Variant report

Variant	nsv456081
Chromosome Location	chr13:95943885-96027507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1539)
CpG islands
(count:732)
Chromatin interactive
region (count:22)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
3	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
4	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
5	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
6	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
9	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
10	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
11	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
12	BACH1	chr13:96001635-96001886	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	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	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	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
19	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
20	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
21	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
22	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
23	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
24	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
25	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
26	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
27	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
28	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
29	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr13:95953565-95953620	HepG2	liver:	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	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr13:95953989-95954014	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
37	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a
38	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
39	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
40	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a
41	CCNT2	chr13:95949924-95950191	K562	blood:	n/a	n/a
42	CCNT2	chr13:95952980-95954262	K562	blood:	n/a	n/a
43	CEBPB	chr13:95973519-95973677	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:95966710-95967200	MCF-7	breast:	n/a	n/a
45	CEBPB	chr13:95951436-95951792	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr13:95948324-95948491	HepG2	liver:	n/a	chr13:95948337-95948348
47	CEBPB	chr13:95949713-95950289	A549	lung:	n/a	n/a
48	CEBPB	chr13:95950014-95950221	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr13:95966626-95967127	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr13:96004765-96005063	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	AG10803	skin:	n/a
2	chr13:95952902-95952952	HUVEC	blood vessel:	n/a
3	chr13:95953482-95953532	SAEC	small airway:	n/a
4	chr13:95953229-95953279	AG09309	skin:	n/a
5	chr13:95954534-95954584	HCM	heart:	n/a
6	chr13:95953505-95953555	HCT-116	colon:	n/a
7	chr13:95953574-95953624	HEK293	kidney:	embryo
8	chr13:95954382-95954432	HEEpiC	esophagus:	n/a
9	chr13:95954534-95954584	MCF10A-Er-Src	breast:	n/a
10	chr13:95953505-95953555	HL-60	blood:	n/a
11	chr13:95953941-95953991	ProgFib	skin:	n/a
12	chr13:95954080-95954130	NT2-D1	testis:	n/a
13	chr13:95953574-95953624	HCT-116	colon:	n/a
14	chr13:95958190-95958240	AG09309	skin:	n/a
15	chr13:95954382-95954432	HIPEpiC	eye:	n/a
16	chr13:95953482-95953532	SK-N-SH	brain:	n/a
17	chr13:95953574-95953624	GM06990	blood:	n/a
18	chr13:95953505-95953555	CMK	blood:	n/a
19	chr13:95953574-95953624	HRPEpiC	eye:	n/a
20	chr13:95953941-95953991	AG04450	lung:	fetal
21	chr13:95958190-95958240	LNCaP	prostate:	n/a
22	chr13:95953574-95953624	SK-N-SH	brain:	n/a
23	chr13:95953482-95953532	NHBE	bronchial:	n/a
24	chr13:95953229-95953279	HMEC	breast:	n/a
25	chr13:95953574-95953624	GM12892	blood:	n/a
26	chr13:95954534-95954584	NHDF-neo	bronchial:	n/a
27	chr13:95953482-95953532	HL-60	blood:	n/a
28	chr13:95953941-95953991	GM12892	blood:	n/a
29	chr13:95952902-95952952	HRPEpiC	eye:	n/a
30	chr13:96008021-96008071	H1-hESC	embryonic stem cell:	embryo
31	chr13:95952937-95952987	SK-N-MC	brain:	n/a
32	chr13:95953229-95953279	AoSMC	blood vessel:	n/a
33	chr13:95958190-95958240	AG04450	lung:	fetal
34	chr13:95953229-95953279	LNCaP	prostate:	n/a
35	chr13:95952902-95952952	HPAEpiC	pulmonary alveolar:	n/a
36	chr13:95954534-95954584	ProgFib	skin:	n/a
37	chr13:95953505-95953555	NT2-D1	testis:	n/a
38	chr13:95954534-95954584	Jurkat	blood:	n/a
39	chr13:95954534-95954584	SAEC	small airway:	n/a
40	chr13:95954382-95954432	HRE	kidney:	n/a
41	chr13:96008021-96008071	HUVEC	blood vessel:	n/a
42	chr13:95954534-95954584	HAEpiC	amniotic membrane:	n/a
43	chr13:95954534-95954584	HUVEC	blood vessel:	n/a
44	chr13:95953505-95953555	MCF-7	breast:	n/a
45	chr13:95953574-95953624	HMEC	breast:	n/a
46	chr13:95954080-95954130	SAEC	small airway:	n/a
47	chr13:96008021-96008071	ovcar-3	ovarian:	n/a
48	chr13:95954382-95954432	NHBE	bronchial:	n/a
49	chr13:95954382-95954432	HRPEpiC	eye:	n/a
50	chr13:95958190-95958240	HPAEpiC	pulmonary alveolar:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
2	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
3	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
4	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
5	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
6	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
7	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
8	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
9	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
10	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
11	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
12	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
13	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
14	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
15	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
16	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
17	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
18	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
19	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
20	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
21	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
22	chr13:95950632..95952981-chr13:95955199..95956850,2	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-CLDN10-6	chr13:95957471-95958654	NONHSAT034755
3	lnc-ABCC4-1	chr13:95954705-95955669	XLOC_010696
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: 3129 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3129 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4771912	chr13:95943885-95943886	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562991977	chr13:95944004-95944005	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576469850	chr13:95944072-95944073	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs367619291	chr13:95944093-95944094	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs140702478	chr13:95944108-95944109	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542215543	chr13:95944109-95944110	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs4773874	chr13:95944156-95944157	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527980982	chr13:95944163-95944164	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs118185478	chr13:95944166-95944167	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564321978	chr13:95944167-95944168	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144885063	chr13:95944183-95944184	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142861031	chr13:95944204-95944205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs367789090	chr13:95944212-95944213	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549432451	chr13:95944245-95944246	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112881780	chr13:95944254-95944255	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35163674	chr13:95944316-95944317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182280075	chr13:95944346-95944347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535060982	chr13:95944350-95944351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369780634	chr13:95944382-95944383	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548961002	chr13:95944394-95944395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565583376	chr13:95944403-95944404	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534905450	chr13:95944428-95944429	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373933025	chr13:95944442-95944443	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558114929	chr13:95944448-95944449	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs8001266	chr13:95944496-95944497	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7999916	chr13:95944509-95944510	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs7999927	chr13:95944520-95944521	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576481274	chr13:95944621-95944622	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs185002508	chr13:95944627-95944628	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562104850	chr13:95944670-95944671	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117001892	chr13:95944704-95944705	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191568790	chr13:95944705-95944706	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73551407	chr13:95944730-95944731	Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533310646	chr13:95944743-95944744	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577099758	chr13:95944803-95944804	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549966251	chr13:95944805-95944806	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528359871	chr13:95944826-95944827	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368306550	chr13:95944840-95944841	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545986959	chr13:95944887-95944888	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182977517	chr13:95944898-95944899	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548841287	chr13:95944926-95944927	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188070066	chr13:95944929-95944930	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534345939	chr13:95944952-95944953	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551665041	chr13:95944970-95944971	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567084912	chr13:95944971-95944972	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576212090	chr13:95944995-95944996	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146743223	chr13:95944999-95945000	Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571551558	chr13:95945000-95945001	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs537193859	chr13:95945080-95945081	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	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

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:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr13:95938800-95945000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr13:95938800-95948800	Weak transcription	Colonic Mucosa	Colon
19	chr13:95938800-95952400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr13:95939000-95951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr13:95939400-95948600	Weak transcription	Fetal Intestine Large	intestine
22	chr13:95940200-95952000	Weak transcription	Left Ventricle	heart
23	chr13:95941800-95944800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr13:95941800-95946400	Weak transcription	GM12878-XiMat	blood
25	chr13:95941800-95952400	Weak transcription	Esophagus	oesophagus
26	chr13:95941800-95952400	Weak transcription	Pancreas	Pancrea
27	chr13:95942000-95945000	Weak transcription	Fetal Intestine Small	intestine
28	chr13:95942000-95946200	Weak transcription	A549	lung
29	chr13:95942000-95948600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr13:95942000-95948800	Weak transcription	Duodenum Mucosa	Duodenum
31	chr13:95942000-95948800	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr13:95942000-95950600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:95942000-95951000	Weak transcription	HUVEC	blood vessel
34	chr13:95943400-95944200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr13:95943600-95945400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr13:95943600-95952400	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr13:95943800-95944000	Genic enhancers	K562	blood
38	chr13:95943800-95944000	ZNF genes & repeats	NHLF	lung
39	chr13:95943800-95945600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr13:95943800-95952400	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr13:95944000-95944800	Weak transcription	K562	blood
42	chr13:95944000-95945000	Weak transcription	NHLF	lung
43	chr13:95944200-95944400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr13:95944200-95945200	Weak transcription	NHEK	skin
45	chr13:95944400-95945400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr13:95944800-95945400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr13:95944800-95945400	Genic enhancers	K562	blood
48	chr13:95945000-95945200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
49	chr13:95945000-95945400	Strong transcription	Fetal Intestine Small	intestine
50	chr13:95945000-95945400	Strong transcription	NHLF	lung

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