Variant report

Variant	esv3445931
Chromosome Location	chr6:133347824-133434532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:524)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:133420786-133421038	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:133361164-133361458	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:133355542-133356273	HepG2	liver:	n/a	n/a
4	ATF1	chr6:133362201-133362491	K562	blood:	n/a	n/a
5	BHLHE40	chr6:133362168-133362430	K562	blood:	n/a	n/a
6	BRCA1	chr6:133408153-133408257	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr6:133420632-133421273	HCT-116	colon:	n/a	n/a
8	CCNT2	chr6:133362206-133362413	K562	blood:	n/a	n/a
9	CEBPB	chr6:133420684-133421027	A549	lung:	n/a	n/a
10	CEBPB	chr6:133379912-133380194	A549	lung:	n/a	chr6:133380067-133380078
11	CEBPB	chr6:133413364-133413718	IMR90	lung:	n/a	chr6:133413530-133413541
12	CEBPB	chr6:133372411-133372758	MCF-7	breast:	n/a	chr6:133372600-133372611
13	CEBPB	chr6:133379918-133380212	IMR90	lung:	n/a	chr6:133380067-133380078
14	CEBPB	chr6:133355592-133356496	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:133372460-133372753	H1-hESC	embryonic stem cell:	n/a	chr6:133372600-133372611
16	CEBPB	chr6:133420609-133421218	IMR90	lung:	n/a	n/a
17	CEBPB	chr6:133420657-133421115	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:133361463-133361740	HepG2	liver:	n/a	chr6:133361621-133361632
19	CEBPB	chr6:133420695-133421066	A549	lung:	n/a	n/a
20	CEBPB	chr6:133384515-133384845	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:133413402-133413711	K562	blood:	n/a	chr6:133413530-133413541
22	CEBPB	chr6:133379895-133380238	HepG2	liver:	n/a	chr6:133380067-133380078
23	CEBPB	chr6:133420684-133421038	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:133384599-133384740	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:133420598-133421307	HCT-116	colon:	n/a	n/a
26	CEBPB	chr6:133413362-133413719	HepG2	liver:	n/a	chr6:133413530-133413541
27	CEBPB	chr6:133413465-133413689	Hela-S3	cervix:	n/a	chr6:133413530-133413541
28	CEBPB	chr6:133365525-133365790	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:133384566-133384833	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:133420681-133421100	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:133402421-133402498	A549	lung:	n/a	n/a
32	CEBPB	chr6:133372424-133372797	HepG2	liver:	n/a	chr6:133372600-133372611
33	CEBPB	chr6:133372433-133372773	IMR90	lung:	n/a	chr6:133372600-133372611
34	CEBPB	chr6:133372446-133372693	Hela-S3	cervix:	n/a	chr6:133372600-133372611
35	CEBPB	chr6:133372429-133372759	A549	lung:	n/a	chr6:133372600-133372611
36	CEBPB	chr6:133420453-133421325	HCT-116	colon:	n/a	n/a
37	CEBPB	chr6:133413391-133413726	A549	lung:	n/a	chr6:133413530-133413541
38	CEBPB	chr6:133413543-133413615	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:133381653-133381862	HepG2	liver:	n/a	chr6:133381745-133381756
40	CEBPB	chr6:133356091-133356329	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:133383291-133383704	IMR90	lung:	n/a	n/a
42	CEBPD	chr6:133362148-133362522	K562	blood:	n/a	n/a
43	CEBPD	chr6:133362128-133362451	K562	blood:	n/a	n/a
44	CHD2	chr6:133413279-133413361	GM12878	blood:	n/a	n/a
45	CHD2	chr6:133376779-133377032	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:133361176-133361461	HepG2	liver:	n/a	chr6:133361328-133361341
47	CTCF	chr6:133361260-133361410	HPAF	blood vessel:	n/a	chr6:133361328-133361341
48	CTCF	chr6:133361130-133361519	K562	blood:	n/a	chr6:133361328-133361341
49	CTCF	chr6:133361241-133361437	ProgFib	skin:	n/a	chr6:133361328-133361341
50	CTCF	chr6:133361300-133361450	GM12865	blood:	n/a	chr6:133361328-133361341

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:133422365-133422415	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:133422365-133422415	AG09309	skin:	n/a
3	chr6:133422365-133422415	PrEC	prostate:	n/a
4	chr6:133376535-133376585	HEK293	kidney:	embryo
5	chr6:133422365-133422415	AG04450	lung:	fetal
6	chr6:133422365-133422415	H1-hESC	embryonic stem cell:	embryo
7	chr6:133422365-133422415	SK-N-MC	brain:	n/a
8	chr6:133422365-133422415	AoSMC	blood vessel:	n/a
9	chr6:133422365-133422415	K562	blood:	n/a
10	chr6:133407909-133407959	GM12878	blood:	n/a
11	chr6:133407909-133407959	HEK293	kidney:	embryo
12	chr6:133422365-133422415	NB4	blood:	n/a
13	chr6:133407909-133407959	HepG2	liver:	n/a
14	chr6:133407909-133407959	BE2_C	brain:	n/a
15	chr6:133422365-133422415	BE2_C	brain:	n/a
16	chr6:133407909-133407959	HAEpiC	amniotic membrane:	n/a
17	chr6:133376535-133376585	SK-N-SH_RA	brain:	n/a
18	chr6:133422365-133422415	NT2-D1	testis:	n/a
19	chr6:133407909-133407959	GM12891	blood:	n/a
20	chr6:133407909-133407959	AoSMC	blood vessel:	n/a
21	chr6:133422365-133422415	Caco-2	colon:	n/a
22	chr6:133376535-133376585	AG04450	lung:	fetal
23	chr6:133407909-133407959	CMK	blood:	n/a
24	chr6:133376535-133376585	NHDF-neo	bronchial:	n/a
25	chr6:133422365-133422415	HIPEpiC	eye:	n/a
26	chr6:133407909-133407959	SAEC	small airway:	n/a
27	chr6:133422365-133422415	NH-A	brain:	n/a
28	chr6:133376535-133376585	SK-N-SH	brain:	n/a
29	chr6:133422365-133422415	HCPEpiC	choroid plexus:	n/a
30	chr6:133407909-133407959	PrEC	prostate:	n/a
31	chr6:133422365-133422415	GM06990	blood:	n/a
32	chr6:133376535-133376585	Hepatocyte	liver:	n/a
33	chr6:133407909-133407959	NH-A	brain:	n/a
34	chr6:133407909-133407959	MCF-7	breast:	n/a
35	chr6:133407909-133407959	ovcar-3	ovarian:	n/a
36	chr6:133422365-133422415	SAEC	small airway:	n/a
37	chr6:133407909-133407959	HEEpiC	esophagus:	n/a
38	chr6:133407909-133407959	ECC-1	luminal epithelium:	n/a
39	chr6:133422365-133422415	SK-N-SH_RA	brain:	n/a
40	chr6:133376535-133376585	LNCaP	prostate:	n/a
41	chr6:133376535-133376585	GM12891	blood:	n/a
42	chr6:133376535-133376585	BE2_C	brain:	n/a
43	chr6:133422365-133422415	MCF10A-Er-Src	breast:	n/a
44	chr6:133407909-133407959	HIPEpiC	eye:	n/a
45	chr6:133376535-133376585	HCT-116	colon:	n/a
46	chr6:133407909-133407959	HCPEpiC	choroid plexus:	n/a
47	chr6:133407909-133407959	SK-N-MC	brain:	n/a
48	chr6:133422365-133422415	HUVEC	blood vessel:	n/a
49	chr6:133376535-133376585	NH-A	brain:	n/a
50	chr6:133422365-133422415	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:133371252..133373949-chr6:133374893..133377251,2	K562	blood:
2	chr6:133134077..133136797-chr6:133382132..133384671,2	MCF-7	breast:
3	chr6:133350605..133352698-chr6:133358690..133361519,2	MCF-7	breast:
4	chr6:133371252..133373949-chr6:133374893..133377251,2	K562	blood:
5	chr6:133432444..133434710-chr6:133454320..133456376,2	K562	blood:
6	chr6:133143184..133145778-chr6:133351555..133353623,2	K562	blood:
7	chr6:133135421..133137439-chr6:133389334..133391072,2	MCF-7	breast:
8	chr6:133350605..133352698-chr6:133358690..133361519,2	MCF-7	breast:
9	chr6:133140267..133142584-chr6:133384243..133385857,2	MCF-7	breast:
10	chr6:133284240..133284797-chr6:133360868..133361418,2	K562	blood:
11	chr6:133417078..133419913-chr6:133422627..133424632,2	MCF-7	breast:
12	chr6:133417078..133419913-chr6:133422627..133424632,2	MCF-7	breast:
13	chr6:133136010..133137577-chr6:133349249..133350798,2	MCF-7	breast:
14	chr6:133418545..133420592-chr6:133429051..133431256,2	MCF-7	breast:
15	chr6:133283886..133284848-chr6:133360811..133361796,7	MCF-7	breast:
16	chr6:133142071..133143902-chr6:133355082..133357821,2	MCF-7	breast:
17	chr6:133298843..133300922-chr6:133348879..133351431,2	MCF-7	breast:
18	chr6:133286155..133286849-chr6:133360880..133361773,3	MCF-7	breast:
19	chr6:133418545..133420592-chr6:133429051..133431256,2	MCF-7	breast:
20	chr6:133352133..133352653-chr9:23112962..23113483,3	MCF-7	breast:
21	chr6:133283881..133284739-chr6:133360893..133361401,2	MCF-7	breast:
22	chr6:133423980..133426292-chr6:133454398..133456094,2	K562	blood:
23	chr6:133399204..133402131-chr6:133405964..133408211,2	MCF-7	breast:
24	chr6:133399204..133402131-chr6:133405964..133408211,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EYA4-1	chr6:133419409-133419457	ENSG00000231023
2	lnc-EYA4-1	chr6:133417649-133417702	ENSG00000231023
3	lnc-EYA4-1	chr6:133427234-133427710	XLOC_005466
4	lnc-EYA4-1	chr6:133411192-133411208	XLOC_005466
5	lnc-EYA4-1	chr6:133421146-133421323	XLOC_005466
6	lnc-EYA4-1	chr6:133421146-133421323	XLOC_005466
7	lnc-EYA4-1	chr6:133409957-133410033	XLOC_005466
8	lnc-EYA4-1	chr6:133417649-133417702	NONHSAT114988
9	lnc-EYA4-1	chr6:133419409-133419457	XLOC_005466
10	lnc-EYA4-1	chr6:133427234-133427691	XLOC_005466
11	lnc-EYA4-1	chr6:133421146-133421323	ENSG00000231023
12	lnc-EYA4-1	chr6:133417649-133417702	XLOC_005466
13	lnc-EYA4-1	chr6:133427234-133427717	NONHSAT114986
14	lnc-EYA4-1	chr6:133427234-133427719	XLOC_005466
15	lnc-EYA4-1	chr6:133409258-133409716	XLOC_005466
16	lnc-EYA4-1	chr6:133417649-133417702	ENSG00000231023
17	lnc-EYA4-1	chr6:133409957-133411208	XLOC_005466
18	lnc-EYA4-1	chr6:133409261-133409716	NONHSAT114988
19	lnc-EYA4-1	chr6:133421146-133421323	XLOC_005466
20	lnc-EYA4-1	chr6:133417649-133417702	NONHSAT114986
21	lnc-EYA4-1	chr6:133417649-133417702	XLOC_005466
22	lnc-EYA4-1	chr6:133419409-133419434	NONHSAT114988
23	lnc-EYA4-1	chr6:133427234-133427717	ENSG00000231023
24	lnc-EYA4-1	chr6:133409219-133409716	NONHSAT114986
25	lnc-EYA4-1	chr6:133409219-133409716	XLOC_005466
26	lnc-EYA4-1	chr6:133421146-133421323	ENSG00000231023
27	lnc-EYA4-1	chr6:133409219-133409716	ENSG00000231023
28	lnc-EYA4-1	chr6:133409219-133409716	XLOC_005466
29	lnc-EYA4-1	chr6:133417649-133417702	XLOC_005466
30	lnc-EYA4-1	chr6:133427234-133427719	XLOC_005466
31	lnc-EYA4-1	chr6:133427234-133427710	XLOC_005466
32	lnc-EYA4-1	chr6:133409957-133411208	ENSG00000231023
33	lnc-EYA4-1	chr6:133409258-133409716	XLOC_005466
34	lnc-EYA4-1	chr6:133421146-133421323	XLOC_005466
35	lnc-EYA4-1	chr6:133421146-133421323	NONHSAT114986
36	lnc-EYA4-1	chr6:133409267-133409716	ENSG00000231023
37	lnc-EYA4-1	chr6:133421017-133421323	XLOC_005466
38	lnc-EYA4-1	chr6:133427234-133427337	ENSG00000231023

No data

Variant related genes	Relation type
LINC00326	TF binding region
LINC00326	CpG island
ENSG00000112306	chromatin interactions
ENSG00000206754	chromatin interactions
TIPARP	miRNA target sites
CNNM2	miRNA target sites
PTEN	miRNA target sites
TJAP1	miRNA target sites
TRIP6	miRNA target sites
TJP2	miRNA target sites
PTCH1	miRNA target sites
CNNM3	miRNA target sites
CNOT2	miRNA target sites
TLE3	miRNA target sites
CNOT6L	miRNA target sites

Extended variants
information (count: 2671 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2671 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541721559	chr6:133349254-133349255	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562033960	chr6:133349271-133349272	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527457678	chr6:133349296-133349297	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144601837	chr6:133349309-133349310	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570349004	chr6:133349310-133349311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533242897	chr6:133349375-133349376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192144365	chr6:133349388-133349389	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183959968	chr6:133349431-133349432	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569904322	chr6:133349439-133349440	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs71742374	chr6:133349530-133349531	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs577535151	chr6:133349537-133349538	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370513842	chr6:133349540-133349541	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370800172	chr6:133349541-133349542	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145534038	chr6:133349557-133349558	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs71989273	chr6:133349559-133349560	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs61078244	chr6:133349568-133349569	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs11303699	chr6:133349569-133349570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs28495111	chr6:133349576-133349577	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs63114762	chr6:133349577-133349578	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs200572595	chr6:133349583-133349584	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189423386	chr6:133349611-133349612	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192617720	chr6:133349612-133349613	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535366026	chr6:133349649-133349650	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558366039	chr6:133349660-133349661	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs578234444	chr6:133349667-133349668	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368911266	chr6:133349684-133349685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539534506	chr6:133349688-133349689	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556237043	chr6:133349722-133349723	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79896715	chr6:133349755-133349756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148839741	chr6:133349762-133349763	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs3012464	chr6:133349769-133349770	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs143552184	chr6:133349850-133349851	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540968949	chr6:133349893-133349894	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563936506	chr6:133349951-133349952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184441400	chr6:133350015-133350016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549966692	chr6:133350041-133350042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111697761	chr6:133350058-133350059	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189867159	chr6:133350059-133350060	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549335728	chr6:133350116-133350117	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536660410	chr6:133350165-133350166	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372390779	chr6:133350168-133350169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182054936	chr6:133350191-133350192	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113826116	chr6:133350236-133350237	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs148026404	chr6:133350261-133350262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111964302	chr6:133350269-133350270	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs62430560	chr6:133350337-133350338	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs143613887	chr6:133350341-133350342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs111871723	chr6:133350352-133350353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535232673	chr6:133350383-133350384	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555334285	chr6:133350391-133350392	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133354600-133355400	Enhancers	HepG2	liver
2	chr6:133355400-133355800	Flanking Active TSS	HepG2	liver
3	chr6:133355600-133356200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:133355600-133356800	Enhancers	A549	lung
5	chr6:133355800-133356000	Enhancers	HepG2	liver
6	chr6:133356000-133356600	Flanking Active TSS	HepG2	liver
7	chr6:133356600-133358000	Enhancers	HepG2	liver
8	chr6:133358000-133372200	Weak transcription	HepG2	liver
9	chr6:133361000-133361600	Enhancers	Fetal Muscle Leg	muscle
10	chr6:133361200-133361400	Enhancers	Fetal Stomach	stomach
11	chr6:133361200-133376200	Weak transcription	Psoas Muscle	Psoas
12	chr6:133361400-133361600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:133361400-133361800	Enhancers	Brain Substantia Nigra	brain
14	chr6:133361400-133362000	Weak transcription	Fetal Stomach	stomach
15	chr6:133361600-133362000	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:133361600-133363800	Enhancers	Fetal Heart	heart
17	chr6:133361800-133376000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:133362000-133362600	Enhancers	Fetal Muscle Leg	muscle
19	chr6:133362000-133362600	Enhancers	Fetal Stomach	stomach
20	chr6:133362200-133362600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:133362600-133363600	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:133362600-133363600	Weak transcription	Fetal Stomach	stomach
23	chr6:133363600-133363800	Enhancers	Fetal Muscle Leg	muscle
24	chr6:133363600-133363800	Enhancers	Fetal Stomach	stomach
25	chr6:133363800-133367800	Weak transcription	Fetal Muscle Leg	muscle
26	chr6:133366800-133367000	Enhancers	Fetal Lung	lung
27	chr6:133367000-133367800	Weak transcription	Fetal Lung	lung
28	chr6:133367800-133368000	Enhancers	Fetal Muscle Leg	muscle
29	chr6:133367800-133368600	Enhancers	Fetal Lung	lung
30	chr6:133367800-133368600	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr6:133368200-133368600	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr6:133368600-133376200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr6:133370600-133371400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr6:133370800-133371400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr6:133371000-133371400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:133371000-133371400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:133371000-133371400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:133371400-133375800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:133371400-133376000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr6:133371400-133376000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr6:133371400-133376000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:133371400-133376200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr6:133372200-133372400	Enhancers	HepG2	liver
44	chr6:133372400-133372600	Bivalent Enhancer	HepG2	liver
45	chr6:133372400-133372800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:133375600-133376600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr6:133375800-133376400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr6:133375800-133376400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:133376000-133376800	Enhancers	H9 Cell Line	embryonic stem cell
50	chr6:133376000-133377400	Enhancers	HUES48 Cell Line	embryonic stem cell

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