Variant report

Variant	nsv965334
Chromosome Location	chr3:49967342-50000012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1178)
CpG islands
(count:1588)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:49977213-49977959	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:49967746-49967786	K562	blood:	n/a	n/a
3	ARID3A	chr3:49967290-49967702	HepG2	liver:	n/a	n/a
4	ATF1	chr3:49998077-49998258	K562	blood:	n/a	n/a
5	ATF1	chr3:49977195-49977837	K562	blood:	n/a	n/a
6	ATF2	chr3:49984110-49984569	GM12878	blood:	n/a	n/a
7	ATF2	chr3:49966802-49967487	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:49977189-49978149	GM12878	blood:	n/a	n/a
9	ATF3	chr3:49967195-49967625	K562	blood:	n/a	n/a
10	ATF3	chr3:49977251-49977657	K562	blood:	n/a	n/a
11	ATF3	chr3:49977192-49977778	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr3:49977110-49977867	GM12878	blood:	n/a	n/a
13	ATF3	chr3:49977205-49977663	HepG2	liver:	n/a	n/a
14	ATF3	chr3:49967192-49967647	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:49977510-49978006	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:49967265-49967614	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr3:49974039-49974263	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:49977194-49977761	K562	blood:	n/a	n/a
19	BCLAF1	chr3:49984582-49984855	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:49977140-49978237	GM12878	blood:	n/a	n/a
21	BCLAF1	chr3:49966932-49967473	GM12878	blood:	n/a	chr3:49967346-49967359
22	BCLAF1	chr3:49977148-49978284	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:49967102-49967544	K562	blood:	n/a	n/a
24	BHLHE40	chr3:49977162-49978070	K562	blood:	n/a	n/a
25	BHLHE40	chr3:49977175-49977857	HepG2	liver:	n/a	n/a
26	BHLHE40	chr3:49977207-49978127	GM12878	blood:	n/a	n/a
27	BRCA1	chr3:49977278-49978146	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:49967382-49967553	GM12878	blood:	n/a	n/a
29	BRCA1	chr3:49977518-49978150	HepG2	liver:	n/a	n/a
30	BRCA1	chr3:49967034-49967443	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr3:49967142-49967728	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr3:49977117-49977499	K562	blood:	n/a	n/a
33	CBX3	chr3:49966704-49967480	K562	blood:	n/a	n/a
34	CBX3	chr3:49976962-49978180	K562	blood:	n/a	n/a
35	CCNT2	chr3:49967026-49967599	K562	blood:	n/a	n/a
36	CCNT2	chr3:49977214-49978065	K562	blood:	n/a	n/a
37	CEBPB	chr3:49977525-49977637	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:49977877-49978190	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:49974598-49974890	K562	blood:	n/a	n/a
40	CEBPB	chr3:49967167-49967666	K562	blood:	n/a	chr3:49967424-49967435
41	CEBPB	chr3:49978408-49978681	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:49967226-49967632	MCF-7	breast:	n/a	chr3:49967424-49967435
43	CEBPB	chr3:49966795-49967729	ECC-1	luminal epithelium:	n/a	chr3:49967424-49967435
44	CEBPB	chr3:49974668-49974805	HepG2	liver:	n/a	n/a
45	CEBPB	chr3:49967222-49967650	HepG2	liver:	n/a	chr3:49967424-49967435
46	CEBPB	chr3:49967318-49967522	K562	blood:	n/a	chr3:49967424-49967435
47	CEBPB	chr3:49967253-49967631	ECC-1	luminal epithelium:	n/a	chr3:49967424-49967435
48	CEBPB	chr3:49995211-49995383	K562	blood:	n/a	chr3:49995320-49995331
49	CEBPB	chr3:49967317-49967653	A549	lung:	n/a	chr3:49967424-49967435
50	CEBPB	chr3:49974652-49974829	Hela-S3	cervix:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49967669-49967719	NH-A	brain:	n/a
2	chr3:49977388-49977438	AG09309	skin:	n/a
3	chr3:49967669-49967719	NH-A	brain:	n/a
4	chr3:49977388-49977438	AG09309	skin:	n/a
5	chr3:49967669-49967719	HL-60	blood:	n/a
6	chr3:49967521-49967571	HMEC	breast:	n/a
7	chr3:49977234-49977284	MCF-7	breast:	n/a
8	chr3:49977428-49977478	LNCaP	prostate:	n/a
9	chr3:49977988-49978038	NT2-D1	testis:	n/a
10	chr3:49967521-49967571	NT2-D1	testis:	n/a
11	chr3:49967416-49967466	SK-N-SH_RA	brain:	n/a
12	chr3:49977234-49977284	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:49977228-49977278	SK-N-SH	brain:	n/a
14	chr3:49977390-49977440	HIPEpiC	eye:	n/a
15	chr3:49967669-49967719	SK-N-SH_RA	brain:	n/a
16	chr3:49977988-49978038	GM06990	blood:	n/a
17	chr3:49967358-49967408	HRE	kidney:	n/a
18	chr3:49967669-49967719	GM19239	blood:	n/a
19	chr3:49977190-49977240	HCPEpiC	choroid plexus:	n/a
20	chr3:49977190-49977240	HIPEpiC	eye:	n/a
21	chr3:49967517-49967567	NT2-D1	testis:	n/a
22	chr3:49977370-49977420	CMK	blood:	n/a
23	chr3:49977591-49977641	SK-N-MC	brain:	n/a
24	chr3:49977234-49977284	AoSMC	blood vessel:	n/a
25	chr3:49987589-49987639	HCF	heart:	n/a
26	chr3:49977390-49977440	SKMC	muscle:	n/a
27	chr3:49987589-49987639	HEEpiC	esophagus:	n/a
28	chr3:49977228-49977278	SK-N-MC	brain:	n/a
29	chr3:49977591-49977641	T-47D	breast:	n/a
30	chr3:49977988-49978038	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:49987589-49987639	HEK293	kidney:	embryo
32	chr3:49977596-49977646	HNPCEpiC	eye:	n/a
33	chr3:49967521-49967571	HRE	kidney:	n/a
34	chr3:49977380-49977430	NH-A	brain:	n/a
35	chr3:49977418-49977468	SK-N-SH_RA	brain:	n/a
36	chr3:49977390-49977440	HEK293	kidney:	embryo
37	chr3:49977418-49977468	NHDF-neo	bronchial:	n/a
38	chr3:49974058-49974108	PFSK-1	brain:	n/a
39	chr3:49977418-49977468	Caco-2	colon:	n/a
40	chr3:49977988-49978038	AG10803	skin:	n/a
41	chr3:49977388-49977438	HAEpiC	amniotic membrane:	n/a
42	chr3:49977390-49977440	Hepatocyte	liver:	n/a
43	chr3:49977370-49977420	LNCaP	prostate:	n/a
44	chr3:49967669-49967719	HAEpiC	amniotic membrane:	n/a
45	chr3:49977591-49977641	HRPEpiC	eye:	n/a
46	chr3:49967669-49967719	T-47D	breast:	n/a
47	chr3:49974058-49974108	HEEpiC	esophagus:	n/a
48	chr3:49977234-49977284	Jurkat	blood:	n/a
49	chr3:49977370-49977420	GM12878	blood:	n/a
50	chr3:49967517-49967567	Caco-2	colon:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49840341..49842910-chr3:49967049..49969753,2	K562	blood:
2	chr3:49978223..49979811-chr3:50003793..50005372,2	K562	blood:
3	chr3:49977058..49978995-chr3:49986374..49988156,2	K562	blood:
4	chr3:49964076..49966567-chr3:49968283..49970694,2	K562	blood:
5	chr3:49966762..49969614-chr3:50125142..50129125,3	K562	blood:
6	chr3:49965568..49971141-chr3:49975411..49979217,7	MCF-7	breast:
7	chr3:49965505..49970003-chr3:49974970..49980028,17	K562	blood:
8	chr3:49970783..49974406-chr3:49975883..49977982,3	K562	blood:
9	chr3:49966817..49967335-chr3:49977017..49977900,2	MCF-7	breast:
10	chr3:49976087..49977817-chr3:49983493..49984999,2	K562	blood:
11	chr3:49977495..49980410-chr3:49985163..49987874,2	K562	blood:
12	chr3:49976777..49979438-chr3:49981879..49983606,2	MCF-7	breast:
13	chr3:49977200..49977809-chr6:41040589..41041439,2	NB4	blood:
14	chr3:49892535..49894935-chr3:49965699..49968471,2	K562	blood:
15	chr1:145438159..145439066-chr3:49977309..49978070,2	Hela-S3	cervix:
16	chr3:49966957..49970009-chr3:49975972..49978983,5	MCF-7	breast:
17	chr3:49965505..49970003-chr3:49975811..49980300,11	K562	blood:
18	chr15:99191647..99192614-chr3:49977517..49978125,2	Hela-S3	cervix:
19	chr3:49823173..49825666-chr3:49976602..49979269,2	MCF-7	breast:
20	chr3:49966957..49970009-chr3:49975972..49978983,5	MCF-7	breast:
21	chr3:49965505..49970003-chr3:49974970..49980028,17	K562	blood:
22	chr3:49977713..49979804-chr3:49979930..49983021,3	K562	blood:
23	chr3:49966031..49968659-chr3:50125180..50127794,3	K562	blood:
24	chr3:49935827..49937610-chr3:49975872..49978554,2	K562	blood:
25	chr3:49977294..49978117-chr3:52007652..52008341,2	HCT-116	colon:
26	chr3:49965505..49970003-chr3:49975811..49980300,11	K562	blood:
27	chr3:49971935..49974638-chr3:49975827..49978010,2	MCF-7	breast:
28	chr3:49977271..49977999-chr3:183903220..183904111,2	Hela-S3	cervix:
29	chr13:111364730..111365670-chr3:49977226..49977814,2	Hela-S3	cervix:
30	chr19:39897402..39898381-chr3:49977408..49978016,3	Hela-S3	cervix:
31	chr3:49977713..49979508-chr3:49980727..49984411,5	K562	blood:
32	chr3:49965568..49971141-chr3:49975411..49979217,7	MCF-7	breast:
33	chr3:49965901..49968488-chr3:49971749..49974859,3	K562	blood:
34	chr3:49750537..49752087-chr3:49966182..49968764,2	K562	blood:
35	chr3:49977095..49978042-chr7:86781332..86782269,3	Hela-S3	cervix:
36	chr3:49975788..49978611-chr3:50125447..50127862,2	MCF-7	breast:
37	chr3:49976300..49979550-chr3:50125389..50128777,3	K562	blood:
38	chr19:16187375..16188133-chr3:49977216..49977859,2	Hela-S3	cervix:
39	chr3:49892284..49895111-chr3:49976165..49977880,2	K562	blood:
40	chr3:49966310..49967243-chr3:49977434..49978106,2	MCF-7	breast:

No data

Variant related genes	Relation type
MON1A	TF binding region
RBM6	TF binding region
MON1A	CpG island
RBM6	CpG island
ENSG00000003756	chromatin interactions
ENSG00000183763	chromatin interactions
ENSG00000161204	chromatin interactions
ENSG00000135164	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000164068	chromatin interactions
ENSG00000140443	chromatin interactions
ENSG00000224046	chromatin interactions
ENSG00000164077	chromatin interactions
ENSG00000272762	chromatin interactions
ENSG00000117289	chromatin interactions
ENSG00000167460	chromatin interactions
ENSG00000248487	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000176095	chromatin interactions
ENSG00000128016	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000230698	chromatin interactions
ENSG00000004534	chromatin interactions
ENSG00000185614	chromatin interactions

Extended variants
information (count: 1152 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535089749	chr3:49967375-49967376	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs550644084	chr3:49967500-49967501	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs568551225	chr3:49967502-49967503	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs539005073	chr3:49967567-49967568	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs199678483	chr3:49967568-49967569	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs368955292	chr3:49967583-49967584	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs572771402	chr3:49967623-49967624	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs533753128	chr3:49967655-49967656	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs375504621	chr3:49967674-49967675	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs371845184	chr3:49967709-49967710	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs573757968	chr3:49967744-49967745	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs188412899	chr3:49967764-49967765	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs542005789	chr3:49967821-49967822	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs557419496	chr3:49967920-49967921	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs575720476	chr3:49968036-49968037	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs546174126	chr3:49968038-49968039	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs76749605	chr3:49968043-49968044	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs145212375	chr3:49968084-49968085	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs372376252	chr3:49968092-49968093	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs555371053	chr3:49968131-49968132	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs564793571	chr3:49968154-49968155	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs528763263	chr3:49968265-49968266	Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs115469655	chr3:49968349-49968350	Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs562175606	chr3:49968373-49968374	Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs529477398	chr3:49968405-49968406	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs550410537	chr3:49968435-49968436	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs556620737	chr3:49968515-49968516	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs191258217	chr3:49968534-49968535	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs6771546	chr3:49968572-49968573	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs140609664	chr3:49968608-49968609	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs566114960	chr3:49968695-49968696	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs9863339	chr3:49968744-49968745	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555632229	chr3:49968749-49968750	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs553949520	chr3:49968770-49968771	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs567390631	chr3:49968812-49968813	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs183150739	chr3:49968938-49968939	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs557495715	chr3:49969003-49969004	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562606929	chr3:49969024-49969025	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs575782824	chr3:49969044-49969045	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs34287901	chr3:49969047-49969048	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs546237503	chr3:49969049-49969050	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs71631035	chr3:49969063-49969064	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546021543	chr3:49969116-49969117	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs79188368	chr3:49969162-49969163	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs558219619	chr3:49969327-49969328	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs187595857	chr3:49969335-49969336	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs534187506	chr3:49969367-49969368	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs573255147	chr3:49969384-49969385	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs191117458	chr3:49969395-49969396	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs112299656	chr3:49969472-49969473	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49966000-49967800	Active TSS	Fetal Kidney	kidney
2	chr3:49966000-49968200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr3:49966200-49967400	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr3:49966200-49967400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr3:49966200-49967400	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr3:49966200-49967400	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr3:49966200-49967400	Active TSS	HSMM	muscle
8	chr3:49966200-49967400	Active TSS	NHLF	lung
9	chr3:49966200-49967800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:49966200-49967800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:49966200-49967800	Active TSS	Brain Hippocampus Middle	brain
12	chr3:49966200-49968000	Active TSS	Psoas Muscle	Psoas
13	chr3:49966200-49968200	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr3:49966400-49967400	Active TSS	H1 Cell Line	embryonic stem cell
15	chr3:49966400-49967400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:49966400-49967400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr3:49966400-49967400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr3:49966400-49967400	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr3:49966400-49967400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:49966400-49967400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr3:49966400-49967400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:49966400-49967400	Active TSS	Muscle Satellite Cultured Cells	--
23	chr3:49966400-49967400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr3:49966400-49967400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr3:49966400-49967400	Active TSS	Duodenum Mucosa	Duodenum
26	chr3:49966400-49967400	Active TSS	Fetal Brain Female	brain
27	chr3:49966400-49967400	Active TSS	Fetal Intestine Large	intestine
28	chr3:49966400-49967400	Active TSS	Fetal Intestine Small	intestine
29	chr3:49966400-49967400	Active TSS	Rectal Smooth Muscle	rectum
30	chr3:49966400-49967400	Active TSS	GM12878-XiMat	blood
31	chr3:49966400-49967400	Active TSS	Hela-S3	cervix
32	chr3:49966400-49967400	Active TSS	HMEC	breast
33	chr3:49966400-49967400	Active TSS	HSMMtube	muscle
34	chr3:49966400-49967400	Active TSS	HUVEC	blood vessel
35	chr3:49966400-49967400	Active TSS	NHEK	skin
36	chr3:49966400-49967400	Active TSS	Osteobl	bone
37	chr3:49966400-49967600	Active TSS	H9 Cell Line	embryonic stem cell
38	chr3:49966400-49967600	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr3:49966400-49967600	Flanking Active TSS	Primary hematopoietic stem cells	blood
40	chr3:49966400-49967600	Active TSS	Primary T killer memory cells from peripheral blood	blood
41	chr3:49966400-49967600	Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr3:49966400-49967600	Active TSS	Brain Angular Gyrus	brain
43	chr3:49966400-49967600	Active TSS	Brain Anterior Caudate	brain
44	chr3:49966400-49967600	Active TSS	Brain Germinal Matrix	brain
45	chr3:49966400-49967600	Active TSS	Colon Smooth Muscle	Colon
46	chr3:49966400-49967600	Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr3:49966400-49967600	Active TSS	A549	lung
48	chr3:49966400-49967600	Active TSS	NHDF-Ad	bronchial
49	chr3:49966400-49967800	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr3:49966400-49968000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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