Variant report

Variant	nsv916394
Chromosome Location	chr9:6055497-6322471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2485)
CpG islands
(count:183)
Chromatin interactive
region (count:49)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2485 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6238753-6239428	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6272234-6272566	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6236398-6236588	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6236968-6237134	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6197394-6197552	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6306047-6306247	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6080499-6080640	HepG2	liver:	n/a	n/a
8	ATF1	chr9:6106923-6107351	K562	blood:	n/a	n/a
9	ATF1	chr9:6080227-6080643	K562	blood:	n/a	n/a
10	ATF1	chr9:6079448-6079725	K562	blood:	n/a	n/a
11	ATF2	chr9:6184846-6185494	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6068923-6069286	GM12878	blood:	n/a	n/a
13	ATF2	chr9:6184965-6185468	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6197314-6197660	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr9:6080194-6080778	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr9:6068794-6069285	GM12878	blood:	n/a	n/a
17	ATF3	chr9:6080243-6080647	K562	blood:	n/a	n/a
18	BACH1	chr9:6212812-6213039	K562	blood:	n/a	n/a
19	BATF	chr9:6185007-6185418	GM12878	blood:	n/a	n/a
20	BATF	chr9:6243750-6244097	GM12878	blood:	n/a	chr9:6243981-6243992
21	BATF	chr9:6096712-6097082	GM12878	blood:	n/a	n/a
22	BATF	chr9:6133370-6133661	GM12878	blood:	n/a	n/a
23	BATF	chr9:6184773-6185635	GM12878	blood:	n/a	n/a
24	BATF	chr9:6243774-6244147	GM12878	blood:	n/a	chr9:6243981-6243992
25	BATF	chr9:6186725-6187026	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:6243799-6244059	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:6185001-6185445	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:6133721-6133994	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:6185090-6185360	GM12878	blood:	n/a	n/a
30	BCLAF1	chr9:6184828-6185523	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:6080512-6080746	K562	blood:	n/a	n/a
32	BHLHE40	chr9:6238901-6239586	HepG2	liver:	n/a	n/a
33	BHLHE40	chr9:6306060-6306216	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:6068939-6069258	GM12878	blood:	n/a	n/a
35	BHLHE40	chr9:6243865-6244064	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:6238263-6238286	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr9:6080147-6080701	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr9:6102464-6102968	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr9:6107086-6107152	GM12878	blood:	n/a	n/a
40	BRCA1	chr9:6215680-6215690	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr9:6152733-6153851	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr9:6305856-6306260	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr9:6218063-6218503	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr9:6055278-6055825	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr9:6070866-6071131	K562	blood:	n/a	n/a
46	CBX3	chr9:6102440-6102981	HCT-116	colon:	n/a	n/a
47	CBX3	chr9:6106944-6107559	HCT-116	colon:	n/a	n/a
48	CBX3	chr9:6173953-6174243	K562	blood:	n/a	n/a
49	CBX3	chr9:6106866-6107334	K562	blood:	n/a	n/a
50	CBX3	chr9:6173999-6174182	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6241371-6241421	ovcar-3	ovarian:	n/a
2	chr9:6252007-6252057	HCM	heart:	n/a
3	chr9:6109415-6109465	HRE	kidney:	n/a
4	chr9:6252007-6252057	HEK293	kidney:	embryo
5	chr9:6252007-6252057	PANC-1	pancreas:	n/a
6	chr9:6109415-6109465	Caco-2	colon:	n/a
7	chr9:6241371-6241421	GM19239	blood:	n/a
8	chr9:6252007-6252057	HNPCEpiC	eye:	n/a
9	chr9:6241371-6241421	NH-A	brain:	n/a
10	chr9:6252007-6252057	MCF10A-Er-Src	breast:	n/a
11	chr9:6241371-6241421	CMK	blood:	n/a
12	chr9:6241371-6241421	NHBE	bronchial:	n/a
13	chr9:6252007-6252057	SK-N-SH	brain:	n/a
14	chr9:6241371-6241421	HEK293	kidney:	embryo
15	chr9:6109415-6109465	U87	brain:	n/a
16	chr9:6241371-6241421	HRE	kidney:	n/a
17	chr9:6241371-6241421	HCPEpiC	choroid plexus:	n/a
18	chr9:6241371-6241421	LNCaP	prostate:	n/a
19	chr9:6109415-6109465	ovcar-3	ovarian:	n/a
20	chr9:6109415-6109465	HNPCEpiC	eye:	n/a
21	chr9:6109415-6109465	NHBE	bronchial:	n/a
22	chr9:6241371-6241421	MCF10A-Er-Src	breast:	n/a
23	chr9:6252007-6252057	HCF	heart:	n/a
24	chr9:6252007-6252057	PrEC	prostate:	n/a
25	chr9:6109415-6109465	HUVEC	blood vessel:	n/a
26	chr9:6109415-6109465	HMEC	breast:	n/a
27	chr9:6252007-6252057	HUVEC	blood vessel:	n/a
28	chr9:6252007-6252057	HepG2	liver:	n/a
29	chr9:6109415-6109465	Hela-S3	cervix:	n/a
30	chr9:6252007-6252057	H1-hESC	embryonic stem cell:	embryo
31	chr9:6109415-6109465	MCF-7	breast:	n/a
32	chr9:6109415-6109465	SAEC	small airway:	n/a
33	chr9:6252007-6252057	A549	lung:	n/a
34	chr9:6109415-6109465	HCPEpiC	choroid plexus:	n/a
35	chr9:6109415-6109465	HepG2	liver:	n/a
36	chr9:6252007-6252057	Caco-2	colon:	n/a
37	chr9:6252007-6252057	HAEpiC	amniotic membrane:	n/a
38	chr9:6241371-6241421	BE2_C	brain:	n/a
39	chr9:6109415-6109465	HL-60	blood:	n/a
40	chr9:6109415-6109465	GM06990	blood:	n/a
41	chr9:6252007-6252057	PFSK-1	brain:	n/a
42	chr9:6109415-6109465	Hepatocyte	liver:	n/a
43	chr9:6241371-6241421	NB4	blood:	n/a
44	chr9:6252007-6252057	NH-A	brain:	n/a
45	chr9:6252007-6252057	SK-N-MC	brain:	n/a
46	chr9:6241371-6241421	PrEC	prostate:	n/a
47	chr9:6109415-6109465	PANC-1	pancreas:	n/a
48	chr9:6252007-6252057	SAEC	small airway:	n/a
49	chr9:6109415-6109465	CMK	blood:	n/a
50	chr9:6109415-6109465	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:6163094..6165877-chr9:6167250..6170974,4	K562	blood:
2	chr9:6266181..6268457-chr9:6269163..6272196,3	K562	blood:
3	chr9:6266181..6268457-chr9:6269163..6272196,3	K562	blood:
4	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
5	chr9:5886117..5886694-chr9:6054993..6055882,2	MCF-7	breast:
6	chr9:6196840..6197620-chr9:6306018..6306519,2	MCF-7	breast:
7	chr9:6107045..6110016-chr9:6112328..6114714,2	K562	blood:
8	chr9:6182316..6185009-chr9:6186082..6187902,2	K562	blood:
9	chr9:6163920..6166108-chr9:6170937..6173147,2	MCF-7	breast:
10	chr9:6067676..6070179-chr9:6077963..6079813,2	MCF-7	breast:
11	chr9:6067676..6070179-chr9:6077963..6079813,2	MCF-7	breast:
12	chr9:6149075..6150608-chr9:6166608..6168151,2	MCF-7	breast:
13	chr9:6194592..6195131-chr9:6305762..6306590,2	MCF-7	breast:
14	chr9:6074105..6076880-chr9:6078281..6080454,2	K562	blood:
15	chr9:6149075..6150608-chr9:6166608..6168151,2	MCF-7	breast:
16	chr9:6055397..6056252-chr9:6305741..6306569,2	K562	blood:
17	chr9:6305170..6307719-chr9:6307772..6310215,2	K562	blood:
18	chr9:6041127..6043265-chr9:6054435..6057249,2	MCF-7	breast:
19	chr9:6307810..6309784-chr9:6311496..6314006,2	K562	blood:
20	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
21	chr9:6163920..6166108-chr9:6170937..6173147,2	MCF-7	breast:
22	chr9:6074105..6076880-chr9:6078281..6080454,2	K562	blood:
23	chr9:6107045..6110016-chr9:6112328..6114714,2	K562	blood:
24	chr9:6241308..6243910-chr9:6245192..6247268,2	MCF-7	breast:
25	chr9:5878375..5880151-chr9:6078401..6080050,2	K562	blood:
26	chr9:6201029..6203540-chr9:6215680..6218483,2	K562	blood:
27	chr9:6163367..6165821-chr9:6169712..6171511,2	K562	blood:
28	chr9:6195102..6195794-chr9:6568308..6568912,2	K562	blood:
29	chr9:6068346..6070215-chr9:6077181..6078766,2	K562	blood:
30	chr9:6055397..6056252-chr9:6305741..6306569,2	K562	blood:
31	chr9:6174199..6177048-chr9:6181572..6183383,2	MCF-7	breast:
32	chr9:6163094..6165877-chr9:6167250..6170974,4	K562	blood:
33	chr9:6196840..6197620-chr9:6306018..6306519,2	MCF-7	breast:
34	chr9:6305170..6307719-chr9:6307772..6310215,2	K562	blood:
35	chr9:6068346..6070215-chr9:6077181..6078766,2	K562	blood:
36	chr9:6244528..6246233-chr9:6251156..6253683,2	MCF-7	breast:
37	chr9:6174199..6177048-chr9:6181572..6183383,2	MCF-7	breast:
38	chr9:6013951..6016263-chr9:6053852..6055883,2	MCF-7	breast:
39	chr9:6054654..6056123-chr9:6305613..6307254,7	MCF-7	breast:
40	chr9:6182316..6185009-chr9:6186082..6187902,2	K562	blood:
41	chr9:6063784..6066146-chr9:6072750..6075401,2	MCF-7	breast:
42	chr9:6163367..6165821-chr9:6169712..6171511,2	K562	blood:
43	chr13:43706108..43706705-chr9:6170816..6171542,2	MCF-7	breast:
44	chr9:6194592..6195131-chr9:6305762..6306590,2	MCF-7	breast:
45	chr9:6063784..6066146-chr9:6072750..6075401,2	MCF-7	breast:
46	chr9:6234179..6236096-chr9:6238826..6241061,2	K562	blood:
47	chr9:6054654..6056123-chr9:6305613..6307254,7	MCF-7	breast:
48	chr9:6307810..6309784-chr9:6311496..6314006,2	K562	blood:
49	chr9:5890360..5891992-chr9:6052880..6055803,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL33-2	chr9:6197158-6197248	NONHSAT130125
2	lnc-TPD52L3-1	chr9:6241693-6241785	NONHSAT130126
3	lnc-IL33-2	chr9:6195934-6196846	NONHSAT130125
4	lnc-MLANA-3	chr9:6056365-6056714	NONHSAT130121
5	lnc-TPD52L3-1	chr9:6242192-6242734	NONHSAT130126
6	lnc-IL33-1	chr9:6276640-6276974	NONHSAT130127
7	lnc-MLANA-1	chr9:6066364-6066714	NONHSAT130122
8	lnc-MLANA-1	chr9:6066365-6066714	XLOC_007273

No data

Variant related genes	Relation type
ENSG00000233846	TF binding region
ENSG00000237274	TF binding region
ENSG00000228132	TF binding region
IL33	TF binding region
ENSG00000233846	CpG island
ENSG00000237274	CpG island
ENSG00000228132	CpG island
IL33	CpG island
ENSG00000137033	chromatin interactions
ENSG00000237158	chromatin interactions
ENSG00000137040	chromatin interactions
ENSG00000120215	chromatin interactions

Extended variants
information (count: 9120 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:9120 , 50 per page) page: 1 2 3 4 5 6 7 ... 183

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs380568	chr9:6055531-6055532	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568862068	chr9:6055532-6055533	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs536585811	chr9:6055562-6055563	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs554588263	chr9:6055656-6055657	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566630702	chr9:6055669-6055670	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189703325	chr9:6055723-6055724	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181346465	chr9:6055807-6055808	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576968032	chr9:6055821-6055822	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576018605	chr9:6055837-6055838	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556170883	chr9:6055867-6055868	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116651629	chr9:6055930-6055931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73639574	chr9:6055931-6055932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76636613	chr9:6055944-6055945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35047870	chr9:6056375-6056376	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs115263613	chr9:6056424-6056425	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs200534051	chr9:6056426-6056427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs201557033	chr9:6056438-6056439	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs374650674	chr9:6056448-6056449	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs393556	chr9:6056468-6056469	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs572697387	chr9:6056482-6056483	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs546467541	chr9:6056489-6056490	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs564705432	chr9:6056510-6056511	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs576690353	chr9:6056517-6056518	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs576782152	chr9:6056518-6056519	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs543997277	chr9:6056519-6056520	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs375803806	chr9:6056525-6056526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs562579315	chr9:6056553-6056554	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs544499527	chr9:6056564-6056565	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs200709437	chr9:6056575-6056576	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs547924580	chr9:6056611-6056612	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs201706657	chr9:6056618-6056619	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs199575252	chr9:6056629-6056630	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs200008462	chr9:6056633-6056634	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs201098938	chr9:6056642-6056643	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs560082049	chr9:6056673-6056674	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs527621714	chr9:6056682-6056683	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs146014724	chr9:6056699-6056700	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs577855190	chr9:6056705-6056706	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs570384269	chr9:6056712-6056713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs567736685	chr9:6062809-6062810	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534861969	chr9:6062817-6062818	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566155551	chr9:6062852-6062853	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184558043	chr9:6062866-6062867	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571768291	chr9:6062894-6062895	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562814152	chr9:6062926-6062927	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577775280	chr9:6062951-6062952	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187027799	chr9:6062965-6062966	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543339568	chr9:6062974-6062975	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373900221	chr9:6062976-6062977	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138322978	chr9:6062982-6062983	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	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
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	18451855	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	21215367	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1594 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6053200-6055800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:6054800-6055800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr9:6054800-6056000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:6054800-6056000	Enhancers	Hela-S3	cervix
5	chr9:6054800-6056000	Enhancers	HMEC	breast
6	chr9:6055000-6056000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:6055400-6055800	Enhancers	NHEK	skin
8	chr9:6055800-6056000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:6062800-6063200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr9:6062800-6063600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr9:6063000-6063600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr9:6063200-6063400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr9:6063200-6063400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr9:6063400-6063600	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr9:6063400-6063800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr9:6063800-6068600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr9:6068200-6068400	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr9:6068200-6068600	Enhancers	Dnd41	blood
19	chr9:6068200-6069000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:6068200-6069000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
21	chr9:6068200-6069400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr9:6068200-6070000	Enhancers	Primary T cells fromperipheralblood	blood
23	chr9:6068200-6070000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr9:6068400-6068600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
25	chr9:6068400-6068600	Enhancers	Duodenum Mucosa	Duodenum
26	chr9:6068400-6068800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr9:6068400-6068800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr9:6068400-6068800	Enhancers	NHDF-Ad	bronchial
29	chr9:6068400-6069000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr9:6068400-6069400	Enhancers	Stomach Mucosa	stomach
31	chr9:6068400-6070000	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr9:6068400-6070000	Enhancers	Primary B cells from peripheral blood	blood
33	chr9:6068400-6070000	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr9:6068400-6070000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr9:6068600-6068800	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr9:6068600-6068800	Enhancers	Spleen	Spleen
37	chr9:6068600-6068800	ZNF genes & repeats	GM12878-XiMat	blood
38	chr9:6068600-6068800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr9:6068600-6069000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr9:6068600-6069000	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr9:6068600-6069400	Flanking Active TSS	Dnd41	blood
42	chr9:6068600-6069600	Enhancers	Primary T cells from cord blood	blood
43	chr9:6068600-6069600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:6068600-6069600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:6068600-6069600	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr9:6068600-6069800	Enhancers	Primary B cells from cord blood	blood
47	chr9:6068600-6069800	Enhancers	Primary hematopoietic stem cells	blood
48	chr9:6068600-6069800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr9:6068600-6070000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr9:6068600-6070200	Enhancers	Rectal Mucosa Donor 29	rectum

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