Variant report

Variant	nsv1047752
Chromosome Location	chr13:69251968-69269284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:69266329-69266484	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:69265322-69265590	K562	blood:	n/a	n/a
3	CEBPB	chr13:69268802-69269108	K562	blood:	n/a	n/a
4	CEBPB	chr13:69268809-69269015	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr13:69268761-69269087	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:69268752-69269047	HepG2	liver:	n/a	n/a
7	CEBPB	chr13:69268765-69268935	A549	lung:	n/a	n/a
8	CTCF	chr13:69259660-69259810	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr13:69256760-69256910	RPTEC	kidney:	n/a	n/a
10	E2F4	chr13:69257947-69257992	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr13:69252919-69253173	GM12878	blood:	n/a	chr13:69253030-69253041
12	EP300	chr13:69268926-69268940	HepG2	liver:	n/a	n/a
13	EP300	chr13:69259993-69261092	MCF-7	breast:	n/a	chr13:69260865-69260875
14	EP300	chr13:69260123-69261010	MCF-7	breast:	n/a	chr13:69260865-69260875
15	FOXM1	chr13:69260159-69261228	MCF-7	breast:	n/a	n/a
16	FOXM1	chr13:69260118-69261026	MCF-7	breast:	n/a	n/a
17	GATA3	chr13:69264612-69264851	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr13:69260124-69261119	MCF-7	breast:	n/a	n/a
19	GATA3	chr13:69260124-69261136	MCF-7	breast:	n/a	n/a
20	GATA3	chr13:69260115-69261157	MCF-7	breast:	n/a	n/a
21	GATA3	chr13:69260086-69261247	MCF-7	breast:	n/a	n/a
22	JUN	chr13:69262695-69262762	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAFF	chr13:69265392-69265521	HepG2	liver:	n/a	chr13:69265408-69265426
24	MAFF	chr13:69266009-69266511	K562	blood:	n/a	chr13:69266361-69266379
25	MAFF	chr13:69266298-69266516	HepG2	liver:	n/a	chr13:69266361-69266379
26	MAFF	chr13:69265294-69265529	K562	blood:	n/a	chr13:69265408-69265426
27	MAFK	chr13:69262835-69263044	HepG2	liver:	n/a	n/a
28	MAFK	chr13:69265297-69265572	HepG2	liver:	n/a	chr13:69265410-69265425
29	MAFK	chr13:69257326-69257358	HepG2	liver:	n/a	chr13:69257347-69257358
30	MAFK	chr13:69266237-69266516	HepG2	liver:	n/a	chr13:69266363-69266378
31	MAFK	chr13:69265309-69265537	HepG2	liver:	n/a	chr13:69265410-69265425
32	MAFK	chr13:69266339-69266437	H1-hESC	embryonic stem cell:	n/a	chr13:69266363-69266378
33	MAFK	chr13:69266231-69266543	HepG2	liver:	n/a	chr13:69266363-69266378
34	MAFK	chr13:69265356-69265500	IMR90	lung:	n/a	chr13:69265410-69265425
35	MAFK	chr13:69262520-69262524	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAFK	chr13:69266223-69266454	IMR90	lung:	n/a	chr13:69266363-69266378
37	MYC	chr13:69264909-69264952	H1-hESC	embryonic stem cell:	n/a	n/a
38	NR2F2	chr13:69260600-69261031	MCF-7	breast:	n/a	n/a
39	NR2F2	chr13:69260141-69261022	MCF-7	breast:	n/a	n/a
40	POLR2A	chr13:69260277-69260582	MCF-7	breast:	n/a	n/a
41	POLR2A	chr13:69265908-69266035	GM12878	blood:	n/a	n/a
42	POLR2A	chr13:69268478-69268601	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr13:69253140-69253174	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr13:69258706-69258712	MCF10A-Er-Src	breast:	n/a	n/a
45	SIN3AK20	chr13:69260006-69260816	MCF-7	breast:	n/a	n/a
46	STAT3	chr13:69256951-69257039	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr13:69260306-69260736	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr13:69255343-69255375	MCF10A-Er-Src	breast:	n/a	n/a
49	TCF12	chr13:69260045-69261067	MCF-7	breast:	n/a	n/a
50	TCF12	chr13:69260087-69261309	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69261665-69261715	NB4	blood:	n/a
2	chr13:69261665-69261715	HUVEC	blood vessel:	n/a
3	chr13:69261665-69261715	PFSK-1	brain:	n/a
4	chr13:69261665-69261715	Jurkat	blood:	n/a
5	chr13:69261665-69261715	HIPEpiC	eye:	n/a
6	chr13:69261665-69261715	HPAEpiC	pulmonary alveolar:	n/a
7	chr13:69261665-69261715	HMEC	breast:	n/a
8	chr13:69261665-69261715	K562	blood:	n/a
9	chr13:69261665-69261715	AG09319	gingival:	n/a
10	chr13:69261665-69261715	HEK293	kidney:	embryo
11	chr13:69261665-69261715	Caco-2	colon:	n/a
12	chr13:69261665-69261715	LNCaP	prostate:	n/a
13	chr13:69261665-69261715	GM12878	blood:	n/a
14	chr13:69261665-69261715	HL-60	blood:	n/a
15	chr13:69261665-69261715	BE2_C	brain:	n/a
16	chr13:69261665-69261715	GM06990	blood:	n/a
17	chr13:69261665-69261715	HNPCEpiC	eye:	n/a
18	chr13:69261665-69261715	SK-N-SH	brain:	n/a
19	chr13:69261665-69261715	MCF-7	breast:	n/a
20	chr13:69261665-69261715	HCF	heart:	n/a
21	chr13:69261665-69261715	HRCEpiC	kidney:	n/a
22	chr13:69261665-69261715	AoSMC	blood vessel:	n/a
23	chr13:69261665-69261715	H1-hESC	embryonic stem cell:	embryo
24	chr13:69261665-69261715	HCT-116	colon:	n/a
25	chr13:69261665-69261715	T-47D	breast:	n/a
26	chr13:69261665-69261715	AG10803	skin:	n/a
27	chr13:69261665-69261715	Hela-S3	cervix:	n/a
28	chr13:69261665-69261715	CMK	blood:	n/a
29	chr13:69261665-69261715	NH-A	brain:	n/a
30	chr13:69261665-69261715	HEEpiC	esophagus:	n/a
31	chr13:69261665-69261715	IMR90	lung:	fetal
32	chr13:69261665-69261715	A549	lung:	n/a
33	chr13:69261665-69261715	ovcar-3	ovarian:	n/a
34	chr13:69261665-69261715	GM12891	blood:	n/a
35	chr13:69261665-69261715	GM12892	blood:	n/a
36	chr13:69261665-69261715	GM19239	blood:	n/a
37	chr13:69261665-69261715	NHBE	bronchial:	n/a
38	chr13:69261665-69261715	HCPEpiC	choroid plexus:	n/a
39	chr13:69261665-69261715	HAEpiC	amniotic membrane:	n/a
40	chr13:69261665-69261715	U87	brain:	n/a
41	chr13:69261665-69261715	HCM	heart:	n/a
42	chr13:69261665-69261715	NT2-D1	testis:	n/a
43	chr13:69261665-69261715	AG09309	skin:	n/a
44	chr13:69261665-69261715	SK-N-MC	brain:	n/a
45	chr13:69261665-69261715	BJ	skin:	n/a
46	chr13:69261665-69261715	AG04449	skin:	fetal
47	chr13:69261665-69261715	PANC-1	pancreas:	n/a
48	chr13:69261665-69261715	ProgFib	skin:	n/a
49	chr13:69261665-69261715	Hepatocyte	liver:	n/a
50	chr13:69261665-69261715	SAEC	small airway:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69259897..69261382-chr13:69319281..69320393,15	MCF-7	breast:
2	chr13:69259900..69260965-chr13:69319275..69320290,3	MCF-7	breast:
3	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
4	chr13:69258057..69262640-chr13:69318281..69322115,7	MCF-7	breast:
5	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
6	chr13:69259986..69260836-chr13:69285583..69286413,2	MCF-7	breast:
7	chr13:69269070..69271450-chr13:69274161..69276898,2	K562	blood:
8	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
9	chr13:69259880..69261273-chr13:69319408..69320273,7	MCF-7	breast:
10	chr13:69260117..69261169-chr13:69319440..69320437,6	MCF-7	breast:
11	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
12	chr13:69259973..69261382-chr13:69319364..69320393,8	MCF-7	breast:
13	chr13:69261144..69263388-chr13:69284618..69286596,2	MCF-7	breast:
14	chr13:69260112..69260846-chr13:69285482..69286306,2	MCF-7	breast:
15	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
16	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL1-8	chr13:69267938-69268213	NONHSAT034237

No data

Variant related genes	Relation type
RN7SL761P	TF binding region
RN7SL761P	CpG island

Extended variants
information (count: 573 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187710198	chr13:69251969-69251970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371255335	chr13:69252013-69252014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561399190	chr13:69252068-69252069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530123813	chr13:69252076-69252077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534606131	chr13:69252127-69252128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547215224	chr13:69252147-69252148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566903115	chr13:69252188-69252189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539326553	chr13:69252206-69252207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192556394	chr13:69252214-69252215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568532929	chr13:69252273-69252274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184592201	chr13:69252319-69252320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554127061	chr13:69252377-69252378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574516153	chr13:69252408-69252409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533647198	chr13:69252414-69252415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573900876	chr13:69252438-69252439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553936650	chr13:69252488-69252489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371382740	chr13:69252518-69252519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34554987	chr13:69252519-69252520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189229518	chr13:69252638-69252639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576923221	chr13:69252641-69252642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192247541	chr13:69252674-69252675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35666206	chr13:69252758-69252759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546151724	chr13:69252831-69252832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9541496	chr13:69252838-69252839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs148829597	chr13:69252864-69252865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143426480	chr13:69252865-69252866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185256088	chr13:69252922-69252923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577225731	chr13:69252927-69252928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565027083	chr13:69252928-69252929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540364471	chr13:69252936-69252937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181107719	chr13:69252952-69252953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532577009	chr13:69252983-69252984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1395674	chr13:69252995-69252996	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185996632	chr13:69253095-69253096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs287418	chr13:69253102-69253103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs556858052	chr13:69253122-69253123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs5804399	chr13:69253124-69253125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150959168	chr13:69253215-69253216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189323929	chr13:69253232-69253233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553569774	chr13:69253250-69253251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140854021	chr13:69253304-69253305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539664034	chr13:69253321-69253322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556357352	chr13:69253341-69253342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117180101	chr13:69253370-69253371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542144544	chr13:69253372-69253373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144669677	chr13:69253394-69253395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35544921	chr13:69253440-69253441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574728294	chr13:69253441-69253442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573304457	chr13:69253463-69253464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540751311	chr13:69253480-69253481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	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
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	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
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69250600-69252000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr13:69251000-69252000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:69251200-69252200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr13:69252000-69253000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr13:69252000-69253000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:69252800-69253200	Enhancers	Placenta Amnion	Placenta Amnion
7	chr13:69253000-69253200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr13:69253000-69253200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:69253000-69253400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:69253200-69256400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr13:69253200-69260200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr13:69258400-69260200	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr13:69260200-69260600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr13:69260200-69260800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr13:69260200-69260800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr13:69260200-69264600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr13:69260400-69260800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr13:69260600-69261400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr13:69260600-69262800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr13:69260800-69262200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr13:69260800-69262200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr13:69260800-69262200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr13:69262000-69262800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr13:69262200-69262400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr13:69262200-69262600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:69262200-69262600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr13:69262200-69262600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr13:69262200-69262800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:69262200-69262800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr13:69262400-69262800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:69262600-69282600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr13:69264600-69265000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:69264600-69265000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr13:69264600-69265000	Enhancers	Brain Germinal Matrix	brain
35	chr13:69266000-69266800	Enhancers	K562	blood
36	chr13:69266800-69272400	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links