Variant report

Variant	esv3315974
Chromosome Location	chr10:94448397-94451545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:656)
CpG islands
(count:794)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94449623-94449834	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:94450472-94450789	K562	blood:	n/a	n/a
3	ARID3A	chr10:94449642-94449923	K562	blood:	n/a	n/a
4	ARID3A	chr10:94448575-94448749	K562	blood:	n/a	n/a
5	BACH1	chr10:94451457-94452071	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:94449756-94450595	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:94450119-94450426	GM12878	blood:	n/a	chr10:94450279-94450290
8	BHLHE40	chr10:94450084-94450434	GM12878	blood:	n/a	chr10:94450146-94450162
9	BHLHE40	chr10:94449745-94450830	K562	blood:	n/a	chr10:94450146-94450162
10	BHLHE40	chr10:94448577-94448982	K562	blood:	n/a	n/a
11	BHLHE40	chr10:94449290-94449318	K562	blood:	n/a	n/a
12	BHLHE40	chr10:94448540-94450445	HepG2	liver:	n/a	chr10:94449270-94449286 chr10:94450146-94450162 chr10:94449642-94449658
13	BRCA1	chr10:94450090-94450104	HepG2	liver:	n/a	n/a
14	CBX3	chr10:94448327-94449135	K562	blood:	n/a	n/a
15	CCNT2	chr10:94448631-94451909	K562	blood:	n/a	chr10:94449521-94449530 chr10:94451255-94451264
16	CEBPB	chr10:94450637-94450895	K562	blood:	n/a	n/a
17	CEBPB	chr10:94448399-94448626	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:94450237-94450353	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:94450133-94450542	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr10:94448390-94448651	K562	blood:	n/a	n/a
21	CEBPD	chr10:94450371-94450938	K562	blood:	n/a	n/a
22	CEBPD	chr10:94449523-94449905	HepG2	liver:	n/a	n/a
23	CEBPD	chr10:94449571-94450015	HepG2	liver:	n/a	n/a
24	CEBPD	chr10:94449168-94449517	HepG2	liver:	n/a	n/a
25	CEBPD	chr10:94450441-94450915	K562	blood:	n/a	n/a
26	CHD1	chr10:94450625-94451087	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr10:94450553-94450647	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr10:94448750-94448936	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr10:94449248-94450546	Hela-S3	cervix:	n/a	chr10:94449522-94449532 chr10:94449385-94449395
30	CHD2	chr10:94451256-94451395	K562	blood:	n/a	n/a
31	CHD2	chr10:94449342-94449343	K562	blood:	n/a	n/a
32	CREB1	chr10:94449053-94450362	A549	lung:	n/a	n/a
33	CTBP2	chr10:94448629-94449382	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr10:94449746-94452477	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr10:94450060-94450210	Hela-S3	cervix:	n/a	chr10:94450145-94450158 chr10:94450142-94450160
36	CTCF	chr10:94448620-94448770	Caco-2	colon:	n/a	n/a
37	CTCF	chr10:94448700-94448850	BJ	skin:	n/a	n/a
38	CTCF	chr10:94448937-94448950	A549	lung:	n/a	n/a
39	CTCF	chr10:94449900-94450050	A549	lung:	n/a	n/a
40	CTCF	chr10:94448820-94448970	HMF	breast:	n/a	n/a
41	CTCF	chr10:94448580-94448730	GM12865	blood:	n/a	n/a
42	CTCF	chr10:94448680-94448830	HFF	foreskin:	n/a	n/a
43	CTCF	chr10:94449469-94449489	GM12878	blood:	n/a	n/a
44	CTCF	chr10:94448580-94448730	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr10:94448860-94449010	GM12873	blood:	n/a	n/a
46	CTCF	chr10:94448380-94448530	BJ	skin:	n/a	n/a
47	CTCF	chr10:94448640-94448790	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr10:94448644-94448820	GM19240	blood:	n/a	n/a
49	CTCF	chr10:94448640-94448790	GM12864	blood:	n/a	n/a
50	CTCF	chr10:94449820-94449970	SK-N-SH_RA	brain:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94449567-94449617	LNCaP	prostate:	n/a
2	chr10:94449567-94449617	LNCaP	prostate:	n/a
3	chr10:94450056-94450106	Hepatocyte	liver:	n/a
4	chr10:94448532-94448582	SKMC	muscle:	n/a
5	chr10:94450056-94450106	SK-N-MC	brain:	n/a
6	chr10:94450994-94451044	HepG2	liver:	n/a
7	chr10:94451351-94451401	NH-A	brain:	n/a
8	chr10:94449250-94449300	HCT-116	colon:	n/a
9	chr10:94450866-94450916	IMR90	lung:	fetal
10	chr10:94450994-94451044	AG04450	lung:	fetal
11	chr10:94449797-94449847	HNPCEpiC	eye:	n/a
12	chr10:94451518-94451568	NB4	blood:	n/a
13	chr10:94450056-94450106	NB4	blood:	n/a
14	chr10:94450531-94450581	LNCaP	prostate:	n/a
15	chr10:94448702-94448752	Caco-2	colon:	n/a
16	chr10:94450531-94450581	AG04450	lung:	fetal
17	chr10:94450866-94450916	HCF	heart:	n/a
18	chr10:94451518-94451568	T-47D	breast:	n/a
19	chr10:94450531-94450581	HL-60	blood:	n/a
20	chr10:94450531-94450581	IMR90	lung:	fetal
21	chr10:94449250-94449300	ovcar-3	ovarian:	n/a
22	chr10:94451518-94451568	HIPEpiC	eye:	n/a
23	chr10:94448728-94448778	NB4	blood:	n/a
24	chr10:94451518-94451568	GM06990	blood:	n/a
25	chr10:94450531-94450581	PANC-1	pancreas:	n/a
26	chr10:94450056-94450106	HCM	heart:	n/a
27	chr10:94450866-94450916	HNPCEpiC	eye:	n/a
28	chr10:94449797-94449847	K562	blood:	n/a
29	chr10:94449250-94449300	A549	lung:	n/a
30	chr10:94448728-94448778	GM06990	blood:	n/a
31	chr10:94450994-94451044	T-47D	breast:	n/a
32	chr10:94451351-94451401	HepG2	liver:	n/a
33	chr10:94448728-94448778	SK-N-MC	brain:	n/a
34	chr10:94448728-94448778	AoSMC	blood vessel:	n/a
35	chr10:94450056-94450106	Caco-2	colon:	n/a
36	chr10:94449567-94449617	NHDF-neo	bronchial:	n/a
37	chr10:94448728-94448778	NT2-D1	testis:	n/a
38	chr10:94451016-94451066	GM06990	blood:	n/a
39	chr10:94450994-94451044	HCM	heart:	n/a
40	chr10:94450531-94450581	PFSK-1	brain:	n/a
41	chr10:94449250-94449300	NHBE	bronchial:	n/a
42	chr10:94448532-94448582	U87	brain:	n/a
43	chr10:94449797-94449847	MCF10A-Er-Src	breast:	n/a
44	chr10:94448728-94448778	NHBE	bronchial:	n/a
45	chr10:94450056-94450106	ProgFib	skin:	n/a
46	chr10:94449797-94449847	HUVEC	blood vessel:	n/a
47	chr10:94451518-94451568	GM12892	blood:	n/a
48	chr10:94451016-94451066	HCPEpiC	choroid plexus:	n/a
49	chr10:94451518-94451568	Jurkat	blood:	n/a
50	chr10:94448702-94448752	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:94449237..94450232-chr6:27805942..27806496,2	NB4	blood:
2	chr10:94449678..94450357-chr11:62359130..62359860,2	Hela-S3	cervix:
3	chr10:94449475..94450112-chr19:14529907..14530785,2	Hela-S3	cervix:
4	chr10:94450024..94450724-chr19:12901932..12902636,2	Hela-S3	cervix:
5	chr10:94449314..94450224-chr16:30388710..30389229,2	NB4	blood:
6	chr10:94449603..94452740-chr10:94589464..94592452,3	K562	blood:
7	chr10:94332371..94335153-chr10:94446165..94448467,2	K562	blood:
8	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
9	chr10:94449913..94450519-chr18:12990641..12991585,2	Hela-S3	cervix:
10	chr10:94349533..94354628-chr10:94448059..94453493,12	K562	blood:
11	chr10:94333616..94336720-chr10:94448718..94451044,3	K562	blood:
12	chr10:94449758..94450309-chr20:30192485..30193219,2	Hela-S3	cervix:
13	chr10:94449635..94450319-chr15:59396946..59397778,2	NB4	blood:
14	chr10:94349533..94356622-chr10:94447410..94453498,11	K562	blood:

No data

Variant related genes	Relation type
HHEX	TF binding region
HHEX	CpG island
ENSG00000138190	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000123136	chromatin interactions
ENSG00000119912	chromatin interactions
ENSG00000101639	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000266969	chromatin interactions
ENSG00000184348	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 70 )

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	rs74149107	chr10:94448475-94448476	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368683939	chr10:94448531-94448532	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs185220612	chr10:94448532-94448533	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs534777764	chr10:94448550-94448551	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs548391548	chr10:94448574-94448575	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs147778208	chr10:94448618-94448619	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs188579373	chr10:94448652-94448653	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs189936100	chr10:94448683-94448684	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs537144231	chr10:94448725-94448726	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs141036674	chr10:94448738-94448739	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs182529846	chr10:94448750-94448751	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs11187135	chr10:94448756-94448757	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149759733	chr10:94448774-94448775	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs76425330	chr10:94448793-94448794	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs573117244	chr10:94448802-94448803	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs556522395	chr10:94448806-94448807	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs542053391	chr10:94448816-94448817	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs117739875	chr10:94448838-94448839	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs562305227	chr10:94448847-94448848	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs113555157	chr10:94448851-94448852	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs544652387	chr10:94448855-94448856	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs564324947	chr10:94448867-94448868	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs533335614	chr10:94448875-94448876	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs552512817	chr10:94448890-94448891	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs34593856	chr10:94448895-94448896	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs559715342	chr10:94448897-94448898	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs528370402	chr10:94448898-94448899	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs181829459	chr10:94448920-94448921	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs548134764	chr10:94448995-94448996	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs568239897	chr10:94449055-94449056	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs536758535	chr10:94449101-94449102	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs188542981	chr10:94449109-94449110	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs371104417	chr10:94449157-94449158	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs114001966	chr10:94449158-94449159	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs12781513	chr10:94449160-94449161	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368448352	chr10:94449193-94449194	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs544628160	chr10:94449198-94449199	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs539013549	chr10:94449199-94449200	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs561307515	chr10:94449206-94449207	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs148939627	chr10:94449214-94449215	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs535737516	chr10:94449228-94449229	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs555690607	chr10:94449286-94449287	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs575746087	chr10:94449287-94449288	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs375280193	chr10:94449305-94449306	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs544399912	chr10:94449334-94449335	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs558196263	chr10:94449416-94449417	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs578130983	chr10:94449438-94449439	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs540657123	chr10:94449448-94449449	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs7475059	chr10:94449469-94449470	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs367580592	chr10:94449475-94449476	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94440600-94448600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:94441800-94448600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:94444400-94448400	Weak transcription	Pancreas	Pancrea
4	chr10:94444600-94448400	Weak transcription	Lung	lung
5	chr10:94446200-94448400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr10:94446600-94448600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:94446800-94448600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr10:94447600-94448600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr10:94447800-94448400	Transcr. at gene 5' and 3'	K562	blood
10	chr10:94447800-94450600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr10:94448000-94448600	Enhancers	Primary B cells from peripheral blood	blood
12	chr10:94448000-94449200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr10:94448000-94449400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:94448200-94448400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr10:94448200-94448400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:94448200-94448400	Enhancers	Colon Smooth Muscle	Colon
17	chr10:94448200-94448400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
18	chr10:94448200-94448400	Bivalent/Poised TSS	Fetal Lung	lung
19	chr10:94448200-94448400	Enhancers	Rectal Smooth Muscle	rectum
20	chr10:94448200-94448400	Enhancers	HUVEC	blood vessel
21	chr10:94448200-94448600	Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr10:94448200-94448600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr10:94448200-94448600	Flanking Active TSS	HepG2	liver
24	chr10:94448200-94448800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
25	chr10:94448200-94448800	Flanking Active TSS	A549	lung
26	chr10:94448200-94449000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr10:94448200-94449000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
28	chr10:94448200-94449000	Flanking Active TSS	Liver	Liver
29	chr10:94448200-94449400	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr10:94448400-94448600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr10:94448400-94448600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
32	chr10:94448400-94448600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
33	chr10:94448400-94448600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr10:94448400-94448600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
35	chr10:94448400-94448600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr10:94448400-94448600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr10:94448400-94448600	Flanking Active TSS	Colon Smooth Muscle	Colon
38	chr10:94448400-94448600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
39	chr10:94448400-94448600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr10:94448400-94448600	Enhancers	Placenta	Placenta
41	chr10:94448400-94448600	Enhancers	Pancreas	Pancrea
42	chr10:94448400-94448600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
43	chr10:94448400-94448600	Flanking Active TSS	K562	blood
44	chr10:94448400-94448600	Bivalent Enhancer	NH-A	brain
45	chr10:94448400-94448600	Flanking Bivalent TSS/Enh	NHDF-Ad	bronchial
46	chr10:94448400-94448800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
47	chr10:94448400-94448800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
48	chr10:94448400-94448800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
49	chr10:94448400-94448800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr10:94448400-94448800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain

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