Variant report

Variant	nsv1040348
Chromosome Location	chr13:95939874-96032829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1606)
CpG islands
(count:733)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
2	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
3	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
6	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
8	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
10	ARID3A	chr13:95952888-95953170	K562	blood:	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	chr13:95969790-95969856	K562	blood:	n/a	n/a
14	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
17	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
18	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
19	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
20	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
21	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
22	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
23	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
24	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
25	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
26	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
27	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
28	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
29	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
30	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr13:95953565-95953620	HepG2	liver:	n/a	n/a
32	BRCA1	chr13:95948905-95949128	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr13:95953989-95954014	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
38	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
39	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a
40	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a
41	CCNT2	chr13:95952980-95954262	K562	blood:	n/a	n/a
42	CCNT2	chr13:95949924-95950191	K562	blood:	n/a	n/a
43	CEBPB	chr13:95949713-95950289	A549	lung:	n/a	n/a
44	CEBPB	chr13:95966667-95967172	MCF-7	breast:	n/a	n/a
45	CEBPB	chr13:96001631-96001874	K562	blood:	n/a	n/a
46	CEBPB	chr13:95966626-95967127	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:95966713-95967073	A549	lung:	n/a	n/a
48	CEBPB	chr13:95966797-95966979	K562	blood:	n/a	n/a
49	CEBPB	chr13:95966527-95967229	HCT-116	colon:	n/a	n/a
50	CEBPB	chr13:95949898-95950255	A549	lung:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95953229-95953279	HCM	heart:	n/a
2	chr13:95953229-95953279	HCM	heart:	n/a
3	chr13:95958190-95958240	HCM	heart:	n/a
4	chr13:95958190-95958240	GM19239	blood:	n/a
5	chr13:95953941-95953991	SK-N-SH	brain:	n/a
6	chr13:95953574-95953624	GM12891	blood:	n/a
7	chr13:95953505-95953555	CMK	blood:	n/a
8	chr13:95954382-95954432	A549	lung:	n/a
9	chr13:95952902-95952952	MCF-7	breast:	n/a
10	chr13:95953505-95953555	HRE	kidney:	n/a
11	chr13:95952902-95952952	GM12878	blood:	n/a
12	chr13:95954382-95954432	T-47D	breast:	n/a
13	chr13:95954080-95954130	Jurkat	blood:	n/a
14	chr13:95954534-95954584	MCF10A-Er-Src	breast:	n/a
15	chr13:95954382-95954432	AoSMC	blood vessel:	n/a
16	chr13:95958190-95958240	SKMC	muscle:	n/a
17	chr13:95954534-95954584	NHDF-neo	bronchial:	n/a
18	chr13:95953574-95953624	ovcar-3	ovarian:	n/a
19	chr13:95954080-95954130	Caco-2	colon:	n/a
20	chr13:95954080-95954130	SK-N-MC	brain:	n/a
21	chr13:95952937-95952987	SKMC	muscle:	n/a
22	chr13:95953941-95953991	HUVEC	blood vessel:	n/a
23	chr13:96008021-96008071	SK-N-SH_RA	brain:	n/a
24	chr13:95953574-95953624	SK-N-MC	brain:	n/a
25	chr13:95954080-95954130	IMR90	lung:	fetal
26	chr13:95958190-95958240	NHBE	bronchial:	n/a
27	chr13:95952937-95952987	GM06990	blood:	n/a
28	chr13:95953482-95953532	IMR90	lung:	fetal
29	chr13:95953229-95953279	K562	blood:	n/a
30	chr13:95953229-95953279	GM12892	blood:	n/a
31	chr13:95953941-95953991	HRPEpiC	eye:	n/a
32	chr13:95954080-95954130	CMK	blood:	n/a
33	chr13:95952937-95952987	T-47D	breast:	n/a
34	chr13:95954534-95954584	GM12891	blood:	n/a
35	chr13:95953574-95953624	Hela-S3	cervix:	n/a
36	chr13:95952937-95952987	ovcar-3	ovarian:	n/a
37	chr13:95958190-95958240	HEK293	kidney:	embryo
38	chr13:95952902-95952952	AG04450	lung:	fetal
39	chr13:95954534-95954584	PFSK-1	brain:	n/a
40	chr13:95952902-95952952	SKMC	muscle:	n/a
41	chr13:95953482-95953532	AG09309	skin:	n/a
42	chr13:95953941-95953991	HIPEpiC	eye:	n/a
43	chr13:95953482-95953532	AG04450	lung:	fetal
44	chr13:95952902-95952952	ovcar-3	ovarian:	n/a
45	chr13:95953574-95953624	HEEpiC	esophagus:	n/a
46	chr13:95953505-95953555	ProgFib	skin:	n/a
47	chr13:95952902-95952952	AG09309	skin:	n/a
48	chr13:95953482-95953532	AG04449	skin:	fetal
49	chr13:95953574-95953624	BE2_C	brain:	n/a
50	chr13:95954382-95954432	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
2	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
3	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
4	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
5	chr13:95841276..95841834-chr13:96032679..96033583,3	K562	blood:
6	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
7	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
8	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
9	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
10	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
11	chr13:95843696..95844640-chr13:96032651..96033707,6	K562	blood:
12	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
13	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
14	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
15	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
16	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
17	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
18	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
19	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
20	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
21	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
22	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
23	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
24	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
25	chr13:95841692..95842231-chr13:96032699..96033435,2	MCF-7	breast:
26	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 3475 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3475 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148788970	chr13:95939886-95939887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142444316	chr13:95939902-95939903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4773872	chr13:95939931-95939932	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147941691	chr13:95939933-95939934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs55750671	chr13:95939960-95939961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556127900	chr13:95939967-95939968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564609601	chr13:95939996-95939997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373383914	chr13:95940031-95940032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141750003	chr13:95940040-95940041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533230589	chr13:95940050-95940051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560852855	chr13:95940059-95940060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376634793	chr13:95940060-95940061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371268064	chr13:95940079-95940080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144311578	chr13:95940080-95940081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546846832	chr13:95940097-95940098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs193297641	chr13:95940103-95940104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532293386	chr13:95940151-95940152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374455200	chr13:95940174-95940175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568759740	chr13:95940204-95940205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185560635	chr13:95940206-95940207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368752306	chr13:95940228-95940229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576405032	chr13:95940234-95940235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147787495	chr13:95940244-95940245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567300006	chr13:95940250-95940251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373865664	chr13:95940251-95940252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562362035	chr13:95940260-95940261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536271886	chr13:95940277-95940278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34404603	chr13:95940322-95940323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs397708656	chr13:95940323-95940324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34824092	chr13:95940366-95940367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562073138	chr13:95940397-95940398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553594630	chr13:95940409-95940410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17235173	chr13:95940466-95940467	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs189294897	chr13:95940469-95940470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559190277	chr13:95940508-95940509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575946857	chr13:95940516-95940517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150289880	chr13:95940536-95940537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560989797	chr13:95940597-95940598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371498694	chr13:95940608-95940609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs137882841	chr13:95940622-95940623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539857093	chr13:95940704-95940705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149120942	chr13:95940792-95940793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143180249	chr13:95940798-95940799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552094307	chr13:95940834-95940835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532409682	chr13:95940835-95940836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568694422	chr13:95940991-95940992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531428919	chr13:95941094-95941095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77483771	chr13:95941150-95941151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567669054	chr13:95941162-95941163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138719284	chr13:95941180-95941181	Weak 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:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
2	chr13:95923800-95941200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr13:95924600-95952600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr13:95926600-95952400	Weak transcription	Brain Hippocampus Middle	brain
5	chr13:95926800-95948600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:95927200-95941600	Weak transcription	Gastric	stomach
7	chr13:95933000-95952600	Weak transcription	Primary T cells from cord blood	blood
8	chr13:95933400-95952600	Weak transcription	Fetal Stomach	stomach
9	chr13:95933600-95951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:95933800-95941800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr13:95933800-95952400	Weak transcription	HSMM	muscle
12	chr13:95933800-95952400	Weak transcription	NHDF-Ad	bronchial
13	chr13:95934000-95941000	Weak transcription	HUVEC	blood vessel
14	chr13:95934000-95941400	Weak transcription	Fetal Kidney	kidney
15	chr13:95934000-95941600	Weak transcription	A549	lung
16	chr13:95934000-95949600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr13:95934000-95951600	Weak transcription	Osteobl	bone
18	chr13:95934200-95941600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr13:95934600-95943600	Weak transcription	NHLF	lung
20	chr13:95935400-95949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:95937600-95948600	Weak transcription	Lung	lung
22	chr13:95938200-95942000	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr13:95938200-95952600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr13:95938400-95941400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr13:95938400-95941600	Weak transcription	Psoas Muscle	Psoas
26	chr13:95938400-95949800	Weak transcription	Colon Smooth Muscle	Colon
27	chr13:95938400-95950800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr13:95938800-95941000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr13:95938800-95945000	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr13:95938800-95948800	Weak transcription	Colonic Mucosa	Colon
31	chr13:95938800-95952400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr13:95939000-95940800	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr13:95939000-95940800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr13:95939000-95941200	Enhancers	K562	blood
35	chr13:95939000-95941200	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr13:95939000-95941400	Weak transcription	Fetal Intestine Small	intestine
37	chr13:95939000-95941600	Weak transcription	GM12878-XiMat	blood
38	chr13:95939000-95951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr13:95939400-95940000	Weak transcription	Left Ventricle	heart
40	chr13:95939400-95943800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr13:95939400-95948600	Weak transcription	Fetal Intestine Large	intestine
42	chr13:95939800-95941600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr13:95940000-95940200	Enhancers	Left Ventricle	heart
44	chr13:95940200-95952000	Weak transcription	Left Ventricle	heart
45	chr13:95940800-95941800	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr13:95940800-95942000	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr13:95941000-95942000	Enhancers	Duodenum Mucosa	Duodenum
48	chr13:95941000-95942000	Enhancers	HUVEC	blood vessel
49	chr13:95941200-95941800	Enhancers	Fetal Lung	lung
50	chr13:95941200-95941800	Enhancers	Small Intestine	intestine

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