Variant report

Variant	nsv562775
Chromosome Location	chr13:95955076-96027507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:123)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr13:95969693-95970101	K562	blood:	n/a	n/a
3	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
4	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
6	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
7	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
8	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
9	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
13	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
14	CCNT2	chr13:95969690-95969892	K562	blood:	n/a	n/a
15	CEBPB	chr13:95966713-95967073	A549	lung:	n/a	n/a
16	CEBPB	chr13:96001631-96001874	K562	blood:	n/a	n/a
17	CEBPB	chr13:95966781-95967036	K562	blood:	n/a	n/a
18	CEBPB	chr13:95966626-95967127	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:95966527-95967229	HCT-116	colon:	n/a	n/a
20	CEBPB	chr13:95966693-95967096	HepG2	liver:	n/a	n/a
21	CEBPB	chr13:95966736-95967046	IMR90	lung:	n/a	n/a
22	CEBPB	chr13:95966589-95967162	HCT-116	colon:	n/a	n/a
23	CEBPB	chr13:95966696-95967048	HepG2	liver:	n/a	n/a
24	CEBPB	chr13:95966676-95967088	HepG2	liver:	n/a	n/a
25	CEBPB	chr13:95973519-95973677	HepG2	liver:	n/a	n/a
26	CEBPB	chr13:95957963-95958022	A549	lung:	n/a	n/a
27	CEBPB	chr13:96022480-96022768	K562	blood:	n/a	chr13:96022629-96022640
28	CEBPB	chr13:95966767-95966976	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:95966667-95967172	MCF-7	breast:	n/a	n/a
30	CEBPB	chr13:96022472-96022715	IMR90	lung:	n/a	chr13:96022629-96022640
31	CEBPB	chr13:96022569-96022728	HepG2	liver:	n/a	chr13:96022629-96022640
32	CEBPB	chr13:96004765-96005063	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr13:95966797-95966979	K562	blood:	n/a	n/a
34	CEBPB	chr13:95971922-95972499	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr13:95966710-95967200	MCF-7	breast:	n/a	n/a
36	CEBPB	chr13:95969679-95969976	Hela-S3	cervix:	n/a	n/a
37	CEBPD	chr13:95966717-95966976	HepG2	liver:	n/a	n/a
38	CEBPD	chr13:95966782-95967001	HepG2	liver:	n/a	n/a
39	CHD2	chr13:95966711-95967026	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr13:95966767-95966967	HepG2	liver:	n/a	n/a
41	CREB1	chr13:95966585-95967155	HepG2	liver:	n/a	n/a
42	CREB1	chr13:95966624-95967070	HepG2	liver:	n/a	n/a
43	CTCF	chr13:96004740-96004890	RPTEC	kidney:	n/a	n/a
44	CTCF	chr13:96004731-96004837	Gliobla	brain:	n/a	n/a
45	CTCF	chr13:96015920-96016070	GM12864	blood:	n/a	n/a
46	CTCF	chr13:96004720-96004870	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr13:96004700-96004850	NHEK	skin:	n/a	n/a
48	CTCF	chr13:96004749-96004822	MCF-7	breast:	n/a	n/a
49	CTCF	chr13:96006337-96006441	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr13:96006440-96006797	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95958190-95958240	NH-A	brain:	n/a
2	chr13:95958190-95958240	NH-A	brain:	n/a
3	chr13:95958190-95958240	GM12892	blood:	n/a
4	chr13:96008021-96008071	HCT-116	colon:	n/a
5	chr13:95958190-95958240	HCT-116	colon:	n/a
6	chr13:96008021-96008071	HRE	kidney:	n/a
7	chr13:96008021-96008071	U87	brain:	n/a
8	chr13:95958190-95958240	AoSMC	blood vessel:	n/a
9	chr13:95958190-95958240	NB4	blood:	n/a
10	chr13:96008021-96008071	HL-60	blood:	n/a
11	chr13:96008021-96008071	GM12878	blood:	n/a
12	chr13:95958190-95958240	HUVEC	blood vessel:	n/a
13	chr13:95958190-95958240	HL-60	blood:	n/a
14	chr13:95958190-95958240	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:95958190-95958240	ovcar-3	ovarian:	n/a
16	chr13:96008021-96008071	GM12891	blood:	n/a
17	chr13:96008021-96008071	CMK	blood:	n/a
18	chr13:95958190-95958240	A549	lung:	n/a
19	chr13:95958190-95958240	HNPCEpiC	eye:	n/a
20	chr13:96008021-96008071	NHBE	bronchial:	n/a
21	chr13:96008021-96008071	HUVEC	blood vessel:	n/a
22	chr13:96008021-96008071	AG04450	lung:	fetal
23	chr13:95958190-95958240	AG09319	gingival:	n/a
24	chr13:95958190-95958240	HIPEpiC	eye:	n/a
25	chr13:95958190-95958240	HMEC	breast:	n/a
26	chr13:96008021-96008071	HRCEpiC	kidney:	n/a
27	chr13:96008021-96008071	RPTEC	kidney:	n/a
28	chr13:96008021-96008071	NH-A	brain:	n/a
29	chr13:95958190-95958240	PrEC	prostate:	n/a
30	chr13:95958190-95958240	GM06990	blood:	n/a
31	chr13:95958190-95958240	HEK293	kidney:	embryo
32	chr13:96008021-96008071	K562	blood:	n/a
33	chr13:95958190-95958240	SK-N-SH	brain:	n/a
34	chr13:95958190-95958240	SKMC	muscle:	n/a
35	chr13:96008021-96008071	HMEC	breast:	n/a
36	chr13:96008021-96008071	HCPEpiC	choroid plexus:	n/a
37	chr13:95958190-95958240	BJ	skin:	n/a
38	chr13:96008021-96008071	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:96008021-96008071	SK-N-SH	brain:	n/a
40	chr13:95958190-95958240	RPTEC	kidney:	n/a
41	chr13:95958190-95958240	Jurkat	blood:	n/a
42	chr13:95958190-95958240	Hepatocyte	liver:	n/a
43	chr13:95958190-95958240	AG04450	lung:	fetal
44	chr13:96008021-96008071	T-47D	breast:	n/a
45	chr13:95958190-95958240	HEEpiC	esophagus:	n/a
46	chr13:96008021-96008071	HCF	heart:	n/a
47	chr13:95958190-95958240	BE2_C	brain:	n/a
48	chr13:96008021-96008071	HCM	heart:	n/a
49	chr13:96008021-96008071	SKMC	muscle:	n/a
50	chr13:96008021-96008071	SAEC	small airway:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
2	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
3	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
4	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
5	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
6	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
7	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
8	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
9	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:

(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-CLDN10-6	chr13:95957471-95958654	NONHSAT034755
3	lnc-ABCC4-1	chr13:95956351-95956401	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
ENSG00000125257	chromatin interactions
SMAD4	miRNA target sites

Extended variants
information (count: 2666 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2666 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs868853	chr13:95955076-95955077	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532826717	chr13:95955163-95955164	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs377213990	chr13:95955196-95955197	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs146199942	chr13:95955262-95955263	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs531829605	chr13:95955294-95955295	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs547842713	chr13:95955339-95955340	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs567821576	chr13:95955373-95955374	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs139107113	chr13:95955414-95955415	Weak transcription Strong transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs111426000	chr13:95955453-95955454	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs112918091	chr13:95955462-95955463	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs546976641	chr13:95955477-95955478	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs570385005	chr13:95955480-95955481	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs58489302	chr13:95955517-95955518	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556205088	chr13:95955538-95955539	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs368102998	chr13:95955547-95955548	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs370241395	chr13:95955548-95955549	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs386380300	chr13:95955552-95955553	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs79287013	chr13:95955553-95955554	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs202198477	chr13:95955558-95955559	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs569797997	chr13:95955562-95955563	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs1766900	chr13:95955602-95955603	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs555647202	chr13:95955610-95955611	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs1764419	chr13:95955619-95955620	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2389235	chr13:95955623-95955624	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554187267	chr13:95955630-95955631	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs56259297	chr13:95955670-95955671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1766901	chr13:95955720-95955721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35303481	chr13:95955742-95955743	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575851405	chr13:95955842-95955843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187817180	chr13:95955843-95955844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531889653	chr13:95955846-95955847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542012629	chr13:95955905-95955906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375421732	chr13:95955935-95955936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191855554	chr13:95955940-95955941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs55950069	chr13:95955966-95955967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61974975	chr13:95956008-95956009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527367755	chr13:95956049-95956050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547116473	chr13:95956061-95956062	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570397746	chr13:95956076-95956077	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs544619167	chr13:95956078-95956079	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs149741661	chr13:95956087-95956088	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs561330903	chr13:95956116-95956117	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs546845322	chr13:95956119-95956120	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535789854	chr13:95956163-95956164	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs555585882	chr13:95956191-95956192	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530063314	chr13:95956207-95956208	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs534259609	chr13:95956212-95956213	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs118172412	chr13:95956263-95956264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577130542	chr13:95956350-95956351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79680935	chr13:95956388-95956389	Weak transcription Enhancers	lncRNA	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:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95953800-95955400	Flanking Active TSS	K562	blood
2	chr13:95954000-95955400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr13:95954400-95955200	Bivalent Enhancer	Brain Germinal Matrix	brain
4	chr13:95954400-95955400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:95954400-95956600	Weak transcription	Right Atrium	heart
6	chr13:95954600-95955200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr13:95954600-95955200	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr13:95954600-95955200	Enhancers	Brain Substantia Nigra	brain
9	chr13:95954600-95955600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr13:95954600-95956000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:95954600-95957800	Enhancers	Fetal Intestine Small	intestine
12	chr13:95954600-95958200	Weak transcription	NHLF	lung
13	chr13:95954800-95955200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr13:95954800-95955400	Enhancers	GM12878-XiMat	blood
15	chr13:95954800-95956000	Weak transcription	Fetal Intestine Large	intestine
16	chr13:95954800-95956200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr13:95954800-95956600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:95954800-95956600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr13:95954800-95968800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr13:95955000-95955400	Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr13:95955000-95955400	Strong transcription	A549	lung
22	chr13:95955200-95956200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr13:95955200-95956400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr13:95955400-95956400	Weak transcription	GM12878-XiMat	blood
25	chr13:95955400-95956600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr13:95955400-95956800	Enhancers	K562	blood
27	chr13:95955400-95957800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr13:95955400-95959600	Weak transcription	A549	lung
29	chr13:95955600-95961400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:95956000-95956800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:95956000-95957800	Enhancers	Fetal Intestine Large	intestine
32	chr13:95956200-95957000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr13:95956200-95957200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr13:95956400-95956600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr13:95956400-95957000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr13:95956400-95957000	Enhancers	GM12878-XiMat	blood
37	chr13:95956600-95956800	Enhancers	Brain Cingulate Gyrus	brain
38	chr13:95956600-95956800	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr13:95956600-95957000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr13:95956600-95957200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr13:95956600-95957400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr13:95956800-95957000	Enhancers	Duodenum Mucosa	Duodenum
43	chr13:95956800-95958000	Weak transcription	K562	blood
44	chr13:95956800-95968800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:95957000-95957400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr13:95957000-95961200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr13:95957200-95958400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr13:95957800-95967000	Weak transcription	Fetal Intestine Small	intestine
49	chr13:95961600-95963800	Weak transcription	K562	blood
50	chr13:95963200-95963600	Enhancers	Rectal Smooth Muscle	rectum

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