Variant report

Variant	nsv831517
Chromosome Location	chr9:14512924-14738206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1986)
CpG islands
(count:793)
Chromatin interactive
region (count:84)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1986 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14524947-14525548	K562	blood:	n/a	n/a
2	ARID3A	chr9:14528249-14529969	K562	blood:	n/a	n/a
3	ARID3A	chr9:14661451-14661789	K562	blood:	n/a	n/a
4	ARID3A	chr9:14652772-14653234	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:14516512-14517029	K562	blood:	n/a	n/a
6	ARID3A	chr9:14538497-14538813	K562	blood:	n/a	n/a
7	ARID3A	chr9:14616384-14616695	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:14522239-14523074	K562	blood:	n/a	n/a
9	ARID3A	chr9:14521846-14521847	K562	blood:	n/a	n/a
10	ARID3A	chr9:14530236-14532723	K562	blood:	n/a	n/a
11	ARID3A	chr9:14525821-14526308	K562	blood:	n/a	n/a
12	ARID3A	chr9:14514181-14514663	K562	blood:	n/a	n/a
13	ARID3A	chr9:14616366-14616729	K562	blood:	n/a	n/a
14	ARID3A	chr9:14527425-14527544	K562	blood:	n/a	n/a
15	ARID3A	chr9:14532898-14533098	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:14523621-14523918	K562	blood:	n/a	n/a
17	ATF1	chr9:14523608-14523943	K562	blood:	n/a	n/a
18	ATF1	chr9:14531098-14532606	K562	blood:	n/a	n/a
19	ATF1	chr9:14661502-14661775	K562	blood:	n/a	n/a
20	ATF2	chr9:14693237-14693620	GM12878	blood:	n/a	n/a
21	ATF2	chr9:14585524-14586203	GM12878	blood:	n/a	n/a
22	ATF2	chr9:14547181-14547669	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr9:14585562-14586344	GM12878	blood:	n/a	n/a
24	ATF2	chr9:14722568-14723014	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr9:14547129-14547833	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr9:14722642-14723053	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
28	BACH1	chr9:14573620-14573628	K562	blood:	n/a	n/a
29	BACH1	chr9:14523611-14523761	K562	blood:	n/a	n/a
30	BACH1	chr9:14693258-14693548	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr9:14585675-14586118	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:14585612-14586175	GM12878	blood:	n/a	chr9:14585907-14585916
33	BCL11A	chr9:14547275-14547658	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr9:14722811-14722999	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr9:14585726-14586068	GM12878	blood:	n/a	chr9:14585907-14585916
36	BCL3	chr9:14585642-14586081	GM12878	blood:	n/a	chr9:14585907-14585916
37	BCLAF1	chr9:14693175-14693606	GM12878	blood:	n/a	n/a
38	BCLAF1	chr9:14693199-14693708	GM12878	blood:	n/a	n/a
39	BCLAF1	chr9:14585603-14586186	GM12878	blood:	n/a	chr9:14585907-14585916
40	BCLAF1	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
41	BHLHE40	chr9:14616435-14616720	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:14531394-14532830	K562	blood:	n/a	n/a
43	BHLHE40	chr9:14585516-14586154	GM12878	blood:	n/a	n/a
44	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
45	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
46	BHLHE40	chr9:14538596-14538834	K562	blood:	n/a	n/a
47	BHLHE40	chr9:14525487-14525576	K562	blood:	n/a	n/a
48	BHLHE40	chr9:14692950-14693814	GM12878	blood:	n/a	chr9:14693117-14693133
49	BHLHE40	chr9:14523316-14523932	K562	blood:	n/a	n/a
50	BRCA1	chr9:14652862-14653081	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14691289-14691339	SK-N-SH_RA	brain:	n/a
2	chr9:14692931-14692981	AG10803	skin:	n/a
3	chr9:14723496-14723546	K562	blood:	n/a
4	chr9:14562893-14562943	HEK293	kidney:	embryo
5	chr9:14690531-14690581	MCF-7	breast:	n/a
6	chr9:14690531-14690581	HepG2	liver:	n/a
7	chr9:14691289-14691339	HepG2	liver:	n/a
8	chr9:14693888-14693938	HEK293	kidney:	embryo
9	chr9:14720244-14720294	SK-N-MC	brain:	n/a
10	chr9:14693504-14693554	SK-N-SH	brain:	n/a
11	chr9:14693648-14693698	ECC-1	luminal epithelium:	n/a
12	chr9:14692931-14692981	HL-60	blood:	n/a
13	chr9:14693888-14693938	U87	brain:	n/a
14	chr9:14723496-14723546	GM19239	blood:	n/a
15	chr9:14692931-14692981	HCM	heart:	n/a
16	chr9:14723496-14723546	NHDF-neo	bronchial:	n/a
17	chr9:14723496-14723546	CMK	blood:	n/a
18	chr9:14722864-14722914	HCPEpiC	choroid plexus:	n/a
19	chr9:14723496-14723546	SK-N-MC	brain:	n/a
20	chr9:14693888-14693938	HCPEpiC	choroid plexus:	n/a
21	chr9:14693504-14693554	GM12891	blood:	n/a
22	chr9:14562893-14562943	MCF-7	breast:	n/a
23	chr9:14693504-14693554	ECC-1	luminal epithelium:	n/a
24	chr9:14722864-14722914	HCT-116	colon:	n/a
25	chr9:14562893-14562943	RPTEC	kidney:	n/a
26	chr9:14693538-14693588	GM19239	blood:	n/a
27	chr9:14690531-14690581	NT2-D1	testis:	n/a
28	chr9:14693504-14693554	AG09319	gingival:	n/a
29	chr9:14693082-14693132	PANC-1	pancreas:	n/a
30	chr9:14693082-14693132	U87	brain:	n/a
31	chr9:14722864-14722914	U87	brain:	n/a
32	chr9:14690531-14690581	HCF	heart:	n/a
33	chr9:14562893-14562943	SK-N-MC	brain:	n/a
34	chr9:14693888-14693938	GM19239	blood:	n/a
35	chr9:14693648-14693698	ovcar-3	ovarian:	n/a
36	chr9:14720244-14720294	ovcar-3	ovarian:	n/a
37	chr9:14693082-14693132	Jurkat	blood:	n/a
38	chr9:14562893-14562943	ProgFib	skin:	n/a
39	chr9:14562893-14562943	GM12891	blood:	n/a
40	chr9:14693538-14693588	BE2_C	brain:	n/a
41	chr9:14723496-14723546	HepG2	liver:	n/a
42	chr9:14643897-14643947	HRE	kidney:	n/a
43	chr9:14693082-14693132	GM12892	blood:	n/a
44	chr9:14690531-14690581	CMK	blood:	n/a
45	chr9:14562893-14562943	AG04449	skin:	fetal
46	chr9:14692931-14692981	A549	lung:	n/a
47	chr9:14720244-14720294	HCPEpiC	choroid plexus:	n/a
48	chr9:14693648-14693698	MCF-7	breast:	n/a
49	chr9:14693888-14693938	Jurkat	blood:	n/a
50	chr9:14643897-14643947	Jurkat	blood:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
2	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
3	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
4	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
5	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
6	chr9:14526618..14530885-chr9:14532603..14534403,3	K562	blood:
7	chr9:14536696..14538433-chr9:14540578..14543493,2	MCF-7	breast:
8	chr9:14465253..14465899-chr9:14652688..14653342,2	MCF-7	breast:
9	chr9:14512951..14515476-chr9:14521722..14523544,2	K562	blood:
10	chr9:14516030..14517919-chr9:14520265..14523157,2	K562	blood:
11	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
12	chr9:14527866..14530461-chr9:14536328..14538766,2	K562	blood:
13	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
14	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
15	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
16	chr9:14536696..14538433-chr9:14540578..14543493,2	MCF-7	breast:
17	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
18	chr9:14723716..14725255-chr9:14725943..14728400,2	K562	blood:
19	chr9:14442114..14442886-chr9:14652552..14653366,4	MCF-7	breast:
20	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
21	chr9:14691643..14693414-chr9:14700745..14703153,2	K562	blood:
22	chr9:14691736..14693392-chr9:14716118..14717957,2	MCF-7	breast:
23	chr9:14527866..14530461-chr9:14536328..14538766,2	K562	blood:
24	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
25	chr9:14553196..14555459-chr9:14557147..14560009,3	K562	blood:
26	chr9:14514179..14519206-chr9:14523722..14526155,4	K562	blood:
27	chr9:14464938..14465658-chr9:14661578..14662250,2	MCF-7	breast:
28	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
29	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
30	chr9:14528313..14531170-chr9:14563342..14566028,2	K562	blood:
31	chr9:14627684..14629345-chr9:14693335..14694855,2	MCF-7	breast:
32	chr9:14551651..14553553-chr9:14553826..14555711,2	K562	blood:
33	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
34	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
35	chr9:14524643..14526362-chr9:14532686..14534400,2	K562	blood:
36	chr9:14511289..14514140-chr9:14516209..14518705,2	K562	blood:
37	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
38	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
39	chr9:14526916..14528634-chr9:14534526..14536593,2	K562	blood:
40	chr9:14508966..14511196-chr9:14560014..14561808,2	K562	blood:
41	chr9:14532036..14533949-chr9:14535107..14537030,2	K562	blood:
42	chr9:14676498..14678344-chr9:14692478..14694843,2	MCF-7	breast:
43	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
44	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
45	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
46	chr9:14513116..14517337-chr9:14529012..14532245,4	K562	blood:
47	chr9:14513208..14515171-chr9:14532827..14534848,2	K562	blood:
48	chr9:14512951..14515476-chr9:14521722..14523544,2	K562	blood:
49	chr9:14531418..14533504-chr9:14535462..14537860,3	K562	blood:
50	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf146-7	chr9:14588065-14588629	NONHSAT130249
2	lnc-C9orf146-7	chr9:14588795-14589277	NONHSAT130249
3	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
4	lnc-C9orf146-7	chr9:14586764-14587315	NONHSAT130249
5	lnc-ZDHHC21-2	chr9:14606167-14606546	NONHSAT130251
6	lnc-CER1-1	chr9:14693227-14693263	NONHSAT130254
7	lnc-ZDHHC21-1	chr9:14611070-14614754	NONHSAT130252
8	lnc-C9orf146-8	chr9:14593575-14594198	NONHSAT130250
9	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
10	lnc-ZDHHC21-2	chr9:14609848-14609996	NONHSAT130251
11	lnc-ZDHHC21-4	chr9:14586767-14587324	ENSG00000273399.1
12	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254
13	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254
14	lnc-ZDHHC21-3	chr9:14588795-14590063	ENSG00000272871.1

No data

Variant related genes	Relation type
ENSG00000237137	TF binding region
ENSG00000229029	TF binding region
CER1	TF binding region
ZDHHC21	TF binding region
ENSG00000272871	TF binding region
ENSG00000273399	TF binding region
ENSG00000237137	CpG island
ENSG00000229029	CpG island
CER1	CpG island
ZDHHC21	CpG island
ENSG00000272871	CpG island
ENSG00000273399	CpG island
ENSG00000237137	chromatin interactions
ENSG00000175893	chromatin interactions

Extended variants
information (count: 10264 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:10264 , 50 per page) page: 1 2 3 4 5 6 7 ... 206

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61071841	chr9:14512930-14512931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs58676728	chr9:14512931-14512932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs149961834	chr9:14513065-14513066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111643142	chr9:14513129-14513130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547044383	chr9:14513163-14513164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10738366	chr9:14513183-14513184	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs13298122	chr9:14513210-14513211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs10738367	chr9:14513221-14513222	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183886907	chr9:14513224-14513225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs199691464	chr9:14513250-14513251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562039320	chr9:14513263-14513264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536185516	chr9:14513266-14513267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555983566	chr9:14513279-14513280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553590826	chr9:14513355-14513356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200656493	chr9:14513383-14513384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538893941	chr9:14513386-14513387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10756562	chr9:14513398-14513399	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575370233	chr9:14513406-14513407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188871084	chr9:14513455-14513456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561144879	chr9:14513477-14513478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574726650	chr9:14513483-14513484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545197800	chr9:14513487-14513488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541512238	chr9:14513495-14513496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540163702	chr9:14513508-14513509	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs9407573	chr9:14513509-14513510	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113144190	chr9:14513557-14513558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552428332	chr9:14513558-14513559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562656840	chr9:14513625-14513626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs71321994	chr9:14513626-14513627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs193069456	chr9:14513630-14513631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200624407	chr9:14513648-14513649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149020861	chr9:14513649-14513650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs71321995	chr9:14513661-14513662	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369590008	chr9:14513667-14513668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs367641899	chr9:14513687-14513688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs146708292	chr9:14513693-14513694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567973780	chr9:14513710-14513711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185315607	chr9:14513726-14513727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10738368	chr9:14513743-14513744	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149191384	chr9:14513773-14513774	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563746812	chr9:14513792-14513793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186974631	chr9:14513821-14513822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377079667	chr9:14513834-14513835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191869662	chr9:14513849-14513850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537952896	chr9:14513936-14513937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371085393	chr9:14513945-14513946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs72702930	chr9:14513999-14514000	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542546851	chr9:14514060-14514061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559086765	chr9:14514130-14514131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs574826674	chr9:14514146-14514147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Chordoma	21215367	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2373 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14504400-14515200	Weak transcription	HSMMtube	muscle
2	chr9:14512200-14514000	Weak transcription	K562	blood
3	chr9:14514000-14515400	Enhancers	K562	blood
4	chr9:14514200-14514400	Enhancers	Fetal Brain Male	brain
5	chr9:14514600-14516000	Weak transcription	Fetal Brain Male	brain
6	chr9:14515000-14515600	Enhancers	HSMM	muscle
7	chr9:14515000-14517800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr9:14515000-14518000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr9:14515200-14515400	Enhancers	HSMMtube	muscle
10	chr9:14515200-14515600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr9:14515200-14515800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr9:14515200-14516200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:14515200-14517200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr9:14515200-14517600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr9:14515200-14517800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr9:14515200-14518000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr9:14515200-14518400	Enhancers	Fetal Muscle Leg	muscle
18	chr9:14515400-14515600	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr9:14515400-14515800	Flanking Active TSS	HSMMtube	muscle
20	chr9:14515400-14516000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:14515400-14516000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr9:14515400-14516200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr9:14515400-14516400	Flanking Active TSS	K562	blood
24	chr9:14515400-14516600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:14515400-14517800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr9:14515400-14519000	Enhancers	Brain Germinal Matrix	brain
27	chr9:14515600-14515800	Bivalent Enhancer	Brain Anterior Caudate	brain
28	chr9:14515600-14516000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr9:14515600-14516000	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr9:14515600-14516000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr9:14515600-14516000	Flanking Active TSS	HSMM	muscle
32	chr9:14515600-14516200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:14515600-14516200	Enhancers	Fetal Muscle Trunk	muscle
34	chr9:14515600-14517600	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr9:14515600-14517800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr9:14515800-14516000	Enhancers	NH-A	brain
37	chr9:14515800-14516200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr9:14515800-14516200	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
39	chr9:14515800-14516200	Enhancers	Brain Hippocampus Middle	brain
40	chr9:14515800-14516200	Enhancers	Esophagus	oesophagus
41	chr9:14515800-14516200	Enhancers	Fetal Stomach	stomach
42	chr9:14515800-14516200	Enhancers	Psoas Muscle	Psoas
43	chr9:14515800-14516200	Active TSS	HSMMtube	muscle
44	chr9:14515800-14516800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr9:14515800-14517200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:14515800-14517800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:14515800-14518000	Enhancers	Fetal Brain Female	brain
48	chr9:14516000-14516200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr9:14516000-14516200	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr9:14516000-14517200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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