Variant report

Variant	esv2829991
Chromosome Location	chr13:95942492-95981856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1379)
CpG islands
(count:671)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1379 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
5	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
6	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
8	ARID3A	chr13:95969693-95970101	K562	blood:	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	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
16	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
17	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
18	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
19	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
20	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
21	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
22	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
23	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
24	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
25	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
26	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
27	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr13:95953565-95953620	HepG2	liver:	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	chr13:95966541-95967031	Hela-S3	cervix:	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	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a
36	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a
37	CCNT2	chr13:95952980-95954262	K562	blood:	n/a	n/a
38	CCNT2	chr13:95949924-95950191	K562	blood:	n/a	n/a
39	CEBPB	chr13:95954091-95954583	GM12878	blood:	n/a	n/a
40	CEBPB	chr13:95966667-95967172	MCF-7	breast:	n/a	n/a
41	CEBPB	chr13:95966781-95967036	K562	blood:	n/a	n/a
42	CEBPB	chr13:95948303-95948484	K562	blood:	n/a	chr13:95948337-95948348
43	CEBPB	chr13:95948243-95948491	IMR90	lung:	n/a	chr13:95948337-95948348
44	CEBPB	chr13:95966736-95967046	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:95966710-95967200	MCF-7	breast:	n/a	n/a
46	CEBPB	chr13:95950014-95950221	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:95966527-95967229	HCT-116	colon:	n/a	n/a
48	CEBPB	chr13:95949868-95950256	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:95949825-95950302	A549	lung:	n/a	n/a
50	CEBPB	chr13:95948906-95949103	H1-hESC	embryonic stem cell:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95953505-95953555	NH-A	brain:	n/a
2	chr13:95953574-95953624	HMEC	breast:	n/a
3	chr13:95953574-95953624	BE2_C	brain:	n/a
4	chr13:95954534-95954584	HCPEpiC	choroid plexus:	n/a
5	chr13:95953229-95953279	AG09319	gingival:	n/a
6	chr13:95954080-95954130	LNCaP	prostate:	n/a
7	chr13:95952937-95952987	MCF10A-Er-Src	breast:	n/a
8	chr13:95953505-95953555	T-47D	breast:	n/a
9	chr13:95953941-95953991	HEEpiC	esophagus:	n/a
10	chr13:95953505-95953555	GM12892	blood:	n/a
11	chr13:95953505-95953555	HCT-116	colon:	n/a
12	chr13:95954080-95954130	HCM	heart:	n/a
13	chr13:95958190-95958240	ECC-1	luminal epithelium:	n/a
14	chr13:95954080-95954130	AG09309	skin:	n/a
15	chr13:95954080-95954130	GM12892	blood:	n/a
16	chr13:95954080-95954130	AG04450	lung:	fetal
17	chr13:95954382-95954432	PANC-1	pancreas:	n/a
18	chr13:95958190-95958240	Hepatocyte	liver:	n/a
19	chr13:95954080-95954130	SK-N-SH_RA	brain:	n/a
20	chr13:95953229-95953279	PFSK-1	brain:	n/a
21	chr13:95953941-95953991	Hela-S3	cervix:	n/a
22	chr13:95953482-95953532	BJ	skin:	n/a
23	chr13:95952937-95952987	U87	brain:	n/a
24	chr13:95954080-95954130	GM12891	blood:	n/a
25	chr13:95958190-95958240	H1-hESC	embryonic stem cell:	embryo
26	chr13:95952937-95952987	HCM	heart:	n/a
27	chr13:95952937-95952987	HCF	heart:	n/a
28	chr13:95952937-95952987	MCF-7	breast:	n/a
29	chr13:95953505-95953555	HepG2	liver:	n/a
30	chr13:95953941-95953991	U87	brain:	n/a
31	chr13:95958190-95958240	PFSK-1	brain:	n/a
32	chr13:95954382-95954432	NHBE	bronchial:	n/a
33	chr13:95954382-95954432	HRCEpiC	kidney:	n/a
34	chr13:95953574-95953624	AG04449	skin:	fetal
35	chr13:95952937-95952987	HRPEpiC	eye:	n/a
36	chr13:95953505-95953555	AG04450	lung:	fetal
37	chr13:95953574-95953624	GM12878	blood:	n/a
38	chr13:95954382-95954432	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:95953229-95953279	SAEC	small airway:	n/a
40	chr13:95953574-95953624	Caco-2	colon:	n/a
41	chr13:95953941-95953991	HL-60	blood:	n/a
42	chr13:95953941-95953991	MCF-7	breast:	n/a
43	chr13:95954534-95954584	PrEC	prostate:	n/a
44	chr13:95953574-95953624	HIPEpiC	eye:	n/a
45	chr13:95953482-95953532	LNCaP	prostate:	n/a
46	chr13:95953941-95953991	AG09319	gingival:	n/a
47	chr13:95954382-95954432	IMR90	lung:	fetal
48	chr13:95953482-95953532	HEK293	kidney:	embryo
49	chr13:95953505-95953555	AoSMC	blood vessel:	n/a
50	chr13:95953505-95953555	HUVEC	blood vessel:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
2	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
3	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
4	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
5	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
6	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
7	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
8	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
9	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
10	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
11	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
12	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
13	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
14	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
15	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
16	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
17	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
18	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
19	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:

(count:3 , 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-CLDN10-6	chr13:95957471-95958654	NONHSAT034755

No data

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

Extended variants
information (count: 1628 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7330673	chr13:95942492-95942493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187130086	chr13:95942536-95942537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534425678	chr13:95942558-95942559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370581819	chr13:95942560-95942561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs9524891	chr13:95942561-95942562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs189978731	chr13:95942598-95942599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs35069836	chr13:95942620-95942621	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140094664	chr13:95942640-95942641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs58280359	chr13:95942696-95942697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575670551	chr13:95942706-95942707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541703942	chr13:95942954-95942955	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs55933951	chr13:95942981-95942982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs71760015	chr13:95942982-95942983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552407747	chr13:95942983-95942984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555658598	chr13:95943011-95943012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7326957	chr13:95943095-95943096	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs9524892	chr13:95943099-95943100	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs7324820	chr13:95943108-95943109	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560340257	chr13:95943117-95943118	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143906200	chr13:95943125-95943126	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7324937	chr13:95943128-95943129	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181616385	chr13:95943144-95943145	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562855832	chr13:95943177-95943178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547849179	chr13:95943184-95943185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531768167	chr13:95943191-95943192	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186300566	chr13:95943222-95943223	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568750642	chr13:95943223-95943224	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527840915	chr13:95943230-95943231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547972463	chr13:95943231-95943232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111945835	chr13:95943263-95943264	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs56291007	chr13:95943264-95943265	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113372006	chr13:95943313-95943314	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535848976	chr13:95943339-95943340	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539135908	chr13:95943405-95943406	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142554572	chr13:95943406-95943407	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569283269	chr13:95943438-95943439	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535451094	chr13:95943486-95943487	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555335355	chr13:95943507-95943508	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572310440	chr13:95943526-95943527	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs75008143	chr13:95943610-95943611	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373703521	chr13:95943626-95943627	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547135059	chr13:95943637-95943638	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34043506	chr13:95943683-95943684	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572740724	chr13:95943694-95943695	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs4773873	chr13:95943731-95943732	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557924900	chr13:95943748-95943749	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563514839	chr13:95943809-95943810	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371137850	chr13:95943825-95943826	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577947098	chr13:95943853-95943854	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539679239	chr13:95943880-95943881	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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

Chromatin state (count:785 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr13:95934600-95943600	Weak transcription	NHLF	lung
13	chr13:95935400-95949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:95937600-95948600	Weak transcription	Lung	lung
15	chr13:95938200-95952600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr13:95938400-95949800	Weak transcription	Colon Smooth Muscle	Colon
17	chr13:95938400-95950800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr13:95938800-95945000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr13:95938800-95948800	Weak transcription	Colonic Mucosa	Colon
20	chr13:95938800-95952400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr13:95939000-95951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr13:95939400-95943800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr13:95939400-95948600	Weak transcription	Fetal Intestine Large	intestine
24	chr13:95940200-95952000	Weak transcription	Left Ventricle	heart
25	chr13:95941800-95943600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr13:95941800-95944800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr13:95941800-95946400	Weak transcription	GM12878-XiMat	blood
28	chr13:95941800-95952400	Weak transcription	Esophagus	oesophagus
29	chr13:95941800-95952400	Weak transcription	Pancreas	Pancrea
30	chr13:95942000-95943600	Weak transcription	K562	blood
31	chr13:95942000-95945000	Weak transcription	Fetal Intestine Small	intestine
32	chr13:95942000-95946200	Weak transcription	A549	lung
33	chr13:95942000-95948600	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr13:95942000-95948800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr13:95942000-95948800	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr13:95942000-95950600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr13:95942000-95951000	Weak transcription	HUVEC	blood vessel
38	chr13:95942200-95943400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr13:95943400-95944200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr13:95943600-95943800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr13:95943600-95943800	Enhancers	K562	blood
42	chr13:95943600-95943800	Strong transcription	NHLF	lung
43	chr13:95943600-95945400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr13:95943600-95952400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr13:95943800-95944000	Genic enhancers	K562	blood
46	chr13:95943800-95944000	ZNF genes & repeats	NHLF	lung
47	chr13:95943800-95945600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr13:95943800-95952400	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr13:95944000-95944800	Weak transcription	K562	blood
50	chr13:95944000-95945000	Weak transcription	NHLF	lung

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