Variant report

Variant	nsv594700
Chromosome Location	chr4:78738089-78740601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:600)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78738551-78739884	HepG2	liver:	n/a	chr4:78739592-78739608
2	ATF2	chr4:78739303-78739934	GM12878	blood:	n/a	n/a
3	BACH1	chr4:78740390-78740590	K562	blood:	n/a	n/a
4	BACH1	chr4:78739516-78740668	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr4:78739244-78740197	GM12878	blood:	n/a	chr4:78740059-78740072 chr4:78739971-78739984 chr4:78740060-78740073
6	BCLAF1	chr4:78740282-78740756	GM12878	blood:	n/a	chr4:78740643-78740656 chr4:78740648-78740657
7	BCLAF1	chr4:78739679-78740049	GM12878	blood:	n/a	chr4:78739971-78739984
8	BHLHE40	chr4:78739710-78740704	GM12878	blood:	n/a	chr4:78740062-78740078
9	BHLHE40	chr4:78739767-78740169	HepG2	liver:	n/a	chr4:78740062-78740078
10	BHLHE40	chr4:78739220-78740500	K562	blood:	n/a	chr4:78740062-78740078
11	BRCA1	chr4:78739324-78739968	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr4:78739990-78740013	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr4:78739878-78739945	HepG2	liver:	n/a	n/a
14	CCNT2	chr4:78739224-78741754	K562	blood:	n/a	chr4:78741442-78741451 chr4:78741506-78741515
15	CEBPB	chr4:78739319-78739929	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:78739401-78739861	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr4:78739304-78740677	GM12878	blood:	n/a	chr4:78740328-78740338
18	CHD1	chr4:78740298-78740471	H1-hESC	embryonic stem cell:	n/a	chr4:78740328-78740338
19	CHD1	chr4:78738659-78742661	IMR90	lung:	n/a	chr4:78741736-78741746 chr4:78740328-78740338
20	CHD1	chr4:78739272-78739971	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:78739261-78741914	Hela-S3	cervix:	n/a	chr4:78741736-78741746 chr4:78740328-78740338
22	CHD2	chr4:78740375-78740503	K562	blood:	n/a	n/a
23	CHD2	chr4:78740314-78740317	HepG2	liver:	n/a	n/a
24	CHD2	chr4:78739752-78740589	GM12878	blood:	n/a	chr4:78740328-78740338
25	CHD2	chr4:78740077-78740138	K562	blood:	n/a	n/a
26	CHD2	chr4:78739781-78739936	HepG2	liver:	n/a	n/a
27	CREB1	chr4:78739676-78739947	A549	lung:	n/a	n/a
28	CTBP2	chr4:78739250-78740791	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:78739380-78739530	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr4:78739856-78739910	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:78739400-78739550	HEK293	kidney:	n/a	n/a
32	CTCF	chr4:78739345-78739596	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:78739480-78739630	HMF	breast:	n/a	n/a
34	CTCF	chr4:78739400-78739550	RPTEC	kidney:	n/a	n/a
35	CTCF	chr4:78739834-78739998	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:78739400-78739550	GM12865	blood:	n/a	n/a
37	CTCF	chr4:78739436-78739551	GM13976	blood:	n/a	n/a
38	CTCF	chr4:78739365-78739603	Medullo	brain:	n/a	n/a
39	CTCF	chr4:78739420-78739570	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr4:78739700-78739850	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr4:78739400-78739550	AG09319	gingival:	n/a	n/a
42	CTCF	chr4:78739402-78739579	LNCaP	prostate:	n/a	n/a
43	CTCF	chr4:78739440-78739590	HepG2	liver:	n/a	n/a
44	CTCF	chr4:78739420-78739570	GM06990	blood:	n/a	n/a
45	CTCF	chr4:78739720-78739870	GM12870	blood:	n/a	n/a
46	CTCF	chr4:78739420-78739570	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr4:78739380-78739583	GM10266	blood:	n/a	n/a
48	CTCF	chr4:78739420-78739570	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:78739380-78739530	NB4	blood:	n/a	n/a
50	CTCF	chr4:78739400-78739550	GM12871	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78740080-78740130	HRE	kidney:	n/a
2	chr4:78740310-78740360	AG04450	lung:	fetal
3	chr4:78740310-78740360	HCPEpiC	choroid plexus:	n/a
4	chr4:78739402-78739452	K562	blood:	n/a
5	chr4:78740080-78740130	HRCEpiC	kidney:	n/a
6	chr4:78740080-78740130	GM12878	blood:	n/a
7	chr4:78739402-78739452	HMEC	breast:	n/a
8	chr4:78740080-78740130	SKMC	muscle:	n/a
9	chr4:78740080-78740130	PFSK-1	brain:	n/a
10	chr4:78740080-78740130	NB4	blood:	n/a
11	chr4:78740310-78740360	HL-60	blood:	n/a
12	chr4:78739402-78739452	Jurkat	blood:	n/a
13	chr4:78740080-78740130	PANC-1	pancreas:	n/a
14	chr4:78739402-78739452	ECC-1	luminal epithelium:	n/a
15	chr4:78739402-78739452	GM12891	blood:	n/a
16	chr4:78739402-78739452	IMR90	lung:	fetal
17	chr4:78739402-78739452	LNCaP	prostate:	n/a
18	chr4:78739402-78739452	HRPEpiC	eye:	n/a
19	chr4:78740080-78740130	GM12892	blood:	n/a
20	chr4:78740080-78740130	Hepatocyte	liver:	n/a
21	chr4:78740080-78740130	AG04449	skin:	fetal
22	chr4:78740310-78740360	GM12892	blood:	n/a
23	chr4:78739402-78739452	HRE	kidney:	n/a
24	chr4:78740080-78740130	HIPEpiC	eye:	n/a
25	chr4:78739402-78739452	HIPEpiC	eye:	n/a
26	chr4:78740080-78740130	Hela-S3	cervix:	n/a
27	chr4:78740080-78740130	LNCaP	prostate:	n/a
28	chr4:78740310-78740360	HRE	kidney:	n/a
29	chr4:78740310-78740360	Hepatocyte	liver:	n/a
30	chr4:78740310-78740360	PrEC	prostate:	n/a
31	chr4:78740080-78740130	NHDF-neo	bronchial:	n/a
32	chr4:78740310-78740360	HRPEpiC	eye:	n/a
33	chr4:78740310-78740360	HNPCEpiC	eye:	n/a
34	chr4:78740080-78740130	GM19239	blood:	n/a
35	chr4:78740080-78740130	MCF-7	breast:	n/a
36	chr4:78739402-78739452	NH-A	brain:	n/a
37	chr4:78739402-78739452	AG04449	skin:	fetal
38	chr4:78740310-78740360	BE2_C	brain:	n/a
39	chr4:78739402-78739452	A549	lung:	n/a
40	chr4:78739402-78739452	NHBE	bronchial:	n/a
41	chr4:78740310-78740360	AG09309	skin:	n/a
42	chr4:78740310-78740360	HAEpiC	amniotic membrane:	n/a
43	chr4:78740080-78740130	HL-60	blood:	n/a
44	chr4:78739402-78739452	AG10803	skin:	n/a
45	chr4:78740080-78740130	BE2_C	brain:	n/a
46	chr4:78740080-78740130	NH-A	brain:	n/a
47	chr4:78739402-78739452	AoSMC	blood vessel:	n/a
48	chr4:78739402-78739452	HL-60	blood:	n/a
49	chr4:78740080-78740130	MCF10A-Er-Src	breast:	n/a
50	chr4:78739402-78739452	HepG2	liver:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78738764..78744926-chr4:78780904..78785516,9	MCF-7	breast:
2	chr4:78739575..78742806-chr4:78977392..78979889,3	MCF-7	breast:
3	chr4:78734703..78743448-chr4:78779372..78785561,20	K562	blood:
4	chr4:78731203..78732890-chr4:78737622..78739382,2	K562	blood:
5	chr4:78738995..78744410-chr4:78782336..78785612,12	K562	blood:
6	chr4:78739575..78741919-chr4:78878334..78880056,2	MCF-7	breast:
7	chr4:78739409..78741307-chr4:83294294..83296166,2	MCF-7	breast:
8	chr4:78740326..78742288-chr4:79472480..79474297,2	MCF-7	breast:
9	chr4:78739289..78742998-chr4:78782109..78787360,12	MCF-7	breast:

No data

Variant related genes	Relation type
CNOT6L	TF binding region
CNOT6L	CpG island
ENSG00000138668	chromatin interactions
ENSG00000250214	chromatin interactions
ENSG00000138759	chromatin interactions
ENSG00000169288	chromatin interactions
ENSG00000272677	chromatin interactions
ENSG00000248926	chromatin interactions
ENSG00000138772	chromatin interactions

Extended variants
information (count: 108 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:108 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1814033	chr4:78738089-78738090	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377261195	chr4:78738096-78738097	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150496927	chr4:78738106-78738107	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs541847297	chr4:78738131-78738132	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189648384	chr4:78738136-78738137	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572129407	chr4:78738140-78738141	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541224066	chr4:78738141-78738142	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530686003	chr4:78738156-78738157	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549362752	chr4:78738204-78738205	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559907783	chr4:78738228-78738229	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114290476	chr4:78738282-78738283	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192541942	chr4:78738358-78738359	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199554999	chr4:78738376-78738377	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544317516	chr4:78738433-78738434	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139467113	chr4:78738495-78738496	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149848670	chr4:78738524-78738525	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549378708	chr4:78738533-78738534	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566005284	chr4:78738544-78738545	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144864056	chr4:78738583-78738584	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148553654	chr4:78738605-78738606	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184228891	chr4:78738666-78738667	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs199546274	chr4:78738706-78738707	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs67118509	chr4:78738707-78738708	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72056365	chr4:78738709-78738710	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200744529	chr4:78738710-78738711	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs537243649	chr4:78738736-78738737	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188956812	chr4:78738747-78738748	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556485435	chr4:78738832-78738833	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550863676	chr4:78738878-78738879	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563436380	chr4:78738898-78738899	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145590013	chr4:78738927-78738928	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181528307	chr4:78738935-78738936	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542526739	chr4:78738986-78738987	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555358968	chr4:78738991-78738992	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571997567	chr4:78739021-78739022	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147724203	chr4:78739034-78739035	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560922362	chr4:78739059-78739060	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs114957072	chr4:78739101-78739102	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535863508	chr4:78739102-78739103	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557467926	chr4:78739134-78739135	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186227379	chr4:78739201-78739202	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115451237	chr4:78739227-78739228	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528123193	chr4:78739229-78739230	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529604945	chr4:78739273-78739274	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542616168	chr4:78739325-78739326	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs62302715	chr4:78739339-78739340	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560664320	chr4:78739343-78739344	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372724349	chr4:78739357-78739358	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs118114195	chr4:78739398-78739399	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs190337289	chr4:78739483-78739484	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78718800-78738600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr4:78722200-78738600	Weak transcription	HSMM	muscle
3	chr4:78722600-78738600	Weak transcription	NHEK	skin
4	chr4:78722600-78739000	Weak transcription	Ovary	ovary
5	chr4:78722600-78739200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:78722800-78738600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:78723000-78738600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:78723200-78738600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:78724400-78738600	Weak transcription	Colonic Mucosa	Colon
10	chr4:78724800-78738600	Weak transcription	Brain Substantia Nigra	brain
11	chr4:78725800-78738600	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr4:78728600-78738600	Weak transcription	Psoas Muscle	Psoas
13	chr4:78728800-78738600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr4:78730400-78738600	Weak transcription	K562	blood
15	chr4:78732200-78738600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:78732400-78738600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:78732800-78738800	Weak transcription	Lung	lung
18	chr4:78733200-78738600	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr4:78733600-78738600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr4:78734800-78738600	Enhancers	Duodenum Mucosa	Duodenum
21	chr4:78735600-78738400	Enhancers	HepG2	liver
22	chr4:78735600-78738600	Enhancers	Liver	Liver
23	chr4:78735800-78738600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:78735800-78738600	Weak transcription	Fetal Kidney	kidney
25	chr4:78735800-78738800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:78736400-78738600	Enhancers	Primary hematopoietic stem cells	blood
27	chr4:78736400-78738600	Weak transcription	A549	lung
28	chr4:78736600-78738600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:78736600-78738800	Enhancers	Primary B cells from cord blood	blood
30	chr4:78736600-78739200	Flanking Active TSS	Primary T cells from cord blood	blood
31	chr4:78736800-78738600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:78736800-78738800	Weak transcription	Brain Germinal Matrix	brain
33	chr4:78737000-78738200	Weak transcription	HUVEC	blood vessel
34	chr4:78737000-78738400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr4:78737000-78738600	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr4:78737000-78738600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr4:78737000-78738600	Weak transcription	Right Ventricle	heart
38	chr4:78737000-78738600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr4:78737000-78738800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr4:78737000-78738800	Weak transcription	Aorta	Aorta
41	chr4:78737000-78738800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr4:78737000-78738800	Weak transcription	Esophagus	oesophagus
43	chr4:78737000-78738800	Weak transcription	Fetal Brain Male	brain
44	chr4:78737000-78738800	Weak transcription	Fetal Brain Female	brain
45	chr4:78737000-78738800	Weak transcription	Fetal Muscle Leg	muscle
46	chr4:78737000-78738800	Weak transcription	Small Intestine	intestine
47	chr4:78737000-78738800	Weak transcription	Spleen	Spleen
48	chr4:78737000-78742400	Active TSS	Thymus	Thymus
49	chr4:78737200-78738600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr4:78737200-78738600	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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