Variant report

Variant	nsv1020067
Chromosome Location	chr6:150730783-150870708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1049)
CpG islands
(count:427)
Chromatin interactive
region (count:70)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1049 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150739351-150739824	K562	blood:	n/a	n/a
2	ARID3A	chr6:150869690-150869835	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:150740211-150740423	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:150856592-150857436	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:150868956-150869252	HepG2	liver:	n/a	n/a
6	ATF1	chr6:150820946-150821189	K562	blood:	n/a	n/a
7	ATF1	chr6:150739202-150739619	K562	blood:	n/a	n/a
8	ATF1	chr6:150767603-150767716	K562	blood:	n/a	n/a
9	ATF2	chr6:150739291-150739724	GM12878	blood:	n/a	n/a
10	ATF2	chr6:150739247-150739780	GM12878	blood:	n/a	n/a
11	BACH1	chr6:150740232-150740513	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr6:150812626-150812895	GM12878	blood:	n/a	chr6:150812742-150812753
13	BATF	chr6:150812652-150812880	GM12878	blood:	n/a	chr6:150812742-150812753
14	BATF	chr6:150804211-150804420	GM12878	blood:	n/a	chr6:150804354-150804364 chr6:150804353-150804364
15	BHLHE40	chr6:150740250-150740590	HepG2	liver:	n/a	chr6:150740427-150740443
16	BHLHE40	chr6:150730961-150731007	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:150772195-150772196	K562	blood:	n/a	n/a
18	BHLHE40	chr6:150740330-150740549	A549	lung:	n/a	chr6:150740427-150740443
19	BHLHE40	chr6:150740226-150740511	GM12878	blood:	n/a	chr6:150740427-150740443
20	BRCA1	chr6:150813075-150813078	HepG2	liver:	n/a	n/a
21	CBX3	chr6:150756959-150757295	K562	blood:	n/a	n/a
22	CBX3	chr6:150746064-150746373	K562	blood:	n/a	n/a
23	CBX3	chr6:150740193-150740740	K562	blood:	n/a	n/a
24	CBX3	chr6:150740231-150740564	K562	blood:	n/a	n/a
25	CEBPB	chr6:150819241-150819564	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:150819309-150819552	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:150739156-150739685	H1-hESC	embryonic stem cell:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
28	CEBPB	chr6:150856392-150856635	A549	lung:	n/a	n/a
29	CEBPB	chr6:150786105-150786330	HepG2	liver:	n/a	chr6:150786191-150786202
30	CEBPB	chr6:150856362-150856807	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:150739101-150739635	HepG2	liver:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
32	CEBPB	chr6:150824853-150825017	K562	blood:	n/a	n/a
33	CEBPB	chr6:150738855-150740583	HCT-116	colon:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
34	CEBPB	chr6:150820940-150821306	Hela-S3	cervix:	n/a	chr6:150821222-150821233 chr6:150821222-150821235 chr6:150821221-150821238
35	CEBPB	chr6:150739133-150739866	A549	lung:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
36	CEBPB	chr6:150836053-150836490	MCF-7	breast:	n/a	n/a
37	CEBPB	chr6:150740292-150740478	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:150739029-150739888	IMR90	lung:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
39	CEBPB	chr6:150870012-150870231	IMR90	lung:	n/a	chr6:150870121-150870132
40	CEBPB	chr6:150738863-150740109	HCT-116	colon:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
41	CEBPB	chr6:150869953-150870272	HepG2	liver:	n/a	chr6:150870121-150870132
42	CEBPB	chr6:150746460-150746514	HepG2	liver:	n/a	chr6:150746471-150746482
43	CEBPB	chr6:150870053-150870191	H1-hESC	embryonic stem cell:	n/a	chr6:150870121-150870132
44	CEBPB	chr6:150739227-150739806	K562	blood:	n/a	chr6:150739263-150739271
45	CEBPB	chr6:150819344-150819544	A549	lung:	n/a	n/a
46	CEBPB	chr6:150836242-150836382	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:150870008-150870165	K562	blood:	n/a	chr6:150870121-150870132
48	CEBPB	chr6:150856420-150856620	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:150739050-150739984	Hela-S3	cervix:	n/a	chr6:150739202-150739213 chr6:150739263-150739271
50	CEBPB	chr6:150813678-150813804	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150738947-150738997	ProgFib	skin:	n/a
2	chr6:150739173-150739223	BE2_C	brain:	n/a
3	chr6:150740393-150740443	HAEpiC	amniotic membrane:	n/a
4	chr6:150800280-150800330	HEEpiC	esophagus:	n/a
5	chr6:150739173-150739223	U87	brain:	n/a
6	chr6:150740393-150740443	AG10803	skin:	n/a
7	chr6:150773917-150773967	NH-A	brain:	n/a
8	chr6:150739173-150739223	AG09309	skin:	n/a
9	chr6:150739173-150739223	NHDF-neo	bronchial:	n/a
10	chr6:150773917-150773967	GM12878	blood:	n/a
11	chr6:150739173-150739223	Caco-2	colon:	n/a
12	chr6:150739173-150739223	SAEC	small airway:	n/a
13	chr6:150740375-150740425	H1-hESC	embryonic stem cell:	embryo
14	chr6:150738947-150738997	NT2-D1	testis:	n/a
15	chr6:150800280-150800330	K562	blood:	n/a
16	chr6:150740375-150740425	HCPEpiC	choroid plexus:	n/a
17	chr6:150740393-150740443	RPTEC	kidney:	n/a
18	chr6:150740393-150740443	HIPEpiC	eye:	n/a
19	chr6:150739454-150739504	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:150738947-150738997	AG09319	gingival:	n/a
21	chr6:150739454-150739504	HEEpiC	esophagus:	n/a
22	chr6:150740375-150740425	AG04450	lung:	fetal
23	chr6:150740375-150740425	HIPEpiC	eye:	n/a
24	chr6:150740375-150740425	AG09309	skin:	n/a
25	chr6:150738947-150738997	HUVEC	blood vessel:	n/a
26	chr6:150738947-150738997	GM06990	blood:	n/a
27	chr6:150800280-150800330	Hepatocyte	liver:	n/a
28	chr6:150739173-150739223	AG09319	gingival:	n/a
29	chr6:150739454-150739504	IMR90	lung:	fetal
30	chr6:150800280-150800330	HIPEpiC	eye:	n/a
31	chr6:150740393-150740443	Hepatocyte	liver:	n/a
32	chr6:150738947-150738997	Hela-S3	cervix:	n/a
33	chr6:150740393-150740443	HRPEpiC	eye:	n/a
34	chr6:150740393-150740443	GM12892	blood:	n/a
35	chr6:150739173-150739223	SK-N-SH_RA	brain:	n/a
36	chr6:150739454-150739504	RPTEC	kidney:	n/a
37	chr6:150773917-150773967	Hepatocyte	liver:	n/a
38	chr6:150739454-150739504	ovcar-3	ovarian:	n/a
39	chr6:150800280-150800330	HMEC	breast:	n/a
40	chr6:150738947-150738997	NB4	blood:	n/a
41	chr6:150738947-150738997	Hepatocyte	liver:	n/a
42	chr6:150740393-150740443	SK-N-SH	brain:	n/a
43	chr6:150739454-150739504	GM12892	blood:	n/a
44	chr6:150739454-150739504	SKMC	muscle:	n/a
45	chr6:150740375-150740425	PANC-1	pancreas:	n/a
46	chr6:150738947-150738997	SK-N-SH	brain:	n/a
47	chr6:150739454-150739504	MCF-7	breast:	n/a
48	chr6:150738947-150738997	SK-N-MC	brain:	n/a
49	chr6:150800280-150800330	GM19239	blood:	n/a
50	chr6:150800280-150800330	A549	lung:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:150672100..150674423-chr6:150737681..150739812,2	K562	blood:
2	chr6:150731412..150734298-chr6:150879211..150881939,2	K562	blood:
3	chr16:85348513..85351058-chr6:150779289..150781438,2	MCF-7	breast:
4	chr6:150820645..150822727-chr6:150824228..150825998,2	K562	blood:
5	chr6:150739022..150740801-chr6:151062707..151063998,9	MCF-7	breast:
6	chr6:150863000..150865080-chr6:150869202..150870709,2	K562	blood:
7	chr6:150854421..150856907-chr6:150860372..150863256,2	MCF-7	breast:
8	chr6:150817308..150819383-chr6:150821139..150822761,2	K562	blood:
9	chr6:150858643..150861809-chr6:150864654..150868383,3	K562	blood:
10	chr6:150858643..150861809-chr6:150864654..150868383,3	K562	blood:
11	chr6:150812964..150816383-chr6:150817541..150822095,5	K562	blood:
12	chr6:150812964..150816383-chr6:150817541..150822095,5	K562	blood:
13	chr6:150807751..150809812-chr6:150811234..150814298,3	K562	blood:
14	chr6:150763305..150765361-chr6:150768135..150769999,2	K562	blood:
15	chr6:150739275..150740853-chr6:151135613..151137022,11	K562	blood:
16	chr6:150739151..150742146-chr6:150742181..150746418,5	K562	blood:
17	chr6:150739007..150740606-chr6:151135993..151137184,5	MCF-7	breast:
18	chr6:150800512..150803479-chr6:150810319..150812165,2	MCF-7	breast:
19	chr6:150753172..150755585-chr6:150755999..150757567,2	K562	blood:
20	chr6:150861044..150862970-chr6:150863595..150866527,2	MCF-7	breast:
21	chr6:150722584..150723485-chr6:150739885..150740902,3	K562	blood:
22	chr6:150835896..150838702-chr6:150854889..150856398,2	MCF-7	breast:
23	chr6:150725228..150728366-chr6:150731535..150733828,3	K562	blood:
24	chr6:150820645..150822727-chr6:150824228..150825998,2	K562	blood:
25	chr6:150846296..150849812-chr6:150852359..150857324,4	K562	blood:
26	chr6:150739171..150740801-chr6:150920989..150922541,9	MCF-7	breast:
27	chr6:150817308..150819383-chr6:150821139..150822761,2	K562	blood:
28	chr6:150863000..150865080-chr6:150869202..150870709,2	K562	blood:
29	chr6:150739625..150740200-chr6:151007043..151007665,2	MCF-7	breast:
30	chr6:150806855..150809448-chr6:150811234..150813450,2	K562	blood:
31	chr6:150830743..150834012-chr6:150835042..150837409,4	K562	blood:
32	chr6:150847959..150850613-chr6:150920501..150922911,2	K562	blood:
33	chr6:150835775..150838453-chr6:150841014..150842645,2	K562	blood:
34	chr6:150720777..150722938-chr6:150732800..150734541,2	MCF-7	breast:
35	chr6:150778759..150781417-chr6:150782165..150783683,2	K562	blood:
36	chr6:150846296..150849812-chr6:150852359..150857324,4	K562	blood:
37	chr6:150832697..150834202-chr6:150837344..150839504,2	K562	blood:
38	chr6:150772857..150774646-chr6:150776022..150779797,3	K562	blood:
39	chr6:150738306..150738871-chr6:151135977..151136495,2	MCF-7	breast:
40	chr6:150835896..150838702-chr6:150854889..150856398,2	MCF-7	breast:
41	chr6:150861044..150862970-chr6:150863595..150866527,2	MCF-7	breast:
42	chr6:150806855..150809448-chr6:150811234..150813450,2	K562	blood:
43	chr6:150739101..150740605-chr6:151135391..151136891,7	MCF-7	breast:
44	chr6:150737527..150738078-chr6:151135893..151136531,2	K562	blood:
45	chr6:150744561..150747232-chr6:150752463..150755073,2	K562	blood:
46	chr6:150856840..150859421-chr6:151018731..151021434,2	MCF-7	breast:
47	chr6:150783745..150786487-chr6:150807804..150809772,2	K562	blood:
48	chr6:150753172..150755585-chr6:150755999..150757567,2	K562	blood:
49	chr6:150863886..150866190-chr6:150885198..150886787,2	K562	blood:
50	chr6:150763305..150765361-chr6:150768135..150769999,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP3-5	chr6:150830742-150831436	NONHSAT115541
2	lnc-ULBP3-5	chr6:150829763-150829820	NONHSAT115541
3	lnc-ULBP3-5	chr6:150825947-150826055	NONHSAT115541

No data

Variant related genes	Relation type
ENSG00000219622	TF binding region
ENSG00000219622	CpG island
ENSG00000120278	chromatin interactions
ENSG00000219622	chromatin interactions
ENSG00000232891	chromatin interactions

Extended variants
information (count: 4083 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4083 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9480385	chr6:150730783-150730784	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373060786	chr6:150730784-150730785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113295166	chr6:150730821-150730822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562165281	chr6:150730836-150730837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575822777	chr6:150730837-150730838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11963221	chr6:150730838-150730839	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs145682307	chr6:150730869-150730870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533054735	chr6:150730913-150730914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546619790	chr6:150730953-150730954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560147546	chr6:150730971-150730972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs650597	chr6:150730975-150730976	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549288926	chr6:150731003-150731004	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs545242978	chr6:150731038-150731039	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs538087584	chr6:150731115-150731116	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs537983777	chr6:150731127-150731128	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs551158076	chr6:150731143-150731144	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs115285900	chr6:150731201-150731202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532330852	chr6:150731213-150731214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73782619	chr6:150731225-150731226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs638990	chr6:150731232-150731233	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs573162349	chr6:150731288-150731289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111415132	chr6:150731330-150731331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111485901	chr6:150731381-150731382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571591906	chr6:150731437-150731438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184680193	chr6:150731441-150731442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534077714	chr6:150731450-150731451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558759032	chr6:150731453-150731454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138347592	chr6:150731471-150731472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370386923	chr6:150731531-150731532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35077610	chr6:150731541-150731542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544863073	chr6:150731627-150731628	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs590179	chr6:150731655-150731656	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs589890	chr6:150731667-150731668	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs62432544	chr6:150731669-150731670	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs372185669	chr6:150731671-150731672	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs76287976	chr6:150731688-150731689	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs374150298	chr6:150731721-150731722	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs12523895	chr6:150731748-150731749	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs575441626	chr6:150731776-150731777	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs9478731	chr6:150731917-150731918	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs548694954	chr6:150731979-150731980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562850734	chr6:150732006-150732007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190172468	chr6:150732043-150732044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551172008	chr6:150732052-150732053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576063996	chr6:150732115-150732116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587982	chr6:150732147-150732148	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs9478732	chr6:150732201-150732202	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546717131	chr6:150732296-150732297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141335400	chr6:150732346-150732347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535883962	chr6:150732379-150732380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150724800-150731000	Weak transcription	Lung	lung
2	chr6:150725400-150731000	Weak transcription	Right Ventricle	heart
3	chr6:150725400-150733000	Weak transcription	Stomach Mucosa	stomach
4	chr6:150725600-150731200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:150727600-150734000	Enhancers	Osteobl	bone
6	chr6:150728400-150732400	Enhancers	Fetal Lung	lung
7	chr6:150728800-150732000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:150729600-150731200	Enhancers	Esophagus	oesophagus
9	chr6:150729800-150731000	Enhancers	NHEK	skin
10	chr6:150729800-150732200	Enhancers	Liver	Liver
11	chr6:150730000-150730800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:150730000-150731200	Enhancers	Gastric	stomach
13	chr6:150730000-150731400	Enhancers	Duodenum Mucosa	Duodenum
14	chr6:150730000-150731400	Enhancers	Left Ventricle	heart
15	chr6:150730000-150731400	Enhancers	Pancreas	Pancrea
16	chr6:150730000-150731400	Enhancers	HMEC	breast
17	chr6:150730000-150732200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:150730200-150731400	Enhancers	Fetal Muscle Trunk	muscle
19	chr6:150730200-150731400	Enhancers	Fetal Muscle Leg	muscle
20	chr6:150730200-150731800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr6:150730200-150732800	Enhancers	Fetal Heart	heart
22	chr6:150730200-150732800	Enhancers	Fetal Kidney	kidney
23	chr6:150730400-150731000	Enhancers	Hela-S3	cervix
24	chr6:150730400-150731200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:150730400-150731200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:150730400-150731200	Enhancers	Stomach Smooth Muscle	stomach
27	chr6:150730400-150731200	Enhancers	Spleen	Spleen
28	chr6:150730400-150731400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:150730400-150731400	Enhancers	Primary B cells from cord blood	blood
30	chr6:150730400-150731400	Enhancers	Right Atrium	heart
31	chr6:150730400-150732000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:150730400-150732000	Enhancers	Adipose Nuclei	Adipose
33	chr6:150730400-150732200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr6:150730400-150732400	Enhancers	Fetal Stomach	stomach
35	chr6:150730400-150733000	Enhancers	HSMMtube	muscle
36	chr6:150730600-150731000	Enhancers	Brain Angular Gyrus	brain
37	chr6:150730600-150731200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:150730600-150731200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:150730600-150731400	Enhancers	Primary hematopoietic stem cells	blood
40	chr6:150730600-150731400	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr6:150730600-150731400	Enhancers	Small Intestine	intestine
42	chr6:150730600-150731800	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr6:150730600-150732400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr6:150730600-150732600	Enhancers	Colon Smooth Muscle	Colon
45	chr6:150730600-150733600	Enhancers	NH-A	brain
46	chr6:150730800-150731000	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr6:150730800-150731200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr6:150730800-150731200	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr6:150730800-150731400	Enhancers	Primary B cells from peripheral blood	blood
50	chr6:150730800-150731400	Enhancers	Fetal Intestine Large	intestine

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