Variant report

Variant	nsv1022714
Chromosome Location	chr6:56729767-56826642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2652)
CpG islands
(count:1405)
Chromatin interactive
region (count:101)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2652 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:56740789-56741128	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:56769406-56769670	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:56819983-56820269	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:56733459-56733856	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:56819871-56820412	K562	blood:	n/a	n/a
6	ATF1	chr6:56771564-56771849	K562	blood:	n/a	n/a
7	ATF1	chr6:56798559-56798632	K562	blood:	n/a	n/a
8	ATF1	chr6:56780628-56781085	K562	blood:	n/a	n/a
9	ATF1	chr6:56755431-56755724	K562	blood:	n/a	n/a
10	ATF1	chr6:56814753-56815136	K562	blood:	n/a	n/a
11	ATF2	chr6:56755239-56756256	GM12878	blood:	n/a	n/a
12	ATF2	chr6:56820294-56820697	GM12878	blood:	n/a	n/a
13	ATF2	chr6:56819836-56820432	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:56818133-56818874	GM12878	blood:	n/a	n/a
15	ATF2	chr6:56755252-56755956	GM12878	blood:	n/a	n/a
16	ATF2	chr6:56819919-56821092	GM12878	blood:	n/a	n/a
17	ATF2	chr6:56819977-56820719	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr6:56818259-56818890	GM12878	blood:	n/a	n/a
19	ATF3	chr6:56755485-56755648	K562	blood:	n/a	n/a
20	ATF3	chr6:56819767-56820311	K562	blood:	n/a	chr6:56819820-56819829 chr6:56819932-56819941
21	ATF3	chr6:56819392-56819722	K562	blood:	n/a	chr6:56819516-56819525
22	ATF3	chr6:56819728-56820242	K562	blood:	n/a	chr6:56819820-56819829 chr6:56819932-56819941
23	ATF3	chr6:56755397-56755867	K562	blood:	n/a	n/a
24	BACH1	chr6:56818233-56820972	H1-hESC	embryonic stem cell:	n/a	chr6:56819593-56819607 chr6:56818672-56818686
25	BACH1	chr6:56815975-56816143	K562	blood:	n/a	n/a
26	BACH1	chr6:56819418-56819736	K562	blood:	n/a	chr6:56819593-56819607
27	BACH1	chr6:56821393-56821426	K562	blood:	n/a	n/a
28	BACH1	chr6:56755369-56755962	K562	blood:	n/a	n/a
29	BACH1	chr6:56803456-56803813	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:56755379-56755755	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:56821894-56822034	K562	blood:	n/a	n/a
32	BATF	chr6:56818395-56818704	GM12878	blood:	n/a	chr6:56818675-56818686
33	BATF	chr6:56755437-56755801	GM12878	blood:	n/a	chr6:56755573-56755583
34	BATF	chr6:56818274-56819000	GM12878	blood:	n/a	chr6:56818675-56818686
35	BATF	chr6:56755432-56755930	GM12878	blood:	n/a	chr6:56755573-56755583
36	BATF	chr6:56820373-56820898	GM12878	blood:	n/a	chr6:56820511-56820521
37	BCL11A	chr6:56818338-56818813	GM12878	blood:	n/a	n/a
38	BCL11A	chr6:56755415-56755814	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:56818245-56818837	GM12878	blood:	n/a	n/a
40	BCL3	chr6:56819954-56820443	A549	lung:	n/a	chr6:56820001-56820014 chr6:56820313-56820322
41	BCL3	chr6:56755419-56755885	GM12878	blood:	n/a	n/a
42	BCL3	chr6:56819927-56820328	GM12878	blood:	n/a	chr6:56820001-56820014 chr6:56820313-56820322
43	BCLAF1	chr6:56820479-56821024	GM12878	blood:	n/a	chr6:56820510-56820519
44	BCLAF1	chr6:56819863-56820348	GM12878	blood:	n/a	chr6:56819877-56819890 chr6:56819880-56819893 chr6:56819882-56819891 chr6:56820001-56820014 chr6:56820313-56820322 chr6:56819885-56819894
45	BCLAF1	chr6:56755418-56756042	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:56819882-56821005	GM12878	blood:	n/a	chr6:56820510-56820519 chr6:56819882-56819891 chr6:56820001-56820014 chr6:56820313-56820322 chr6:56819885-56819894
47	BCLAF1	chr6:56818137-56818833	GM12878	blood:	n/a	chr6:56818176-56818185
48	BHLHE40	chr6:56740732-56741167	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:56779736-56780104	K562	blood:	n/a	n/a
50	BHLHE40	chr6:56815889-56816082	K562	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56819432-56819482	HNPCEpiC	eye:	n/a
2	chr6:56777045-56777095	AG09309	skin:	n/a
3	chr6:56819432-56819482	HNPCEpiC	eye:	n/a
4	chr6:56777045-56777095	AG09309	skin:	n/a
5	chr6:56792931-56792981	SKMC	muscle:	n/a
6	chr6:56818479-56818529	A549	lung:	n/a
7	chr6:56818479-56818529	GM19239	blood:	n/a
8	chr6:56755566-56755616	GM12891	blood:	n/a
9	chr6:56733060-56733110	MCF-7	breast:	n/a
10	chr6:56820087-56820137	HEEpiC	esophagus:	n/a
11	chr6:56820808-56820858	Hepatocyte	liver:	n/a
12	chr6:56820286-56820336	HRCEpiC	kidney:	n/a
13	chr6:56819612-56819662	Caco-2	colon:	n/a
14	chr6:56777045-56777095	Hepatocyte	liver:	n/a
15	chr6:56765087-56765137	T-47D	breast:	n/a
16	chr6:56819432-56819482	NB4	blood:	n/a
17	chr6:56820386-56820436	SK-N-SH_RA	brain:	n/a
18	chr6:56815929-56815979	HCT-116	colon:	n/a
19	chr6:56820386-56820436	GM12891	blood:	n/a
20	chr6:56733060-56733110	HepG2	liver:	n/a
21	chr6:56819432-56819482	PANC-1	pancreas:	n/a
22	chr6:56819615-56819665	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:56819912-56819962	SK-N-MC	brain:	n/a
24	chr6:56815929-56815979	U87	brain:	n/a
25	chr6:56815929-56815979	ovcar-3	ovarian:	n/a
26	chr6:56820869-56820919	GM12891	blood:	n/a
27	chr6:56765087-56765137	GM19239	blood:	n/a
28	chr6:56765087-56765137	AG04450	lung:	fetal
29	chr6:56820869-56820919	HCPEpiC	choroid plexus:	n/a
30	chr6:56820778-56820828	HCT-116	colon:	n/a
31	chr6:56733060-56733110	GM19239	blood:	n/a
32	chr6:56818479-56818529	HCPEpiC	choroid plexus:	n/a
33	chr6:56819623-56819673	SAEC	small airway:	n/a
34	chr6:56820808-56820858	H1-hESC	embryonic stem cell:	embryo
35	chr6:56819612-56819662	ECC-1	luminal epithelium:	n/a
36	chr6:56820869-56820919	HepG2	liver:	n/a
37	chr6:56755566-56755616	ECC-1	luminal epithelium:	n/a
38	chr6:56792931-56792981	GM12892	blood:	n/a
39	chr6:56819615-56819665	GM12892	blood:	n/a
40	chr6:56819432-56819482	AG09309	skin:	n/a
41	chr6:56820286-56820336	BE2_C	brain:	n/a
42	chr6:56819615-56819665	HRCEpiC	kidney:	n/a
43	chr6:56820286-56820336	GM12891	blood:	n/a
44	chr6:56820869-56820919	BJ	skin:	n/a
45	chr6:56820087-56820137	HMEC	breast:	n/a
46	chr6:56777045-56777095	K562	blood:	n/a
47	chr6:56820778-56820828	NHDF-neo	bronchial:	n/a
48	chr6:56755566-56755616	Caco-2	colon:	n/a
49	chr6:56777045-56777095	PANC-1	pancreas:	n/a
50	chr6:56818409-56818459	H1-hESC	embryonic stem cell:	embryo

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:56821886..56823483-chr6:56846659..56848373,2	MCF-7	breast:
2	chr6:56813560..56816424-chr6:56821895..56824578,2	K562	blood:
3	chr6:56818586..56820160-chr6:56954804..56956394,2	K562	blood:
4	chr6:56795022..56797639-chr6:56802844..56804905,2	K562	blood:
5	chr6:56799400..56801740-chr6:56804250..56805836,2	K562	blood:
6	chr6:56820267..56822074-chr6:56879367..56881411,2	K562	blood:
7	chr6:56743268..56744831-chr6:56747772..56749482,2	MCF-7	breast:
8	chr6:56777418..56779642-chr6:56786166..56787815,2	MCF-7	breast:
9	chr6:56777926..56779935-chr6:56789816..56792167,2	K562	blood:
10	chr6:56818015..56821855-chr6:57180367..57183028,4	K562	blood:
11	chr6:56780041..56782514-chr6:56808634..56811006,2	K562	blood:
12	chr6:56820330..56821970-chr6:56922226..56924549,2	MCF-7	breast:
13	chr6:56716516..56717082-chr6:56820161..56820759,2	MCF-7	breast:
14	chr6:56807429..56808990-chr6:56818714..56821233,2	MCF-7	breast:
15	chr6:56785340..56787401-chr6:56789206..56791573,2	MCF-7	breast:
16	chr6:56779944..56782895-chr6:56786364..56788046,2	MCF-7	breast:
17	chr6:56769451..56770050-chr6:56819340..56821302,7	MCF-7	breast:
18	chr6:56763562..56765199-chr6:56770424..56772449,2	MCF-7	breast:
19	chr6:56819016..56821758-chr6:56822095..56823994,2	K562	blood:
20	chr6:56767464..56768319-chr6:56820397..56821373,5	MCF-7	breast:
21	chr6:56792046..56794849-chr6:56818085..56820101,2	K562	blood:
22	chr6:56825122..56826633-chr6:56914497..56917347,2	K562	blood:
23	chr6:56767335..56769579-chr6:56770902..56774646,3	K562	blood:
24	chr6:56809927..56811973-chr6:56817461..56820564,4	MCF-7	breast:
25	chr6:56795022..56797639-chr6:56802844..56804905,2	K562	blood:
26	chr6:56799400..56801740-chr6:56804250..56805836,2	K562	blood:
27	chr6:56777418..56779642-chr6:56786166..56787815,2	MCF-7	breast:
28	chr6:56726286..56729119-chr6:56729880..56733046,4	MCF-7	breast:
29	chr6:56773027..56775523-chr6:56776633..56778873,3	K562	blood:
30	chr6:56765319..56768240-chr6:56782219..56784389,2	K562	blood:
31	chr3:53925577..53926163-chr6:56819278..56819811,2	Hela-S3	cervix:
32	chr6:56767464..56768319-chr6:56820397..56821373,5	MCF-7	breast:
33	chr6:56817930..56821539-chr6:56909452..56912838,6	K562	blood:
34	chr6:56785340..56787401-chr6:56789206..56791573,2	MCF-7	breast:
35	chr6:56767380..56768433-chr6:56825743..56826632,5	MCF-7	breast:
36	chr6:56725702..56727982-chr6:56732126..56734324,2	K562	blood:
37	chr6:56793845..56796346-chr6:150069714..150072289,2	MCF-7	breast:
38	chr6:56790222..56793074-chr6:56811865..56815272,3	K562	blood:
39	chr6:56767335..56769579-chr6:56770902..56774646,3	K562	blood:
40	chr6:56769038..56769893-chr6:57181008..57181695,4	K562	blood:
41	chr6:56722965..56725223-chr6:56732847..56735248,2	K562	blood:
42	chr6:56819190..56819889-chr8:141520799..141521484,2	Hela-S3	cervix:
43	chr6:56817328..56823856-chr6:56824167..56831366,18	K562	blood:
44	chr6:56790222..56793074-chr6:56811865..56815272,3	K562	blood:
45	chr6:56741671..56743522-chr6:56818559..56820649,2	K562	blood:
46	chr6:56714424..56718313-chr6:56818301..56821248,4	MCF-7	breast:
47	chr6:56748557..56750730-chr6:57036166..57038744,2	K562	blood:
48	chr6:56821970..56823839-chr6:57043056..57044628,2	K562	blood:
49	chr10:101380540..101381425-chr6:56819022..56819785,2	NB4	blood:
50	chr6:56770313..56772562-chr6:56773630..56775659,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BEND6-2	chr6:56735989-56736541	NONHSAT113251
2	lnc-RAB23-10	chr6:56817639-56818372	NONHSAT113254

No data

Variant related genes	Relation type
BEND6	TF binding region
RNU6-626P	TF binding region
RPL17P26	TF binding region
DST	TF binding region
BEND6	CpG island
RNU6-626P	CpG island
RPL17P26	CpG island
DST	CpG island
ENSG00000151914	chromatin interactions
ENSG00000168116	chromatin interactions
ENSG00000260475	chromatin interactions
ENSG00000112200	chromatin interactions
ENSG00000135829	chromatin interactions
ENSG00000120253	chromatin interactions
ENSG00000226803	chromatin interactions
ENSG00000146143	chromatin interactions
ENSG00000104472	chromatin interactions
ENSG00000200224	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000216854	chromatin interactions
ENSG00000151917	chromatin interactions
ENSG00000120265	chromatin interactions
ENSG00000113811	chromatin interactions
ENSG00000231441	chromatin interactions
ENSG00000112208	chromatin interactions

Extended variants
information (count: 3256 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3256 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75130396	chr6:56729817-56729818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546232683	chr6:56729887-56729888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150959895	chr6:56729939-56729940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181776003	chr6:56729982-56729983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556755190	chr6:56730014-56730015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113135780	chr6:56730036-56730037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112001266	chr6:56730060-56730061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539218166	chr6:56730064-56730065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556653605	chr6:56730074-56730075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558086627	chr6:56730087-56730088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs60584138	chr6:56730089-56730090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576756554	chr6:56730099-56730100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187325119	chr6:56730172-56730173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190984392	chr6:56730192-56730193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140868483	chr6:56730215-56730216	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs13214893	chr6:56730223-56730224	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs544711608	chr6:56730246-56730247	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs144616384	chr6:56730276-56730277	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs111767134	chr6:56730430-56730431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138517822	chr6:56730515-56730516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565525409	chr6:56730523-56730524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78722810	chr6:56730570-56730571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116205429	chr6:56730585-56730586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75542424	chr6:56730597-56730598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561746946	chr6:56730601-56730602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550671802	chr6:56730632-56730633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528849892	chr6:56730685-56730686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183089576	chr6:56730691-56730692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377547286	chr6:56730732-56730733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140442489	chr6:56730742-56730743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150374250	chr6:56730754-56730755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113110138	chr6:56730766-56730767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113356339	chr6:56730770-56730771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs60337113	chr6:56730786-56730787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189698551	chr6:56730826-56730827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35440408	chr6:56730853-56730854	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs113220966	chr6:56730860-56730861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149511501	chr6:56730926-56730927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556519538	chr6:56730970-56730971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114364785	chr6:56730997-56730998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188190057	chr6:56731016-56731017	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143999229	chr6:56731034-56731035	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572278040	chr6:56731038-56731039	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375004304	chr6:56731077-56731078	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138407278	chr6:56731094-56731095	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561384314	chr6:56731140-56731141	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192953507	chr6:56731144-56731145	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550350939	chr6:56731192-56731193	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562495439	chr6:56731195-56731196	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533094071	chr6:56731217-56731218	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56717400-56730200	Weak transcription	Ovary	ovary
2	chr6:56717800-56730400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:56718200-56731000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:56721800-56731200	Weak transcription	Brain Hippocampus Middle	brain
5	chr6:56723000-56732600	Weak transcription	Small Intestine	intestine
6	chr6:56724200-56733800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr6:56724600-56730400	Enhancers	Fetal Intestine Small	intestine
8	chr6:56725000-56730400	Enhancers	HUVEC	blood vessel
9	chr6:56725600-56730000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:56725600-56730200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr6:56725600-56731000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr6:56725600-56731200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:56725600-56734800	Enhancers	Hela-S3	cervix
14	chr6:56725800-56730400	Enhancers	Fetal Intestine Large	intestine
15	chr6:56726600-56730000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:56727000-56729800	Weak transcription	Colonic Mucosa	Colon
17	chr6:56727200-56734600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:56727400-56730600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:56727400-56730600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr6:56727600-56730600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:56727600-56730600	Enhancers	NHEK	skin
22	chr6:56727600-56734400	Enhancers	HMEC	breast
23	chr6:56727800-56734800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:56728000-56730000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:56728000-56730200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:56728000-56731800	Weak transcription	Spleen	Spleen
27	chr6:56728000-56734800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:56728000-56735000	Enhancers	HSMM	muscle
29	chr6:56728000-56735000	Enhancers	NHDF-Ad	bronchial
30	chr6:56728200-56730800	Enhancers	NHLF	lung
31	chr6:56728200-56733800	Enhancers	HSMMtube	muscle
32	chr6:56728200-56733800	Enhancers	Osteobl	bone
33	chr6:56728400-56729800	Weak transcription	Right Atrium	heart
34	chr6:56728400-56730200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:56728600-56730000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:56728800-56730000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:56728800-56734800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:56729000-56730200	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr6:56729000-56730400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr6:56729000-56733000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr6:56729200-56731800	Weak transcription	GM12878-XiMat	blood
42	chr6:56729200-56733000	Enhancers	A549	lung
43	chr6:56729400-56729800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr6:56729400-56731600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:56729400-56731800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:56729400-56731800	Weak transcription	NH-A	brain
47	chr6:56729600-56732200	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr6:56729800-56730000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr6:56729800-56730200	Enhancers	Colonic Mucosa	Colon
50	chr6:56729800-56730400	Enhancers	Right Atrium	heart

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