Variant report

Variant	esv1806734
Chromosome Location	chr6:133125643-133168582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1878)
CpG islands
(count:1708)
Chromatin interactive
region (count:123)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1878 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:133144140-133144418	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:133164461-133164874	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:133133546-133134814	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:133135176-133136074	K562	blood:	n/a	n/a
5	ARID3A	chr6:133135183-133135945	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:133151422-133151653	K562	blood:	n/a	n/a
7	ARID3A	chr6:133151397-133151695	HepG2	liver:	n/a	n/a
8	ATF1	chr6:133154119-133154349	K562	blood:	n/a	n/a
9	ATF1	chr6:133144166-133144463	K562	blood:	n/a	n/a
10	ATF2	chr6:133141042-133141394	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:133138596-133141032	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:133140519-133141387	GM12878	blood:	n/a	n/a
13	ATF2	chr6:133139322-133140019	GM12878	blood:	n/a	n/a
14	ATF2	chr6:133136568-133136991	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr6:133138592-133141523	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:133141648-133142284	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:133133920-133136221	GM12878	blood:	n/a	n/a
18	ATF2	chr6:133134163-133135006	GM12878	blood:	n/a	n/a
19	ATF2	chr6:133135123-133137131	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:133137238-133138580	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr6:133140542-133141381	GM12878	blood:	n/a	n/a
22	ATF2	chr6:133137549-133138050	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:133135064-133136140	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:133135112-133136032	GM12878	blood:	n/a	n/a
25	ATF3	chr6:133135100-133135580	A549	lung:	n/a	n/a
26	ATF3	chr6:133135201-133135832	K562	blood:	n/a	n/a
27	ATF3	chr6:133135099-133135938	A549	lung:	n/a	n/a
28	BACH1	chr6:133135475-133135974	K562	blood:	n/a	n/a
29	BACH1	chr6:133141800-133142743	K562	blood:	n/a	n/a
30	BACH1	chr6:133133404-133133766	K562	blood:	n/a	n/a
31	BATF	chr6:133134714-133135000	GM12878	blood:	n/a	n/a
32	BATF	chr6:133133912-133134498	GM12878	blood:	n/a	chr6:133134171-133134182
33	BATF	chr6:133134664-133135001	GM12878	blood:	n/a	n/a
34	BCL11A	chr6:133134668-133135043	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:133135530-133135950	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:133135567-133135850	GM12878	blood:	n/a	n/a
37	BCL3	chr6:133139072-133140029	K562	blood:	n/a	n/a
38	BCL3	chr6:133135314-133135961	GM12878	blood:	n/a	n/a
39	BCL3	chr6:133141699-133142239	GM12878	blood:	n/a	n/a
40	BCL3	chr6:133141639-133142381	A549	lung:	n/a	n/a
41	BCL3	chr6:133135074-133135954	A549	lung:	n/a	n/a
42	BCL3	chr6:133140220-133141232	K562	blood:	n/a	chr6:133140480-133140489
43	BCL3	chr6:133135109-133136146	A549	lung:	n/a	n/a
44	BCL3	chr6:133139176-133142713	A549	lung:	n/a	chr6:133140480-133140489
45	BCL3	chr6:133140179-133141582	GM12878	blood:	n/a	chr6:133140480-133140489
46	BCL3	chr6:133140130-133141392	K562	blood:	n/a	chr6:133140480-133140489
47	BCL3	chr6:133140081-133141503	A549	lung:	n/a	chr6:133140480-133140489
48	BCL3	chr6:133138857-133140029	K562	blood:	n/a	n/a
49	BCLAF1	chr6:133138595-133141450	K562	blood:	n/a	chr6:133140480-133140489
50	BCLAF1	chr6:133140168-133141402	GM12878	blood:	n/a	chr6:133140480-133140489

(count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:133138774-133138824	CMK	blood:	n/a
2	chr6:133138165-133138215	AG04449	skin:	fetal
3	chr6:133137827-133137877	HL-60	blood:	n/a
4	chr6:133141956-133142006	ECC-1	luminal epithelium:	n/a
5	chr6:133136266-133136316	GM12878	blood:	n/a
6	chr6:133135828-133135878	HEEpiC	esophagus:	n/a
7	chr6:133137119-133137169	NB4	blood:	n/a
8	chr6:133141956-133142006	HCM	heart:	n/a
9	chr6:133131884-133131934	Caco-2	colon:	n/a
10	chr6:133135564-133135614	BJ	skin:	n/a
11	chr6:133135904-133135954	HUVEC	blood vessel:	n/a
12	chr6:133137119-133137169	SK-N-MC	brain:	n/a
13	chr6:133135492-133135542	HMEC	breast:	n/a
14	chr6:133135557-133135607	HCT-116	colon:	n/a
15	chr6:133135524-133135574	GM12892	blood:	n/a
16	chr6:133136317-133136367	PFSK-1	brain:	n/a
17	chr6:133138774-133138824	HAEpiC	amniotic membrane:	n/a
18	chr6:133137119-133137169	BE2_C	brain:	n/a
19	chr6:133135687-133135737	SKMC	muscle:	n/a
20	chr6:133135579-133135629	MCF10A-Er-Src	breast:	n/a
21	chr6:133135564-133135614	AG10803	skin:	n/a
22	chr6:133138774-133138824	GM12891	blood:	n/a
23	chr6:133137827-133137877	ProgFib	skin:	n/a
24	chr6:133135579-133135629	SK-N-MC	brain:	n/a
25	chr6:133134704-133134754	NB4	blood:	n/a
26	chr6:133135564-133135614	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:133138210-133138260	ECC-1	luminal epithelium:	n/a
28	chr6:133136135-133136185	HNPCEpiC	eye:	n/a
29	chr6:133137827-133137877	HAEpiC	amniotic membrane:	n/a
30	chr6:133136317-133136367	CMK	blood:	n/a
31	chr6:133137810-133137860	HNPCEpiC	eye:	n/a
32	chr6:133137810-133137860	HUVEC	blood vessel:	n/a
33	chr6:133137893-133137943	H1-hESC	embryonic stem cell:	embryo
34	chr6:133138210-133138260	IMR90	lung:	fetal
35	chr6:133135492-133135542	MCF10A-Er-Src	breast:	n/a
36	chr6:133134704-133134754	SK-N-SH_RA	brain:	n/a
37	chr6:133131884-133131934	PrEC	prostate:	n/a
38	chr6:133135828-133135878	GM19239	blood:	n/a
39	chr6:133136015-133136065	Jurkat	blood:	n/a
40	chr6:133136135-133136185	PrEC	prostate:	n/a
41	chr6:133137167-133137217	T-47D	breast:	n/a
42	chr6:133138210-133138260	SK-N-SH	brain:	n/a
43	chr6:133136266-133136316	AG04449	skin:	fetal
44	chr6:133135904-133135954	T-47D	breast:	n/a
45	chr6:133138774-133138824	GM12892	blood:	n/a
46	chr6:133134704-133134754	Caco-2	colon:	n/a
47	chr6:133137119-133137169	Hepatocyte	liver:	n/a
48	chr6:133134704-133134754	BE2_C	brain:	n/a
49	chr6:133138165-133138215	Jurkat	blood:	n/a
50	chr6:133135579-133135629	AG09319	gingival:	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:133132887..133135811-chr6:134273188..134277510,5	K562	blood:
2	chr6:133141835..133144313-chr6:133156927..133159674,3	K562	blood:
3	chr1:33429448..33430407-chr6:133134991..133135963,2	Hela-S3	cervix:
4	chr6:133146833..133149424-chr6:133152798..133154698,2	K562	blood:
5	chr6:133135395..133135910-chr9:102668805..102669502,2	MCF-7	breast:
6	chr6:133134186..133135888-chr6:133168555..133170762,2	K562	blood:
7	chr17:79479507..79480059-chr6:133135411..133136304,2	HCT-116	colon:
8	chr6:132774346..132776472-chr6:133129139..133131123,2	MCF-7	breast:
9	chr6:133133722..133135487-chr6:133500551..133504315,3	K562	blood:
10	chr6:133139023..133140882-chr6:133238687..133240373,2	MCF-7	breast:
11	chr6:132832873..132835191-chr6:133139473..133141127,2	K562	blood:
12	chr6:133139563..133143378-chr6:133869645..133873437,4	K562	blood:
13	chr22:42739071..42740021-chr6:133135515..133136044,2	HCT-116	colon:
14	chr6:133151552..133152231-chr6:133505787..133506589,2	MCF-7	breast:
15	chr6:132849284..132852259-chr6:133140271..133142677,3	MCF-7	breast:
16	chr6:133118738..133121936-chr6:133122452..133126687,7	K562	blood:
17	chr6:133146833..133149424-chr6:133152798..133154698,2	K562	blood:
18	chr19:2163733..2164433-chr6:133135620..133136388,2	HCT-116	colon:
19	chr11:18417141..18419717-chr6:133139653..133142088,2	K562	blood:
20	chr6:133084415..133087080-chr6:133134762..133137402,2	MCF-7	breast:
21	chr6:133083233..133085227-chr6:133144108..133145647,2	K562	blood:
22	chr6:133142048..133144415-chr6:133161174..133163996,2	MCF-7	breast:
23	chr6:133140267..133142584-chr6:133384243..133385857,2	MCF-7	breast:
24	chr6:133102182..133104847-chr6:133124000..133126674,2	K562	blood:
25	chr19:1478974..1479621-chr6:133135658..133136245,2	Hela-S3	cervix:
26	chr6:132860709..132862896-chr6:133144372..133146096,2	K562	blood:
27	chr6:133141835..133144313-chr6:133156927..133159674,3	K562	blood:
28	chr6:133125209..133127039-chr6:133127242..133130510,3	MCF-7	breast:
29	chr6:133151897..133155334-chr6:133156928..133160559,4	K562	blood:
30	chr6:133054032..133057251-chr6:133136548..133139421,3	K562	blood:
31	chr6:133135683..133136351-chr9:130547259..130548177,2	Hela-S3	cervix:
32	chr6:133135604..133137467-chr6:144606007..144608305,2	K562	blood:
33	chr11:122932373..122933017-chr6:133135657..133136205,2	Hela-S3	cervix:
34	chr6:133049609..133052376-chr6:133137041..133138744,2	MCF-7	breast:
35	chr6:133117688..133126502-chr6:133133829..133139054,19	MCF-7	breast:
36	chr6:133139979..133142138-chr6:133214137..133215920,2	MCF-7	breast:
37	chr6:133135224..133137195-chr7:86974442..86977103,2	MCF-7	breast:
38	chr6:133142071..133143902-chr6:133355082..133357821,2	MCF-7	breast:
39	chr6:133122629..133124869-chr6:133126190..133128532,2	MCF-7	breast:
40	chr6:132855902..132859597-chr6:133135974..133139810,3	K562	blood:
41	chr6:133132907..133137002-chr6:133163874..133168278,4	MCF-7	breast:
42	chr19:33608688..33609467-chr6:133154061..133154906,2	MCF-7	breast:
43	chr19:12885475..12887158-chr6:133138358..133141147,2	K562	blood:
44	chr17:73083843..73084453-chr6:133135605..133136113,2	Hela-S3	cervix:
45	chr6:133140432..133142390-chr6:133219540..133222428,2	MCF-7	breast:
46	chr6:133133823..133137064-chr6:133152471..133155832,4	K562	blood:
47	chr3:64145733..64148089-chr6:133139687..133142420,2	MCF-7	breast:
48	chr1:853806..855355-chr6:133134480..133137289,2	MCF-7	breast:
49	chr6:133133683..133137845-chr6:133157752..133163297,5	K562	blood:
50	chr19:58873348..58874285-chr6:133135194..133136031,2	Hela-S3	cervix:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf192-1	chr6:133134432-133134602	XLOC_005834
2	lnc-C6orf192-1	chr6:133125513-133125727	XLOC_005834
3	lnc-C6orf192-1	chr6:133125837-133126090	XLOC_005834

No data

Variant related genes	Relation type
SNORD101	TF binding region
RPS12	TF binding region
SNORA33	TF binding region
SNORD100	TF binding region
SNORD101	CpG island
RPS12	CpG island
SNORA33	CpG island
SNORD100	CpG island
ENSG00000136631	chromatin interactions
ENSG00000269054	chromatin interactions
ENSG00000146409	chromatin interactions
ENSG00000106399	chromatin interactions
ENSG00000238059	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000227954	chromatin interactions
ENSG00000200534	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000136807	chromatin interactions
ENSG00000079950	chromatin interactions
ENSG00000206754	chromatin interactions
ENSG00000170190	chromatin interactions
ENSG00000146399	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000085365	chromatin interactions
ENSG00000100207	chromatin interactions
ENSG00000258429	chromatin interactions
ENSG00000012048	chromatin interactions
ENSG00000234484	chromatin interactions
ENSG00000158710	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000028839	chromatin interactions
ENSG00000095066	chromatin interactions
ENSG00000005469	chromatin interactions
ENSG00000174586	chromatin interactions
ENSG00000131725	chromatin interactions
ENSG00000266070	chromatin interactions
ENSG00000152818	chromatin interactions
ENSG00000182165	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000119559	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000255145	chromatin interactions
ENSG00000268050	chromatin interactions
ENSG00000104885	chromatin interactions
ENSG00000245556	chromatin interactions
ENSG00000223764	chromatin interactions
ENSG00000268230	chromatin interactions
ENSG00000146410	chromatin interactions
ENSG00000219545	chromatin interactions
ENSG00000112303	chromatin interactions
ENSG00000185088	chromatin interactions
ENSG00000187595	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000093134	chromatin interactions
ENSG00000271488	chromatin interactions
ENSG00000204055	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000237110	chromatin interactions
ENSG00000235415	chromatin interactions
ENSG00000218194	chromatin interactions
ENSG00000136874	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000273015	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000116514	chromatin interactions
ENSG00000221500	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000072786	chromatin interactions
SMAD5	miRNA target sites
SFRS5	miRNA target sites
LPP	miRNA target sites

Extended variants
information (count: 1929 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9493446	chr6:133125643-133125644	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548866251	chr6:133125645-133125646	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs147949682	chr6:133125687-133125688	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs183141317	chr6:133125741-133125742	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs551472073	chr6:133125743-133125744	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs571744034	chr6:133125844-133125845	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs9493447	chr6:133125900-133125901	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs9493448	chr6:133125933-133125934	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567869610	chr6:133125936-133125937	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs572552324	chr6:133126043-133126044	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs553056056	chr6:133126055-133126056	Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs536796851	chr6:133126101-133126102	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs1073511	chr6:133126110-133126111	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574897670	chr6:133126156-133126157	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs1073512	chr6:133126158-133126159	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs9493449	chr6:133126179-133126180	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557464337	chr6:133126194-133126195	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs375938726	chr6:133126199-133126200	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs140150170	chr6:133126216-133126217	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs36123789	chr6:133126220-133126221	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs397887956	chr6:133126221-133126222	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs562996608	chr6:133126223-133126224	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs546149373	chr6:133126227-133126228	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs141131496	chr6:133126275-133126276	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs559636840	chr6:133126291-133126292	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs528356549	chr6:133126313-133126314	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs371775140	chr6:133126328-133126329	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs192970035	chr6:133126368-133126369	Weak transcription Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs528342021	chr6:133126414-133126415	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs184262521	chr6:133126420-133126421	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs59646391	chr6:133126438-133126439	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs530887983	chr6:133126556-133126557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200118958	chr6:133126587-133126588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530333883	chr6:133126591-133126592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546857175	chr6:133126610-133126611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371851102	chr6:133126611-133126612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538953188	chr6:133126620-133126621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559163409	chr6:133126631-133126632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570912411	chr6:133126642-133126643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs188325946	chr6:133126682-133126683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs556649826	chr6:133126721-133126722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573384203	chr6:133126740-133126741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149066604	chr6:133126752-133126753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12195249	chr6:133126763-133126764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs550254074	chr6:133126799-133126800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12215084	chr6:133126801-133126802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs148117059	chr6:133126808-133126809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544986961	chr6:133126810-133126811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62425110	chr6:133126819-133126820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs12201540	chr6:133126857-133126858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:82)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133120400-133126200	Weak transcription	Fetal Heart	heart
2	chr6:133120800-133134000	Weak transcription	Pancreas	Pancrea
3	chr6:133121200-133128000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:133121200-133129000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:133121200-133133600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:133126200-133126400	Active TSS	Fetal Heart	heart
7	chr6:133128000-133131200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:133129000-133129200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:133129200-133129800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:133129400-133130000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr6:133129800-133130000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:133130000-133130600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr6:133130000-133133600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr6:133130600-133131000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:133131000-133131200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr6:133131200-133131600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:133131200-133133200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr6:133131600-133133600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:133131800-133133400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:133132200-133132800	Enhancers	K562	blood
21	chr6:133132200-133133000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:133132200-133133600	Enhancers	Adipose Nuclei	Adipose
23	chr6:133132400-133132800	Enhancers	Fetal Lung	lung
24	chr6:133132400-133133200	Enhancers	Liver	Liver
25	chr6:133132400-133133400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr6:133132600-133132800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr6:133132600-133132800	Enhancers	Small Intestine	intestine
28	chr6:133132600-133133400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr6:133132600-133133600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:133132600-133133600	Enhancers	HepG2	liver
31	chr6:133132800-133133000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:133132800-133133000	Flanking Active TSS	K562	blood
33	chr6:133132800-133133400	Enhancers	Stomach Mucosa	stomach
34	chr6:133132800-133133600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:133132800-133133600	Weak transcription	Fetal Lung	lung
36	chr6:133132800-133133600	Weak transcription	Small Intestine	intestine
37	chr6:133133000-133133200	Enhancers	Fetal Muscle Trunk	muscle
38	chr6:133133000-133133400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr6:133133000-133133400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:133133000-133133600	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:133133000-133133600	Enhancers	Duodenum Mucosa	Duodenum
42	chr6:133133000-133133600	Enhancers	K562	blood
43	chr6:133133000-133133600	Enhancers	NHLF	lung
44	chr6:133133200-133133400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:133133200-133133400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr6:133133200-133133400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr6:133133200-133133400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:133133200-133133400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr6:133133200-133133400	Flanking Active TSS	Liver	Liver
50	chr6:133133200-133133400	Enhancers	NHEK	skin

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