Variant report

Variant	nsv8423
Chromosome Location	chr9:19125975-19128690
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:480)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:19127264-19127726	HepG2	liver:	n/a	n/a
2	ATF2	chr9:19126871-19127725	GM12878	blood:	n/a	n/a
3	ATF2	chr9:19128464-19128720	GM12878	blood:	n/a	n/a
4	ATF2	chr9:19126887-19127266	GM12878	blood:	n/a	n/a
5	ATF3	chr9:19127382-19127679	K562	blood:	n/a	n/a
6	ATF3	chr9:19127310-19127776	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr9:19127439-19127606	GM12878	blood:	n/a	n/a
8	ATF3	chr9:19127394-19127634	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr9:19127427-19127709	HepG2	liver:	n/a	n/a
10	ATF3	chr9:19127327-19127661	HepG2	liver:	n/a	n/a
11	BACH1	chr9:19128611-19128947	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:19127170-19127647	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr9:19126919-19127957	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:19127057-19127851	K562	blood:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
15	BHLHE40	chr9:19127320-19127727	A549	lung:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
16	BHLHE40	chr9:19127397-19127709	HepG2	liver:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
17	BHLHE40	chr9:19125993-19126344	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:19127069-19127972	HepG2	liver:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
19	BHLHE40	chr9:19126637-19126650	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:19127346-19127734	HepG2	liver:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
21	BHLHE40	chr9:19127045-19128054	GM12878	blood:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
22	BHLHE40	chr9:19128618-19129000	GM12878	blood:	n/a	chr9:19128969-19128985
23	BRCA1	chr9:19127095-19127242	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr9:19127219-19127831	GM12878	blood:	n/a	n/a
25	CCNT2	chr9:19127172-19127848	K562	blood:	n/a	chr9:19127346-19127355
26	CEBPB	chr9:19128640-19128819	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr9:19127153-19127849	HepG2	liver:	n/a	n/a
28	CEBPD	chr9:19127367-19127763	HepG2	liver:	n/a	n/a
29	CHD1	chr9:19127525-19128757	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr9:19127033-19128972	GM12878	blood:	n/a	chr9:19128894-19128904 chr9:19127523-19127533
31	CHD1	chr9:19127011-19127301	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr9:19127081-19127759	HepG2	liver:	n/a	chr9:19127523-19127533
33	CHD2	chr9:19128344-19128426	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr9:19127424-19127752	K562	blood:	n/a	chr9:19127523-19127533
35	CHD2	chr9:19127042-19127968	GM12878	blood:	n/a	chr9:19127523-19127533
36	CHD2	chr9:19128673-19128943	GM12878	blood:	n/a	chr9:19128894-19128904
37	CHD2	chr9:19127099-19127742	H1-hESC	embryonic stem cell:	n/a	chr9:19127523-19127533
38	CHD2	chr9:19127544-19127801	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr9:19127021-19127972	HepG2	liver:	n/a	n/a
40	CREB1	chr9:19127241-19127729	A549	lung:	n/a	n/a
41	CTCF	chr9:19126928-19127063	GM10266	blood:	n/a	n/a
42	CTCF	chr9:19126980-19127130	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr9:19128358-19128375	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:19127020-19127170	GM12871	blood:	n/a	n/a
45	CTCF	chr9:19127480-19127630	GM12868	blood:	n/a	n/a
46	CTCF	chr9:19126984-19126998	A549	lung:	n/a	n/a
47	CTCF	chr9:19126922-19127074	GM12891	blood:	n/a	n/a
48	CTCF	chr9:19126440-19126590	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr9:19128320-19128470	GM06990	blood:	n/a	n/a
50	CTCF	chr9:19126940-19127003	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:19127549-19127599	T-47D	breast:	n/a
2	chr9:19126294-19126344	AG04450	lung:	fetal
3	chr9:19127804-19127854	AG10803	skin:	n/a
4	chr9:19126294-19126344	ECC-1	luminal epithelium:	n/a
5	chr9:19126294-19126344	Caco-2	colon:	n/a
6	chr9:19126294-19126344	HCM	heart:	n/a
7	chr9:19127549-19127599	HepG2	liver:	n/a
8	chr9:19127549-19127599	GM06990	blood:	n/a
9	chr9:19127549-19127599	AG09319	gingival:	n/a
10	chr9:19127804-19127854	GM12892	blood:	n/a
11	chr9:19127549-19127599	SAEC	small airway:	n/a
12	chr9:19126294-19126344	AG09309	skin:	n/a
13	chr9:19126294-19126344	HL-60	blood:	n/a
14	chr9:19127804-19127854	IMR90	lung:	fetal
15	chr9:19127549-19127599	BE2_C	brain:	n/a
16	chr9:19127549-19127599	K562	blood:	n/a
17	chr9:19127549-19127599	HCT-116	colon:	n/a
18	chr9:19127549-19127599	PrEC	prostate:	n/a
19	chr9:19126294-19126344	HepG2	liver:	n/a
20	chr9:19127549-19127599	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:19126294-19126344	HMEC	breast:	n/a
22	chr9:19127804-19127854	NH-A	brain:	n/a
23	chr9:19127549-19127599	Caco-2	colon:	n/a
24	chr9:19127549-19127599	HRPEpiC	eye:	n/a
25	chr9:19127804-19127854	HMEC	breast:	n/a
26	chr9:19127804-19127854	SK-N-SH	brain:	n/a
27	chr9:19127549-19127599	MCF10A-Er-Src	breast:	n/a
28	chr9:19127549-19127599	GM12892	blood:	n/a
29	chr9:19126294-19126344	NHDF-neo	bronchial:	n/a
30	chr9:19127549-19127599	IMR90	lung:	fetal
31	chr9:19126294-19126344	HEK293	kidney:	embryo
32	chr9:19126294-19126344	HRE	kidney:	n/a
33	chr9:19126294-19126344	MCF10A-Er-Src	breast:	n/a
34	chr9:19127804-19127854	U87	brain:	n/a
35	chr9:19127549-19127599	CMK	blood:	n/a
36	chr9:19127804-19127854	RPTEC	kidney:	n/a
37	chr9:19126294-19126344	IMR90	lung:	fetal
38	chr9:19126294-19126344	GM12878	blood:	n/a
39	chr9:19126294-19126344	HEEpiC	esophagus:	n/a
40	chr9:19127804-19127854	ECC-1	luminal epithelium:	n/a
41	chr9:19127804-19127854	SK-N-MC	brain:	n/a
42	chr9:19127804-19127854	NHBE	bronchial:	n/a
43	chr9:19127549-19127599	GM12891	blood:	n/a
44	chr9:19127804-19127854	GM12878	blood:	n/a
45	chr9:19127549-19127599	AG10803	skin:	n/a
46	chr9:19127804-19127854	T-47D	breast:	n/a
47	chr9:19127804-19127854	GM12891	blood:	n/a
48	chr9:19127804-19127854	ovcar-3	ovarian:	n/a
49	chr9:19126294-19126344	GM19239	blood:	n/a
50	chr9:19127804-19127854	AG09319	gingival:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:19124716..19129711-chr9:19378738..19382022,6	K562	blood:
2	chr9:19125987..19127822-chr9:19460752..19462438,2	MCF-7	breast:
3	chr9:19101429..19104985-chr9:19125580..19131342,7	K562	blood:
4	chr9:19128414..19130954-chr9:19155486..19158249,2	MCF-7	breast:
5	chr9:19101057..19103224-chr9:19126510..19128425,2	MCF-7	breast:
6	chr9:19102335..19104420-chr9:19127605..19129443,2	MCF-7	breast:
7	chr9:19127609..19129220-chr9:19207374..19210036,2	MCF-7	breast:
8	chr9:19125652..19127211-chr9:19148540..19150962,2	K562	blood:
9	chr9:19128630..19131218-chr9:19137487..19139302,2	K562	blood:
10	chr9:19047688..19050062-chr9:19125989..19129041,3	K562	blood:
11	chr9:19126615..19131871-chr9:19228040..19232542,7	MCF-7	breast:
12	chr9:19127602..19130118-chr9:19378923..19381565,2	MCF-7	breast:
13	chr9:19047624..19049710-chr9:19124952..19127835,2	MCF-7	breast:
14	chr9:19126391..19130012-chr9:19228888..19231863,3	MCF-7	breast:

No data

Variant related genes	Relation type
PLIN2	TF binding region
PLIN2	CpG island
ENSG00000137154	chromatin interactions
ENSG00000231909	chromatin interactions
ENSG00000147872	chromatin interactions
ENSG00000137145	chromatin interactions
ENSG00000147874	chromatin interactions
ENSG00000155876	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538707374	chr9:19126026-19126027	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs371542285	chr9:19126064-19126065	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs145379948	chr9:19126065-19126066	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs534384463	chr9:19126071-19126072	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs369552243	chr9:19126074-19126075	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs60329524	chr9:19126082-19126083	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs34801012	chr9:19126123-19126124	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs149124591	chr9:19126124-19126125	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs537861405	chr9:19126132-19126133	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs556486821	chr9:19126139-19126140	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs11555396	chr9:19126170-19126171	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs369960006	chr9:19126185-19126186	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs200362155	chr9:19126271-19126272	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs2228416	chr9:19126281-19126282	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs202143072	chr9:19126285-19126286	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs201024699	chr9:19126295-19126296	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs142216441	chr9:19126307-19126308	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs41269017	chr9:19126313-19126314	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs55918606	chr9:19126361-19126362	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs377347620	chr9:19126364-19126365	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs151198176	chr9:19126372-19126373	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs151104975	chr9:19126395-19126396	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs72561717	chr9:19126396-19126397	Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs201349928	chr9:19126424-19126425	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs111903968	chr9:19126431-19126432	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs373607837	chr9:19126452-19126453	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs377389478	chr9:19126470-19126471	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs561034741	chr9:19126472-19126473	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs531596979	chr9:19126473-19126474	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs3802335	chr9:19126476-19126477	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs564899921	chr9:19126479-19126480	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs558943812	chr9:19126494-19126495	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs182894266	chr9:19126502-19126503	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs565779277	chr9:19126526-19126527	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs375319845	chr9:19126529-19126530	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs187446738	chr9:19126562-19126563	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs3824369	chr9:19126565-19126566	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs113861614	chr9:19126584-19126585	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs191029143	chr9:19126599-19126600	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs113038645	chr9:19126604-19126605	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs556844782	chr9:19126605-19126606	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs556559570	chr9:19126643-19126644	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs577651170	chr9:19126671-19126672	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs538643942	chr9:19126675-19126676	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs553851261	chr9:19126678-19126679	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs372302800	chr9:19126700-19126701	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs182824767	chr9:19126714-19126715	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs187074954	chr9:19126723-19126724	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs574956373	chr9:19126738-19126739	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs574856365	chr9:19126765-19126766	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Myelofibrosis	22110671	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	21811587	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:19103400-19126400	Weak transcription	Fetal Brain Male	brain
2	chr9:19110600-19126400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:19113400-19126200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:19114000-19126000	Strong transcription	Rectal Mucosa Donor 29	rectum
5	chr9:19114200-19126200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:19114800-19126000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
7	chr9:19114800-19126000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr9:19116400-19127000	Weak transcription	Stomach Mucosa	stomach
9	chr9:19116600-19126000	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr9:19116600-19126000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:19117000-19127000	Weak transcription	HSMMtube	muscle
12	chr9:19118000-19126600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:19118400-19126600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr9:19120600-19126600	Weak transcription	Fetal Brain Female	brain
15	chr9:19121200-19126000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr9:19121200-19126200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr9:19121200-19126400	Weak transcription	Brain Germinal Matrix	brain
18	chr9:19121200-19127000	Weak transcription	Brain Angular Gyrus	brain
19	chr9:19121400-19126200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr9:19121400-19127000	Weak transcription	Brain Anterior Caudate	brain
21	chr9:19121600-19126600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr9:19121800-19126000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr9:19121800-19127000	Weak transcription	Aorta	Aorta
24	chr9:19122400-19126000	Weak transcription	Hela-S3	cervix
25	chr9:19122400-19126400	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:19122800-19126400	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:19123000-19126000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr9:19123000-19126000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr9:19123000-19126000	Weak transcription	Colonic Mucosa	Colon
30	chr9:19123000-19126200	Transcr. at gene 5' and 3'	HepG2	liver
31	chr9:19123000-19126400	Weak transcription	Brain Hippocampus Middle	brain
32	chr9:19123000-19127000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr9:19123200-19126200	Weak transcription	Colon Smooth Muscle	Colon
34	chr9:19123400-19126000	Genic enhancers	Dnd41	blood
35	chr9:19123400-19126400	Weak transcription	Ovary	ovary
36	chr9:19123600-19126000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:19123600-19126200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr9:19123600-19126200	Weak transcription	Brain Substantia Nigra	brain
39	chr9:19123600-19126400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr9:19123600-19126400	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
41	chr9:19123600-19126400	Genic enhancers	Fetal Thymus	thymus
42	chr9:19123600-19126400	Weak transcription	Stomach Smooth Muscle	stomach
43	chr9:19123600-19126600	Weak transcription	Fetal Lung	lung
44	chr9:19123600-19126600	Weak transcription	A549	lung
45	chr9:19123600-19126600	Weak transcription	HSMM	muscle
46	chr9:19123600-19126800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr9:19123800-19126200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr9:19123800-19126200	Weak transcription	Fetal Kidney	kidney
49	chr9:19123800-19126600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:19124000-19126000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland

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