Variant report

Variant	nsv537825
Chromosome Location	chr5:99745775-100133140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3286)
CpG islands
(count:1405)
Chromatin interactive
region (count:87)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3286 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:99990630-99990941	K562	blood:	n/a	n/a
2	ARID3A	chr5:99983489-99983958	K562	blood:	n/a	n/a
3	ARID3A	chr5:99982017-99982085	K562	blood:	n/a	n/a
4	ARID3A	chr5:99977601-99977922	K562	blood:	n/a	n/a
5	ARID3A	chr5:99913247-99913398	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:99931174-99931491	HepG2	liver:	n/a	n/a
7	ATF1	chr5:99870740-99871206	K562	blood:	n/a	n/a
8	ATF1	chr5:99990201-99990376	K562	blood:	n/a	n/a
9	ATF1	chr5:99931269-99931451	K562	blood:	n/a	n/a
10	ATF2	chr5:100113239-100113801	GM12878	blood:	n/a	n/a
11	ATF2	chr5:99870603-99871255	GM12878	blood:	n/a	chr5:99870979-99870990
12	ATF2	chr5:100115814-100116618	GM12878	blood:	n/a	n/a
13	ATF2	chr5:99805499-99805973	GM12878	blood:	n/a	n/a
14	ATF2	chr5:100113254-100113986	GM12878	blood:	n/a	n/a
15	ATF2	chr5:99870731-99871119	H1-hESC	embryonic stem cell:	n/a	chr5:99870979-99870990
16	ATF2	chr5:99870721-99871127	H1-hESC	embryonic stem cell:	n/a	chr5:99870979-99870990
17	ATF2	chr5:99870739-99871221	GM12878	blood:	n/a	chr5:99870979-99870990
18	ATF3	chr5:99870861-99871135	K562	blood:	n/a	chr5:99870978-99870988 chr5:99870981-99870989 chr5:99870978-99870988 chr5:99870981-99870988 chr5:99870979-99870990 chr5:99870981-99870992 chr5:99870977-99870992 chr5:99870979-99870990 chr5:99870978-99870991 chr5:99870981-99870991 chr5:99870977-99870990 chr5:99870978-99870989
19	BACH1	chr5:100000078-100000111	K562	blood:	n/a	n/a
20	BACH1	chr5:100096929-100097209	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:99929015-99929033	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr5:99963124-99963144	K562	blood:	n/a	n/a
23	BACH1	chr5:100096973-100097266	K562	blood:	n/a	n/a
24	BATF	chr5:100124193-100124393	GM12878	blood:	n/a	n/a
25	BATF	chr5:100067561-100067816	GM12878	blood:	n/a	n/a
26	BATF	chr5:99886169-99886390	GM12878	blood:	n/a	n/a
27	BATF	chr5:100113325-100113660	GM12878	blood:	n/a	n/a
28	BATF	chr5:99805639-99805821	GM12878	blood:	n/a	n/a
29	BATF	chr5:100113362-100113705	GM12878	blood:	n/a	n/a
30	BATF	chr5:99805585-99805811	GM12878	blood:	n/a	n/a
31	BCL11A	chr5:99886437-99886629	GM12878	blood:	n/a	n/a
32	BCL11A	chr5:99805514-99805830	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:99919773-99920253	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:99805489-99805819	GM12878	blood:	n/a	n/a
35	BCL11A	chr5:100113452-100113629	GM12878	blood:	n/a	n/a
36	BCL11A	chr5:100113380-100113701	GM12878	blood:	n/a	n/a
37	BCL11A	chr5:99919820-99920240	GM12878	blood:	n/a	n/a
38	BCL3	chr5:100113343-100113674	GM12878	blood:	n/a	n/a
39	BCLAF1	chr5:100113272-100113938	GM12878	blood:	n/a	n/a
40	BCLAF1	chr5:100067447-100067934	GM12878	blood:	n/a	n/a
41	BCLAF1	chr5:100113279-100113876	GM12878	blood:	n/a	n/a
42	BCLAF1	chr5:99886248-99886772	GM12878	blood:	n/a	n/a
43	BCLAF1	chr5:99870672-99871419	GM12878	blood:	n/a	chr5:99871059-99871068
44	BCLAF1	chr5:100116020-100116573	GM12878	blood:	n/a	n/a
45	BCLAF1	chr5:99765967-99766325	GM12878	blood:	n/a	n/a
46	BCLAF1	chr5:100115920-100116600	GM12878	blood:	n/a	n/a
47	BHLHE40	chr5:99980080-99980171	HepG2	liver:	n/a	n/a
48	BHLHE40	chr5:99978352-99978517	K562	blood:	n/a	n/a
49	BHLHE40	chr5:99919902-99920215	GM12878	blood:	n/a	n/a
50	BHLHE40	chr5:99983105-99983921	K562	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99870955-99871005	A549	lung:	n/a
2	chr5:99871651-99871701	ovcar-3	ovarian:	n/a
3	chr5:99870955-99871005	A549	lung:	n/a
4	chr5:99871651-99871701	ovcar-3	ovarian:	n/a
5	chr5:99886768-99886818	PANC-1	pancreas:	n/a
6	chr5:99870961-99871011	GM06990	blood:	n/a
7	chr5:99875156-99875206	PrEC	prostate:	n/a
8	chr5:99870957-99871007	PFSK-1	brain:	n/a
9	chr5:99871683-99871733	GM12891	blood:	n/a
10	chr5:100108624-100108674	H1-hESC	embryonic stem cell:	embryo
11	chr5:99871233-99871283	T-47D	breast:	n/a
12	chr5:99870955-99871005	GM12892	blood:	n/a
13	chr5:99871683-99871733	HRE	kidney:	n/a
14	chr5:99870961-99871011	GM12878	blood:	n/a
15	chr5:99871026-99871076	PFSK-1	brain:	n/a
16	chr5:99869840-99869890	BJ	skin:	n/a
17	chr5:99871065-99871115	HCM	heart:	n/a
18	chr5:99979316-99979366	AG04449	skin:	fetal
19	chr5:99871073-99871123	LNCaP	prostate:	n/a
20	chr5:99931437-99931487	SAEC	small airway:	n/a
21	chr5:99870887-99870937	CMK	blood:	n/a
22	chr5:99886768-99886818	T-47D	breast:	n/a
23	chr5:99871555-99871605	IMR90	lung:	fetal
24	chr5:100126093-100126143	A549	lung:	n/a
25	chr5:99871065-99871115	HEEpiC	esophagus:	n/a
26	chr5:100024634-100024684	LNCaP	prostate:	n/a
27	chr5:99871233-99871283	Hela-S3	cervix:	n/a
28	chr5:99875156-99875206	HCPEpiC	choroid plexus:	n/a
29	chr5:99869796-99869846	Caco-2	colon:	n/a
30	chr5:100108624-100108674	MCF-7	breast:	n/a
31	chr5:99871555-99871605	NH-A	brain:	n/a
32	chr5:99870961-99871011	MCF-7	breast:	n/a
33	chr5:99871555-99871605	Hepatocyte	liver:	n/a
34	chr5:99870926-99870976	H1-hESC	embryonic stem cell:	embryo
35	chr5:99871651-99871701	GM19239	blood:	n/a
36	chr5:99869796-99869846	ProgFib	skin:	n/a
37	chr5:99979316-99979366	SK-N-MC	brain:	n/a
38	chr5:100108624-100108674	AoSMC	blood vessel:	n/a
39	chr5:99922152-99922202	HCPEpiC	choroid plexus:	n/a
40	chr5:99870926-99870976	NHBE	bronchial:	n/a
41	chr5:99922152-99922202	HCF	heart:	n/a
42	chr5:99993323-99993373	HCM	heart:	n/a
43	chr5:99871233-99871283	NT2-D1	testis:	n/a
44	chr5:99871065-99871115	K562	blood:	n/a
45	chr5:99869796-99869846	AG09319	gingival:	n/a
46	chr5:99870957-99871007	AG09319	gingival:	n/a
47	chr5:100126093-100126143	H1-hESC	embryonic stem cell:	embryo
48	chr5:99871683-99871733	HepG2	liver:	n/a
49	chr5:99871073-99871123	PANC-1	pancreas:	n/a
50	chr5:99870961-99871011	CMK	blood:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:99880455..99883115-chr5:99884041..99887018,2	MCF-7	breast:
2	chr5:100129066..100130718-chr5:100133106..100136007,2	MCF-7	breast:
3	chr5:99979324..99981672-chr5:99983886..99985398,2	K562	blood:
4	chr5:99763910..99766552-chr5:99768110..99770337,2	MCF-7	breast:
5	chr5:100088083..100090255-chr5:100094028..100097000,2	MCF-7	breast:
6	chr5:99968617..99971336-chr5:99974828..99976431,2	K562	blood:
7	chr5:99840638..99843580-chr5:99851710..99854340,2	MCF-7	breast:
8	chr5:99813306..99815252-chr5:99818447..99820144,2	K562	blood:
9	chr5:99982875..99983980-chr5:100090231..100091716,20	MCF-7	breast:
10	chr5:100073871..100076252-chrX:117692329..117695024,2	MCF-7	breast:
11	chr5:99979051..99981832-chr5:99981912..99985691,4	MCF-7	breast:
12	chr5:99948806..99952463-chr5:99954515..99956491,4	K562	blood:
13	chr5:100043067..100045245-chr5:100047793..100049309,2	K562	blood:
14	chr5:99861679..99863597-chr5:99869149..99871005,2	MCF-7	breast:
15	chr5:99983062..99983901-chr5:100090730..100091412,3	MCF-7	breast:
16	chr5:99983045..99983930-chr5:100117214..100117742,2	MCF-7	breast:
17	chr5:99979051..99981832-chr5:99981912..99985691,4	MCF-7	breast:
18	chr5:99993129..99995264-chr5:100001992..100004177,2	K562	blood:
19	chr5:99763910..99766552-chr5:99768110..99770337,2	MCF-7	breast:
20	chr5:99989812..99991852-chr5:99993776..99996637,2	K562	blood:
21	chr5:99975585..99977874-chr5:99980709..99983188,3	K562	blood:
22	chr5:99969436..99971759-chr5:99981835..99984130,2	MCF-7	breast:
23	chr5:99862444..99865055-chr5:99868858..99871762,2	K562	blood:
24	chr5:99978477..99981448-chr5:99989522..99992251,2	MCF-7	breast:
25	chr5:99978017..99980273-chr5:99982713..99984242,2	MCF-7	breast:
26	chr5:99943979..99946598-chr5:99951467..99953484,2	K562	blood:
27	chr5:99983062..99983901-chr5:100090730..100091412,3	MCF-7	breast:
28	chr5:99969436..99971759-chr5:99981835..99984130,2	MCF-7	breast:
29	chr5:99994840..99996773-chr5:99998173..100000130,2	K562	blood:
30	chr5:100088083..100090255-chr5:100094028..100097000,2	MCF-7	breast:
31	chr5:100032298..100033924-chr5:100061965..100063557,2	K562	blood:
32	chr5:99982908..99983980-chr5:100090394..100091716,11	MCF-7	breast:
33	chr5:25503170..25504042-chr5:99982844..99983480,2	MCF-7	breast:
34	chr5:99872854..99874470-chr5:99877624..99879735,2	K562	blood:
35	chr5:99813306..99815252-chr5:99818447..99820144,2	K562	blood:
36	chr5:99871520..99873605-chr5:99874648..99876676,2	MCF-7	breast:
37	chr5:99814495..99815041-chr5:100726099..100726630,2	MCF-7	breast:
38	chr5:100081411..100083893-chr5:100102856..100104705,2	MCF-7	breast:
39	chr5:99978477..99981448-chr5:99989522..99992251,2	MCF-7	breast:
40	chr5:100081411..100083893-chr5:100102856..100104705,2	MCF-7	breast:
41	chr5:100084872..100087123-chr5:100099781..100102264,2	MCF-7	breast:
42	chr5:100091660..100093864-chr5:100095640..100097485,2	MCF-7	breast:
43	chr5:99978017..99980273-chr5:99982713..99984242,2	MCF-7	breast:
44	chr5:100084872..100087123-chr5:100099781..100102264,2	MCF-7	breast:
45	chr2:61371675..61372208-chr5:99870468..99871213,2	NB4	blood:
46	chr5:100129066..100130718-chr5:100133106..100136007,2	MCF-7	breast:
47	chr5:100056227..100057850-chr5:100061884..100063603,2	K562	blood:
48	chr4:32147186..32148048-chr5:99775915..99776706,2	MCF-7	breast:
49	chr20:52739790..52740546-chr5:100102888..100103739,2	MCF-7	breast:
50	chr5:100079826..100081841-chr5:100089952..100091943,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-3	chr5:99785458-99786801	NONHSAT103002
2	lnc-FAM174A-1	chr5:99755954-99756151	NONHSAT103000
3	lnc-ST8SIA4-3	chr5:99785458-99786801	ENSG00000247877
4	lnc-ST8SIA4-3	chr5:99786639-99786801	ENSG00000247877
5	lnc-ST8SIA4-3	chr5:99854234-99854315	ENSG00000247877
6	lnc-FAM174A-3	chr5:100117459-100117529	NONHSAT103010
7	lnc-FAM174A-1	chr5:99755954-99756452	XLOC_004490
8	lnc-ST8SIA4-3	chr5:99862010-99862053	ENSG00000247877
9	lnc-FAM174A-2	chr5:100068762-100069090	NONHSAT103009
10	lnc-ST8SIA4-3	chr5:99792761-99792828	ENSG00000247877
11	lnc-ST8SIA4-2	chr5:99993523-99993674	XLOC_004939
12	lnc-ST8SIA4-3	chr5:99862010-99862053	NONHSAT103002
13	lnc-ST8SIA4-3	chr5:99870865-99870966	ENSG00000247877
14	lnc-ST8SIA4-3	chr5:99869784-99869856	NONHSAT103002
15	lnc-ST8SIA4-2	chr5:99989816-99990096	XLOC_004939
16	lnc-ST8SIA4-2	chr5:99991144-99991208	XLOC_004939
17	lnc-ST8SIA4-2	chr5:99993523-99993674	XLOC_004939
18	lnc-ST8SIA4-3	chr5:99854234-99854315	ENSG00000247877
19	lnc-FAM174A-1	chr5:99759095-99759158	NONHSAT103000
20	lnc-ST8SIA4-2	chr5:99991144-99991179	XLOC_004939
21	lnc-ST8SIA4-2	chr5:99992117-99992230	XLOC_004939
22	lnc-ST8SIA4-2	chr5:99989792-99990096	XLOC_004939
23	lnc-ST8SIA4-3	chr5:99869784-99869856	ENSG00000247877
24	lnc-ST8SIA4-3	chr5:99854234-99854315	NONHSAT103002
25	lnc-FAM174A-1	chr5:99755149-99755217	XLOC_004490
26	lnc-ST8SIA4-3	chr5:99869784-99869856	ENSG00000247877
27	lnc-FAM174A-3	chr5:100128634-100128791	NONHSAT103010
28	lnc-FAM174A-1	chr5:99755149-99755217	NONHSAT103000
29	lnc-ST8SIA4-3	chr5:99870865-99870890	ENSG00000247877

No data

Variant related genes	Relation type
FAM174A	TF binding region
RN7SKP62	TF binding region
ENSG00000250806	TF binding region
ENSG00000247877	TF binding region
FAM174A	CpG island
RN7SKP62	CpG island
ENSG00000250806	CpG island
ENSG00000247877	CpG island
ENSG00000212994	chromatin interactions
ENSG00000180917	chromatin interactions
ENSG00000250806	chromatin interactions
ENSG00000212978	chromatin interactions
ENSG00000247877	chromatin interactions
ENSG00000174132	chromatin interactions
TJAP1	miRNA target sites
RBFOX2	miRNA target sites
ZBTB38	miRNA target sites
NOTCH2	miRNA target sites
FRZB	miRNA target sites
LPGAT1	miRNA target sites
CLDN12	miRNA target sites
EIF2B1	miRNA target sites
RLF	miRNA target sites
FAM190B	miRNA target sites
HSPC159	miRNA target sites
TTLL12	miRNA target sites

Extended variants
information (count: 9532 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:9532 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77798373	chr5:99745798-99745799	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs538957973	chr5:99745838-99745839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116112419	chr5:99745864-99745865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192569809	chr5:99745923-99745924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113995853	chr5:99745933-99745934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550421031	chr5:99745995-99745996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183253276	chr5:99746001-99746002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201029629	chr5:99746010-99746011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199559970	chr5:99746011-99746012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72060945	chr5:99746012-99746013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78660727	chr5:99746013-99746014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535611638	chr5:99746059-99746060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553935127	chr5:99746100-99746101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572349067	chr5:99746146-99746147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539496198	chr5:99746165-99746166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557598802	chr5:99746168-99746169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575967071	chr5:99746184-99746185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146768297	chr5:99746189-99746190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561979340	chr5:99746190-99746191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569881347	chr5:99746196-99746197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140227110	chr5:99746214-99746215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541385589	chr5:99746261-99746262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116420639	chr5:99746262-99746263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145276454	chr5:99746290-99746291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552606484	chr5:99746336-99746337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564445378	chr5:99746432-99746433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188170614	chr5:99746462-99746463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6866895	chr5:99746472-99746473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549915565	chr5:99746473-99746474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531045262	chr5:99746484-99746485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568154805	chr5:99746489-99746490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374395645	chr5:99746506-99746507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564673718	chr5:99746508-99746509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535741163	chr5:99746528-99746529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535110815	chr5:99746532-99746533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202169341	chr5:99746639-99746640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192652651	chr5:99746668-99746669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565915798	chr5:99746678-99746679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539669696	chr5:99746695-99746696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578180065	chr5:99746700-99746701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573811515	chr5:99746702-99746703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115873703	chr5:99746739-99746740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137895412	chr5:99746778-99746779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537193161	chr5:99746822-99746823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149050362	chr5:99746827-99746828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112255396	chr5:99746831-99746832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541318007	chr5:99746858-99746859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183737826	chr5:99746859-99746860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577738226	chr5:99746863-99746864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544879623	chr5:99746871-99746872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99744600-99746000	Enhancers	Fetal Lung	lung
2	chr5:99745400-99745800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:99745400-99745800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:99745400-99745800	Flanking Active TSS	Brain Germinal Matrix	brain
5	chr5:99745400-99745800	Flanking Active TSS	Fetal Brain Male	brain
6	chr5:99745600-99746000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr5:99745800-99746000	Enhancers	Brain Germinal Matrix	brain
8	chr5:99745800-99747200	Enhancers	Fetal Brain Male	brain
9	chr5:99746000-99753200	Weak transcription	Fetal Lung	lung
10	chr5:99753200-99753400	Enhancers	Fetal Lung	lung
11	chr5:99753400-99760000	Weak transcription	Fetal Lung	lung
12	chr5:99753800-99765000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:99754000-99754200	Enhancers	Brain Germinal Matrix	brain
14	chr5:99754200-99756400	Weak transcription	Brain Germinal Matrix	brain
15	chr5:99754400-99755600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:99755600-99756400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:99758200-99758400	Enhancers	HSMM	muscle
18	chr5:99758200-99759200	Enhancers	HSMMtube	muscle
19	chr5:99758600-99759000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:99758800-99759200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr5:99759000-99759200	Enhancers	HSMM	muscle
22	chr5:99759000-99759600	Enhancers	Hela-S3	cervix
23	chr5:99759000-99759600	Enhancers	HUVEC	blood vessel
24	chr5:99759000-99760200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:99759600-99760000	Weak transcription	Hela-S3	cervix
26	chr5:99759600-99760000	Weak transcription	HUVEC	blood vessel
27	chr5:99760000-99760400	Enhancers	Hela-S3	cervix
28	chr5:99760000-99760400	Enhancers	HUVEC	blood vessel
29	chr5:99760000-99761000	ZNF genes & repeats	Fetal Lung	lung
30	chr5:99760000-99761600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
31	chr5:99760200-99760600	ZNF genes & repeats	Fetal Kidney	kidney
32	chr5:99760200-99761400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:99761600-99762200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr5:99762200-99762400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr5:99766200-99767000	Enhancers	Fetal Lung	lung
36	chr5:99766200-99767400	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr5:99767400-99769000	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr5:99769000-99770800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr5:99770400-99770800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr5:99770400-99770800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr5:99776400-99776800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:99782600-99786400	Enhancers	Fetal Lung	lung
43	chr5:99783800-99784400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr5:99783800-99784600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:99790200-99790800	Enhancers	HUVEC	blood vessel
46	chr5:99799600-99800000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:99800000-99800600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:99800000-99800600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:99800000-99800600	Enhancers	Osteobl	bone
50	chr5:99800600-99801000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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