Variant report

Variant	esv3420339
Chromosome Location	chr3:49505548-49510046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:550)
Chromatin interactive
region (count:28)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:49507229-49507663	K562	blood:	n/a	n/a
2	ARID3A	chr3:49507921-49507987	K562	blood:	n/a	n/a
3	ARID3A	chr3:49506649-49506704	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:49508127-49508140	HepG2	liver:	n/a	n/a
5	ATF2	chr3:49507039-49507498	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr3:49506787-49507344	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:49506859-49507457	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr3:49507111-49507464	A549	lung:	n/a	n/a
9	BCLAF1	chr3:49507220-49508257	GM12878	blood:	n/a	chr3:49507529-49507542 chr3:49507531-49507544
10	BHLHE40	chr3:49507119-49508162	GM12878	blood:	n/a	chr3:49507920-49507936 chr3:49507598-49507614
11	BHLHE40	chr3:49509368-49509744	K562	blood:	n/a	n/a
12	BHLHE40	chr3:49507265-49508115	K562	blood:	n/a	chr3:49507920-49507936 chr3:49507598-49507614
13	BHLHE40	chr3:49507202-49507815	HepG2	liver:	n/a	chr3:49507598-49507614
14	BRCA1	chr3:49506884-49507757	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr3:49507195-49507387	HepG2	liver:	n/a	n/a
16	BRCA1	chr3:49506988-49507393	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr3:49507921-49507954	HepG2	liver:	n/a	n/a
18	CBX3	chr3:49507754-49508255	K562	blood:	n/a	n/a
19	CBX3	chr3:49509312-49509769	K562	blood:	n/a	n/a
20	CCNT2	chr3:49509460-49509753	K562	blood:	n/a	n/a
21	CCNT2	chr3:49507283-49508340	K562	blood:	n/a	chr3:49507353-49507362
22	CEBPB	chr3:49506788-49507351	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:49507151-49507483	GM12878	blood:	n/a	n/a
24	CEBPB	chr3:49507475-49507767	HepG2	liver:	n/a	chr3:49507491-49507499
25	CEBPB	chr3:49506379-49508231	Hela-S3	cervix:	n/a	chr3:49507491-49507499
26	CEBPB	chr3:49507520-49507716	IMR90	lung:	n/a	n/a
27	CEBPD	chr3:49507006-49508138	HepG2	liver:	n/a	n/a
28	CHD1	chr3:49507009-49507283	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr3:49506442-49506605	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr3:49508285-49508485	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr3:49506945-49508260	GM12878	blood:	n/a	n/a
32	CHD1	chr3:49508478-49508783	GM12878	blood:	n/a	n/a
33	CHD2	chr3:49507126-49507772	K562	blood:	n/a	n/a
34	CHD2	chr3:49506965-49508193	GM12878	blood:	n/a	n/a
35	CHD2	chr3:49507748-49507975	HepG2	liver:	n/a	n/a
36	CHD2	chr3:49506968-49507072	HepG2	liver:	n/a	n/a
37	CHD2	chr3:49506858-49507971	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr3:49506826-49508138	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr3:49507322-49507451	HepG2	liver:	n/a	n/a
40	CREB1	chr3:49507077-49508289	GM12878	blood:	n/a	n/a
41	CREB1	chr3:49506478-49508467	HepG2	liver:	n/a	n/a
42	CREB1	chr3:49506796-49508185	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr3:49507038-49507937	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr3:49506770-49508199	A549	lung:	n/a	n/a
45	CTBP2	chr3:49507721-49508261	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr3:49508200-49508350	HMF	breast:	n/a	n/a
47	CTCF	chr3:49508200-49508350	HCM	heart:	n/a	n/a
48	CTCF	chr3:49507740-49507890	GM12865	blood:	n/a	n/a
49	CTCF	chr3:49508160-49508310	AG04450	lung:	n/a	chr3:49508177-49508190
50	CTCF	chr3:49508840-49508990	HCPEpiC	choroid plexus:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49507545-49507595	HUVEC	blood vessel:	n/a
2	chr3:49507545-49507595	HUVEC	blood vessel:	n/a
3	chr3:49509320-49509370	Hepatocyte	liver:	n/a
4	chr3:49509320-49509370	A549	lung:	n/a
5	chr3:49507266-49507316	BE2_C	brain:	n/a
6	chr3:49507266-49507316	GM12892	blood:	n/a
7	chr3:49507478-49507528	AoSMC	blood vessel:	n/a
8	chr3:49507266-49507316	GM12891	blood:	n/a
9	chr3:49507385-49507435	AG09319	gingival:	n/a
10	chr3:49509320-49509370	Jurkat	blood:	n/a
11	chr3:49507844-49507894	GM12892	blood:	n/a
12	chr3:49507186-49507236	HepG2	liver:	n/a
13	chr3:49507844-49507894	Caco-2	colon:	n/a
14	chr3:49507385-49507435	RPTEC	kidney:	n/a
15	chr3:49507844-49507894	SK-N-SH	brain:	n/a
16	chr3:49509320-49509370	GM06990	blood:	n/a
17	chr3:49508289-49508339	HEEpiC	esophagus:	n/a
18	chr3:49507478-49507528	HRE	kidney:	n/a
19	chr3:49508289-49508339	AG10803	skin:	n/a
20	chr3:49507266-49507316	AG04450	lung:	fetal
21	chr3:49507844-49507894	H1-hESC	embryonic stem cell:	embryo
22	chr3:49508289-49508339	NT2-D1	testis:	n/a
23	chr3:49507291-49507341	H1-hESC	embryonic stem cell:	embryo
24	chr3:49507291-49507341	BE2_C	brain:	n/a
25	chr3:49507545-49507595	HepG2	liver:	n/a
26	chr3:49507291-49507341	AG04449	skin:	fetal
27	chr3:49507478-49507528	HNPCEpiC	eye:	n/a
28	chr3:49507545-49507595	Hela-S3	cervix:	n/a
29	chr3:49507545-49507595	GM12892	blood:	n/a
30	chr3:49507844-49507894	T-47D	breast:	n/a
31	chr3:49507385-49507435	BE2_C	brain:	n/a
32	chr3:49507545-49507595	GM19239	blood:	n/a
33	chr3:49507478-49507528	AG09309	skin:	n/a
34	chr3:49507385-49507435	GM06990	blood:	n/a
35	chr3:49507186-49507236	NH-A	brain:	n/a
36	chr3:49508289-49508339	HCT-116	colon:	n/a
37	chr3:49507545-49507595	GM12891	blood:	n/a
38	chr3:49507478-49507528	K562	blood:	n/a
39	chr3:49508289-49508339	Hepatocyte	liver:	n/a
40	chr3:49507385-49507435	Hepatocyte	liver:	n/a
41	chr3:49507844-49507894	MCF10A-Er-Src	breast:	n/a
42	chr3:49507385-49507435	HUVEC	blood vessel:	n/a
43	chr3:49507266-49507316	GM06990	blood:	n/a
44	chr3:49507266-49507316	MCF10A-Er-Src	breast:	n/a
45	chr3:49507186-49507236	HUVEC	blood vessel:	n/a
46	chr3:49507545-49507595	K562	blood:	n/a
47	chr3:49508289-49508339	NB4	blood:	n/a
48	chr3:49507545-49507595	Jurkat	blood:	n/a
49	chr3:49509320-49509370	HCM	heart:	n/a
50	chr3:49507844-49507894	NHBE	bronchial:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49507518..49508282-chr5:43515171..43515703,2	Hela-S3	cervix:
2	chr3:49460325..49461920-chr3:49506460..49509220,2	MCF-7	breast:
3	chr3:49448236..49450769-chr3:49505936..49509558,3	MCF-7	breast:
4	chr3:49506494..49510419-chr3:49709515..49713189,4	MCF-7	breast:
5	chr3:49065352..49067075-chr3:49506284..49508355,2	K562	blood:
6	chr3:49447402..49451449-chr3:49505916..49509646,7	K562	blood:
7	chr3:49506879..49507449-chr7:45018883..45019516,2	Hela-S3	cervix:
8	chr3:49505441..49508480-chr3:49710122..49713377,5	MCF-7	breast:
9	chr3:49455358..49458192-chr3:49507443..49509538,2	MCF-7	breast:
10	chr3:49507200..49507717-chr5:65440276..65440998,2	Hela-S3	cervix:
11	chr3:49448736..49451146-chr3:49507489..49509395,2	MCF-7	breast:
12	chr3:49506481..49509131-chr3:49546764..49549304,2	MCF-7	breast:
13	chr3:49507938..49509712-chr3:49512685..49515016,2	K562	blood:
14	chr3:49043383..49045852-chr3:49505855..49507402,2	MCF-7	breast:
15	chr3:49506444..49509653-chr3:49710909..49714606,3	K562	blood:
16	chr16:30536975..30539864-chr3:49506980..49509217,2	MCF-7	breast:
17	chr3:49508269..49511222-chr3:49551619..49554342,2	K562	blood:
18	chr3:49501861..49505109-chr3:49505439..49508808,5	K562	blood:
19	chr3:49376524..49378988-chr3:49507303..49509521,2	MCF-7	breast:
20	chr3:49507449..49508233-chr9:131940290..131940960,2	Hela-S3	cervix:
21	chr3:49056423..49060378-chr3:49506507..49510634,4	K562	blood:
22	chr3:49130007..49132020-chr3:49507888..49509693,2	K562	blood:
23	chr3:49507807..49509484-chr3:49555798..49559257,3	MCF-7	breast:
24	chr3:49447402..49452044-chr3:49506038..49509646,9	K562	blood:
25	chr3:49507792..49509395-chr3:49538517..49540372,2	MCF-7	breast:
26	chr3:49506988..49509379-chr3:49529279..49532110,2	MCF-7	breast:
27	chr3:49503012..49504721-chr3:49506646..49509185,2	MCF-7	breast:
28	chr16:68056858..68057446-chr3:49507615..49508193,2	NB4	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAG1-1	chr3:49507787-49507866	NONHSAT089700
2	lnc-DAG1-1	chr3:49507722-49507866	NONHSAT089697
3	lnc-DAG1-1	chr3:49507735-49507866	NONHSAT089698
4	lnc-DAG1-1	chr3:49506146-49506488	NONHSAT089696

No data

Variant related genes	Relation type
DAG1	TF binding region
RNA5SP130	TF binding region
DAG1	CpG island
RNA5SP130	CpG island
ENSG00000272434	chromatin interactions
ENSG00000164062	chromatin interactions
ENSG00000145020	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000173402	chromatin interactions
ENSG00000248240	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000207605	chromatin interactions
ENSG00000167264	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000201301	chromatin interactions
ENSG00000153914	chromatin interactions
ENSG00000253744	chromatin interactions
ENSG00000198218	chromatin interactions
ENSG00000199032	chromatin interactions
ENSG00000169957	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000178252	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000235261	chromatin interactions
ENSG00000114316	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144641752	chr3:49505554-49505555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs35974337	chr3:49505586-49505587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs181554741	chr3:49505670-49505671	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186255704	chr3:49505676-49505677	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs540014047	chr3:49505694-49505695	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs546692813	chr3:49505710-49505711	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568073611	chr3:49505730-49505731	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535473769	chr3:49505787-49505788	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557102615	chr3:49505805-49505806	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558422698	chr3:49505831-49505832	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569517112	chr3:49505908-49505909	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs539785921	chr3:49505915-49505916	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs191304968	chr3:49505942-49505943	Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs182622580	chr3:49506008-49506009	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs540288753	chr3:49506039-49506040	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs555516510	chr3:49506154-49506155	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
17	rs573652372	chr3:49506167-49506168	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs143195513	chr3:49506269-49506270	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
19	rs71080520	chr3:49506273-49506274	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
20	rs13095470	chr3:49506274-49506275	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	mRNA abundance
21	rs6797164	chr3:49506299-49506300	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs562381412	chr3:49506360-49506361	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
23	rs533249846	chr3:49506365-49506366	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
24	rs545021398	chr3:49506401-49506402	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
25	rs560246793	chr3:49506404-49506405	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
26	rs184908276	chr3:49506450-49506451	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
27	rs527494345	chr3:49506452-49506453	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
28	rs546656076	chr3:49506492-49506493	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs564660712	chr3:49506532-49506533	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs561823561	chr3:49506580-49506581	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs529380172	chr3:49506597-49506598	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs190901772	chr3:49506607-49506608	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs569201567	chr3:49506612-49506613	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs540074560	chr3:49506732-49506733	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs376732249	chr3:49506745-49506746	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs34653951	chr3:49506806-49506807	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs537587017	chr3:49506810-49506811	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs9860055	chr3:49506900-49506901	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs142658338	chr3:49506917-49506918	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs556026576	chr3:49506949-49506950	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs573767415	chr3:49506981-49506982	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs542074164	chr3:49506988-49506989	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs77012634	chr3:49507020-49507021	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs150568866	chr3:49507030-49507031	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs577568671	chr3:49507084-49507085	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
46	rs545248266	chr3:49507159-49507160	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
47	rs545326373	chr3:49507193-49507194	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
48	rs139896371	chr3:49507204-49507205	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
49	rs183225398	chr3:49507322-49507323	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
50	rs542395993	chr3:49507409-49507410	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49490600-49506600	Enhancers	Fetal Muscle Leg	muscle
2	chr3:49491800-49506200	Enhancers	Placenta	Placenta
3	chr3:49497400-49506400	Weak transcription	Brain Germinal Matrix	brain
4	chr3:49498000-49506000	Weak transcription	Fetal Stomach	stomach
5	chr3:49499600-49506600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr3:49500000-49505600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr3:49500000-49505600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:49500000-49506200	Weak transcription	Adipose Nuclei	Adipose
9	chr3:49500000-49506400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr3:49500000-49506400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr3:49500000-49506400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr3:49500000-49506400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr3:49500000-49506400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:49500000-49506400	Weak transcription	Psoas Muscle	Psoas
15	chr3:49500000-49506400	Weak transcription	NH-A	brain
16	chr3:49500000-49506400	Weak transcription	NHDF-Ad	bronchial
17	chr3:49500000-49506600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:49501400-49506600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:49502200-49506600	Enhancers	Fetal Muscle Trunk	muscle
20	chr3:49502400-49506400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:49502600-49506800	Enhancers	Fetal Heart	heart
22	chr3:49503000-49506600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:49503400-49505600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr3:49503400-49505800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr3:49503400-49506000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:49503400-49506200	Weak transcription	A549	lung
27	chr3:49503400-49506400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr3:49503400-49506400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:49503400-49506400	Weak transcription	Colonic Mucosa	Colon
30	chr3:49503400-49506400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr3:49503600-49505600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr3:49503600-49505600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:49503600-49505800	Weak transcription	Right Ventricle	heart
34	chr3:49503600-49505800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr3:49503600-49506000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr3:49503600-49506000	Enhancers	Hela-S3	cervix
37	chr3:49503600-49506400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:49503600-49506400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr3:49503600-49506400	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr3:49503600-49506400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:49503600-49506400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr3:49503600-49506400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr3:49503600-49506400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr3:49503600-49506400	Weak transcription	Brain Anterior Caudate	brain
45	chr3:49503600-49506400	Weak transcription	Fetal Intestine Large	intestine
46	chr3:49503600-49506400	Weak transcription	HSMM	muscle
47	chr3:49503600-49506400	Weak transcription	NHEK	skin
48	chr3:49503600-49506600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr3:49503600-49506600	Weak transcription	Brain Angular Gyrus	brain
50	chr3:49503600-49507200	Weak transcription	Spleen	Spleen

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