Variant report

Variant	nsv882389
Chromosome Location	chr5:95144952-95173887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1372)
CpG islands
(count:1038)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:95158181-95158443	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:95170684-95170932	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:95159281-95159700	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:95159302-95159649	K562	blood:	n/a	n/a
5	ARID3A	chr5:95162875-95163278	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:95157945-95158819	K562	blood:	n/a	n/a
7	ATF2	chr5:95170026-95170881	GM12878	blood:	n/a	n/a
8	ATF2	chr5:95144257-95144985	GM12878	blood:	n/a	n/a
9	ATF2	chr5:95169802-95171042	GM12878	blood:	n/a	n/a
10	ATF2	chr5:95159257-95160051	GM12878	blood:	n/a	n/a
11	ATF2	chr5:95172123-95172700	GM12878	blood:	n/a	n/a
12	ATF2	chr5:95172148-95172612	GM12878	blood:	n/a	n/a
13	BACH1	chr5:95158633-95158901	K562	blood:	n/a	n/a
14	BACH1	chr5:95158536-95158853	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr5:95170025-95170408	GM12878	blood:	n/a	n/a
16	BATF	chr5:95170067-95170428	GM12878	blood:	n/a	n/a
17	BATF	chr5:95157110-95157375	GM12878	blood:	n/a	n/a
18	BATF	chr5:95172192-95172615	GM12878	blood:	n/a	n/a
19	BATF	chr5:95172247-95172565	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:95170091-95170366	GM12878	blood:	n/a	n/a
21	BCL3	chr5:95151004-95151329	GM12878	blood:	n/a	n/a
22	BCL3	chr5:95159189-95159848	A549	lung:	n/a	n/a
23	BCLAF1	chr5:95157006-95157464	GM12878	blood:	n/a	n/a
24	BCLAF1	chr5:95170509-95171071	GM12878	blood:	n/a	chr5:95170809-95170822
25	BCLAF1	chr5:95170454-95170940	GM12878	blood:	n/a	chr5:95170809-95170822
26	BCLAF1	chr5:95158075-95158725	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:95159458-95160310	GM12878	blood:	n/a	n/a
28	BCLAF1	chr5:95144291-95145176	GM12878	blood:	n/a	n/a
29	BCLAF1	chr5:95170109-95170478	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:95147872-95148096	K562	blood:	n/a	n/a
31	BHLHE40	chr5:95163513-95163615	K562	blood:	n/a	n/a
32	BHLHE40	chr5:95170139-95170951	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:95157178-95157394	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:95157735-95158918	GM12878	blood:	n/a	n/a
35	BHLHE40	chr5:95159309-95160421	K562	blood:	n/a	n/a
36	BHLHE40	chr5:95162863-95163372	HepG2	liver:	n/a	n/a
37	BHLHE40	chr5:95161244-95161853	K562	blood:	n/a	n/a
38	BHLHE40	chr5:95159087-95160368	HepG2	liver:	n/a	n/a
39	BHLHE40	chr5:95144377-95145294	GM12878	blood:	n/a	n/a
40	BHLHE40	chr5:95157794-95158388	K562	blood:	n/a	n/a
41	BHLHE40	chr5:95159538-95160256	GM12878	blood:	n/a	n/a
42	BRCA1	chr5:95156942-95157093	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr5:95170855-95170862	HepG2	liver:	n/a	n/a
44	BRCA1	chr5:95159419-95160173	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr5:95159612-95160031	HepG2	liver:	n/a	n/a
46	BRCA1	chr5:95170689-95170919	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr5:95157680-95157695	HepG2	liver:	n/a	n/a
48	BRCA1	chr5:95162861-95163241	HepG2	liver:	n/a	n/a
49	CBX3	chr5:95157700-95158284	K562	blood:	n/a	n/a
50	CCNT2	chr5:95170704-95170915	K562	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:95158523-95158573	MCF-7	breast:	n/a
2	chr5:95158523-95158573	MCF-7	breast:	n/a
3	chr5:95170798-95170848	HEEpiC	esophagus:	n/a
4	chr5:95158068-95158118	Jurkat	blood:	n/a
5	chr5:95170684-95170734	GM06990	blood:	n/a
6	chr5:95170684-95170734	SAEC	small airway:	n/a
7	chr5:95170684-95170734	HMEC	breast:	n/a
8	chr5:95159639-95159689	HRE	kidney:	n/a
9	chr5:95159365-95159415	SKMC	muscle:	n/a
10	chr5:95158141-95158191	GM19239	blood:	n/a
11	chr5:95159365-95159415	GM12878	blood:	n/a
12	chr5:95170684-95170734	Caco-2	colon:	n/a
13	chr5:95145218-95145268	SKMC	muscle:	n/a
14	chr5:95166697-95166747	HRPEpiC	eye:	n/a
15	chr5:95159614-95159664	HAEpiC	amniotic membrane:	n/a
16	chr5:95158141-95158191	HRE	kidney:	n/a
17	chr5:95159423-95159473	NT2-D1	testis:	n/a
18	chr5:95158523-95158573	HCPEpiC	choroid plexus:	n/a
19	chr5:95145218-95145268	PANC-1	pancreas:	n/a
20	chr5:95159423-95159473	ECC-1	luminal epithelium:	n/a
21	chr5:95158141-95158191	HUVEC	blood vessel:	n/a
22	chr5:95170684-95170734	PANC-1	pancreas:	n/a
23	chr5:95151391-95151441	Caco-2	colon:	n/a
24	chr5:95159614-95159664	NHDF-neo	bronchial:	n/a
25	chr5:95153995-95154045	MCF-7	breast:	n/a
26	chr5:95170684-95170734	H1-hESC	embryonic stem cell:	embryo
27	chr5:95171699-95171749	A549	lung:	n/a
28	chr5:95159614-95159664	HRPEpiC	eye:	n/a
29	chr5:95159614-95159664	HRCEpiC	kidney:	n/a
30	chr5:95166697-95166747	HCF	heart:	n/a
31	chr5:95169805-95169855	AG09309	skin:	n/a
32	chr5:95158523-95158573	A549	lung:	n/a
33	chr5:95169805-95169855	HRE	kidney:	n/a
34	chr5:95159423-95159473	NHDF-neo	bronchial:	n/a
35	chr5:95166697-95166747	ECC-1	luminal epithelium:	n/a
36	chr5:95159614-95159664	BJ	skin:	n/a
37	chr5:95159365-95159415	ProgFib	skin:	n/a
38	chr5:95170798-95170848	CMK	blood:	n/a
39	chr5:95166697-95166747	NH-A	brain:	n/a
40	chr5:95170798-95170848	AoSMC	blood vessel:	n/a
41	chr5:95158068-95158118	HEEpiC	esophagus:	n/a
42	chr5:95159365-95159415	ovcar-3	ovarian:	n/a
43	chr5:95158433-95158483	AG10803	skin:	n/a
44	chr5:95159365-95159415	HIPEpiC	eye:	n/a
45	chr5:95171699-95171749	PrEC	prostate:	n/a
46	chr5:95151391-95151441	GM12892	blood:	n/a
47	chr5:95145218-95145268	SAEC	small airway:	n/a
48	chr5:95158068-95158118	AG04449	skin:	fetal
49	chr5:95153995-95154045	IMR90	lung:	fetal
50	chr5:95170798-95170848	ovcar-3	ovarian:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:95152970..95154938-chr5:95156399..95158380,2	MCF-7	breast:
2	chr5:95149457..95151084-chr5:95151205..95153172,2	K562	blood:
3	chr5:95168597..95170209-chr5:95172089..95173618,2	K562	blood:
4	chr5:95156501..95159437-chr5:95167856..95170336,2	MCF-7	breast:
5	chr5:95159839..95161506-chr5:95164819..95166390,2	MCF-7	breast:
6	chr5:94981172..94985318-chr5:95169805..95176246,5	MCF-7	breast:
7	chr5:95097577..95099971-chr5:95142843..95145150,2	K562	blood:
8	chr5:95157133..95161008-chr5:95170364..95173601,6	MCF-7	breast:
9	chr5:95168597..95170209-chr5:95172089..95173618,2	K562	blood:
10	chr5:95129490..95131493-chr5:95145014..95147003,2	K562	blood:
11	chr5:95167615..95170613-chr5:95172553..95174092,2	MCF-7	breast:
12	chr5:95148182..95149810-chr5:95152162..95154421,2	MCF-7	breast:
13	chr5:95140024..95141907-chr5:95144179..95145770,2	MCF-7	breast:
14	chr5:94890695..94892363-chr5:95148648..95150304,2	K562	blood:
15	chr5:95144281..95145870-chr5:95178022..95180919,2	MCF-7	breast:
16	chr5:95162262..95164257-chr5:95169999..95171533,2	MCF-7	breast:
17	chr5:95164709..95167343-chr5:95169252..95170958,2	MCF-7	breast:
18	chr5:95165646..95168602-chr5:95177618..95179620,3	MCF-7	breast:
19	chr16:31191124..31191940-chr5:95158038..95158783,2	Hela-S3	cervix:
20	chr5:95151960..95154634-chr5:95154994..95157886,2	K562	blood:
21	chr5:95159650..95161680-chr5:95169175..95170926,2	MCF-7	breast:
22	chr5:95157133..95161008-chr5:95170364..95173601,6	MCF-7	breast:
23	chr5:95156277..95158130-chr5:95161683..95164482,2	K562	blood:
24	chr5:95141198..95143249-chr5:95146319..95147835,2	K562	blood:
25	chr5:95152689..95154883-chr5:95158180..95160300,2	K562	blood:
26	chr1:29352126..29352937-chr5:95144638..95145200,2	NB4	blood:
27	chr5:95167615..95170613-chr5:95172553..95174092,2	MCF-7	breast:
28	chr5:95149457..95151084-chr5:95151205..95153172,2	K562	blood:
29	chr5:95159839..95161506-chr5:95164819..95166390,2	MCF-7	breast:
30	chr5:94997987..94999624-chr5:95155659..95157984,2	K562	blood:
31	chr5:95131346..95133321-chr5:95171352..95173975,2	MCF-7	breast:
32	chr5:95156076..95158959-chr5:95159159..95161216,2	MCF-7	breast:
33	chr5:95148182..95149810-chr5:95152162..95154421,2	MCF-7	breast:
34	chr5:95145254..95146894-chr5:95156475..95158183,2	K562	blood:
35	chr5:158649..159235-chr5:95159285..95159785,2	Hela-S3	cervix:
36	chr5:95160713..95163370-chr5:95164070..95166105,2	MCF-7	breast:
37	chr5:95147817..95150624-chr5:95169490..95171087,2	K562	blood:
38	chr5:95065571..95068096-chr5:95150283..95152215,2	MCF-7	breast:
39	chr5:95158093..95160900-chr5:95173063..95176588,5	MCF-7	breast:
40	chr5:95149187..95152215-chr5:95156568..95159390,5	MCF-7	breast:
41	chr5:94890265..94891768-chr5:95158248..95160600,2	K562	blood:
42	chr5:95137694..95139720-chr5:95158837..95160612,2	MCF-7	breast:
43	chr5:95160713..95163370-chr5:95164070..95166105,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLRX-2	chr5:95170128-95170405	NONHSAT102864
2	lnc-GLRX-2	chr5:95170611-95170750	NONHSAT102864
3	lnc-GLRX-1	chr5:95171647-95171960	ENSG00000251409.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	GLRX	hsa-miR-128-3p	chr5:95149599-95149619
2	GLRX	hsa-miR-16-5p	chr5:95149556-95149577
3	GLRX	hsa-miR-16-5p	chr5:95150243-95150264
4	GLRX	hsa-miR-128-3p	chr5:95149915-95149937

Variant related genes	Relation type
ENSG00000251000	TF binding region
GLRX	TF binding region
ENSG00000251000	CpG island
GLRX	CpG island
ENSG00000251000	chromatin interactions
ENSG00000175449	chromatin interactions
ENSG00000198677	chromatin interactions
ENSG00000173221	chromatin interactions
ENSG00000250240	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000164292	chromatin interactions
ENSG00000164291	chromatin interactions

Extended variants
information (count: 1035 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17085122	chr5:95144952-95144953	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548264985	chr5:95144978-95144979	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs56727798	chr5:95144994-95144995	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs112343313	chr5:95145011-95145012	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537030872	chr5:95145030-95145031	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538814184	chr5:95145050-95145051	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111477991	chr5:95145058-95145059	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550525228	chr5:95145065-95145066	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570328172	chr5:95145075-95145076	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73138405	chr5:95145076-95145077	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558835193	chr5:95145084-95145085	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566257394	chr5:95145086-95145087	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148355247	chr5:95145118-95145119	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17085125	chr5:95145133-95145134	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116688917	chr5:95145193-95145194	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141674581	chr5:95145211-95145212	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs186094200	chr5:95145218-95145219	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs576687342	chr5:95145219-95145220	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs538274549	chr5:95145230-95145231	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545981710	chr5:95145294-95145295	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs75791184	chr5:95145310-95145311	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559331759	chr5:95145404-95145405	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150544033	chr5:95145424-95145425	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574921968	chr5:95145505-95145506	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs189761259	chr5:95145769-95145770	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561747644	chr5:95145786-95145787	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530543857	chr5:95145797-95145798	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550552100	chr5:95145798-95145799	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs10042284	chr5:95145802-95145803	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532737933	chr5:95145840-95145841	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372359721	chr5:95145890-95145891	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368937327	chr5:95145894-95145895	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552822871	chr5:95145925-95145926	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566176269	chr5:95145935-95145936	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181459190	chr5:95145978-95145979	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112113790	chr5:95146049-95146050	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115610208	chr5:95146078-95146079	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142721817	chr5:95146089-95146090	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556890883	chr5:95146114-95146115	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576824863	chr5:95146130-95146131	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545993101	chr5:95146174-95146175	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546311938	chr5:95146186-95146187	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143093631	chr5:95146222-95146223	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372116837	chr5:95146227-95146228	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545819194	chr5:95146228-95146229	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553220578	chr5:95146244-95146245	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572983939	chr5:95146270-95146271	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs5869694	chr5:95146284-95146285	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs397882807	chr5:95146290-95146291	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs576240353	chr5:95146316-95146317	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2230 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95115400-95157000	Weak transcription	Aorta	Aorta
2	chr5:95121000-95156800	Weak transcription	Brain Germinal Matrix	brain
3	chr5:95124600-95154400	Weak transcription	Brain Angular Gyrus	brain
4	chr5:95125000-95154400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr5:95127800-95149200	Weak transcription	Fetal Brain Female	brain
6	chr5:95130000-95145000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr5:95130000-95145000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr5:95130000-95157400	Weak transcription	Ovary	ovary
9	chr5:95130400-95146000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr5:95133600-95147800	Weak transcription	K562	blood
11	chr5:95139600-95145400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:95139800-95154200	Weak transcription	Pancreas	Pancrea
13	chr5:95141200-95145000	Weak transcription	Brain Hippocampus Middle	brain
14	chr5:95141400-95145400	Weak transcription	HepG2	liver
15	chr5:95142800-95148000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr5:95143000-95148600	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr5:95143200-95145600	Enhancers	Fetal Muscle Leg	muscle
18	chr5:95143200-95147600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr5:95143200-95148400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:95143200-95153600	Genic enhancers	Fetal Thymus	thymus
21	chr5:95143400-95148000	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr5:95143600-95146000	Genic enhancers	Fetal Intestine Small	intestine
23	chr5:95143600-95146600	Enhancers	Fetal Stomach	stomach
24	chr5:95143600-95146800	Enhancers	Colonic Mucosa	Colon
25	chr5:95143600-95147000	Enhancers	Small Intestine	intestine
26	chr5:95143600-95147800	Enhancers	Primary hematopoietic stem cells	blood
27	chr5:95143800-95145000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:95143800-95145000	Flanking Active TSS	Primary T cells from cord blood	blood
29	chr5:95143800-95145000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
30	chr5:95143800-95145600	Genic enhancers	HSMM	muscle
31	chr5:95143800-95145800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr5:95143800-95145800	Enhancers	Brain Anterior Caudate	brain
33	chr5:95143800-95146200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr5:95143800-95146200	Enhancers	A549	lung
35	chr5:95143800-95146600	Enhancers	Placenta	Placenta
36	chr5:95143800-95146800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:95143800-95147200	Enhancers	Stomach Mucosa	stomach
38	chr5:95143800-95147800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:95143800-95147800	Enhancers	Fetal Intestine Large	intestine
40	chr5:95143800-95148400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:95143800-95149600	Enhancers	Fetal Lung	lung
42	chr5:95144000-95145200	Enhancers	Brain Substantia Nigra	brain
43	chr5:95144000-95145600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr5:95144000-95145600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
45	chr5:95144000-95145600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr5:95144000-95145600	Enhancers	NHEK	skin
47	chr5:95144000-95146200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:95144000-95146600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:95144000-95146800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr5:95144200-95145000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood

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