Variant report

Variant	nsv428162
Chromosome Location	chr7:11085784-11359333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1406)
CpG islands
(count:489)
Chromatin interactive
region (count:152)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:11251750-11252065	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:11122472-11122755	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:11321430-11322312	K562	blood:	n/a	n/a
4	ARID3A	chr7:11287818-11288185	HepG2	liver:	n/a	n/a
5	ATF1	chr7:11321603-11321938	K562	blood:	n/a	n/a
6	ATF1	chr7:11128773-11128831	K562	blood:	n/a	n/a
7	ATF1	chr7:11295980-11296164	K562	blood:	n/a	n/a
8	ATF1	chr7:11221045-11221594	K562	blood:	n/a	n/a
9	ATF2	chr7:11224807-11225248	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:11122404-11123057	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:11224855-11225204	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:11232775-11233077	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:11231364-11231607	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:11102229-11102429	K562	blood:	n/a	n/a
15	BACH1	chr7:11175371-11175473	K562	blood:	n/a	n/a
16	BACH1	chr7:11296612-11296698	K562	blood:	n/a	n/a
17	BACH1	chr7:11321579-11321959	K562	blood:	n/a	n/a
18	BACH1	chr7:11232750-11233085	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr7:11118081-11118314	GM12878	blood:	n/a	chr7:11118255-11118265
20	BATF	chr7:11118139-11118345	GM12878	blood:	n/a	chr7:11118255-11118265
21	BATF	chr7:11160374-11160600	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:11224826-11225121	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr7:11224931-11225119	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr7:11195043-11195271	GM12878	blood:	n/a	n/a
25	BCLAF1	chr7:11251750-11252062	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:11228287-11228806	K562	blood:	n/a	n/a
27	BHLHE40	chr7:11297291-11297301	K562	blood:	n/a	n/a
28	BHLHE40	chr7:11258948-11259424	K562	blood:	n/a	n/a
29	BHLHE40	chr7:11253041-11253054	HepG2	liver:	n/a	n/a
30	BHLHE40	chr7:11321620-11321922	K562	blood:	n/a	n/a
31	BHLHE40	chr7:11305072-11305074	K562	blood:	n/a	n/a
32	BHLHE40	chr7:11251822-11252032	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:11215693-11215816	K562	blood:	n/a	n/a
34	BHLHE40	chr7:11210726-11210891	GM12878	blood:	n/a	n/a
35	BRCA1	chr7:11167087-11167179	GM12878	blood:	n/a	n/a
36	BRCA1	chr7:11254177-11254219	GM12878	blood:	n/a	n/a
37	CBX3	chr7:11321519-11321993	K562	blood:	n/a	n/a
38	CCNT2	chr7:11321665-11322011	K562	blood:	n/a	n/a
39	CCNT2	chr7:11217186-11217420	K562	blood:	n/a	n/a
40	CEBPB	chr7:11108217-11108264	H1-hESC	embryonic stem cell:	n/a	chr7:11108241-11108252
41	CEBPB	chr7:11341101-11341408	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:11124794-11124970	HepG2	liver:	n/a	chr7:11124881-11124894
43	CEBPB	chr7:11115589-11115882	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:11301110-11301336	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:11300941-11301574	MCF-7	breast:	n/a	n/a
46	CEBPB	chr7:11210530-11210811	Hela-S3	cervix:	n/a	chr7:11210690-11210701
47	CEBPB	chr7:11115591-11115952	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:11210548-11210824	A549	lung:	n/a	chr7:11210690-11210701
49	CEBPB	chr7:11321149-11321368	K562	blood:	n/a	n/a
50	CEBPB	chr7:11122652-11122903	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11292672-11292722	H1-hESC	embryonic stem cell:	embryo
2	chr7:11292672-11292722	H1-hESC	embryonic stem cell:	embryo
3	chr7:11101436-11101486	NH-A	brain:	n/a
4	chr7:11232035-11232085	SK-N-SH	brain:	n/a
5	chr7:11101436-11101486	HCF	heart:	n/a
6	chr7:11315835-11315885	SAEC	small airway:	n/a
7	chr7:11232035-11232085	GM12891	blood:	n/a
8	chr7:11279531-11279581	Hela-S3	cervix:	n/a
9	chr7:11232035-11232085	HIPEpiC	eye:	n/a
10	chr7:11291686-11291736	HIPEpiC	eye:	n/a
11	chr7:11291686-11291736	SK-N-SH_RA	brain:	n/a
12	chr7:11232035-11232085	NB4	blood:	n/a
13	chr7:11091695-11091745	SAEC	small airway:	n/a
14	chr7:11091695-11091745	HEEpiC	esophagus:	n/a
15	chr7:11292672-11292722	HRPEpiC	eye:	n/a
16	chr7:11279531-11279581	HMEC	breast:	n/a
17	chr7:11315835-11315885	HNPCEpiC	eye:	n/a
18	chr7:11291686-11291736	SKMC	muscle:	n/a
19	chr7:11232035-11232085	GM19239	blood:	n/a
20	chr7:11292672-11292722	HCPEpiC	choroid plexus:	n/a
21	chr7:11101436-11101486	HL-60	blood:	n/a
22	chr7:11315835-11315885	GM12891	blood:	n/a
23	chr7:11315835-11315885	A549	lung:	n/a
24	chr7:11091695-11091745	Hela-S3	cervix:	n/a
25	chr7:11292672-11292722	HIPEpiC	eye:	n/a
26	chr7:11292672-11292722	GM12892	blood:	n/a
27	chr7:11292672-11292722	HCM	heart:	n/a
28	chr7:11101436-11101486	AG04449	skin:	fetal
29	chr7:11273481-11273531	SK-N-MC	brain:	n/a
30	chr7:11292672-11292722	T-47D	breast:	n/a
31	chr7:11091695-11091745	K562	blood:	n/a
32	chr7:11315835-11315885	Jurkat	blood:	n/a
33	chr7:11279531-11279581	GM12878	blood:	n/a
34	chr7:11291686-11291736	BJ	skin:	n/a
35	chr7:11101436-11101486	PFSK-1	brain:	n/a
36	chr7:11232035-11232085	NH-A	brain:	n/a
37	chr7:11315835-11315885	T-47D	breast:	n/a
38	chr7:11273481-11273531	BE2_C	brain:	n/a
39	chr7:11232035-11232085	NHBE	bronchial:	n/a
40	chr7:11273481-11273531	U87	brain:	n/a
41	chr7:11101436-11101486	AG09309	skin:	n/a
42	chr7:11273481-11273531	GM06990	blood:	n/a
43	chr7:11315835-11315885	HRE	kidney:	n/a
44	chr7:11232035-11232085	PrEC	prostate:	n/a
45	chr7:11091695-11091745	NHBE	bronchial:	n/a
46	chr7:11091695-11091745	Hepatocyte	liver:	n/a
47	chr7:11291686-11291736	Hepatocyte	liver:	n/a
48	chr7:11279531-11279581	SK-N-SH_RA	brain:	n/a
49	chr7:11315835-11315885	Caco-2	colon:	n/a
50	chr7:11291686-11291736	A549	lung:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:11193047..11193912-chr7:11250807..11251473,2	MCF-7	breast:
2	chr7:11141677..11144293-chr7:11222755..11224742,2	K562	blood:
3	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
4	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
5	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
6	chr7:11292499..11294774-chr7:11295925..11298788,3	K562	blood:
7	chr7:11328573..11331475-chr7:11331531..11334464,2	K562	blood:
8	chr7:11328573..11331475-chr7:11331531..11334464,2	K562	blood:
9	chr7:11012344..11014924-chr7:11251730..11254367,2	MCF-7	breast:
10	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
11	chr7:11136221..11139675-chr7:11144358..11148872,4	K562	blood:
12	chr7:11012606..11015240-chr7:11166727..11169294,2	MCF-7	breast:
13	chr7:11175308..11177163-chr7:11367863..11369367,2	MCF-7	breast:
14	chr7:11346706..11349910-chr7:11350007..11353700,4	K562	blood:
15	chr7:11113760..11116450-chr7:11117895..11120001,2	MCF-7	breast:
16	chr7:11325170..11327885-chr7:11339729..11342510,2	K562	blood:
17	chr7:11349044..11351457-chr7:11357652..11360171,2	MCF-7	breast:
18	chr7:11267687..11270680-chr7:11271994..11274932,4	K562	blood:
19	chr7:10977336..10979714-chr7:11321113..11323195,2	K562	blood:
20	chr7:11073711..11075320-chr7:11100379..11102062,2	K562	blood:
21	chr7:11121943..11123973-chr7:11130475..11132999,2	K562	blood:
22	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
23	chr7:11283625..11286458-chr7:11299427..11301201,2	MCF-7	breast:
24	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
25	chr7:11256893..11259555-chr7:11260673..11263509,2	K562	blood:
26	chr7:11249621..11251321-chr7:11263470..11265207,2	K562	blood:
27	chr7:11251355..11252341-chr7:11383095..11384072,2	K562	blood:
28	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
29	chr7:11300390..11302568-chr7:11306434..11309079,2	K562	blood:
30	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
31	chr7:11252043..11254339-chr7:11287708..11289525,2	MCF-7	breast:
32	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
33	chr7:11141677..11144293-chr7:11222755..11224742,2	K562	blood:
34	chr7:11287653..11289211-chr7:11291988..11294174,2	MCF-7	breast:
35	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
36	chr7:11108681..11111650-chr7:11117427..11119548,2	K562	blood:
37	chr7:11305179..11307568-chr7:11307740..11310059,2	K562	blood:
38	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
39	chr7:11349044..11351457-chr7:11357652..11360171,2	MCF-7	breast:
40	chr7:11337762..11340036-chr7:11346341..11348579,2	K562	blood:
41	chr7:11270835..11273820-chr7:11282821..11286972,3	MCF-7	breast:
42	chr7:11149421..11151035-chr7:11153801..11157843,3	K562	blood:
43	chr7:11271122..11274578-chr7:11276351..11278199,3	MCF-7	breast:
44	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
45	chr7:11242328..11245146-chr7:11247823..11250208,3	K562	blood:
46	chr6:101927489..101928280-chr7:11251597..11252397,2	MCF-7	breast:
47	chr7:11310747..11312959-chr7:11363468..11365814,2	MCF-7	breast:
48	chr7:11197789..11199466-chr7:11199534..11202480,2	K562	blood:
49	chr7:11205391..11208108-chr7:11211440..11214054,2	MCF-7	breast:
50	chr7:11317077..11318618-chr7:11320125..11322658,2	K562	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-1	chr7:11228166-11228261	ENSG00000230333.2
2	lnc-PHF14-1	chr7:11221359-11221463	ENSG00000230333.2
3	lnc-PHF14-1	chr7:11283885-11284106	ENSG00000230333.1
4	lnc-PHF14-7	chr7:11349080-11349292	NONHSAT119217
5	lnc-PHF14-7	chr7:11348441-11348653	FPKM1_group_29119_transcript_1
6	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.1
7	lnc-PHF14-1	chr7:11232993-11233049	ENSG00000230333.1
8	lnc-PHF14-1	chr7:11236934-11237071	ENSG00000230333.1
9	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.1
10	lnc-PHF14-1	chr7:11267144-11267456	ENSG00000230333.1
11	lnc-PHF14-1	chr7:11236937-11237071	ENSG00000230333.1
12	lnc-PHF14-1	chr7:11267144-11267282	ENSG00000230333.1
13	lnc-PHF14-1	chr7:11236937-11237071	ENSG00000230333.2
14	lnc-PHF14-1	chr7:11232622-11232677	ENSG00000230333.2
15	lnc-PHF14-1	chr7:11287920-11288002	ENSG00000230333.1
16	lnc-PHF14-1	chr7:11292607-11292852	ENSG00000230333.1
17	lnc-PHF14-1	chr7:11267144-11267282	ENSG00000230333.2
18	lnc-PHF14-1	chr7:11236934-11237071	ENSG00000230333.1
19	lnc-PHF14-1	chr7:11232993-11233049	ENSG00000230333.1
20	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.2
21	lnc-PHF14-1	chr7:11283885-11284106	ENSG00000230333.1
22	lnc-PHF14-1	chr7:11293826-11295704	NONHSAT119212
23	lnc-PHF14-7	chr7:11348370-11348437	NONHSAT119217
24	lnc-PHF14-6	chr7:11342306-11343759	NONHSAT119216
25	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.2
26	lnc-THSD7A-2	chr7:11297308-11298162	NONHSAT119215
27	lnc-PHF14-9	chr7:11259265-11259377	ucscGeneNc_uc003ssb_2
28	lnc-PHF14-1	chr7:11267144-11267282	ENSG00000230333.2
29	lnc-PHF14-1	chr7:11292257-11293759	NONHSAT119212
30	lnc-PHF14-1	chr7:11236937-11237071	ENSG00000230333.1
31	lnc-PHF14-7	chr7:11348370-11348437	FPKM1_group_29119_transcript_1
32	lnc-PHF14-6	chr7:11344275-11345327	NONHSAT119216
33	lnc-PHF14-1	chr7:11292740-11292852	ENSG00000230333.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF14	hsa-miR-155-5p	chr7:11142799-11142820
2	PHF14	hsa-miR-155-5p	chr7:11148709-11148731
3	PHF14	hsa-miR-155-5p	chr7:11142813-11142835

Variant related genes	Relation type
PHF14	TF binding region
ENSG00000230333	TF binding region
NPM1P11	TF binding region
PHF14	CpG island
ENSG00000230333	CpG island
NPM1P11	CpG island
ENSG00000271185	chromatin interactions
ENSG00000106443	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000226827	chromatin interactions
ENSG00000230333	chromatin interactions
ENSG00000196204	chromatin interactions

Extended variants
information (count: 11295 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:11295 , 50 per page) page: 1 2 3 4 5 6 7 ... 226

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545767786	chr7:11085788-11085789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562735004	chr7:11085792-11085793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561532569	chr7:11085795-11085796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3779410	chr7:11085801-11085802	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs376549304	chr7:11085868-11085869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34033654	chr7:11085873-11085874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547950999	chr7:11085880-11085881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561860929	chr7:11085881-11085882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527738705	chr7:11085900-11085901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547389447	chr7:11085909-11085910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535396699	chr7:11085916-11085917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570754317	chr7:11085923-11085924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60979082	chr7:11085956-11085957	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs74722607	chr7:11085994-11085995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534591680	chr7:11086058-11086059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536078533	chr7:11086067-11086068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187575753	chr7:11086202-11086203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568172373	chr7:11086248-11086249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200519414	chr7:11086272-11086273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs66936990	chr7:11086273-11086274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533827459	chr7:11086286-11086287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558364791	chr7:11086291-11086292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192059393	chr7:11086321-11086322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576744714	chr7:11086357-11086358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138135496	chr7:11086363-11086364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556203238	chr7:11086379-11086380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553011069	chr7:11086413-11086414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541630548	chr7:11086460-11086461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561498438	chr7:11086479-11086480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs202056727	chr7:11086494-11086495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181780589	chr7:11086495-11086496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6967802	chr7:11086499-11086500	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564539774	chr7:11086511-11086512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186257455	chr7:11086539-11086540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552511372	chr7:11086560-11086561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58148239	chr7:11086565-11086566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564448531	chr7:11086583-11086584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs55976132	chr7:11086616-11086617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs60123000	chr7:11086617-11086618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11323530	chr7:11086656-11086657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142703380	chr7:11086668-11086669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570271155	chr7:11086675-11086676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201862196	chr7:11086676-11086677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529573013	chr7:11086693-11086694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568888491	chr7:11086706-11086707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190237305	chr7:11086727-11086728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182689708	chr7:11086741-11086742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34033198	chr7:11086743-11086744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374602064	chr7:11086754-11086755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553561750	chr7:11086762-11086763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD

Chromatin state (count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11014600-11092000	Weak transcription	Colonic Mucosa	Colon
2	chr7:11014800-11117400	Weak transcription	HSMMtube	muscle
3	chr7:11015200-11108200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr7:11031600-11103800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:11035800-11092600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:11035800-11113000	Weak transcription	Esophagus	oesophagus
7	chr7:11035800-11113200	Weak transcription	Lung	lung
8	chr7:11035800-11123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:11036000-11101600	Weak transcription	Placenta	Placenta
10	chr7:11036600-11100800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:11039000-11090600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:11039000-11108800	Weak transcription	Psoas Muscle	Psoas
13	chr7:11046000-11128600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:11046200-11175000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:11046600-11103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr7:11046600-11122600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:11046600-11167800	Weak transcription	Thymus	Thymus
18	chr7:11048200-11098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:11048200-11113400	Weak transcription	Aorta	Aorta
20	chr7:11054400-11101800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:11054400-11113200	Weak transcription	Pancreas	Pancrea
22	chr7:11057800-11190200	Weak transcription	Fetal Brain Male	brain
23	chr7:11064200-11093600	Weak transcription	Hela-S3	cervix
24	chr7:11064400-11088400	Weak transcription	Brain Anterior Caudate	brain
25	chr7:11064400-11104200	Weak transcription	NHEK	skin
26	chr7:11064400-11112400	Weak transcription	Brain Germinal Matrix	brain
27	chr7:11064400-11112400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr7:11064400-11122800	Weak transcription	Rectal Smooth Muscle	rectum
29	chr7:11064600-11091600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:11064600-11101400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr7:11064600-11101600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:11064600-11111800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr7:11065000-11101600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr7:11065000-11101800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:11066400-11106800	Weak transcription	Fetal Kidney	kidney
36	chr7:11066600-11104400	Weak transcription	NHDF-Ad	bronchial
37	chr7:11068400-11102800	Weak transcription	Small Intestine	intestine
38	chr7:11071800-11103800	Weak transcription	Right Ventricle	heart
39	chr7:11071800-11113000	Weak transcription	Fetal Intestine Small	intestine
40	chr7:11071800-11113000	Weak transcription	Fetal Stomach	stomach
41	chr7:11073600-11093600	Weak transcription	NHLF	lung
42	chr7:11074800-11086400	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr7:11075000-11086600	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr7:11076400-11090800	Weak transcription	Left Ventricle	heart
45	chr7:11076400-11095600	Weak transcription	Fetal Heart	heart
46	chr7:11076400-11101600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr7:11076400-11101600	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr7:11076400-11193200	Weak transcription	Ovary	ovary
49	chr7:11076600-11091400	Weak transcription	Fetal Brain Female	brain
50	chr7:11076800-11091200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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