Variant report

Variant	nsv613651
Chromosome Location	chr9:15296355-15358157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1050)
CpG islands
(count:367)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15307077-15307551	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15333319-15333669	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15351035-15351548	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15306129-15306386	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:15357028-15357575	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:15350374-15350711	HepG2	liver:	n/a	n/a
7	ATF1	chr9:15299673-15299858	K562	blood:	n/a	n/a
8	BACH1	chr9:15328520-15328827	K562	blood:	n/a	n/a
9	BACH1	chr9:15306339-15306925	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:15328555-15328874	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:15306084-15306387	GM12878	blood:	n/a	n/a
12	BATF	chr9:15299577-15299867	GM12878	blood:	n/a	chr9:15299785-15299794
13	BCL3	chr9:15331510-15331929	GM12878	blood:	n/a	n/a
14	BCL3	chr9:15331480-15331831	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:15299556-15300027	GM12878	blood:	n/a	chr9:15299645-15299654
16	BHLHE40	chr9:15357545-15357594	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:15351043-15351484	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:15318021-15318086	K562	blood:	n/a	n/a
19	BHLHE40	chr9:15307159-15307687	K562	blood:	n/a	n/a
20	BHLHE40	chr9:15306190-15306323	K562	blood:	n/a	n/a
21	BHLHE40	chr9:15315454-15315624	K562	blood:	n/a	n/a
22	BHLHE40	chr9:15307178-15307437	GM12878	blood:	n/a	n/a
23	BRCA1	chr9:15307498-15307506	HepG2	liver:	n/a	n/a
24	BRCA1	chr9:15299127-15299177	GM12878	blood:	n/a	n/a
25	CBX3	chr9:15323298-15323578	K562	blood:	n/a	n/a
26	CCNT2	chr9:15307181-15307674	K562	blood:	n/a	n/a
27	CEBPB	chr9:15296111-15296452	HepG2	liver:	n/a	chr9:15296245-15296258 chr9:15296246-15296257
28	CEBPB	chr9:15328968-15329272	A549	lung:	n/a	chr9:15329145-15329156
29	CEBPB	chr9:15328993-15329312	IMR90	lung:	n/a	chr9:15329145-15329156
30	CEBPB	chr9:15307255-15307554	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:15305873-15306429	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
32	CEBPB	chr9:15307099-15307605	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:15305925-15306284	ECC-1	luminal epithelium:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
34	CEBPB	chr9:15305959-15306418	A549	lung:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
35	CEBPB	chr9:15300306-15300673	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:15328741-15329330	K562	blood:	n/a	chr9:15329145-15329156
37	CEBPB	chr9:15350317-15350793	MCF-7	breast:	n/a	chr9:15350602-15350613
38	CEBPB	chr9:15299423-15299459	A549	lung:	n/a	n/a
39	CEBPB	chr9:15350429-15350771	Hela-S3	cervix:	n/a	chr9:15350602-15350613
40	CEBPB	chr9:15350420-15351443	HepG2	liver:	n/a	chr9:15350602-15350613
41	CEBPB	chr9:15357033-15357492	MCF-7	breast:	n/a	chr9:15357245-15357256
42	CEBPB	chr9:15350328-15350801	A549	lung:	n/a	chr9:15350602-15350613
43	CEBPB	chr9:15350535-15350767	A549	lung:	n/a	chr9:15350602-15350613
44	CEBPB	chr9:15357187-15357345	Hela-S3	cervix:	n/a	chr9:15357245-15357256
45	CEBPB	chr9:15296139-15296371	HepG2	liver:	n/a	chr9:15296245-15296258 chr9:15296246-15296257
46	CEBPB	chr9:15331605-15331805	HepG2	liver:	n/a	chr9:15331667-15331678
47	CEBPB	chr9:15357101-15357410	A549	lung:	n/a	chr9:15357245-15357256
48	CEBPB	chr9:15357101-15357372	HepG2	liver:	n/a	chr9:15357245-15357256
49	CEBPB	chr9:15357075-15357432	K562	blood:	n/a	chr9:15357245-15357256
50	CEBPB	chr9:15305937-15306278	K562	blood:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15310979-15311029	SKMC	muscle:	n/a
2	chr9:15310979-15311029	SKMC	muscle:	n/a
3	chr9:15305873-15305923	HRPEpiC	eye:	n/a
4	chr9:15306337-15306387	GM06990	blood:	n/a
5	chr9:15306736-15306786	GM19239	blood:	n/a
6	chr9:15305873-15305923	K562	blood:	n/a
7	chr9:15306337-15306387	SAEC	small airway:	n/a
8	chr9:15306736-15306786	NT2-D1	testis:	n/a
9	chr9:15310979-15311029	GM19239	blood:	n/a
10	chr9:15307376-15307426	HRE	kidney:	n/a
11	chr9:15306337-15306387	Jurkat	blood:	n/a
12	chr9:15306337-15306387	NT2-D1	testis:	n/a
13	chr9:15306736-15306786	PrEC	prostate:	n/a
14	chr9:15307376-15307426	LNCaP	prostate:	n/a
15	chr9:15306736-15306786	AG04450	lung:	fetal
16	chr9:15310979-15311029	HRPEpiC	eye:	n/a
17	chr9:15307376-15307426	HCF	heart:	n/a
18	chr9:15306736-15306786	SK-N-MC	brain:	n/a
19	chr9:15307376-15307426	AG09319	gingival:	n/a
20	chr9:15307873-15307923	GM12878	blood:	n/a
21	chr9:15307376-15307426	NH-A	brain:	n/a
22	chr9:15306337-15306387	A549	lung:	n/a
23	chr9:15307873-15307923	NT2-D1	testis:	n/a
24	chr9:15310979-15311029	RPTEC	kidney:	n/a
25	chr9:15307873-15307923	AG09319	gingival:	n/a
26	chr9:15305873-15305923	RPTEC	kidney:	n/a
27	chr9:15306337-15306387	GM12892	blood:	n/a
28	chr9:15306736-15306786	Hela-S3	cervix:	n/a
29	chr9:15310979-15311029	Hela-S3	cervix:	n/a
30	chr9:15305873-15305923	BJ	skin:	n/a
31	chr9:15307376-15307426	BE2_C	brain:	n/a
32	chr9:15307376-15307426	ovcar-3	ovarian:	n/a
33	chr9:15307376-15307426	K562	blood:	n/a
34	chr9:15306736-15306786	AG09319	gingival:	n/a
35	chr9:15307376-15307426	SK-N-SH	brain:	n/a
36	chr9:15306736-15306786	NH-A	brain:	n/a
37	chr9:15307376-15307426	PANC-1	pancreas:	n/a
38	chr9:15305873-15305923	LNCaP	prostate:	n/a
39	chr9:15307376-15307426	GM12892	blood:	n/a
40	chr9:15306736-15306786	GM12892	blood:	n/a
41	chr9:15306736-15306786	GM06990	blood:	n/a
42	chr9:15305873-15305923	AG10803	skin:	n/a
43	chr9:15310979-15311029	HepG2	liver:	n/a
44	chr9:15310979-15311029	Caco-2	colon:	n/a
45	chr9:15307873-15307923	GM12892	blood:	n/a
46	chr9:15310979-15311029	ProgFib	skin:	n/a
47	chr9:15305873-15305923	AG09309	skin:	n/a
48	chr9:15307376-15307426	SK-N-SH_RA	brain:	n/a
49	chr9:15306736-15306786	T-47D	breast:	n/a
50	chr9:15306736-15306786	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:15356402..15356902-chr9:134721602..134722134,2	NB4	blood:
2	chr9:15305709..15307336-chr9:15348928..15350627,2	MCF-7	breast:
3	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
4	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
5	chr9:15293831..15297894-chr9:15305171..15308300,4	MCF-7	breast:
6	chr9:15357011..15359248-chr9:15422187..15424051,2	MCF-7	breast:
7	chr9:15306963..15308773-chr9:15314988..15318754,3	MCF-7	breast:
8	chr9:15332011..15334775-chr9:15347128..15349228,2	MCF-7	breast:
9	chr9:15277443..15278337-chr9:15356714..15357650,2	MCF-7	breast:
10	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
11	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
12	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
13	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
14	chr9:15211338..15211919-chr9:15356761..15357369,2	MCF-7	breast:
15	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
16	chr9:15305128..15307154-chr9:15417021..15419951,2	MCF-7	breast:
17	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
18	chr9:15352501..15354066-chr9:15419261..15422025,2	MCF-7	breast:
19	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-2	chr9:15348166-15348453	NONHSAT130262

No data

Variant related genes	Relation type
RPL7P33	TF binding region
RN7SL157P	TF binding region
TTC39B	TF binding region
RPL7P33	CpG island
RN7SL157P	CpG island
TTC39B	CpG island
ENSG00000164975	chromatin interactions
ENSG00000263817	chromatin interactions
ENSG00000155158	chromatin interactions

Extended variants
information (count: 2920 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2920 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10961965	chr9:15296355-15296356	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562423795	chr9:15296358-15296359	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs10118629	chr9:15296450-15296451	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs548213462	chr9:15296456-15296457	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569657998	chr9:15296512-15296513	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10115392	chr9:15296526-15296527	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs192028615	chr9:15296562-15296563	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182637556	chr9:15296617-15296618	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs13293198	chr9:15296640-15296641	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113343843	chr9:15296647-15296648	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574678162	chr9:15296656-15296657	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs10121558	chr9:15296674-15296675	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556976904	chr9:15296680-15296681	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575219096	chr9:15296757-15296758	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545922055	chr9:15296787-15296788	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3905247	chr9:15296845-15296846	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10121612	chr9:15296852-15296853	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs540833373	chr9:15296885-15296886	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564792874	chr9:15296905-15296906	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529664047	chr9:15296911-15296912	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs386733006	chr9:15296931-15296932	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs115472341	chr9:15296932-15296933	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377287179	chr9:15296938-15296939	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113925513	chr9:15296946-15296947	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570535542	chr9:15296966-15296967	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140477243	chr9:15296998-15296999	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs386733007	chr9:15297007-15297008	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs71323933	chr9:15297008-15297009	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528126913	chr9:15297009-15297010	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs28444701	chr9:15297020-15297021	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs370125511	chr9:15297027-15297028	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs3905248	chr9:15297028-15297029	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs370587048	chr9:15297069-15297070	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535394987	chr9:15297075-15297076	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556815348	chr9:15297081-15297082	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147631625	chr9:15297160-15297161	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539464653	chr9:15297171-15297172	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs75435571	chr9:15297188-15297189	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78945410	chr9:15297189-15297190	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs80132871	chr9:15297190-15297191	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557828117	chr9:15297191-15297192	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192794049	chr9:15297288-15297289	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540370677	chr9:15297317-15297318	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555958472	chr9:15297340-15297341	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376441705	chr9:15297344-15297345	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574260738	chr9:15297368-15297369	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544786889	chr9:15297373-15297374	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563189291	chr9:15297393-15297394	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4087078	chr9:15297398-15297399	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs549228300	chr9:15297461-15297462	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
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
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
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
Intellectual disability	22102821	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
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1305 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15277600-15296800	Weak transcription	Gastric	stomach
2	chr9:15287400-15303600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:15290800-15305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:15290800-15306000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:15291200-15305600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:15292200-15296800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:15293400-15296400	Enhancers	Fetal Intestine Large	intestine
8	chr9:15294200-15296600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr9:15294400-15306200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:15294600-15297600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:15294800-15297000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr9:15294800-15297200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:15294800-15297600	Enhancers	Lung	lung
14	chr9:15295000-15296800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr9:15295000-15297000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr9:15295200-15297800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr9:15295400-15296800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:15295400-15297200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:15295400-15297200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:15295400-15297200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:15295400-15297400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:15295600-15296600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr9:15295600-15296600	Flanking Active TSS	GM12878-XiMat	blood
24	chr9:15295600-15297400	Flanking Active TSS	Primary T cells from cord blood	blood
25	chr9:15295800-15296400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr9:15295800-15296400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
27	chr9:15295800-15296400	Flanking Active TSS	HepG2	liver
28	chr9:15295800-15296600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
29	chr9:15295800-15296600	Flanking Active TSS	Fetal Kidney	kidney
30	chr9:15295800-15296800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
31	chr9:15295800-15296800	Flanking Active TSS	Fetal Thymus	thymus
32	chr9:15295800-15297000	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr9:15295800-15297200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr9:15295800-15297200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr9:15295800-15297200	Flanking Active TSS	Dnd41	blood
36	chr9:15295800-15297600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr9:15295800-15298400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr9:15296000-15296400	Active TSS	Muscle Satellite Cultured Cells	--
39	chr9:15296000-15296400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr9:15296000-15296400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr9:15296000-15296400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:15296000-15296400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
43	chr9:15296000-15296400	Flanking Active TSS	Fetal Lung	lung
44	chr9:15296000-15296400	Active TSS	Small Intestine	intestine
45	chr9:15296000-15296400	Flanking Active TSS	Hela-S3	cervix
46	chr9:15296000-15296600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr9:15296000-15296600	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr9:15296000-15296600	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr9:15296000-15296600	Flanking Active TSS	Primary hematopoietic stem cells	blood
50	chr9:15296000-15296600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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