Variant report

Variant	nsv880750
Chromosome Location	chr4:188159641-188416501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:753)
CpG islands
(count:671)
Chromatin interactive
region (count:20)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:753 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	BCL3	chr4:188193059-188193371	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:188162982-188163057	A549	lung:	n/a	n/a
5	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
6	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
8	CEBPB	chr4:188337488-188337650	K562	blood:	n/a	chr4:188337610-188337621
9	CEBPB	chr4:188337419-188337771	IMR90	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
10	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
11	CEBPB	chr4:188263083-188263269	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:188254254-188254599	IMR90	lung:	n/a	chr4:188254404-188254415
14	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
15	CEBPB	chr4:188167868-188168162	IMR90	lung:	n/a	chr4:188168001-188168012 chr4:188168002-188168013 chr4:188168052-188168065
16	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:188234147-188234350	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
19	CEBPB	chr4:188190202-188190454	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:188254340-188254476	A549	lung:	n/a	chr4:188254404-188254415
21	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
22	CEBPB	chr4:188301252-188301594	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:188309832-188310058	IMR90	lung:	n/a	chr4:188309977-188309986
25	CEBPB	chr4:188183122-188183182	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:188301254-188301599	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:188254417-188254534	K562	blood:	n/a	n/a
28	CEBPB	chr4:188213364-188213403	K562	blood:	n/a	n/a
29	CEBPB	chr4:188167859-188168183	HepG2	liver:	n/a	chr4:188168001-188168012 chr4:188168002-188168013 chr4:188168052-188168065
30	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
31	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
32	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
33	CEBPB	chr4:188190130-188190519	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
35	CEBPB	chr4:188223685-188224011	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:188253393-188253593	HepG2	liver:	n/a	chr4:188253450-188253461
37	CEBPB	chr4:188253347-188253499	Hela-S3	cervix:	n/a	chr4:188253450-188253461
38	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
39	CEBPB	chr4:188317722-188317931	HepG2	liver:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
40	CEBPB	chr4:188301323-188301523	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:188254264-188254489	HepG2	liver:	n/a	chr4:188254404-188254415
42	CEBPB	chr4:188295952-188296114	HepG2	liver:	n/a	chr4:188296003-188296014 chr4:188296003-188296016
43	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
44	CEBPB	chr4:188184825-188185024	IMR90	lung:	n/a	n/a
45	CTCF	chr4:188171360-188171510	HMEC	breast:	n/a	n/a
46	CTCF	chr4:188301340-188301490	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr4:188301287-188301469	K562	blood:	n/a	n/a
48	CTCF	chr4:188301320-188301470	K562	blood:	n/a	n/a
49	CTCF	chr4:188301200-188301350	A549	lung:	n/a	n/a
50	CTCF	chr4:188301260-188301410	MCF-7	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188230390-188230440	IMR90	lung:	fetal
2	chr4:188256637-188256687	HEEpiC	esophagus:	n/a
3	chr4:188208070-188208120	K562	blood:	n/a
4	chr4:188256765-188256815	ECC-1	luminal epithelium:	n/a
5	chr4:188391387-188391437	HCM	heart:	n/a
6	chr4:188256765-188256815	HAEpiC	amniotic membrane:	n/a
7	chr4:188391387-188391437	GM12892	blood:	n/a
8	chr4:188391387-188391437	NB4	blood:	n/a
9	chr4:188230390-188230440	Caco-2	colon:	n/a
10	chr4:188223108-188223158	NHDF-neo	bronchial:	n/a
11	chr4:188314314-188314364	GM19239	blood:	n/a
12	chr4:188223108-188223158	HAEpiC	amniotic membrane:	n/a
13	chr4:188398437-188398487	AG09319	gingival:	n/a
14	chr4:188314314-188314364	HNPCEpiC	eye:	n/a
15	chr4:188256765-188256815	HCT-116	colon:	n/a
16	chr4:188208070-188208120	AG04450	lung:	fetal
17	chr4:188256708-188256758	ECC-1	luminal epithelium:	n/a
18	chr4:188401038-188401088	Caco-2	colon:	n/a
19	chr4:188256765-188256815	NH-A	brain:	n/a
20	chr4:188401038-188401088	HEEpiC	esophagus:	n/a
21	chr4:188401038-188401088	AG10803	skin:	n/a
22	chr4:188190184-188190234	HIPEpiC	eye:	n/a
23	chr4:188230390-188230440	GM12878	blood:	n/a
24	chr4:188256637-188256687	A549	lung:	n/a
25	chr4:188256765-188256815	NHBE	bronchial:	n/a
26	chr4:188391387-188391437	AG10803	skin:	n/a
27	chr4:188208070-188208120	HEK293	kidney:	embryo
28	chr4:188401038-188401088	NHDF-neo	bronchial:	n/a
29	chr4:188401038-188401088	HCT-116	colon:	n/a
30	chr4:188256708-188256758	U87	brain:	n/a
31	chr4:188208070-188208120	ECC-1	luminal epithelium:	n/a
32	chr4:188208070-188208120	NH-A	brain:	n/a
33	chr4:188190184-188190234	ProgFib	skin:	n/a
34	chr4:188190184-188190234	HCM	heart:	n/a
35	chr4:188314314-188314364	HAEpiC	amniotic membrane:	n/a
36	chr4:188401038-188401088	HRE	kidney:	n/a
37	chr4:188223108-188223158	AoSMC	blood vessel:	n/a
38	chr4:188398437-188398487	HCM	heart:	n/a
39	chr4:188398437-188398487	BE2_C	brain:	n/a
40	chr4:188208070-188208120	HepG2	liver:	n/a
41	chr4:188401038-188401088	HCM	heart:	n/a
42	chr4:188256765-188256815	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:188230390-188230440	GM06990	blood:	n/a
44	chr4:188190184-188190234	BE2_C	brain:	n/a
45	chr4:188256765-188256815	HRE	kidney:	n/a
46	chr4:188190184-188190234	IMR90	lung:	fetal
47	chr4:188256637-188256687	K562	blood:	n/a
48	chr4:188208070-188208120	MCF10A-Er-Src	breast:	n/a
49	chr4:188230390-188230440	PANC-1	pancreas:	n/a
50	chr4:188223108-188223158	SK-N-SH_RA	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
2	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
3	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
4	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
5	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
6	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
7	chr4:188177128..188179488-chr4:188187474..188190252,2	MCF-7	breast:
8	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
9	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
10	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
11	chr4:188169327..188171194-chr4:188181076..188182965,2	K562	blood:
12	chr4:188136808..188139497-chr4:188168223..188169981,2	K562	blood:
13	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
14	chr4:188177128..188179488-chr4:188187474..188190252,2	MCF-7	breast:
15	chr4:188261472..188262979-chr4:188266588..188269425,2	K562	blood:
16	chr4:188169327..188171194-chr4:188181076..188182965,2	K562	blood:
17	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:
18	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
19	chr4:188278385..188280812-chr4:188281318..188282901,2	K562	blood:
20	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
2	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
3	lnc-ZFP42-13	chr4:188251486-188251546	NONHSAT099691
4	lnc-ZFP42-6	chr4:188291802-188291929	XLOC_003826
5	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
6	lnc-FAT1-3	chr4:188225237-188225621	XLOC_004217
7	lnc-ZFP42-5	chr4:188334718-188334865	ENSG00000250620
8	lnc-ZFP42-13	chr4:188252448-188253478	NONHSAT099691
9	lnc-ZFP42-6	chr4:188292449-188292580	XLOC_003826
10	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
11	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
12	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
13	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828
14	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
15	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691
16	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
17	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
18	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
19	lnc-ZFP42-13	chr4:188237423-188237596	NONHSAT099691
20	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217
21	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
22	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
23	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
24	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
25	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
26	lnc-ZFP42-6	chr4:188292838-188293075	XLOC_003826

No data

Variant related genes	Relation type
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ENSG00000250042	TF binding region
ENSG00000250658	TF binding region
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ENSG00000250042	CpG island
ENSG00000250658	CpG island
ENSG00000251643	chromatin interactions

Extended variants
information (count: 8165 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:8165 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1532021	chr4:188159641-188159642	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565211537	chr4:188159678-188159679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531129563	chr4:188159684-188159685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187197766	chr4:188159727-188159728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10009680	chr4:188159768-188159769	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs80343854	chr4:188159801-188159802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10032227	chr4:188159821-188159822	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs143765073	chr4:188159831-188159832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532097498	chr4:188159844-188159845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552223607	chr4:188159854-188159855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151101954	chr4:188159880-188159881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374501944	chr4:188159939-188159940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192133349	chr4:188159952-188159953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28674939	chr4:188159974-188159975	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs28542768	chr4:188160002-188160003	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs28539295	chr4:188160054-188160055	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553004755	chr4:188160056-188160057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573023777	chr4:188160116-188160117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183833023	chr4:188160194-188160195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542865719	chr4:188160199-188160200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558515279	chr4:188160201-188160202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140984645	chr4:188160208-188160209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188058404	chr4:188160240-188160241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561667230	chr4:188160242-188160243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574896286	chr4:188160257-188160258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570427231	chr4:188160333-188160334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540830830	chr4:188160362-188160363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192234933	chr4:188160423-188160424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532260475	chr4:188160442-188160443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150227691	chr4:188160501-188160502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138699620	chr4:188160514-188160515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553359645	chr4:188160520-188160521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531380855	chr4:188160522-188160523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182800750	chr4:188160545-188160546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141976666	chr4:188160571-188160572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73014176	chr4:188160591-188160592	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557499830	chr4:188160601-188160602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114241818	chr4:188160697-188160698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538727556	chr4:188160706-188160707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558673621	chr4:188160714-188160715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12513370	chr4:188160716-188160717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs66522372	chr4:188160724-188160725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111841164	chr4:188160726-188160727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10678036	chr4:188160740-188160741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533616984	chr4:188160752-188160753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376821424	chr4:188160753-188160754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368644361	chr4:188160755-188160756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116462469	chr4:188160816-188160817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368768269	chr4:188160832-188160833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540793963	chr4:188160840-188160841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD

Chromatin state (count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188158400-188160200	Weak transcription	HMEC	breast
2	chr4:188158600-188160000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:188158600-188161000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:188159600-188160400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:188160000-188162000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:188160200-188160400	Enhancers	Ovary	ovary
7	chr4:188160200-188160400	Enhancers	HMEC	breast
8	chr4:188160400-188160800	Weak transcription	HMEC	breast
9	chr4:188160400-188164600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:188160800-188161200	Enhancers	HMEC	breast
11	chr4:188161000-188161200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:188164600-188166400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:188165600-188177000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr4:188166400-188190000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:188171000-188171800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:188171000-188172000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:188171200-188171800	Enhancers	Adipose Nuclei	Adipose
18	chr4:188171400-188171800	Enhancers	Fetal Lung	lung
19	chr4:188172000-188172400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr4:188172400-188173400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:188176600-188177000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:188176600-188177000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:188176600-188177000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:188176600-188177200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr4:188176600-188177200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:188176800-188177000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:188176800-188177200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:188177000-188177200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr4:188177000-188178000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:188177000-188179600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr4:188177200-188179600	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr4:188177400-188178200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr4:188178000-188178200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:188178000-188178600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:188178000-188179000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr4:188178200-188178400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:188178400-188179600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr4:188178800-188180400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:188179000-188179400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:188179400-188180600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:188179400-188180600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:188179600-188180400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:188179600-188180400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:188179600-188180400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:188179600-188180600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:188179600-188180600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:188179800-188180000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr4:188180000-188180600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:188180400-188180600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
50	chr4:188183800-188185400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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