Variant report

Variant	nsv1020692
Chromosome Location	chr6:101136992-101426071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1826)
CpG islands
(count:916)
Chromatin interactive
region (count:148)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:101309874-101310730	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:101339060-101339651	K562	blood:	n/a	n/a
3	ARID3A	chr6:101167786-101168649	K562	blood:	n/a	n/a
4	ARID3A	chr6:101361710-101361821	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:101329171-101329282	K562	blood:	n/a	n/a
6	ARID3A	chr6:101328160-101329909	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:101396557-101397017	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:101416990-101417029	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:101328295-101328654	K562	blood:	n/a	n/a
10	ARID3A	chr6:101396704-101396823	K562	blood:	n/a	n/a
11	ARID3A	chr6:101167807-101168113	HepG2	liver:	n/a	n/a
12	ATF1	chr6:101329007-101329734	K562	blood:	n/a	n/a
13	ATF1	chr6:101249683-101249708	K562	blood:	n/a	n/a
14	ATF1	chr6:101168207-101168524	K562	blood:	n/a	n/a
15	ATF2	chr6:101340639-101340959	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:101328989-101329579	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:101328781-101329644	GM12878	blood:	n/a	n/a
18	ATF3	chr6:101329035-101329383	K562	blood:	n/a	chr6:101329222-101329236 chr6:101329076-101329085 chr6:101329299-101329308 chr6:101329222-101329242
19	BACH1	chr6:101307789-101307792	K562	blood:	n/a	n/a
20	BACH1	chr6:101329023-101329589	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr6:101298141-101298334	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:101328965-101329677	GM12878	blood:	n/a	chr6:101329234-101329247
23	BCLAF1	chr6:101328702-101329584	GM12878	blood:	n/a	chr6:101329234-101329247
24	BCLAF1	chr6:101328830-101329530	K562	blood:	n/a	chr6:101329234-101329247
25	BHLHE40	chr6:101328597-101329538	GM12878	blood:	n/a	chr6:101328973-101328989
26	BHLHE40	chr6:101396832-101396917	K562	blood:	n/a	n/a
27	BHLHE40	chr6:101328625-101329968	K562	blood:	n/a	chr6:101328973-101328989
28	BHLHE40	chr6:101330212-101330739	K562	blood:	n/a	n/a
29	BHLHE40	chr6:101257262-101257586	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:101167814-101167956	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:101328724-101329517	HepG2	liver:	n/a	chr6:101328973-101328989
32	BRCA1	chr6:101328995-101329495	GM12878	blood:	n/a	n/a
33	BRCA1	chr6:101372001-101373154	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr6:101329474-101329674	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr6:101396520-101396961	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr6:101329003-101329597	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr6:101328942-101329318	HepG2	liver:	n/a	n/a
38	BRCA1	chr6:101329902-101330016	HepG2	liver:	n/a	n/a
39	CBX3	chr6:101328683-101329649	HCT-116	colon:	n/a	n/a
40	CBX3	chr6:101328828-101329742	K562	blood:	n/a	n/a
41	CBX3	chr6:101346149-101346415	K562	blood:	n/a	n/a
42	CBX3	chr6:101346136-101346464	K562	blood:	n/a	n/a
43	CCNT2	chr6:101328683-101329932	K562	blood:	n/a	chr6:101328716-101328725
44	CCNT2	chr6:101168200-101168648	K562	blood:	n/a	n/a
45	CCNT2	chr6:101339079-101339553	K562	blood:	n/a	n/a
46	CCNT2	chr6:101396629-101397041	K562	blood:	n/a	n/a
47	CEBPB	chr6:101328247-101328744	A549	lung:	n/a	chr6:101328477-101328488 chr6:101328477-101328490 chr6:101328449-101328460 chr6:101328479-101328488 chr6:101328479-101328488 chr6:101328479-101328488 chr6:101328477-101328490
48	CEBPB	chr6:101162157-101162478	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:101338981-101339623	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:101350968-101351234	A549	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:101328941-101328991	Caco-2	colon:	n/a
2	chr6:101328941-101328991	Caco-2	colon:	n/a
3	chr6:101329504-101329554	AG10803	skin:	n/a
4	chr6:101329408-101329458	Hela-S3	cervix:	n/a
5	chr6:101325415-101325465	NHDF-neo	bronchial:	n/a
6	chr6:101329408-101329458	T-47D	breast:	n/a
7	chr6:101325415-101325465	Caco-2	colon:	n/a
8	chr6:101329408-101329458	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:101329304-101329354	SK-N-SH	brain:	n/a
10	chr6:101331608-101331658	HEEpiC	esophagus:	n/a
11	chr6:101308372-101308422	AG09309	skin:	n/a
12	chr6:101328941-101328991	SAEC	small airway:	n/a
13	chr6:101306732-101306782	BE2_C	brain:	n/a
14	chr6:101277371-101277421	MCF-7	breast:	n/a
15	chr6:101277371-101277421	SAEC	small airway:	n/a
16	chr6:101329504-101329554	AG09309	skin:	n/a
17	chr6:101329504-101329554	ovcar-3	ovarian:	n/a
18	chr6:101329304-101329354	ovcar-3	ovarian:	n/a
19	chr6:101329304-101329354	AoSMC	blood vessel:	n/a
20	chr6:101329307-101329357	AG09309	skin:	n/a
21	chr6:101325415-101325465	RPTEC	kidney:	n/a
22	chr6:101329408-101329458	GM19239	blood:	n/a
23	chr6:101328506-101328556	NH-A	brain:	n/a
24	chr6:101328941-101328991	HL-60	blood:	n/a
25	chr6:101331608-101331658	HepG2	liver:	n/a
26	chr6:101328941-101328991	ovcar-3	ovarian:	n/a
27	chr6:101308372-101308422	HRCEpiC	kidney:	n/a
28	chr6:101329169-101329219	AG04450	lung:	fetal
29	chr6:101329119-101329169	HRPEpiC	eye:	n/a
30	chr6:101329307-101329357	HMEC	breast:	n/a
31	chr6:101329504-101329554	LNCaP	prostate:	n/a
32	chr6:101211671-101211721	PrEC	prostate:	n/a
33	chr6:101329169-101329219	NT2-D1	testis:	n/a
34	chr6:101306732-101306782	PANC-1	pancreas:	n/a
35	chr6:101277371-101277421	IMR90	lung:	fetal
36	chr6:101308372-101308422	HEK293	kidney:	embryo
37	chr6:101325415-101325465	H1-hESC	embryonic stem cell:	embryo
38	chr6:101211671-101211721	HMEC	breast:	n/a
39	chr6:101308372-101308422	HAEpiC	amniotic membrane:	n/a
40	chr6:101308372-101308422	PFSK-1	brain:	n/a
41	chr6:101328506-101328556	BE2_C	brain:	n/a
42	chr6:101211671-101211721	RPTEC	kidney:	n/a
43	chr6:101331608-101331658	HEK293	kidney:	embryo
44	chr6:101306732-101306782	HNPCEpiC	eye:	n/a
45	chr6:101329304-101329354	AG10803	skin:	n/a
46	chr6:101328506-101328556	HNPCEpiC	eye:	n/a
47	chr6:101329504-101329554	MCF10A-Er-Src	breast:	n/a
48	chr6:101329504-101329554	HIPEpiC	eye:	n/a
49	chr6:101308372-101308422	BJ	skin:	n/a
50	chr6:101329504-101329554	HCT-116	colon:	n/a

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:100557223..100558887-chr6:101377861..101380025,2	K562	blood:
2	chr6:101379567..101381723-chr6:101382355..101385002,3	K562	blood:
3	chr6:101057024..101059544-chr6:101398692..101400539,2	K562	blood:
4	chr6:101333586..101335134-chr6:101338753..101340690,2	K562	blood:
5	chr6:101327650..101330005-chr6:101331234..101332758,2	K562	blood:
6	chr6:101316563..101319212-chr6:101321882..101324252,3	K562	blood:
7	chr6:101326886..101330925-chr6:101337161..101339877,4	MCF-7	breast:
8	chr6:101271641..101274156-chr6:101276043..101277591,3	K562	blood:
9	chr6:101321078..101323999-chr6:101327365..101330497,3	K562	blood:
10	chr6:101163027..101165840-chr6:101165855..101168378,2	K562	blood:
11	chr6:101151355..101153775-chr6:101154853..101157255,2	K562	blood:
12	chr6:101209490..101212282-chr6:101220701..101222580,2	MCF-7	breast:
13	chr6:101166704..101169523-chr6:101191232..101192828,2	K562	blood:
14	chr6:101162028..101164995-chr6:101165855..101170689,5	K562	blood:
15	chr6:101167975..101170318-chr6:101170858..101173669,2	MCF-7	breast:
16	chr6:101177164..101179781-chr6:101180643..101183395,2	K562	blood:
17	chr6:101302750..101305645-chr6:101307403..101308925,2	K562	blood:
18	chr6:101328331..101330007-chr6:101341794..101343997,2	K562	blood:
19	chr6:101151240..101154082-chr6:101158096..101159766,2	K562	blood:
20	chr6:101411504..101413327-chr6:101470844..101473368,2	MCF-7	breast:
21	chr6:101184266..101186701-chr6:101321079..101322607,2	K562	blood:
22	chr6:101309386..101311336-chr6:101316442..101318776,3	K562	blood:
23	chr6:101184266..101186701-chr6:101321079..101322607,2	K562	blood:
24	chr6:101309650..101312548-chr6:101313030..101314755,2	MCF-7	breast:
25	chr6:101227439..101228979-chr6:101229862..101232635,2	MCF-7	breast:
26	chr6:101232498..101235152-chr6:101238676..101241489,3	K562	blood:
27	chr6:101315511..101317723-chr6:101321403..101323944,2	K562	blood:
28	chr6:101243998..101244878-chr6:101416721..101417385,2	MCF-7	breast:
29	chr6:101166704..101169523-chr6:101191232..101192828,2	K562	blood:
30	chr6:101165938..101169618-chr6:101169739..101172714,3	K562	blood:
31	chr6:101209793..101211666-chr6:101212559..101214654,2	MCF-7	breast:
32	chr6:101141922..101144028-chr6:101167838..101169583,2	MCF-7	breast:
33	chr16:18801227..18802129-chr6:101329291..101329807,2	Hela-S3	cervix:
34	chr6:101221571..101223322-chr6:101224245..101227065,4	K562	blood:
35	chr6:101134397..101137375-chr6:101141087..101145140,3	K562	blood:
36	chr6:101239952..101241770-chr6:101249281..101252213,2	K562	blood:
37	chr6:101341802..101344010-chr6:101345674..101348065,2	K562	blood:
38	chr6:101286243..101289209-chr6:101295205..101297234,2	K562	blood:
39	chr6:101235770..101239248-chr6:101239414..101244156,4	K562	blood:
40	chr6:101309650..101312548-chr6:101313030..101314755,2	MCF-7	breast:
41	chr6:101167975..101170318-chr6:101170858..101173669,2	MCF-7	breast:
42	chr6:101302750..101305984-chr6:101307403..101310104,4	K562	blood:
43	chr6:101302750..101305645-chr6:101307403..101308925,2	K562	blood:
44	chr6:101341802..101344010-chr6:101345674..101348065,2	K562	blood:
45	chr6:101337316..101339556-chr6:101341141..101344086,2	K562	blood:
46	chr6:101139725..101141428-chr6:101141736..101143273,2	K562	blood:
47	chr6:101333586..101335134-chr6:101338753..101340690,2	K562	blood:
48	chr6:101155893..101159033-chr6:101162373..101164963,3	K562	blood:
49	chr6:101315815..101318038-chr6:101328933..101331740,2	MCF-7	breast:
50	chr6:101221571..101223322-chr6:101224245..101227065,4	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRIK2-5	chr6:101337479-101338214	NONHSAT114165
2	lnc-ASCC3-2	chr6:101334755-101334895	NONHSAT114164
3	lnc-ASCC3-2	chr6:101334427-101334598	NONHSAT114164
4	lnc-GRIK2-5	chr6:101336895-101338371	NONHSAT114163
5	lnc-GRIK2-5	chr6:101346251-101346864	NONHSAT114163
6	lnc-GRIK2-5	chr6:101332648-101334181	NONHSAT114163
7	lnc-GRIK2-2	chr6:101329347-101330863	ENSG00000260000.2
8	lnc-ASCC3-2	chr6:101335104-101335291	NONHSAT114164
9	lnc-GRIK2-4	chr6:101377136-101377267	NONHSAT114166
10	lnc-GRIK2-4	chr6:101391882-101391952	NONHSAT114166
11	lnc-GRIK2-2	chr6:101329347-101330847	ENSG00000260000.1
12	lnc-GRIK2-1	chr6:101410735-101411032	XLOC_005405
13	lnc-GRIK2-1	chr6:101410581-101410627	XLOC_005405

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ASCC3	hsa-miR-16-5p	chr6:101304922-101304942
2	ASCC3	hsa-miR-30a-5p	chr6:101305993-101306014

Variant related genes	Relation type
ENSG00000238999	TF binding region
ENSG00000260000	TF binding region
ENSG00000270987	TF binding region
ASCC3	TF binding region
ENSG00000238999	CpG island
ENSG00000260000	CpG island
ENSG00000270987	CpG island
ASCC3	CpG island
ENSG00000260000	chromatin interactions
ENSG00000149679	chromatin interactions
ENSG00000270987	chromatin interactions
ENSG00000250312	chromatin interactions
ENSG00000112249	chromatin interactions
ENSG00000134419	chromatin interactions
ENSG00000164465	chromatin interactions

Extended variants
information (count: 9386 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:9386 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572284011	chr6:101136994-101136995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573835833	chr6:101137022-101137023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540906999	chr6:101137025-101137026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559494064	chr6:101137050-101137051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371801419	chr6:101137104-101137105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541743359	chr6:101137106-101137107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577691405	chr6:101137146-101137147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564612996	chr6:101137179-101137180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147205687	chr6:101137180-101137181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189974225	chr6:101137281-101137282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs239206	chr6:101137332-101137333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs561434028	chr6:101137337-101137338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139573136	chr6:101137366-101137367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183331499	chr6:101137382-101137383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74355197	chr6:101137424-101137425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539172322	chr6:101137441-101137442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551111639	chr6:101137527-101137528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188071293	chr6:101137542-101137543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557144845	chr6:101137551-101137552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200438079	chr6:101137564-101137565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72941282	chr6:101137577-101137578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563252467	chr6:101137604-101137605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9498091	chr6:101137727-101137728	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs573896353	chr6:101137731-101137732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78634839	chr6:101137747-101137748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117112986	chr6:101137751-101137752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577431255	chr6:101137757-101137758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs239207	chr6:101137765-101137766	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs192807868	chr6:101137856-101137857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34174259	chr6:101137894-101137895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542718641	chr6:101137896-101137897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370084635	chr6:101137917-101137918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574952717	chr6:101138061-101138062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77712553	chr6:101138102-101138103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539737424	chr6:101138142-101138143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559618118	chr6:101138151-101138152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528282470	chr6:101138152-101138153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74978926	chr6:101138153-101138154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185318520	chr6:101138177-101138178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34807833	chr6:101138184-101138185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565406705	chr6:101138201-101138202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374662297	chr6:101138217-101138218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187843465	chr6:101138263-101138264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551150444	chr6:101138270-101138271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569412804	chr6:101138289-101138290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530787561	chr6:101138293-101138294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192870012	chr6:101138305-101138306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199644578	chr6:101138351-101138352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530212474	chr6:101138417-101138418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549917672	chr6:101138421-101138422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	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
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	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
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Autism	22543975	CNVD

Chromatin state (count:3419 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101093000-101145800	Weak transcription	Fetal Thymus	thymus
2	chr6:101100600-101149800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:101100800-101147600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:101100800-101164600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:101103800-101143600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:101110000-101147600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:101110400-101146800	Weak transcription	Primary T cells from cord blood	blood
8	chr6:101111200-101168200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:101111600-101168000	Weak transcription	NHDF-Ad	bronchial
10	chr6:101111800-101139800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:101111800-101147200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:101111800-101147200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:101111800-101168200	Weak transcription	Osteobl	bone
14	chr6:101112000-101161200	Weak transcription	HMEC	breast
15	chr6:101118600-101168000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr6:101118800-101147400	Weak transcription	GM12878-XiMat	blood
17	chr6:101119000-101147000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr6:101119200-101165600	Weak transcription	NH-A	brain
19	chr6:101119400-101181200	Weak transcription	Left Ventricle	heart
20	chr6:101119800-101146800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:101119800-101146800	Weak transcription	Primary B cells from cord blood	blood
22	chr6:101120000-101146800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:101120000-101147000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:101120000-101148000	Weak transcription	HSMMtube	muscle
25	chr6:101121000-101137600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:101122000-101148000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:101124600-101146800	Weak transcription	Dnd41	blood
28	chr6:101124800-101147400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr6:101126200-101147000	Weak transcription	Fetal Intestine Small	intestine
30	chr6:101127400-101146800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:101128800-101168000	Weak transcription	NHLF	lung
32	chr6:101130600-101148000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:101132600-101145000	Weak transcription	HSMM	muscle
34	chr6:101133200-101147000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr6:101133200-101149400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr6:101134000-101146800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:101134000-101149600	Weak transcription	Fetal Heart	heart
38	chr6:101137600-101138600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:101137800-101148000	Weak transcription	Esophagus	oesophagus
40	chr6:101138600-101143200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:101139800-101140200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr6:101140200-101149800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:101141400-101147800	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr6:101142200-101147800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:101142200-101148000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr6:101142400-101189600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr6:101142800-101147000	Weak transcription	Liver	Liver
48	chr6:101143000-101143200	Enhancers	K562	blood
49	chr6:101143000-101149400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:101143200-101143800	Flanking Active TSS	K562	blood

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