Variant report

Variant	nsv1047902
Chromosome Location	chr13:95945118-96032829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1594)
CpG islands
(count:732)
Chromatin interactive
region (count:24)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1594 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
5	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
6	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
7	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
8	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
9	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
10	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
11	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
12	BACH1	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
16	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
17	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
18	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
19	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
20	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
21	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
22	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
23	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
24	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
25	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
26	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
27	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
28	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
29	BRCA1	chr13:95953565-95953620	HepG2	liver:	n/a	n/a
30	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr13:95948905-95949128	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr13:95953989-95954014	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
36	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
38	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a
39	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
40	CCNT2	chr13:95952980-95954262	K562	blood:	n/a	n/a
41	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a
42	CCNT2	chr13:95949924-95950191	K562	blood:	n/a	n/a
43	CEBPB	chr13:95966797-95966979	K562	blood:	n/a	n/a
44	CEBPB	chr13:95948243-95948491	IMR90	lung:	n/a	chr13:95948337-95948348
45	CEBPB	chr13:96001631-96001874	K562	blood:	n/a	n/a
46	CEBPB	chr13:95949879-95950546	HepG2	liver:	n/a	n/a
47	CEBPB	chr13:95948906-95949103	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr13:95973519-95973677	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:96022480-96022768	K562	blood:	n/a	chr13:96022629-96022640
50	CEBPB	chr13:95969679-95969976	Hela-S3	cervix:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95954382-95954432	BJ	skin:	n/a
2	chr13:95958190-95958240	HCT-116	colon:	n/a
3	chr13:95958190-95958240	Jurkat	blood:	n/a
4	chr13:95953505-95953555	ovcar-3	ovarian:	n/a
5	chr13:95954382-95954432	LNCaP	prostate:	n/a
6	chr13:95954080-95954130	SKMC	muscle:	n/a
7	chr13:95952937-95952987	Hepatocyte	liver:	n/a
8	chr13:95953941-95953991	HPAEpiC	pulmonary alveolar:	n/a
9	chr13:95954382-95954432	AG04450	lung:	fetal
10	chr13:95953229-95953279	SKMC	muscle:	n/a
11	chr13:95953505-95953555	HUVEC	blood vessel:	n/a
12	chr13:96008021-96008071	HCPEpiC	choroid plexus:	n/a
13	chr13:95958190-95958240	AG09319	gingival:	n/a
14	chr13:95953229-95953279	HRE	kidney:	n/a
15	chr13:95953482-95953532	ovcar-3	ovarian:	n/a
16	chr13:95953482-95953532	HL-60	blood:	n/a
17	chr13:95954382-95954432	GM12878	blood:	n/a
18	chr13:95952937-95952987	AG10803	skin:	n/a
19	chr13:95958190-95958240	GM12892	blood:	n/a
20	chr13:95952902-95952952	HCF	heart:	n/a
21	chr13:95958190-95958240	Hela-S3	cervix:	n/a
22	chr13:96008021-96008071	NT2-D1	testis:	n/a
23	chr13:95953574-95953624	ECC-1	luminal epithelium:	n/a
24	chr13:95953574-95953624	SK-N-SH_RA	brain:	n/a
25	chr13:95954382-95954432	Hela-S3	cervix:	n/a
26	chr13:95953941-95953991	BE2_C	brain:	n/a
27	chr13:95954382-95954432	AG10803	skin:	n/a
28	chr13:95958190-95958240	CMK	blood:	n/a
29	chr13:95953574-95953624	AoSMC	blood vessel:	n/a
30	chr13:95958190-95958240	AG04449	skin:	fetal
31	chr13:95952937-95952987	HepG2	liver:	n/a
32	chr13:95953505-95953555	HCF	heart:	n/a
33	chr13:95952937-95952987	H1-hESC	embryonic stem cell:	embryo
34	chr13:96008021-96008071	Hela-S3	cervix:	n/a
35	chr13:95953229-95953279	ECC-1	luminal epithelium:	n/a
36	chr13:95954080-95954130	U87	brain:	n/a
37	chr13:95952902-95952952	HUVEC	blood vessel:	n/a
38	chr13:95953482-95953532	AG10803	skin:	n/a
39	chr13:95953482-95953532	BE2_C	brain:	n/a
40	chr13:95953574-95953624	AG09319	gingival:	n/a
41	chr13:95954382-95954432	ECC-1	luminal epithelium:	n/a
42	chr13:95953229-95953279	HPAEpiC	pulmonary alveolar:	n/a
43	chr13:95952902-95952952	HEEpiC	esophagus:	n/a
44	chr13:95952937-95952987	HCPEpiC	choroid plexus:	n/a
45	chr13:95953505-95953555	HIPEpiC	eye:	n/a
46	chr13:95958190-95958240	AG04450	lung:	fetal
47	chr13:95953574-95953624	HRCEpiC	kidney:	n/a
48	chr13:95952902-95952952	MCF-7	breast:	n/a
49	chr13:95953574-95953624	HCM	heart:	n/a
50	chr13:95953941-95953991	PANC-1	pancreas:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
2	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
3	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
4	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
5	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
6	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
7	chr13:95841276..95841834-chr13:96032679..96033583,3	K562	blood:
8	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
9	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
10	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
11	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
12	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
13	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
14	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
15	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
16	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
17	chr13:95843696..95844640-chr13:96032651..96033707,6	K562	blood:
18	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
19	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
20	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
21	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
22	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
23	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
24	chr13:95841692..95842231-chr13:96032699..96033435,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-1	chr13:95954705-95955669	XLOC_010696
2	lnc-ABCC4-1	chr13:95956351-95956401	XLOC_010696
3	lnc-ABCC4-2	chr13:96003796-96003967	NONHSAT034758
4	lnc-CLDN10-6	chr13:95957471-95958654	NONHSAT034755

No data

Variant related genes	Relation type
RNY4P27	TF binding region
ABCC4	TF binding region
RNY3P8	TF binding region
RNY4P27	CpG island
ABCC4	CpG island
RNY3P8	CpG island
ENSG00000083544	chromatin interactions
ENSG00000125257	chromatin interactions
ENSG00000206737	chromatin interactions
SMAD4	miRNA target sites

Extended variants
information (count: 3270 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3270 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7981095	chr13:95945118-95945119	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573795075	chr13:95945119-95945120	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs192916297	chr13:95945156-95945157	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs140348411	chr13:95945191-95945192	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs572375693	chr13:95945208-95945209	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs145419692	chr13:95945236-95945237	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs370304740	chr13:95945255-95945256	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs557983068	chr13:95945263-95945264	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs577914337	chr13:95945282-95945283	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs543747325	chr13:95945287-95945288	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs563894078	chr13:95945359-95945360	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs377269967	chr13:95945446-95945447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368702212	chr13:95945458-95945459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529494389	chr13:95945515-95945516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542681020	chr13:95945536-95945537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs137998141	chr13:95945543-95945544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528046518	chr13:95945589-95945590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149596876	chr13:95945590-95945591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571307778	chr13:95945591-95945592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61974961	chr13:95945641-95945642	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550927670	chr13:95945643-95945644	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567432242	chr13:95945682-95945683	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536077952	chr13:95945688-95945689	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143289642	chr13:95945696-95945697	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540708977	chr13:95945698-95945699	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566045035	chr13:95945701-95945702	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534838374	chr13:95945709-95945710	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557720846	chr13:95945720-95945721	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577653160	chr13:95945723-95945724	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563803350	chr13:95945770-95945771	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9561831	chr13:95945782-95945783	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9561832	chr13:95945789-95945790	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9302055	chr13:95945798-95945799	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10467345	chr13:95945803-95945804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71433013	chr13:95945806-95945807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182900643	chr13:95945813-95945814	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12870819	chr13:95945817-95945818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9561833	chr13:95945824-95945825	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187979147	chr13:95945845-95945846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147668069	chr13:95945848-95945849	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542861071	chr13:95945865-95945866	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559351673	chr13:95945868-95945869	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528188941	chr13:95945869-95945870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545161461	chr13:95945870-95945871	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564858746	chr13:95945871-95945872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192449030	chr13:95945874-95945875	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550864286	chr13:95945877-95945878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141394086	chr13:95945882-95945883	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375197426	chr13:95945887-95945888	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550058497	chr13:95945909-95945910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	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
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
2	chr13:95924600-95952600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr13:95926600-95952400	Weak transcription	Brain Hippocampus Middle	brain
4	chr13:95926800-95948600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr13:95933000-95952600	Weak transcription	Primary T cells from cord blood	blood
6	chr13:95933400-95952600	Weak transcription	Fetal Stomach	stomach
7	chr13:95933600-95951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr13:95933800-95952400	Weak transcription	HSMM	muscle
9	chr13:95933800-95952400	Weak transcription	NHDF-Ad	bronchial
10	chr13:95934000-95949600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr13:95934000-95951600	Weak transcription	Osteobl	bone
12	chr13:95935400-95949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr13:95937600-95948600	Weak transcription	Lung	lung
14	chr13:95938200-95952600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr13:95938400-95949800	Weak transcription	Colon Smooth Muscle	Colon
16	chr13:95938400-95950800	Weak transcription	Stomach Smooth Muscle	stomach
17	chr13:95938800-95948800	Weak transcription	Colonic Mucosa	Colon
18	chr13:95938800-95952400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr13:95939000-95951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr13:95939400-95948600	Weak transcription	Fetal Intestine Large	intestine
21	chr13:95940200-95952000	Weak transcription	Left Ventricle	heart
22	chr13:95941800-95946400	Weak transcription	GM12878-XiMat	blood
23	chr13:95941800-95952400	Weak transcription	Esophagus	oesophagus
24	chr13:95941800-95952400	Weak transcription	Pancreas	Pancrea
25	chr13:95942000-95946200	Weak transcription	A549	lung
26	chr13:95942000-95948600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr13:95942000-95948800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr13:95942000-95948800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr13:95942000-95950600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr13:95942000-95951000	Weak transcription	HUVEC	blood vessel
31	chr13:95943600-95945400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr13:95943600-95952400	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr13:95943800-95945600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr13:95943800-95952400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr13:95944200-95945200	Weak transcription	NHEK	skin
36	chr13:95944400-95945400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr13:95944800-95945400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr13:95944800-95945400	Genic enhancers	K562	blood
39	chr13:95945000-95945200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
40	chr13:95945000-95945400	Strong transcription	Fetal Intestine Small	intestine
41	chr13:95945000-95945400	Strong transcription	NHLF	lung
42	chr13:95945200-95945400	ZNF genes & repeats	NHEK	skin
43	chr13:95945200-95948600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr13:95945400-95945600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr13:95945400-95946600	Weak transcription	Fetal Intestine Small	intestine
46	chr13:95945400-95946600	Weak transcription	K562	blood
47	chr13:95945400-95946800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr13:95945400-95950800	Weak transcription	NHEK	skin
49	chr13:95945400-95951000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr13:95945400-95951000	Weak transcription	NHLF	lung

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