Variant report

Variant	nsv871097
Chromosome Location	chr1:94850443-94941890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1284)
CpG islands
(count:976)
Chromatin interactive
region (count:39)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94884708-94885136	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94882733-94884031	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94890686-94890723	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:94891126-94891987	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:94849296-94850774	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:94882968-94884005	K562	blood:	n/a	n/a
7	ARID3A	chr1:94929310-94929611	HepG2	liver:	n/a	n/a
8	ATF1	chr1:94882859-94883854	K562	blood:	n/a	n/a
9	ATF1	chr1:94872091-94872184	K562	blood:	n/a	n/a
10	BACH1	chr1:94884883-94884897	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:94883363-94884230	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:94882928-94883108	K562	blood:	n/a	n/a
13	BATF	chr1:94876808-94877148	GM12878	blood:	n/a	n/a
14	BATF	chr1:94876823-94877077	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:94876806-94877085	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:94876815-94877104	GM12878	blood:	n/a	n/a
17	BCL3	chr1:94883321-94883829	A549	lung:	n/a	chr1:94883748-94883757 chr1:94883742-94883750
18	BCL3	chr1:94883389-94883838	A549	lung:	n/a	chr1:94883748-94883757 chr1:94883742-94883750
19	BCLAF1	chr1:94883459-94883903	GM12878	blood:	n/a	chr1:94883748-94883757 chr1:94883742-94883750
20	BCLAF1	chr1:94876832-94877125	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:94876747-94877119	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:94888141-94888148	K562	blood:	n/a	n/a
23	BHLHE40	chr1:94862003-94862207	K562	blood:	n/a	n/a
24	BHLHE40	chr1:94882881-94884204	K562	blood:	n/a	chr1:94884179-94884195
25	BHLHE40	chr1:94883427-94884257	GM12878	blood:	n/a	chr1:94884179-94884195
26	BHLHE40	chr1:94884879-94884917	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:94891372-94891730	HepG2	liver:	n/a	n/a
28	BHLHE40	chr1:94883176-94884119	HepG2	liver:	n/a	n/a
29	BHLHE40	chr1:94850606-94850686	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:94850417-94851103	HepG2	liver:	n/a	n/a
31	BRCA1	chr1:94850787-94850892	HepG2	liver:	n/a	n/a
32	BRCA1	chr1:94882208-94882219	HepG2	liver:	n/a	n/a
33	BRCA1	chr1:94882874-94883852	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr1:94884389-94884943	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr1:94883522-94883767	HepG2	liver:	n/a	n/a
36	BRCA1	chr1:94883483-94883931	GM12878	blood:	n/a	n/a
37	CBX3	chr1:94910438-94910682	K562	blood:	n/a	n/a
38	CBX3	chr1:94915770-94915943	K562	blood:	n/a	n/a
39	CBX3	chr1:94915685-94916228	K562	blood:	n/a	n/a
40	CBX3	chr1:94915954-94916165	K562	blood:	n/a	n/a
41	CBX3	chr1:94882841-94884223	K562	blood:	n/a	n/a
42	CCNT2	chr1:94883491-94884832	K562	blood:	n/a	n/a
43	CEBPB	chr1:94884737-94885264	A549	lung:	n/a	n/a
44	CEBPB	chr1:94854380-94854593	HepG2	liver:	n/a	chr1:94854441-94854452
45	CEBPB	chr1:94882984-94883155	HepG2	liver:	n/a	chr1:94883071-94883088
46	CEBPB	chr1:94882684-94883856	HepG2	liver:	n/a	chr1:94883654-94883665 chr1:94883071-94883088
47	CEBPB	chr1:94937794-94938064	IMR90	lung:	n/a	chr1:94937930-94937943
48	CEBPB	chr1:94882684-94884080	Hela-S3	cervix:	n/a	chr1:94883654-94883665 chr1:94883071-94883088
49	CEBPB	chr1:94883428-94883825	H1-hESC	embryonic stem cell:	n/a	chr1:94883654-94883665
50	CEBPB	chr1:94884315-94885194	Hela-S3	cervix:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94883526-94883576	AG09319	gingival:	n/a
2	chr1:94884060-94884110	PANC-1	pancreas:	n/a
3	chr1:94883752-94883802	BJ	skin:	n/a
4	chr1:94860295-94860345	HRCEpiC	kidney:	n/a
5	chr1:94883754-94883804	ovcar-3	ovarian:	n/a
6	chr1:94883536-94883586	AoSMC	blood vessel:	n/a
7	chr1:94883546-94883596	HepG2	liver:	n/a
8	chr1:94883536-94883586	HL-60	blood:	n/a
9	chr1:94860295-94860345	SKMC	muscle:	n/a
10	chr1:94884039-94884089	HL-60	blood:	n/a
11	chr1:94883581-94883631	HUVEC	blood vessel:	n/a
12	chr1:94929484-94929534	PrEC	prostate:	n/a
13	chr1:94884189-94884239	ProgFib	skin:	n/a
14	chr1:94884189-94884239	AG04449	skin:	fetal
15	chr1:94884060-94884110	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:94883752-94883802	AG10803	skin:	n/a
17	chr1:94883526-94883576	MCF10A-Er-Src	breast:	n/a
18	chr1:94883752-94883802	NT2-D1	testis:	n/a
19	chr1:94888188-94888238	HIPEpiC	eye:	n/a
20	chr1:94883526-94883576	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:94884039-94884089	AG04450	lung:	fetal
22	chr1:94882585-94882635	HRPEpiC	eye:	n/a
23	chr1:94883754-94883804	HCF	heart:	n/a
24	chr1:94888188-94888238	PFSK-1	brain:	n/a
25	chr1:94882585-94882635	GM12892	blood:	n/a
26	chr1:94884060-94884110	SKMC	muscle:	n/a
27	chr1:94888188-94888238	GM06990	blood:	n/a
28	chr1:94883536-94883586	ECC-1	luminal epithelium:	n/a
29	chr1:94883754-94883804	HepG2	liver:	n/a
30	chr1:94929484-94929534	AG09319	gingival:	n/a
31	chr1:94884541-94884591	CMK	blood:	n/a
32	chr1:94883526-94883576	HNPCEpiC	eye:	n/a
33	chr1:94883581-94883631	NHBE	bronchial:	n/a
34	chr1:94929484-94929534	SK-N-MC	brain:	n/a
35	chr1:94884039-94884089	PANC-1	pancreas:	n/a
36	chr1:94883526-94883576	HCPEpiC	choroid plexus:	n/a
37	chr1:94884541-94884591	LNCaP	prostate:	n/a
38	chr1:94883469-94883519	HNPCEpiC	eye:	n/a
39	chr1:94860295-94860345	NB4	blood:	n/a
40	chr1:94884541-94884591	HCF	heart:	n/a
41	chr1:94883526-94883576	Caco-2	colon:	n/a
42	chr1:94888188-94888238	AG09319	gingival:	n/a
43	chr1:94883752-94883802	A549	lung:	n/a
44	chr1:94888188-94888238	HCPEpiC	choroid plexus:	n/a
45	chr1:94883752-94883802	MCF10A-Er-Src	breast:	n/a
46	chr1:94929484-94929534	AG04449	skin:	fetal
47	chr1:94929484-94929534	ProgFib	skin:	n/a
48	chr1:94884060-94884110	HAEpiC	amniotic membrane:	n/a
49	chr1:94888188-94888238	MCF-7	breast:	n/a
50	chr1:94883581-94883631	Caco-2	colon:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94882805..94885755-chr1:94886317..94890931,5	MCF-7	breast:
2	chr1:94866195..94867958-chr1:94884183..94886223,2	K562	blood:
3	chr1:94941332..94943153-chr1:94956990..94959761,2	MCF-7	breast:
4	chr1:94883956..94884476-chr11:109963954..109964551,2	Hela-S3	cervix:
5	chr1:94883408..94885801-chr1:94885846..94888306,2	K562	blood:
6	chr1:94871621..94873674-chr1:94882130..94885368,3	MCF-7	breast:
7	chr1:94878270..94880710-chr1:94881581..94884110,3	MCF-7	breast:
8	chr1:94870652..94872761-chr1:94882197..94884699,2	MCF-7	breast:
9	chr1:94870652..94872761-chr1:94882197..94884699,2	MCF-7	breast:
10	chr1:94883768..94885488-chr1:94926929..94929559,2	MCF-7	breast:
11	chr1:94899881..94901992-chr1:94904934..94907266,2	MCF-7	breast:
12	chr1:94816155..94817816-chr1:94928944..94931018,2	MCF-7	breast:
13	chr1:94851431..94853630-chr1:94859546..94862192,3	K562	blood:
14	chr1:94899881..94901992-chr1:94904934..94907266,2	MCF-7	breast:
15	chr1:94859969..94862064-chr1:94864707..94866674,2	MCF-7	breast:
16	chr1:94901652..94904489-chr1:94917080..94919308,2	MCF-7	breast:
17	chr1:94311158..94313376-chr1:94883814..94886511,2	K562	blood:
18	chr1:94859969..94862064-chr1:94864707..94866674,2	MCF-7	breast:
19	chr1:94851431..94853630-chr1:94859546..94862192,3	K562	blood:
20	chr1:94510948..94511922-chr1:94929239..94929819,2	K562	blood:
21	chr1:94883223..94885583-chr1:94928116..94929855,2	MCF-7	breast:
22	chr1:94883107..94885464-chr1:94890446..94893482,3	MCF-7	breast:
23	chr1:94851431..94853630-chr1:94859624..94862192,2	K562	blood:
24	chr1:94883693..94884231-chr19:56110193..56110901,2	Hela-S3	cervix:
25	chr1:94901652..94904489-chr1:94917080..94919308,2	MCF-7	breast:
26	chr1:94883202..94883857-chr12:10365795..10366377,2	Hela-S3	cervix:
27	chr1:94879263..94881471-chr1:94882275..94884256,2	K562	blood:
28	chr1:94871621..94873674-chr1:94882130..94885368,3	MCF-7	breast:
29	chr1:94871659..94875955-chr1:94882402..94885551,3	K562	blood:
30	chr1:94851431..94853630-chr1:94859624..94862192,2	K562	blood:
31	chr1:94923038..94925155-chr1:94932732..94934568,2	K562	blood:
32	chr1:94864885..94867606-chr1:94871384..94874031,2	K562	blood:
33	chr1:94871659..94875955-chr1:94882402..94885551,3	K562	blood:
34	chr1:94884761..94885689-chr8:37898104..37898745,2	HCT-116	colon:
35	chr1:94883231..94883773-chr6:27860386..27861366,2	Hela-S3	cervix:
36	chr1:94883202..94883926-chr16:87351047..87352034,2	Hela-S3	cervix:
37	chr1:94526680..94527603-chr1:94928967..94929584,2	K562	blood:
38	chr1:94923038..94925155-chr1:94932732..94934568,2	K562	blood:
39	chr1:94883602..94885258-chr1:94893153..94895561,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP29-6	chr1:94859295-94860100	NONHSAT004590
2	lnc-ARHGAP29-6	chr1:94860863-94862328	NONHSAT004590
3	lnc-F3-3	chr1:94917576-94917751	l_89_chr1:94917575-94970548_76bGuttman_hLF
4	lnc-F3-5	chr1:94871951-94872438	NONHSAT004591

No data

Variant related genes	Relation type
ABCD3	TF binding region
ENSG00000232918	TF binding region
ABCD3	CpG island
ENSG00000232918	CpG island
ENSG00000197153	chromatin interactions
ENSG00000179943	chromatin interactions
ENSG00000198691	chromatin interactions
ENSG00000270006	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000117528	chromatin interactions
ENSG00000260464	chromatin interactions
ENSG00000232918	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000211575	chromatin interactions
ENSG00000149289	chromatin interactions
ENSG00000139112	chromatin interactions
ENSG00000233224	chromatin interactions

Extended variants
information (count: 3339 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3339 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2391467	chr1:94850443-94850444	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191393818	chr1:94850455-94850456	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566346505	chr1:94850488-94850489	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1765617	chr1:94850526-94850527	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553690442	chr1:94850544-94850545	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567193037	chr1:94850557-94850558	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1765618	chr1:94850575-94850576	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs141924976	chr1:94850597-94850598	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575817392	chr1:94850605-94850606	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544770923	chr1:94850610-94850611	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558353037	chr1:94850636-94850637	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546798589	chr1:94850646-94850647	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372758522	chr1:94850648-94850649	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541005614	chr1:94850669-94850670	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561331058	chr1:94850719-94850720	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560377096	chr1:94850722-94850723	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150828076	chr1:94850743-94850744	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543881131	chr1:94850768-94850769	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532214472	chr1:94850811-94850812	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs728862	chr1:94850829-94850830	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532672662	chr1:94850876-94850877	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552756223	chr1:94850878-94850879	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114758878	chr1:94850911-94850912	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75472886	chr1:94850941-94850942	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569158968	chr1:94850950-94850951	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201710515	chr1:94850961-94850962	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548651319	chr1:94850981-94850982	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567235341	chr1:94851063-94851064	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs76170359	chr1:94851068-94851069	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs549073559	chr1:94851069-94851070	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs118059180	chr1:94851074-94851075	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs569220363	chr1:94851095-94851096	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs537881593	chr1:94851155-94851156	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs569384824	chr1:94851217-94851218	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183198522	chr1:94851234-94851235	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs558320047	chr1:94851242-94851243	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs902338	chr1:94851310-94851311	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs5776218	chr1:94851319-94851320	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs541296073	chr1:94851332-94851333	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs374977455	chr1:94851337-94851338	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs902337	chr1:94851376-94851377	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs374066880	chr1:94851447-94851448	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574688550	chr1:94851450-94851451	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs543809052	chr1:94851461-94851462	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs902336	chr1:94851498-94851499	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs35282342	chr1:94851512-94851513	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs563674272	chr1:94851537-94851538	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs577369590	chr1:94851578-94851579	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs201172897	chr1:94851580-94851581	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs144895986	chr1:94851601-94851602	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2220 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94846000-94850600	Enhancers	Fetal Thymus	thymus
2	chr1:94846200-94854400	Enhancers	Fetal Intestine Small	intestine
3	chr1:94846600-94851200	Enhancers	Primary hematopoietic stem cells	blood
4	chr1:94846600-94851400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:94847400-94850600	Enhancers	Stomach Mucosa	stomach
6	chr1:94847400-94851800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:94849200-94851000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr1:94849200-94851200	Enhancers	Fetal Kidney	kidney
9	chr1:94849400-94851200	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr1:94849400-94851600	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr1:94849600-94850600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:94849600-94850800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:94849600-94851200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:94849600-94851200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:94849600-94851400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr1:94849600-94851800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr1:94849600-94852200	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr1:94849800-94851000	Weak transcription	Esophagus	oesophagus
19	chr1:94849800-94851200	Enhancers	Right Atrium	heart
20	chr1:94850000-94850600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:94850000-94851200	Flanking Active TSS	Duodenum Mucosa	Duodenum
22	chr1:94850000-94851200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr1:94850000-94851400	Flanking Active TSS	HepG2	liver
24	chr1:94850000-94854000	Enhancers	Fetal Intestine Large	intestine
25	chr1:94850200-94850600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr1:94850200-94850800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:94850200-94850800	Enhancers	Primary B cells from peripheral blood	blood
28	chr1:94850200-94850800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr1:94850200-94850800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr1:94850200-94850800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr1:94850200-94850800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:94850200-94850800	Flanking Active TSS	Liver	Liver
33	chr1:94850200-94850800	Enhancers	Lung	lung
34	chr1:94850200-94850800	Enhancers	HSMM	muscle
35	chr1:94850200-94851000	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr1:94850200-94851200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr1:94850200-94851200	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr1:94850200-94851200	Enhancers	Pancreas	Pancrea
39	chr1:94850200-94851200	Flanking Active TSS	Thymus	Thymus
40	chr1:94850200-94851200	Enhancers	Spleen	Spleen
41	chr1:94850200-94851200	Flanking Active TSS	Dnd41	blood
42	chr1:94850200-94851400	Active TSS	Rectal Smooth Muscle	rectum
43	chr1:94850200-94851400	Flanking Active TSS	A549	lung
44	chr1:94850400-94850800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
45	chr1:94850400-94850800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr1:94850400-94850800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:94850400-94850800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr1:94850400-94850800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr1:94850400-94851000	Enhancers	Primary B cells from cord blood	blood
50	chr1:94850400-94851200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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