Variant report

Variant	nsv1032961
Chromosome Location	chr6:76343575-76788852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2766)
CpG islands
(count:1526)
Chromatin interactive
region (count:203)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:2766 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76601370-76601603	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:76484978-76485281	K562	blood:	n/a	n/a
3	ARID3A	chr6:76562512-76562787	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:76643375-76643655	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
10	ARID3A	chr6:76532773-76532821	HepG2	liver:	n/a	n/a
11	ATF1	chr6:76562615-76562871	K562	blood:	n/a	n/a
12	ATF1	chr6:76517943-76518107	K562	blood:	n/a	n/a
13	ATF1	chr6:76757267-76757352	K562	blood:	n/a	n/a
14	ATF2	chr6:76540581-76541147	GM12878	blood:	n/a	n/a
15	ATF2	chr6:76540625-76541135	GM12878	blood:	n/a	n/a
16	ATF2	chr6:76703028-76703778	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:76636098-76636563	GM12878	blood:	n/a	n/a
18	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
19	BACH1	chr6:76523240-76523470	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:76644723-76645282	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:76603125-76603698	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
25	BACH1	chr6:76783062-76783350	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:76783055-76783343	K562	blood:	n/a	n/a
27	BACH1	chr6:76407134-76407232	K562	blood:	n/a	n/a
28	BATF	chr6:76540606-76541165	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
29	BATF	chr6:76641889-76642089	GM12878	blood:	n/a	n/a
30	BATF	chr6:76713845-76714245	GM12878	blood:	n/a	chr6:76714006-76714015
31	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a
32	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
33	BATF	chr6:76491591-76491869	GM12878	blood:	n/a	chr6:76491779-76491789
34	BATF	chr6:76540656-76541080	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
35	BATF	chr6:76636006-76636350	GM12878	blood:	n/a	n/a
36	BATF	chr6:76713883-76714156	GM12878	blood:	n/a	chr6:76714006-76714015
37	BCL11A	chr6:76540633-76541116	GM12878	blood:	n/a	chr6:76541003-76541012
38	BCL11A	chr6:76453680-76454055	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:76540692-76541027	GM12878	blood:	n/a	chr6:76541003-76541012
40	BCL11A	chr6:76453638-76454028	GM12878	blood:	n/a	n/a
41	BCL3	chr6:76540681-76541141	GM12878	blood:	n/a	chr6:76541003-76541012
42	BCLAF1	chr6:76540594-76541163	GM12878	blood:	n/a	chr6:76541003-76541012
43	BCLAF1	chr6:76540610-76541170	GM12878	blood:	n/a	chr6:76541003-76541012
44	BHLHE40	chr6:76716529-76716801	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:76644694-76645145	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:76486318-76486449	K562	blood:	n/a	n/a
47	BHLHE40	chr6:76458636-76459067	K562	blood:	n/a	chr6:76459001-76459017
48	BHLHE40	chr6:76485025-76485362	K562	blood:	n/a	n/a
49	BHLHE40	chr6:76463942-76463968	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:76533999-76534219	GM12878	blood:	n/a	n/a

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76459077-76459127	GM12878	blood:	n/a
2	chr6:76459077-76459127	GM12878	blood:	n/a
3	chr6:76631383-76631433	CMK	blood:	n/a
4	chr6:76702942-76702992	SK-N-SH	brain:	n/a
5	chr6:76762173-76762223	HRCEpiC	kidney:	n/a
6	chr6:76458633-76458683	HEEpiC	esophagus:	n/a
7	chr6:76583931-76583981	SK-N-SH	brain:	n/a
8	chr6:76459077-76459127	T-47D	breast:	n/a
9	chr6:76458005-76458055	NHDF-neo	bronchial:	n/a
10	chr6:76762173-76762223	HIPEpiC	eye:	n/a
11	chr6:76461321-76461371	Hepatocyte	liver:	n/a
12	chr6:76702942-76702992	HIPEpiC	eye:	n/a
13	chr6:76644807-76644857	HCF	heart:	n/a
14	chr6:76456187-76456237	HIPEpiC	eye:	n/a
15	chr6:76645123-76645173	A549	lung:	n/a
16	chr6:76645016-76645066	HEK293	kidney:	embryo
17	chr6:76724431-76724481	HNPCEpiC	eye:	n/a
18	chr6:76636725-76636775	GM12892	blood:	n/a
19	chr6:76645008-76645058	SK-N-SH_RA	brain:	n/a
20	chr6:76702942-76702992	A549	lung:	n/a
21	chr6:76644222-76644272	HepG2	liver:	n/a
22	chr6:76603364-76603414	AG10803	skin:	n/a
23	chr6:76645016-76645066	BJ	skin:	n/a
24	chr6:76645123-76645173	HL-60	blood:	n/a
25	chr6:76456187-76456237	ProgFib	skin:	n/a
26	chr6:76461321-76461371	GM06990	blood:	n/a
27	chr6:76456187-76456237	Caco-2	colon:	n/a
28	chr6:76458633-76458683	AG10803	skin:	n/a
29	chr6:76696290-76696340	AG09319	gingival:	n/a
30	chr6:76696290-76696340	HL-60	blood:	n/a
31	chr6:76645016-76645066	HL-60	blood:	n/a
32	chr6:76583931-76583981	HNPCEpiC	eye:	n/a
33	chr6:76603364-76603414	K562	blood:	n/a
34	chr6:76644790-76644840	HCPEpiC	choroid plexus:	n/a
35	chr6:76696290-76696340	AG09309	skin:	n/a
36	chr6:76702942-76702992	HEEpiC	esophagus:	n/a
37	chr6:76425457-76425507	HRE	kidney:	n/a
38	chr6:76645008-76645058	K562	blood:	n/a
39	chr6:76645123-76645173	RPTEC	kidney:	n/a
40	chr6:76644807-76644857	HAEpiC	amniotic membrane:	n/a
41	chr6:76645016-76645066	BE2_C	brain:	n/a
42	chr6:76631383-76631433	LNCaP	prostate:	n/a
43	chr6:76636725-76636775	MCF10A-Er-Src	breast:	n/a
44	chr6:76456187-76456237	CMK	blood:	n/a
45	chr6:76645008-76645058	HIPEpiC	eye:	n/a
46	chr6:76644790-76644840	NHBE	bronchial:	n/a
47	chr6:76696290-76696340	NB4	blood:	n/a
48	chr6:76459077-76459127	HUVEC	blood vessel:	n/a
49	chr6:76458633-76458683	HCF	heart:	n/a
50	chr6:76459511-76459561	HAEpiC	amniotic membrane:	n/a

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:76564297..76564995-chr6:76602725..76603462,2	MCF-7	breast:
2	chr6:76354605..76357480-chr6:76358370..76361189,2	MCF-7	breast:
3	chr3:150479690..150481282-chr6:76352345..76354574,2	MCF-7	breast:
4	chr6:76457614..76459414-chr6:76469003..76470756,2	K562	blood:
5	chr6:76457754..76460582-chr6:76467683..76471676,6	MCF-7	breast:
6	chr6:76423467..76426296-chr6:76461021..76463732,3	MCF-7	breast:
7	chr6:76416198..76418365-chr6:76457940..76460718,3	MCF-7	breast:
8	chr6:76348520..76350771-chr6:76351491..76354055,3	K562	blood:
9	chr6:76465017..76467292-chr6:76472497..76474825,2	K562	blood:
10	chr6:76519784..76521479-chr6:76528977..76530844,2	MCF-7	breast:
11	chr6:76617686..76620159-chr6:76629560..76631488,2	MCF-7	breast:
12	chr6:76441614..76445337-chr6:76457792..76459831,5	MCF-7	breast:
13	chr6:76445351..76447592-chr6:76454801..76459037,4	MCF-7	breast:
14	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
15	chr6:76463940..76466517-chr6:76472497..76474287,2	K562	blood:
16	chr5:151542542..151543442-chr6:76603129..76603708,2	MCF-7	breast:
17	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
18	chr6:76431586..76433985-chr6:76438066..76440225,2	MCF-7	breast:
19	chr6:76465017..76467292-chr6:76472497..76474825,2	K562	blood:
20	chr6:76330148..76333811-chr6:76341672..76344273,3	K562	blood:
21	chr6:76310839..76313480-chr6:76354672..76356986,2	MCF-7	breast:
22	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
23	chr6:76369470..76371755-chr6:76372281..76373933,2	K562	blood:
24	chr6:76522682..76525185-chr6:76527621..76531483,3	MCF-7	breast:
25	chr6:76456988..76460628-chr6:76493059..76496718,4	MCF-7	breast:
26	chr6:76467679..76470814-chr6:76472807..76475124,3	K562	blood:
27	chr6:76456486..76459516-chr6:76469446..76471432,3	MCF-7	breast:
28	chr6:76426836..76429906-chr6:76458673..76460595,3	MCF-7	breast:
29	chr6:76478606..76481168-chr6:76482628..76484653,2	MCF-7	breast:
30	chr6:76458193..76461486-chr6:76482230..76486067,4	MCF-7	breast:
31	chr6:76465841..76467549-chr6:76494669..76496179,2	MCF-7	breast:
32	chr6:76711975..76713621-chr6:76719761..76721754,2	K562	blood:
33	chr6:76459866..76461619-chr6:76483545..76486040,2	K562	blood:
34	chr6:76467679..76470814-chr6:76472807..76475124,3	K562	blood:
35	chr6:76461303..76463860-chr6:76468925..76471220,2	K562	blood:
36	chr6:76371815..76374314-chr6:76380785..76382399,2	MCF-7	breast:
37	chr6:76402073..76403999-chr6:76420565..76422699,2	MCF-7	breast:
38	chr6:76348810..76350607-chr6:76352555..76355121,2	K562	blood:
39	chr6:76457017..76459821-chr6:76526945..76528874,2	MCF-7	breast:
40	chr6:76408144..76410485-chr6:76410972..76412755,2	MCF-7	breast:
41	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:
42	chr6:76472032..76473906-chr6:76480774..76483408,2	MCF-7	breast:
43	chr6:76312117..76313931-chr6:76346420..76348406,2	K562	blood:
44	chr6:76459866..76461619-chr6:76483545..76486040,2	K562	blood:
45	chr6:76600564..76603457-chr6:76615084..76617457,2	MCF-7	breast:
46	chr6:76310966..76312781-chr6:76360511..76362036,2	MCF-7	breast:
47	chr6:76423467..76426296-chr6:76461021..76463732,3	MCF-7	breast:
48	chr6:76310342..76312305-chr6:76373129..76377244,3	K562	blood:
49	chr6:76530548..76533502-chr6:76541265..76544166,2	K562	blood:
50	chr6:76458666..76460451-chr6:76537768..76540622,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-6	chr6:76372937-76373221	NONHSAT113627
2	lnc-FILIP1-3	chr6:76364686-76365015	NONHSAT113628
3	lnc-MYO6-1	chr6:76359931-76362040	ENSG00000249080
4	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
5	lnc-MYO6-6	chr6:76368978-76369123	NONHSAT113627
6	lnc-MYO6-1	chr6:76362140-76362390	ENSG00000249080
7	lnc-MYO6-7	chr6:76344423-76344772	NONHSAT113624
8	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632
9	lnc-MYO6-6	chr6:76357008-76357517	NONHSAT113627
10	lnc-MYO6-4	chr6:76673631-76673965	expReg_chr6_7326_+

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MYO6	hsa-miR-143-3p	chr6:76625556-76625576
2	MYO6	hsa-miR-145-5p	chr6:76625088-76625110
3	MYO6	hsa-miR-320a	chr6:76625812-76625831
4	MYO6	hsa-miR-143-3p	chr6:76625569-76625576
5	MYO6	hsa-miR-145-5p	chr6:76625538-76625544
6	MYO6	hsa-miR-145-5p	chr6:76625103-76625109

Variant related genes	Relation type
RN7SKP163	TF binding region
SENP6	TF binding region
IMPG1	TF binding region
ENSG00000200040	TF binding region
MYO6	TF binding region
RNU6-1016P	TF binding region
ENSG00000239132	TF binding region
RNU6-155P	TF binding region
RNA5SP209	TF binding region
RN7SKP163	CpG island
SENP6	CpG island
IMPG1	CpG island
ENSG00000200040	CpG island
MYO6	CpG island
RNU6-1016P	CpG island
ENSG00000239132	CpG island
RNU6-155P	CpG island
RNA5SP209	CpG island
ENSG00000001167	chromatin interactions
ENSG00000181788	chromatin interactions
ENSG00000244265	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000252498	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000217488	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000196586	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000155903	chromatin interactions
NR4A2	miRNA target sites
KRAS	miRNA target sites

Extended variants
information (count: 13895 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:13895 , 50 per page) page: 1 2 3 4 5 6 7 ... 278

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191975357	chr6:76343646-76343647	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577297252	chr6:76343653-76343654	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35191416	chr6:76343655-76343656	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371941676	chr6:76343739-76343740	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182649202	chr6:76343771-76343772	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562939003	chr6:76343774-76343775	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12214738	chr6:76343783-76343784	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548554774	chr6:76343829-76343830	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72654719	chr6:76343916-76343917	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527968220	chr6:76343962-76343963	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552782109	chr6:76343987-76343988	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570933867	chr6:76344000-76344001	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372321074	chr6:76344056-76344057	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537978967	chr6:76344087-76344088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs9360928	chr6:76344148-76344149	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532535579	chr6:76344184-76344185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141935560	chr6:76344204-76344205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567770458	chr6:76344238-76344239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs17529743	chr6:76344267-76344268	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs112881123	chr6:76344285-76344286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553344063	chr6:76344332-76344333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79980437	chr6:76344355-76344356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573057877	chr6:76344356-76344357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187652360	chr6:76344387-76344388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199617972	chr6:76344394-76344395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557969144	chr6:76344406-76344407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576175671	chr6:76344419-76344420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17414086	chr6:76344431-76344432	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs191685973	chr6:76344432-76344433	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs371315357	chr6:76344446-76344447	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs374561849	chr6:76344447-76344448	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs574943056	chr6:76344449-76344450	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs531966562	chr6:76344476-76344477	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs199794830	chr6:76344490-76344491	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs542282733	chr6:76344496-76344497	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs150751620	chr6:76344504-76344505	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs374768053	chr6:76344523-76344524	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs72654720	chr6:76344543-76344544	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371550363	chr6:76344556-76344557	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs575371402	chr6:76344588-76344589	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs559499945	chr6:76344599-76344600	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs139075507	chr6:76344647-76344648	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs545297820	chr6:76344650-76344651	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs549923112	chr6:76344684-76344685	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs567856465	chr6:76344700-76344701	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs535174558	chr6:76344717-76344718	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs547019296	chr6:76344738-76344739	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs116745924	chr6:76344794-76344795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75680264	chr6:76344823-76344824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149460546	chr6:76344875-76344876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
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	21293372	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5448 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76319800-76348400	Weak transcription	NHEK	skin
2	chr6:76320200-76351800	Weak transcription	HSMMtube	muscle
3	chr6:76320200-76391600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr6:76321200-76348400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:76321800-76370400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:76322600-76361000	Weak transcription	Thymus	Thymus
7	chr6:76330400-76349600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:76330400-76349800	Weak transcription	Colonic Mucosa	Colon
9	chr6:76330400-76361000	Weak transcription	Esophagus	oesophagus
10	chr6:76330600-76346600	Weak transcription	Left Ventricle	heart
11	chr6:76330600-76361200	Weak transcription	Spleen	Spleen
12	chr6:76330600-76368600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr6:76330600-76369800	Weak transcription	Right Ventricle	heart
14	chr6:76330600-76370200	Weak transcription	Aorta	Aorta
15	chr6:76330600-76381600	Weak transcription	Stomach Mucosa	stomach
16	chr6:76330600-76390400	Weak transcription	Gastric	stomach
17	chr6:76330800-76348400	Weak transcription	Fetal Brain Female	brain
18	chr6:76331000-76349600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr6:76331400-76352600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr6:76331600-76356200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:76331800-76361000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr6:76331800-76361200	Weak transcription	Brain Germinal Matrix	brain
23	chr6:76332000-76357400	Weak transcription	Brain Anterior Caudate	brain
24	chr6:76332000-76368400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:76332200-76356400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:76332800-76389000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:76333000-76365800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr6:76333000-76366000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:76333200-76349600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr6:76333200-76391000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:76333600-76361000	Weak transcription	Fetal Brain Male	brain
32	chr6:76333800-76358400	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr6:76335200-76343800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:76335200-76345200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr6:76335200-76370600	Weak transcription	Psoas Muscle	Psoas
36	chr6:76335400-76348200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr6:76335400-76354400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr6:76335400-76388800	Weak transcription	Small Intestine	intestine
39	chr6:76335600-76348600	Weak transcription	Pancreas	Pancrea
40	chr6:76335600-76370400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:76336200-76344400	Strong transcription	Fetal Thymus	thymus
42	chr6:76336400-76354800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:76337400-76347000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr6:76337600-76346600	Weak transcription	Lung	lung
45	chr6:76337600-76347600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr6:76338800-76346400	Weak transcription	Ovary	ovary
47	chr6:76338800-76346600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr6:76339200-76366400	Strong transcription	Dnd41	blood
49	chr6:76339400-76346400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr6:76339400-76402000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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