Variant report

Variant	nsv832635
Chromosome Location	chr13:65419368-65574767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:65503121-65503331	GM12878	blood:	n/a	n/a
2	BCL11A	chr13:65512818-65513084	GM12878	blood:	n/a	n/a
3	BCL11A	chr13:65512859-65513178	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:65512810-65513130	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:65423279-65423659	IMR90	lung:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
6	CEBPB	chr13:65499086-65499312	A549	lung:	n/a	chr13:65499202-65499213
7	CEBPB	chr13:65424238-65424548	HepG2	liver:	n/a	chr13:65424398-65424409
8	CEBPB	chr13:65423280-65423696	A549	lung:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
9	CEBPB	chr13:65549489-65549824	HepG2	liver:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
10	CEBPB	chr13:65424222-65424546	IMR90	lung:	n/a	chr13:65424398-65424409
11	CEBPB	chr13:65549486-65549834	IMR90	lung:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
12	CEBPB	chr13:65449988-65450076	H1-hESC	embryonic stem cell:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
13	CEBPB	chr13:65463368-65463605	IMR90	lung:	n/a	n/a
14	CEBPB	chr13:65423288-65423653	Hela-S3	cervix:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
15	CEBPB	chr13:65423344-65423632	A549	lung:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
16	CEBPB	chr13:65424220-65424578	A549	lung:	n/a	chr13:65424398-65424409
17	CEBPB	chr13:65423231-65423769	A549	lung:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
18	CEBPB	chr13:65423316-65423630	H1-hESC	embryonic stem cell:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
19	CEBPB	chr13:65503142-65503716	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:65423282-65423649	HepG2	liver:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
21	CEBPB	chr13:65503090-65503733	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:65423323-65423606	K562	blood:	n/a	chr13:65423466-65423479 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423477 chr13:65423468-65423479 chr13:65423466-65423479 chr13:65423466-65423477 chr13:65423468-65423477 chr13:65423466-65423479
23	CEBPB	chr13:65486134-65486601	A549	lung:	n/a	n/a
24	CEBPB	chr13:65499086-65499360	HepG2	liver:	n/a	chr13:65499202-65499213
25	CEBPB	chr13:65449866-65450161	HepG2	liver:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
26	CEBPB	chr13:65449858-65450171	IMR90	lung:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
27	CEBPB	chr13:65530999-65531037	HepG2	liver:	n/a	chr13:65531013-65531026 chr13:65531015-65531026 chr13:65531010-65531027 chr13:65531013-65531024 chr13:65531013-65531026
28	CHD1	chr13:65568223-65568415	GM12878	blood:	n/a	n/a
29	CHD2	chr13:65567966-65568470	GM12878	blood:	n/a	n/a
30	CHD2	chr13:65499635-65499713	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr13:65571680-65571830	AG04450	lung:	n/a	n/a
32	CTCF	chr13:65532436-65532505	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr13:65571700-65571850	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr13:65502048-65502064	Fibrobl	skin:	n/a	n/a
35	CTCF	chr13:65571800-65571950	HMEC	breast:	n/a	n/a
36	CTCF	chr13:65519300-65519450	AG10803	skin:	n/a	chr13:65519402-65519423
37	CTCF	chr13:65552346-65552377	GM13976	blood:	n/a	n/a
38	CTCF	chr13:65559841-65559911	Lung_OC	lung:	n/a	n/a
39	CTCF	chr13:65571760-65571910	HMEC	breast:	n/a	n/a
40	CTCF	chr13:65571760-65571910	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr13:65434969-65435038	Lung_OC	lung:	n/a	n/a
42	CTCF	chr13:65445940-65446090	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr13:65571780-65571930	AG10803	skin:	n/a	n/a
44	CTCF	chr13:65571780-65571930	AG04450	lung:	n/a	n/a
45	CTCF	chr13:65571760-65571910	Caco-2	colon:	n/a	n/a
46	CTCF	chr13:65571700-65571850	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr13:65475340-65475433	NHEK	skin:	n/a	n/a
48	CTCF	chr13:65446280-65446290	ProgFib	skin:	n/a	n/a
49	CTCF	chr13:65571760-65571910	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr13:65571800-65571950	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65532796-65532846	HEK293	kidney:	embryo
2	chr13:65500072-65500122	SK-N-SH_RA	brain:	n/a
3	chr13:65532408-65532458	HepG2	liver:	n/a
4	chr13:65500141-65500191	SKMC	muscle:	n/a
5	chr13:65532796-65532846	HEK293	kidney:	embryo
6	chr13:65500072-65500122	SK-N-SH_RA	brain:	n/a
7	chr13:65532408-65532458	HepG2	liver:	n/a
8	chr13:65500141-65500191	SKMC	muscle:	n/a
9	chr13:65532408-65532458	HNPCEpiC	eye:	n/a
10	chr13:65533139-65533189	MCF10A-Er-Src	breast:	n/a
11	chr13:65500072-65500122	AoSMC	blood vessel:	n/a
12	chr13:65532408-65532458	GM06990	blood:	n/a
13	chr13:65500072-65500122	U87	brain:	n/a
14	chr13:65500072-65500122	AG04450	lung:	fetal
15	chr13:65532408-65532458	HRPEpiC	eye:	n/a
16	chr13:65532273-65532323	Hepatocyte	liver:	n/a
17	chr13:65532820-65532870	AG04449	skin:	fetal
18	chr13:65532820-65532870	HNPCEpiC	eye:	n/a
19	chr13:65532796-65532846	CMK	blood:	n/a
20	chr13:65500072-65500122	NHBE	bronchial:	n/a
21	chr13:65532581-65532631	HEEpiC	esophagus:	n/a
22	chr13:65532878-65532928	GM12891	blood:	n/a
23	chr13:65532820-65532870	Hepatocyte	liver:	n/a
24	chr13:65532796-65532846	HCT-116	colon:	n/a
25	chr13:65532273-65532323	A549	lung:	n/a
26	chr13:65532273-65532323	NT2-D1	testis:	n/a
27	chr13:65533139-65533189	HCPEpiC	choroid plexus:	n/a
28	chr13:65532581-65532631	PFSK-1	brain:	n/a
29	chr13:65500124-65500174	HEEpiC	esophagus:	n/a
30	chr13:65532796-65532846	AG10803	skin:	n/a
31	chr13:65532878-65532928	BJ	skin:	n/a
32	chr13:65533139-65533189	HCF	heart:	n/a
33	chr13:65500124-65500174	HAEpiC	amniotic membrane:	n/a
34	chr13:65532408-65532458	ProgFib	skin:	n/a
35	chr13:65533500-65533550	CMK	blood:	n/a
36	chr13:65532878-65532928	SKMC	muscle:	n/a
37	chr13:65532820-65532870	NT2-D1	testis:	n/a
38	chr13:65532820-65532870	LNCaP	prostate:	n/a
39	chr13:65532878-65532928	CMK	blood:	n/a
40	chr13:65533500-65533550	GM12891	blood:	n/a
41	chr13:65533500-65533550	AoSMC	blood vessel:	n/a
42	chr13:65532820-65532870	SKMC	muscle:	n/a
43	chr13:65532820-65532870	AoSMC	blood vessel:	n/a
44	chr13:65532820-65532870	HIPEpiC	eye:	n/a
45	chr13:65532273-65532323	HCM	heart:	n/a
46	chr13:65532878-65532928	PANC-1	pancreas:	n/a
47	chr13:65532796-65532846	NT2-D1	testis:	n/a
48	chr13:65532820-65532870	HAEpiC	amniotic membrane:	n/a
49	chr13:65500124-65500174	CMK	blood:	n/a
50	chr13:65500141-65500191	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
2	chr13:65452228..65453752-chr13:65456863..65459026,2	MCF-7	breast:
3	chr13:65490694..65491214-chr8:101576105..101576870,2	K562	blood:
4	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
5	chr13:65501243..65504224-chr17:41399641..41402005,2	K562	blood:
6	chr13:65502724..65504224-chr17:41400395..41402648,2	MCF-7	breast:
7	chr13:65501223..65502743-chr17:41399641..41401888,2	K562	blood:
8	chr13:65452228..65453752-chr13:65456863..65459026,2	MCF-7	breast:

Variant related genes	Relation type
LGMNP1	TF binding region
LGMNP1	CpG island

Extended variants
information (count: 1734 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147279504	chr13:65419401-65419402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576229165	chr13:65419405-65419406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs61950123	chr13:65419424-65419425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376186774	chr13:65419430-65419431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183401444	chr13:65419504-65419505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187937303	chr13:65419577-65419578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564047313	chr13:65419598-65419599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1040018	chr13:65419623-65419624	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs140836971	chr13:65419677-65419678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563406275	chr13:65419701-65419702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149789038	chr13:65419702-65419703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549482874	chr13:65419714-65419715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559687564	chr13:65419746-65419747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192499904	chr13:65419761-65419762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184551524	chr13:65419764-65419765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562597744	chr13:65419771-65419772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571973515	chr13:65419785-65419786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35976693	chr13:65419807-65419808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539412721	chr13:65419844-65419845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549820626	chr13:65419868-65419869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9598841	chr13:65419872-65419873	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553127420	chr13:65419914-65419915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535180625	chr13:65419943-65419944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186705220	chr13:65419975-65419976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572103325	chr13:65419988-65419989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534817951	chr13:65419998-65419999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9571290	chr13:65420059-65420060	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs192204002	chr13:65420064-65420065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35568891	chr13:65420070-65420071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543346318	chr13:65420078-65420079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557327759	chr13:65420083-65420084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184984904	chr13:65420109-65420110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9571291	chr13:65420200-65420201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180808476	chr13:65421651-65421652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533120575	chr13:65421655-65421656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545517431	chr13:65421658-65421659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150104423	chr13:65421660-65421661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111310747	chr13:65421730-65421731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544840227	chr13:65421764-65421765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561386408	chr13:65421790-65421791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530402566	chr13:65421796-65421797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34481740	chr13:65421804-65421805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9571292	chr13:65421829-65421830	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559296993	chr13:65421834-65421835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563433641	chr13:65421844-65421845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377511403	chr13:65421867-65421868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528116233	chr13:65421923-65421924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551020913	chr13:65421924-65421925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571012967	chr13:65421961-65421962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530590820	chr13:65421962-65421963	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65418200-65420200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:65419400-65419800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:65421600-65423600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:65421800-65422200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:65421800-65422600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr13:65422000-65422200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr13:65422000-65423400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr13:65422000-65423400	Enhancers	Fetal Intestine Small	intestine
9	chr13:65422200-65423400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr13:65423400-65423800	Enhancers	Adipose Nuclei	Adipose
11	chr13:65423600-65424800	Enhancers	Fetal Lung	lung
12	chr13:65426400-65426800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:65428400-65430000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr13:65432400-65432800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr13:65435000-65436400	Enhancers	Liver	Liver
16	chr13:65440600-65441000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:65440600-65441000	Enhancers	Fetal Stomach	stomach
18	chr13:65443400-65443800	Enhancers	HUVEC	blood vessel
19	chr13:65443800-65445800	Weak transcription	HUVEC	blood vessel
20	chr13:65445800-65446200	Enhancers	HUVEC	blood vessel
21	chr13:65446200-65446400	ZNF genes & repeats	Pancreas	Pancrea
22	chr13:65446200-65446600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr13:65446600-65451400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr13:65451400-65451600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr13:65470000-65470400	Active TSS	Gastric	stomach
26	chr13:65474200-65474400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:65482800-65483800	Enhancers	HUVEC	blood vessel
28	chr13:65483000-65483400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr13:65483000-65483400	Enhancers	HMEC	breast
30	chr13:65483000-65483600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr13:65483400-65484400	Weak transcription	HMEC	breast
32	chr13:65483400-65485600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:65483600-65485600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr13:65483800-65485600	Weak transcription	HUVEC	blood vessel
35	chr13:65484400-65485000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr13:65484400-65487000	Enhancers	HMEC	breast
37	chr13:65485000-65485400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr13:65485400-65486200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr13:65485600-65485800	Enhancers	A549	lung
40	chr13:65485600-65486200	Enhancers	NHEK	skin
41	chr13:65485600-65487000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr13:65485600-65487000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr13:65485600-65487000	Enhancers	HUVEC	blood vessel
44	chr13:65485600-65487200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr13:65485600-65487200	Enhancers	NH-A	brain
46	chr13:65485800-65486000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr13:65485800-65486000	Flanking Active TSS	A549	lung
48	chr13:65486000-65486400	Active TSS	A549	lung
49	chr13:65486200-65489000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr13:65486400-65486800	Enhancers	A549	lung

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