Variant report

Variant	nsv964740
Chromosome Location	chr4:69137797-69159003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:69137557-69138352	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr4:69138568-69138734	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:69151973-69151987	GM12878	blood:	n/a	n/a
4	CBX3	chr4:69147378-69147755	K562	blood:	n/a	n/a
5	CEBPB	chr4:69151511-69151639	K562	blood:	n/a	n/a
6	CEBPB	chr4:69138149-69138405	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:69151434-69151642	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:69151515-69151974	HepG2	liver:	n/a	chr4:69151832-69151845 chr4:69151833-69151844 chr4:69151832-69151845 chr4:69151832-69151843
9	CEBPB	chr4:69154789-69154925	K562	blood:	n/a	n/a
10	CEBPD	chr4:69147413-69147936	K562	blood:	n/a	n/a
11	CHD1	chr4:69137913-69138143	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr4:69137523-69138304	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:69137476-69137982	HCT-116	colon:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
14	CTCF	chr4:69137524-69137873	A549	lung:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
15	CTCF	chr4:69137426-69137945	MCF-7	breast:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
16	CTCF	chr4:69137518-69137811	Kidney_OC	kidney:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
17	CTCF	chr4:69137569-69137803	GM13977	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
18	CTCF	chr4:69137660-69137810	HA-sp	spinal cord:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
19	CTCF	chr4:69137404-69138072	SK-N-SH	brain:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
20	CTCF	chr4:69137524-69137828	Medullo	brain:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
21	CTCF	chr4:69137555-69137802	K562	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
22	CTCF	chr4:69137660-69137810	HAc	cerebellar:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
23	CTCF	chr4:69137414-69137982	HCT-116	colon:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
24	CTCF	chr4:69137449-69137888	K562	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
25	CTCF	chr4:69137532-69137838	Spleen_OC	spleen:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
26	CTCF	chr4:69137540-69137820	HUVEC	blood vessel:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
27	CTCF	chr4:69137564-69137807	GM12878	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
28	CTCF	chr4:69137363-69138002	A549	lung:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
29	CTCF	chr4:69137531-69137802	SK-N-SH_RA	brain:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
30	CTCF	chr4:69137563-69137819	Lung_OC	lung:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
31	CTCF	chr4:69137479-69137879	H1-hESC	embryonic stem cell:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
32	CTCF	chr4:69143618-69143648	GM13976	blood:	n/a	n/a
33	CTCF	chr4:69137482-69137940	IMR90	lung:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
34	CTCF	chr4:69144760-69144910	GM12865	blood:	n/a	n/a
35	CTCF	chr4:69137566-69137808	Pancreas_OC	pancreas:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
36	CTCF	chr4:69137660-69137810	GM12872	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
37	CTCF	chr4:69137493-69137865	ECC-1	luminal epithelium:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
38	CTCF	chr4:69137660-69137810	BJ	skin:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
39	CTCF	chr4:69137660-69137810	NHDF-neo	bronchial:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
40	CTCF	chr4:69137532-69137847	T-47D	breast:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
41	CTCF	chr4:69158820-69158828	K562	blood:	n/a	n/a
42	CTCF	chr4:69138400-69138610	GM12801	blood:	n/a	n/a
43	CTCF	chr4:69137660-69137810	BE2_C	brain:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
44	CTCF	chr4:69137503-69137863	K562	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
45	CTCF	chr4:69137660-69137810	HRE	kidney:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
46	CTCF	chr4:69137462-69137801	MCF-7	breast:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
47	CTCF	chr4:69137544-69137806	HepG2	liver:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
48	CTCF	chr4:69137485-69137915	GM12878	blood:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
49	CTCF	chr4:69137465-69137881	HepG2	liver:	n/a	chr4:69137686-69137702 chr4:69137690-69137698
50	E2F4	chr4:69158403-69158603	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69138730-69138780	Hepatocyte	liver:	n/a
2	chr4:69138730-69138780	BJ	skin:	n/a
3	chr4:69138730-69138780	HAEpiC	amniotic membrane:	n/a
4	chr4:69138730-69138780	HRCEpiC	kidney:	n/a
5	chr4:69138730-69138780	PFSK-1	brain:	n/a
6	chr4:69138730-69138780	AoSMC	blood vessel:	n/a
7	chr4:69138730-69138780	MCF10A-Er-Src	breast:	n/a
8	chr4:69138730-69138780	K562	blood:	n/a
9	chr4:69138730-69138780	HL-60	blood:	n/a
10	chr4:69138730-69138780	HMEC	breast:	n/a
11	chr4:69138730-69138780	Jurkat	blood:	n/a
12	chr4:69138730-69138780	CMK	blood:	n/a
13	chr4:69138730-69138780	SKMC	muscle:	n/a
14	chr4:69138730-69138780	HRE	kidney:	n/a
15	chr4:69138730-69138780	Caco-2	colon:	n/a
16	chr4:69138730-69138780	H1-hESC	embryonic stem cell:	embryo
17	chr4:69138730-69138780	NT2-D1	testis:	n/a
18	chr4:69138730-69138780	NB4	blood:	n/a
19	chr4:69138730-69138780	MCF-7	breast:	n/a
20	chr4:69138730-69138780	T-47D	breast:	n/a
21	chr4:69138730-69138780	NHBE	bronchial:	n/a
22	chr4:69138730-69138780	SK-N-MC	brain:	n/a
23	chr4:69138730-69138780	PrEC	prostate:	n/a
24	chr4:69138730-69138780	GM06990	blood:	n/a
25	chr4:69138730-69138780	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:69138730-69138780	AG10803	skin:	n/a
27	chr4:69138730-69138780	AG04450	lung:	fetal
28	chr4:69138730-69138780	GM12878	blood:	n/a
29	chr4:69138730-69138780	SK-N-SH_RA	brain:	n/a
30	chr4:69138730-69138780	NHDF-neo	bronchial:	n/a
31	chr4:69138730-69138780	HepG2	liver:	n/a
32	chr4:69138730-69138780	RPTEC	kidney:	n/a
33	chr4:69138730-69138780	PANC-1	pancreas:	n/a
34	chr4:69138730-69138780	A549	lung:	n/a
35	chr4:69138730-69138780	GM19239	blood:	n/a
36	chr4:69138730-69138780	ovcar-3	ovarian:	n/a
37	chr4:69138730-69138780	HUVEC	blood vessel:	n/a
38	chr4:69138730-69138780	ProgFib	skin:	n/a
39	chr4:69138730-69138780	NH-A	brain:	n/a
40	chr4:69138730-69138780	HRPEpiC	eye:	n/a
41	chr4:69138730-69138780	LNCaP	prostate:	n/a
42	chr4:69138730-69138780	Hela-S3	cervix:	n/a
43	chr4:69138730-69138780	HCF	heart:	n/a
44	chr4:69138730-69138780	HCM	heart:	n/a
45	chr4:69138730-69138780	IMR90	lung:	fetal
46	chr4:69138730-69138780	GM12891	blood:	n/a
47	chr4:69138730-69138780	GM12892	blood:	n/a
48	chr4:69138730-69138780	HCT-116	colon:	n/a
49	chr4:69138730-69138780	HIPEpiC	eye:	n/a
50	chr4:69138730-69138780	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:69148927..69150978-chr4:69199918..69202560,2	K562	blood:
2	chr1:180884197..180885718-chr4:69153705..69156603,2	MCF-7	breast:
3	chr4:69152138..69154955-chr4:69200554..69203200,2	K562	blood:
4	chr4:69143211..69145096-chr4:69239415..69241951,2	K562	blood:
5	chr4:69137297..69138672-chr4:69241345..69242423,9	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YTHDC1-2	chr4:69151533-69151677	NONHSAT096728
2	lnc-YTHDC1-2	chr4:69149523-69149595	NONHSAT096728
3	lnc-YTHDC1-2	chr4:69148179-69148398	NONHSAT096728

Variant related genes	Relation type
ENSG00000248639	TF binding region
ENSG00000250642	TF binding region
ENSG00000248639	CpG island
ENSG00000250642	CpG island
ENSG00000162840	chromatin interactions

Extended variants
information (count: 866 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562004336	chr4:69137801-69137802	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549385464	chr4:69137804-69137805	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs545780282	chr4:69137806-69137807	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568075860	chr4:69137862-69137863	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527993643	chr4:69137874-69137875	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72856446	chr4:69137905-69137906	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs145248098	chr4:69137926-69137927	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147263588	chr4:69137946-69137947	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530131251	chr4:69137970-69137971	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549804695	chr4:69137988-69137989	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373155613	chr4:69138016-69138017	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs34945022	chr4:69138035-69138036	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs371089260	chr4:69138061-69138062	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188757334	chr4:69138139-69138140	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549573138	chr4:69138172-69138173	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538977389	chr4:69138205-69138206	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs113631128	chr4:69138246-69138247	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540042533	chr4:69138253-69138254	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144593781	chr4:69138279-69138280	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7674768	chr4:69138292-69138293	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs576627628	chr4:69138303-69138304	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555181714	chr4:69138307-69138308	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7691074	chr4:69138386-69138387	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537150730	chr4:69138429-69138430	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs192136748	chr4:69138450-69138451	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576783927	chr4:69138491-69138492	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368273894	chr4:69138516-69138517	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552510000	chr4:69138523-69138524	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145725940	chr4:69138580-69138581	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7670560	chr4:69138643-69138644	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs573070991	chr4:69138645-69138646	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149004049	chr4:69138653-69138654	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185455735	chr4:69138654-69138655	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530580215	chr4:69138696-69138697	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76892741	chr4:69138823-69138824	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs190293433	chr4:69138869-69138870	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs374743071	chr4:69138920-69138921	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs182520394	chr4:69138967-69138968	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs151116964	chr4:69138984-69138985	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs548226044	chr4:69138999-69139000	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs568337490	chr4:69139046-69139047	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367775165	chr4:69139050-69139051	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548856541	chr4:69139051-69139052	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185814655	chr4:69139117-69139118	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537611523	chr4:69139126-69139127	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552873970	chr4:69139152-69139153	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570511334	chr4:69139160-69139161	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145116975	chr4:69139195-69139196	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7676366	chr4:69139236-69139237	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs137921254	chr4:69139273-69139274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ollier disease	21235737	CNVD
Autism	21865298	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Medulloblastoma	21163964	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69133600-69137800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:69134000-69137800	Weak transcription	NHLF	lung
3	chr4:69134200-69137800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:69134200-69137800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr4:69134200-69137800	Weak transcription	Ovary	ovary
6	chr4:69134200-69137800	Weak transcription	HMEC	breast
7	chr4:69134200-69137800	Weak transcription	HSMM	muscle
8	chr4:69136200-69138200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:69137000-69138400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:69137200-69137800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:69137200-69137800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:69137200-69137800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:69137400-69138800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:69137600-69137800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:69137600-69137800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:69137600-69137800	Enhancers	Fetal Intestine Large	intestine
17	chr4:69137600-69137800	Active TSS	NH-A	brain
18	chr4:69137600-69138200	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr4:69137600-69138200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:69137600-69138200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:69137600-69138200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:69137600-69138200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:69137600-69138200	Active TSS	Osteobl	bone
24	chr4:69137800-69138000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr4:69137800-69138000	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr4:69137800-69138000	Active TSS	Primary hematopoietic stem cells	blood
27	chr4:69137800-69138000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:69137800-69138000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:69137800-69138000	Flanking Active TSS	NH-A	brain
30	chr4:69137800-69138000	Active TSS	NHEK	skin
31	chr4:69137800-69138200	Active TSS	H9 Cell Line	embryonic stem cell
32	chr4:69137800-69138200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:69137800-69138200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:69137800-69138200	Active TSS	HUES64 Cell Line	embryonic stem cell
35	chr4:69137800-69138200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:69137800-69138200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr4:69137800-69138200	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr4:69137800-69138200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:69137800-69138200	Active TSS	Muscle Satellite Cultured Cells	--
40	chr4:69137800-69138200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:69137800-69138200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr4:69137800-69138200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:69137800-69138200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr4:69137800-69138200	Active TSS	Brain Substantia Nigra	brain
45	chr4:69137800-69138200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
46	chr4:69137800-69138200	Flanking Active TSS	Fetal Intestine Large	intestine
47	chr4:69137800-69138200	Active TSS	Fetal Kidney	kidney
48	chr4:69137800-69138200	Active TSS	Fetal Muscle Trunk	muscle
49	chr4:69137800-69138200	Active TSS	Fetal Stomach	stomach
50	chr4:69137800-69138200	Active TSS	Ovary	ovary

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