Variant report

Variant	nsv831501
Chromosome Location	chr9:6868099-7058526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1939)
CpG islands
(count:246)
Chromatin interactive
region (count:49)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1939 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6877521-6878180	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6932065-6932168	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:7055642-7055921	K562	blood:	n/a	n/a
4	ARID3A	chr9:6986412-6986867	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6871154-6871863	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6899014-6899731	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6931921-6932276	K562	blood:	n/a	n/a
8	ARID3A	chr9:6900480-6901015	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:6927709-6928185	K562	blood:	n/a	n/a
10	ARID3A	chr9:7052706-7052906	K562	blood:	n/a	n/a
11	ARID3A	chr9:6896535-6896910	K562	blood:	n/a	n/a
12	ARID3A	chr9:6955127-6955771	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:6910048-6910291	K562	blood:	n/a	n/a
14	ARID3A	chr9:6896614-6898522	HepG2	liver:	n/a	chr9:6897723-6897739 chr9:6897724-6897740
15	ATF1	chr9:6896588-6896942	K562	blood:	n/a	n/a
16	ATF1	chr9:6927695-6928152	K562	blood:	n/a	n/a
17	ATF1	chr9:7011743-7011938	K562	blood:	n/a	n/a
18	ATF1	chr9:6931877-6932320	K562	blood:	n/a	n/a
19	ATF1	chr9:6894414-6894608	K562	blood:	n/a	n/a
20	ATF2	chr9:6973498-6974318	GM12878	blood:	n/a	n/a
21	ATF2	chr9:6893660-6894746	GM12878	blood:	n/a	n/a
22	ATF2	chr9:6960665-6961260	GM12878	blood:	n/a	n/a
23	ATF2	chr9:6973706-6974207	GM12878	blood:	n/a	n/a
24	ATF2	chr9:6917103-6917695	GM12878	blood:	n/a	n/a
25	ATF2	chr9:6893949-6894575	GM12878	blood:	n/a	n/a
26	ATF2	chr9:6902404-6902842	GM12878	blood:	n/a	n/a
27	ATF2	chr9:7055504-7055907	GM12878	blood:	n/a	n/a
28	ATF3	chr9:6931886-6932304	K562	blood:	n/a	n/a
29	ATF3	chr9:6896530-6896937	K562	blood:	n/a	n/a
30	BACH1	chr9:6955248-6955617	H1-hESC	embryonic stem cell:	n/a	chr9:6955424-6955438
31	BATF	chr9:6973808-6974185	GM12878	blood:	n/a	chr9:6973978-6973989
32	BATF	chr9:6973758-6974189	GM12878	blood:	n/a	chr9:6973978-6973989
33	BATF	chr9:6923191-6923398	GM12878	blood:	n/a	n/a
34	BATF	chr9:6894106-6894608	GM12878	blood:	n/a	n/a
35	BATF	chr9:7055521-7055844	GM12878	blood:	n/a	n/a
36	BATF	chr9:6894207-6894592	GM12878	blood:	n/a	n/a
37	BATF	chr9:7055473-7055753	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:6894214-6894574	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:6973811-6974164	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:6973797-6974200	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:6917243-6917586	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:6893817-6893964	GM12878	blood:	n/a	n/a
43	BCLAF1	chr9:6973634-6974239	GM12878	blood:	n/a	n/a
44	BCLAF1	chr9:6894120-6894571	GM12878	blood:	n/a	n/a
45	BHLHE40	chr9:6931869-6932449	K562	blood:	n/a	n/a
46	BHLHE40	chr9:6896595-6896959	K562	blood:	n/a	n/a
47	BHLHE40	chr9:6955450-6955720	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:6925145-6925210	K562	blood:	n/a	n/a
49	BHLHE40	chr9:6894236-6894572	GM12878	blood:	n/a	n/a
50	BHLHE40	chr9:6955289-6955945	HepG2	liver:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6932042-6932092	HRPEpiC	eye:	n/a
2	chr9:6921930-6921980	SK-N-MC	brain:	n/a
3	chr9:6932042-6932092	HRPEpiC	eye:	n/a
4	chr9:6921930-6921980	SK-N-MC	brain:	n/a
5	chr9:6932042-6932092	HepG2	liver:	n/a
6	chr9:6932042-6932092	NT2-D1	testis:	n/a
7	chr9:6869699-6869749	ECC-1	luminal epithelium:	n/a
8	chr9:6932042-6932092	LNCaP	prostate:	n/a
9	chr9:6955559-6955609	GM12891	blood:	n/a
10	chr9:6869699-6869749	HIPEpiC	eye:	n/a
11	chr9:6932042-6932092	AG09309	skin:	n/a
12	chr9:6921930-6921980	AG04449	skin:	fetal
13	chr9:6932042-6932092	HCPEpiC	choroid plexus:	n/a
14	chr9:6869699-6869749	GM12892	blood:	n/a
15	chr9:6869699-6869749	NT2-D1	testis:	n/a
16	chr9:6869699-6869749	PrEC	prostate:	n/a
17	chr9:6921930-6921980	HCT-116	colon:	n/a
18	chr9:6921930-6921980	GM12878	blood:	n/a
19	chr9:6932042-6932092	AG10803	skin:	n/a
20	chr9:6932042-6932092	HL-60	blood:	n/a
21	chr9:6921930-6921980	NHDF-neo	bronchial:	n/a
22	chr9:6921930-6921980	ECC-1	luminal epithelium:	n/a
23	chr9:6955559-6955609	SK-N-SH_RA	brain:	n/a
24	chr9:6955559-6955609	NHDF-neo	bronchial:	n/a
25	chr9:6869699-6869749	HRPEpiC	eye:	n/a
26	chr9:6869699-6869749	SK-N-SH_RA	brain:	n/a
27	chr9:6955559-6955609	NB4	blood:	n/a
28	chr9:6869699-6869749	HPAEpiC	pulmonary alveolar:	n/a
29	chr9:6955559-6955609	Hepatocyte	liver:	n/a
30	chr9:6921930-6921980	HIPEpiC	eye:	n/a
31	chr9:6869699-6869749	ProgFib	skin:	n/a
32	chr9:6869699-6869749	HRCEpiC	kidney:	n/a
33	chr9:6869699-6869749	MCF10A-Er-Src	breast:	n/a
34	chr9:6955559-6955609	LNCaP	prostate:	n/a
35	chr9:6921930-6921980	HUVEC	blood vessel:	n/a
36	chr9:6869699-6869749	Caco-2	colon:	n/a
37	chr9:6955559-6955609	A549	lung:	n/a
38	chr9:6921930-6921980	PrEC	prostate:	n/a
39	chr9:6921930-6921980	LNCaP	prostate:	n/a
40	chr9:6955559-6955609	H1-hESC	embryonic stem cell:	embryo
41	chr9:6932042-6932092	A549	lung:	n/a
42	chr9:6869699-6869749	HCPEpiC	choroid plexus:	n/a
43	chr9:6955559-6955609	SAEC	small airway:	n/a
44	chr9:6932042-6932092	HRCEpiC	kidney:	n/a
45	chr9:6869699-6869749	SAEC	small airway:	n/a
46	chr9:6869699-6869749	T-47D	breast:	n/a
47	chr9:6932042-6932092	HIPEpiC	eye:	n/a
48	chr9:6921930-6921980	GM19239	blood:	n/a
49	chr9:6869699-6869749	HEEpiC	esophagus:	n/a
50	chr9:6869699-6869749	HNPCEpiC	eye:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
2	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
3	chr9:6890515..6892207-chr9:6893663..6895984,2	K562	blood:
4	chr9:6909294..6911452-chr9:6925149..6926696,2	K562	blood:
5	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
6	chr9:6919963..6921657-chr9:6923857..6925524,2	K562	blood:
7	chr9:6902386..6904166-chr9:6906939..6908570,2	K562	blood:
8	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
9	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
10	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
11	chr9:6756573..6759030-chr9:6894279..6896008,2	K562	blood:
12	chr9:6978865..6981054-chr9:6982708..6984588,2	K562	blood:
13	chr9:6923976..6925853-chr9:6926210..6927942,2	K562	blood:
14	chr9:7028131..7030409-chr9:7036098..7038098,2	MCF-7	breast:
15	chr9:6876130..6878078-chr9:6891371..6893102,2	K562	blood:
16	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
17	chr9:6892256..6893815-chr9:6903780..6905360,2	MCF-7	breast:
18	chr9:7028131..7030409-chr9:7036098..7038098,2	MCF-7	breast:
19	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
20	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
21	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
22	chr9:7052698..7053251-chr9:7360197..7360994,2	K562	blood:
23	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
24	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
25	chr9:6890515..6892207-chr9:6893663..6895984,2	K562	blood:
26	chr9:7051581..7054293-chr9:7055466..7057984,2	MCF-7	breast:
27	chr9:7046839..7049487-chr9:7050524..7052607,2	K562	blood:
28	chr9:6876130..6878078-chr9:6891371..6893102,2	K562	blood:
29	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
30	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
31	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
32	chr9:6888137..6890891-chr9:6891909..6894488,2	K562	blood:
33	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
34	chr9:7052337..7053367-chr9:7536144..7537120,3	MCF-7	breast:
35	chr5:35003633..35004245-chr9:7020432..7021432,2	K562	blood:
36	chr9:6755920..6758663-chr9:6904149..6906669,2	K562	blood:
37	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
38	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
39	chr9:6881706..6883676-chr9:6890777..6893621,2	K562	blood:
40	chr9:6896046..6898374-chr9:6899883..6901481,2	K562	blood:
41	chr9:7052501..7053186-chr9:7233839..7234508,2	MCF-7	breast:
42	chr9:6896046..6898374-chr9:6899883..6901481,2	K562	blood:
43	chr9:7052132..7053116-chr9:7186335..7186921,2	K562	blood:
44	chr9:7051581..7054293-chr9:7055466..7057984,2	MCF-7	breast:
45	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
46	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
47	chr9:6896445..6898374-chr9:6899981..6902743,2	K562	blood:
48	chr9:7052694..7053246-chr9:7259513..7260136,3	MCF-7	breast:
49	chr9:6920289..6921801-chr9:7142294..7145025,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-6	chr9:6948033-6948214	NONHSAT130166
2	lnc-UHRF2-6	chr9:6893123-6893232	NONHSAT130166
3	lnc-UHRF2-2	chr9:6978625-6978859	ENSG00000224972.1
4	lnc-UHRF2-2	chr9:6974766-6974939	ENSG00000224972.1
5	lnc-UHRF2-6	chr9:6941586-6941815	NONHSAT130166
6	lnc-UHRF2-2	chr9:6973827-6973887	ENSG00000224972.1
7	lnc-UHRF2-6	chr9:6942460-6942634	NONHSAT130166
8	lnc-UHRF2-2	chr9:6902670-6902752	ENSG00000224972.1

No data

Variant related genes	Relation type
KDM4C	TF binding region
ENSG00000224972	TF binding region
KDM4C	CpG island
ENSG00000224972	CpG island
ENSG00000107077	chromatin interactions
ENSG00000224972	chromatin interactions

Extended variants
information (count: 9877 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:9877 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552295022	chr9:6868111-6868112	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146458283	chr9:6868112-6868113	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370764704	chr9:6868114-6868115	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549763123	chr9:6868128-6868129	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549995944	chr9:6868131-6868132	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568615226	chr9:6868166-6868167	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12235676	chr9:6868177-6868178	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs143407158	chr9:6868178-6868179	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569805006	chr9:6868197-6868198	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565934281	chr9:6868208-6868209	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146755176	chr9:6868211-6868212	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188672899	chr9:6868216-6868217	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200170013	chr9:6868217-6868218	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537023780	chr9:6868249-6868250	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555734798	chr9:6868254-6868255	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574604391	chr9:6868266-6868267	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542136063	chr9:6868296-6868297	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545056114	chr9:6868298-6868299	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560477234	chr9:6868315-6868316	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376016563	chr9:6868325-6868326	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370836675	chr9:6868343-6868344	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572245613	chr9:6868359-6868360	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140413658	chr9:6868361-6868362	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535523759	chr9:6868378-6868379	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370372983	chr9:6868383-6868384	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548777673	chr9:6868413-6868414	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565688972	chr9:6868416-6868417	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563989203	chr9:6868419-6868420	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180769445	chr9:6868472-6868473	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113780301	chr9:6868489-6868490	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186148120	chr9:6868502-6868503	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192264613	chr9:6868508-6868509	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537290169	chr9:6868551-6868552	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181956208	chr9:6868562-6868563	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145676594	chr9:6868587-6868588	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537884485	chr9:6868608-6868609	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374445078	chr9:6868623-6868624	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539613176	chr9:6868627-6868628	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551582193	chr9:6868631-6868632	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10975865	chr9:6868645-6868646	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs10975866	chr9:6868649-6868650	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555619211	chr9:6868655-6868656	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573972118	chr9:6868667-6868668	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187409718	chr9:6868668-6868669	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557462027	chr9:6868684-6868685	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554092919	chr9:6868685-6868686	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115380655	chr9:6868688-6868689	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148934006	chr9:6868693-6868694	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190528010	chr9:6868730-6868731	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77366980	chr9:6868737-6868738	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD

Chromatin state (count:3879 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6824400-6892000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr9:6835400-6869200	Weak transcription	Right Ventricle	heart
3	chr9:6835400-6893200	Weak transcription	Colonic Mucosa	Colon
4	chr9:6835600-6870600	Weak transcription	Esophagus	oesophagus
5	chr9:6850400-6869600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr9:6852800-6868600	Weak transcription	Fetal Heart	heart
7	chr9:6852800-6869200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr9:6853000-6874000	Weak transcription	Gastric	stomach
9	chr9:6853600-6869400	Weak transcription	Lung	lung
10	chr9:6863400-6868200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:6863800-6868400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr9:6864000-6868400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr9:6864000-6868400	Weak transcription	Thymus	Thymus
14	chr9:6864000-6869200	Weak transcription	Left Ventricle	heart
15	chr9:6864000-6869200	Weak transcription	Pancreas	Pancrea
16	chr9:6864000-6880400	Weak transcription	Aorta	Aorta
17	chr9:6864200-6877400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:6864400-6868400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr9:6864400-6868600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr9:6864400-6869200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:6864400-6869400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr9:6864400-6869400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr9:6864400-6869600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:6864400-6870200	Weak transcription	Brain Angular Gyrus	brain
25	chr9:6864400-6874600	Weak transcription	Spleen	Spleen
26	chr9:6864400-6880200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr9:6864400-6880400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr9:6864400-6885400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr9:6864600-6869400	Weak transcription	Stomach Smooth Muscle	stomach
30	chr9:6864600-6869600	Weak transcription	HMEC	breast
31	chr9:6864600-6870600	Weak transcription	Liver	Liver
32	chr9:6864600-6870600	Weak transcription	Brain Anterior Caudate	brain
33	chr9:6864600-6870800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:6864600-6871400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr9:6864600-6873400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:6864600-6873800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr9:6864600-6873800	Weak transcription	HSMMtube	muscle
38	chr9:6864600-6874600	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr9:6864600-6874600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr9:6864600-6875200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:6864600-6887200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr9:6864600-6889600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr9:6864800-6869000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr9:6865000-6868200	Weak transcription	Primary T cells from cord blood	blood
45	chr9:6865000-6869200	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr9:6865000-6877800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr9:6865000-6887200	Weak transcription	Fetal Intestine Large	intestine
48	chr9:6865400-6869200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr9:6865600-6868400	Weak transcription	Fetal Thymus	thymus
50	chr9:6865600-6870600	Weak transcription	Primary B cells from cord blood	blood

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