Variant report

Variant	nsv1019328
Chromosome Location	chr6:76154751-76604197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4453)
CpG islands
(count:1893)
Chromatin interactive
region (count:311)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4453 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:76484978-76485281	K562	blood:	n/a	n/a
3	ARID3A	chr6:76532773-76532821	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76331504-76331869	K562	blood:	n/a	n/a
6	ARID3A	chr6:76339500-76339892	K562	blood:	n/a	n/a
7	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
8	ARID3A	chr6:76312666-76313021	K562	blood:	n/a	n/a
9	ARID3A	chr6:76233632-76234708	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:76342477-76343204	K562	blood:	n/a	chr6:76342662-76342678
11	ARID3A	chr6:76601370-76601603	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:76272954-76273059	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:76333004-76333194	K562	blood:	n/a	n/a
14	ARID3A	chr6:76315396-76315502	K562	blood:	n/a	n/a
15	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:76337921-76337975	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:76562512-76562787	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:76311201-76311902	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:76322881-76323353	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:76313655-76313921	K562	blood:	n/a	n/a
21	ARID3A	chr6:76236274-76236597	HepG2	liver:	n/a	n/a
22	ARID3A	chr6:76320480-76320552	K562	blood:	n/a	n/a
23	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
24	ATF1	chr6:76342790-76343022	K562	blood:	n/a	n/a
25	ATF1	chr6:76244545-76244659	K562	blood:	n/a	n/a
26	ATF1	chr6:76203452-76203656	K562	blood:	n/a	n/a
27	ATF1	chr6:76562615-76562871	K562	blood:	n/a	n/a
28	ATF1	chr6:76517943-76518107	K562	blood:	n/a	n/a
29	ATF2	chr6:76205641-76206490	GM12878	blood:	n/a	n/a
30	ATF2	chr6:76260226-76260768	GM12878	blood:	n/a	n/a
31	ATF2	chr6:76540581-76541147	GM12878	blood:	n/a	n/a
32	ATF2	chr6:76205848-76206431	GM12878	blood:	n/a	n/a
33	ATF2	chr6:76311636-76312501	GM12878	blood:	n/a	n/a
34	ATF2	chr6:76202373-76202963	GM12878	blood:	n/a	n/a
35	ATF2	chr6:76260318-76260565	GM12878	blood:	n/a	n/a
36	ATF2	chr6:76540625-76541135	GM12878	blood:	n/a	n/a
37	ATF3	chr6:76234032-76234712	A549	lung:	n/a	n/a
38	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
39	ATF3	chr6:76206011-76206395	K562	blood:	n/a	n/a
40	ATF3	chr6:76233899-76234696	A549	lung:	n/a	n/a
41	ATF3	chr6:76168471-76169059	A549	lung:	n/a	n/a
42	ATF3	chr6:76168492-76169062	A549	lung:	n/a	n/a
43	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
44	BACH1	chr6:76318040-76318256	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr6:76523240-76523470	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr6:76311710-76311864	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr6:76603125-76603698	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr6:76261204-76261211	K562	blood:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76458005-76458055	PANC-1	pancreas:	n/a
2	chr6:76459511-76459561	NHDF-neo	bronchial:	n/a
3	chr6:76458005-76458055	PANC-1	pancreas:	n/a
4	chr6:76459511-76459561	NHDF-neo	bronchial:	n/a
5	chr6:76315197-76315247	BJ	skin:	n/a
6	chr6:76311363-76311413	BJ	skin:	n/a
7	chr6:76456187-76456237	SK-N-MC	brain:	n/a
8	chr6:76203225-76203275	CMK	blood:	n/a
9	chr6:76191813-76191863	HL-60	blood:	n/a
10	chr6:76341733-76341783	AG04449	skin:	fetal
11	chr6:76311363-76311413	AG10803	skin:	n/a
12	chr6:76458005-76458055	HCM	heart:	n/a
13	chr6:76603364-76603414	A549	lung:	n/a
14	chr6:76312378-76312428	AG10803	skin:	n/a
15	chr6:76203530-76203580	HNPCEpiC	eye:	n/a
16	chr6:76311636-76311686	ovcar-3	ovarian:	n/a
17	chr6:76319793-76319843	H1-hESC	embryonic stem cell:	embryo
18	chr6:76203675-76203725	LNCaP	prostate:	n/a
19	chr6:76311363-76311413	SK-N-SH	brain:	n/a
20	chr6:76198240-76198290	SK-N-SH	brain:	n/a
21	chr6:76425457-76425507	K562	blood:	n/a
22	chr6:76603364-76603414	NB4	blood:	n/a
23	chr6:76203642-76203692	SKMC	muscle:	n/a
24	chr6:76330505-76330555	NB4	blood:	n/a
25	chr6:76203530-76203580	NT2-D1	testis:	n/a
26	chr6:76459077-76459127	K562	blood:	n/a
27	chr6:76425457-76425507	GM06990	blood:	n/a
28	chr6:76425457-76425507	BJ	skin:	n/a
29	chr6:76203225-76203275	HMEC	breast:	n/a
30	chr6:76203597-76203647	GM12878	blood:	n/a
31	chr6:76203666-76203716	BE2_C	brain:	n/a
32	chr6:76203225-76203275	GM12878	blood:	n/a
33	chr6:76203675-76203725	MCF10A-Er-Src	breast:	n/a
34	chr6:76311331-76311381	RPTEC	kidney:	n/a
35	chr6:76603364-76603414	SK-N-SH	brain:	n/a
36	chr6:76204308-76204358	A549	lung:	n/a
37	chr6:76309300-76309350	ECC-1	luminal epithelium:	n/a
38	chr6:76315197-76315247	ovcar-3	ovarian:	n/a
39	chr6:76203597-76203647	PANC-1	pancreas:	n/a
40	chr6:76459511-76459561	NH-A	brain:	n/a
41	chr6:76311920-76311970	SK-N-SH_RA	brain:	n/a
42	chr6:76319793-76319843	GM19239	blood:	n/a
43	chr6:76311331-76311381	HUVEC	blood vessel:	n/a
44	chr6:76319793-76319843	AG04449	skin:	fetal
45	chr6:76330505-76330555	HCF	heart:	n/a
46	chr6:76203597-76203647	HMEC	breast:	n/a
47	chr6:76311331-76311381	GM12878	blood:	n/a
48	chr6:76311920-76311970	HRCEpiC	kidney:	n/a
49	chr6:76603364-76603414	NT2-D1	testis:	n/a
50	chr6:76203225-76203275	SAEC	small airway:	n/a

(count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr6:76271916..76274380-chr6:76310344..76312548,2	MCF-7	breast:
2	chr6:76405218..76407618-chr6:76430939..76433858,2	MCF-7	breast:
3	chr6:76359039..76361608-chr6:76376741..76379401,2	MCF-7	breast:
4	chr6:76458966..76460939-chr6:76574214..76577179,2	MCF-7	breast:
5	chr6:76316110..76319023-chr6:76339771..76341687,2	K562	blood:
6	chr6:76006607..76007140-chr6:76236090..76236641,2	MCF-7	breast:
7	chr6:76318407..76320592-chr6:76330257..76332672,2	K562	blood:
8	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:
9	chr6:76424657..76427289-chr6:76428050..76430901,3	MCF-7	breast:
10	chr6:76228629..76230410-chr6:76233743..76235799,2	K562	blood:
11	chr6:76267023..76268550-chr6:76287027..76288640,2	K562	blood:
12	chr6:76286862..76288767-chr6:76289048..76291040,2	MCF-7	breast:
13	chr1:149223806..149225375-chr6:76310132..76311971,2	MCF-7	breast:
14	chr6:76457754..76460582-chr6:76467683..76471676,6	MCF-7	breast:
15	chr6:76426476..76430048-chr6:76457436..76461171,5	MCF-7	breast:
16	chr6:76222296..76224632-chr6:76225087..76227864,2	K562	blood:
17	chr6:76361046..76364656-chr6:76366287..76368782,3	K562	blood:
18	chr6:76234510..76236120-chr6:76239992..76242407,2	MCF-7	breast:
19	chr6:76373474..76375579-chr6:76380760..76383330,2	K562	blood:
20	chr6:76337128..76338933-chr6:76358786..76360573,2	K562	blood:
21	chr6:76307687..76309384-chr6:76493357..76494955,2	K562	blood:
22	chr6:76370677..76372880-chr6:76377007..76378733,2	K562	blood:
23	chr6:76310717..76312305-chr6:76374454..76377244,2	K562	blood:
24	chr2:233562031..233562988-chr6:76458771..76459462,2	Hela-S3	cervix:
25	chr6:76458866..76461215-chr6:76472496..76475519,3	MCF-7	breast:
26	chr6:76348810..76350607-chr6:76352555..76355121,2	K562	blood:
27	chr6:76457060..76461197-chr6:76473704..76478813,6	MCF-7	breast:
28	chr6:76348520..76350771-chr6:76351491..76354055,3	K562	blood:
29	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
30	chr6:76320486..76323287-chr6:76327522..76329955,3	K562	blood:
31	chr6:76238154..76239955-chr6:76258308..76260923,2	K562	blood:
32	chr6:76006957..76007653-chr6:76235682..76236264,3	MCF-7	breast:
33	chr6:76238349..76239999-chr6:76240837..76242447,2	MCF-7	breast:
34	chr11:93474252..93474772-chr6:76458412..76459090,2	Hela-S3	cervix:
35	chr6:76527031..76529550-chr6:76557950..76559452,2	MCF-7	breast:
36	chr6:76456486..76459516-chr6:76469446..76471432,3	MCF-7	breast:
37	chr6:75952178..75953795-chr6:76311805..76314377,2	K562	blood:
38	chr1:148241338..148242027-chr6:76183482..76183984,2	MCF-7	breast:
39	chr6:76564297..76564995-chr6:76602725..76603462,2	MCF-7	breast:
40	chr6:76327323..76329622-chr6:76330394..76331981,2	K562	blood:
41	chr6:76446062..76448644-chr6:76456702..76459457,3	MCF-7	breast:
42	chr1:149223711..149224233-chr6:76183458..76183978,3	HCT-116	colon:
43	chr6:76457017..76459821-chr6:76526945..76528874,2	MCF-7	breast:
44	chr6:76329104..76331316-chr6:76370800..76373283,2	K562	blood:
45	chr3:141205080..141206779-chr6:76458156..76460847,2	MCF-7	breast:
46	chr6:76522682..76525185-chr6:76527621..76531483,3	MCF-7	breast:
47	chr6:76310342..76312305-chr6:76373129..76377244,3	K562	blood:
48	chr6:76354799..76357581-chr6:76387845..76390206,2	K562	blood:
49	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:
50	chr6:76522682..76525185-chr6:76527621..76531483,3	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-6	chr6:76372937-76373221	NONHSAT113627
2	lnc-SENP6-1	chr6:76164893-76165024	ENSG00000238156
3	lnc-SENP6-9	chr6:76174839-76175286	NONHSAT113617
4	lnc-MYO6-6	chr6:76357008-76357517	NONHSAT113627
5	lnc-FILIP1-2	chr6:76320674-76321504	NONHSAT113622
6	lnc-MYO6-7	chr6:76343366-76343442	NONHSAT113624
7	lnc-MYO6-1	chr6:76362140-76362390	ENSG00000249080
8	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
9	lnc-SENP6-1	chr6:76167878-76167952	ENSG00000238156
10	lnc-SENP6-7	chr6:76209421-76209852	NONHSAT113619
11	lnc-FILIP1-3	chr6:76364686-76365015	NONHSAT113628
12	lnc-FILIP1-2	chr6:76320906-76321661	NONHSAT113623
13	lnc-MYO6-1	chr6:76359931-76362040	ENSG00000249080
14	lnc-MYO6-6	chr6:76368978-76369123	NONHSAT113627
15	lnc-SENP6-1	chr6:76168421-76168616	ENSG00000238156
16	lnc-SENP6-6	chr6:76295838-76296177	NONHSAT113620
17	lnc-SENP6-1	chr6:76164660-76164717	ENSG00000238156
18	lnc-MYO6-7	chr6:76344423-76344772	NONHSAT113624
19	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632

No data

Variant related genes	Relation type
ENSG00000220730	TF binding region
RNU6-1016P	TF binding region
ENSG00000239132	TF binding region
RNU6-1338P	TF binding region
ENSG00000238156	TF binding region
RN7SKP163	TF binding region
FILIP1	TF binding region
SENP6	TF binding region
RNU1-34P	TF binding region
MYO6	TF binding region
ENSG00000217488	TF binding region
RNU6-155P	TF binding region
ENSG00000217680	TF binding region
RPL26P20	TF binding region
RNA5SP209	TF binding region
ENSG00000220730	CpG island
RNU6-1016P	CpG island
ENSG00000239132	CpG island
RNU6-1338P	CpG island
ENSG00000238156	CpG island
RN7SKP163	CpG island
FILIP1	CpG island
SENP6	CpG island
RNU1-34P	CpG island
MYO6	CpG island
ENSG00000217488	CpG island
RNU6-155P	CpG island
ENSG00000217680	CpG island
RPL26P20	CpG island
RNA5SP209	CpG island
ENSG00000225793	chromatin interactions
ENSG00000169715	chromatin interactions
ENSG00000217488	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000252498	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000101447	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000118407	chromatin interactions
ENSG00000231652	chromatin interactions
ENSG00000112695	chromatin interactions
ENSG00000244265	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000181788	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000108854	chromatin interactions
ENSG00000252137	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000123505	chromatin interactions
ENSG00000220730	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000196586	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000164430	chromatin interactions
ENSG00000156535	chromatin interactions
KRAS	miRNA target sites
NR4A2	miRNA target sites

Extended variants
information (count: 14601 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:14601 , 50 per page) page: 1 2 3 4 5 6 7 ... 293

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142891034	chr6:76154825-76154826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546132277	chr6:76154827-76154828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571204900	chr6:76154878-76154879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150785673	chr6:76154901-76154902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576745699	chr6:76154923-76154924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544010533	chr6:76154935-76154936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187114416	chr6:76154950-76154951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528973559	chr6:76155003-76155004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541033436	chr6:76155132-76155133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559042923	chr6:76155327-76155328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200129252	chr6:76155334-76155335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543787073	chr6:76155374-76155375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112631704	chr6:76155442-76155443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184241034	chr6:76155450-76155451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139206581	chr6:76155501-76155502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530644089	chr6:76155506-76155507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35140892	chr6:76155565-76155566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185052421	chr6:76155592-76155593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568255750	chr6:76155625-76155626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535536797	chr6:76155628-76155629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189758281	chr6:76155651-76155652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555783581	chr6:76155709-76155710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574109610	chr6:76155716-76155717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182384433	chr6:76155784-76155785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539805678	chr6:76155793-76155794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187099051	chr6:76155916-76155917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559552692	chr6:76155917-76155918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576806428	chr6:76155919-76155920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111401618	chr6:76156084-76156085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537684590	chr6:76156090-76156091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372032587	chr6:76156096-76156097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541717051	chr6:76156160-76156161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555959195	chr6:76156278-76156279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34747139	chr6:76156294-76156295	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558676764	chr6:76156362-76156363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540743578	chr6:76156419-76156420	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559313728	chr6:76156461-76156462	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577598249	chr6:76156499-76156500	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111718931	chr6:76156524-76156525	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191548398	chr6:76156550-76156551	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578093267	chr6:76156556-76156557	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149501850	chr6:76156587-76156588	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144063022	chr6:76156633-76156634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370351336	chr6:76156728-76156729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529409198	chr6:76156805-76156806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547610734	chr6:76156831-76156832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6930208	chr6:76156851-76156852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140066170	chr6:76156874-76156875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375611046	chr6:76156892-76156893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551237889	chr6:76156902-76156903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Chronic lymphocytic leukemia	21546498	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelodysplastic syndrome	18508791	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:7291 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76146400-76171600	Weak transcription	Right Ventricle	heart
2	chr6:76148000-76156200	Weak transcription	Aorta	Aorta
3	chr6:76148400-76173600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:76148600-76156200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr6:76148800-76177000	Weak transcription	Fetal Muscle Leg	muscle
6	chr6:76149000-76154800	Weak transcription	Psoas Muscle	Psoas
7	chr6:76150400-76154800	Weak transcription	A549	lung
8	chr6:76150400-76156200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:76150400-76168800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:76150600-76156200	Weak transcription	Left Ventricle	heart
11	chr6:76154200-76155200	Enhancers	Colon Smooth Muscle	Colon
12	chr6:76154400-76155400	Enhancers	Rectal Smooth Muscle	rectum
13	chr6:76154600-76155200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:76154600-76155400	Weak transcription	Fetal Heart	heart
15	chr6:76154600-76155600	Enhancers	Fetal Lung	lung
16	chr6:76154800-76155200	Enhancers	Psoas Muscle	Psoas
17	chr6:76154800-76158000	Enhancers	A549	lung
18	chr6:76154800-76159200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:76155000-76155400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:76155200-76156200	Weak transcription	Psoas Muscle	Psoas
21	chr6:76155200-76156400	Weak transcription	Colon Smooth Muscle	Colon
22	chr6:76155200-76159000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:76155400-76155600	Enhancers	Fetal Heart	heart
24	chr6:76155400-76155800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr6:76155400-76159000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:76155600-76156000	Weak transcription	Fetal Heart	heart
27	chr6:76155600-76168000	Weak transcription	Fetal Lung	lung
28	chr6:76155800-76157200	Enhancers	Rectal Smooth Muscle	rectum
29	chr6:76156000-76157400	Enhancers	Fetal Heart	heart
30	chr6:76156200-76156400	Enhancers	Left Ventricle	heart
31	chr6:76156200-76156400	Enhancers	NHDF-Ad	bronchial
32	chr6:76156200-76156600	Enhancers	Aorta	Aorta
33	chr6:76156200-76156600	Enhancers	Psoas Muscle	Psoas
34	chr6:76156200-76156600	Enhancers	Right Atrium	heart
35	chr6:76156200-76156800	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr6:76156200-76156800	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr6:76156400-76156600	Genic enhancers	Left Ventricle	heart
38	chr6:76156400-76156800	Enhancers	Colon Smooth Muscle	Colon
39	chr6:76156400-76159200	Weak transcription	NHDF-Ad	bronchial
40	chr6:76156600-76159600	Weak transcription	Aorta	Aorta
41	chr6:76156600-76167600	Weak transcription	Psoas Muscle	Psoas
42	chr6:76156600-76171400	Weak transcription	Left Ventricle	heart
43	chr6:76156800-76159200	Weak transcription	Colon Smooth Muscle	Colon
44	chr6:76156800-76169800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:76156800-76170800	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr6:76157400-76164800	Weak transcription	Fetal Heart	heart
47	chr6:76158000-76159200	Weak transcription	A549	lung
48	chr6:76159000-76160000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:76159000-76160000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:76159200-76159400	Enhancers	Colon Smooth Muscle	Colon

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