Variant report

Variant	nsv967451
Chromosome Location	chr7:6417630-6427589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6424825-6425475	HepG2	liver:	n/a	n/a
2	ATF1	chr7:6425094-6425398	K562	blood:	n/a	n/a
3	ATF2	chr7:6425006-6425405	GM12878	blood:	n/a	n/a
4	ATF3	chr7:6424925-6425559	HCT-116	colon:	n/a	n/a
5	ATF3	chr7:6424947-6425510	A549	lung:	n/a	n/a
6	ATF3	chr7:6424850-6425553	HCT-116	colon:	n/a	n/a
7	BACH1	chr7:6425804-6426093	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:6422631-6422760	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr7:6424879-6425528	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:6424951-6425487	A549	lung:	n/a	n/a
11	CEBPB	chr7:6425032-6425491	MCF-7	breast:	n/a	n/a
12	CEBPB	chr7:6424964-6425459	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr7:6423398-6423580	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:6424817-6425521	HCT-116	colon:	n/a	n/a
15	CEBPB	chr7:6425062-6425411	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:6425041-6425490	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:6424935-6425654	A549	lung:	n/a	n/a
18	CEBPB	chr7:6424933-6425451	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:6422439-6422701	K562	blood:	n/a	n/a
20	CEBPB	chr7:6425041-6425417	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr7:6423332-6423653	K562	blood:	n/a	n/a
22	CEBPB	chr7:6423800-6423913	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:6424918-6425507	A549	lung:	n/a	n/a
24	CEBPB	chr7:6425000-6425484	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:6424858-6425631	HCT-116	colon:	n/a	n/a
26	CHD1	chr7:6425847-6425849	GM12878	blood:	n/a	n/a
27	CHD2	chr7:6422785-6422842	GM12878	blood:	n/a	n/a
28	CHD2	chr7:6425025-6425431	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr7:6424700-6424850	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr7:6424880-6425030	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr7:6425700-6425850	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr7:6424740-6424890	HCFaa	heart:	n/a	n/a
33	E2F4	chr7:6425098-6425382	MCF10A-Er-Src	breast:	n/a	n/a
34	ELF1	chr7:6425016-6425419	HepG2	liver:	n/a	n/a
35	ELF1	chr7:6424964-6425417	A549	lung:	n/a	n/a
36	ELF1	chr7:6424910-6425424	A549	lung:	n/a	n/a
37	ELF1	chr7:6424867-6425621	SK-N-SH	brain:	n/a	n/a
38	ELF1	chr7:6424702-6425561	HCT-116	colon:	n/a	n/a
39	ELF1	chr7:6424889-6425624	MCF-7	breast:	n/a	n/a
40	ELF1	chr7:6425025-6425393	HepG2	liver:	n/a	n/a
41	ELK1	chr7:6425053-6425134	GM12878	blood:	n/a	n/a
42	EP300	chr7:6424950-6425423	HepG2	liver:	n/a	chr7:6425233-6425241 chr7:6425182-6425191 chr7:6425181-6425190
43	EP300	chr7:6425177-6425326	HepG2	liver:	n/a	chr7:6425233-6425241 chr7:6425182-6425191 chr7:6425181-6425190
44	EP300	chr7:6424821-6425586	ECC-1	luminal epithelium:	n/a	chr7:6425233-6425241 chr7:6425451-6425458 chr7:6425182-6425191 chr7:6425181-6425190
45	EP300	chr7:6424750-6425724	T-47D	breast:	n/a	chr7:6425233-6425241 chr7:6425451-6425458 chr7:6425182-6425191 chr7:6425181-6425190
46	EP300	chr7:6424760-6424815	GM12878	blood:	n/a	n/a
47	EP300	chr7:6424868-6425475	Hela-S3	cervix:	n/a	chr7:6425233-6425241 chr7:6425451-6425458 chr7:6425182-6425191 chr7:6425181-6425190
48	EP300	chr7:6424903-6425491	T-47D	breast:	n/a	chr7:6425233-6425241 chr7:6425451-6425458 chr7:6425182-6425191 chr7:6425181-6425190
49	EP300	chr7:6424855-6425567	A549	lung:	n/a	chr7:6425233-6425241 chr7:6425451-6425458 chr7:6425182-6425191 chr7:6425181-6425190
50	EP300	chr7:6425491-6425586	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6418440-6418490	HL-60	blood:	n/a
2	chr7:6418440-6418490	HEEpiC	esophagus:	n/a
3	chr7:6418440-6418490	AG04450	lung:	fetal
4	chr7:6418440-6418490	AG10803	skin:	n/a
5	chr7:6418440-6418490	HCT-116	colon:	n/a
6	chr7:6418440-6418490	RPTEC	kidney:	n/a
7	chr7:6418440-6418490	Hepatocyte	liver:	n/a
8	chr7:6418440-6418490	HCM	heart:	n/a
9	chr7:6418440-6418490	SKMC	muscle:	n/a
10	chr7:6418440-6418490	MCF10A-Er-Src	breast:	n/a
11	chr7:6418440-6418490	ovcar-3	ovarian:	n/a
12	chr7:6418440-6418490	HNPCEpiC	eye:	n/a
13	chr7:6418440-6418490	NB4	blood:	n/a
14	chr7:6418440-6418490	PANC-1	pancreas:	n/a
15	chr7:6418440-6418490	HepG2	liver:	n/a
16	chr7:6418440-6418490	NT2-D1	testis:	n/a
17	chr7:6418440-6418490	GM19239	blood:	n/a
18	chr7:6418440-6418490	MCF-7	breast:	n/a
19	chr7:6418440-6418490	Hela-S3	cervix:	n/a
20	chr7:6418440-6418490	GM06990	blood:	n/a
21	chr7:6418440-6418490	HRCEpiC	kidney:	n/a
22	chr7:6418440-6418490	NH-A	brain:	n/a
23	chr7:6418440-6418490	LNCaP	prostate:	n/a
24	chr7:6418440-6418490	GM12891	blood:	n/a
25	chr7:6418440-6418490	U87	brain:	n/a
26	chr7:6418440-6418490	AG09319	gingival:	n/a
27	chr7:6418440-6418490	BJ	skin:	n/a
28	chr7:6418440-6418490	HCF	heart:	n/a
29	chr7:6418440-6418490	AG04449	skin:	fetal
30	chr7:6418440-6418490	HUVEC	blood vessel:	n/a
31	chr7:6418440-6418490	GM12878	blood:	n/a
32	chr7:6418440-6418490	A549	lung:	n/a
33	chr7:6418440-6418490	T-47D	breast:	n/a
34	chr7:6418440-6418490	Caco-2	colon:	n/a
35	chr7:6418440-6418490	HAEpiC	amniotic membrane:	n/a
36	chr7:6418440-6418490	CMK	blood:	n/a
37	chr7:6418440-6418490	ProgFib	skin:	n/a
38	chr7:6418440-6418490	AG09309	skin:	n/a
39	chr7:6418440-6418490	BE2_C	brain:	n/a
40	chr7:6418440-6418490	HMEC	breast:	n/a
41	chr7:6418440-6418490	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:6418440-6418490	HRE	kidney:	n/a
43	chr7:6418440-6418490	IMR90	lung:	fetal
44	chr7:6418440-6418490	NHBE	bronchial:	n/a
45	chr7:6418440-6418490	H1-hESC	embryonic stem cell:	embryo
46	chr7:6418440-6418490	SK-N-SH_RA	brain:	n/a
47	chr7:6418440-6418490	HCPEpiC	choroid plexus:	n/a
48	chr7:6418440-6418490	HIPEpiC	eye:	n/a
49	chr7:6418440-6418490	GM12892	blood:	n/a
50	chr7:6418440-6418490	PrEC	prostate:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6421014..6424482-chr7:6430347..6433930,4	K562	blood:
2	chr7:6420289..6422847-chr7:6423300..6426069,2	K562	blood:
3	chr7:6414882..6417650-chr7:6542443..6546000,3	MCF-7	breast:
4	chr7:6421413..6423710-chr7:6424469..6426937,2	MCF-7	breast:
5	chr7:6413899..6414665-chr7:6424418..6425315,2	MCF-7	breast:
6	chr7:6425587..6427672-chr7:6434203..6435980,2	K562	blood:
7	chr7:6425290..6426951-chr7:6443487..6445552,2	MCF-7	breast:
8	chr7:6425039..6427961-chr7:6431283..6434070,6	K562	blood:
9	chr7:6423918..6426061-chr7:6486090..6487608,2	K562	blood:
10	chr7:6423770..6428087-chr7:6429749..6432812,3	MCF-7	breast:
11	chr7:6421014..6427961-chr7:6430347..6436546,11	K562	blood:
12	chr7:6386938..6388709-chr7:6422840..6425617,3	MCF-7	breast:
13	chr7:6421340..6424107-chr7:6434003..6435791,2	MCF-7	breast:
14	chr7:6423125..6425686-chr7:6428295..6430313,2	K562	blood:
15	chr7:6413015..6417903-chr7:6435938..6439469,5	MCF-7	breast:
16	chr5:33550176..33550968-chr7:6425037..6425801,2	MCF-7	breast:
17	chr7:6421913..6424520-chr7:6475642..6477904,2	MCF-7	breast:
18	chr7:6424186..6426386-chr7:6428771..6430313,2	K562	blood:
19	chr7:6408313..6409948-chr7:6425652..6428069,2	MCF-7	breast:
20	chr7:6420289..6422847-chr7:6423300..6426069,2	K562	blood:
21	chr7:6415178..6416975-chr7:6426266..6428182,2	MCF-7	breast:
22	chr7:6421413..6423710-chr7:6424469..6426937,2	MCF-7	breast:
23	chr7:6412400..6417963-chr7:6418207..6425853,16	MCF-7	breast:
24	chr7:6420136..6422492-chr7:6433519..6436270,2	MCF-7	breast:

No data

Variant related genes	Relation type
RAC1	TF binding region
RAC1	CpG island
ENSG00000178397	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000136238	chromatin interactions

Extended variants
information (count: 572 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553369134	chr7:6417635-6417636	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs188647771	chr7:6417638-6417639	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192267257	chr7:6417642-6417643	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375846749	chr7:6417643-6417644	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555814266	chr7:6417676-6417677	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544140037	chr7:6417677-6417678	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368455826	chr7:6417678-6417679	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144307127	chr7:6417718-6417719	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534692871	chr7:6417723-6417724	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553472078	chr7:6417735-6417736	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs578030992	chr7:6417781-6417782	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545596623	chr7:6417791-6417792	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183185698	chr7:6417802-6417803	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111972443	chr7:6417808-6417809	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201398381	chr7:6417809-6417810	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560165955	chr7:6417811-6417812	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187838576	chr7:6417819-6417820	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543282896	chr7:6417822-6417823	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561811567	chr7:6417830-6417831	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs79686877	chr7:6417836-6417837	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575391665	chr7:6417844-6417845	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540661095	chr7:6417891-6417892	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542482920	chr7:6417925-6417926	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs561220794	chr7:6417942-6417943	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs528334681	chr7:6417943-6417944	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369972999	chr7:6417951-6417952	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs191141193	chr7:6417952-6417953	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552015549	chr7:6417971-6417972	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs570231508	chr7:6417972-6417973	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs184512519	chr7:6417975-6417976	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs546508958	chr7:6418008-6418009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs564491262	chr7:6418025-6418026	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs531987937	chr7:6418042-6418043	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs550639592	chr7:6418082-6418083	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs568908452	chr7:6418108-6418109	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567853087	chr7:6418109-6418110	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs372726815	chr7:6418121-6418122	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189382019	chr7:6418156-6418157	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148744555	chr7:6418159-6418160	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs2017198	chr7:6418166-6418167	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549349277	chr7:6418167-6418168	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs567875732	chr7:6418170-6418171	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs557552908	chr7:6418171-6418172	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs575859921	chr7:6418187-6418188	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs35551995	chr7:6418198-6418199	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553707359	chr7:6418247-6418248	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7784465	chr7:6418275-6418276	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs2347338	chr7:6418278-6418279	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs192901831	chr7:6418288-6418289	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184926078	chr7:6418291-6418292	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Ependymoma	20639864	CNVD
Autism	20685689	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6415600-6417800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:6415600-6418000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr7:6415600-6418200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:6415600-6423800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:6415800-6417800	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr7:6415800-6417800	Enhancers	Fetal Heart	heart
7	chr7:6415800-6417800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr7:6415800-6418000	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr7:6415800-6418000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr7:6415800-6418800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:6415800-6419400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr7:6415800-6419400	Weak transcription	Aorta	Aorta
13	chr7:6415800-6419600	Weak transcription	HSMMtube	muscle
14	chr7:6415800-6422400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:6415800-6422600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr7:6415800-6427400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr7:6416000-6417800	Enhancers	Fetal Intestine Large	intestine
18	chr7:6416000-6418400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:6416000-6418400	Enhancers	Primary T cells from cord blood	blood
20	chr7:6416000-6419600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:6416000-6424800	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr7:6416200-6417800	Genic enhancers	Fetal Thymus	thymus
23	chr7:6416200-6418000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:6416200-6418800	Enhancers	Primary B cells from cord blood	blood
25	chr7:6416200-6421200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr7:6416200-6422600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:6416400-6417800	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr7:6416400-6418400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr7:6416400-6420600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:6416400-6422400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr7:6416600-6417800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:6416600-6417800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:6416600-6417800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr7:6416600-6417800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr7:6416600-6417800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr7:6416600-6417800	Genic enhancers	Fetal Brain Female	brain
37	chr7:6416600-6417800	Genic enhancers	Gastric	stomach
38	chr7:6416600-6417800	Genic enhancers	Small Intestine	intestine
39	chr7:6416600-6418000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
40	chr7:6416600-6423800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:6416800-6418600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
42	chr7:6416800-6418600	Enhancers	Right Ventricle	heart
43	chr7:6416800-6418800	Genic enhancers	Fetal Intestine Small	intestine
44	chr7:6416800-6419200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr7:6416800-6419400	Weak transcription	NH-A	brain
46	chr7:6416800-6419600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:6417000-6417800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:6417000-6417800	Enhancers	Brain Germinal Matrix	brain
49	chr7:6417000-6417800	Genic enhancers	Fetal Stomach	stomach
50	chr7:6417000-6417800	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach

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