Variant report

Variant	esv3407876
Chromosome Location	chr3:48774454-48823998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:908)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:48814408-48814608	K562	blood:	n/a	n/a
2	ARID3A	chr3:48779668-48779965	K562	blood:	n/a	n/a
3	ARID3A	chr3:48781280-48781445	K562	blood:	n/a	n/a
4	ATF1	chr3:48779668-48779977	K562	blood:	n/a	n/a
5	ATF1	chr3:48822258-48822259	K562	blood:	n/a	n/a
6	ATF1	chr3:48814440-48814647	K562	blood:	n/a	n/a
7	ATF1	chr3:48781255-48781554	K562	blood:	n/a	n/a
8	ATF1	chr3:48820750-48821116	K562	blood:	n/a	n/a
9	ATF3	chr3:48820746-48820936	K562	blood:	n/a	n/a
10	ATF3	chr3:48779630-48779931	K562	blood:	n/a	n/a
11	BACH1	chr3:48777408-48777782	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr3:48779664-48780098	K562	blood:	n/a	n/a
13	BHLHE40	chr3:48820701-48821008	K562	blood:	n/a	n/a
14	BHLHE40	chr3:48777369-48778071	HepG2	liver:	n/a	chr3:48777530-48777546
15	BHLHE40	chr3:48777426-48777738	A549	lung:	n/a	chr3:48777530-48777546
16	BHLHE40	chr3:48777376-48777820	K562	blood:	n/a	chr3:48777530-48777546
17	BHLHE40	chr3:48794081-48794272	HepG2	liver:	n/a	n/a
18	BHLHE40	chr3:48777350-48777743	GM12878	blood:	n/a	chr3:48777530-48777546
19	BRCA1	chr3:48777406-48777603	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr3:48777470-48778000	HepG2	liver:	n/a	n/a
21	CBX3	chr3:48779586-48780061	K562	blood:	n/a	n/a
22	CBX3	chr3:48777341-48777994	K562	blood:	n/a	n/a
23	CBX3	chr3:48779651-48780019	K562	blood:	n/a	n/a
24	CCNT2	chr3:48814406-48814529	K562	blood:	n/a	n/a
25	CCNT2	chr3:48779727-48779995	K562	blood:	n/a	n/a
26	CCNT2	chr3:48777371-48777722	K562	blood:	n/a	n/a
27	CEBPB	chr3:48806963-48806995	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:48803911-48803986	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:48802104-48802134	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr3:48779627-48779888	A549	lung:	n/a	chr3:48779748-48779761
31	CEBPB	chr3:48782286-48782445	K562	blood:	n/a	n/a
32	CEBPB	chr3:48806927-48806999	A549	lung:	n/a	n/a
33	CEBPB	chr3:48779529-48779990	K562	blood:	n/a	chr3:48779748-48779761
34	CEBPB	chr3:48779570-48779959	K562	blood:	n/a	chr3:48779748-48779761
35	CEBPB	chr3:48779685-48779892	Hela-S3	cervix:	n/a	chr3:48779748-48779761
36	CEBPB	chr3:48800208-48800209	IMR90	lung:	n/a	n/a
37	CEBPB	chr3:48779618-48779927	IMR90	lung:	n/a	chr3:48779748-48779761
38	CEBPB	chr3:48815500-48815546	K562	blood:	n/a	n/a
39	CEBPB	chr3:48782925-48782960	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:48806965-48806993	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:48782998-48783120	HepG2	liver:	n/a	chr3:48783027-48783038
42	CEBPB	chr3:48821765-48822187	IMR90	lung:	n/a	n/a
43	CEBPB	chr3:48781386-48781441	K562	blood:	n/a	n/a
44	CEBPB	chr3:48800079-48800237	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:48782888-48783187	K562	blood:	n/a	chr3:48783027-48783038
46	CEBPB	chr3:48777479-48777640	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:48802121-48802132	IMR90	lung:	n/a	n/a
48	CEBPD	chr3:48779647-48780073	K562	blood:	n/a	n/a
49	CEBPD	chr3:48779661-48780145	K562	blood:	n/a	n/a
50	CHD2	chr3:48777192-48777709	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:48788345-48788395	Jurkat	blood:	n/a
2	chr3:48788345-48788395	NHDF-neo	bronchial:	n/a
3	chr3:48788345-48788395	HRE	kidney:	n/a
4	chr3:48776948-48776998	HRCEpiC	kidney:	n/a
5	chr3:48776948-48776998	MCF-7	breast:	n/a
6	chr3:48776948-48776998	HRPEpiC	eye:	n/a
7	chr3:48788345-48788395	Hela-S3	cervix:	n/a
8	chr3:48788345-48788395	AG04449	skin:	fetal
9	chr3:48776948-48776998	MCF10A-Er-Src	breast:	n/a
10	chr3:48788345-48788395	HCF	heart:	n/a
11	chr3:48788345-48788395	AG04450	lung:	fetal
12	chr3:48788345-48788395	SAEC	small airway:	n/a
13	chr3:48788345-48788395	ovcar-3	ovarian:	n/a
14	chr3:48776948-48776998	AoSMC	blood vessel:	n/a
15	chr3:48776948-48776998	LNCaP	prostate:	n/a
16	chr3:48776948-48776998	HMEC	breast:	n/a
17	chr3:48788345-48788395	AG09309	skin:	n/a
18	chr3:48788345-48788395	U87	brain:	n/a
19	chr3:48788345-48788395	GM12878	blood:	n/a
20	chr3:48788345-48788395	HepG2	liver:	n/a
21	chr3:48788345-48788395	HUVEC	blood vessel:	n/a
22	chr3:48776948-48776998	SK-N-MC	brain:	n/a
23	chr3:48788345-48788395	HMEC	breast:	n/a
24	chr3:48776948-48776998	BE2_C	brain:	n/a
25	chr3:48776948-48776998	NH-A	brain:	n/a
26	chr3:48776948-48776998	AG09319	gingival:	n/a
27	chr3:48776948-48776998	H1-hESC	embryonic stem cell:	embryo
28	chr3:48776948-48776998	HepG2	liver:	n/a
29	chr3:48776948-48776998	HIPEpiC	eye:	n/a
30	chr3:48776948-48776998	HNPCEpiC	eye:	n/a
31	chr3:48776948-48776998	GM19239	blood:	n/a
32	chr3:48788345-48788395	PrEC	prostate:	n/a
33	chr3:48788345-48788395	MCF10A-Er-Src	breast:	n/a
34	chr3:48788345-48788395	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:48788345-48788395	PANC-1	pancreas:	n/a
36	chr3:48776948-48776998	HEK293	kidney:	embryo
37	chr3:48776948-48776998	U87	brain:	n/a
38	chr3:48788345-48788395	H1-hESC	embryonic stem cell:	embryo
39	chr3:48776948-48776998	GM12892	blood:	n/a
40	chr3:48788345-48788395	SK-N-SH	brain:	n/a
41	chr3:48776948-48776998	AG10803	skin:	n/a
42	chr3:48776948-48776998	NT2-D1	testis:	n/a
43	chr3:48776948-48776998	HL-60	blood:	n/a
44	chr3:48776948-48776998	ProgFib	skin:	n/a
45	chr3:48788345-48788395	ProgFib	skin:	n/a
46	chr3:48788345-48788395	HAEpiC	amniotic membrane:	n/a
47	chr3:48776948-48776998	HAEpiC	amniotic membrane:	n/a
48	chr3:48788345-48788395	SK-N-MC	brain:	n/a
49	chr3:48776948-48776998	HEEpiC	esophagus:	n/a
50	chr3:48776948-48776998	PANC-1	pancreas:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:48800799..48802746-chr3:48804382..48806917,2	K562	blood:
2	chr3:48722717..48723318-chr3:48802553..48803080,2	MCF-7	breast:
3	chr3:48777794..48779364-chr3:49056466..49058458,2	K562	blood:
4	chr3:48781538..48784352-chr3:48787212..48789298,3	K562	blood:
5	chr3:48774382..48777198-chr3:48777431..48780356,3	K562	blood:
6	chr3:48776467..48778976-chr3:48782002..48785742,3	K562	blood:
7	chr3:48778330..48780434-chr3:48788133..48790019,2	K562	blood:
8	chr3:48778919..48781292-chr3:49044225..49047223,2	K562	blood:
9	chr3:48752126..48754626-chr3:48784750..48786261,2	MCF-7	breast:
10	chr3:48781538..48784352-chr3:48787212..48789298,3	K562	blood:
11	chr3:48816757..48818353-chr3:48820387..48821948,2	K562	blood:
12	chr3:48754698..48757669-chr3:48775875..48778896,4	K562	blood:
13	chr3:48698968..48701587-chr3:48778820..48781194,2	K562	blood:
14	chr3:48807713..48809774-chr3:48894172..48896397,2	K562	blood:
15	chr3:48777544..48781186-chr3:48954650..48958375,5	K562	blood:
16	chr3:48776050..48777733-chr3:48988339..48990662,2	MCF-7	breast:
17	chr3:48792219..48794491-chr3:48797284..48799439,2	K562	blood:
18	chr3:48783500..48786885-chr3:48790129..48792388,3	K562	blood:
19	chr3:48783500..48786885-chr3:48790129..48792388,3	K562	blood:
20	chr3:48788421..48790694-chr3:48794526..48796243,3	K562	blood:
21	chr3:48722733..48723520-chr3:48777126..48777745,2	MCF-7	breast:
22	chr3:48754326..48756420-chr3:48796799..48799099,2	K562	blood:
23	chr3:48816757..48818353-chr3:48820387..48821948,2	K562	blood:
24	chr3:48777662..48781214-chr3:48954479..48957215,3	K562	blood:
25	chr3:48800799..48802746-chr3:48804382..48806917,2	K562	blood:
26	chr3:48792219..48794491-chr3:48797284..48799439,2	K562	blood:

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PRKAR2A	hsa-miR-16-5p	chr3:48788676-48788669
2	PRKAR2A	hsa-miR-16-5p	chr3:48788670-48788691

Variant related genes	Relation type
IP6K2	TF binding region
PRKAR2A	TF binding region
IP6K2	CpG island
PRKAR2A	CpG island
ENSG00000178252	chromatin interactions
ENSG00000114302	chromatin interactions
ENSG00000228350	chromatin interactions
ENSG00000221883	chromatin interactions
ENSG00000213672	chromatin interactions
ENSG00000207605	chromatin interactions
ENSG00000008300	chromatin interactions
ENSG00000199032	chromatin interactions
ENSG00000178537	chromatin interactions
ENSG00000068745	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000177479	chromatin interactions

Extended variants
information (count: 1634 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540778244	chr3:48774463-48774464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141502160	chr3:48774512-48774513	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74283328	chr3:48774648-48774649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376618756	chr3:48774673-48774674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575596377	chr3:48774744-48774745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370236050	chr3:48774750-48774751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115007916	chr3:48774757-48774758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142372052	chr3:48774768-48774769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577562366	chr3:48774798-48774799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181416983	chr3:48774895-48774896	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545016266	chr3:48774981-48774982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534885037	chr3:48774989-48774990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552873820	chr3:48775067-48775068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373743783	chr3:48775088-48775089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536283128	chr3:48775114-48775115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377438649	chr3:48775130-48775131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs554635927	chr3:48775175-48775176	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576433916	chr3:48775213-48775214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543559870	chr3:48775217-48775218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559071537	chr3:48775225-48775226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184273368	chr3:48775282-48775283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541688293	chr3:48775347-48775348	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs560123741	chr3:48775351-48775352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs529704901	chr3:48775408-48775409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541893021	chr3:48775412-48775413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563276369	chr3:48775413-48775414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530587514	chr3:48775426-48775427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs188643955	chr3:48775475-48775476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570598108	chr3:48775580-48775581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs528305468	chr3:48775591-48775592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546476091	chr3:48775600-48775601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs563937724	chr3:48775628-48775629	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77798571	chr3:48775639-48775640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574019131	chr3:48775640-48775641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77329203	chr3:48775655-48775656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568057202	chr3:48775704-48775705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531253993	chr3:48775718-48775719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181333028	chr3:48775772-48775773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571851752	chr3:48775842-48775843	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554500634	chr3:48775844-48775845	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569963557	chr3:48775846-48775847	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572772744	chr3:48775869-48775870	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543198067	chr3:48775877-48775878	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561477466	chr3:48775884-48775885	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544603524	chr3:48775995-48775996	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537522849	chr3:48776010-48776011	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371205549	chr3:48776041-48776042	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186106845	chr3:48776113-48776114	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577352171	chr3:48776172-48776173	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138538213	chr3:48776193-48776194	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1680 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48770800-48774600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr3:48771000-48776200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:48771200-48776000	Weak transcription	HMEC	breast
4	chr3:48772800-48777200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr3:48772800-48780200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr3:48773000-48776400	Weak transcription	NHEK	skin
7	chr3:48773200-48775000	Weak transcription	Fetal Lung	lung
8	chr3:48773200-48775000	Weak transcription	Left Ventricle	heart
9	chr3:48773200-48775000	Weak transcription	Stomach Mucosa	stomach
10	chr3:48773200-48775000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr3:48773200-48775600	Weak transcription	Placenta	Placenta
12	chr3:48773200-48776000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr3:48773200-48776000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr3:48773200-48777000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:48773200-48777000	Weak transcription	HSMMtube	muscle
16	chr3:48773200-48777200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:48773400-48774800	Weak transcription	Adipose Nuclei	Adipose
18	chr3:48773400-48775000	Weak transcription	Brain Anterior Caudate	brain
19	chr3:48773400-48775000	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr3:48773400-48775000	Weak transcription	Fetal Stomach	stomach
21	chr3:48773400-48775200	Weak transcription	Fetal Intestine Large	intestine
22	chr3:48773400-48775800	Weak transcription	Colon Smooth Muscle	Colon
23	chr3:48773400-48776200	Weak transcription	Colonic Mucosa	Colon
24	chr3:48773400-48776200	Weak transcription	Small Intestine	intestine
25	chr3:48773400-48776400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr3:48773400-48776800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:48773400-48777000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:48773400-48777000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr3:48773400-48777000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr3:48773600-48774800	Weak transcription	Liver	Liver
31	chr3:48773600-48774800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr3:48773600-48775000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:48773600-48775000	Weak transcription	Fetal Kidney	kidney
34	chr3:48773600-48776000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr3:48773600-48777200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr3:48773600-48777200	Weak transcription	NHDF-Ad	bronchial
37	chr3:48773800-48777000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:48774000-48777000	Enhancers	Duodenum Mucosa	Duodenum
39	chr3:48774200-48775000	Weak transcription	Fetal Intestine Small	intestine
40	chr3:48774200-48776400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr3:48774200-48777200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:48774400-48775000	Weak transcription	HepG2	liver
43	chr3:48774600-48775400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr3:48774600-48776200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr3:48774800-48775200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr3:48774800-48775400	Enhancers	GM12878-XiMat	blood
47	chr3:48774800-48775400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr3:48774800-48775800	Enhancers	Adipose Nuclei	Adipose
49	chr3:48774800-48776000	Enhancers	Right Atrium	heart
50	chr3:48774800-48776800	Enhancers	Rectal Mucosa Donor 29	rectum

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