Variant report

Variant	nsv881584
Chromosome Location	chr4:187969329-188480913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1361)
CpG islands
(count:3603)
Chromatin interactive
region (count:49)
LncRNA
region (count:67)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1361 , 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	chr4:188172278-188172408	HepG2	liver:	n/a	n/a
2	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
3	BACH1	chr4:188129816-188130163	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:188008250-188008420	K562	blood:	n/a	n/a
5	BACH1	chr4:188068202-188068264	K562	blood:	n/a	n/a
6	BACH1	chr4:188129825-188130039	K562	blood:	n/a	n/a
7	BACH1	chr4:188009756-188009863	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr4:188193059-188193371	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
10	BHLHE40	chr4:188162982-188163057	A549	lung:	n/a	n/a
11	BHLHE40	chr4:188078752-188079118	K562	blood:	n/a	n/a
12	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:188254254-188254599	IMR90	lung:	n/a	chr4:188254404-188254415
14	CEBPB	chr4:188223685-188224011	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:188301252-188301594	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:188184825-188185024	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
18	CEBPB	chr4:188190130-188190519	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:188158501-188158795	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:188018970-188019044	HepG2	liver:	n/a	chr4:188018994-188019005
21	CEBPB	chr4:188023857-188024454	HepG2	liver:	n/a	chr4:188023987-188023998
22	CEBPB	chr4:188100977-188101137	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:188253393-188253593	HepG2	liver:	n/a	chr4:188253450-188253461
24	CEBPB	chr4:188026962-188027291	HepG2	liver:	n/a	chr4:188027103-188027114
25	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
26	CEBPB	chr4:188301323-188301523	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr4:188254417-188254534	K562	blood:	n/a	n/a
28	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
29	CEBPB	chr4:188295952-188296114	HepG2	liver:	n/a	chr4:188296003-188296014 chr4:188296003-188296016
30	CEBPB	chr4:188440459-188440698	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:188153426-188153626	A549	lung:	n/a	n/a
32	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
34	CEBPB	chr4:188167859-188168183	HepG2	liver:	n/a	chr4:188168001-188168012 chr4:188168002-188168013 chr4:188168052-188168065
35	CEBPB	chr4:188151952-188152262	HepG2	liver:	n/a	chr4:188152090-188152101 chr4:188152090-188152103 chr4:188152092-188152103 chr4:188152230-188152243 chr4:188152092-188152101
36	CEBPB	chr4:188158488-188158792	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:188011726-188011964	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:188026969-188027265	IMR90	lung:	n/a	chr4:188027103-188027114
39	CEBPB	chr4:188153356-188153615	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:188254340-188254476	A549	lung:	n/a	chr4:188254404-188254415
41	CEBPB	chr4:188253347-188253499	Hela-S3	cervix:	n/a	chr4:188253450-188253461
42	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:188153348-188153608	IMR90	lung:	n/a	n/a
45	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
46	CEBPB	chr4:188167868-188168162	IMR90	lung:	n/a	chr4:188168001-188168012 chr4:188168002-188168013 chr4:188168052-188168065
47	CEBPB	chr4:188056837-188057059	A549	lung:	n/a	n/a
48	CEBPB	chr4:188301254-188301599	MCF-7	breast:	n/a	n/a
49	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
50	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890

(count:3603 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188208070-188208120	HepG2	liver:	n/a
2	chr4:188149410-188149460	GM12892	blood:	n/a
3	chr4:188139877-188139927	T-47D	breast:	n/a
4	chr4:187985377-187985427	AoSMC	blood vessel:	n/a
5	chr4:188208070-188208120	HepG2	liver:	n/a
6	chr4:188149410-188149460	GM12892	blood:	n/a
7	chr4:188139877-188139927	T-47D	breast:	n/a
8	chr4:187985377-187985427	AoSMC	blood vessel:	n/a
9	chr4:188097683-188097733	AG09319	gingival:	n/a
10	chr4:188391387-188391437	RPTEC	kidney:	n/a
11	chr4:187985377-187985427	T-47D	breast:	n/a
12	chr4:188256765-188256815	IMR90	lung:	fetal
13	chr4:187982852-187982902	NHDF-neo	bronchial:	n/a
14	chr4:188156675-188156725	A549	lung:	n/a
15	chr4:188097967-188098017	Hepatocyte	liver:	n/a
16	chr4:187981566-187981616	HCT-116	colon:	n/a
17	chr4:187984506-187984556	HCPEpiC	choroid plexus:	n/a
18	chr4:188097774-188097824	Caco-2	colon:	n/a
19	chr4:188256765-188256815	HRE	kidney:	n/a
20	chr4:188139877-188139927	SK-N-MC	brain:	n/a
21	chr4:187985472-187985522	MCF10A-Er-Src	breast:	n/a
22	chr4:188045368-188045418	NHBE	bronchial:	n/a
23	chr4:188139877-188139927	SAEC	small airway:	n/a
24	chr4:188426278-188426328	HCT-116	colon:	n/a
25	chr4:188423066-188423116	IMR90	lung:	fetal
26	chr4:188149410-188149460	H1-hESC	embryonic stem cell:	embryo
27	chr4:188131622-188131672	Jurkat	blood:	n/a
28	chr4:188462685-188462735	LNCaP	prostate:	n/a
29	chr4:188045495-188045545	SK-N-MC	brain:	n/a
30	chr4:188045368-188045418	GM06990	blood:	n/a
31	chr4:188314314-188314364	K562	blood:	n/a
32	chr4:188046350-188046400	Caco-2	colon:	n/a
33	chr4:188423066-188423116	GM12891	blood:	n/a
34	chr4:188256765-188256815	NT2-D1	testis:	n/a
35	chr4:188423066-188423116	U87	brain:	n/a
36	chr4:187992866-187992916	HCT-116	colon:	n/a
37	chr4:188045689-188045739	LNCaP	prostate:	n/a
38	chr4:188256637-188256687	NH-A	brain:	n/a
39	chr4:188046350-188046400	SAEC	small airway:	n/a
40	chr4:188156675-188156725	RPTEC	kidney:	n/a
41	chr4:188230390-188230440	HIPEpiC	eye:	n/a
42	chr4:187985452-187985502	ProgFib	skin:	n/a
43	chr4:187984958-187985008	HMEC	breast:	n/a
44	chr4:188104526-188104576	NHBE	bronchial:	n/a
45	chr4:188097683-188097733	ProgFib	skin:	n/a
46	chr4:187985472-187985522	H1-hESC	embryonic stem cell:	embryo
47	chr4:188256637-188256687	HIPEpiC	eye:	n/a
48	chr4:188046444-188046494	SK-N-SH	brain:	n/a
49	chr4:187982852-187982902	HEK293	kidney:	embryo
50	chr4:188046444-188046494	T-47D	breast:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:
2	chr4:187645367..187647070-chr4:188073656..188075512,2	K562	blood:
3	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
4	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
5	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
6	chr4:188177128..188179488-chr4:188187474..188190252,2	MCF-7	breast:
7	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
8	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
9	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
10	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
11	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
12	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
13	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
14	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
15	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
16	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
17	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
18	chr4:188021348..188024236-chr4:188025948..188027821,2	K562	blood:
19	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
20	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
21	chr4:188082742..188084382-chr4:188084801..188086705,2	K562	blood:
22	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
23	chr4:187646533..187648100-chr4:188156626..188159035,2	MCF-7	breast:
24	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
25	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
26	chr4:188169327..188171194-chr4:188181076..188182965,2	K562	blood:
27	chr4:188083083..188085833-chr4:188087348..188090241,2	MCF-7	breast:
28	chr4:188177128..188179488-chr4:188187474..188190252,2	MCF-7	breast:
29	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:
30	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
31	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
32	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:
33	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
34	chr4:188169327..188171194-chr4:188181076..188182965,2	K562	blood:
35	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
36	chr4:188127890..188130779-chr4:188137377..188140053,2	K562	blood:
37	chr4:187987739..187989795-chr4:187999500..188002033,2	MCF-7	breast:
38	chr4:188100330..188101980-chr4:188105667..188107214,2	K562	blood:
39	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
40	chr4:188056141..188059135-chr4:188062494..188064650,2	K562	blood:
41	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
42	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
43	chr4:188077660..188079789-chr4:188085671..188087696,2	K562	blood:
44	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
45	chr4:188066477..188068496-chr4:188071988..188074466,2	K562	blood:
46	chr4:187647654..187649416-chr4:188063013..188065311,2	MCF-7	breast:
47	chr4:188016055..188017615-chr4:188020801..188022830,2	MCF-7	breast:
48	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
49	chr4:188127890..188131303-chr4:188136198..188140053,3	K562	blood:

(count:67 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-7	chr4:188134283-188134810	XLOC_003825
2	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
3	lnc-ZFP42-7	chr4:188134283-188135298	XLOC_003825
4	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
5	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
6	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828
7	lnc-ZFP42-7	chr4:188123145-188123296	XLOC_003825
8	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
9	lnc-ZFP42-7	chr4:188134283-188134753	NONHSAT099688
10	lnc-ZFP42-7	chr4:188129941-188130201	XLOC_003825
11	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217
12	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
13	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
14	lnc-ZFP42-7	chr4:188133530-188134139	XLOC_003825
15	lnc-F11-3	chr4:187981829-187982019	NONHSAT099680
16	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
17	lnc-F11-3	chr4:187980530-187980856	XLOC_003823
18	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
19	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
20	lnc-ZFP42-7	chr4:188123187-188123296	XLOC_003825
21	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
22	lnc-ZFP42-7	chr4:188133499-188133581	NONHSAT099688
23	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
24	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691
25	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
26	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
27	lnc-F11-3	chr4:187980348-187980402	XLOC_003823
28	lnc-ZFP42-13	chr4:188252448-188253478	NONHSAT099691
29	lnc-ZFP42-7	chr4:188133530-188134139	XLOC_003825
30	lnc-ZFP42-5	chr4:188334718-188334865	ENSG00000250620
31	lnc-ZFP42-7	chr4:188124136-188124768	XLOC_003825
32	lnc-ZFP42-7	chr4:188123140-188123296	XLOC_003825
33	lnc-ZFP42-7	chr4:188123217-188123296	XLOC_003825
34	lnc-ZFP42-6	chr4:188291802-188291929	XLOC_003826
35	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
36	lnc-ZFP42-7	chr4:188133984-188134139	NONHSAT099688
37	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
38	lnc-FAT1-2	chr4:188122781-188123084	XLOC_004216
39	lnc-FAT1-2	chr4:188119427-188119745	XLOC_004216
40	lnc-F11-3	chr4:187980278-187980644	NONHSAT099680
41	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
42	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
43	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
44	lnc-ZFP42-13	chr4:188237423-188237596	NONHSAT099691
45	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
46	lnc-F11-4	chr4:187981253-187981417	XLOC_003824
47	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
48	lnc-F11-4	chr4:187981829-187982084	XLOC_003824
49	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
50	lnc-ZFP42-13	chr4:188251486-188251546	NONHSAT099691

No data

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ENSG00000250042	TF binding region
ENSG00000250590	TF binding region
ENSG00000249747	TF binding region
ENSG00000250971	TF binding region
ENSG00000250658	TF binding region
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ENSG00000250042	CpG island
ENSG00000250590	CpG island
ENSG00000249747	CpG island
ENSG00000250971	CpG island
ENSG00000250658	CpG island
ENSG00000029993	chromatin interactions
ENSG00000083857	chromatin interactions
ENSG00000251643	chromatin interactions
UBXN1	miRNA target sites
ANTXR1	miRNA target sites
LMNB1	miRNA target sites
ANKRD57	miRNA target sites
ANP32E	miRNA target sites
OSBPL1A	miRNA target sites
CCND1	miRNA target sites
ZFYVE26	miRNA target sites

Extended variants
information (count: 16146 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:16146 , 50 per page) page: 1 2 3 4 5 6 7 ... 323

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538658354	chr4:187971466-187971467	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188523787	chr4:187971467-187971468	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141442500	chr4:187971483-187971484	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs12644996	chr4:187971503-187971504	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4573171	chr4:187971507-187971508	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7791791	chr4:187971535-187971536	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555182869	chr4:187971540-187971541	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376481791	chr4:187971550-187971551	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370932216	chr4:187971580-187971581	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575104502	chr4:187971588-187971589	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551206323	chr4:187971632-187971633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368325670	chr4:187971663-187971664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143751680	chr4:187971693-187971694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554512269	chr4:187971710-187971711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577601197	chr4:187971716-187971717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545860419	chr4:187971717-187971718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562322751	chr4:187971721-187971722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28524953	chr4:187971754-187971755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541575321	chr4:187971755-187971756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112051427	chr4:187971759-187971760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149664180	chr4:187971760-187971761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547150960	chr4:187971762-187971763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527486443	chr4:187971770-187971771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193107872	chr4:187971795-187971796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370153282	chr4:187978065-187978066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs570187274	chr4:187978086-187978087	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs537257956	chr4:187978087-187978088	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs79099074	chr4:187978095-187978096	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs116422742	chr4:187980301-187980302	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs139865615	chr4:187980314-187980315	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs534704359	chr4:187980332-187980333	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs557523513	chr4:187980374-187980375	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs186730239	chr4:187980403-187980404	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs528348819	chr4:187980416-187980417	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs10019973	chr4:187980423-187980424	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190188833	chr4:187980476-187980477	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs78511104	chr4:187980488-187980489	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs143225614	chr4:187980500-187980501	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs368179381	chr4:187980505-187980506	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs562055142	chr4:187980541-187980542	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs572309855	chr4:187980606-187980607	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs150670580	chr4:187980656-187980657	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs564395297	chr4:187980686-187980687	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs3923586	chr4:187980711-187980712	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs549945954	chr4:187980721-187980722	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs117705658	chr4:187980791-187980792	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs139851573	chr4:187980817-187980818	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs374581074	chr4:187980834-187980835	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs77029919	chr4:187980864-187980865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4241838	chr4:187980880-187980881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Pancreatic cancer	17952125	CNVD
Oral cancer	17325662	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD

Chromatin state (count:1304 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187971400-187971600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:187971400-187971600	Enhancers	HSMM	muscle
3	chr4:187971400-187971800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:187971400-187971800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:187971400-187971800	Enhancers	HUVEC	blood vessel
6	chr4:187971400-187971800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr4:187971400-187971800	Enhancers	NHDF-Ad	bronchial
8	chr4:187980400-187980600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:187980400-187980600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:187980400-187982000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:187981000-187981800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:187982000-187991800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:187982000-187995200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:187984600-187985600	Bivalent Enhancer	Placenta	Placenta
15	chr4:187984800-187985800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:187985000-187985200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:187985200-187986600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr4:187985800-187986000	Enhancers	Rectal Smooth Muscle	rectum
19	chr4:187985800-187990600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:187986000-187987000	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:187986200-187986400	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr4:187986200-187986600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:187986200-187986800	Enhancers	Brain Germinal Matrix	brain
24	chr4:187986200-187987000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:187986200-187987200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:187986200-187987600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:187986400-187987000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:187986600-187986800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:187986600-187987400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:187986600-187991800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr4:187987000-187987200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr4:187987000-187987200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr4:187987000-187987400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:187987000-187987400	Enhancers	Rectal Smooth Muscle	rectum
35	chr4:187987000-187987400	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr4:187987000-187993000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:187987200-187987400	Enhancers	Fetal Muscle Trunk	muscle
38	chr4:187987200-187987800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:187987200-187990600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:187987400-187990600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr4:187987400-187990600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:187987400-187990600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr4:187987600-187991800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr4:187990200-187990600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:187990400-187991200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:187990600-187991000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:187990600-187991000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:187990600-187991000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:187990600-187991000	Active TSS	Adipose Nuclei	Adipose
50	chr4:187990600-187991000	Enhancers	Fetal Muscle Trunk	muscle

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