Variant report

Variant	esv2757308
Chromosome Location	chr9:6743440-6845561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1825)
CpG islands
(count:916)
Chromatin interactive
region (count:45)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6758992-6759444	K562	blood:	n/a	n/a
2	ARID3A	chr9:6819233-6819386	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6756811-6758201	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6779811-6780274	K562	blood:	n/a	n/a
5	ARID3A	chr9:6755672-6755722	K562	blood:	n/a	n/a
6	ARID3A	chr9:6788815-6789003	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6845117-6845374	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:6779378-6780217	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:6756891-6757253	K562	blood:	n/a	n/a
10	ARID3A	chr9:6787981-6788483	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:6781433-6781998	HepG2	liver:	n/a	n/a
12	ATF1	chr9:6756990-6758095	K562	blood:	n/a	n/a
13	ATF1	chr9:6753060-6753144	K562	blood:	n/a	n/a
14	ATF1	chr9:6779901-6780225	K562	blood:	n/a	n/a
15	ATF2	chr9:6771687-6772129	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr9:6777168-6777670	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:6757293-6758094	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr9:6758832-6759575	GM12878	blood:	n/a	n/a
19	ATF2	chr9:6750387-6751234	GM12878	blood:	n/a	n/a
20	ATF2	chr9:6771753-6772027	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr9:6758832-6759588	GM12878	blood:	n/a	n/a
22	ATF2	chr9:6750570-6751254	GM12878	blood:	n/a	n/a
23	ATF2	chr9:6756928-6758082	GM12878	blood:	n/a	n/a
24	ATF2	chr9:6757315-6757912	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr9:6756759-6758392	GM12878	blood:	n/a	n/a
26	ATF3	chr9:6757628-6758216	HepG2	liver:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
27	ATF3	chr9:6757154-6757557	K562	blood:	n/a	n/a
28	ATF3	chr9:6757468-6758055	A549	lung:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
29	ATF3	chr9:6757549-6758137	H1-hESC	embryonic stem cell:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
30	ATF3	chr9:6757789-6758049	GM12878	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
31	ATF3	chr9:6757570-6758187	GM12878	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
32	ATF3	chr9:6757524-6758154	A549	lung:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
33	ATF3	chr9:6757772-6758138	K562	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
34	ATF3	chr9:6757790-6758075	K562	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
35	ATF3	chr9:6757652-6758141	HepG2	liver:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
36	ATF3	chr9:6757678-6758138	H1-hESC	embryonic stem cell:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
37	ATF3	chr9:6757514-6757784	K562	blood:	n/a	n/a
38	ATF3	chr9:6779898-6780160	K562	blood:	n/a	n/a
39	BACH1	chr9:6764615-6764768	H1-hESC	embryonic stem cell:	n/a	chr9:6764754-6764768
40	BACH1	chr9:6765406-6765470	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr9:6757224-6758261	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr9:6758576-6759166	H1-hESC	embryonic stem cell:	n/a	n/a
43	BATF	chr9:6816627-6816816	GM12878	blood:	n/a	n/a
44	BATF	chr9:6750653-6751296	GM12878	blood:	n/a	n/a
45	BATF	chr9:6759129-6759503	GM12878	blood:	n/a	n/a
46	BATF	chr9:6757171-6757975	GM12878	blood:	n/a	n/a
47	BCL11A	chr9:6750696-6750991	GM12878	blood:	n/a	chr9:6750723-6750732
48	BCL11A	chr9:6750615-6751060	GM12878	blood:	n/a	chr9:6750723-6750732
49	BCL11A	chr9:6771770-6772048	H1-hESC	embryonic stem cell:	n/a	n/a
50	BCL3	chr9:6757389-6758173	GM12878	blood:	n/a	chr9:6757996-6758009

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6835001-6835051	GM12878	blood:	n/a
2	chr9:6835001-6835051	GM12878	blood:	n/a
3	chr9:6757781-6757831	Caco-2	colon:	n/a
4	chr9:6757146-6757196	HAEpiC	amniotic membrane:	n/a
5	chr9:6755109-6755159	HEEpiC	esophagus:	n/a
6	chr9:6758935-6758985	HL-60	blood:	n/a
7	chr9:6758935-6758985	HRPEpiC	eye:	n/a
8	chr9:6835001-6835051	AoSMC	blood vessel:	n/a
9	chr9:6836634-6836684	HCPEpiC	choroid plexus:	n/a
10	chr9:6758935-6758985	GM06990	blood:	n/a
11	chr9:6779450-6779500	MCF10A-Er-Src	breast:	n/a
12	chr9:6836634-6836684	AG04449	skin:	fetal
13	chr9:6779450-6779500	SAEC	small airway:	n/a
14	chr9:6758853-6758903	HMEC	breast:	n/a
15	chr9:6758853-6758903	SK-N-MC	brain:	n/a
16	chr9:6755109-6755159	AG04450	lung:	fetal
17	chr9:6779450-6779500	CMK	blood:	n/a
18	chr9:6836634-6836684	AG09309	skin:	n/a
19	chr9:6835001-6835051	K562	blood:	n/a
20	chr9:6779450-6779500	ovcar-3	ovarian:	n/a
21	chr9:6835001-6835051	LNCaP	prostate:	n/a
22	chr9:6757781-6757831	HRCEpiC	kidney:	n/a
23	chr9:6757146-6757196	PrEC	prostate:	n/a
24	chr9:6757347-6757397	HCF	heart:	n/a
25	chr9:6758140-6758190	SK-N-MC	brain:	n/a
26	chr9:6758935-6758985	GM19239	blood:	n/a
27	chr9:6757781-6757831	IMR90	lung:	fetal
28	chr9:6836634-6836684	Hela-S3	cervix:	n/a
29	chr9:6836634-6836684	PrEC	prostate:	n/a
30	chr9:6757781-6757831	NHBE	bronchial:	n/a
31	chr9:6757146-6757196	AG04450	lung:	fetal
32	chr9:6757781-6757831	U87	brain:	n/a
33	chr9:6758853-6758903	GM12892	blood:	n/a
34	chr9:6758853-6758903	HRCEpiC	kidney:	n/a
35	chr9:6758683-6758733	A549	lung:	n/a
36	chr9:6757347-6757397	Hepatocyte	liver:	n/a
37	chr9:6757146-6757196	NHBE	bronchial:	n/a
38	chr9:6755109-6755159	HRE	kidney:	n/a
39	chr9:6758546-6758596	PANC-1	pancreas:	n/a
40	chr9:6836634-6836684	GM06990	blood:	n/a
41	chr9:6755109-6755159	NT2-D1	testis:	n/a
42	chr9:6758546-6758596	NB4	blood:	n/a
43	chr9:6758853-6758903	LNCaP	prostate:	n/a
44	chr9:6757781-6757831	SK-N-SH	brain:	n/a
45	chr9:6757347-6757397	HIPEpiC	eye:	n/a
46	chr9:6757347-6757397	AG04449	skin:	fetal
47	chr9:6757781-6757831	HAEpiC	amniotic membrane:	n/a
48	chr9:6757912-6757962	HCPEpiC	choroid plexus:	n/a
49	chr9:6758853-6758903	HCPEpiC	choroid plexus:	n/a
50	chr9:6757146-6757196	NT2-D1	testis:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6702391..6705446-chr9:6756717..6760058,5	MCF-7	breast:
2	chr1:201979647..201980421-chr9:6757390..6758317,2	HCT-116	colon:
3	chr9:6706468..6709007-chr9:6764056..6766511,2	MCF-7	breast:
4	chr9:6751679..6753304-chr9:6755614..6757783,2	MCF-7	breast:
5	chr9:6747740..6749345-chr9:6756036..6758918,2	MCF-7	breast:
6	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
7	chr9:6749197..6752825-chr9:6755235..6757236,4	K562	blood:
8	chr9:6413251..6414875-chr9:6756450..6759044,2	K562	blood:
9	chr12:49245554..49246083-chr9:6757387..6757976,2	Hela-S3	cervix:
10	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
11	chr9:6765179..6766927-chr9:6770237..6771845,2	K562	blood:
12	chr9:6749158..6750730-chr9:6754623..6757370,3	K562	blood:
13	chr11:57102959..57103791-chr9:6757018..6757636,2	NB4	blood:
14	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
15	chr1:78469866..78470559-chr9:6757407..6758029,2	NB4	blood:
16	chr22:39077394..39078187-chr9:6757291..6757887,2	HCT-116	colon:
17	chr9:6757021..6759532-chr9:6768470..6771017,3	K562	blood:
18	chr1:24117621..24118528-chr9:6757285..6757921,2	Hela-S3	cervix:
19	chr1:63833144..63833741-chr9:6757006..6757570,2	NB4	blood:
20	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
21	chr9:6749158..6750730-chr9:6754623..6757370,3	K562	blood:
22	chr9:6751286..6753075-chr9:6755508..6757503,2	MCF-7	breast:
23	chr9:6747740..6749345-chr9:6756036..6758918,2	MCF-7	breast:
24	chr9:6757388..6759261-chr9:6764601..6766785,2	MCF-7	breast:
25	chr9:6711589..6718151-chr9:6755774..6759657,12	MCF-7	breast:
26	chr9:6756506..6759336-chr9:6761694..6766158,6	MCF-7	breast:
27	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
28	chr9:6680103..6682666-chr9:6784102..6786978,2	K562	blood:
29	chr2:219187766..219188395-chr9:6757084..6757687,2	NB4	blood:
30	chr11:88070952..88071704-chr9:6757255..6758140,2	NB4	blood:
31	chr9:6757938..6759489-chr9:6817335..6820629,3	MCF-7	breast:
32	chr9:6765179..6766927-chr9:6770237..6771845,2	K562	blood:
33	chr9:6757988..6759532-chr9:6768470..6771009,2	K562	blood:
34	chr9:6714844..6717578-chr9:6754943..6759087,4	MCF-7	breast:
35	chr17:45727006..45727831-chr9:6757854..6758764,2	HCT-116	colon:
36	chr17:4458410..4459064-chr9:6757173..6757817,2	NB4	blood:
37	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
38	chr9:6411580..6414419-chr9:6755713..6757647,2	K562	blood:
39	chr9:6722888..6726785-chr9:6754807..6757177,3	K562	blood:
40	chr7:86781908..86782653-chr9:6757524..6758733,3	Hela-S3	cervix:
41	chr9:6749197..6752825-chr9:6755235..6757236,4	K562	blood:
42	chr6:26216402..26217347-chr9:6757097..6757962,2	Hela-S3	cervix:
43	chr9:6751286..6753075-chr9:6755508..6757503,2	MCF-7	breast:
44	chr9:6668807..6671531-chr9:6755488..6757060,2	K562	blood:
45	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLDC-1	chr9:6748703-6748981	NONHSAT130164
2	lnc-UHRF2-1	chr9:6785601-6785929	ENSG00000236563.1
3	lnc-UHRF2-1	chr9:6780333-6780490	ENSG00000236563.1

No data

Variant related genes	Relation type
SNRPEP2	TF binding region
KDM4C	TF binding region
ENSG00000230581	TF binding region
SNRPEP2	CpG island
KDM4C	CpG island
ENSG00000230581	CpG island
ENSG00000168274	chromatin interactions
ENSG00000132382	chromatin interactions
ENSG00000135164	chromatin interactions
ENSG00000273338	chromatin interactions
ENSG00000011009	chromatin interactions
ENSG00000127838	chromatin interactions
ENSG00000225489	chromatin interactions
ENSG00000109861	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000147854	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000231381	chromatin interactions
ENSG00000256968	chromatin interactions
ENSG00000088035	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000149136	chromatin interactions
ENSG00000107077	chromatin interactions
ENSG00000100216	chromatin interactions
ENSG00000228274	chromatin interactions
ENSG00000229611	chromatin interactions
ENSG00000174243	chromatin interactions

Extended variants
information (count: 5478 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5478 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4008332	chr9:6743440-6743441	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563400875	chr9:6743477-6743478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184552935	chr9:6743481-6743482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542710767	chr9:6743532-6743533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561554469	chr9:6743554-6743555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142028576	chr9:6743567-6743568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369806455	chr9:6743583-6743584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188156778	chr9:6743613-6743614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150508201	chr9:6743670-6743671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550542801	chr9:6743688-6743689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116435953	chr9:6743698-6743699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs820521	chr9:6743705-6743706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201960626	chr9:6743706-6743707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548231607	chr9:6743744-6743745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192734902	chr9:6743761-6743762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534511514	chr9:6743787-6743788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374784207	chr9:6743826-6743827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35581518	chr9:6743917-6743918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550314190	chr9:6743918-6743919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537932440	chr9:6743940-6743941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs702280	chr9:6743963-6743964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372757618	chr9:6743973-6743974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184401544	chr9:6743979-6743980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115193634	chr9:6744035-6744036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542751589	chr9:6744059-6744060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560809823	chr9:6744124-6744125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115875226	chr9:6744152-6744153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142743054	chr9:6744161-6744162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539126108	chr9:6744168-6744169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555764475	chr9:6744176-6744177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532679547	chr9:6744263-6744264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550832819	chr9:6744266-6744267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562544586	chr9:6744275-6744276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529998067	chr9:6744296-6744297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548707044	chr9:6744299-6744300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386732150	chr9:6744330-6744331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139581748	chr9:6744331-6744332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546462836	chr9:6744335-6744336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574771901	chr9:6744381-6744382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542559021	chr9:6744382-6744383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571386864	chr9:6744385-6744386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113291848	chr9:6744386-6744387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144048566	chr9:6744393-6744394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575350990	chr9:6744394-6744395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189284006	chr9:6744395-6744396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148688406	chr9:6744398-6744399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545230169	chr9:6744405-6744406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34597969	chr9:6744447-6744448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs7048014	chr9:6744448-6744449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576975962	chr9:6744457-6744458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:2924 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6724200-6749200	Weak transcription	Primary B cells from cord blood	blood
2	chr9:6742800-6743600	Enhancers	HepG2	liver
3	chr9:6743600-6747800	Weak transcription	HepG2	liver
4	chr9:6749200-6750200	Enhancers	Primary B cells from cord blood	blood
5	chr9:6749200-6750200	Enhancers	Primary T cells fromperipheralblood	blood
6	chr9:6749400-6750200	Enhancers	Primary B cells from peripheral blood	blood
7	chr9:6749800-6750400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr9:6750000-6750200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:6750000-6750400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr9:6750000-6750400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr9:6750000-6750400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr9:6750000-6750400	Enhancers	GM12878-XiMat	blood
13	chr9:6750000-6750600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:6750000-6751000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:6750000-6751200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr9:6750200-6750400	Active TSS	Monocytes-CD14+_RO01746	blood
17	chr9:6750200-6750600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
18	chr9:6750200-6751000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
19	chr9:6750200-6751000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr9:6750200-6751000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr9:6750200-6751000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:6750200-6751200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:6750200-6751200	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr9:6750200-6751200	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr9:6750200-6751400	Enhancers	Fetal Thymus	thymus
26	chr9:6750400-6750600	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr9:6750400-6750600	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr9:6750400-6750600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr9:6750400-6750800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr9:6750400-6750800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr9:6750400-6750800	Active TSS	GM12878-XiMat	blood
32	chr9:6750400-6751000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr9:6750400-6751000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr9:6750400-6751000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr9:6750400-6751000	Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr9:6750400-6751000	Active TSS	Rectal Mucosa Donor 29	rectum
37	chr9:6750400-6751000	Enhancers	HMEC	breast
38	chr9:6750400-6751000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr9:6750400-6751200	Enhancers	Primary T cells from cord blood	blood
40	chr9:6750400-6751200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr9:6750600-6750800	Active TSS	Primary hematopoietic stem cells	blood
42	chr9:6750600-6750800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:6750600-6751000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr9:6750600-6751000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr9:6750600-6751000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:6750600-6751000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:6750600-6751000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:6750600-6751000	Active TSS	Duodenum Mucosa	Duodenum
49	chr9:6750600-6751200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr9:6750600-6751200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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