Variant report

Variant	nsv428779
Chromosome Location	chr4:188285249-188439933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:529)
CpG islands
(count:612)
Chromatin interactive
region (count:12)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
2	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
3	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
4	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
5	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
6	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
7	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
8	CEBPB	chr4:188337419-188337771	IMR90	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
9	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
10	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:188295952-188296114	HepG2	liver:	n/a	chr4:188296003-188296014 chr4:188296003-188296016
12	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
13	CEBPB	chr4:188309832-188310058	IMR90	lung:	n/a	chr4:188309977-188309986
14	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
15	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
16	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
17	CEBPB	chr4:188337488-188337650	K562	blood:	n/a	chr4:188337610-188337621
18	CEBPB	chr4:188301323-188301523	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:188317722-188317931	HepG2	liver:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
20	CEBPB	chr4:188301254-188301599	MCF-7	breast:	n/a	n/a
21	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
23	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
24	CEBPB	chr4:188301252-188301594	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
26	CTCF	chr4:188301320-188301470	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr4:188301271-188301530	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:188301179-188301619	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:188301320-188301470	HMEC	breast:	n/a	n/a
30	CTCF	chr4:188301320-188301470	HL-60	blood:	n/a	n/a
31	CTCF	chr4:188301287-188301469	K562	blood:	n/a	n/a
32	CTCF	chr4:188301340-188301490	HEK293	kidney:	n/a	n/a
33	CTCF	chr4:188301360-188301510	GM12878	blood:	n/a	n/a
34	CTCF	chr4:188338000-188338150	K562	blood:	n/a	n/a
35	CTCF	chr4:188301180-188301330	WI-38	lung:	n/a	n/a
36	CTCF	chr4:188301320-188301470	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr4:188301260-188301410	HEK293	kidney:	n/a	n/a
38	CTCF	chr4:188301400-188301550	WI-38	lung:	n/a	n/a
39	CTCF	chr4:188338000-188338150	GM12866	blood:	n/a	n/a
40	CTCF	chr4:188338000-188338150	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:188301347-188301449	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr4:188301301-188301509	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:188301380-188301530	A549	lung:	n/a	n/a
44	CTCF	chr4:188301218-188301736	HCT-116	colon:	n/a	n/a
45	CTCF	chr4:188301320-188301470	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:188301280-188301430	AG04450	lung:	n/a	n/a
47	CTCF	chr4:188301300-188301450	BJ	skin:	n/a	n/a
48	CTCF	chr4:188301280-188301430	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr4:188301320-188301470	BE2_C	brain:	n/a	n/a
50	CTCF	chr4:188338024-188338072	HepG2	liver:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188428637-188428687	GM12891	blood:	n/a
2	chr4:188426437-188426487	A549	lung:	n/a
3	chr4:188428637-188428687	GM12891	blood:	n/a
4	chr4:188426437-188426487	A549	lung:	n/a
5	chr4:188401038-188401088	RPTEC	kidney:	n/a
6	chr4:188423066-188423116	BE2_C	brain:	n/a
7	chr4:188423066-188423116	RPTEC	kidney:	n/a
8	chr4:188401038-188401088	SK-N-SH	brain:	n/a
9	chr4:188423066-188423116	GM12892	blood:	n/a
10	chr4:188426437-188426487	NT2-D1	testis:	n/a
11	chr4:188426506-188426556	AG04449	skin:	fetal
12	chr4:188428637-188428687	MCF10A-Er-Src	breast:	n/a
13	chr4:188391387-188391437	AG09319	gingival:	n/a
14	chr4:188427966-188428016	AG10803	skin:	n/a
15	chr4:188428637-188428687	NT2-D1	testis:	n/a
16	chr4:188428637-188428687	HCM	heart:	n/a
17	chr4:188391387-188391437	NT2-D1	testis:	n/a
18	chr4:188426278-188426328	ovcar-3	ovarian:	n/a
19	chr4:188426506-188426556	HCPEpiC	choroid plexus:	n/a
20	chr4:188391387-188391437	IMR90	lung:	fetal
21	chr4:188428637-188428687	NHBE	bronchial:	n/a
22	chr4:188426506-188426556	NHDF-neo	bronchial:	n/a
23	chr4:188423066-188423116	HL-60	blood:	n/a
24	chr4:188423066-188423116	HepG2	liver:	n/a
25	chr4:188391387-188391437	ProgFib	skin:	n/a
26	chr4:188423066-188423116	GM19239	blood:	n/a
27	chr4:188428637-188428687	Jurkat	blood:	n/a
28	chr4:188391387-188391437	RPTEC	kidney:	n/a
29	chr4:188401038-188401088	NB4	blood:	n/a
30	chr4:188401038-188401088	Jurkat	blood:	n/a
31	chr4:188426437-188426487	Hela-S3	cervix:	n/a
32	chr4:188314314-188314364	HEEpiC	esophagus:	n/a
33	chr4:188426278-188426328	SKMC	muscle:	n/a
34	chr4:188423066-188423116	ECC-1	luminal epithelium:	n/a
35	chr4:188391387-188391437	HL-60	blood:	n/a
36	chr4:188428637-188428687	GM06990	blood:	n/a
37	chr4:188398437-188398487	NHDF-neo	bronchial:	n/a
38	chr4:188314314-188314364	Jurkat	blood:	n/a
39	chr4:188426437-188426487	Hepatocyte	liver:	n/a
40	chr4:188314314-188314364	HCT-116	colon:	n/a
41	chr4:188426506-188426556	GM12891	blood:	n/a
42	chr4:188314314-188314364	IMR90	lung:	fetal
43	chr4:188428637-188428687	PrEC	prostate:	n/a
44	chr4:188391387-188391437	LNCaP	prostate:	n/a
45	chr4:188426278-188426328	NT2-D1	testis:	n/a
46	chr4:188423066-188423116	AG09319	gingival:	n/a
47	chr4:188398437-188398487	GM12878	blood:	n/a
48	chr4:188314314-188314364	HIPEpiC	eye:	n/a
49	chr4:188428637-188428687	HUVEC	blood vessel:	n/a
50	chr4:188423066-188423116	ovcar-3	ovarian:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
2	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
3	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
4	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
5	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:
6	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
7	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
8	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
9	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
10	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
11	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
12	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
2	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
3	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
4	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
5	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
6	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
7	lnc-ZFP42-6	chr4:188292838-188293075	XLOC_003826
8	lnc-ZFP42-6	chr4:188292449-188292580	XLOC_003826
9	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
10	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
11	lnc-ZFP42-5	chr4:188334718-188334865	ENSG00000250620
12	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
13	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
14	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
15	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
16	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828
17	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
18	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
19	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
20	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
21	lnc-ZFP42-6	chr4:188291802-188291929	XLOC_003826
22	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219

No data

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ENSG00000250042	TF binding region
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ENSG00000250042	CpG island
ENSG00000251643	chromatin interactions
ENSG00000029993	chromatin interactions
ANP32E	miRNA target sites
ANTXR1	miRNA target sites

Extended variants
information (count: 3738 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:3738 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545712399	chr4:188286211-188286212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188376794	chr4:188286226-188286227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560914558	chr4:188286227-188286228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542496168	chr4:188286229-188286230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560888592	chr4:188286230-188286231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544830120	chr4:188286246-188286247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560921895	chr4:188286293-188286294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552183101	chr4:188286297-188286298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529847460	chr4:188286298-188286299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62353221	chr4:188286371-188286372	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs114785283	chr4:188286406-188286407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs55966066	chr4:188286456-188286457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150433727	chr4:188286470-188286471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372734624	chr4:188286481-188286482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568818846	chr4:188286511-188286512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537600478	chr4:188286526-188286527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565141549	chr4:188286527-188286528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532602522	chr4:188286555-188286556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536785646	chr4:188286643-188286644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180743524	chr4:188286667-188286668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573164501	chr4:188286679-188286680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538671732	chr4:188286801-188286802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559253879	chr4:188286846-188286847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367633013	chr4:188286861-188286862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76127543	chr4:188286887-188286888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550485596	chr4:188286893-188286894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566258245	chr4:188286909-188286910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73019955	chr4:188286949-188286950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145922600	chr4:188286983-188286984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530354079	chr4:188287010-188287011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13136532	chr4:188287111-188287112	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561507762	chr4:188287136-188287137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12503292	chr4:188287137-188287138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13108880	chr4:188287153-188287154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs13108881	chr4:188287158-188287159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560004830	chr4:188287226-188287227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184413866	chr4:188287236-188287237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189705968	chr4:188287239-188287240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562439551	chr4:188287256-188287257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181337869	chr4:188287310-188287311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143838555	chr4:188287320-188287321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201679862	chr4:188287334-188287335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112970956	chr4:188287364-188287365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147258566	chr4:188287384-188287385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140604171	chr4:188287396-188287397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547037600	chr4:188287414-188287415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373091664	chr4:188287435-188287436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538988531	chr4:188287439-188287440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375975396	chr4:188287442-188287443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559042438	chr4:188287502-188287503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188286200-188286400	Enhancers	Pancreas	Pancrea
2	chr4:188286400-188287800	Weak transcription	Pancreas	Pancrea
3	chr4:188286600-188288000	Enhancers	HepG2	liver
4	chr4:188287800-188288400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr4:188287800-188288600	Enhancers	Pancreas	Pancrea
6	chr4:188288000-188288400	Enhancers	Fetal Lung	lung
7	chr4:188291800-188292600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:188291800-188292800	Enhancers	Fetal Heart	heart
9	chr4:188292000-188292200	Enhancers	Fetal Intestine Large	intestine
10	chr4:188292600-188294800	Weak transcription	Fetal Intestine Large	intestine
11	chr4:188292600-188304000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:188294600-188295200	Enhancers	Adipose Nuclei	Adipose
13	chr4:188294800-188295000	Enhancers	Fetal Intestine Large	intestine
14	chr4:188294800-188295000	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr4:188295000-188295600	Weak transcription	Fetal Intestine Large	intestine
16	chr4:188295200-188299200	Weak transcription	Adipose Nuclei	Adipose
17	chr4:188295600-188295800	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr4:188295600-188296600	Enhancers	Fetal Intestine Large	intestine
19	chr4:188297800-188298400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:188299200-188300000	Enhancers	Adipose Nuclei	Adipose
21	chr4:188301400-188301800	Enhancers	Pancreas	Pancrea
22	chr4:188301800-188304000	Weak transcription	Pancreas	Pancrea
23	chr4:188304000-188304600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:188304000-188304600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:188304200-188304800	Enhancers	HMEC	breast
26	chr4:188308400-188308600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr4:188308400-188309000	Enhancers	A549	lung
28	chr4:188308600-188309200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr4:188309000-188309400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:188309000-188309400	Flanking Active TSS	A549	lung
31	chr4:188309000-188309800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:188309200-188310000	Enhancers	Placenta Amnion	Placenta Amnion
33	chr4:188309400-188309600	Enhancers	A549	lung
34	chr4:188309800-188311000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:188310000-188310400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr4:188310400-188310800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr4:188311000-188311200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:188314200-188316000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:188314400-188315600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr4:188314800-188315000	Enhancers	NHLF	lung
41	chr4:188314800-188315600	Enhancers	NHDF-Ad	bronchial
42	chr4:188319600-188319800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:188321400-188322000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:188323200-188338800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:188329000-188329600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:188329400-188330000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:188335600-188337800	Enhancers	Fetal Brain Male	brain
48	chr4:188335800-188336000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:188335800-188336200	Enhancers	Fetal Muscle Leg	muscle
50	chr4:188335800-188339400	Enhancers	Fetal Lung	lung

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