Variant report

Variant	nsv830901
Chromosome Location	chr7:11093455-11272219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1020)
CpG islands
(count:122)
Chromatin interactive
region (count:107)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	ATF1	chr7:11128773-11128831	K562	blood:	n/a	n/a
4	ATF1	chr7:11221045-11221594	K562	blood:	n/a	n/a
5	ATF2	chr7:11232775-11233077	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:11224855-11225204	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:11122404-11123057	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:11224807-11225248	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:11231364-11231607	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:11102229-11102429	K562	blood:	n/a	n/a
11	BACH1	chr7:11232750-11233085	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:11175371-11175473	K562	blood:	n/a	n/a
13	BATF	chr7:11118139-11118345	GM12878	blood:	n/a	chr7:11118255-11118265
14	BATF	chr7:11160374-11160600	GM12878	blood:	n/a	n/a
15	BATF	chr7:11118081-11118314	GM12878	blood:	n/a	chr7:11118255-11118265
16	BCL11A	chr7:11224826-11225121	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr7:11224931-11225119	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr7:11195043-11195271	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:11251750-11252062	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:11228287-11228806	K562	blood:	n/a	n/a
21	BHLHE40	chr7:11258948-11259424	K562	blood:	n/a	n/a
22	BHLHE40	chr7:11253041-11253054	HepG2	liver:	n/a	n/a
23	BHLHE40	chr7:11210726-11210891	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:11215693-11215816	K562	blood:	n/a	n/a
25	BHLHE40	chr7:11251822-11252032	GM12878	blood:	n/a	n/a
26	BRCA1	chr7:11167087-11167179	GM12878	blood:	n/a	n/a
27	BRCA1	chr7:11254177-11254219	GM12878	blood:	n/a	n/a
28	CCNT2	chr7:11217186-11217420	K562	blood:	n/a	n/a
29	CEBPB	chr7:11247274-11247517	K562	blood:	n/a	n/a
30	CEBPB	chr7:11115591-11115931	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:11210550-11210871	HepG2	liver:	n/a	chr7:11210690-11210701
32	CEBPB	chr7:11108137-11108367	K562	blood:	n/a	chr7:11108241-11108252
33	CEBPB	chr7:11235249-11235455	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:11169609-11170090	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:11115591-11115952	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:11122652-11122903	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:11252949-11253321	HepG2	liver:	n/a	chr7:11253104-11253115 chr7:11253103-11253116
38	CEBPB	chr7:11115581-11115979	MCF-7	breast:	n/a	n/a
39	CEBPB	chr7:11108116-11108371	HepG2	liver:	n/a	chr7:11108241-11108252
40	CEBPB	chr7:11233120-11233482	MCF-7	breast:	n/a	n/a
41	CEBPB	chr7:11210526-11210841	IMR90	lung:	n/a	chr7:11210690-11210701
42	CEBPB	chr7:11210548-11210824	A549	lung:	n/a	chr7:11210690-11210701
43	CEBPB	chr7:11124748-11125014	K562	blood:	n/a	chr7:11124881-11124894
44	CEBPB	chr7:11261510-11261710	HepG2	liver:	n/a	chr7:11261549-11261560
45	CEBPB	chr7:11115586-11115929	A549	lung:	n/a	n/a
46	CEBPB	chr7:11122659-11123159	A549	lung:	n/a	n/a
47	CEBPB	chr7:11115611-11115936	K562	blood:	n/a	n/a
48	CEBPB	chr7:11115583-11115943	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:11232885-11233417	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:11210530-11210811	Hela-S3	cervix:	n/a	chr7:11210690-11210701

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11232035-11232085	HEEpiC	esophagus:	n/a
2	chr7:11232035-11232085	NHDF-neo	bronchial:	n/a
3	chr7:11101436-11101486	AG04449	skin:	fetal
4	chr7:11232035-11232085	AG10803	skin:	n/a
5	chr7:11232035-11232085	GM19239	blood:	n/a
6	chr7:11232035-11232085	NB4	blood:	n/a
7	chr7:11101436-11101486	AG04450	lung:	fetal
8	chr7:11101436-11101486	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:11232035-11232085	H1-hESC	embryonic stem cell:	embryo
10	chr7:11101436-11101486	H1-hESC	embryonic stem cell:	embryo
11	chr7:11232035-11232085	BE2_C	brain:	n/a
12	chr7:11101436-11101486	IMR90	lung:	fetal
13	chr7:11232035-11232085	SKMC	muscle:	n/a
14	chr7:11232035-11232085	AG04450	lung:	fetal
15	chr7:11101436-11101486	HepG2	liver:	n/a
16	chr7:11101436-11101486	HEEpiC	esophagus:	n/a
17	chr7:11232035-11232085	Hepatocyte	liver:	n/a
18	chr7:11232035-11232085	SK-N-SH	brain:	n/a
19	chr7:11101436-11101486	GM12891	blood:	n/a
20	chr7:11101436-11101486	HCM	heart:	n/a
21	chr7:11232035-11232085	HIPEpiC	eye:	n/a
22	chr7:11232035-11232085	A549	lung:	n/a
23	chr7:11101436-11101486	GM19239	blood:	n/a
24	chr7:11232035-11232085	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:11101436-11101486	AoSMC	blood vessel:	n/a
26	chr7:11232035-11232085	HCF	heart:	n/a
27	chr7:11101436-11101486	PrEC	prostate:	n/a
28	chr7:11232035-11232085	NT2-D1	testis:	n/a
29	chr7:11101436-11101486	HRCEpiC	kidney:	n/a
30	chr7:11232035-11232085	HRCEpiC	kidney:	n/a
31	chr7:11101436-11101486	MCF-7	breast:	n/a
32	chr7:11101436-11101486	HCF	heart:	n/a
33	chr7:11232035-11232085	NHBE	bronchial:	n/a
34	chr7:11101436-11101486	SK-N-MC	brain:	n/a
35	chr7:11101436-11101486	T-47D	breast:	n/a
36	chr7:11232035-11232085	PrEC	prostate:	n/a
37	chr7:11232035-11232085	MCF-7	breast:	n/a
38	chr7:11232035-11232085	RPTEC	kidney:	n/a
39	chr7:11232035-11232085	SK-N-MC	brain:	n/a
40	chr7:11101436-11101486	GM12892	blood:	n/a
41	chr7:11232035-11232085	AG04449	skin:	fetal
42	chr7:11101436-11101486	Hepatocyte	liver:	n/a
43	chr7:11232035-11232085	AG09309	skin:	n/a
44	chr7:11101436-11101486	AG09319	gingival:	n/a
45	chr7:11101436-11101486	PANC-1	pancreas:	n/a
46	chr7:11101436-11101486	BE2_C	brain:	n/a
47	chr7:11232035-11232085	ECC-1	luminal epithelium:	n/a
48	chr7:11101436-11101486	SK-N-SH_RA	brain:	n/a
49	chr7:11232035-11232085	ProgFib	skin:	n/a
50	chr7:11232035-11232085	HAEpiC	amniotic membrane:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:11187936..11191247-chr7:11191383..11194500,4	K562	blood:
2	chr7:11128812..11130687-chr7:11131248..11133734,2	MCF-7	breast:
3	chr7:11149421..11151035-chr7:11153801..11157843,3	K562	blood:
4	chr7:11229782..11232630-chr7:11260914..11263136,3	K562	blood:
5	chr7:11256893..11259555-chr7:11260673..11263509,2	K562	blood:
6	chr7:11251355..11252341-chr7:11383095..11384072,2	K562	blood:
7	chr7:11192916..11193961-chr7:11251567..11252421,4	MCF-7	breast:
8	chr7:11108681..11111650-chr7:11117427..11119548,2	K562	blood:
9	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
10	chr7:11140028..11142682-chr7:11145035..11147597,3	K562	blood:
11	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
12	chr6:101927489..101928280-chr7:11251597..11252397,2	MCF-7	breast:
13	chr7:11022666..11024973-chr7:11118639..11120820,2	K562	blood:
14	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
15	chr7:11193309..11193972-chr7:11380975..11381751,3	MCF-7	breast:
16	chr7:5013239..5014028-chr7:11185489..11186384,2	NB4	blood:
17	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
18	chr7:11136221..11139675-chr7:11144358..11148872,4	K562	blood:
19	chr7:11187936..11191247-chr7:11191383..11194500,4	K562	blood:
20	chr7:11271128..11274673-chr7:11275122..11277135,3	MCF-7	breast:
21	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
22	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
23	chr7:10978704..10980840-chr7:11097948..11100485,2	MCF-7	breast:
24	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
25	chr7:11193047..11193912-chr7:11250807..11251473,2	MCF-7	breast:
26	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
27	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
28	chr7:11113760..11116450-chr7:11117895..11120001,2	MCF-7	breast:
29	chr7:10978313..10981160-chr7:11099563..11101890,2	K562	blood:
30	chr7:11244458..11249354-chr7:11252765..11256676,5	MCF-7	breast:
31	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
32	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
33	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
34	chr7:11141677..11144293-chr7:11222755..11224742,2	K562	blood:
35	chr7:11242328..11245146-chr7:11247823..11250208,3	K562	blood:
36	chr7:11230694..11232235-chr7:11241525..11243997,2	MCF-7	breast:
37	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
38	chr7:11245322..11247054-chr7:11253506..11255264,2	K562	blood:
39	chr17:78500461..78501088-chr7:11221500..11222496,2	HCT-116	colon:
40	chr7:11193379..11193920-chr7:11380707..11381612,2	MCF-7	breast:
41	chr7:11124384..11127270-chr7:11131542..11136731,4	K562	blood:
42	chr7:11193091..11193870-chr7:11383205..11383845,2	MCF-7	breast:
43	chr7:11162789..11165137-chr7:11166828..11168631,2	K562	blood:
44	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
45	chr7:11130768..11133783-chr7:11134322..11137393,4	K562	blood:
46	chr7:11179754..11182412-chr7:11187476..11189973,2	K562	blood:
47	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
48	chr7:11270835..11273820-chr7:11282821..11286972,3	MCF-7	breast:
49	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
50	chr7:11086741..11089284-chr7:11093452..11095479,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-1	chr7:11221359-11221463	ENSG00000230333.2
2	lnc-PHF14-1	chr7:11228166-11228261	ENSG00000230333.2
3	lnc-PHF14-1	chr7:11236934-11237071	ENSG00000230333.1
4	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.1
5	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.2
6	lnc-PHF14-1	chr7:11267144-11267282	ENSG00000230333.2
7	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.2
8	lnc-PHF14-1	chr7:11266645-11266691	ENSG00000230333.1
9	lnc-PHF14-1	chr7:11236934-11237071	ENSG00000230333.1
10	lnc-PHF14-1	chr7:11232993-11233049	ENSG00000230333.1
11	lnc-PHF14-1	chr7:11236937-11237071	ENSG00000230333.1
12	lnc-PHF14-1	chr7:11267144-11267282	ENSG00000230333.1
13	lnc-PHF14-1	chr7:11267144-11267456	ENSG00000230333.1
14	lnc-PHF14-9	chr7:11259265-11259377	ucscGeneNc_uc003ssb_2
15	lnc-PHF14-1	chr7:11236937-11237071	ENSG00000230333.2
16	lnc-PHF14-1	chr7:11267144-11267282	ENSG00000230333.2
17	lnc-PHF14-1	chr7:11232993-11233049	ENSG00000230333.1
18	lnc-PHF14-1	chr7:11232622-11232677	ENSG00000230333.2
19	lnc-PHF14-1	chr7:11236937-11237071	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	chr7:11142813-11142835
3	PHF14	hsa-miR-155-5p	chr7:11148709-11148731

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

Extended variants
information (count: 7285 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:7285 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547454928	chr7:11093470-11093471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371086514	chr7:11093479-11093480	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80193059	chr7:11093496-11093497	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536814564	chr7:11093503-11093504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551619131	chr7:11093572-11093573	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372969091	chr7:11093614-11093615	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114878529	chr7:11093638-11093639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62440478	chr7:11093649-11093650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76528857	chr7:11093651-11093652	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs3801441	chr7:11093709-11093710	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs540482385	chr7:11093730-11093731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555319143	chr7:11093733-11093734	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370105877	chr7:11093736-11093737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565845664	chr7:11093740-11093741	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549363007	chr7:11093744-11093745	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531057915	chr7:11093825-11093826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377657481	chr7:11093878-11093879	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192823359	chr7:11093891-11093892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150177066	chr7:11093919-11093920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558247366	chr7:11093931-11093932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371034221	chr7:11094001-11094002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs578121753	chr7:11094026-11094027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570326238	chr7:11094064-11094065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4720932	chr7:11094126-11094127	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567582233	chr7:11094128-11094129	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114911240	chr7:11094136-11094137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536548018	chr7:11094138-11094139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574424200	chr7:11094199-11094200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543287369	chr7:11094240-11094241	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559733299	chr7:11094252-11094253	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528701672	chr7:11094258-11094259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183048120	chr7:11094307-11094308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564213318	chr7:11094318-11094319	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76259824	chr7:11094460-11094461	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549407607	chr7:11094492-11094493	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370439873	chr7:11094530-11094531	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10487898	chr7:11094579-11094580	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs57281048	chr7:11094600-11094601	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565552896	chr7:11094654-11094655	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565800325	chr7:11094690-11094691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116499849	chr7:11094732-11094733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187740956	chr7:11094803-11094804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111786067	chr7:11094854-11094855	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6965290	chr7:11094865-11094866	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs557422184	chr7:11094912-11094913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574070940	chr7:11094922-11094923	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542624008	chr7:11094940-11094941	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553653524	chr7:11094951-11094952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192402791	chr7:11094964-11094965	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs372241731	chr7:11094985-11094986	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	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:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11014800-11117400	Weak transcription	HSMMtube	muscle
2	chr7:11015200-11108200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr7:11031600-11103800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:11035800-11113000	Weak transcription	Esophagus	oesophagus
5	chr7:11035800-11113200	Weak transcription	Lung	lung
6	chr7:11035800-11123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:11036000-11101600	Weak transcription	Placenta	Placenta
8	chr7:11036600-11100800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:11039000-11108800	Weak transcription	Psoas Muscle	Psoas
10	chr7:11046000-11128600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr7:11046200-11175000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr7:11046600-11103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:11046600-11122600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:11046600-11167800	Weak transcription	Thymus	Thymus
15	chr7:11048200-11098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:11048200-11113400	Weak transcription	Aorta	Aorta
17	chr7:11054400-11101800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:11054400-11113200	Weak transcription	Pancreas	Pancrea
19	chr7:11057800-11190200	Weak transcription	Fetal Brain Male	brain
20	chr7:11064200-11093600	Weak transcription	Hela-S3	cervix
21	chr7:11064400-11104200	Weak transcription	NHEK	skin
22	chr7:11064400-11112400	Weak transcription	Brain Germinal Matrix	brain
23	chr7:11064400-11112400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr7:11064400-11122800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:11064600-11101400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr7:11064600-11101600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr7:11064600-11111800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr7:11065000-11101600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr7:11065000-11101800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:11066400-11106800	Weak transcription	Fetal Kidney	kidney
31	chr7:11066600-11104400	Weak transcription	NHDF-Ad	bronchial
32	chr7:11068400-11102800	Weak transcription	Small Intestine	intestine
33	chr7:11071800-11103800	Weak transcription	Right Ventricle	heart
34	chr7:11071800-11113000	Weak transcription	Fetal Intestine Small	intestine
35	chr7:11071800-11113000	Weak transcription	Fetal Stomach	stomach
36	chr7:11073600-11093600	Weak transcription	NHLF	lung
37	chr7:11076400-11095600	Weak transcription	Fetal Heart	heart
38	chr7:11076400-11101600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr7:11076400-11101600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr7:11076400-11193200	Weak transcription	Ovary	ovary
41	chr7:11076800-11122200	Weak transcription	HMEC	breast
42	chr7:11077000-11102800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr7:11077000-11130600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr7:11077000-11162400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr7:11077200-11097200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr7:11077200-11108800	Weak transcription	Colon Smooth Muscle	Colon
47	chr7:11077600-11097400	Weak transcription	A549	lung
48	chr7:11077600-11100800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:11077600-11106400	Weak transcription	NH-A	brain
50	chr7:11078600-11122400	Weak transcription	Fetal Muscle Leg	muscle

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