Variant report

Variant	esv3414236
Chromosome Location	chr9:17577977-17580825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:17578879-17579258	H1-hESC	embryonic stem cell:	n/a	chr9:17579056-17579070
2	BACH1	chr9:17579465-17579665	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:17578520-17578521	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr9:17578871-17579210	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr9:17579040-17579237	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr9:17578952-17579084	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:17578893-17579163	Hela-S3	cervix:	n/a	n/a
8	CHD1	chr9:17579305-17579446	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr9:17578731-17579704	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr9:17578780-17579235	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr9:17578888-17579286	HepG2	liver:	n/a	n/a
12	CREB1	chr9:17578794-17579273	ECC-1	luminal epithelium:	n/a	n/a
13	CREB1	chr9:17578899-17579312	A549	lung:	n/a	n/a
14	CREB1	chr9:17578927-17579150	A549	lung:	n/a	n/a
15	CREB1	chr9:17578738-17579751	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr9:17578881-17579269	ECC-1	luminal epithelium:	n/a	n/a
17	CREB1	chr9:17578652-17579375	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr9:17578745-17579933	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:17578918-17578982	H1-hESC	embryonic stem cell:	n/a	chr9:17578919-17578932 chr9:17578922-17578935
20	CTCF	chr9:17578945-17578987	LNCaP	prostate:	n/a	n/a
21	CTCF	chr9:17579502-17579546	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr9:17578851-17579027	H1-hESC	embryonic stem cell:	n/a	chr9:17578919-17578932 chr9:17578922-17578935
23	CTCF	chr9:17579097-17579105	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr9:17578904-17578951	Hela-S3	cervix:	n/a	chr9:17578919-17578932 chr9:17578922-17578935
25	CTCF	chr9:17578970-17579091	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr9:17578900-17579050	WERI-Rb-1	eye:	n/a	chr9:17578919-17578932 chr9:17578922-17578935
27	E2F1	chr9:17578726-17579522	Hela-S3	cervix:	n/a	chr9:17579058-17579067 chr9:17579359-17579369 chr9:17579020-17579031 chr9:17579473-17579482 chr9:17578952-17578963 chr9:17578852-17578862 chr9:17578999-17579010 chr9:17579060-17579069
28	E2F4	chr9:17578860-17579153	MCF10A-Er-Src	breast:	n/a	chr9:17579058-17579067 chr9:17579060-17579069
29	E2F6	chr9:17578913-17579180	A549	lung:	n/a	chr9:17579058-17579067 chr9:17579060-17579069
30	E2F6	chr9:17578483-17579540	H1-hESC	embryonic stem cell:	n/a	chr9:17579058-17579067 chr9:17579359-17579369 chr9:17579473-17579482 chr9:17578852-17578862 chr9:17579060-17579069
31	E2F6	chr9:17578686-17579532	H1-hESC	embryonic stem cell:	n/a	chr9:17579058-17579067 chr9:17579359-17579369 chr9:17579473-17579482 chr9:17578852-17578862 chr9:17579060-17579069
32	EGR1	chr9:17579292-17579753	ECC-1	luminal epithelium:	n/a	chr9:17579541-17579551 chr9:17579541-17579554 chr9:17579542-17579553 chr9:17579729-17579739 chr9:17579540-17579554 chr9:17579472-17579482 chr9:17579541-17579554 chr9:17579542-17579552 chr9:17579542-17579551 chr9:17579541-17579554 chr9:17579541-17579554 chr9:17579536-17579558 chr9:17579542-17579552 chr9:17579540-17579555
33	EGR1	chr9:17578860-17579706	H1-hESC	embryonic stem cell:	n/a	chr9:17579541-17579551 chr9:17579541-17579554 chr9:17579542-17579553 chr9:17579540-17579554 chr9:17579472-17579482 chr9:17579541-17579554 chr9:17579542-17579552 chr9:17579542-17579551 chr9:17579541-17579554 chr9:17579541-17579554 chr9:17579536-17579558 chr9:17579542-17579552 chr9:17579540-17579555
34	EGR1	chr9:17579253-17579792	ECC-1	luminal epithelium:	n/a	chr9:17579541-17579551 chr9:17579541-17579554 chr9:17579542-17579553 chr9:17579729-17579739 chr9:17579540-17579554 chr9:17579472-17579482 chr9:17579541-17579554 chr9:17579542-17579552 chr9:17579542-17579551 chr9:17579541-17579554 chr9:17579541-17579554 chr9:17579536-17579558 chr9:17579542-17579552 chr9:17579540-17579555
35	EGR1	chr9:17579330-17579724	H1-hESC	embryonic stem cell:	n/a	chr9:17579541-17579551 chr9:17579541-17579554 chr9:17579542-17579553 chr9:17579540-17579554 chr9:17579472-17579482 chr9:17579541-17579554 chr9:17579542-17579552 chr9:17579542-17579551 chr9:17579541-17579554 chr9:17579541-17579554 chr9:17579536-17579558 chr9:17579542-17579552 chr9:17579540-17579555
36	ELK1	chr9:17578948-17579014	Hela-S3	cervix:	n/a	n/a
37	EP300	chr9:17578743-17579225	H1-hESC	embryonic stem cell:	n/a	chr9:17578852-17578868 chr9:17578853-17578869
38	GABPA	chr9:17578838-17579225	H1-hESC	embryonic stem cell:	n/a	n/a
39	GABPA	chr9:17579222-17579662	H1-hESC	embryonic stem cell:	n/a	chr9:17579473-17579482
40	GTF2F1	chr9:17578927-17579231	Hela-S3	cervix:	n/a	n/a
41	GTF2F1	chr9:17578921-17579250	H1-hESC	embryonic stem cell:	n/a	n/a
42	HA-E2F1	chr9:17578683-17579606	Hela-S3	cervix:	n/a	chr9:17579058-17579067 chr9:17579359-17579369 chr9:17579020-17579031 chr9:17579541-17579551 chr9:17579473-17579482 chr9:17578952-17578963 chr9:17578852-17578862 chr9:17578999-17579010 chr9:17579060-17579069
43	HCFC1	chr9:17578579-17579706	Hela-S3	cervix:	n/a	n/a
44	JUND	chr9:17579226-17579363	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr9:17578877-17579470	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr9:17578941-17579185	H1-hESC	embryonic stem cell:	n/a	n/a
47	KAP1	chr9:17579323-17579569	HEK293	kidney:	n/a	n/a
48	MAFK	chr9:17578902-17579105	Hela-S3	cervix:	n/a	n/a
49	MAX	chr9:17578811-17579206	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAX	chr9:17578610-17579756	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17579026-17579076	HUVEC	blood vessel:	n/a
2	chr9:17578725-17578775	SAEC	small airway:	n/a
3	chr9:17579734-17579784	SK-N-MC	brain:	n/a
4	chr9:17579026-17579076	HCPEpiC	choroid plexus:	n/a
5	chr9:17578779-17578829	HCM	heart:	n/a
6	chr9:17579227-17579277	PrEC	prostate:	n/a
7	chr9:17578174-17578224	HEK293	kidney:	embryo
8	chr9:17578779-17578829	SAEC	small airway:	n/a
9	chr9:17578174-17578224	ProgFib	skin:	n/a
10	chr9:17578779-17578829	AG10803	skin:	n/a
11	chr9:17578174-17578224	MCF-7	breast:	n/a
12	chr9:17579227-17579277	RPTEC	kidney:	n/a
13	chr9:17578725-17578775	HRE	kidney:	n/a
14	chr9:17579026-17579076	HCM	heart:	n/a
15	chr9:17578174-17578224	PANC-1	pancreas:	n/a
16	chr9:17578174-17578224	IMR90	lung:	fetal
17	chr9:17578779-17578829	NHBE	bronchial:	n/a
18	chr9:17579734-17579784	HL-60	blood:	n/a
19	chr9:17578779-17578829	SK-N-SH_RA	brain:	n/a
20	chr9:17579734-17579784	PrEC	prostate:	n/a
21	chr9:17579734-17579784	BE2_C	brain:	n/a
22	chr9:17579734-17579784	T-47D	breast:	n/a
23	chr9:17578725-17578775	AG09309	skin:	n/a
24	chr9:17579734-17579784	HRCEpiC	kidney:	n/a
25	chr9:17579227-17579277	HCM	heart:	n/a
26	chr9:17578779-17578829	HCPEpiC	choroid plexus:	n/a
27	chr9:17578725-17578775	HCPEpiC	choroid plexus:	n/a
28	chr9:17579026-17579076	HEK293	kidney:	embryo
29	chr9:17579026-17579076	ProgFib	skin:	n/a
30	chr9:17579227-17579277	AG10803	skin:	n/a
31	chr9:17578725-17578775	NHDF-neo	bronchial:	n/a
32	chr9:17578725-17578775	HepG2	liver:	n/a
33	chr9:17579026-17579076	NT2-D1	testis:	n/a
34	chr9:17578779-17578829	PANC-1	pancreas:	n/a
35	chr9:17579026-17579076	RPTEC	kidney:	n/a
36	chr9:17578174-17578224	MCF10A-Er-Src	breast:	n/a
37	chr9:17578174-17578224	NHBE	bronchial:	n/a
38	chr9:17579026-17579076	AG09319	gingival:	n/a
39	chr9:17578725-17578775	HCT-116	colon:	n/a
40	chr9:17579734-17579784	U87	brain:	n/a
41	chr9:17578174-17578224	HCF	heart:	n/a
42	chr9:17578725-17578775	HUVEC	blood vessel:	n/a
43	chr9:17578174-17578224	GM19239	blood:	n/a
44	chr9:17579227-17579277	SK-N-MC	brain:	n/a
45	chr9:17578779-17578829	HCT-116	colon:	n/a
46	chr9:17579227-17579277	HCF	heart:	n/a
47	chr9:17579227-17579277	LNCaP	prostate:	n/a
48	chr9:17579734-17579784	NHDF-neo	bronchial:	n/a
49	chr9:17578779-17578829	AG09309	skin:	n/a
50	chr9:17578174-17578224	SK-N-SH_RA	brain:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTLN-5	chr9:17579080-17579285	NONHSAT130304

Variant related genes	Relation type
SH3GL2	TF binding region
SH3GL2	CpG island

Extended variants
information (count: 155 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:155 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369142626	chr9:17578021-17578022	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs577272774	chr9:17578040-17578041	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs541225477	chr9:17578060-17578061	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs141187299	chr9:17578093-17578094	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs182768710	chr9:17578118-17578119	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542088062	chr9:17578136-17578137	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs373688374	chr9:17578159-17578160	Bivalent/Poised TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564022344	chr9:17578186-17578187	Bivalent/Poised TSS Bivalent Enhancer Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs185814893	chr9:17578229-17578230	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs556866985	chr9:17578318-17578319	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552153819	chr9:17578337-17578338	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs564555185	chr9:17578347-17578348	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs376105721	chr9:17578386-17578387	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs79458795	chr9:17578392-17578393	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs528235052	chr9:17578403-17578404	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs76140046	chr9:17578454-17578455	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs147382180	chr9:17578466-17578467	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190615972	chr9:17578477-17578478	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs556941663	chr9:17578483-17578484	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184052518	chr9:17578493-17578494	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs3758217	chr9:17578502-17578503	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558959812	chr9:17578503-17578504	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530457328	chr9:17578524-17578525	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs3780254	chr9:17578554-17578555	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541153179	chr9:17578571-17578572	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs3780253	chr9:17578609-17578610	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574655993	chr9:17578618-17578619	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs10810810	chr9:17578645-17578646	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs563782245	chr9:17578653-17578654	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs531282293	chr9:17578673-17578674	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs117746011	chr9:17578691-17578692	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs3758216	chr9:17578707-17578708	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528174543	chr9:17578708-17578709	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs115146901	chr9:17578709-17578710	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568178106	chr9:17578807-17578808	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs529058347	chr9:17578819-17578820	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs370377512	chr9:17578861-17578862	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs188947590	chr9:17578863-17578864	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs558666580	chr9:17578876-17578877	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs3758215	chr9:17578882-17578883	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534711292	chr9:17578957-17578958	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs566549763	chr9:17578966-17578967	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs553006618	chr9:17578968-17578969	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs574592937	chr9:17578974-17578975	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535667622	chr9:17578985-17578986	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs529114333	chr9:17578997-17578998	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs557572518	chr9:17579012-17579013	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs575830720	chr9:17579014-17579015	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs546504038	chr9:17579028-17579029	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs564648266	chr9:17579043-17579044	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	21364760	CNVD
Cancer	22183965	CNVD
Lung adenocarcinoma	21935476	CNVD
Thoracic aortic aneurysm	21698135	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17577800-17578000	Enhancers	Esophagus	oesophagus
2	chr9:17577800-17578200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:17577800-17578200	Active TSS	Spleen	Spleen
4	chr9:17577800-17580000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
5	chr9:17578000-17578200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
6	chr9:17578200-17578400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr9:17578200-17578400	Enhancers	Hela-S3	cervix
8	chr9:17578200-17578600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
9	chr9:17578200-17578600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
10	chr9:17578200-17578600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
11	chr9:17578200-17578600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr9:17578200-17578800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
13	chr9:17578200-17579000	Bivalent/Poised TSS	Ovary	ovary
14	chr9:17578200-17580000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:17578200-17580600	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr9:17578400-17578600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
17	chr9:17578400-17578600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:17578400-17578600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
19	chr9:17578400-17578600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:17578400-17578600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr9:17578400-17578600	Bivalent Enhancer	Adipose Nuclei	Adipose
22	chr9:17578400-17578600	Enhancers	Brain Hippocampus Middle	brain
23	chr9:17578400-17578600	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr9:17578400-17578600	Enhancers	Brain Substantia Nigra	brain
25	chr9:17578400-17578600	Bivalent Enhancer	Fetal Kidney	kidney
26	chr9:17578400-17578600	Bivalent Enhancer	Fetal Lung	lung
27	chr9:17578400-17578600	Enhancers	Right Ventricle	heart
28	chr9:17578400-17578600	Bivalent Enhancer	HUVEC	blood vessel
29	chr9:17578400-17579000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
30	chr9:17578400-17579000	Flanking Active TSS	Hela-S3	cervix
31	chr9:17578400-17579800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
32	chr9:17578400-17580000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
33	chr9:17578400-17580000	Active TSS	H9 Cell Line	embryonic stem cell
34	chr9:17578400-17580000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr9:17578400-17580000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:17578400-17580000	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
37	chr9:17578400-17580200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
38	chr9:17578400-17580200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr9:17578400-17580400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
40	chr9:17578400-17580800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr9:17578400-17580800	Active TSS	Fetal Brain Female	brain
42	chr9:17578600-17578800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:17578600-17578800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:17578600-17578800	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:17578600-17578800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
46	chr9:17578600-17578800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
47	chr9:17578600-17578800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:17578600-17578800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr9:17578600-17578800	Flanking Active TSS	Brain Angular Gyrus	brain
50	chr9:17578600-17578800	Flanking Active TSS	Brain Anterior Caudate	brain

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