Variant report

Variant	nsv1026827
Chromosome Location	chr9:26693515-26904699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2196)
CpG islands
(count:305)
Chromatin interactive
region (count:76)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2196 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:26892177-26893347	K562	blood:	n/a	n/a
2	ARID3A	chr9:26892213-26892999	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:26890942-26891193	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:26746655-26746928	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:26744401-26744755	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:26891400-26891881	HepG2	liver:	n/a	n/a
7	ATF1	chr9:26779126-26779512	K562	blood:	n/a	n/a
8	ATF1	chr9:26892115-26893225	K562	blood:	n/a	n/a
9	ATF2	chr9:26892198-26893098	GM12878	blood:	n/a	n/a
10	ATF2	chr9:26892013-26893122	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr9:26892559-26893227	GM12878	blood:	n/a	n/a
12	ATF2	chr9:26746311-26747148	GM12878	blood:	n/a	n/a
13	ATF3	chr9:26892673-26892938	K562	blood:	n/a	chr9:26892808-26892822
14	ATF3	chr9:26892257-26893018	A549	lung:	n/a	chr9:26892808-26892822
15	ATF3	chr9:26892552-26893020	H1-hESC	embryonic stem cell:	n/a	chr9:26892808-26892822
16	ATF3	chr9:26892598-26892975	GM12878	blood:	n/a	chr9:26892808-26892822
17	ATF3	chr9:26892496-26892918	HepG2	liver:	n/a	chr9:26892808-26892822
18	BACH1	chr9:26746447-26747018	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr9:26892276-26892919	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr9:26892616-26892987	GM12878	blood:	n/a	n/a
21	BATF	chr9:26812328-26812593	GM12878	blood:	n/a	chr9:26812496-26812507
22	BATF	chr9:26812281-26812601	GM12878	blood:	n/a	chr9:26812496-26812507
23	BCL11A	chr9:26813340-26813512	GM12878	blood:	n/a	n/a
24	BCL3	chr9:26892474-26893160	A549	lung:	n/a	chr9:26892820-26892829
25	BCL3	chr9:26892270-26893005	GM12878	blood:	n/a	chr9:26892820-26892829
26	BCL3	chr9:26892108-26893104	A549	lung:	n/a	chr9:26892820-26892829
27	BCL3	chr9:26898323-26898654	GM12878	blood:	n/a	n/a
28	BCLAF1	chr9:26892196-26893074	GM12878	blood:	n/a	chr9:26892820-26892829
29	BCLAF1	chr9:26892105-26893182	GM12878	blood:	n/a	chr9:26892820-26892829
30	BHLHE40	chr9:26746185-26747145	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:26892210-26893289	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:26892227-26893079	HepG2	liver:	n/a	n/a
33	BHLHE40	chr9:26892236-26893061	K562	blood:	n/a	n/a
34	BHLHE40	chr9:26790082-26790647	K562	blood:	n/a	n/a
35	BRCA1	chr9:26892303-26892816	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:26779130-26779354	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr9:26863222-26863417	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr9:26892305-26893025	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr9:26892689-26893084	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr9:26892062-26892479	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr9:26891346-26891824	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr9:26892612-26892935	HepG2	liver:	n/a	n/a
43	CBX3	chr9:26746383-26747096	HCT-116	colon:	n/a	n/a
44	CBX3	chr9:26892605-26893010	K562	blood:	n/a	n/a
45	CBX3	chr9:26882181-26882467	K562	blood:	n/a	n/a
46	CBX3	chr9:26746522-26747086	HCT-116	colon:	n/a	n/a
47	CCNT2	chr9:26892240-26892960	K562	blood:	n/a	n/a
48	CEBPB	chr9:26892142-26892457	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr9:26851012-26851387	K562	blood:	n/a	chr9:26851190-26851201 chr9:26851191-26851200 chr9:26851189-26851202 chr9:26851191-26851200 chr9:26851191-26851200 chr9:26851189-26851202
50	CEBPB	chr9:26850957-26851469	A549	lung:	n/a	chr9:26851190-26851201 chr9:26851191-26851200 chr9:26851189-26851202 chr9:26851191-26851200 chr9:26851191-26851200 chr9:26851189-26851202

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:26722560-26722610	NH-A	brain:	n/a
2	chr9:26892919-26892969	RPTEC	kidney:	n/a
3	chr9:26892479-26892529	HAEpiC	amniotic membrane:	n/a
4	chr9:26892479-26892529	PANC-1	pancreas:	n/a
5	chr9:26761746-26761796	SK-N-SH	brain:	n/a
6	chr9:26892069-26892119	PANC-1	pancreas:	n/a
7	chr9:26892919-26892969	AoSMC	blood vessel:	n/a
8	chr9:26892069-26892119	NHBE	bronchial:	n/a
9	chr9:26892069-26892119	HRCEpiC	kidney:	n/a
10	chr9:26892919-26892969	PrEC	prostate:	n/a
11	chr9:26892919-26892969	SK-N-MC	brain:	n/a
12	chr9:26761746-26761796	SAEC	small airway:	n/a
13	chr9:26892919-26892969	Hela-S3	cervix:	n/a
14	chr9:26892069-26892119	HEEpiC	esophagus:	n/a
15	chr9:26722560-26722610	PrEC	prostate:	n/a
16	chr9:26722560-26722610	MCF10A-Er-Src	breast:	n/a
17	chr9:26892069-26892119	BE2_C	brain:	n/a
18	chr9:26892479-26892529	AG04449	skin:	fetal
19	chr9:26892919-26892969	K562	blood:	n/a
20	chr9:26892919-26892969	HRPEpiC	eye:	n/a
21	chr9:26892069-26892119	HCF	heart:	n/a
22	chr9:26892479-26892529	SK-N-MC	brain:	n/a
23	chr9:26892919-26892969	T-47D	breast:	n/a
24	chr9:26761746-26761796	HEEpiC	esophagus:	n/a
25	chr9:26892479-26892529	LNCaP	prostate:	n/a
26	chr9:26722560-26722610	SKMC	muscle:	n/a
27	chr9:26761746-26761796	H1-hESC	embryonic stem cell:	embryo
28	chr9:26892479-26892529	RPTEC	kidney:	n/a
29	chr9:26892919-26892969	BJ	skin:	n/a
30	chr9:26892919-26892969	Hepatocyte	liver:	n/a
31	chr9:26722560-26722610	H1-hESC	embryonic stem cell:	embryo
32	chr9:26722560-26722610	HCT-116	colon:	n/a
33	chr9:26892479-26892529	SK-N-SH	brain:	n/a
34	chr9:26892479-26892529	BJ	skin:	n/a
35	chr9:26761746-26761796	NT2-D1	testis:	n/a
36	chr9:26892919-26892969	GM06990	blood:	n/a
37	chr9:26892069-26892119	ECC-1	luminal epithelium:	n/a
38	chr9:26892479-26892529	HL-60	blood:	n/a
39	chr9:26722560-26722610	HAEpiC	amniotic membrane:	n/a
40	chr9:26761746-26761796	HEK293	kidney:	embryo
41	chr9:26722560-26722610	HMEC	breast:	n/a
42	chr9:26892479-26892529	MCF10A-Er-Src	breast:	n/a
43	chr9:26892919-26892969	SK-N-SH	brain:	n/a
44	chr9:26892069-26892119	RPTEC	kidney:	n/a
45	chr9:26892069-26892119	AG04449	skin:	fetal
46	chr9:26722560-26722610	HEEpiC	esophagus:	n/a
47	chr9:26892919-26892969	NHBE	bronchial:	n/a
48	chr9:26892479-26892529	HRCEpiC	kidney:	n/a
49	chr9:26892919-26892969	ProgFib	skin:	n/a
50	chr9:26892479-26892529	A549	lung:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:17739272..17740133-chr9:26892437..26893088,2	Hela-S3	cervix:
2	chr9:26894759..26896593-chr9:26898391..26900808,2	K562	blood:
3	chr9:26884245..26886305-chr9:26888073..26890557,2	K562	blood:
4	chr9:26762229..26764985-chr9:26768189..26769709,2	MCF-7	breast:
5	chr9:26889862..26894629-chr9:26953159..26958871,9	K562	blood:
6	chr9:26859892..26862595-chr9:26891089..26892734,2	MCF-7	breast:
7	chr9:26890425..26894629-chr9:26953159..26958312,6	K562	blood:
8	chr15:93443364..93444002-chr9:26892582..26893189,2	HCT-116	colon:
9	chr9:26904433..26907115-chr9:26907974..26909867,2	K562	blood:
10	chr12:39299074..39299955-chr9:26892301..26892993,2	Hela-S3	cervix:
11	chr9:26873222..26876012-chr9:26876055..26878747,3	K562	blood:
12	chr9:26886474..26888568-chr9:26890678..26892880,3	MCF-7	breast:
13	chr9:26890972..26893985-chr9:26945405..26948624,3	MCF-7	breast:
14	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
15	chr9:26891285..26894088-chr9:26896175..26900385,5	K562	blood:
16	chr9:26867603..26870334-chr9:26891418..26893651,2	MCF-7	breast:
17	chr9:26744400..26745094-chr9:26856160..26856966,3	MCF-7	breast:
18	chr6:47937522..47938139-chr9:26854193..26854937,2	MCF-7	breast:
19	chr9:26865662..26868224-chr9:26870486..26872108,2	MCF-7	breast:
20	chr9:26890485..26893190-chr9:26945159..26948755,7	MCF-7	breast:
21	chr9:26900485..26902697-chr9:26902754..26904663,2	K562	blood:
22	chr9:26898930..26900769-chr9:26941051..26942769,2	MCF-7	breast:
23	chr9:26886338..26888156-chr9:26890310..26892766,2	MCF-7	breast:
24	chr9:26744169..26744992-chr9:26856156..26857045,4	MCF-7	breast:
25	chr9:26886338..26888156-chr9:26890310..26892766,2	MCF-7	breast:
26	chr9:26879503..26881932-chr9:26883463..26885436,2	K562	blood:
27	chr9:26326443..26327103-chr9:26862889..26863559,2	MCF-7	breast:
28	chr9:26899122..26901033-chr9:26907283..26909966,2	K562	blood:
29	chr9:26892381..26894407-chr9:26894414..26897617,3	MCF-7	breast:
30	chr9:26865662..26868224-chr9:26870486..26872108,2	MCF-7	breast:
31	chr9:26888414..26890276-chr9:26890319..26892503,2	MCF-7	breast:
32	chr9:26893520..26896311-chr9:26900470..26903160,2	MCF-7	breast:
33	chr9:26863201..26866107-chr9:26870458..26872508,2	K562	blood:
34	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
35	chr9:26697199..26699954-chr9:26703852..26705743,2	K562	blood:
36	chr9:26723206..26723920-chr9:26975181..26975897,2	K562	blood:
37	chr9:26744400..26745007-chr9:26975049..26975918,2	MCF-7	breast:
38	chr9:26863059..26863690-chr9:26975381..26976202,2	MCF-7	breast:
39	chr9:26901868..26903390-chr9:26945608..26947352,2	MCF-7	breast:
40	chr9:26744400..26745094-chr9:26856160..26856966,3	MCF-7	breast:
41	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
42	chr19:58694769..58695737-chr9:26892467..26893064,2	Hela-S3	cervix:
43	chr9:26892381..26894407-chr9:26894414..26897617,3	MCF-7	breast:
44	chr9:26863201..26866107-chr9:26870458..26872508,2	K562	blood:
45	chr9:26882668..26884290-chr9:26943587..26946347,2	MCF-7	breast:
46	chr9:26894775..26896593-chr9:26898921..26900808,2	K562	blood:
47	chr9:26891080..26893894-chr9:26901411..26904515,3	MCF-7	breast:
48	chr9:26697199..26699954-chr9:26703852..26705743,2	K562	blood:
49	chr9:26745009..26745599-chr9:26856133..26856633,2	MCF-7	breast:
50	chr9:26891080..26895841-chr9:26945501..26948974,8	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFT74-1	chr9:26801731-26802058	NONHSAT130596
2	lnc-IFT74-1	chr9:26805818-26805860	ENSG00000253400
3	lnc-PLAA-2	chr9:26880176-26880547	NONHSAT130599
4	lnc-C9orf82-1	chr9:26718906-26718917	XLOC_007661
5	lnc-IFT74-1	chr9:26801731-26802058	ENSG00000253400
6	lnc-C9orf82-1	chr9:26716406-26716605	XLOC_007661
7	lnc-IFT74-1	chr9:26805818-26806505	NONHSAT130596
8	lnc-IFT74-5	chr9:26895676-26895968	NONHSAT130600
9	lnc-IFT74-1	chr9:26800918-26800938	NONHSAT130596

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C9orf82	hsa-miR-16-5p	chr9:26840784-26840804
2	C9orf82	hsa-miR-16-5p	chr9:26841116-26841137

Variant related genes	Relation type
ENSG00000232466	TF binding region
ENSG00000253400	TF binding region
CAAP1	TF binding region
ENSG00000252580	TF binding region
ENSG00000254261	TF binding region
RN7SL100P	TF binding region
ENSG00000232466	CpG island
ENSG00000253400	CpG island
CAAP1	CpG island
ENSG00000252580	CpG island
ENSG00000254261	CpG island
RN7SL100P	CpG island
ENSG00000072310	chromatin interactions
ENSG00000171606	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000139117	chromatin interactions
ENSG00000234676	chromatin interactions
ENSG00000137055	chromatin interactions
ENSG00000232466	chromatin interactions
ENSG00000173575	chromatin interactions
ENSG00000096872	chromatin interactions
ENSG00000240306	chromatin interactions
ENSG00000120159	chromatin interactions

Extended variants
information (count: 6829 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:6829 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184319348	chr9:26693550-26693551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566081653	chr9:26693583-26693584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552573054	chr9:26693653-26693654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577533268	chr9:26693677-26693678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189301983	chr9:26693680-26693681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180872736	chr9:26693691-26693692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557176431	chr9:26693710-26693711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575387038	chr9:26693712-26693713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186405565	chr9:26693723-26693724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188605660	chr9:26693726-26693727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536745872	chr9:26693810-26693811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573395011	chr9:26693869-26693870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13289000	chr9:26693890-26693891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs10217512	chr9:26693902-26693903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs202242957	chr9:26693959-26693960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200490910	chr9:26693960-26693961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532489524	chr9:26693963-26693964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544625256	chr9:26693983-26693984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181482871	chr9:26693988-26693989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148908804	chr9:26694008-26694009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114487002	chr9:26694056-26694057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73425855	chr9:26694059-26694060	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs528191320	chr9:26694062-26694063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577496289	chr9:26694121-26694122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571162307	chr9:26694122-26694123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185971444	chr9:26694126-26694127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557006699	chr9:26694151-26694152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569109440	chr9:26694156-26694157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7871815	chr9:26694184-26694185	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs553925012	chr9:26694206-26694207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572095055	chr9:26694254-26694255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112676060	chr9:26694286-26694287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71508693	chr9:26694299-26694300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190873338	chr9:26694303-26694304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573033245	chr9:26694354-26694355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540732695	chr9:26694392-26694393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559005551	chr9:26694436-26694437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184202325	chr9:26694437-26694438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544578982	chr9:26694439-26694440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563068757	chr9:26694486-26694487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530349169	chr9:26694500-26694501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73425860	chr9:26694551-26694552	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs187209048	chr9:26694586-26694587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143585486	chr9:26694609-26694610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542664562	chr9:26694637-26694638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546427979	chr9:26694650-26694651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150984584	chr9:26694662-26694663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532036338	chr9:26694701-26694702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550570633	chr9:26694717-26694718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568723588	chr9:26694735-26694736	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2325 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26687800-26694200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:26694000-26696600	Enhancers	Fetal Brain Male	brain
3	chr9:26694200-26695000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:26694200-26695000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:26695000-26697000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:26697400-26697600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:26702200-26703800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:26702400-26703000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr9:26706200-26706400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:26708000-26708400	Enhancers	Small Intestine	intestine
11	chr9:26708000-26708400	Enhancers	Stomach Mucosa	stomach
12	chr9:26708200-26708600	Enhancers	Duodenum Mucosa	Duodenum
13	chr9:26712000-26712800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:26713000-26714800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:26715000-26715200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:26715200-26716400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:26715200-26720400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:26715800-26716400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr9:26718600-26719000	Active TSS	Aorta	Aorta
20	chr9:26720400-26720600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:26720600-26726600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:26721600-26723400	Enhancers	Brain Germinal Matrix	brain
23	chr9:26722200-26723000	Enhancers	Fetal Lung	lung
24	chr9:26722200-26723600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr9:26722200-26723800	Enhancers	Duodenum Mucosa	Duodenum
26	chr9:26722400-26723000	Enhancers	Fetal Brain Female	brain
27	chr9:26722400-26723400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr9:26722600-26722800	Enhancers	Fetal Stomach	stomach
29	chr9:26722600-26723000	Bivalent Enhancer	Brain Hippocampus Middle	brain
30	chr9:26722800-26723000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr9:26722800-26723200	Enhancers	Brain Anterior Caudate	brain
32	chr9:26722800-26723600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr9:26723000-26723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr9:26723000-26723400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:26723000-26723400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:26723000-26723800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
37	chr9:26723000-26723800	Active TSS	Fetal Brain Female	brain
38	chr9:26723000-26724000	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr9:26723200-26723400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr9:26723200-26723600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr9:26723200-26723600	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr9:26723200-26723600	Active TSS	Fetal Kidney	kidney
43	chr9:26723200-26723800	Active TSS	Brain Anterior Caudate	brain
44	chr9:26723200-26723800	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr9:26723400-26723600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr9:26723400-26723600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr9:26723400-26723600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr9:26723400-26723800	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr9:26723400-26723800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr9:26723400-26723800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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