Variant report

Variant	nsv510585
Chromosome Location	chr13:51057884-51083783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51083366-51083443	HepG2	liver:	n/a	n/a
2	BACH1	chr13:51068926-51068942	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr13:51058929-51058939	K562	blood:	n/a	n/a
4	CEBPB	chr13:51059623-51060088	HepG2	liver:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
5	CEBPB	chr13:51059956-51060137	IMR90	lung:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
6	CEBPB	chr13:51059624-51060125	A549	lung:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
7	CEBPB	chr13:51059998-51060183	K562	blood:	n/a	chr13:51060048-51060061 chr13:51060048-51060059 chr13:51060048-51060061 chr13:51060048-51060061
8	CTCF	chr13:51066171-51066200	Lung_OC	lung:	n/a	n/a
9	CTCF	chr13:51061180-51061330	HPF	lung:	n/a	n/a
10	CTCF	chr13:51075620-51075770	MCF-7	breast:	n/a	n/a
11	CTCF	chr13:51065369-51065395	MCF-7	breast:	n/a	n/a
12	E2F4	chr13:51065769-51065810	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr13:51066794-51066832	MCF10A-Er-Src	breast:	n/a	n/a
14	ELK1	chr13:51058885-51059063	K562	blood:	n/a	n/a
15	EP300	chr13:51060449-51060932	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr13:51083358-51083597	HepG2	liver:	n/a	n/a
17	EP300	chr13:51060698-51061000	K562	blood:	n/a	chr13:51060983-51060996
18	EP300	chr13:51059843-51059983	K562	blood:	n/a	n/a
19	EP300	chr13:51060390-51060894	SK-N-SH_RA	brain:	n/a	n/a
20	GATA2	chr13:51060631-51061048	SH-SY5Y	brain:	n/a	chr13:51060835-51060847 chr13:51060836-51060845 chr13:51060833-51060849 chr13:51060836-51060846 chr13:51060838-51060845 chr13:51060907-51060916
21	GATA3	chr13:51060408-51060844	SH-SY5Y	brain:	n/a	n/a
22	HNF4A	chr13:51083245-51083584	HepG2	liver:	n/a	chr13:51083376-51083384
23	JUND	chr13:51068432-51068493	K562	blood:	n/a	n/a
24	JUND	chr13:51060319-51060364	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUND	chr13:51063711-51063809	HepG2	liver:	n/a	n/a
26	JUND	chr13:51060761-51060953	K562	blood:	n/a	n/a
27	KAP1	chr13:51060252-51061047	HEK293	kidney:	n/a	n/a
28	MAFF	chr13:51061049-51061357	HepG2	liver:	n/a	chr13:51061190-51061208
29	MAFK	chr13:51061040-51061373	HepG2	liver:	n/a	n/a
30	MAFK	chr13:51061044-51061318	IMR90	lung:	n/a	n/a
31	MAFK	chr13:51058854-51059032	K562	blood:	n/a	chr13:51058860-51058871 chr13:51058859-51058870 chr13:51058860-51058871
32	MAFK	chr13:51061073-51061352	HepG2	liver:	n/a	n/a
33	MAFK	chr13:51059734-51059799	K562	blood:	n/a	n/a
34	MAFK	chr13:51064019-51064227	HepG2	liver:	n/a	chr13:51064120-51064135
35	MAFK	chr13:51064012-51064278	HepG2	liver:	n/a	chr13:51064120-51064135
36	MAX	chr13:51075469-51075780	NB4	blood:	n/a	chr13:51075623-51075633
37	MAZ	chr13:51058706-51058957	K562	blood:	n/a	n/a
38	MAZ	chr13:51066308-51066416	HepG2	liver:	n/a	n/a
39	MAZ	chr13:51060811-51061118	K562	blood:	n/a	n/a
40	MYC	chr13:51075519-51075686	NB4	blood:	n/a	chr13:51075623-51075633
41	MYC	chr13:51060735-51060991	K562	blood:	n/a	n/a
42	MYC	chr13:51060786-51060990	H1-hESC	embryonic stem cell:	n/a	n/a
43	MYC	chr13:51060876-51061076	K562	blood:	n/a	n/a
44	POLR2A	chr13:51065349-51065519	Gliobla	brain:	n/a	n/a
45	POLR2A	chr13:51057879-51058072	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr13:51065805-51065838	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr13:51060151-51060581	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr13:51075987-51076067	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr13:51065337-51065533	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr13:51075559-51075590	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51060599-51060649	BJ	skin:	n/a
2	chr13:51060599-51060649	HCM	heart:	n/a
3	chr13:51060599-51060649	HCPEpiC	choroid plexus:	n/a
4	chr13:51060599-51060649	SK-N-SH	brain:	n/a
5	chr13:51060599-51060649	HL-60	blood:	n/a
6	chr13:51060599-51060649	NHDF-neo	bronchial:	n/a
7	chr13:51060599-51060649	CMK	blood:	n/a
8	chr13:51060599-51060649	AG04450	lung:	fetal
9	chr13:51060599-51060649	Caco-2	colon:	n/a
10	chr13:51060599-51060649	Hepatocyte	liver:	n/a
11	chr13:51060599-51060649	ovcar-3	ovarian:	n/a
12	chr13:51060599-51060649	NHBE	bronchial:	n/a
13	chr13:51060599-51060649	GM06990	blood:	n/a
14	chr13:51060599-51060649	HCT-116	colon:	n/a
15	chr13:51060599-51060649	HNPCEpiC	eye:	n/a
16	chr13:51060599-51060649	AoSMC	blood vessel:	n/a
17	chr13:51060599-51060649	NT2-D1	testis:	n/a
18	chr13:51060599-51060649	PFSK-1	brain:	n/a
19	chr13:51060599-51060649	GM12892	blood:	n/a
20	chr13:51060599-51060649	SKMC	muscle:	n/a
21	chr13:51060599-51060649	HEK293	kidney:	embryo
22	chr13:51060599-51060649	AG09309	skin:	n/a
23	chr13:51060599-51060649	NH-A	brain:	n/a
24	chr13:51060599-51060649	RPTEC	kidney:	n/a
25	chr13:51060599-51060649	PANC-1	pancreas:	n/a
26	chr13:51060599-51060649	NB4	blood:	n/a
27	chr13:51060599-51060649	HRE	kidney:	n/a
28	chr13:51060599-51060649	HUVEC	blood vessel:	n/a
29	chr13:51060599-51060649	GM12878	blood:	n/a
30	chr13:51060599-51060649	HEEpiC	esophagus:	n/a
31	chr13:51060599-51060649	PrEC	prostate:	n/a
32	chr13:51060599-51060649	H1-hESC	embryonic stem cell:	embryo
33	chr13:51060599-51060649	HPAEpiC	pulmonary alveolar:	n/a
34	chr13:51060599-51060649	MCF10A-Er-Src	breast:	n/a
35	chr13:51060599-51060649	AG04449	skin:	fetal
36	chr13:51060599-51060649	HRPEpiC	eye:	n/a
37	chr13:51060599-51060649	HepG2	liver:	n/a
38	chr13:51060599-51060649	LNCaP	prostate:	n/a
39	chr13:51060599-51060649	HMEC	breast:	n/a
40	chr13:51060599-51060649	BE2_C	brain:	n/a
41	chr13:51060599-51060649	AG09319	gingival:	n/a
42	chr13:51060599-51060649	HRCEpiC	kidney:	n/a
43	chr13:51060599-51060649	HAEpiC	amniotic membrane:	n/a
44	chr13:51060599-51060649	A549	lung:	n/a
45	chr13:51060599-51060649	GM12891	blood:	n/a
46	chr13:51060599-51060649	T-47D	breast:	n/a
47	chr13:51060599-51060649	ECC-1	luminal epithelium:	n/a
48	chr13:51060599-51060649	Hela-S3	cervix:	n/a
49	chr13:51060599-51060649	K562	blood:	n/a
50	chr13:51060599-51060649	HCF	heart:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
2	chr12:132987438..132988105-chr13:51062911..51063480,2	MCF-7	breast:
3	chr13:51057495..51060887-chr13:51065845..51068156,3	K562	blood:
4	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
5	chr13:51065916..51068221-chr13:51075145..51077143,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASEH2B-3	chr13:51067608-51067670	NONHSAT033856
2	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
3	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033817
4	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033856
5	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
6	lnc-RNASEH2B-3	chr13:51069312-51069605	NONHSAT033856
7	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033827
8	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033819
9	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033821
10	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033812
11	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033855
12	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT140131
13	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033825
14	lnc-RNASEH2B-3	chr13:51076948-51077016	XLOC_010390
15	lnc-RNASEH2B-3	chr13:51066787-51066897	NR_109974
16	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033815
17	lnc-RNASEH2B-3	chr13:51066787-51067189	NONHSAT033842
18	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033850
19	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
20	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033846
21	lnc-RNASEH2B-3	chr13:51066780-51066897	NONHSAT033861

No data

Variant related genes	Relation type
DLEU1	TF binding region
DLEU1	CpG island
ENSG00000176124	chromatin interactions
NAGK	miRNA target sites

Extended variants
information (count: 724 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574465595	chr13:51057936-51057937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs114029091	chr13:51057951-51057952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184690025	chr13:51057970-51057971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561495264	chr13:51058015-51058016	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534371341	chr13:51058077-51058078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369693470	chr13:51058138-51058139	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10467505	chr13:51058179-51058180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548554066	chr13:51058227-51058228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143641871	chr13:51058235-51058236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531051616	chr13:51058236-51058237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552351401	chr13:51058239-51058240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570639489	chr13:51058263-51058264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs111548968	chr13:51058387-51058388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs146874438	chr13:51058404-51058405	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189335692	chr13:51058411-51058412	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568334274	chr13:51058418-51058419	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535741772	chr13:51058499-51058500	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs75681961	chr13:51058516-51058517	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556505989	chr13:51058560-51058561	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs180700628	chr13:51058716-51058717	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554342590	chr13:51058745-51058746	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183661573	chr13:51058793-51058794	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572992608	chr13:51058852-51058853	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545809543	chr13:51058855-51058856	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140721284	chr13:51058856-51058857	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188424741	chr13:51058882-51058883	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573517966	chr13:51058893-51058894	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544187453	chr13:51058900-51058901	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563686966	chr13:51058910-51058911	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12584728	chr13:51058942-51058943	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs79442997	chr13:51058962-51058963	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150442888	chr13:51058963-51058964	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564305471	chr13:51059016-51059017	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559929947	chr13:51059078-51059079	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369352085	chr13:51059095-51059096	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546730901	chr13:51059159-51059160	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568449698	chr13:51059161-51059162	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs182187	chr13:51059256-51059257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374928047	chr13:51059314-51059315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550988799	chr13:51059350-51059351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569200700	chr13:51059363-51059364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539725910	chr13:51059381-51059382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558008442	chr13:51059411-51059412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372815833	chr13:51059422-51059423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114151014	chr13:51059460-51059461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533898977	chr13:51059487-51059488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs555213356	chr13:51059555-51059556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368170696	chr13:51059578-51059579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs138283317	chr13:51059606-51059607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112524680	chr13:51059651-51059652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51041800-51060600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:51053000-51058600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr13:51053400-51058400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr13:51053400-51060200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr13:51053600-51058400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr13:51056400-51060200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:51057200-51058000	Enhancers	Fetal Heart	heart
8	chr13:51057400-51058400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:51057600-51058600	Enhancers	Brain Cingulate Gyrus	brain
10	chr13:51058000-51058400	Weak transcription	Fetal Heart	heart
11	chr13:51058400-51058600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr13:51058400-51058600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr13:51058400-51058600	Enhancers	Ovary	ovary
14	chr13:51058400-51058600	Enhancers	K562	blood
15	chr13:51058400-51059000	Active TSS	Brain Anterior Caudate	brain
16	chr13:51058400-51059000	Active TSS	Brain Hippocampus Middle	brain
17	chr13:51058400-51059000	Active TSS	Brain Substantia Nigra	brain
18	chr13:51058400-51059200	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr13:51058400-51059200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr13:51058400-51061400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr13:51058400-51061400	Enhancers	Fetal Heart	heart
22	chr13:51058600-51058800	Flanking Active TSS	Brain Angular Gyrus	brain
23	chr13:51058600-51058800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr13:51058600-51058800	Flanking Active TSS	Ovary	ovary
25	chr13:51058600-51058800	Active TSS	NH-A	brain
26	chr13:51058600-51058800	Active TSS	Osteobl	bone
27	chr13:51058600-51059000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:51058600-51059000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr13:51058600-51059000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr13:51058600-51059000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr13:51058600-51059000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr13:51058600-51059000	Active TSS	Brain Cingulate Gyrus	brain
33	chr13:51058600-51059000	Enhancers	Esophagus	oesophagus
34	chr13:51058600-51059000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr13:51058600-51059000	Flanking Active TSS	K562	blood
36	chr13:51058600-51059200	Enhancers	HMEC	breast
37	chr13:51058600-51060200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr13:51058800-51059000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr13:51058800-51059000	Active TSS	Brain Angular Gyrus	brain
40	chr13:51058800-51059000	Enhancers	Fetal Lung	lung
41	chr13:51058800-51059000	Enhancers	Ovary	ovary
42	chr13:51058800-51059000	Enhancers	Right Atrium	heart
43	chr13:51058800-51059000	Flanking Active TSS	NH-A	brain
44	chr13:51058800-51059000	Enhancers	NHLF	lung
45	chr13:51058800-51059000	Flanking Active TSS	Osteobl	bone
46	chr13:51058800-51059200	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr13:51058800-51059200	Enhancers	Fetal Stomach	stomach
48	chr13:51059000-51059200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr13:51059000-51059200	Flanking Active TSS	Brain Angular Gyrus	brain
50	chr13:51059000-51059200	Flanking Active TSS	Brain Anterior Caudate	brain

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