Variant report

Variant	esv3345776
Chromosome Location	chr13:111356851-111361549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:794)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111358502-111358688	HepG2	liver:	n/a	n/a
2	ATF2	chr13:111358404-111358906	GM12878	blood:	n/a	n/a
3	BACH1	chr13:111358564-111358921	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:111357933-111358316	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr13:111358321-111358947	GM12878	blood:	n/a	chr13:111358653-111358662
6	BCL3	chr13:111359273-111359700	GM12878	blood:	n/a	n/a
7	BCLAF1	chr13:111358471-111359475	GM12878	blood:	n/a	chr13:111358653-111358662
8	BCLAF1	chr13:111358123-111358873	GM12878	blood:	n/a	chr13:111358653-111358662
9	BHLHE40	chr13:111358088-111359042	K562	blood:	n/a	chr13:111358181-111358197
10	BHLHE40	chr13:111358083-111359001	GM12878	blood:	n/a	chr13:111358181-111358197
11	BHLHE40	chr13:111358350-111359050	HepG2	liver:	n/a	n/a
12	BHLHE40	chr13:111359523-111359649	K562	blood:	n/a	n/a
13	BHLHE40	chr13:111357294-111357378	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:111358426-111358827	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr13:111357097-111357890	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr13:111358559-111358744	HepG2	liver:	n/a	n/a
17	CBX3	chr13:111358407-111359006	K562	blood:	n/a	n/a
18	CCNT2	chr13:111358123-111358920	K562	blood:	n/a	n/a
19	CEBPB	chr13:111358060-111358836	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:111357100-111357696	HCT-116	colon:	n/a	chr13:111357227-111357238
21	CEBPB	chr13:111356593-111357855	Hela-S3	cervix:	n/a	chr13:111357227-111357238
22	CEBPB	chr13:111357191-111357794	A549	lung:	n/a	chr13:111357227-111357238
23	CEBPB	chr13:111357166-111357640	IMR90	lung:	n/a	chr13:111357227-111357238
24	CEBPB	chr13:111357102-111357884	HCT-116	colon:	n/a	chr13:111357227-111357238
25	CEBPB	chr13:111357252-111357498	K562	blood:	n/a	n/a
26	CEBPB	chr13:111357234-111357545	MCF-7	breast:	n/a	n/a
27	CEBPB	chr13:111357213-111357523	HepG2	liver:	n/a	chr13:111357227-111357238
28	CEBPB	chr13:111357054-111357595	A549	lung:	n/a	chr13:111357227-111357238
29	CEBPB	chr13:111357163-111357524	K562	blood:	n/a	chr13:111357227-111357238
30	CEBPB	chr13:111357119-111357556	K562	blood:	n/a	chr13:111357227-111357238
31	CEBPB	chr13:111357218-111357414	HepG2	liver:	n/a	chr13:111357227-111357238
32	CEBPB	chr13:111358752-111358816	K562	blood:	n/a	n/a
33	CEBPD	chr13:111358200-111358914	HepG2	liver:	n/a	n/a
34	CEBPD	chr13:111359305-111359625	HepG2	liver:	n/a	n/a
35	CHD1	chr13:111358740-111358941	GM12878	blood:	n/a	n/a
36	CHD1	chr13:111358187-111358261	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr13:111357649-111357949	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr13:111358070-111359069	GM12878	blood:	n/a	n/a
39	CHD2	chr13:111357831-111357840	GM12878	blood:	n/a	n/a
40	CHD2	chr13:111358256-111359009	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr13:111358156-111358874	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr13:111358575-111358963	HepG2	liver:	n/a	n/a
43	CHD2	chr13:111358651-111358913	K562	blood:	n/a	n/a
44	CHD2	chr13:111357161-111357837	Hela-S3	cervix:	n/a	n/a
45	CREB1	chr13:111357982-111359292	HepG2	liver:	n/a	n/a
46	CREB1	chr13:111358182-111359028	A549	lung:	n/a	n/a
47	CREB1	chr13:111358236-111359102	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr13:111358195-111359143	GM12878	blood:	n/a	n/a
49	CTCF	chr13:111358500-111358650	HMF	breast:	n/a	n/a
50	CTCF	chr13:111358580-111358730	HCM	heart:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111358924-111358974	NB4	blood:	n/a
2	chr13:111358924-111358974	NB4	blood:	n/a
3	chr13:111358803-111358853	HL-60	blood:	n/a
4	chr13:111358532-111358582	CMK	blood:	n/a
5	chr13:111358538-111358588	AG09309	skin:	n/a
6	chr13:111358924-111358974	AG09319	gingival:	n/a
7	chr13:111357885-111357935	BJ	skin:	n/a
8	chr13:111358885-111358935	ProgFib	skin:	n/a
9	chr13:111358885-111358935	AG04450	lung:	fetal
10	chr13:111358527-111358577	IMR90	lung:	fetal
11	chr13:111358522-111358572	HMEC	breast:	n/a
12	chr13:111358862-111358912	HNPCEpiC	eye:	n/a
13	chr13:111358924-111358974	Hepatocyte	liver:	n/a
14	chr13:111358532-111358582	NT2-D1	testis:	n/a
15	chr13:111358522-111358572	Caco-2	colon:	n/a
16	chr13:111358552-111358602	NH-A	brain:	n/a
17	chr13:111358924-111358974	K562	blood:	n/a
18	chr13:111358885-111358935	NT2-D1	testis:	n/a
19	chr13:111358552-111358602	MCF-7	breast:	n/a
20	chr13:111358862-111358912	K562	blood:	n/a
21	chr13:111358552-111358602	CMK	blood:	n/a
22	chr13:111358803-111358853	HEK293	kidney:	embryo
23	chr13:111358516-111358566	HRPEpiC	eye:	n/a
24	chr13:111358803-111358853	HepG2	liver:	n/a
25	chr13:111358516-111358566	MCF-7	breast:	n/a
26	chr13:111358522-111358572	T-47D	breast:	n/a
27	chr13:111358924-111358974	AG04450	lung:	fetal
28	chr13:111358862-111358912	CMK	blood:	n/a
29	chr13:111358862-111358912	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:111358538-111358588	MCF-7	breast:	n/a
31	chr13:111358291-111358341	RPTEC	kidney:	n/a
32	chr13:111358803-111358853	CMK	blood:	n/a
33	chr13:111358522-111358572	GM12891	blood:	n/a
34	chr13:111358862-111358912	PFSK-1	brain:	n/a
35	chr13:111358552-111358602	HRPEpiC	eye:	n/a
36	chr13:111358862-111358912	SK-N-SH_RA	brain:	n/a
37	chr13:111358862-111358912	HRE	kidney:	n/a
38	chr13:111357885-111357935	ProgFib	skin:	n/a
39	chr13:111358924-111358974	GM19239	blood:	n/a
40	chr13:111357885-111357935	HMEC	breast:	n/a
41	chr13:111358527-111358577	MCF10A-Er-Src	breast:	n/a
42	chr13:111358885-111358935	HCT-116	colon:	n/a
43	chr13:111358552-111358602	SAEC	small airway:	n/a
44	chr13:111361529-111361579	ovcar-3	ovarian:	n/a
45	chr13:111358803-111358853	NHDF-neo	bronchial:	n/a
46	chr13:111358862-111358912	PANC-1	pancreas:	n/a
47	chr13:111358516-111358566	MCF10A-Er-Src	breast:	n/a
48	chr13:111358552-111358602	SK-N-SH	brain:	n/a
49	chr13:111358291-111358341	PrEC	prostate:	n/a
50	chr13:111358885-111358935	GM12892	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179718648..179719326-chr13:111357431..111357953,2	Hela-S3	cervix:
2	chr13:111358233..111358789-chr17:61904375..61905309,2	HCT-116	colon:
3	chr13:111357144..111360099-chr13:111360341..111362234,3	K562	blood:
4	chr13:111354377..111357375-chr13:111522032..111524115,2	K562	blood:
5	chr12:52444794..52445706-chr13:111357930..111358458,2	Hela-S3	cervix:
6	chr13:111266746..111269387-chr13:111357064..111359748,3	MCF-7	breast:
7	chr13:111357509..111359061-chr13:111566329..111568110,2	MCF-7	breast:
8	chr13:111266587..111269692-chr13:111357018..111359356,4	K562	blood:

No data

Variant related genes	Relation type
CARS2	TF binding region
ING1	TF binding region
CARS2	CpG island
ING1	CpG island
ENSG00000255874	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000087191	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000108592	chromatin interactions
ENSG00000213995	chromatin interactions

Extended variants
information (count: 196 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:196 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565372447	chr13:111356891-111356892	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs539025625	chr13:111356899-111356900	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs6492304	chr13:111356964-111356965	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs561520346	chr13:111356998-111356999	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576024586	chr13:111357053-111357054	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs187298899	chr13:111357065-111357066	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192190228	chr13:111357073-111357074	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs75052651	chr13:111357087-111357088	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs77933657	chr13:111357088-111357089	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs184547976	chr13:111357122-111357123	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs117806869	chr13:111357147-111357148	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541001726	chr13:111357187-111357188	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs74125058	chr13:111357197-111357198	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs149702757	chr13:111357206-111357207	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs7986286	chr13:111357207-111357208	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs548665928	chr13:111357218-111357219	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs563781085	chr13:111357233-111357234	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs72663405	chr13:111357253-111357254	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549454037	chr13:111357351-111357352	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561362226	chr13:111357364-111357365	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs528670725	chr13:111357369-111357370	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546917197	chr13:111357371-111357372	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs145521801	chr13:111357389-111357390	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571582887	chr13:111357482-111357483	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556126136	chr13:111357508-111357509	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187762212	chr13:111357531-111357532	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375224575	chr13:111357569-111357570	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550923052	chr13:111357570-111357571	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569737007	chr13:111357689-111357690	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536796122	chr13:111357716-111357717	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs78589951	chr13:111357753-111357754	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573779083	chr13:111357760-111357761	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs148422353	chr13:111357783-111357784	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs371386312	chr13:111357828-111357829	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376640710	chr13:111357845-111357846	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369920147	chr13:111357849-111357850	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529804222	chr13:111357873-111357874	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553318183	chr13:111357885-111357886	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201240343	chr13:111357888-111357889	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs142620615	chr13:111357890-111357891	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs117788141	chr13:111357899-111357900	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372279480	chr13:111357915-111357916	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs563580081	chr13:111357917-111357918	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs45518835	chr13:111357937-111357938	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs575585160	chr13:111357959-111357960	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs542789745	chr13:111357965-111357966	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs561412165	chr13:111357987-111357988	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs9521906	chr13:111358000-111358001	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546757676	chr13:111358018-111358019	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs565249603	chr13:111358071-111358072	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111312800-111357400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr13:111352400-111357200	Weak transcription	HUVEC	blood vessel
3	chr13:111353200-111357200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr13:111353400-111357200	Weak transcription	Brain Anterior Caudate	brain
5	chr13:111353400-111357600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr13:111353600-111357200	Weak transcription	Brain Substantia Nigra	brain
7	chr13:111353800-111357200	Weak transcription	Colonic Mucosa	Colon
8	chr13:111354000-111357200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr13:111354200-111357200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr13:111354200-111357200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr13:111354200-111357200	Weak transcription	Liver	Liver
12	chr13:111354200-111357400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr13:111354200-111357400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr13:111354400-111357400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr13:111354400-111357600	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr13:111354600-111357400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr13:111354600-111357400	Enhancers	Fetal Heart	heart
18	chr13:111354800-111357200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr13:111355000-111357000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr13:111355000-111357600	Enhancers	Stomach Mucosa	stomach
21	chr13:111355400-111357000	Weak transcription	Adipose Nuclei	Adipose
22	chr13:111355400-111357200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr13:111355400-111357200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr13:111355600-111357200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr13:111355600-111357200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr13:111355600-111357400	Weak transcription	Brain Angular Gyrus	brain
27	chr13:111355600-111357800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:111355600-111357800	Weak transcription	Aorta	Aorta
29	chr13:111355600-111358000	Weak transcription	Small Intestine	intestine
30	chr13:111355800-111357000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr13:111355800-111357200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr13:111355800-111357200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr13:111355800-111357200	Weak transcription	Fetal Brain Male	brain
34	chr13:111355800-111357200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr13:111355800-111357200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr13:111355800-111357200	Enhancers	HepG2	liver
37	chr13:111355800-111357400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr13:111355800-111357400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr13:111355800-111357400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr13:111355800-111357400	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr13:111355800-111357400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr13:111355800-111357400	Weak transcription	Left Ventricle	heart
43	chr13:111355800-111357400	Weak transcription	Right Ventricle	heart
44	chr13:111355800-111357600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr13:111355800-111357600	Weak transcription	Right Atrium	heart
46	chr13:111355800-111358000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:111355800-111358000	Weak transcription	Gastric	stomach
48	chr13:111356000-111357200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr13:111356000-111357200	Weak transcription	Fetal Brain Female	brain
50	chr13:111356000-111357200	Enhancers	Skeletal Muscle Male	skeletal muscle

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