Variant report

Variant	nsv1026162
Chromosome Location	chr6:64639580-65470828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3032)
CpG islands
(count:734)
Chromatin interactive
region (count:61)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3032 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:64794125-64794597	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:65011400-65012086	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:64964536-64964856	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:65013819-65014100	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:64646417-64646756	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:64968244-64968998	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:64990489-64990795	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:64756462-64757064	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:64651577-64651929	HepG2	liver:	n/a	n/a
10	ATF1	chr6:65390020-65390161	K562	blood:	n/a	n/a
11	ATF1	chr6:64976496-64976720	K562	blood:	n/a	n/a
12	ATF2	chr6:64964815-64965334	GM12878	blood:	n/a	n/a
13	ATF2	chr6:65179383-65179633	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:64976091-64976606	GM12878	blood:	n/a	n/a
15	ATF2	chr6:64976044-64976744	GM12878	blood:	n/a	n/a
16	BACH1	chr6:64837165-64837183	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:64943636-64943644	K562	blood:	n/a	n/a
18	BACH1	chr6:65376528-65376582	K562	blood:	n/a	n/a
19	BATF	chr6:64791421-64791660	GM12878	blood:	n/a	chr6:64791565-64791576
20	BATF	chr6:64966228-64966667	GM12878	blood:	n/a	n/a
21	BATF	chr6:65042852-65043055	GM12878	blood:	n/a	n/a
22	BATF	chr6:65042855-65043015	GM12878	blood:	n/a	n/a
23	BATF	chr6:64976180-64976789	GM12878	blood:	n/a	n/a
24	BATF	chr6:64976172-64976684	GM12878	blood:	n/a	n/a
25	BATF	chr6:65230010-65230290	GM12878	blood:	n/a	chr6:65230189-65230200 chr6:65230190-65230200 chr6:65230168-65230179
26	BATF	chr6:64791435-64791721	GM12878	blood:	n/a	chr6:64791565-64791576
27	BATF	chr6:65229975-65230316	GM12878	blood:	n/a	chr6:65230189-65230200 chr6:65230190-65230200 chr6:65230168-65230179
28	BATF	chr6:64964929-64965262	GM12878	blood:	n/a	chr6:64965092-64965103
29	BCL11A	chr6:65230019-65230255	GM12878	blood:	n/a	chr6:65230192-65230201
30	BCL11A	chr6:65230000-65230227	GM12878	blood:	n/a	chr6:65230192-65230201
31	BCL11A	chr6:64976133-64976749	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:64966422-64966651	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:64976470-64976780	GM12878	blood:	n/a	n/a
34	BCL3	chr6:64976137-64976578	GM12878	blood:	n/a	n/a
35	BCL3	chr6:64964914-64965159	GM12878	blood:	n/a	n/a
36	BCL3	chr6:65230007-65230285	GM12878	blood:	n/a	chr6:65230192-65230201
37	BCLAF1	chr6:64976165-64976706	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:64755076-64755129	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:64791352-64791756	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:64794285-64794421	HepG2	liver:	n/a	n/a
41	BHLHE40	chr6:64975549-64975596	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:64756591-64756906	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:64990141-64990705	GM12878	blood:	n/a	chr6:64990410-64990419 chr6:64990410-64990419 chr6:64990404-64990425
44	BHLHE40	chr6:64976000-64976860	GM12878	blood:	n/a	n/a
45	BRCA1	chr6:64959800-64960357	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr6:65443446-65443561	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr6:64674214-64674223	H1-hESC	embryonic stem cell:	n/a	n/a
48	CBX3	chr6:64664226-64664434	K562	blood:	n/a	n/a
49	CCNT2	chr6:64677255-64677405	K562	blood:	n/a	n/a
50	CCNT2	chr6:65382053-65382189	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:65341479-65341529	NT2-D1	testis:	n/a
2	chr6:64733737-64733787	HIPEpiC	eye:	n/a
3	chr6:65341479-65341529	NT2-D1	testis:	n/a
4	chr6:64733737-64733787	HIPEpiC	eye:	n/a
5	chr6:65099958-65100008	Hepatocyte	liver:	n/a
6	chr6:64928665-64928715	PANC-1	pancreas:	n/a
7	chr6:65214835-65214885	AG10803	skin:	n/a
8	chr6:64654929-64654979	Jurkat	blood:	n/a
9	chr6:64734868-64734918	AG09309	skin:	n/a
10	chr6:64654929-64654979	PrEC	prostate:	n/a
11	chr6:64654929-64654979	Caco-2	colon:	n/a
12	chr6:64989895-64989945	HNPCEpiC	eye:	n/a
13	chr6:65341479-65341529	SK-N-SH	brain:	n/a
14	chr6:64989895-64989945	HIPEpiC	eye:	n/a
15	chr6:65099958-65100008	HCF	heart:	n/a
16	chr6:64729109-64729159	MCF10A-Er-Src	breast:	n/a
17	chr6:64928665-64928715	SAEC	small airway:	n/a
18	chr6:64654929-64654979	HCT-116	colon:	n/a
19	chr6:65214835-65214885	HepG2	liver:	n/a
20	chr6:64734868-64734918	PFSK-1	brain:	n/a
21	chr6:64729109-64729159	ProgFib	skin:	n/a
22	chr6:64989895-64989945	HL-60	blood:	n/a
23	chr6:64729109-64729159	HEK293	kidney:	embryo
24	chr6:64734868-64734918	GM12878	blood:	n/a
25	chr6:64734843-64734893	SAEC	small airway:	n/a
26	chr6:64733737-64733787	HUVEC	blood vessel:	n/a
27	chr6:64734868-64734918	Hepatocyte	liver:	n/a
28	chr6:65230924-65230974	ProgFib	skin:	n/a
29	chr6:65099958-65100008	AG04450	lung:	fetal
30	chr6:64729109-64729159	LNCaP	prostate:	n/a
31	chr6:65099958-65100008	GM12891	blood:	n/a
32	chr6:65099958-65100008	SK-N-SH	brain:	n/a
33	chr6:65230924-65230974	BE2_C	brain:	n/a
34	chr6:64742105-64742155	LNCaP	prostate:	n/a
35	chr6:64729109-64729159	NHBE	bronchial:	n/a
36	chr6:65214835-65214885	IMR90	lung:	fetal
37	chr6:64928665-64928715	GM12892	blood:	n/a
38	chr6:65341479-65341529	AoSMC	blood vessel:	n/a
39	chr6:65214835-65214885	NHBE	bronchial:	n/a
40	chr6:64734868-64734918	NT2-D1	testis:	n/a
41	chr6:65230924-65230974	NB4	blood:	n/a
42	chr6:64742105-64742155	GM12892	blood:	n/a
43	chr6:64654929-64654979	K562	blood:	n/a
44	chr6:64654929-64654979	AG04450	lung:	fetal
45	chr6:65214835-65214885	Caco-2	colon:	n/a
46	chr6:64734843-64734893	U87	brain:	n/a
47	chr6:64928665-64928715	CMK	blood:	n/a
48	chr6:64734868-64734918	SAEC	small airway:	n/a
49	chr6:64989895-64989945	GM12878	blood:	n/a
50	chr6:64742105-64742155	PANC-1	pancreas:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:14919049..14919953-chr6:65270014..65270629,2	MCF-7	breast:
2	chr6:65277767..65280603-chr6:65309612..65311226,2	K562	blood:
3	chr6:65190711..65192538-chr6:65195530..65197362,2	K562	blood:
4	chr6:65375121..65377112-chr6:65391704..65393357,2	K562	blood:
5	chr6:64748612..64751041-chr6:64751525..64753155,2	MCF-7	breast:
6	chr6:65070131..65072480-chr6:65075607..65077474,2	MCF-7	breast:
7	chr6:65294576..65297046-chr6:65300065..65301851,2	K562	blood:
8	chr6:64898967..64901155-chr6:64903465..64905780,2	K562	blood:
9	chr6:65126062..65128864-chr6:65133526..65135852,2	MCF-7	breast:
10	chr6:64825086..64826621-chr6:64878332..64879949,2	K562	blood:
11	chr6:64990450..64991143-chr6:65442394..65443437,5	MCF-7	breast:
12	chr6:65219986..65221958-chr6:65240490..65242186,2	K562	blood:
13	chr6:64990450..64991143-chr6:65442394..65443437,5	MCF-7	breast:
14	chr10:107790162..107791057-chr6:65201703..65202502,2	MCF-7	breast:
15	chr6:65190711..65192538-chr6:65195530..65197362,2	K562	blood:
16	chr20:46132660..46133356-chr6:64886601..64887388,2	MCF-7	breast:
17	chr3:192405286..192405824-chr6:65200917..65201417,2	HCT-116	colon:
18	chr12:81340169..81340734-chr6:64895212..64895734,2	MCF-7	breast:
19	chr6:64814684..64816252-chr6:64820717..64823220,2	MCF-7	breast:
20	chr6:65372691..65375418-chr6:65377989..65379580,2	MCF-7	breast:
21	chr6:65105555..65108214-chr6:65112608..65114216,2	K562	blood:
22	chr6:64968428..64970654-chr6:64971597..64973561,2	MCF-7	breast:
23	chr6:65423336..65423981-chr6:160399331..160400281,2	MCF-7	breast:
24	chr6:64683925..64686124-chr6:64690938..64693074,3	K562	blood:
25	chr6:65383707..65386242-chr6:65386286..65389127,2	MCF-7	breast:
26	chr6:65287761..65289568-chr6:65291145..65293984,2	K562	blood:
27	chr6:65375121..65377112-chr6:65391704..65393357,2	K562	blood:
28	chr10:122595797..122596436-chr6:65107139..65107964,2	MCF-7	breast:
29	chr6:64825086..64826621-chr6:64878332..64879949,2	K562	blood:
30	chr6:64822184..64824629-chr6:64828164..64830437,2	K562	blood:
31	chr6:65294576..65297046-chr6:65300065..65301851,2	K562	blood:
32	chr6:64722104..64722842-chr6:65040545..65041404,3	MCF-7	breast:
33	chr6:64722104..64722842-chr6:65040545..65041404,3	MCF-7	breast:
34	chr6:65429271..65430989-chr6:65432501..65434234,2	K562	blood:
35	chr6:65213276..65216079-chr6:65219368..65221151,2	K562	blood:
36	chr6:65090547..65093920-chr6:65096939..65100016,3	MCF-7	breast:
37	chr6:64814684..64816252-chr6:64820717..64823220,2	MCF-7	breast:
38	chr6:65213231..65215666-chr6:65222700..65224711,2	K562	blood:
39	chr6:65219986..65221958-chr6:65240490..65242186,2	K562	blood:
40	chr6:65090547..65093920-chr6:65096939..65100016,3	MCF-7	breast:
41	chr6:64968428..64970654-chr6:64971597..64973561,2	MCF-7	breast:
42	chr6:64748612..64751041-chr6:64751525..64753155,2	MCF-7	breast:
43	chr6:65372691..65375418-chr6:65377989..65379580,2	MCF-7	breast:
44	chr6:65277767..65280603-chr6:65309612..65311226,2	K562	blood:
45	chr6:65429271..65430989-chr6:65432501..65434234,2	K562	blood:
46	chr6:64898967..64901155-chr6:64903465..64905780,2	K562	blood:
47	chr6:65006449..65008476-chr6:65012080..65014134,2	K562	blood:
48	chr6:64683925..64686124-chr6:64690938..64693074,3	K562	blood:
49	chr6:64523219..64524103-chr6:65442776..65443345,2	MCF-7	breast:
50	chr6:65126062..65128864-chr6:65133526..65135852,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF3-2	chr6:65110209-65110322	ENSG00000232120.1
2	lnc-PHF3-2	chr6:65089477-65089605	ENSG00000232120.1
3	lnc-PHF3-10	chr6:65145647-65145784	NONHSAT113362
4	lnc-PHF3-10	chr6:65179250-65179393	NONHSAT113362
5	lnc-LGSN-5	chr6:65423165-65423228	NONHSAT113363
6	lnc-LGSN-4	chr6:65341098-65341575	NONHSAT113364
7	lnc-LGSN-1	chr6:65443266-65443460	ENSG00000243828.1
8	lnc-PHF3-10	chr6:65166930-65167043	NONHSAT113362
9	lnc-PHF3-2	chr6:65122529-65122672	ENSG00000232120.1
10	lnc-LGSN-5	chr6:65303024-65303202	NONHSAT113363
11	lnc-LGSN-1	chr6:65443266-65443438	ENSG00000243828.1
12	lnc-LGSN-1	chr6:65438730-65438951	ENSG00000243828.1
13	lnc-LGSN-1	chr6:65440706-65440885	ENSG00000243828.1
14	lnc-PHF3-2	chr6:65087688-65087825	ENSG00000232120.1
15	lnc-LGSN-5	chr6:65327311-65327426	NONHSAT113363
16	lnc-PHF3-10	chr6:65147436-65147564	NONHSAT113362
17	lnc-LGSN-5	chr6:65336014-65336138	NONHSAT113363

No data

Variant related genes	Relation type
ENSG00000232120	TF binding region
HNRNPDP2	TF binding region
ENSG00000243828	TF binding region
EYS	TF binding region
ENSG00000232120	CpG island
HNRNPDP2	CpG island
ENSG00000243828	CpG island
EYS	CpG island

Extended variants
information (count: 11210 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:11210 , 50 per page) page: 1 2 3 4 5 6 7 ... 225

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564396029	chr6:64639630-64639631	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528408876	chr6:64639637-64639638	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546750688	chr6:64639640-64639641	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190910816	chr6:64639707-64639708	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542292396	chr6:64639732-64639733	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536577980	chr6:64639737-64639738	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550272187	chr6:64639851-64639852	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568468949	chr6:64639870-64639871	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539044120	chr6:64639875-64639876	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141505142	chr6:64639908-64639909	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376731098	chr6:64639909-64639910	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144465495	chr6:64639942-64639943	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116057416	chr6:64639965-64639966	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575094461	chr6:64639979-64639980	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148795581	chr6:64639996-64639997	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557485388	chr6:64640010-64640011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575848377	chr6:64640046-64640047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141582125	chr6:64640056-64640057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532092214	chr6:64640063-64640064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150866021	chr6:64640065-64640066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183902347	chr6:64640067-64640068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140108309	chr6:64640101-64640102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561506244	chr6:64640115-64640116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200022520	chr6:64640173-64640174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs66675060	chr6:64640174-64640175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115062271	chr6:64640179-64640180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397777229	chr6:64640181-64640182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550409145	chr6:64640218-64640219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145414585	chr6:64640226-64640227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186944070	chr6:64640235-64640236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191840955	chr6:64640302-64640303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566368480	chr6:64640310-64640311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552734813	chr6:64640330-64640331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546979870	chr6:64640338-64640339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs58947090	chr6:64640339-64640340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568815285	chr6:64640350-64640351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115312666	chr6:64640405-64640406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550422372	chr6:64640473-64640474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575786968	chr6:64640493-64640494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539570756	chr6:64640530-64640531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558098117	chr6:64640606-64640607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573166266	chr6:64640630-64640631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs36123296	chr6:64640640-64640641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540475470	chr6:64640672-64640673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561646023	chr6:64640698-64640699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565487139	chr6:64640701-64640702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147689748	chr6:64640714-64640715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543989340	chr6:64640717-64640718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562374259	chr6:64640725-64640726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183119556	chr6:64640789-64640790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19114987	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64635800-64640000	Enhancers	Fetal Heart	heart
2	chr6:64637200-64644800	Weak transcription	Fetal Intestine Large	intestine
3	chr6:64637200-64645000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr6:64637400-64639800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:64637400-64640600	Weak transcription	Liver	Liver
6	chr6:64637800-64641000	Weak transcription	Fetal Intestine Small	intestine
7	chr6:64638800-64639600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:64639000-64639800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:64639200-64639800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:64639200-64640000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr6:64639800-64640000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:64639800-64640000	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr6:64640000-64640400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:64640000-64641000	Weak transcription	Fetal Heart	heart
15	chr6:64640000-64652000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:64640400-64641200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr6:64640600-64641600	Enhancers	Liver	Liver
18	chr6:64640600-64642600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:64640800-64641600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr6:64640800-64642000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr6:64641000-64641200	Enhancers	Fetal Heart	heart
22	chr6:64641000-64641400	Enhancers	Fetal Intestine Small	intestine
23	chr6:64641200-64642600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr6:64641400-64644800	Weak transcription	Fetal Intestine Small	intestine
25	chr6:64641600-64644800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:64641600-64645000	Weak transcription	Liver	Liver
27	chr6:64642000-64645000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:64642600-64643000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr6:64642600-64645000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:64643000-64645000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr6:64644800-64645800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:64644800-64647000	Enhancers	Fetal Intestine Large	intestine
33	chr6:64644800-64647200	Enhancers	Fetal Intestine Small	intestine
34	chr6:64645000-64645600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr6:64645000-64646000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:64645000-64647200	Enhancers	Liver	Liver
37	chr6:64645000-64647200	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr6:64645000-64647200	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr6:64645200-64647000	Enhancers	HepG2	liver
40	chr6:64645800-64646600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr6:64645800-64648800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:64646000-64646400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:64646200-64646400	Weak transcription	Fetal Lung	lung
44	chr6:64646400-64646600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:64646600-64647000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr6:64646600-64648000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:64647000-64647200	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr6:64647000-64651400	Weak transcription	HepG2	liver
49	chr6:64647000-64651600	Weak transcription	Fetal Intestine Large	intestine
50	chr6:64647200-64648200	Weak transcription	Liver	Liver

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