Variant report

Variant	nsv561701
Chromosome Location	chr13:54711276-54826104
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:427)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:54815858-54816140	ECC-1	luminal epithelium:	n/a	n/a
2	CEBPB	chr13:54784761-54785163	MCF-7	breast:	n/a	n/a
3	CEBPB	chr13:54750821-54751091	ECC-1	luminal epithelium:	n/a	chr13:54750934-54750945
4	CEBPB	chr13:54813135-54813273	H1-hESC	embryonic stem cell:	n/a	chr13:54813217-54813228
5	CEBPB	chr13:54728675-54728972	HepG2	liver:	n/a	chr13:54728830-54728841
6	CEBPB	chr13:54784873-54785176	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr13:54753352-54753369	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:54784939-54785095	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:54725214-54725221	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:54744391-54744583	H1-hESC	embryonic stem cell:	n/a	chr13:54744558-54744571
11	CEBPB	chr13:54784789-54785162	MCF-7	breast:	n/a	n/a
12	CEBPB	chr13:54737712-54737752	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr13:54813050-54813332	HepG2	liver:	n/a	chr13:54813217-54813228
14	CEBPB	chr13:54750785-54751096	HepG2	liver:	n/a	chr13:54750934-54750945
15	CEBPB	chr13:54815763-54816209	ECC-1	luminal epithelium:	n/a	chr13:54815801-54815812
16	CEBPB	chr13:54784834-54785264	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr13:54719060-54719258	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr13:54790997-54791189	HepG2	liver:	n/a	chr13:54791043-54791054
19	CHD1	chr13:54791943-54791973	GM12878	blood:	n/a	n/a
20	CHD2	chr13:54750152-54750176	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr13:54736308-54736478	MCF-7	breast:	n/a	n/a
22	CTCF	chr13:54760180-54760330	GM12873	blood:	n/a	n/a
23	CTCF	chr13:54760020-54760170	HMEC	breast:	n/a	n/a
24	CTCF	chr13:54760060-54760210	NHEK	skin:	n/a	n/a
25	CTCF	chr13:54760084-54760102	GM12878	blood:	n/a	n/a
26	CTCF	chr13:54760040-54760190	Caco-2	colon:	n/a	n/a
27	CTCF	chr13:54793848-54793875	GM13976	blood:	n/a	n/a
28	CTCF	chr13:54759855-54760337	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:54760040-54760190	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr13:54759380-54759530	WERI-Rb-1	eye:	n/a	chr13:54759422-54759440
31	CTCF	chr13:54760000-54760150	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr13:54736335-54736448	MCF-7	breast:	n/a	n/a
33	CTCF	chr13:54760020-54760170	HRE	kidney:	n/a	n/a
34	CTCF	chr13:54759860-54760010	NHEK	skin:	n/a	n/a
35	CTCF	chr13:54736200-54736350	RPTEC	kidney:	n/a	n/a
36	CTCF	chr13:54760060-54760210	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr13:54759968-54760230	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:54736320-54736470	Caco-2	colon:	n/a	n/a
39	CTCF	chr13:54759980-54760130	HRE	kidney:	n/a	n/a
40	CTCF	chr13:54759960-54760110	NHEK	skin:	n/a	n/a
41	CTCF	chr13:54759920-54760070	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr13:54736300-54736450	HEK293	kidney:	n/a	n/a
43	CTCF	chr13:54760020-54760170	Caco-2	colon:	n/a	n/a
44	CTCF	chr13:54736280-54736430	NHEK	skin:	n/a	n/a
45	CTCF	chr13:54759970-54760169	Medullo	brain:	n/a	n/a
46	CTCF	chr13:54724500-54724650	HL-60	blood:	n/a	n/a
47	CTCF	chr13:54736320-54736470	HL-60	blood:	n/a	n/a
48	CTCF	chr13:54759980-54760130	HL-60	blood:	n/a	n/a
49	CTCF	chr13:54759949-54760266	GM12878	blood:	n/a	n/a
50	CTCF	chr13:54760080-54760154	Kidney_OC	kidney:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54725166-54725216	HRE	kidney:	n/a
2	chr13:54817511-54817561	HCPEpiC	choroid plexus:	n/a
3	chr13:54774189-54774239	HCPEpiC	choroid plexus:	n/a
4	chr13:54719190-54719240	HAEpiC	amniotic membrane:	n/a
5	chr13:54758149-54758199	CMK	blood:	n/a
6	chr13:54774189-54774239	NT2-D1	testis:	n/a
7	chr13:54719190-54719240	GM06990	blood:	n/a
8	chr13:54740236-54740286	HRE	kidney:	n/a
9	chr13:54719190-54719240	Hepatocyte	liver:	n/a
10	chr13:54740236-54740286	NHBE	bronchial:	n/a
11	chr13:54821786-54821836	HUVEC	blood vessel:	n/a
12	chr13:54821786-54821836	HRE	kidney:	n/a
13	chr13:54740236-54740286	HepG2	liver:	n/a
14	chr13:54758149-54758199	NT2-D1	testis:	n/a
15	chr13:54774189-54774239	T-47D	breast:	n/a
16	chr13:54774189-54774239	GM12892	blood:	n/a
17	chr13:54758149-54758199	Hela-S3	cervix:	n/a
18	chr13:54740236-54740286	Hela-S3	cervix:	n/a
19	chr13:54740236-54740286	HIPEpiC	eye:	n/a
20	chr13:54725166-54725216	HCPEpiC	choroid plexus:	n/a
21	chr13:54821786-54821836	HCM	heart:	n/a
22	chr13:54740236-54740286	HRCEpiC	kidney:	n/a
23	chr13:54719190-54719240	RPTEC	kidney:	n/a
24	chr13:54774189-54774239	SAEC	small airway:	n/a
25	chr13:54817511-54817561	NB4	blood:	n/a
26	chr13:54719190-54719240	MCF-7	breast:	n/a
27	chr13:54740236-54740286	Hepatocyte	liver:	n/a
28	chr13:54817511-54817561	SK-N-MC	brain:	n/a
29	chr13:54758149-54758199	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:54821786-54821836	SK-N-SH	brain:	n/a
31	chr13:54821786-54821836	U87	brain:	n/a
32	chr13:54821786-54821836	MCF-7	breast:	n/a
33	chr13:54719190-54719240	LNCaP	prostate:	n/a
34	chr13:54758149-54758199	T-47D	breast:	n/a
35	chr13:54774189-54774239	HIPEpiC	eye:	n/a
36	chr13:54725166-54725216	MCF-7	breast:	n/a
37	chr13:54740236-54740286	HCF	heart:	n/a
38	chr13:54719190-54719240	PrEC	prostate:	n/a
39	chr13:54740236-54740286	AG10803	skin:	n/a
40	chr13:54758149-54758199	HL-60	blood:	n/a
41	chr13:54817511-54817561	CMK	blood:	n/a
42	chr13:54817511-54817561	AoSMC	blood vessel:	n/a
43	chr13:54821786-54821836	Caco-2	colon:	n/a
44	chr13:54719190-54719240	NT2-D1	testis:	n/a
45	chr13:54740236-54740286	PFSK-1	brain:	n/a
46	chr13:54725166-54725216	HMEC	breast:	n/a
47	chr13:54740236-54740286	HCT-116	colon:	n/a
48	chr13:54821786-54821836	SKMC	muscle:	n/a
49	chr13:54821786-54821836	HCPEpiC	choroid plexus:	n/a
50	chr13:54758149-54758199	NH-A	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:54758846..54760838-chr13:54765685..54768244,2	K562	blood:
2	chr13:54758846..54760838-chr13:54765685..54768244,2	K562	blood:
3	chr13:54780172..54782257-chr13:54783482..54785302,2	MCF-7	breast:
4	chr13:54766693..54769398-chr13:54785918..54788383,2	MCF-7	breast:
5	chr13:54759630..54760543-chr13:55804447..55805083,2	MCF-7	breast:
6	chr13:54780172..54782257-chr13:54783482..54785302,2	MCF-7	breast:
7	chr13:54766693..54769398-chr13:54785918..54788383,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-4	chr13:54813174-54813188	NONHSAT034030
2	lnc-OLFM4-4	chr13:54817929-54818572	NONHSAT034030
3	lnc-OLFM4-4	chr13:54812998-54813118	NONHSAT034030
4	lnc-OLFM4-4	chr13:54813124-54813153	NONHSAT034030
5	lnc-OLFM4-4	chr13:54817928-54819360	NONHSAT034031

No data

Variant related genes	Relation type
LINC00458	TF binding region
LINC00458	CpG island

Extended variants
information (count: 3630 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3630 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2576147	chr13:54711276-54711277	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562116907	chr13:54711282-54711283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80112331	chr13:54711289-54711290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181541061	chr13:54711298-54711299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538755779	chr13:54711310-54711311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527929771	chr13:54711312-54711313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547963255	chr13:54711378-54711379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548107461	chr13:54711387-54711388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186408327	chr13:54711409-54711410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190003590	chr13:54711424-54711425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371252293	chr13:54711459-54711460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550218281	chr13:54711474-54711475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570030093	chr13:54711488-54711489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566125226	chr13:54711529-54711530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117867279	chr13:54711555-54711556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs933101	chr13:54711570-54711571	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531477581	chr13:54711571-54711572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555320533	chr13:54711582-54711583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369786287	chr13:54711706-54711707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553886696	chr13:54711717-54711718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549900213	chr13:54711784-54711785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573677312	chr13:54711806-54711807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181566197	chr13:54711847-54711848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73199650	chr13:54711866-54711867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555825808	chr13:54711909-54711910	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575662563	chr13:54711910-54711911	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs142420073	chr13:54711930-54711931	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs185715074	chr13:54711936-54711937	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs150874102	chr13:54711943-54711944	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs572660536	chr13:54711954-54711955	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs543449046	chr13:54711955-54711956	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs541266520	chr13:54712027-54712028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561503088	chr13:54712034-54712035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530230858	chr13:54712075-54712076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556634960	chr13:54712128-54712129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373378399	chr13:54712142-54712143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563750001	chr13:54712150-54712151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139341585	chr13:54712158-54712159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552532552	chr13:54712163-54712164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536032024	chr13:54712200-54712201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576912947	chr13:54712219-54712220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571460235	chr13:54712244-54712245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370769913	chr13:54712246-54712247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527555340	chr13:54712261-54712262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2576148	chr13:54712264-54712265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs546058179	chr13:54712357-54712358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567488720	chr13:54712365-54712366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536017203	chr13:54712373-54712374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555889425	chr13:54712374-54712375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149698599	chr13:54712417-54712418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54708000-54712000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr13:54708400-54711600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr13:54708600-54718800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr13:54710600-54711400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:54714400-54714800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr13:54714800-54721200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr13:54716800-54717000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr13:54717000-54718600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr13:54718600-54719200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr13:54718800-54719400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:54718800-54719400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr13:54718800-54719600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr13:54718800-54719600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr13:54719000-54719400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr13:54719000-54719600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr13:54719000-54719600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr13:54719000-54719600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:54719200-54719400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr13:54719200-54719400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr13:54719400-54720800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr13:54719400-54720800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr13:54719600-54721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr13:54719600-54721000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr13:54719600-54721200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr13:54720800-54721800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr13:54720800-54722000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr13:54721000-54721600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:54721000-54722600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:54721200-54721400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr13:54721200-54721600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr13:54721200-54722000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr13:54721400-54724600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:54721600-54724600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr13:54721600-54724800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr13:54721800-54724800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr13:54722000-54722400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr13:54722000-54724800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:54722400-54722600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr13:54722400-54722600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr13:54722600-54736200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr13:54722600-54741200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr13:54724600-54725000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr13:54724600-54725200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr13:54724800-54725400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr13:54724800-54725400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr13:54724800-54725400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr13:54725200-54725600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr13:54725400-54726200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr13:54725800-54726200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr13:54726200-54726400	Enhancers	HUES48 Cell Line	embryonic stem cell

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