Variant report

Variant	nsv900926
Chromosome Location	chr13:95927386-95972496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1633)
CpG islands
(count:796)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1633 , 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	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95931642-95931648	K562	blood:	n/a	n/a
3	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
5	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
6	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
7	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
9	ARID3A	chr13:95937866-95938402	K562	blood:	n/a	n/a
10	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
11	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
12	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
13	ATF1	chr13:95938012-95938442	K562	blood:	n/a	n/a
14	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
15	ATF2	chr13:95932888-95933441	GM12878	blood:	n/a	n/a
16	ATF2	chr13:95933714-95934499	GM12878	blood:	n/a	n/a
17	ATF2	chr13:95932871-95933559	GM12878	blood:	n/a	n/a
18	ATF3	chr13:95938112-95938426	K562	blood:	n/a	n/a
19	BACH1	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
21	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr13:95933185-95933517	GM12878	blood:	n/a	chr13:95933299-95933308
23	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
24	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
25	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
26	BCLAF1	chr13:95937861-95938393	K562	blood:	n/a	n/a
27	BCLAF1	chr13:95933136-95933564	GM12878	blood:	n/a	chr13:95933299-95933308
28	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
29	BHLHE40	chr13:95931372-95931664	K562	blood:	n/a	n/a
30	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
31	BHLHE40	chr13:95937918-95938449	K562	blood:	n/a	n/a
32	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
33	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
34	BHLHE40	chr13:95934235-95934425	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
36	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
37	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
38	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
39	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
40	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
43	BRCA1	chr13:95953989-95954014	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr13:95948905-95949128	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:95953565-95953620	HepG2	liver:	n/a	n/a
47	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr13:95938077-95938390	K562	blood:	n/a	n/a
49	CBX3	chr13:95937978-95938484	K562	blood:	n/a	n/a
50	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95954534-95954584	NT2-D1	testis:	n/a
2	chr13:95932467-95932517	PFSK-1	brain:	n/a
3	chr13:95954382-95954432	AG10803	skin:	n/a
4	chr13:95954534-95954584	NT2-D1	testis:	n/a
5	chr13:95932467-95932517	PFSK-1	brain:	n/a
6	chr13:95954382-95954432	AG10803	skin:	n/a
7	chr13:95953229-95953279	NH-A	brain:	n/a
8	chr13:95958190-95958240	T-47D	breast:	n/a
9	chr13:95952902-95952952	NHDF-neo	bronchial:	n/a
10	chr13:95932467-95932517	GM19239	blood:	n/a
11	chr13:95952902-95952952	HIPEpiC	eye:	n/a
12	chr13:95933097-95933147	SK-N-SH_RA	brain:	n/a
13	chr13:95953229-95953279	MCF10A-Er-Src	breast:	n/a
14	chr13:95958190-95958240	SK-N-MC	brain:	n/a
15	chr13:95953574-95953624	AG09319	gingival:	n/a
16	chr13:95952902-95952952	GM19239	blood:	n/a
17	chr13:95958190-95958240	CMK	blood:	n/a
18	chr13:95953229-95953279	HNPCEpiC	eye:	n/a
19	chr13:95953505-95953555	GM12892	blood:	n/a
20	chr13:95958190-95958240	Jurkat	blood:	n/a
21	chr13:95933097-95933147	HCT-116	colon:	n/a
22	chr13:95953941-95953991	HRCEpiC	kidney:	n/a
23	chr13:95954534-95954584	PANC-1	pancreas:	n/a
24	chr13:95953229-95953279	HRPEpiC	eye:	n/a
25	chr13:95952937-95952987	Caco-2	colon:	n/a
26	chr13:95954080-95954130	HEEpiC	esophagus:	n/a
27	chr13:95933097-95933147	PANC-1	pancreas:	n/a
28	chr13:95932467-95932517	SKMC	muscle:	n/a
29	chr13:95954382-95954432	RPTEC	kidney:	n/a
30	chr13:95953574-95953624	HCF	heart:	n/a
31	chr13:95953482-95953532	HCT-116	colon:	n/a
32	chr13:95953229-95953279	Jurkat	blood:	n/a
33	chr13:95958190-95958240	A549	lung:	n/a
34	chr13:95953574-95953624	AG04449	skin:	fetal
35	chr13:95954534-95954584	SK-N-SH	brain:	n/a
36	chr13:95958190-95958240	HCF	heart:	n/a
37	chr13:95953229-95953279	HUVEC	blood vessel:	n/a
38	chr13:95953941-95953991	HEEpiC	esophagus:	n/a
39	chr13:95954080-95954130	AG04449	skin:	fetal
40	chr13:95954080-95954130	HUVEC	blood vessel:	n/a
41	chr13:95932467-95932517	NHBE	bronchial:	n/a
42	chr13:95953574-95953624	HEEpiC	esophagus:	n/a
43	chr13:95952902-95952952	NH-A	brain:	n/a
44	chr13:95953941-95953991	NB4	blood:	n/a
45	chr13:95952937-95952987	PANC-1	pancreas:	n/a
46	chr13:95954534-95954584	HRPEpiC	eye:	n/a
47	chr13:95932467-95932517	GM06990	blood:	n/a
48	chr13:95953482-95953532	AG04449	skin:	fetal
49	chr13:95953574-95953624	GM12892	blood:	n/a
50	chr13:95953574-95953624	GM12878	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
2	chr13:95922109..95924473-chr13:95936856..95939759,2	K562	blood:
3	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
4	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
5	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
6	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
7	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
8	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
9	chr13:95923828..95925504-chr13:95926180..95928122,2	K562	blood:
10	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
11	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
12	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
13	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
14	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
15	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
16	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
17	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
18	chr13:95924370..95928427-chr13:95951382..95954630,5	K562	blood:
19	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
20	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
21	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
22	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
23	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
24	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
25	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
26	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
27	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:

(count:3 , 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

No data

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

Extended variants
information (count: 1852 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1852 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9524873	chr13:95927386-95927387	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575781669	chr13:95927394-95927395	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544623320	chr13:95927405-95927406	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191584691	chr13:95927414-95927415	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530376366	chr13:95927421-95927422	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184462431	chr13:95927463-95927464	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566210994	chr13:95927471-95927472	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9524874	chr13:95927481-95927482	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs6492775	chr13:95927494-95927495	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs558139597	chr13:95927532-95927533	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs370084970	chr13:95927540-95927541	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568997549	chr13:95927596-95927597	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145159856	chr13:95927719-95927720	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9524875	chr13:95927759-95927760	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs17300935	chr13:95927856-95927857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs533805173	chr13:95927863-95927864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369797876	chr13:95927866-95927867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35693009	chr13:95927867-95927868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs111281355	chr13:95927868-95927869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7320811	chr13:95927876-95927877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs113117255	chr13:95927941-95927942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9590231	chr13:95927989-95927990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367943630	chr13:95928003-95928004	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs66477891	chr13:95928004-95928005	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs61446542	chr13:95928018-95928019	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs367995187	chr13:95928064-95928065	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538785197	chr13:95928125-95928126	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs73548855	chr13:95928127-95928128	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575600564	chr13:95928162-95928163	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576288216	chr13:95928331-95928332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544798802	chr13:95928499-95928500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561289846	chr13:95928523-95928524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575231666	chr13:95928554-95928555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540906225	chr13:95928559-95928560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541626114	chr13:95928576-95928577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561939160	chr13:95928594-95928595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560224270	chr13:95928637-95928638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199606184	chr13:95928669-95928670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75340412	chr13:95928678-95928679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs398024028	chr13:95928687-95928688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572199282	chr13:95928693-95928694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11840532	chr13:95928696-95928697	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138983720	chr13:95928739-95928740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567401564	chr13:95928760-95928761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs58632827	chr13:95928761-95928762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs397960778	chr13:95928773-95928774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377610778	chr13:95928774-95928775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541324899	chr13:95928776-95928777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563727910	chr13:95928866-95928867	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531269292	chr13:95928871-95928872	Weak transcription Enhancers Genic enhancers	n/a	n/a	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:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95897000-95927400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr13:95910200-95927400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr13:95913600-95932800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr13:95917000-95931400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr13:95919000-95930000	Weak transcription	Esophagus	oesophagus
6	chr13:95919800-95928000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr13:95920200-95928800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
9	chr13:95920400-95927400	Weak transcription	Hela-S3	cervix
10	chr13:95920600-95928200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr13:95921600-95927600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:95922400-95927600	Weak transcription	Brain Anterior Caudate	brain
13	chr13:95922400-95927800	Weak transcription	NHEK	skin
14	chr13:95922800-95928200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr13:95923800-95941200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr13:95924000-95927400	Weak transcription	NHDF-Ad	bronchial
17	chr13:95924200-95927400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr13:95924200-95927600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:95924200-95927600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr13:95924200-95928000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:95924200-95930800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr13:95924200-95932800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr13:95924400-95927400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr13:95924400-95927800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr13:95924400-95927800	Weak transcription	Brain Substantia Nigra	brain
26	chr13:95924400-95927800	Weak transcription	NH-A	brain
27	chr13:95924600-95927400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr13:95924600-95927400	Weak transcription	HSMM	muscle
29	chr13:95924600-95927600	Weak transcription	Fetal Muscle Leg	muscle
30	chr13:95924600-95928000	Weak transcription	Osteobl	bone
31	chr13:95924600-95928400	Weak transcription	Fetal Muscle Trunk	muscle
32	chr13:95924600-95952600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr13:95924800-95927400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr13:95924800-95927400	Weak transcription	HSMMtube	muscle
35	chr13:95924800-95928000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:95924800-95932200	Weak transcription	HUVEC	blood vessel
37	chr13:95925400-95927400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr13:95925400-95927600	Genic enhancers	A549	lung
39	chr13:95925400-95929000	Enhancers	Colon Smooth Muscle	Colon
40	chr13:95925600-95928200	Enhancers	Stomach Mucosa	stomach
41	chr13:95925600-95929000	Enhancers	NHLF	lung
42	chr13:95925800-95928600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr13:95925800-95928800	Enhancers	Fetal Stomach	stomach
44	chr13:95925800-95929000	Enhancers	Fetal Lung	lung
45	chr13:95925800-95932200	Weak transcription	Psoas Muscle	Psoas
46	chr13:95926000-95927800	Enhancers	Ovary	ovary
47	chr13:95926200-95927800	Enhancers	Duodenum Mucosa	Duodenum
48	chr13:95926200-95928400	Enhancers	Stomach Smooth Muscle	stomach
49	chr13:95926200-95928600	Enhancers	Fetal Intestine Large	intestine
50	chr13:95926200-95928600	Enhancers	Pancreas	Pancrea

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