Variant report

Variant	nsv613637
Chromosome Location	chr9:14524438-15011915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3996)
CpG islands
(count:1404)
Chromatin interactive
region (count:102)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3996 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14661451-14661789	K562	blood:	n/a	n/a
2	ARID3A	chr9:14616366-14616729	K562	blood:	n/a	n/a
3	ARID3A	chr9:14528249-14529969	K562	blood:	n/a	n/a
4	ARID3A	chr9:14893420-14893599	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:14960946-14962339	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:14530236-14532723	K562	blood:	n/a	n/a
7	ARID3A	chr9:14527425-14527544	K562	blood:	n/a	n/a
8	ARID3A	chr9:14882074-14882476	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:14908366-14908878	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:14868526-14869963	HepG2	liver:	n/a	chr9:14869168-14869184 chr9:14869167-14869183
11	ARID3A	chr9:14525821-14526308	K562	blood:	n/a	n/a
12	ARID3A	chr9:14652772-14653234	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:14616384-14616695	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:14532898-14533098	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:14768583-14768889	K562	blood:	n/a	n/a
16	ARID3A	chr9:14913278-14913856	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:14925038-14925148	HepG2	liver:	n/a	n/a
18	ARID3A	chr9:14888518-14888791	HepG2	liver:	n/a	n/a
19	ARID3A	chr9:14524947-14525548	K562	blood:	n/a	n/a
20	ARID3A	chr9:14967513-14968337	HepG2	liver:	n/a	n/a
21	ARID3A	chr9:14899812-14900038	HepG2	liver:	n/a	n/a
22	ARID3A	chr9:14538497-14538813	K562	blood:	n/a	n/a
23	ATF1	chr9:14797561-14797747	K562	blood:	n/a	n/a
24	ATF1	chr9:14531098-14532606	K562	blood:	n/a	n/a
25	ATF1	chr9:14993152-14993450	K562	blood:	n/a	n/a
26	ATF1	chr9:14992118-14992479	K562	blood:	n/a	n/a
27	ATF1	chr9:14926973-14927434	K562	blood:	n/a	n/a
28	ATF1	chr9:14661502-14661775	K562	blood:	n/a	n/a
29	ATF1	chr9:14779539-14779966	K562	blood:	n/a	n/a
30	ATF2	chr9:14693237-14693620	GM12878	blood:	n/a	n/a
31	ATF2	chr9:14722568-14723014	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr9:14722642-14723053	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr9:14585524-14586203	GM12878	blood:	n/a	n/a
34	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
35	ATF2	chr9:14547181-14547669	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr9:14585562-14586344	GM12878	blood:	n/a	n/a
37	ATF2	chr9:14547129-14547833	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF3	chr9:14779743-14779981	K562	blood:	n/a	n/a
39	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr9:14573620-14573628	K562	blood:	n/a	n/a
41	BACH1	chr9:14693258-14693548	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr9:14585675-14586118	GM12878	blood:	n/a	n/a
43	BATF	chr9:14992095-14992275	GM12878	blood:	n/a	n/a
44	BCL11A	chr9:14585612-14586175	GM12878	blood:	n/a	chr9:14585907-14585916
45	BCL11A	chr9:14585726-14586068	GM12878	blood:	n/a	chr9:14585907-14585916
46	BCL11A	chr9:14547275-14547658	H1-hESC	embryonic stem cell:	n/a	n/a
47	BCL11A	chr9:14722811-14722999	H1-hESC	embryonic stem cell:	n/a	n/a
48	BCL3	chr9:14812818-14813170	GM12878	blood:	n/a	n/a
49	BCL3	chr9:14974056-14974338	GM12878	blood:	n/a	n/a
50	BCL3	chr9:14585642-14586081	GM12878	blood:	n/a	chr9:14585907-14585916

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14978400-14978450	Caco-2	colon:	n/a
2	chr9:14978400-14978450	Caco-2	colon:	n/a
3	chr9:14723496-14723546	GM12891	blood:	n/a
4	chr9:14993584-14993634	HCT-116	colon:	n/a
5	chr9:14720244-14720294	HCM	heart:	n/a
6	chr9:14992172-14992222	K562	blood:	n/a
7	chr9:14992172-14992222	GM12891	blood:	n/a
8	chr9:14883945-14883995	HRPEpiC	eye:	n/a
9	chr9:14910315-14910365	HRPEpiC	eye:	n/a
10	chr9:14693538-14693588	MCF-7	breast:	n/a
11	chr9:14993584-14993634	SK-N-SH_RA	brain:	n/a
12	chr9:14838752-14838802	AG09309	skin:	n/a
13	chr9:14691289-14691339	SK-N-MC	brain:	n/a
14	chr9:14838752-14838802	SK-N-SH_RA	brain:	n/a
15	chr9:14692931-14692981	NT2-D1	testis:	n/a
16	chr9:14723496-14723546	HEEpiC	esophagus:	n/a
17	chr9:14720244-14720294	BJ	skin:	n/a
18	chr9:14693538-14693588	RPTEC	kidney:	n/a
19	chr9:14562893-14562943	NB4	blood:	n/a
20	chr9:14749903-14749953	GM12878	blood:	n/a
21	chr9:14720244-14720294	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:14693538-14693588	HAEpiC	amniotic membrane:	n/a
23	chr9:14693504-14693554	HEEpiC	esophagus:	n/a
24	chr9:14992172-14992222	ovcar-3	ovarian:	n/a
25	chr9:14691289-14691339	SK-N-SH	brain:	n/a
26	chr9:14908132-14908182	HCPEpiC	choroid plexus:	n/a
27	chr9:14693888-14693938	HEK293	kidney:	embryo
28	chr9:14693648-14693698	SK-N-MC	brain:	n/a
29	chr9:14693648-14693698	HIPEpiC	eye:	n/a
30	chr9:14690531-14690581	BJ	skin:	n/a
31	chr9:14723496-14723546	GM12892	blood:	n/a
32	chr9:14993466-14993516	HUVEC	blood vessel:	n/a
33	chr9:14908132-14908182	GM19239	blood:	n/a
34	chr9:14992172-14992222	GM12878	blood:	n/a
35	chr9:14691289-14691339	HNPCEpiC	eye:	n/a
36	chr9:14690531-14690581	SK-N-SH_RA	brain:	n/a
37	chr9:14910315-14910365	Hepatocyte	liver:	n/a
38	chr9:14720244-14720294	NH-A	brain:	n/a
39	chr9:14562893-14562943	HNPCEpiC	eye:	n/a
40	chr9:14693888-14693938	CMK	blood:	n/a
41	chr9:14749903-14749953	BJ	skin:	n/a
42	chr9:14722864-14722914	NT2-D1	testis:	n/a
43	chr9:14693888-14693938	AG09309	skin:	n/a
44	chr9:14978400-14978450	SK-N-MC	brain:	n/a
45	chr9:14692931-14692981	GM06990	blood:	n/a
46	chr9:14693082-14693132	HCM	heart:	n/a
47	chr9:14910689-14910739	SK-N-MC	brain:	n/a
48	chr9:14838752-14838802	LNCaP	prostate:	n/a
49	chr9:14910689-14910739	GM12892	blood:	n/a
50	chr9:14883945-14883995	LNCaP	prostate:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:14531418..14533504-chr9:14535462..14537860,3	K562	blood:
2	chr9:14692215..14694584-chr9:14703998..14706013,2	MCF-7	breast:
3	chr9:14532036..14533949-chr9:14535107..14537030,2	K562	blood:
4	chr9:14527866..14530461-chr9:14536328..14538766,2	K562	blood:
5	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
6	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:
7	chr9:14528961..14530611-chr9:14536905..14538766,2	K562	blood:
8	chr9:14508966..14511196-chr9:14560014..14561808,2	K562	blood:
9	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
10	chr9:14524643..14526362-chr9:14532686..14534400,2	K562	blood:
11	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
12	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
13	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
14	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
15	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
16	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
17	chr9:14513208..14515171-chr9:14532827..14534848,2	K562	blood:
18	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
19	chr9:14692712..14694901-chr9:14767288..14769707,2	MCF-7	breast:
20	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
21	chr20:52274228..52274993-chr9:14900093..14900641,2	MCF-7	breast:
22	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
23	chr9:14442256..14442845-chr9:14661275..14662107,4	K562	blood:
24	chr21:20745898..20746419-chr9:14747590..14748110,2	MCF-7	breast:
25	chr9:14441846..14442823-chr9:14768420..14769609,5	MCF-7	breast:
26	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
27	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
28	chr9:14514179..14519206-chr9:14523722..14526155,4	K562	blood:
29	chr9:14528961..14530611-chr9:14536905..14538766,2	K562	blood:
30	chr9:14627684..14629345-chr9:14693335..14694855,2	MCF-7	breast:
31	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
32	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
33	chr9:14526916..14528634-chr9:14534526..14536593,2	K562	blood:
34	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
35	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
36	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:
37	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
38	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
39	chr9:14785127..14787393-chr9:14791653..14793787,2	MCF-7	breast:
40	chr9:14527866..14530461-chr9:14536328..14538766,2	K562	blood:
41	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
42	chr9:14488421..14491052-chr9:14527490..14530260,2	K562	blood:
43	chr9:14553196..14555459-chr9:14557147..14560009,3	K562	blood:
44	chr9:14534376..14536312-chr9:14538392..14540360,2	K562	blood:
45	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
46	chr9:14534376..14536312-chr9:14538392..14540360,2	K562	blood:
47	chr9:14528313..14531170-chr9:14563342..14566028,2	K562	blood:
48	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
49	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
50	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
2	lnc-C9orf146-7	chr9:14586764-14587315	NONHSAT130249
3	lnc-C9orf146-7	chr9:14588065-14588629	NONHSAT130249
4	lnc-ZDHHC21-3	chr9:14588795-14590063	ENSG00000272871.1
5	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254
6	lnc-FREM1-1	chr9:14979298-14979338	l_3739_chr9:14977433-14983179_testes
7	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254
8	lnc-ZDHHC21-2	chr9:14606167-14606546	NONHSAT130251
9	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
10	lnc-ZDHHC21-4	chr9:14586767-14587324	ENSG00000273399.1
11	lnc-FREM1-1	chr9:14977434-14977699	l_3739_chr9:14977433-14983179_testes
12	lnc-CER1-1	chr9:14693227-14693263	NONHSAT130254
13	lnc-FREM1-1	chr9:14977891-14977954	l_3739_chr9:14977433-14983179_testes
14	lnc-ZDHHC21-1	chr9:14611070-14614754	NONHSAT130252
15	lnc-ZDHHC21-2	chr9:14609848-14609996	NONHSAT130251
16	lnc-C9orf146-7	chr9:14588795-14589277	NONHSAT130249
17	lnc-FREM1-1	chr9:14980226-14980343	l_3739_chr9:14977433-14983179_testes
18	lnc-FREM1-1	chr9:14983147-14983179	l_3739_chr9:14977433-14983179_testes
19	lnc-C9orf146-8	chr9:14593575-14594198	NONHSAT130250

No data

Variant related genes	Relation type
ZDHHC21	TF binding region
LDHAP4	TF binding region
FREM1	TF binding region
ENSG00000215237	TF binding region
ENSG00000237137	TF binding region
RNU6-1260P	TF binding region
ENSG00000272871	TF binding region
ENSG00000273399	TF binding region
ENSG00000229029	TF binding region
CER1	TF binding region
ZDHHC21	CpG island
LDHAP4	CpG island
FREM1	CpG island
ENSG00000215237	CpG island
ENSG00000237137	CpG island
RNU6-1260P	CpG island
ENSG00000272871	CpG island
ENSG00000273399	CpG island
ENSG00000229029	CpG island
CER1	CpG island
ENSG00000175893	chromatin interactions
ENSG00000164946	chromatin interactions
ENSG00000199814	chromatin interactions
ENSG00000251960	chromatin interactions
ENSG00000237137	chromatin interactions

Extended variants
information (count: 23086 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:23086 , 50 per page) page: 1 2 3 4 5 6 7 ... 462

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs927969	chr9:14524438-14524439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538232043	chr9:14524505-14524506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554948855	chr9:14524530-14524531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183761396	chr9:14524536-14524537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540470178	chr9:14524550-14524551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560057682	chr9:14524562-14524563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576896398	chr9:14524599-14524600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147720107	chr9:14524661-14524662	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs545534690	chr9:14524703-14524704	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189311154	chr9:14524719-14524720	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs16931893	chr9:14524741-14524742	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs531247419	chr9:14524742-14524743	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs397978752	chr9:14524783-14524784	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs4741390	chr9:14524784-14524785	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs4741391	chr9:14524810-14524811	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530295576	chr9:14524832-14524833	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs547193169	chr9:14524912-14524913	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs181718477	chr9:14524915-14524916	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs539130269	chr9:14524948-14524949	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs187419209	chr9:14524994-14524995	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs569329182	chr9:14524996-14524997	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs191435316	chr9:14525008-14525009	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs539232753	chr9:14525025-14525026	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs557558980	chr9:14525040-14525041	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs575926987	chr9:14525049-14525050	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs554989343	chr9:14525050-14525051	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs373179917	chr9:14525115-14525116	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs112652066	chr9:14525151-14525152	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs11790649	chr9:14525156-14525157	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs561258203	chr9:14525289-14525290	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs530369369	chr9:14525307-14525308	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182058831	chr9:14525318-14525319	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs553936504	chr9:14525322-14525323	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs559847220	chr9:14525343-14525344	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs576923086	chr9:14525416-14525417	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs545969418	chr9:14525484-14525485	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs186302461	chr9:14525499-14525500	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs377452466	chr9:14525531-14525532	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs574751196	chr9:14525565-14525566	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs541439255	chr9:14525572-14525573	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs146910414	chr9:14525623-14525624	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs530330934	chr9:14525629-14525630	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369906437	chr9:14525665-14525666	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs560828417	chr9:14525682-14525683	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532641484	chr9:14525705-14525706	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs190414990	chr9:14525720-14525721	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs182294685	chr9:14525762-14525763	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs569410662	chr9:14525763-14525764	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs545851353	chr9:14525765-14525766	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs186624182	chr9:14525772-14525773	Weak transcription Active TSS	n/a	n/a	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
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	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
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:4661 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14521000-14529000	Weak transcription	Brain Germinal Matrix	brain
2	chr9:14521400-14525800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:14521400-14527400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:14524200-14524600	Enhancers	K562	blood
5	chr9:14524600-14525600	Flanking Active TSS	K562	blood
6	chr9:14525600-14525800	Active TSS	K562	blood
7	chr9:14525800-14526000	Flanking Active TSS	K562	blood
8	chr9:14525800-14526200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:14526000-14526800	Active TSS	K562	blood
10	chr9:14526200-14530200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr9:14526800-14527000	Enhancers	K562	blood
12	chr9:14527000-14528000	Weak transcription	K562	blood
13	chr9:14527400-14527600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:14527600-14528000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr9:14528000-14531400	Active TSS	K562	blood
16	chr9:14528000-14531800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:14528400-14529000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr9:14528600-14528800	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr9:14528600-14529400	Enhancers	Fetal Heart	heart
20	chr9:14528800-14529200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr9:14528800-14529400	Bivalent Enhancer	Fetal Lung	lung
22	chr9:14529000-14529400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr9:14529000-14529400	Enhancers	Fetal Kidney	kidney
24	chr9:14529000-14529400	Enhancers	Rectal Smooth Muscle	rectum
25	chr9:14529000-14529400	Active TSS	Right Atrium	heart
26	chr9:14529000-14530400	Enhancers	Brain Germinal Matrix	brain
27	chr9:14529000-14532200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr9:14529200-14529400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr9:14529200-14529400	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr9:14529200-14533000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr9:14529400-14530200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:14529400-14530600	Enhancers	Fetal Brain Female	brain
33	chr9:14529400-14531600	Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr9:14529400-14531800	Weak transcription	Fetal Heart	heart
35	chr9:14529400-14532200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:14529400-14532600	Weak transcription	Fetal Kidney	kidney
37	chr9:14529400-14534000	Weak transcription	Right Atrium	heart
38	chr9:14529400-14534000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr9:14529800-14535600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:14530200-14530600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:14530200-14531000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:14530200-14532000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:14530200-14532600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr9:14530200-14533600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr9:14530200-14534400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr9:14530200-14535000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr9:14530200-14535600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr9:14530400-14530600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:14530400-14530600	Active TSS	Brain Anterior Caudate	brain
50	chr9:14530400-14530600	Bivalent Enhancer	Brain Substantia Nigra	brain

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