Variant report

Variant	nsv538391
Chromosome Location	chr6:101225650-101623140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2144)
CpG islands
(count:1037)
Chromatin interactive
region (count:106)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2144 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:101329171-101329282	K562	blood:	n/a	n/a
2	ARID3A	chr6:101361710-101361821	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:101328295-101328654	K562	blood:	n/a	n/a
4	ARID3A	chr6:101328160-101329909	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:101309874-101310730	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:101416990-101417029	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:101339060-101339651	K562	blood:	n/a	n/a
8	ARID3A	chr6:101396557-101397017	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:101396704-101396823	K562	blood:	n/a	n/a
10	ATF1	chr6:101329007-101329734	K562	blood:	n/a	n/a
11	ATF1	chr6:101249683-101249708	K562	blood:	n/a	n/a
12	ATF2	chr6:101328781-101329644	GM12878	blood:	n/a	n/a
13	ATF2	chr6:101340639-101340959	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:101328989-101329579	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr6:101531241-101531839	A549	lung:	n/a	n/a
16	ATF3	chr6:101528370-101528764	A549	lung:	n/a	n/a
17	ATF3	chr6:101329035-101329383	K562	blood:	n/a	chr6:101329222-101329236 chr6:101329076-101329085 chr6:101329299-101329308 chr6:101329222-101329242
18	ATF3	chr6:101531317-101531784	A549	lung:	n/a	n/a
19	BACH1	chr6:101329023-101329589	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:101307789-101307792	K562	blood:	n/a	n/a
21	BATF	chr6:101298141-101298334	GM12878	blood:	n/a	n/a
22	BCL3	chr6:101531281-101531958	A549	lung:	n/a	n/a
23	BCL3	chr6:101531326-101531819	A549	lung:	n/a	n/a
24	BCL3	chr6:101528350-101529074	A549	lung:	n/a	chr6:101528799-101528808 chr6:101528625-101528634 chr6:101528708-101528717 chr6:101528707-101528716
25	BCLAF1	chr6:101328702-101329584	GM12878	blood:	n/a	chr6:101329234-101329247
26	BCLAF1	chr6:101328965-101329677	GM12878	blood:	n/a	chr6:101329234-101329247
27	BCLAF1	chr6:101328830-101329530	K562	blood:	n/a	chr6:101329234-101329247
28	BHLHE40	chr6:101330212-101330739	K562	blood:	n/a	n/a
29	BHLHE40	chr6:101573310-101573328	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:101328724-101329517	HepG2	liver:	n/a	chr6:101328973-101328989
31	BHLHE40	chr6:101396832-101396917	K562	blood:	n/a	n/a
32	BHLHE40	chr6:101257262-101257586	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:101328625-101329968	K562	blood:	n/a	chr6:101328973-101328989
34	BHLHE40	chr6:101462027-101462064	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:101328597-101329538	GM12878	blood:	n/a	chr6:101328973-101328989
36	BRCA1	chr6:101396520-101396961	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr6:101329474-101329674	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr6:101328995-101329495	GM12878	blood:	n/a	n/a
39	BRCA1	chr6:101329902-101330016	HepG2	liver:	n/a	n/a
40	BRCA1	chr6:101328942-101329318	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:101467887-101468048	GM12878	blood:	n/a	n/a
42	BRCA1	chr6:101372001-101373154	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr6:101329003-101329597	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr6:101346149-101346415	K562	blood:	n/a	n/a
45	CBX3	chr6:101328828-101329742	K562	blood:	n/a	n/a
46	CBX3	chr6:101346136-101346464	K562	blood:	n/a	n/a
47	CBX3	chr6:101328683-101329649	HCT-116	colon:	n/a	n/a
48	CCNT2	chr6:101328683-101329932	K562	blood:	n/a	chr6:101328716-101328725
49	CCNT2	chr6:101339079-101339553	K562	blood:	n/a	n/a
50	CCNT2	chr6:101396629-101397041	K562	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:101329119-101329169	A549	lung:	n/a
2	chr6:101329408-101329458	K562	blood:	n/a
3	chr6:101308372-101308422	HIPEpiC	eye:	n/a
4	chr6:101331608-101331658	Hela-S3	cervix:	n/a
5	chr6:101277371-101277421	BE2_C	brain:	n/a
6	chr6:101328941-101328991	HCM	heart:	n/a
7	chr6:101277371-101277421	HEK293	kidney:	embryo
8	chr6:101306732-101306782	AG10803	skin:	n/a
9	chr6:101331608-101331658	GM12891	blood:	n/a
10	chr6:101329169-101329219	RPTEC	kidney:	n/a
11	chr6:101448078-101448128	HCF	heart:	n/a
12	chr6:101329504-101329554	HCPEpiC	choroid plexus:	n/a
13	chr6:101329304-101329354	HCT-116	colon:	n/a
14	chr6:101325415-101325465	K562	blood:	n/a
15	chr6:101597928-101597978	GM06990	blood:	n/a
16	chr6:101329504-101329554	HMEC	breast:	n/a
17	chr6:101331608-101331658	HUVEC	blood vessel:	n/a
18	chr6:101306732-101306782	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:101448078-101448128	AG09319	gingival:	n/a
20	chr6:101329169-101329219	A549	lung:	n/a
21	chr6:101329169-101329219	ECC-1	luminal epithelium:	n/a
22	chr6:101605940-101605990	CMK	blood:	n/a
23	chr6:101329307-101329357	SK-N-SH	brain:	n/a
24	chr6:101325415-101325465	GM12892	blood:	n/a
25	chr6:101331608-101331658	RPTEC	kidney:	n/a
26	chr6:101277371-101277421	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:101448078-101448128	SK-N-SH	brain:	n/a
28	chr6:101329502-101329552	GM12878	blood:	n/a
29	chr6:101329307-101329357	HRCEpiC	kidney:	n/a
30	chr6:101329408-101329458	HEK293	kidney:	embryo
31	chr6:101329502-101329552	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:101448078-101448128	HCPEpiC	choroid plexus:	n/a
33	chr6:101329307-101329357	HEEpiC	esophagus:	n/a
34	chr6:101448078-101448128	MCF-7	breast:	n/a
35	chr6:101329307-101329357	HRE	kidney:	n/a
36	chr6:101329408-101329458	BJ	skin:	n/a
37	chr6:101597928-101597978	AoSMC	blood vessel:	n/a
38	chr6:101329119-101329169	MCF-7	breast:	n/a
39	chr6:101277371-101277421	U87	brain:	n/a
40	chr6:101329502-101329552	GM06990	blood:	n/a
41	chr6:101329119-101329169	GM12878	blood:	n/a
42	chr6:101448078-101448128	HRCEpiC	kidney:	n/a
43	chr6:101329307-101329357	NT2-D1	testis:	n/a
44	chr6:101329307-101329357	PANC-1	pancreas:	n/a
45	chr6:101308372-101308422	ECC-1	luminal epithelium:	n/a
46	chr6:101605940-101605990	H1-hESC	embryonic stem cell:	embryo
47	chr6:101306732-101306782	AG04450	lung:	fetal
48	chr6:101329119-101329169	Jurkat	blood:	n/a
49	chr6:101308372-101308422	BJ	skin:	n/a
50	chr6:101329408-101329458	AG04450	lung:	fetal

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:101271307..101273305-chr6:101294411..101297319,2	K562	blood:
2	chr6:101532278..101533905-chr6:101535075..101537157,2	K562	blood:
3	chr6:101325336..101331866-chr6:101332086..101337094,13	K562	blood:
4	chr6:101162432..101165009-chr6:101330194..101333113,2	K562	blood:
5	chr6:101452622..101455428-chr6:101458387..101460104,2	MCF-7	breast:
6	chr6:101328129..101329755-chr6:101606100..101609085,2	MCF-7	breast:
7	chr6:101286650..101289518-chr6:101298601..101300535,2	K562	blood:
8	chr6:101227439..101228979-chr6:101229862..101232635,2	MCF-7	breast:
9	chr6:101328640..101330753-chr6:101345381..101346977,2	MCF-7	breast:
10	chr6:101324614..101326514-chr6:101327615..101329304,2	MCF-7	breast:
11	chr6:101302214..101305047-chr6:101327915..101330416,2	MCF-7	breast:
12	chr6:101317284..101319189-chr6:101327814..101329949,3	K562	blood:
13	chr6:101269410..101270925-chr6:101275181..101277439,2	MCF-7	breast:
14	chr6:101319726..101322538-chr6:101323434..101327261,5	K562	blood:
15	chr6:101269410..101270925-chr6:101275181..101277439,2	MCF-7	breast:
16	chr6:101243854..101246024-chr6:101258576..101260117,2	K562	blood:
17	chr6:101286243..101289209-chr6:101295205..101297234,2	K562	blood:
18	chr6:101311227..101314088-chr6:101316060..101317818,2	MCF-7	breast:
19	chr6:101302750..101305645-chr6:101307403..101308925,2	K562	blood:
20	chr6:101327650..101330005-chr6:101331234..101332758,2	K562	blood:
21	chr6:101327181..101330084-chr6:117801293..117803939,2	K562	blood:
22	chr6:101333797..101336056-chr6:101337811..101340573,2	MCF-7	breast:
23	chr6:101232498..101235152-chr6:101238676..101241489,3	K562	blood:
24	chr6:101309386..101311336-chr6:101316442..101318776,3	K562	blood:
25	chr6:101294725..101296598-chr6:101316147..101318633,2	K562	blood:
26	chr6:101271307..101273305-chr6:101294411..101297319,2	K562	blood:
27	chr6:101341802..101344010-chr6:101345674..101348065,2	K562	blood:
28	chr6:101239952..101241770-chr6:101249281..101252213,2	K562	blood:
29	chr6:101184266..101186701-chr6:101321079..101322607,2	K562	blood:
30	chr6:101555646..101557341-chr6:101557571..101560206,2	MCF-7	breast:
31	chr6:101299454..101302050-chr6:101304670..101307311,3	MCF-7	breast:
32	chr6:101327681..101329866-chr6:101349579..101352191,2	K562	blood:
33	chr4:124242..124909-chr6:101328965..101329469,2	NB4	blood:
34	chr6:101467552..101469829-chr6:101470681..101473630,2	MCF-7	breast:
35	chr6:101271641..101274156-chr6:101276043..101277591,3	K562	blood:
36	chr6:101467552..101469829-chr6:101470681..101473630,2	MCF-7	breast:
37	chr6:101316563..101319212-chr6:101321882..101324252,3	K562	blood:
38	chr6:101315511..101317723-chr6:101321403..101323944,2	K562	blood:
39	chr6:101309650..101312548-chr6:101313030..101314755,2	MCF-7	breast:
40	chr6:101321078..101323999-chr6:101327365..101330497,3	K562	blood:
41	chr6:101302750..101305984-chr6:101307403..101310104,4	K562	blood:
42	chr6:101307908..101309612-chr6:101327803..101330133,2	K562	blood:
43	chr6:101235770..101239248-chr6:101239414..101244156,4	K562	blood:
44	chr6:101239952..101241770-chr6:101249281..101252213,2	K562	blood:
45	chr6:101319726..101322538-chr6:101323434..101327261,5	K562	blood:
46	chr6:101341802..101344010-chr6:101345674..101348065,2	K562	blood:
47	chr6:101271641..101274156-chr6:101276043..101277591,3	K562	blood:
48	chr6:101333797..101336056-chr6:101337811..101340573,2	MCF-7	breast:
49	chr6:101328507..101330711-chr6:101341226..101343294,2	K562	blood:
50	chr6:101286650..101289518-chr6:101298601..101300535,2	K562	blood:

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

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

No data

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

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

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
ENSG00000164465	chromatin interactions
ENSG00000270987	chromatin interactions
ENSG00000149679	chromatin interactions
ENSG00000260000	chromatin interactions
ENSG00000250312	chromatin interactions
ENSG00000112249	chromatin interactions
ENSG00000134419	chromatin interactions

Extended variants
information (count: 9323 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:9323 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573460428	chr6:101225665-101225666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72945181	chr6:101225682-101225683	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs375551074	chr6:101225696-101225697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115788346	chr6:101225705-101225706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4840154	chr6:101225723-101225724	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564522582	chr6:101225867-101225868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572128163	chr6:101225914-101225915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199904452	chr6:101225979-101225980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397728053	chr6:101225990-101225991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532708060	chr6:101225992-101225993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551260002	chr6:101226009-101226010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532163196	chr6:101226126-101226127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184009426	chr6:101226209-101226210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369501471	chr6:101226226-101226227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545658433	chr6:101226241-101226242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548468365	chr6:101226276-101226277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs66466404	chr6:101226283-101226284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71547413	chr6:101226284-101226285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs67314064	chr6:101226286-101226287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs398002428	chr6:101226290-101226291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188741627	chr6:101226299-101226300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9404041	chr6:101226300-101226301	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs552647834	chr6:101226394-101226395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570853478	chr6:101226398-101226399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180772413	chr6:101226413-101226414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568306792	chr6:101226433-101226434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184230219	chr6:101226437-101226438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575413438	chr6:101226452-101226453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536467661	chr6:101226455-101226456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144928671	chr6:101226474-101226475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189604216	chr6:101226569-101226570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377571413	chr6:101226579-101226580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111747385	chr6:101226580-101226581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539930794	chr6:101226588-101226589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564591576	chr6:101226617-101226618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182072760	chr6:101226629-101226630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375323099	chr6:101226705-101226706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536733008	chr6:101226709-101226710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186451010	chr6:101226713-101226714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530308583	chr6:101226718-101226719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140669043	chr6:101226719-101226720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560661908	chr6:101226822-101226823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553664134	chr6:101227093-101227094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74472233	chr6:101227102-101227103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552705048	chr6:101227134-101227135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570915986	chr6:101227150-101227151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190321582	chr6:101227166-101227167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549876974	chr6:101227289-101227290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368010861	chr6:101227360-101227361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569160256	chr6:101227401-101227402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101184400-101304600	Weak transcription	Hela-S3	cervix
2	chr6:101191400-101277000	Weak transcription	Esophagus	oesophagus
3	chr6:101211800-101231800	Weak transcription	Pancreas	Pancrea
4	chr6:101212000-101246400	Weak transcription	Psoas Muscle	Psoas
5	chr6:101212000-101276200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:101212000-101281400	Weak transcription	Aorta	Aorta
7	chr6:101213200-101227400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:101213200-101242800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:101213400-101244000	Weak transcription	HSMMtube	muscle
10	chr6:101213600-101241600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr6:101213600-101256000	Weak transcription	Ovary	ovary
12	chr6:101213600-101281600	Weak transcription	Gastric	stomach
13	chr6:101213800-101237000	Weak transcription	Primary T cells from cord blood	blood
14	chr6:101213800-101250800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:101213800-101254200	Weak transcription	Fetal Thymus	thymus
16	chr6:101214600-101236400	Weak transcription	GM12878-XiMat	blood
17	chr6:101214800-101281600	Weak transcription	Left Ventricle	heart
18	chr6:101215200-101228200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:101215200-101237000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:101215200-101237400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:101215200-101242200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr6:101215200-101244000	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr6:101215200-101244000	Weak transcription	Liver	Liver
24	chr6:101215200-101244000	Weak transcription	Placenta	Placenta
25	chr6:101215200-101247000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr6:101215200-101252600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:101215200-101256200	Weak transcription	Osteobl	bone
28	chr6:101215200-101263000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr6:101215200-101311400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr6:101215400-101234800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:101215400-101239800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr6:101215400-101242000	Weak transcription	Primary B cells from cord blood	blood
33	chr6:101215400-101243400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:101215400-101243400	Weak transcription	NHDF-Ad	bronchial
35	chr6:101215400-101243600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:101215400-101243600	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr6:101215400-101244000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr6:101215400-101244000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr6:101215400-101258600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr6:101215600-101242400	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr6:101215600-101242600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr6:101216200-101241800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:101217400-101231200	Weak transcription	Dnd41	blood
44	chr6:101223000-101244200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:101223000-101256800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:101223400-101242200	Weak transcription	NH-A	brain
47	chr6:101223400-101243600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:101225200-101226000	Strong transcription	HSMM	muscle
49	chr6:101225200-101226000	Strong transcription	HUVEC	blood vessel
50	chr6:101225400-101226600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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