Variant report

Variant	esv2752289
Chromosome Location	chr9:21361957-21499624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1944)
CpG islands
(count:367)
Chromatin interactive
region (count:11)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1944 , 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	chr9:21382111-21382396	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:21396319-21396369	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:21461370-21461829	HepG2	liver:	n/a	n/a
4	ATF2	chr9:21381480-21382315	GM12878	blood:	n/a	n/a
5	ATF2	chr9:21444211-21444704	GM12878	blood:	n/a	n/a
6	ATF2	chr9:21381554-21382273	GM12878	blood:	n/a	n/a
7	ATF2	chr9:21444183-21444612	GM12878	blood:	n/a	n/a
8	BACH1	chr9:21396047-21396543	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:21415559-21415776	H1-hESC	embryonic stem cell:	n/a	chr9:21415684-21415698
10	BATF	chr9:21367253-21367565	GM12878	blood:	n/a	chr9:21367396-21367407
11	BATF	chr9:21381702-21382092	GM12878	blood:	n/a	n/a
12	BATF	chr9:21381625-21382187	GM12878	blood:	n/a	n/a
13	BATF	chr9:21367292-21367542	GM12878	blood:	n/a	chr9:21367396-21367407
14	BCL11A	chr9:21381619-21382272	GM12878	blood:	n/a	chr9:21381986-21381995
15	BCL11A	chr9:21381656-21382167	GM12878	blood:	n/a	chr9:21381986-21381995
16	BCL11A	chr9:21367236-21367595	GM12878	blood:	n/a	chr9:21367349-21367358
17	BCL3	chr9:21381640-21382241	GM12878	blood:	n/a	chr9:21381986-21381995
18	BCL3	chr9:21498490-21499615	A549	lung:	n/a	n/a
19	BCLAF1	chr9:21381621-21382291	GM12878	blood:	n/a	chr9:21381986-21381995
20	BCLAF1	chr9:21381612-21382254	GM12878	blood:	n/a	chr9:21381986-21381995
21	BCLAF1	chr9:21396108-21396541	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:21404025-21404312	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:21382053-21382377	HepG2	liver:	n/a	n/a
24	BHLHE40	chr9:21396259-21396485	A549	lung:	n/a	n/a
25	BHLHE40	chr9:21395908-21396562	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:21444209-21444535	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:21396169-21396483	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:21381496-21382354	GM12878	blood:	n/a	n/a
29	BRCA1	chr9:21396110-21396494	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr9:21396248-21396483	GM12878	blood:	n/a	n/a
31	CBX3	chr9:21465829-21466378	HCT-116	colon:	n/a	n/a
32	CEBPB	chr9:21455331-21455661	Hela-S3	cervix:	n/a	chr9:21455473-21455484
33	CEBPB	chr9:21450742-21451060	IMR90	lung:	n/a	chr9:21450902-21450913
34	CEBPB	chr9:21415765-21416076	A549	lung:	n/a	n/a
35	CEBPB	chr9:21493662-21493841	A549	lung:	n/a	n/a
36	CEBPB	chr9:21372342-21372396	A549	lung:	n/a	n/a
37	CEBPB	chr9:21444379-21444606	IMR90	lung:	n/a	chr9:21444494-21444505
38	CEBPB	chr9:21444352-21444627	A549	lung:	n/a	chr9:21444494-21444505
39	CEBPB	chr9:21444339-21444652	HepG2	liver:	n/a	chr9:21444494-21444505
40	CEBPB	chr9:21415312-21415515	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:21450737-21451128	Hela-S3	cervix:	n/a	chr9:21450902-21450913
42	CEBPB	chr9:21478670-21478870	A549	lung:	n/a	chr9:21478675-21478688
43	CEBPB	chr9:21495278-21495540	IMR90	lung:	n/a	n/a
44	CEBPB	chr9:21455421-21455617	HepG2	liver:	n/a	chr9:21455473-21455484
45	CEBPB	chr9:21414255-21414455	HepG2	liver:	n/a	chr9:21414408-21414421 chr9:21414408-21414419 chr9:21414405-21414422
46	CEBPB	chr9:21450783-21450983	H1-hESC	embryonic stem cell:	n/a	chr9:21450902-21450913
47	CEBPB	chr9:21454162-21454564	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:21461343-21461732	HepG2	liver:	n/a	chr9:21461511-21461522
49	CEBPB	chr9:21396167-21396488	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:21414300-21414550	A549	lung:	n/a	chr9:21414408-21414421 chr9:21414408-21414419 chr9:21414405-21414422

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21396078-21396128	SK-N-MC	brain:	n/a
2	chr9:21396078-21396128	SK-N-MC	brain:	n/a
3	chr9:21393116-21393166	T-47D	breast:	n/a
4	chr9:21396119-21396169	K562	blood:	n/a
5	chr9:21396119-21396169	NB4	blood:	n/a
6	chr9:21396107-21396157	HMEC	breast:	n/a
7	chr9:21396078-21396128	HCF	heart:	n/a
8	chr9:21396107-21396157	HRPEpiC	eye:	n/a
9	chr9:21368292-21368342	HRPEpiC	eye:	n/a
10	chr9:21393116-21393166	AG04450	lung:	fetal
11	chr9:21409505-21409555	PANC-1	pancreas:	n/a
12	chr9:21409505-21409555	Caco-2	colon:	n/a
13	chr9:21396078-21396128	HepG2	liver:	n/a
14	chr9:21409505-21409555	CMK	blood:	n/a
15	chr9:21409505-21409555	HUVEC	blood vessel:	n/a
16	chr9:21396078-21396128	HL-60	blood:	n/a
17	chr9:21393116-21393166	AG09319	gingival:	n/a
18	chr9:21396078-21396128	HRE	kidney:	n/a
19	chr9:21396107-21396157	NHBE	bronchial:	n/a
20	chr9:21409505-21409555	SKMC	muscle:	n/a
21	chr9:21396119-21396169	HAEpiC	amniotic membrane:	n/a
22	chr9:21396119-21396169	HCF	heart:	n/a
23	chr9:21396119-21396169	HCM	heart:	n/a
24	chr9:21396119-21396169	HEK293	kidney:	embryo
25	chr9:21396078-21396128	ProgFib	skin:	n/a
26	chr9:21396078-21396128	U87	brain:	n/a
27	chr9:21393116-21393166	MCF10A-Er-Src	breast:	n/a
28	chr9:21393116-21393166	NHBE	bronchial:	n/a
29	chr9:21396107-21396157	SK-N-MC	brain:	n/a
30	chr9:21393116-21393166	H1-hESC	embryonic stem cell:	embryo
31	chr9:21396107-21396157	AoSMC	blood vessel:	n/a
32	chr9:21409505-21409555	LNCaP	prostate:	n/a
33	chr9:21409505-21409555	NB4	blood:	n/a
34	chr9:21396107-21396157	AG04450	lung:	fetal
35	chr9:21409505-21409555	GM12891	blood:	n/a
36	chr9:21396119-21396169	IMR90	lung:	fetal
37	chr9:21396107-21396157	SAEC	small airway:	n/a
38	chr9:21409505-21409555	Hepatocyte	liver:	n/a
39	chr9:21396078-21396128	NHDF-neo	bronchial:	n/a
40	chr9:21396119-21396169	RPTEC	kidney:	n/a
41	chr9:21368292-21368342	AG04449	skin:	fetal
42	chr9:21396107-21396157	RPTEC	kidney:	n/a
43	chr9:21409505-21409555	HRCEpiC	kidney:	n/a
44	chr9:21396107-21396157	HEEpiC	esophagus:	n/a
45	chr9:21409505-21409555	BJ	skin:	n/a
46	chr9:21396107-21396157	AG09319	gingival:	n/a
47	chr9:21368292-21368342	PFSK-1	brain:	n/a
48	chr9:21396119-21396169	SKMC	muscle:	n/a
49	chr9:21368292-21368342	PANC-1	pancreas:	n/a
50	chr9:21396119-21396169	HNPCEpiC	eye:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:21464451..21467378-chr9:21800569..21802345,2	MCF-7	breast:
2	chr9:21496297..21498448-chr9:21802383..21804700,2	MCF-7	breast:
3	chr9:21491433..21492444-chr9:21789127..21790263,7	MCF-7	breast:
4	chr9:21465480..21466871-chr9:21788898..21790282,6	MCF-7	breast:
5	chr9:21348973..21351463-chr9:21362839..21365132,2	MCF-7	breast:
6	chr9:21465639..21466595-chr9:21789434..21790168,4	MCF-7	breast:
7	chr17:56707046..56709120-chr9:21394171..21396091,2	MCF-7	breast:
8	chr9:21434162..21434698-chr9:21455012..21455833,2	MCF-7	breast:
9	chr9:21492643..21493283-chr9:21789425..21789929,2	MCF-7	breast:
10	chr9:21332702..21335919-chr9:21391741..21394424,4	MCF-7	breast:
11	chr9:21326559..21327137-chr9:21413703..21414313,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNE-1	chr9:21477168-21477292	NONHSAT130388
2	lnc-IFNE-1	chr9:21477168-21477291	ENSG00000171889
3	lnc-IFNE-1	chr9:21455641-21455943	ENSG00000171889
4	lnc-IFNE-1	chr9:21454267-21455943	NONHSAT130386
5	lnc-IFNE-1	chr9:21477168-21477291	NONHSAT130385
6	lnc-IFNE-1	chr9:21476898-21477034	ENSG00000171889
7	lnc-IFNE-1	chr9:21477168-21477292	NONHSAT130389
8	lnc-IFNE-1	chr9:21477168-21477291	NONHSAT130386
9	lnc-IFNA1-1	chr9:21455483-21456048	NONHSAT130387
10	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130388
11	lnc-IFNA8-1	chr9:21403080-21403650	NONHSAT130383
12	lnc-IFNE-1	chr9:21455587-21455943	NONHSAT130388
13	lnc-IFNA2-2	chr9:21398613-21399138	NONHSAT130382
14	lnc-IFNE-1	chr9:21454267-21455943	NONHSAT130385
15	lnc-IFNE-1	chr9:21476873-21477034	NONHSAT130389
16	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130386
17	lnc-IFNA8-2	chr9:21420233-21420812	NONHSAT130384
18	lnc-IFNA2-1	chr9:21394887-21396345	ENSG00000261696.1
19	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130385

No data

Variant related genes	Relation type
IFNA13	TF binding region
ENSG00000261696	TF binding region
IFNA12P	TF binding region
IFNWP2	TF binding region
IFNA8	TF binding region
IFNWP19	TF binding region
IFNA1	TF binding region
IFNA2	TF binding region
IFNA11P	TF binding region
IFNE	TF binding region
IFNA13	CpG island
ENSG00000261696	CpG island
IFNA12P	CpG island
IFNWP2	CpG island
IFNA8	CpG island
IFNWP19	CpG island
IFNA1	CpG island
IFNA2	CpG island
IFNA11P	CpG island
IFNE	CpG island
ENSG00000238271	chromatin interactions
ENSG00000264545	chromatin interactions
ENSG00000120235	chromatin interactions
ENSG00000198642	chromatin interactions
ENSG00000099810	chromatin interactions
EEF1A1	miRNA target sites
RAB14	miRNA target sites
RPP40	miRNA target sites

Extended variants
information (count: 4700 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:4700 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs597408	chr9:21361957-21361958	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs16938357	chr9:21361973-21361974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs597440	chr9:21361976-21361977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs553134907	chr9:21361981-21361982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs667214	chr9:21362014-21362015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535961389	chr9:21362015-21362016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189143234	chr9:21362065-21362066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142120510	chr9:21362088-21362089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544184832	chr9:21362123-21362124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558072976	chr9:21362131-21362132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113009547	chr9:21362133-21362134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192812381	chr9:21362134-21362135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538476404	chr9:21362147-21362148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78244368	chr9:21362154-21362155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574122272	chr9:21362209-21362210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140353236	chr9:21362211-21362212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111531385	chr9:21362235-21362236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185462989	chr9:21362243-21362244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550592577	chr9:21362251-21362252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560898453	chr9:21362283-21362284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189592807	chr9:21362285-21362286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533265228	chr9:21362289-21362290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144112470	chr9:21362293-21362294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566682032	chr9:21362311-21362312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181485191	chr9:21362320-21362321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117999022	chr9:21362343-21362344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575419155	chr9:21362378-21362379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146514065	chr9:21362398-21362399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10964972	chr9:21362409-21362410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs186169755	chr9:21362446-21362447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs16938415	chr9:21362518-21362519	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150180747	chr9:21362545-21362546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111460536	chr9:21362558-21362559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375210042	chr9:21362559-21362560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539834295	chr9:21362565-21362566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574208665	chr9:21362574-21362575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs600118	chr9:21362582-21362583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs138726465	chr9:21362597-21362598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575413196	chr9:21362605-21362606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544282559	chr9:21362608-21362609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564084860	chr9:21362615-21362616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34629117	chr9:21362699-21362700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376391991	chr9:21362719-21362720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529172483	chr9:21362725-21362726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188492711	chr9:21362740-21362741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10964973	chr9:21362772-21362773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113534214	chr9:21362792-21362793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181310976	chr9:21362794-21362795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529127275	chr9:21362801-21362802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7851654	chr9:21362802-21362803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:160)

Disease	PMID	Source
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
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
Oral cancer	21386901	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
Breast cancer	21858162	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
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	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
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Ovarian cancer	21781307	CNVD
Cancer	20164920	CNVD

Chromatin state (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21358600-21363400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr9:21360200-21367000	Weak transcription	GM12878-XiMat	blood
3	chr9:21363400-21364000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr9:21364000-21366000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr9:21366000-21366800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr9:21366600-21367200	Bivalent Enhancer	Primary B cells from cord blood	blood
7	chr9:21367000-21367200	Enhancers	GM12878-XiMat	blood
8	chr9:21367200-21367600	Weak transcription	GM12878-XiMat	blood
9	chr9:21367600-21368200	Enhancers	GM12878-XiMat	blood
10	chr9:21367800-21368000	Bivalent Enhancer	Primary B cells from cord blood	blood
11	chr9:21378800-21379000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
12	chr9:21378800-21379200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr9:21378800-21379400	Enhancers	GM12878-XiMat	blood
14	chr9:21379000-21379400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
15	chr9:21379200-21381000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr9:21379400-21379600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:21379400-21380400	Weak transcription	GM12878-XiMat	blood
18	chr9:21380400-21380800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
19	chr9:21380400-21381400	Enhancers	GM12878-XiMat	blood
20	chr9:21380400-21382600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
21	chr9:21381000-21381400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:21381000-21381400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:21381000-21382600	Enhancers	Primary B cells from cord blood	blood
24	chr9:21381200-21381400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr9:21381200-21381600	Enhancers	Primary hematopoietic stem cells	blood
26	chr9:21381400-21381600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr9:21381400-21381600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
28	chr9:21381400-21381600	Enhancers	Duodenum Mucosa	Duodenum
29	chr9:21381400-21381800	Bivalent Enhancer	Brain Anterior Caudate	brain
30	chr9:21381400-21381800	Flanking Active TSS	GM12878-XiMat	blood
31	chr9:21381400-21382000	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr9:21381400-21382000	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr9:21381400-21382000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
34	chr9:21381400-21382200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
35	chr9:21381400-21382200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:21381400-21382200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:21381400-21382200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr9:21381400-21382400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:21381400-21382400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:21381400-21382400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr9:21381400-21382400	Enhancers	Primary B cells from peripheral blood	blood
42	chr9:21381400-21382400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
43	chr9:21381400-21382400	Enhancers	Placenta	Placenta
44	chr9:21381400-21382600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr9:21381400-21382600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:21381400-21382600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
47	chr9:21381400-21382800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr9:21381400-21383000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr9:21381400-21386000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr9:21381600-21381800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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