Variant report

Variant	nsv491784
Chromosome Location	chr1:79146141-79853482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3430)
CpG islands
(count:1408)
Chromatin interactive
region (count:36)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3430 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:79305459-79305734	K562	blood:	n/a	n/a
2	ARID3A	chr1:79305438-79305769	HepG2	liver:	n/a	n/a
3	ATF1	chr1:79259668-79259884	K562	blood:	n/a	n/a
4	ATF2	chr1:79507719-79508191	GM12878	blood:	n/a	n/a
5	ATF2	chr1:79506114-79506881	GM12878	blood:	n/a	n/a
6	ATF2	chr1:79507696-79508185	GM12878	blood:	n/a	n/a
7	ATF2	chr1:79658867-79659458	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:79505821-79506890	GM12878	blood:	n/a	n/a
9	ATF2	chr1:79350690-79350993	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:79728345-79728782	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:79507950-79508076	K562	blood:	n/a	n/a
12	BACH1	chr1:79508075-79508122	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:79658878-79659483	H1-hESC	embryonic stem cell:	n/a	chr1:79659052-79659066
14	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:79545497-79545905	H1-hESC	embryonic stem cell:	n/a	chr1:79545669-79545683
16	BATF	chr1:79186923-79187193	GM12878	blood:	n/a	chr1:79187031-79187042
17	BATF	chr1:79507758-79508057	GM12878	blood:	n/a	n/a
18	BATF	chr1:79320756-79321223	GM12878	blood:	n/a	chr1:79320825-79320834
19	BATF	chr1:79507747-79508138	GM12878	blood:	n/a	n/a
20	BATF	chr1:79506304-79506770	GM12878	blood:	n/a	n/a
21	BATF	chr1:79658862-79659246	GM12878	blood:	n/a	chr1:79659055-79659066
22	BATF	chr1:79186827-79187216	GM12878	blood:	n/a	chr1:79187031-79187042
23	BATF	chr1:79658879-79659230	GM12878	blood:	n/a	chr1:79659055-79659066
24	BATF	chr1:79506383-79506726	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:79659126-79659356	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr1:79506346-79506753	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:79728386-79728591	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr1:79300086-79300356	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:79603898-79604245	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr1:79507862-79508010	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:79604022-79604167	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL11A	chr1:79262911-79263285	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr1:79507836-79508150	GM12878	blood:	n/a	n/a
34	BCL3	chr1:79158093-79158327	GM12878	blood:	n/a	n/a
35	BCL3	chr1:79507766-79508061	GM12878	blood:	n/a	n/a
36	BCL3	chr1:79506306-79506801	GM12878	blood:	n/a	n/a
37	BCLAF1	chr1:79507869-79508207	GM12878	blood:	n/a	n/a
38	BCLAF1	chr1:79506260-79506789	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:79655568-79655570	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:79297522-79297765	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:79158440-79158519	HepG2	liver:	n/a	n/a
43	BHLHE40	chr1:79320988-79321254	GM12878	blood:	n/a	n/a
44	BRCA1	chr1:79617796-79617801	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr1:79509475-79509505	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr1:79262865-79262987	H1-hESC	embryonic stem cell:	n/a	n/a
49	CBX3	chr1:79297275-79297897	HCT-116	colon:	n/a	n/a
50	CBX3	chr1:79658842-79659475	HCT-116	colon:	n/a	n/a

(count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79594960-79595010	AG09319	gingival:	n/a
2	chr1:79350918-79350968	LNCaP	prostate:	n/a
3	chr1:79726633-79726683	AoSMC	blood vessel:	n/a
4	chr1:79472408-79472458	PFSK-1	brain:	n/a
5	chr1:79726633-79726683	HepG2	liver:	n/a
6	chr1:79594960-79595010	AG09319	gingival:	n/a
7	chr1:79350918-79350968	LNCaP	prostate:	n/a
8	chr1:79726633-79726683	AoSMC	blood vessel:	n/a
9	chr1:79472408-79472458	PFSK-1	brain:	n/a
10	chr1:79726633-79726683	HepG2	liver:	n/a
11	chr1:79830414-79830464	HL-60	blood:	n/a
12	chr1:79472532-79472582	NT2-D1	testis:	n/a
13	chr1:79726633-79726683	IMR90	lung:	fetal
14	chr1:79472408-79472458	ECC-1	luminal epithelium:	n/a
15	chr1:79726633-79726683	SAEC	small airway:	n/a
16	chr1:79726633-79726683	MCF-7	breast:	n/a
17	chr1:79801791-79801841	Hepatocyte	liver:	n/a
18	chr1:79307043-79307093	BJ	skin:	n/a
19	chr1:79627622-79627672	SK-N-SH_RA	brain:	n/a
20	chr1:79472361-79472411	HCT-116	colon:	n/a
21	chr1:79473783-79473833	SAEC	small airway:	n/a
22	chr1:79726633-79726683	K562	blood:	n/a
23	chr1:79472643-79472693	GM12891	blood:	n/a
24	chr1:79471984-79472034	GM06990	blood:	n/a
25	chr1:79472643-79472693	NB4	blood:	n/a
26	chr1:79472532-79472582	Hepatocyte	liver:	n/a
27	chr1:79728608-79728658	AG04449	skin:	fetal
28	chr1:79594960-79595010	H1-hESC	embryonic stem cell:	embryo
29	chr1:79472532-79472582	HCT-116	colon:	n/a
30	chr1:79472282-79472332	GM19239	blood:	n/a
31	chr1:79658903-79658953	K562	blood:	n/a
32	chr1:79472643-79472693	T-47D	breast:	n/a
33	chr1:79474718-79474768	HIPEpiC	eye:	n/a
34	chr1:79472452-79472502	HCPEpiC	choroid plexus:	n/a
35	chr1:79627622-79627672	PrEC	prostate:	n/a
36	chr1:79658903-79658953	Jurkat	blood:	n/a
37	chr1:79307043-79307093	HepG2	liver:	n/a
38	chr1:79728608-79728658	Hela-S3	cervix:	n/a
39	chr1:79830414-79830464	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:79658903-79658953	HAEpiC	amniotic membrane:	n/a
41	chr1:79801791-79801841	A549	lung:	n/a
42	chr1:79472643-79472693	NHBE	bronchial:	n/a
43	chr1:79350918-79350968	AG09319	gingival:	n/a
44	chr1:79350918-79350968	AoSMC	blood vessel:	n/a
45	chr1:79472558-79472608	GM06990	blood:	n/a
46	chr1:79728608-79728658	AG10803	skin:	n/a
47	chr1:79726633-79726683	SK-N-MC	brain:	n/a
48	chr1:79471984-79472034	A549	lung:	n/a
49	chr1:79472452-79472502	U87	brain:	n/a
50	chr1:79307043-79307093	HRPEpiC	eye:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
2	chr1:79717844..79719500-chr13:74206627..74209123,2	MCF-7	breast:
3	chr1:79304951..79305958-chr1:79662942..79663752,3	MCF-7	breast:
4	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
5	chr1:79299275..79301209-chr1:79305174..79307511,2	K562	blood:
6	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
7	chr1:79702123..79704938-chr10:125479865..125482682,2	MCF-7	breast:
8	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:
9	chr1:79744482..79747181-chr12:54772744..54775487,2	MCF-7	breast:
10	chr1:79154179..79155005-chr1:79663219..79663974,2	MCF-7	breast:
11	chr1:79826260..79828689-chr6:111008268..111010656,2	MCF-7	breast:
12	chr1:79281703..79284146-chr1:79308021..79310225,2	K562	blood:
13	chr1:79728080..79730865-chr1:79731789..79734341,2	K562	blood:
14	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
15	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:
16	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
17	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
18	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
19	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
20	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:
21	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
22	chr1:79728080..79730865-chr1:79731789..79734341,2	K562	blood:
23	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
24	chr1:79281703..79284146-chr1:79308021..79310225,2	K562	blood:
25	chr1:79304951..79305958-chr1:79662942..79663752,3	MCF-7	breast:
26	chr1:79266346..79267150-chr1:79858034..79858765,3	MCF-7	breast:
27	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
28	chr1:79154179..79155005-chr1:79663219..79663974,2	MCF-7	breast:
29	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
30	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
31	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
32	chr1:79299275..79301209-chr1:79305174..79307511,2	K562	blood:
33	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
34	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:
35	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:
36	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-2	chr1:79735991-79736371	NONHSAT004088
2	lnc-IFI44-7	chr1:79562042-79562232	NONHSAT004086
3	lnc-IFI44-2	chr1:79775231-79775405	XLOC_000266
4	lnc-IFI44-2	chr1:79775371-79775405	XLOC_000266
5	lnc-IFI44-1	chr1:79790385-79790548	ENSG00000235011.2
6	lnc-ELTD1-4	chr1:79787090-79787278	XLOC_000880
7	lnc-IFI44-2	chr1:79775231-79775346	XLOC_000266
8	lnc-IFI44-2	chr1:79775230-79775405	NONHSAT004088
9	lnc-ELTD1-5	chr1:79789342-79789745	XLOC_000881
10	lnc-IFI44-2	chr1:79842763-79842816	XLOC_000266
11	lnc-ELTD1-5	chr1:79789429-79789745	NONHSAT004093
12	lnc-IFI44-1	chr1:79789454-79789644	XLOC_000267
13	lnc-ELTD1-5	chr1:79790271-79790416	NONHSAT004093
14	lnc-ELTD1-3	chr1:79778966-79779074	XLOC_000879
15	lnc-ELTD1-2	chr1:79490858-79491009	XLOC_000877
16	lnc-IFI44-1	chr1:79789454-79789644	ENSG00000235011.2
17	lnc-ELTD1-1	chr1:79351642-79351681	NONHSAT004083
18	lnc-ELTD1-4	chr1:79786813-79786877	XLOC_000880
19	lnc-ELTD1-1	chr1:79346569-79346750	NONHSAT004083
20	lnc-IFI44-7	chr1:79562972-79563122	NONHSAT004086
21	lnc-ELTD1-2	chr1:79493775-79493876	XLOC_000877
22	lnc-IFI44-1	chr1:79790384-79790534	XLOC_000267
23	lnc-ELTD1-5	chr1:79790271-79790552	XLOC_000881
24	lnc-ELTD1-5	chr1:79788603-79788631	NONHSAT004093
25	lnc-ELTD1-3	chr1:79775130-79775346	XLOC_000879
26	lnc-IFI44-1	chr1:79790270-79790552	NONHSAT004094
27	lnc-IFI44-2	chr1:79735992-79736371	XLOC_000266
28	lnc-IFI44-1	chr1:79789341-79789745	NONHSAT004094
29	lnc-IFI44-2	chr1:79736086-79736371	XLOC_000266

No data

Variant related genes	Relation type
ENSG00000266388	TF binding region
ENSG00000235011	TF binding region
ENSG00000221683	TF binding region
ENSG00000235400	TF binding region
ELTD1	TF binding region
PSAT1P3	TF binding region
ENSG00000266388	CpG island
ENSG00000235011	CpG island
ENSG00000221683	CpG island
ENSG00000235400	CpG island
ELTD1	CpG island
PSAT1P3	CpG island
ENSG00000161642	chromatin interactions
DYRK2	miRNA target sites
RELA	miRNA target sites
BCL11A	miRNA target sites
IGSF1	miRNA target sites
C9orf5	miRNA target sites
TCF7L2	miRNA target sites
ZNF652	miRNA target sites

Extended variants
information (count: 18730 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:18730 , 50 per page) page: 1 2 3 4 5 6 7 ... 375

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187577012	chr1:79146151-79146152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75712493	chr1:79146184-79146185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375337107	chr1:79146224-79146225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566810406	chr1:79146233-79146234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547576275	chr1:79146351-79146352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572568118	chr1:79146416-79146417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142955309	chr1:79146417-79146418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1547181	chr1:79146434-79146435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs578120930	chr1:79146457-79146458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192791807	chr1:79146481-79146482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563966961	chr1:79146495-79146496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538664497	chr1:79146513-79146514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549363020	chr1:79146517-79146518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368392363	chr1:79146552-79146553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528525075	chr1:79146577-79146578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182914203	chr1:79146578-79146579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151121298	chr1:79146583-79146584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538787783	chr1:79146593-79146594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113858080	chr1:79146596-79146597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569103055	chr1:79146613-79146614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77496307	chr1:79146655-79146656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554476118	chr1:79146689-79146690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377251475	chr1:79146698-79146699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12755937	chr1:79146699-79146700	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs146796321	chr1:79146709-79146710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541168692	chr1:79146718-79146719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113638719	chr1:79146748-79146749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140603320	chr1:79146774-79146775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375748174	chr1:79146808-79146809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145738091	chr1:79146840-79146841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146711362	chr1:79146873-79146874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563745510	chr1:79146878-79146879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111716197	chr1:79146893-79146894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6695058	chr1:79146909-79146910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs561616278	chr1:79146921-79146922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528487310	chr1:79146928-79146929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188157245	chr1:79146961-79146962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565336170	chr1:79146971-79146972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375968453	chr1:79146984-79146985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556279864	chr1:79147003-79147004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550713067	chr1:79147032-79147033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191754425	chr1:79147057-79147058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536067307	chr1:79147058-79147059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199941617	chr1:79147102-79147103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377593301	chr1:79147130-79147131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548075071	chr1:79147166-79147167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566469815	chr1:79147189-79147190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370564081	chr1:79147194-79147195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377396044	chr1:79147195-79147196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374327936	chr1:79147199-79147200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1787 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79117600-79153000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:79126600-79148000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr1:79138600-79148200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:79143600-79151200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:79144200-79148000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:79144200-79148000	Weak transcription	Osteobl	bone
7	chr1:79144400-79148200	Weak transcription	HSMM	muscle
8	chr1:79148000-79148400	Enhancers	Osteobl	bone
9	chr1:79148000-79148600	Enhancers	NHDF-Ad	bronchial
10	chr1:79148000-79149000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:79148000-79149000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr1:79148000-79149200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:79148200-79148400	Enhancers	HMEC	breast
14	chr1:79148200-79148600	Enhancers	HSMM	muscle
15	chr1:79148200-79149000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:79148200-79149000	Enhancers	NHLF	lung
17	chr1:79148200-79149800	Enhancers	HUVEC	blood vessel
18	chr1:79148400-79153000	Weak transcription	Osteobl	bone
19	chr1:79148600-79153000	Weak transcription	HSMM	muscle
20	chr1:79148600-79153000	Weak transcription	NHDF-Ad	bronchial
21	chr1:79149000-79152800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr1:79149000-79153200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:79149000-79153400	Weak transcription	NHLF	lung
24	chr1:79149200-79152800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:79149600-79149800	Enhancers	Right Atrium	heart
26	chr1:79149800-79153400	Weak transcription	HUVEC	blood vessel
27	chr1:79150000-79152600	Weak transcription	Liver	Liver
28	chr1:79150800-79151400	Enhancers	Brain Germinal Matrix	brain
29	chr1:79151200-79156400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:79152600-79154600	Enhancers	Liver	Liver
31	chr1:79152800-79153400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr1:79152800-79159000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:79153000-79153600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:79153000-79155000	Enhancers	Fetal Brain Male	brain
35	chr1:79153000-79155000	Enhancers	HSMM	muscle
36	chr1:79153000-79155200	Enhancers	Osteobl	bone
37	chr1:79153000-79159000	Enhancers	NHDF-Ad	bronchial
38	chr1:79153200-79154200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:79153200-79158800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:79153400-79153800	Enhancers	NHEK	skin
41	chr1:79153400-79154000	Enhancers	HUVEC	blood vessel
42	chr1:79153400-79154400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr1:79153400-79154400	Enhancers	HMEC	breast
44	chr1:79153400-79154400	Enhancers	NHLF	lung
45	chr1:79153400-79154600	Enhancers	NH-A	brain
46	chr1:79153400-79155000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:79153400-79155000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:79153600-79154400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr1:79153800-79154400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:79154200-79154400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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