Variant report

Variant	nsv881568
Chromosome Location	chr4:187848075-188237194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1542)
CpG islands
(count:4278)
Chromatin interactive
region (count:55)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1542 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187861751-187861928	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187857788-187858659	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:188172278-188172408	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:187868629-187868925	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:187853628-187853802	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:187867829-187868202	HepG2	liver:	n/a	n/a
7	ATF1	chr4:187861013-187861279	K562	blood:	n/a	n/a
8	BACH1	chr4:188008250-188008420	K562	blood:	n/a	n/a
9	BACH1	chr4:188129816-188130163	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:187938365-187938620	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:188068202-188068264	K562	blood:	n/a	n/a
12	BACH1	chr4:187870229-187870474	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:188129825-188130039	K562	blood:	n/a	n/a
14	BACH1	chr4:188009756-188009863	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr4:188193059-188193371	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:188162982-188163057	A549	lung:	n/a	n/a
17	BHLHE40	chr4:188078752-188079118	K562	blood:	n/a	n/a
18	BHLHE40	chr4:187867852-187868124	HepG2	liver:	n/a	n/a
19	CBX3	chr4:187853176-187854694	HCT-116	colon:	n/a	n/a
20	CBX3	chr4:187857745-187858737	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:187850180-187850774	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:187853152-187854568	HCT-116	colon:	n/a	n/a
23	CBX3	chr4:187848532-187849172	HCT-116	colon:	n/a	n/a
24	CEBPB	chr4:187869806-187870313	IMR90	lung:	n/a	chr4:187869972-187869984
25	CEBPB	chr4:187951852-187952028	HepG2	liver:	n/a	chr4:187951939-187951950
26	CEBPB	chr4:187863984-187864144	HepG2	liver:	n/a	chr4:187864080-187864091
27	CEBPB	chr4:188148708-188148996	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:187863884-187864367	IMR90	lung:	n/a	chr4:187864080-187864091
29	CEBPB	chr4:187930239-187930492	HepG2	liver:	n/a	chr4:187930359-187930370
30	CEBPB	chr4:187951890-187952101	K562	blood:	n/a	chr4:187951939-187951950
31	CEBPB	chr4:187949036-187949236	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:188130901-188131533	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:187950987-187951100	H1-hESC	embryonic stem cell:	n/a	chr4:187951044-187951061
34	CEBPB	chr4:187863784-187864213	A549	lung:	n/a	chr4:187864080-187864091
35	CEBPB	chr4:188026988-188027296	A549	lung:	n/a	chr4:188027103-188027114
36	CEBPB	chr4:188158514-188158784	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:188167859-188168183	HepG2	liver:	n/a	chr4:188168001-188168012 chr4:188168002-188168013 chr4:188168052-188168065
38	CEBPB	chr4:187856204-187856429	HepG2	liver:	n/a	chr4:187856291-187856302
39	CEBPB	chr4:188100977-188101137	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:188023857-188024454	HepG2	liver:	n/a	chr4:188023987-188023998
41	CEBPB	chr4:187862226-187862465	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:187858205-187858555	A549	lung:	n/a	n/a
43	CEBPB	chr4:188026962-188027291	HepG2	liver:	n/a	chr4:188027103-188027114
44	CEBPB	chr4:187861713-187861987	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:187864692-187864880	IMR90	lung:	n/a	chr4:187864774-187864785
46	CEBPB	chr4:188026969-188027265	IMR90	lung:	n/a	chr4:188027103-188027114
47	CEBPB	chr4:188153426-188153626	A549	lung:	n/a	n/a
48	CEBPB	chr4:187852834-187853004	HepG2	liver:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
49	CEBPB	chr4:187857692-187858706	HCT-116	colon:	n/a	n/a
50	CEBPB	chr4:188011726-188011964	IMR90	lung:	n/a	n/a

(count:4278 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188156675-188156725	AoSMC	blood vessel:	n/a
2	chr4:188078724-188078774	RPTEC	kidney:	n/a
3	chr4:187984506-187984556	GM19239	blood:	n/a
4	chr4:188149410-188149460	SK-N-SH_RA	brain:	n/a
5	chr4:188230390-188230440	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:188097683-188097733	HIPEpiC	eye:	n/a
7	chr4:187893119-187893169	RPTEC	kidney:	n/a
8	chr4:188046350-188046400	NHDF-neo	bronchial:	n/a
9	chr4:188156675-188156725	AoSMC	blood vessel:	n/a
10	chr4:188078724-188078774	RPTEC	kidney:	n/a
11	chr4:187984506-187984556	GM19239	blood:	n/a
12	chr4:188149410-188149460	SK-N-SH_RA	brain:	n/a
13	chr4:188230390-188230440	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:188097683-188097733	HIPEpiC	eye:	n/a
15	chr4:187893119-187893169	RPTEC	kidney:	n/a
16	chr4:188046350-188046400	NHDF-neo	bronchial:	n/a
17	chr4:187877218-187877268	HRPEpiC	eye:	n/a
18	chr4:188078724-188078774	NH-A	brain:	n/a
19	chr4:188140291-188140341	HUVEC	blood vessel:	n/a
20	chr4:188046350-188046400	LNCaP	prostate:	n/a
21	chr4:188140222-188140272	GM12878	blood:	n/a
22	chr4:188078670-188078720	PANC-1	pancreas:	n/a
23	chr4:187869873-187869923	HEK293	kidney:	embryo
24	chr4:187894704-187894754	SKMC	muscle:	n/a
25	chr4:188097967-188098017	AG09309	skin:	n/a
26	chr4:188140291-188140341	GM06990	blood:	n/a
27	chr4:187982852-187982902	A549	lung:	n/a
28	chr4:187981566-187981616	Jurkat	blood:	n/a
29	chr4:187882934-187882984	GM06990	blood:	n/a
30	chr4:187984718-187984768	HL-60	blood:	n/a
31	chr4:187882934-187882984	AG09319	gingival:	n/a
32	chr4:187959224-187959274	BE2_C	brain:	n/a
33	chr4:188190184-188190234	SK-N-SH_RA	brain:	n/a
34	chr4:188045689-188045739	A549	lung:	n/a
35	chr4:187984718-187984768	HepG2	liver:	n/a
36	chr4:188131622-188131672	RPTEC	kidney:	n/a
37	chr4:187984506-187984556	HepG2	liver:	n/a
38	chr4:187894704-187894754	GM12878	blood:	n/a
39	chr4:187982852-187982902	MCF-7	breast:	n/a
40	chr4:187851405-187851455	HEK293	kidney:	embryo
41	chr4:187851405-187851455	IMR90	lung:	fetal
42	chr4:188097683-188097733	MCF10A-Er-Src	breast:	n/a
43	chr4:187985377-187985427	U87	brain:	n/a
44	chr4:187880263-187880313	NH-A	brain:	n/a
45	chr4:188097967-188098017	PrEC	prostate:	n/a
46	chr4:188046444-188046494	NB4	blood:	n/a
47	chr4:188101115-188101165	MCF-7	breast:	n/a
48	chr4:187884817-187884867	NHBE	bronchial:	n/a
49	chr4:188034964-188035014	PrEC	prostate:	n/a
50	chr4:187851586-187851636	AG09319	gingival:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:187759553..187761639-chr4:187893343..187896166,2	K562	blood:
2	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
3	chr4:187646533..187648100-chr4:188156626..188159035,2	MCF-7	breast:
4	chr4:187867875..187869719-chr4:187871363..187873618,2	MCF-7	breast:
5	chr4:188177128..188179488-chr4:188187474..188190252,2	MCF-7	breast:
6	chr4:187848247..187850848-chr4:187854272..187856829,2	K562	blood:
7	chr4:187676723..187679624-chr4:187847276..187848972,2	K562	blood:
8	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
9	chr4:187939165..187941494-chr4:187941726..187943652,2	K562	blood:
10	chr4:187844136..187846877-chr4:187850742..187852747,2	K562	blood:
11	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
12	chr4:187867875..187869719-chr4:187871363..187873618,2	MCF-7	breast:
13	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:
14	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
15	chr4:187648031..187648672-chr4:187867515..187868384,2	MCF-7	breast:
16	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
17	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
18	chr4:187647203..187650083-chr4:187858614..187861044,2	MCF-7	breast:
19	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
20	chr4:187641888..187650885-chr4:187865376..187870322,9	MCF-7	breast:
21	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
22	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
23	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
24	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
25	chr4:187647654..187649416-chr4:188063013..188065311,2	MCF-7	breast:
26	chr4:187702948..187705032-chr4:187853740..187855963,2	K562	blood:
27	chr4:187910556..187913594-chr4:187916872..187920065,3	K562	blood:
28	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
29	chr4:187645972..187647664-chr4:187867143..187868450,8	MCF-7	breast:
30	chr4:188169327..188171194-chr4:188181076..188182965,2	K562	blood:
31	chr4:188169327..188171194-chr4:188181076..188182965,2	K562	blood:
32	chr4:187658603..187659281-chr4:187867789..187868472,2	MCF-7	breast:
33	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
34	chr4:187838828..187841268-chr4:187853169..187855944,2	K562	blood:
35	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
36	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
37	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
38	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
39	chr4:187648351..187650879-chr4:187855816..187858244,2	MCF-7	breast:
40	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
41	chr4:187644629..187648780-chr4:187865976..187870182,7	MCF-7	breast:
42	chr4:187867684..187870026-chr4:187872421..187875152,2	MCF-7	breast:
43	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
44	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
45	chr4:187646857..187647583-chr4:187867241..187868105,3	MCF-7	breast:
46	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
47	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
48	chr4:187645367..187647070-chr4:188073656..188075512,2	K562	blood:
49	chr4:187867684..187870026-chr4:187872421..187875152,2	MCF-7	breast:
50	chr4:187848247..187850848-chr4:187854272..187856829,2	K562	blood:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-7	chr4:188133530-188134139	XLOC_003825
2	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691
3	lnc-ZFP42-7	chr4:188133499-188133581	NONHSAT099688
4	lnc-ZFP42-7	chr4:188123140-188123296	XLOC_003825
5	lnc-ZFP42-7	chr4:188129941-188130201	XLOC_003825
6	lnc-ZFP42-7	chr4:188134283-188134753	NONHSAT099688
7	lnc-F11-3	chr4:187981371-187981417	NONHSAT099680
8	lnc-ZFP42-7	chr4:188130341-188130500	XLOC_003825
9	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
10	lnc-F11-3	chr4:187981829-187982019	NONHSAT099680
11	lnc-FAT1-1	chr4:187900644-187900886	XLOC_004215
12	lnc-F11-3	chr4:187980348-187980402	XLOC_003823
13	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217
14	lnc-ZFP42-7	chr4:188124136-188124768	XLOC_003825
15	lnc-F11-3	chr4:187980530-187980856	XLOC_003823
16	lnc-F11-4	chr4:187981829-187982084	XLOC_003824
17	lnc-ZFP42-7	chr4:188123145-188123296	XLOC_003825
18	lnc-ZFP42-7	chr4:188134283-188134810	XLOC_003825
19	lnc-FAT1-2	chr4:188122781-188123084	XLOC_004216
20	lnc-ZFP42-7	chr4:188133530-188134139	XLOC_003825
21	lnc-FAT1-2	chr4:188119427-188119745	XLOC_004216
22	lnc-F11-4	chr4:187981253-187981417	XLOC_003824
23	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
24	lnc-FAT1-1	chr4:187917410-187917592	XLOC_004215
25	lnc-F11-3	chr4:187980278-187980644	NONHSAT099680
26	lnc-FAT1-3	chr4:188225237-188225621	XLOC_004217
27	lnc-ZFP42-7	chr4:188129941-188130201	XLOC_003825
28	lnc-ZFP42-7	chr4:188123217-188123296	XLOC_003825
29	lnc-FAT1-1	chr4:187943080-187943127	XLOC_004215
30	lnc-ZFP42-7	chr4:188123187-188123296	XLOC_003825
31	lnc-ZFP42-7	chr4:188123178-188123296	XLOC_003825
32	lnc-ZFP42-7	chr4:188134283-188135298	XLOC_003825
33	lnc-ZFP42-7	chr4:188133984-188134139	NONHSAT099688
34	lnc-ZFP42-7	chr4:188133530-188133630	XLOC_003825

No data

Variant related genes	Relation type
ENSG00000249747	TF binding region
ENSG00000250971	TF binding region
ENSG00000249742	TF binding region
ENSG00000250658	TF binding region
ENSG00000249747	CpG island
ENSG00000250971	CpG island
ENSG00000249742	CpG island
ENSG00000250658	CpG island
ENSG00000083857	chromatin interactions
ENSG00000249742	chromatin interactions
ANKRD57	miRNA target sites
LMNB1	miRNA target sites
UBXN1	miRNA target sites
OSBPL1A	miRNA target sites
ZFYVE26	miRNA target sites
CCND1	miRNA target sites

Extended variants
information (count: 13886 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:13886 , 50 per page) page: 1 2 3 4 5 6 7 ... 278

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6829485	chr4:187848075-187848076	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540965076	chr4:187848078-187848079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550188704	chr4:187848088-187848089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6829689	chr4:187848143-187848144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs111380799	chr4:187848158-187848159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2162197	chr4:187848172-187848173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148055002	chr4:187848190-187848191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541879206	chr4:187848328-187848329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538795672	chr4:187848347-187848348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552512703	chr4:187848467-187848468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569141762	chr4:187848473-187848474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538118836	chr4:187848486-187848487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs80057766	chr4:187848494-187848495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191034040	chr4:187848509-187848510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141648763	chr4:187848519-187848520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183171889	chr4:187848549-187848550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs55857581	chr4:187848550-187848551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs55769031	chr4:187848564-187848565	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs545163072	chr4:187848585-187848586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565259806	chr4:187848600-187848601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547068386	chr4:187848616-187848617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186050386	chr4:187848621-187848622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190905377	chr4:187848634-187848635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs56292228	chr4:187848652-187848653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs34007261	chr4:187848659-187848660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111897764	chr4:187848679-187848680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150507669	chr4:187848700-187848701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139542630	chr4:187848705-187848706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56364281	chr4:187848731-187848732	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs4241836	chr4:187848793-187848794	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs183048055	chr4:187848803-187848804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538185350	chr4:187848963-187848964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62343123	chr4:187848979-187848980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs73873957	chr4:187849063-187849064	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs73873958	chr4:187849084-187849085	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs188082134	chr4:187849110-187849111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572973649	chr4:187849134-187849135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538731402	chr4:187849161-187849162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113653881	chr4:187849165-187849166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558766629	chr4:187849173-187849174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10532855	chr4:187849180-187849181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199735150	chr4:187849181-187849182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs397880625	chr4:187849182-187849183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575428984	chr4:187849195-187849196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536218356	chr4:187849196-187849197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547895997	chr4:187849211-187849212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146767393	chr4:187849231-187849232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569374063	chr4:187849261-187849262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553016629	chr4:187849300-187849301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191774454	chr4:187849338-187849339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oral cancer	17325662	CNVD
Autism	20808228	CNVD

Chromatin state (count:1632 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187837200-187863800	Weak transcription	Right Atrium	heart
2	chr4:187840000-187853400	Weak transcription	Fetal Kidney	kidney
3	chr4:187842000-187852400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:187842600-187848600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:187842600-187852200	Weak transcription	HMEC	breast
6	chr4:187845800-187851200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:187846000-187850400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:187846200-187848600	Weak transcription	NHEK	skin
9	chr4:187846200-187851400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:187846200-187851800	Weak transcription	Osteobl	bone
11	chr4:187846400-187848600	Weak transcription	NHDF-Ad	bronchial
12	chr4:187846400-187849800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:187846400-187851200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:187846400-187851200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:187846400-187853400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:187846800-187848600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:187847800-187848800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr4:187848600-187848800	Enhancers	NHDF-Ad	bronchial
19	chr4:187848600-187849000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:187848600-187849000	Enhancers	NHEK	skin
21	chr4:187848600-187850600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:187848800-187849200	Weak transcription	NHDF-Ad	bronchial
23	chr4:187849000-187852000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:187849200-187850600	Enhancers	NHDF-Ad	bronchial
25	chr4:187849800-187850800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:187850200-187850400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:187850400-187850800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:187850400-187852200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:187850600-187851800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:187850600-187852000	Weak transcription	NHDF-Ad	bronchial
31	chr4:187850800-187852200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:187850800-187852200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr4:187851200-187851400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:187851200-187851800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:187851200-187851800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:187851400-187854000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr4:187851800-187853000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:187851800-187853400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:187851800-187855800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:187851800-187857800	Enhancers	Osteobl	bone
41	chr4:187852000-187853000	Enhancers	NHDF-Ad	bronchial
42	chr4:187852000-187854200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:187852000-187854400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:187852000-187855000	Enhancers	HSMM	muscle
45	chr4:187852200-187853000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:187852200-187853800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:187852200-187854400	Enhancers	HMEC	breast
48	chr4:187852200-187854600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:187852400-187853400	Enhancers	NHLF	lung
50	chr4:187852400-187855000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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