Variant report

Variant	nsv1031745
Chromosome Location	chr6:76257913-76493355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2418)
CpG islands
(count:1098)
Chromatin interactive
region (count:226)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2418 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76337921-76337975	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:76339500-76339892	K562	blood:	n/a	n/a
4	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76320480-76320552	K562	blood:	n/a	n/a
6	ARID3A	chr6:76322881-76323353	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:76312666-76313021	K562	blood:	n/a	n/a
8	ARID3A	chr6:76342477-76343204	K562	blood:	n/a	chr6:76342662-76342678
9	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:76272954-76273059	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:76311201-76311902	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:76333004-76333194	K562	blood:	n/a	n/a
13	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
14	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:76484978-76485281	K562	blood:	n/a	n/a
16	ARID3A	chr6:76331504-76331869	K562	blood:	n/a	n/a
17	ARID3A	chr6:76313655-76313921	K562	blood:	n/a	n/a
18	ARID3A	chr6:76315396-76315502	K562	blood:	n/a	n/a
19	ATF1	chr6:76342790-76343022	K562	blood:	n/a	n/a
20	ATF2	chr6:76311636-76312501	GM12878	blood:	n/a	n/a
21	ATF2	chr6:76260318-76260565	GM12878	blood:	n/a	n/a
22	ATF2	chr6:76260226-76260768	GM12878	blood:	n/a	n/a
23	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
24	BACH1	chr6:76261204-76261211	K562	blood:	n/a	n/a
25	BACH1	chr6:76312675-76312783	K562	blood:	n/a	n/a
26	BACH1	chr6:76311710-76311864	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:76318040-76318256	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
31	BACH1	chr6:76407134-76407232	K562	blood:	n/a	n/a
32	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a
33	BATF	chr6:76260251-76260762	GM12878	blood:	n/a	chr6:76260414-76260423
34	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
35	BATF	chr6:76289645-76290038	GM12878	blood:	n/a	n/a
36	BATF	chr6:76491591-76491869	GM12878	blood:	n/a	chr6:76491779-76491789
37	BCL11A	chr6:76289736-76289977	GM12878	blood:	n/a	n/a
38	BCL11A	chr6:76289699-76289966	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:76453638-76454028	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:76453680-76454055	GM12878	blood:	n/a	n/a
41	BCL3	chr6:76311339-76311837	GM12878	blood:	n/a	chr6:76311730-76311739 chr6:76311800-76311813 chr6:76311732-76311745 chr6:76311798-76311807
42	BCLAF1	chr6:76289601-76290063	GM12878	blood:	n/a	n/a
43	BCLAF1	chr6:76311198-76312444	GM12878	blood:	n/a	chr6:76311730-76311739 chr6:76311800-76311813 chr6:76311732-76311745 chr6:76311798-76311807
44	BCLAF1	chr6:76311127-76312480	GM12878	blood:	n/a	chr6:76311730-76311739 chr6:76311800-76311813 chr6:76311732-76311745 chr6:76311798-76311807
45	BHLHE40	chr6:76312095-76312309	K562	blood:	n/a	n/a
46	BHLHE40	chr6:76289720-76290070	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:76397729-76398031	K562	blood:	n/a	n/a
48	BHLHE40	chr6:76311300-76311866	K562	blood:	n/a	chr6:76311797-76311813
49	BHLHE40	chr6:76485025-76485362	K562	blood:	n/a	n/a
50	BHLHE40	chr6:76311312-76311822	GM12878	blood:	n/a	chr6:76311797-76311813

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76312378-76312428	PFSK-1	brain:	n/a
2	chr6:76311363-76311413	AoSMC	blood vessel:	n/a
3	chr6:76458633-76458683	AG09309	skin:	n/a
4	chr6:76309300-76309350	SK-N-SH	brain:	n/a
5	chr6:76461321-76461371	LNCaP	prostate:	n/a
6	chr6:76310551-76310601	AG04449	skin:	fetal
7	chr6:76341733-76341783	U87	brain:	n/a
8	chr6:76458005-76458055	HRE	kidney:	n/a
9	chr6:76319793-76319843	H1-hESC	embryonic stem cell:	embryo
10	chr6:76456187-76456237	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:76315197-76315247	CMK	blood:	n/a
12	chr6:76311363-76311413	NHBE	bronchial:	n/a
13	chr6:76458633-76458683	HCF	heart:	n/a
14	chr6:76459077-76459127	NH-A	brain:	n/a
15	chr6:76309300-76309350	BE2_C	brain:	n/a
16	chr6:76310551-76310601	HL-60	blood:	n/a
17	chr6:76341733-76341783	HMEC	breast:	n/a
18	chr6:76330505-76330555	HCPEpiC	choroid plexus:	n/a
19	chr6:76458005-76458055	PANC-1	pancreas:	n/a
20	chr6:76330505-76330555	NHDF-neo	bronchial:	n/a
21	chr6:76311363-76311413	GM12891	blood:	n/a
22	chr6:76330505-76330555	HEEpiC	esophagus:	n/a
23	chr6:76311331-76311381	CMK	blood:	n/a
24	chr6:76310551-76310601	PrEC	prostate:	n/a
25	chr6:76330505-76330555	HEK293	kidney:	embryo
26	chr6:76311636-76311686	HCPEpiC	choroid plexus:	n/a
27	chr6:76311363-76311413	MCF10A-Er-Src	breast:	n/a
28	chr6:76309300-76309350	AG04450	lung:	fetal
29	chr6:76310551-76310601	HRPEpiC	eye:	n/a
30	chr6:76309300-76309350	GM12878	blood:	n/a
31	chr6:76312378-76312428	SK-N-SH	brain:	n/a
32	chr6:76458005-76458055	GM19239	blood:	n/a
33	chr6:76311331-76311381	HCF	heart:	n/a
34	chr6:76341733-76341783	HepG2	liver:	n/a
35	chr6:76312378-76312428	NT2-D1	testis:	n/a
36	chr6:76459077-76459127	ovcar-3	ovarian:	n/a
37	chr6:76311331-76311381	U87	brain:	n/a
38	chr6:76309300-76309350	PFSK-1	brain:	n/a
39	chr6:76458005-76458055	Jurkat	blood:	n/a
40	chr6:76310551-76310601	SK-N-MC	brain:	n/a
41	chr6:76311363-76311413	NH-A	brain:	n/a
42	chr6:76458005-76458055	PrEC	prostate:	n/a
43	chr6:76459077-76459127	AG09319	gingival:	n/a
44	chr6:76311636-76311686	HEEpiC	esophagus:	n/a
45	chr6:76312378-76312428	HUVEC	blood vessel:	n/a
46	chr6:76461321-76461371	IMR90	lung:	fetal
47	chr6:76312378-76312428	AoSMC	blood vessel:	n/a
48	chr6:76312378-76312428	NHBE	bronchial:	n/a
49	chr6:76341733-76341783	NHBE	bronchial:	n/a
50	chr6:76341733-76341783	HCF	heart:	n/a

(count:226 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:76295830..76298564-chr6:76308288..76310113,2	MCF-7	breast:
2	chr6:76373474..76375579-chr6:76380760..76383330,2	K562	blood:
3	chr6:76406647..76409621-chr6:76410785..76413589,2	K562	blood:
4	chr6:76458193..76461486-chr6:76482230..76486067,4	MCF-7	breast:
5	chr6:76310717..76312305-chr6:76374454..76377244,2	K562	blood:
6	chr6:76424657..76427289-chr6:76428050..76430901,3	MCF-7	breast:
7	chr6:74405547..74407236-chr6:76311267..76312799,2	MCF-7	breast:
8	chr6:76337128..76338933-chr6:76358786..76360573,2	K562	blood:
9	chr6:76431586..76433985-chr6:76438066..76440225,2	MCF-7	breast:
10	chr6:76397986..76399777-chr6:76458759..76460559,2	MCF-7	breast:
11	chr6:76306113..76308673-chr6:76313720..76315996,2	K562	blood:
12	chr6:76457060..76461197-chr6:76473704..76478813,6	MCF-7	breast:
13	chr14:21923624..21924407-chr6:76311791..76312313,2	MCF-7	breast:
14	chr6:76354605..76357480-chr6:76358370..76361189,2	MCF-7	breast:
15	chr6:76458966..76460939-chr6:76574214..76577179,2	MCF-7	breast:
16	chr6:76348810..76350607-chr6:76352555..76355121,2	K562	blood:
17	chr6:76312246..76314943-chr6:76370644..76373354,2	MCF-7	breast:
18	chr6:76456505..76458923-chr6:76460845..76462733,2	K562	blood:
19	chr6:76310925..76313590-chr6:76457201..76459634,2	K562	blood:
20	chr6:76325725..76327529-chr6:76327837..76330229,2	K562	blood:
21	chr6:76457017..76459821-chr6:76526945..76528874,2	MCF-7	breast:
22	chr6:76361046..76364656-chr6:76366287..76368782,3	K562	blood:
23	chr6:76310839..76313480-chr6:76354672..76356986,2	MCF-7	breast:
24	chr6:76312467..76314027-chr6:76330257..76332737,2	K562	blood:
25	chr6:76467679..76470814-chr6:76472807..76475124,3	K562	blood:
26	chr6:76301594..76304347-chr6:76310698..76312348,3	MCF-7	breast:
27	chr6:76286862..76288767-chr6:76289048..76291040,2	MCF-7	breast:
28	chr6:76311276..76313926-chr6:76328791..76332406,4	MCF-7	breast:
29	chr6:76469142..76471151-chr6:76480358..76482124,2	MCF-7	breast:
30	chr6:76415966..76418474-chr6:76457642..76460557,4	MCF-7	breast:
31	chr6:76465841..76467549-chr6:76494669..76496179,2	MCF-7	breast:
32	chr6:76312117..76313931-chr6:76346420..76348406,2	K562	blood:
33	chr11:93474252..93474772-chr6:76458412..76459090,2	Hela-S3	cervix:
34	chr6:76359039..76361608-chr6:76376741..76379401,2	MCF-7	breast:
35	chr17:56735238..56737884-chr6:76312067..76314109,2	MCF-7	breast:
36	chr6:76348163..76350859-chr6:76356641..76358719,2	K562	blood:
37	chr6:76316110..76319023-chr6:76339771..76341687,2	K562	blood:
38	chr6:76330148..76333811-chr6:76341672..76344273,3	K562	blood:
39	chr6:76310342..76312305-chr6:76373129..76377244,3	K562	blood:
40	chr6:76356613..76358787-chr6:76370587..76373323,2	K562	blood:
41	chr6:76366871..76369155-chr6:76374703..76377343,2	MCF-7	breast:
42	chr6:76369769..76371871-chr6:76379242..76380946,2	K562	blood:
43	chr6:76316605..76319587-chr6:76326249..76328171,2	MCF-7	breast:
44	chr6:76463940..76466517-chr6:76472497..76474287,2	K562	blood:
45	chr6:75973426..75975778-chr6:76313491..76316125,2	K562	blood:
46	chr2:67624427..67625159-chr6:76458926..76459754,2	Hela-S3	cervix:
47	chr6:76314618..76316766-chr6:76326972..76330457,3	K562	blood:
48	chr6:74229402..74231607-chr6:76310929..76313785,2	K562	blood:
49	chr17:62658047..62658828-chr6:76312151..76312940,2	Hela-S3	cervix:
50	chr6:76298381..76301021-chr6:76312234..76315010,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FILIP1-2	chr6:76320674-76321504	NONHSAT113622
2	lnc-MYO6-6	chr6:76372937-76373221	NONHSAT113627
3	lnc-FILIP1-2	chr6:76320906-76321661	NONHSAT113623
4	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
5	lnc-SENP6-6	chr6:76295838-76296177	NONHSAT113620
6	lnc-FILIP1-3	chr6:76364686-76365015	NONHSAT113628
7	lnc-MYO6-7	chr6:76343366-76343442	NONHSAT113624
8	lnc-MYO6-6	chr6:76368978-76369123	NONHSAT113627
9	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632
10	lnc-MYO6-7	chr6:76344423-76344772	NONHSAT113624
11	lnc-MYO6-6	chr6:76357008-76357517	NONHSAT113627
12	lnc-MYO6-1	chr6:76362140-76362390	ENSG00000249080
13	lnc-MYO6-1	chr6:76359931-76362040	ENSG00000249080

No data

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

Extended variants
information (count: 8052 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8052 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547897745	chr6:76261101-76261102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566190008	chr6:76261172-76261173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6940127	chr6:76261177-76261178	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558263570	chr6:76261187-76261188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35128224	chr6:76261203-76261204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13204866	chr6:76261244-76261245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528795215	chr6:76261298-76261299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78202191	chr6:76261359-76261360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182529968	chr6:76261363-76261364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535608531	chr6:76261445-76261446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534234324	chr6:76261500-76261501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12196108	chr6:76261529-76261530	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs61234544	chr6:76261562-76261563	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs58183765	chr6:76261564-76261565	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370455364	chr6:76261565-76261566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72380277	chr6:76261566-76261567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528906510	chr6:76264255-76264256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540981807	chr6:76264256-76264257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559435497	chr6:76264257-76264258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533247687	chr6:76264263-76264264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376543649	chr6:76264265-76264266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546076132	chr6:76264317-76264318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199642669	chr6:76264351-76264352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545878303	chr6:76264378-76264379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371678922	chr6:76265342-76265343	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552063246	chr6:76265347-76265348	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11755821	chr6:76265360-76265361	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570316973	chr6:76265429-76265430	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs34246595	chr6:76265433-76265434	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184884767	chr6:76265434-76265435	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs62414234	chr6:76265455-76265456	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188222549	chr6:76265471-76265472	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138984453	chr6:76265483-76265484	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181099167	chr6:76265538-76265539	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534692453	chr6:76265546-76265547	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530663207	chr6:76265612-76265613	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9360921	chr6:76265642-76265643	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
38	rs140443709	chr6:76265705-76265706	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544635660	chr6:76265719-76265720	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs55971756	chr6:76265724-76265725	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs548179119	chr6:76265754-76265755	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186275257	chr6:76265759-76265760	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114450249	chr6:76265826-76265827	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529283901	chr6:76265839-76265840	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191571012	chr6:76265889-76265890	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112047229	chr6:76265942-76265943	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144358531	chr6:76265944-76265945	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566488288	chr6:76265945-76265946	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs57285115	chr6:76265961-76265962	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560730377	chr6:76266012-76266013	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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	18451855	CNVD

Chromatin state (count:4992 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76261000-76261600	Enhancers	GM12878-XiMat	blood
2	chr6:76264200-76264400	Enhancers	Esophagus	oesophagus
3	chr6:76265400-76266200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:76265400-76266200	Enhancers	Fetal Intestine Large	intestine
5	chr6:76265400-76266600	Enhancers	Fetal Intestine Small	intestine
6	chr6:76265600-76266200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:76265600-76266600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:76265800-76266200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr6:76265800-76266200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:76265800-76266200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:76265800-76266600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:76266000-76266400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:76266600-76266800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:76266800-76267000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:76268400-76268600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:76276000-76276200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:76276000-76276600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:76276800-76277200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:76280600-76281000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:76281000-76289000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:76289000-76291400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:76289400-76290000	Enhancers	GM12878-XiMat	blood
23	chr6:76289400-76290200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:76289400-76290200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr6:76289600-76290000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr6:76290200-76291600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr6:76290600-76291200	Enhancers	NHDF-Ad	bronchial
28	chr6:76291800-76292000	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr6:76298800-76305600	Weak transcription	Fetal Intestine Small	intestine
30	chr6:76302600-76303200	Enhancers	Fetal Intestine Large	intestine
31	chr6:76303200-76305600	Weak transcription	Fetal Intestine Large	intestine
32	chr6:76305600-76306000	Enhancers	Fetal Intestine Large	intestine
33	chr6:76305600-76306200	Enhancers	Fetal Intestine Small	intestine
34	chr6:76305600-76306800	Enhancers	HepG2	liver
35	chr6:76306000-76310000	Weak transcription	Fetal Intestine Large	intestine
36	chr6:76306200-76309000	Weak transcription	Fetal Intestine Small	intestine
37	chr6:76306600-76306800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:76306600-76307800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:76306600-76308200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr6:76306600-76308200	Enhancers	Colon Smooth Muscle	Colon
41	chr6:76306800-76307600	Enhancers	Primary B cells from peripheral blood	blood
42	chr6:76306800-76307600	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr6:76306800-76308000	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr6:76306800-76308200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr6:76306800-76308200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:76306800-76308400	Enhancers	Rectal Smooth Muscle	rectum
47	chr6:76306800-76310400	Weak transcription	HepG2	liver
48	chr6:76307000-76308200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr6:76307200-76308200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr6:76307200-76308200	Enhancers	Primary T helper cells PMA-I stimulated	--

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