	MCF-7	breast:
8	chr11:82612183..82613162-chr7:97600612..97601573,2	HCT-116	colon:
9	chr7:97612509..97614900-chr7:97617695..97620194,2	K562	blood:
10	chr7:97499263..97502446-chr7:97599755..97603082,5	K562	blood:
11	chr7:97592453..97595469-chr7:97599396..97602015,3	K562	blood:
12	chr7:97499451..97501256-chr7:97634003..97636766,2	K562	blood:
13	chr7:97499263..97501796-chr7:97600194..97603082,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LMTK2-3	chr7:97627637-97627932	NONHSAT122168

No data

Variant related genes	Relation type
OR7E38P	TF binding region
RN7SL478P	TF binding region
OCM2	TF binding region
ENSG00000243554	TF binding region
OR7E38P	CpG island
RN7SL478P	CpG island
OCM2	CpG island
ENSG00000243554	CpG island
ENSG00000137509	chromatin interactions
ENSG00000070669	chromatin interactions
ENSG00000243554	chromatin interactions
ENSG00000135175	chromatin interactions
ENSG00000266668	chromatin interactions
ENSG00000226744	chromatin interactions
ENSG00000183444	chromatin interactions
ENSG00000266318	chromatin interactions
ENSG00000165490	chromatin interactions

Extended variants
information (count: 709 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371222095	chr7:97601079-97601080	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs553179248	chr7:97601121-97601122	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs147448280	chr7:97601190-97601191	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs139989467	chr7:97601213-97601214	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs557215388	chr7:97601215-97601216	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs116192794	chr7:97601223-97601224	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs114775729	chr7:97601233-97601234	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs530150779	chr7:97601252-97601253	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs377549681	chr7:97601260-97601261	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs540332659	chr7:97601283-97601284	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs548250228	chr7:97601293-97601294	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs193154088	chr7:97601309-97601310	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs544527169	chr7:97601356-97601357	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs3832500	chr7:97601401-97601402	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs397840740	chr7:97601406-97601407	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs184997599	chr7:97601421-97601422	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs533491850	chr7:97601482-97601483	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs552170475	chr7:97601534-97601535	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs3735259	chr7:97601571-97601572	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528148195	chr7:97601605-97601606	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs374164148	chr7:97601619-97601620	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs189896787	chr7:97601629-97601630	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs535614477	chr7:97601658-97601659	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs181169500	chr7:97601698-97601699	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs377277519	chr7:97601725-97601726	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs371027928	chr7:97601777-97601778	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs143889569	chr7:97601798-97601799	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs539368706	chr7:97601823-97601824	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs375480879	chr7:97601831-97601832	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs35069412	chr7:97601835-97601836	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372951977	chr7:97601839-97601840	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs529597665	chr7:97601842-97601843	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs372638234	chr7:97601856-97601857	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs540272049	chr7:97601866-97601867	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs555438070	chr7:97601884-97601885	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs150640603	chr7:97601888-97601889	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs34123558	chr7:97601937-97601938	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs139926296	chr7:97601989-97601990	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs562958401	chr7:97601991-97601992	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs77400454	chr7:97602012-97602013	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs545721786	chr7:97602028-97602029	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs564033497	chr7:97602087-97602088	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs528086812	chr7:97602107-97602108	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs375531994	chr7:97602118-97602119	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs149821493	chr7:97602130-97602131	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs200867477	chr7:97602155-97602156	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs202003241	chr7:97602158-97602159	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs375855968	chr7:97602159-97602160	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs568129437	chr7:97602207-97602208	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs145881903	chr7:97602221-97602222	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97600200-97601800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr7:97600200-97602200	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr7:97600200-97602200	Active TSS	HSMMtube	muscle
4	chr7:97600200-97602400	Active TSS	Stomach Smooth Muscle	stomach
5	chr7:97600200-97602800	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr7:97600400-97601200	Flanking Active TSS	Primary T cells from cord blood	blood
7	chr7:97600400-97601800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:97600400-97601800	Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr7:97600400-97601800	Active TSS	NHEK	skin
10	chr7:97600400-97602000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:97600400-97602000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:97600400-97602200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:97600400-97602200	Active TSS	Thymus	Thymus
14	chr7:97600400-97602200	Active TSS	HSMM	muscle
15	chr7:97600400-97602200	Active TSS	Osteobl	bone
16	chr7:97600400-97602600	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr7:97600400-97602800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:97600400-97602800	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr7:97600400-97602800	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr7:97600600-97601200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
21	chr7:97600600-97601200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:97600600-97601200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:97600600-97601200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:97600600-97601200	Flanking Active TSS	Fetal Thymus	thymus
25	chr7:97600600-97601400	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr7:97600600-97601800	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr7:97600600-97601800	Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr7:97600600-97601800	Active TSS	Lung	lung
29	chr7:97600600-97602000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:97600600-97602000	Active TSS	Colon Smooth Muscle	Colon
31	chr7:97600600-97602000	Active TSS	Esophagus	oesophagus
32	chr7:97600600-97602000	Active TSS	Rectal Smooth Muscle	rectum
33	chr7:97600600-97602000	Active TSS	K562	blood
34	chr7:97600600-97602000	Active TSS	NH-A	brain
35	chr7:97600600-97602200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:97600600-97602200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:97600600-97602200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr7:97600600-97602200	Active TSS	Left Ventricle	heart
39	chr7:97600600-97602200	Active TSS	Psoas Muscle	Psoas
40	chr7:97600600-97602200	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr7:97600600-97602200	Active TSS	NHLF	lung
42	chr7:97600600-97602600	Active TSS	H1 Cell Line	embryonic stem cell
43	chr7:97600600-97602600	Active TSS	H9 Cell Line	embryonic stem cell
44	chr7:97600600-97602600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:97600600-97602600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr7:97600600-97602600	Active TSS	Pancreas	Pancrea
47	chr7:97600600-97602600	Active TSS	A549	lung
48	chr7:97600600-97602600	Active TSS	GM12878-XiMat	blood
49	chr7:97600600-97602600	Active TSS	Hela-S3	cervix
50	chr7:97600600-97602800	Active TSS	HUES6 Cell Line	embryonic stem cell

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