Variant report

Variant	nsv871144
Chromosome Location	chr1:92380302-92641607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1521)
CpG islands
(count:2686)
Chromatin interactive
region (count:51)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92463047-92463494	K562	blood:	n/a	n/a
2	ARID3A	chr1:92463265-92463529	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:92424619-92424819	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:92545681-92545684	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:92392911-92393150	K562	blood:	n/a	n/a
6	ARID3A	chr1:92392821-92393186	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:92545717-92545724	K562	blood:	n/a	n/a
8	ARID3A	chr1:92504254-92504757	HepG2	liver:	n/a	n/a
9	ATF1	chr1:92608669-92608727	K562	blood:	n/a	n/a
10	ATF1	chr1:92591884-92591960	K562	blood:	n/a	n/a
11	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
12	ATF3	chr1:92414808-92414936	K562	blood:	n/a	chr1:92414878-92414887 chr1:92414867-92414887
13	BACH1	chr1:92494875-92495995	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:92458760-92458932	K562	blood:	n/a	n/a
15	BHLHE40	chr1:92545583-92546606	K562	blood:	n/a	n/a
16	BHLHE40	chr1:92407219-92407552	K562	blood:	n/a	n/a
17	BHLHE40	chr1:92414729-92414870	K562	blood:	n/a	n/a
18	BRCA1	chr1:92548328-92548357	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:92495150-92495489	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr1:92620422-92620917	HCT-116	colon:	n/a	n/a
21	CBX3	chr1:92545636-92546410	K562	blood:	n/a	n/a
22	CBX3	chr1:92551256-92551644	K562	blood:	n/a	n/a
23	CBX3	chr1:92620575-92620818	HCT-116	colon:	n/a	n/a
24	CBX3	chr1:92551261-92551662	HCT-116	colon:	n/a	n/a
25	CBX3	chr1:92551278-92551743	HCT-116	colon:	n/a	n/a
26	CBX3	chr1:92551214-92551741	K562	blood:	n/a	n/a
27	CCNT2	chr1:92545770-92546292	K562	blood:	n/a	chr1:92545783-92545792
28	CCNT2	chr1:92629723-92629923	K562	blood:	n/a	n/a
29	CEBPB	chr1:92414332-92414701	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:92504657-92504803	H1-hESC	embryonic stem cell:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
31	CEBPB	chr1:92517024-92517137	HepG2	liver:	n/a	chr1:92517083-92517094
32	CEBPB	chr1:92414400-92414603	MCF-7	breast:	n/a	n/a
33	CEBPB	chr1:92557276-92557559	A549	lung:	n/a	n/a
34	CEBPB	chr1:92380856-92381040	Hela-S3	cervix:	n/a	chr1:92380948-92380959
35	CEBPB	chr1:92557199-92557564	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:92414360-92414677	A549	lung:	n/a	n/a
37	CEBPB	chr1:92380799-92381201	HepG2	liver:	n/a	chr1:92380948-92380959
38	CEBPB	chr1:92398696-92398710	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:92504509-92504831	A549	lung:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
40	CEBPB	chr1:92562014-92562256	Hela-S3	cervix:	n/a	chr1:92562163-92562174
41	CEBPB	chr1:92455971-92456232	HepG2	liver:	n/a	chr1:92456098-92456109
42	CEBPB	chr1:92557218-92557555	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:92557333-92557513	K562	blood:	n/a	n/a
44	CEBPB	chr1:92448101-92448201	K562	blood:	n/a	n/a
45	CEBPB	chr1:92496162-92496469	IMR90	lung:	n/a	chr1:92496303-92496314
46	CEBPB	chr1:92424510-92424800	HepG2	liver:	n/a	chr1:92424646-92424655 chr1:92424645-92424656 chr1:92424644-92424655
47	CEBPB	chr1:92400251-92400417	K562	blood:	n/a	chr1:92400319-92400330
48	CEBPB	chr1:92561500-92561678	K562	blood:	n/a	n/a
49	CEBPB	chr1:92561470-92562295	IMR90	lung:	n/a	chr1:92562163-92562174
50	CEBPB	chr1:92414333-92414714	K562	blood:	n/a	n/a

(count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92494997-92495047	Caco-2	colon:	n/a
2	chr1:92546135-92546185	AoSMC	blood vessel:	n/a
3	chr1:92494997-92495047	Caco-2	colon:	n/a
4	chr1:92546135-92546185	AoSMC	blood vessel:	n/a
5	chr1:92545580-92545630	SKMC	muscle:	n/a
6	chr1:92413007-92413057	LNCaP	prostate:	n/a
7	chr1:92546040-92546090	HCF	heart:	n/a
8	chr1:92414737-92414787	GM19239	blood:	n/a
9	chr1:92545650-92545700	GM12891	blood:	n/a
10	chr1:92491486-92491536	Jurkat	blood:	n/a
11	chr1:92491486-92491536	HCT-116	colon:	n/a
12	chr1:92495818-92495868	GM12891	blood:	n/a
13	chr1:92631249-92631299	ProgFib	skin:	n/a
14	chr1:92414782-92414832	Caco-2	colon:	n/a
15	chr1:92495083-92495133	HCPEpiC	choroid plexus:	n/a
16	chr1:92414295-92414345	IMR90	lung:	fetal
17	chr1:92417998-92418048	AoSMC	blood vessel:	n/a
18	chr1:92545768-92545818	GM12892	blood:	n/a
19	chr1:92414221-92414271	PFSK-1	brain:	n/a
20	chr1:92546040-92546090	CMK	blood:	n/a
21	chr1:92494997-92495047	NHBE	bronchial:	n/a
22	chr1:92495877-92495927	BE2_C	brain:	n/a
23	chr1:92414737-92414787	H1-hESC	embryonic stem cell:	embryo
24	chr1:92415048-92415098	Hela-S3	cervix:	n/a
25	chr1:92494997-92495047	BJ	skin:	n/a
26	chr1:92545662-92545712	AG10803	skin:	n/a
27	chr1:92495004-92495054	ProgFib	skin:	n/a
28	chr1:92495877-92495927	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:92545888-92545938	LNCaP	prostate:	n/a
30	chr1:92416320-92416370	HEK293	kidney:	embryo
31	chr1:92414737-92414787	CMK	blood:	n/a
32	chr1:92545224-92545274	Jurkat	blood:	n/a
33	chr1:92546135-92546185	Jurkat	blood:	n/a
34	chr1:92495877-92495927	HUVEC	blood vessel:	n/a
35	chr1:92417998-92418048	GM12892	blood:	n/a
36	chr1:92545888-92545938	NHDF-neo	bronchial:	n/a
37	chr1:92545888-92545938	HEEpiC	esophagus:	n/a
38	chr1:92415145-92415195	HMEC	breast:	n/a
39	chr1:92414221-92414271	H1-hESC	embryonic stem cell:	embryo
40	chr1:92546470-92546520	MCF10A-Er-Src	breast:	n/a
41	chr1:92549234-92549284	AG10803	skin:	n/a
42	chr1:92414520-92414570	GM12878	blood:	n/a
43	chr1:92545768-92545818	SKMC	muscle:	n/a
44	chr1:92495877-92495927	HAEpiC	amniotic membrane:	n/a
45	chr1:92414520-92414570	PFSK-1	brain:	n/a
46	chr1:92495818-92495868	Hepatocyte	liver:	n/a
47	chr1:92546447-92546497	H1-hESC	embryonic stem cell:	embryo
48	chr1:92494898-92494948	SK-N-SH	brain:	n/a
49	chr1:92413007-92413057	AG09309	skin:	n/a
50	chr1:92546135-92546185	Hepatocyte	liver:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:92529998..92532866-chr1:92545519..92547678,2	MCF-7	breast:
2	chr1:92532650..92534894-chr1:92538818..92540475,2	K562	blood:
3	chr1:91964010..91966765-chr1:92464590..92467417,2	K562	blood:
4	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
5	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
6	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
7	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
8	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
9	chr1:91869631..91870341-chr1:92392565..92393108,2	K562	blood:
10	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
11	chr1:92531679..92534472-chr1:92536505..92538325,2	K562	blood:
12	chr1:91995716..91996502-chr1:92392369..92393018,2	MCF-7	breast:
13	chr1:92628189..92630728-chr1:92634090..92636512,2	K562	blood:
14	chr1:92628189..92630728-chr1:92634090..92636512,2	K562	blood:
15	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
16	chr1:92500741..92502488-chr1:92762793..92765174,2	MCF-7	breast:
17	chr1:92597223..92599261-chr1:92601215..92603024,2	K562	blood:
18	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
19	chr1:92202754..92203402-chr1:92392489..92393086,2	MCF-7	breast:
20	chr1:92545812..92549091-chr1:92549918..92553923,4	K562	blood:
21	chr1:92398059..92398985-chr1:92756667..92757204,2	MCF-7	breast:
22	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
23	chr1:92532650..92534894-chr1:92538818..92540475,2	K562	blood:
24	chr1:92082754..92083639-chr1:92392516..92393512,4	MCF-7	breast:
25	chr1:92640592..92643432-chr1:92648038..92650855,3	K562	blood:
26	chr1:91994551..91996997-chr1:92385610..92388191,2	K562	blood:
27	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
28	chr1:92624229..92626147-chr1:92633625..92636572,2	K562	blood:
29	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
30	chr1:92463193..92463783-chr1:92756674..92757244,2	MCF-7	breast:
31	chr1:92636751..92638708-chr14:23652231..23655007,2	MCF-7	breast:
32	chr1:92490161..92492607-chr1:92493368..92497617,3	K562	blood:
33	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
34	chr1:92411395..92413821-chr1:92420439..92422796,2	K562	blood:
35	chr1:91978918..91979433-chr1:92392533..92393092,2	K562	blood:
36	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
37	chr1:92542913..92545844-chr1:92825979..92827706,2	K562	blood:
38	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
39	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
40	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
41	chr1:92544652..92546280-chr1:92558053..92559585,2	K562	blood:
42	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
43	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
44	chr1:91976686..91977638-chr1:92392584..92393518,2	K562	blood:
45	chr1:91966529..91968334-chr1:92639534..92641055,2	K562	blood:
46	chr1:92411395..92413821-chr1:92420439..92422796,2	K562	blood:
47	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
48	chr1:92529998..92532866-chr1:92545519..92547678,2	MCF-7	breast:
49	chr1:91966132..91968252-chr1:92404869..92406833,2	K562	blood:
50	chr1:92624229..92626147-chr1:92633625..92636572,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004443
2	lnc-EPHX4-2	chr1:92414960-92415076	NONHSAT004446
3	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004445
4	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004445
5	lnc-EPHX4-2	chr1:92415457-92415856	NONHSAT004444
6	lnc-BRDT-1	chr1:92404826-92405131	NONHSAT004442
7	lnc-EPHX4-2	chr1:92414955-92415076	NONHSAT004444
8	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004444
9	lnc-EPHX4-2	chr1:92415447-92415869	NONHSAT004446
10	lnc-EPHX4-2	chr1:92415447-92415889	NONHSAT004445
11	lnc-EPHX4-2	chr1:92415457-92415859	NONHSAT004443
12	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004443
13	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004446

No data

Variant related genes	Relation type
KIAA1107	TF binding region
LPCAT2BP	TF binding region
GAPDHP46	TF binding region
BTBD8	TF binding region
SETSIP	TF binding region
BRDT	TF binding region
EPHX4	TF binding region
RN7SL235P	TF binding region
PRKAR1AP	TF binding region
KIAA1107	CpG island
LPCAT2BP	CpG island
GAPDHP46	CpG island
BTBD8	CpG island
SETSIP	CpG island
BRDT	CpG island
EPHX4	CpG island
RN7SL235P	CpG island
PRKAR1AP	CpG island
ENSG00000122484	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000189195	chromatin interactions
ENSG00000162669	chromatin interactions
ENSG00000215277	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000092068	chromatin interactions
ENSG00000233228	chromatin interactions

Extended variants
information (count: 7222 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:7222 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs883873	chr1:92380302-92380303	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561521668	chr1:92380351-92380352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115688512	chr1:92380356-92380357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551916665	chr1:92380384-92380385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570294906	chr1:92380479-92380480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532665458	chr1:92380515-92380516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs877277	chr1:92380523-92380524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11165785	chr1:92380549-92380550	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs536213087	chr1:92380565-92380566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56323961	chr1:92380571-92380572	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs184769303	chr1:92380580-92380581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542084904	chr1:92380581-92380582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147890674	chr1:92380588-92380589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577346935	chr1:92380590-92380591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541159995	chr1:92380609-92380610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141768446	chr1:92380661-92380662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552061676	chr1:92380668-92380669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2770185	chr1:92380670-92380671	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113606933	chr1:92380694-92380695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563257192	chr1:92380778-92380779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373490698	chr1:92380794-92380795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113556513	chr1:92380813-92380814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565590394	chr1:92380856-92380857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2799532	chr1:92380859-92380860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1810795	chr1:92380868-92380869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561727999	chr1:92380911-92380912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528266391	chr1:92380920-92380921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189133404	chr1:92380930-92380931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559542249	chr1:92380969-92380970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191309877	chr1:92381043-92381044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141652275	chr1:92381056-92381057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184426753	chr1:92381119-92381120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149227735	chr1:92381147-92381148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs80108812	chr1:92381161-92381162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537770880	chr1:92381258-92381259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58796125	chr1:92381259-92381260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189713772	chr1:92381260-92381261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568227702	chr1:92381292-92381293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534856929	chr1:92381416-92381417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553051217	chr1:92381445-92381446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574415008	chr1:92381479-92381480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11165787	chr1:92381483-92381484	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556566618	chr1:92381492-92381493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556586845	chr1:92381499-92381500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138553306	chr1:92381521-92381522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527611296	chr1:92381576-92381577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376659953	chr1:92381615-92381616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181244887	chr1:92381621-92381622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572997631	chr1:92381622-92381623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540024948	chr1:92381646-92381647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1764 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92378400-92391400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:92379000-92389400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr1:92379200-92383600	Enhancers	Placenta	Placenta
4	chr1:92379400-92384200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:92379800-92380600	Weak transcription	HepG2	liver
6	chr1:92379800-92381800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr1:92379800-92383000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr1:92380200-92380800	Enhancers	Hela-S3	cervix
9	chr1:92380600-92381600	Enhancers	HepG2	liver
10	chr1:92380800-92381200	Weak transcription	Hela-S3	cervix
11	chr1:92381200-92381400	Enhancers	Hela-S3	cervix
12	chr1:92381400-92385400	Weak transcription	Hela-S3	cervix
13	chr1:92381600-92389800	Weak transcription	HepG2	liver
14	chr1:92381800-92382600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:92381800-92383000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:92382400-92383000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:92382400-92383000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:92382400-92383200	Enhancers	Fetal Heart	heart
19	chr1:92382600-92383200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr1:92382800-92383200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:92383000-92383200	Enhancers	Placenta Amnion	Placenta Amnion
22	chr1:92383200-92383600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:92383600-92383800	Enhancers	Placenta Amnion	Placenta Amnion
24	chr1:92383600-92386600	Weak transcription	Placenta	Placenta
25	chr1:92383800-92386800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr1:92384200-92384400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:92385400-92385800	Enhancers	Hela-S3	cervix
28	chr1:92385600-92386000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:92385800-92386600	Weak transcription	Hela-S3	cervix
30	chr1:92386000-92393200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:92386600-92387200	Enhancers	Hela-S3	cervix
32	chr1:92386600-92387800	Enhancers	Placenta	Placenta
33	chr1:92386800-92387600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr1:92387200-92389400	Weak transcription	Hela-S3	cervix
35	chr1:92387600-92389600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr1:92387800-92391800	Weak transcription	Placenta	Placenta
37	chr1:92388800-92389800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:92389200-92389400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:92389200-92389400	Enhancers	NHDF-Ad	bronchial
40	chr1:92389400-92389600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:92389400-92389600	Enhancers	Hela-S3	cervix
42	chr1:92389400-92389800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:92389400-92390000	Enhancers	NHLF	lung
44	chr1:92389400-92390200	Enhancers	HMEC	breast
45	chr1:92389400-92390200	Flanking Active TSS	NHDF-Ad	bronchial
46	chr1:92389400-92390400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr1:92389400-92390400	Enhancers	NH-A	brain
48	chr1:92389400-92392000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:92389600-92389800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:92389600-92389800	Enhancers	Placenta Amnion	Placenta Amnion

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