Variant report

Variant	nsv1037954
Chromosome Location	chr13:61319533-61395907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:61361279-61361584	HepG2	liver:	n/a	n/a
2	CEBPB	chr13:61361169-61361614	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr13:61369765-61370051	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr13:61364067-61364277	H1-hESC	embryonic stem cell:	n/a	chr13:61364200-61364211
5	CEBPB	chr13:61361234-61361617	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr13:61361366-61361530	A549	lung:	n/a	n/a
7	CEBPB	chr13:61361158-61361658	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr13:61361259-61361594	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:61369761-61370052	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr13:61365495-61365763	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr13:61328609-61328626	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr13:61329579-61329691	A549	lung:	n/a	chr13:61329638-61329646
13	CTCF	chr13:61329529-61329752	MCF-7	breast:	n/a	chr13:61329638-61329646
14	CTCF	chr13:61329560-61329710	NB4	blood:	n/a	chr13:61329638-61329646
15	CTCF	chr13:61329543-61329752	HUVEC	blood vessel:	n/a	chr13:61329638-61329646
16	CTCF	chr13:61329648-61329691	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr13:61329540-61329690	Hela-S3	cervix:	n/a	chr13:61329638-61329646
18	CTCF	chr13:61329580-61329730	HAc	cerebellar:	n/a	chr13:61329638-61329646
19	CTCF	chr13:61368620-61368770	GM06990	blood:	n/a	n/a
20	CTCF	chr13:61329554-61329681	LNCaP	prostate:	n/a	chr13:61329638-61329646
21	CTCF	chr13:61329480-61329630	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr13:61329480-61329630	RPTEC	kidney:	n/a	n/a
23	CTCF	chr13:61329580-61329730	HUVEC	blood vessel:	n/a	chr13:61329638-61329646
24	CTCF	chr13:61390140-61390290	GM06990	blood:	n/a	n/a
25	CTCF	chr13:61329560-61329710	NHEK	skin:	n/a	chr13:61329638-61329646
26	CTCF	chr13:61329560-61329710	MCF-7	breast:	n/a	chr13:61329638-61329646
27	CTCF	chr13:61329579-61329710	HepG2	liver:	n/a	chr13:61329638-61329646
28	CTCF	chr13:61329480-61329630	HCT-116	colon:	n/a	n/a
29	CTCF	chr13:61329460-61329610	BE2_C	brain:	n/a	n/a
30	CTCF	chr13:61329476-61329797	MCF-7	breast:	n/a	chr13:61329638-61329646
31	CTCF	chr13:61329554-61329698	Medullo	brain:	n/a	chr13:61329638-61329646
32	CTCF	chr13:61329562-61329684	HepG2	liver:	n/a	chr13:61329638-61329646
33	CTCF	chr13:61329520-61329670	HRE	kidney:	n/a	chr13:61329638-61329646
34	CTCF	chr13:61329460-61329610	HMEC	breast:	n/a	n/a
35	CTCF	chr13:61329580-61329730	RPTEC	kidney:	n/a	chr13:61329638-61329646
36	CTCF	chr13:61329480-61329630	MCF-7	breast:	n/a	n/a
37	CTCF	chr13:61329540-61329690	HEEpiC	esophagus:	n/a	chr13:61329638-61329646
38	CTCF	chr13:61329520-61329670	NHEK	skin:	n/a	chr13:61329638-61329646
39	CTCF	chr13:61329532-61329768	NHEK	skin:	n/a	chr13:61329638-61329646
40	CTCF	chr13:61329500-61329650	HCT-116	colon:	n/a	chr13:61329638-61329646
41	CTCF	chr13:61329500-61329650	HEK293	kidney:	n/a	chr13:61329638-61329646
42	CTCF	chr13:61329560-61329736	MCF-7	breast:	n/a	chr13:61329638-61329646
43	CTCF	chr13:61364834-61364895	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr13:61329577-61329726	MCF-7	breast:	n/a	chr13:61329638-61329646
45	CTCF	chr13:61329580-61329730	SAEC	small airway:	n/a	chr13:61329638-61329646
46	CTCF	chr13:61329586-61329698	Hela-S3	cervix:	n/a	chr13:61329638-61329646
47	CTCF	chr13:61329560-61329710	Caco-2	colon:	n/a	chr13:61329638-61329646
48	CTCF	chr13:61379985-61380081	GM10248	blood:	n/a	n/a
49	CTCF	chr13:61329600-61329750	WERI-Rb-1	eye:	n/a	chr13:61329638-61329646
50	CTCF	chr13:61329560-61329710	HEEpiC	esophagus:	n/a	chr13:61329638-61329646

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:61330581-61330631	HNPCEpiC	eye:	n/a
2	chr13:61330581-61330631	HEEpiC	esophagus:	n/a
3	chr13:61330581-61330631	Jurkat	blood:	n/a
4	chr13:61330581-61330631	HUVEC	blood vessel:	n/a
5	chr13:61330581-61330631	HPAEpiC	pulmonary alveolar:	n/a
6	chr13:61330581-61330631	SK-N-SH_RA	brain:	n/a
7	chr13:61330581-61330631	ECC-1	luminal epithelium:	n/a
8	chr13:61330581-61330631	SK-N-MC	brain:	n/a
9	chr13:61330581-61330631	U87	brain:	n/a
10	chr13:61330581-61330631	AG04449	skin:	fetal
11	chr13:61330581-61330631	HRCEpiC	kidney:	n/a
12	chr13:61330581-61330631	AG10803	skin:	n/a
13	chr13:61330581-61330631	HRPEpiC	eye:	n/a
14	chr13:61330581-61330631	SAEC	small airway:	n/a
15	chr13:61330581-61330631	NH-A	brain:	n/a
16	chr13:61330581-61330631	T-47D	breast:	n/a
17	chr13:61330581-61330631	AG04450	lung:	fetal
18	chr13:61330581-61330631	RPTEC	kidney:	n/a
19	chr13:61330581-61330631	HMEC	breast:	n/a
20	chr13:61330581-61330631	Hepatocyte	liver:	n/a
21	chr13:61330581-61330631	HCPEpiC	choroid plexus:	n/a
22	chr13:61330581-61330631	HCF	heart:	n/a
23	chr13:61330581-61330631	AG09309	skin:	n/a
24	chr13:61330581-61330631	BJ	skin:	n/a
25	chr13:61330581-61330631	MCF-7	breast:	n/a
26	chr13:61330581-61330631	NT2-D1	testis:	n/a
27	chr13:61330581-61330631	HCT-116	colon:	n/a
28	chr13:61330581-61330631	GM12892	blood:	n/a
29	chr13:61330581-61330631	HEK293	kidney:	embryo
30	chr13:61330581-61330631	ProgFib	skin:	n/a
31	chr13:61330581-61330631	HepG2	liver:	n/a
32	chr13:61330581-61330631	HRE	kidney:	n/a
33	chr13:61330581-61330631	GM06990	blood:	n/a
34	chr13:61330581-61330631	H1-hESC	embryonic stem cell:	embryo
35	chr13:61330581-61330631	PrEC	prostate:	n/a
36	chr13:61330581-61330631	NHBE	bronchial:	n/a
37	chr13:61330581-61330631	HCM	heart:	n/a
38	chr13:61330581-61330631	LNCaP	prostate:	n/a
39	chr13:61330581-61330631	ovcar-3	ovarian:	n/a
40	chr13:61330581-61330631	GM12878	blood:	n/a
41	chr13:61330581-61330631	CMK	blood:	n/a
42	chr13:61330581-61330631	Hela-S3	cervix:	n/a
43	chr13:61330581-61330631	GM12891	blood:	n/a
44	chr13:61330581-61330631	SKMC	muscle:	n/a
45	chr13:61330581-61330631	AoSMC	blood vessel:	n/a
46	chr13:61330581-61330631	IMR90	lung:	fetal
47	chr13:61330581-61330631	SK-N-SH	brain:	n/a
48	chr13:61330581-61330631	AG09319	gingival:	n/a
49	chr13:61330581-61330631	K562	blood:	n/a
50	chr13:61330581-61330631	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:61329166..61329692-chr13:62259510..62260157,2	MCF-7	breast:
2	chr13:61228521..61229179-chr13:61368487..61369171,2	MCF-7	breast:

Variant related genes	Relation type
RNY4P31	TF binding region
RNY3P5	TF binding region
RNY4P31	CpG island
RNY3P5	CpG island

Extended variants
information (count: 1727 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1727 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17058769	chr13:61319533-61319534	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545188338	chr13:61319540-61319541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563661489	chr13:61319543-61319544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184824694	chr13:61319577-61319578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542145359	chr13:61319584-61319585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3914422	chr13:61319605-61319606	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561956482	chr13:61319632-61319633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529241666	chr13:61319635-61319636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530838807	chr13:61319666-61319667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148762950	chr13:61319694-61319695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565906350	chr13:61319708-61319709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10595293	chr13:61319760-61319761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570621562	chr13:61319783-61319784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566978288	chr13:61319798-61319799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188789597	chr13:61319804-61319805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551189923	chr13:61319867-61319868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569775899	chr13:61319874-61319875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142472895	chr13:61319876-61319877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554978181	chr13:61319936-61319937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573971603	chr13:61319942-61319943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368350339	chr13:61319966-61319967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181588162	chr13:61319971-61319972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553117240	chr13:61319973-61319974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs578117646	chr13:61319991-61319992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12861751	chr13:61319995-61319996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566540159	chr13:61320030-61320031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535768929	chr13:61320031-61320032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552850159	chr13:61320060-61320061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147953384	chr13:61320098-61320099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139917139	chr13:61320132-61320133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569139351	chr13:61320144-61320145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543031275	chr13:61320155-61320156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561295825	chr13:61320190-61320191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537849337	chr13:61320215-61320216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141707918	chr13:61320216-61320217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529176317	chr13:61320234-61320235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145349793	chr13:61320279-61320280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147655924	chr13:61320285-61320286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559450779	chr13:61320311-61320312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140997520	chr13:61320318-61320319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368381347	chr13:61320320-61320321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569634286	chr13:61320336-61320337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537177200	chr13:61320339-61320340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150211465	chr13:61320342-61320343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566937705	chr13:61320363-61320364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372279644	chr13:61320400-61320401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534947246	chr13:61320448-61320449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186251904	chr13:61320463-61320464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145015053	chr13:61320479-61320480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149080990	chr13:61320498-61320499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
small cell lung cancer	20016488	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	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
Non-small cell lung cancer	16651412	CNVD
Esophageal squamous carcinoma	20200074	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61314600-61327800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:61319400-61319800	Enhancers	Fetal Heart	heart
3	chr13:61321600-61322200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:61321800-61322400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr13:61322200-61322400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:61322200-61322400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:61322400-61328400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:61323800-61324800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:61323800-61326000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr13:61324800-61325800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:61325400-61326000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr13:61325600-61325800	Enhancers	Fetal Brain Female	brain
13	chr13:61325600-61326000	Enhancers	Fetal Brain Male	brain
14	chr13:61325800-61326000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr13:61326000-61328400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr13:61326000-61329000	Weak transcription	Fetal Brain Male	brain
17	chr13:61326000-61330200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:61326200-61330400	Weak transcription	Fetal Brain Female	brain
19	chr13:61327800-61328400	Enhancers	Primary hematopoietic stem cells	blood
20	chr13:61327800-61331600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr13:61328000-61328600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr13:61328000-61328800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr13:61328000-61330800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr13:61328000-61330800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr13:61328000-61331000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr13:61328200-61329400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr13:61328200-61330800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr13:61328200-61334400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr13:61328400-61328600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr13:61328400-61328800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr13:61328400-61329000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:61328400-61330600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:61328400-61330600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr13:61328400-61330800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr13:61328400-61331000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr13:61328600-61328800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr13:61328600-61329000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr13:61328600-61329000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr13:61328600-61329600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr13:61328600-61329800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr13:61328600-61330400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr13:61328800-61329000	Enhancers	Primary hematopoietic stem cells	blood
43	chr13:61328800-61329400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:61328800-61329600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:61328800-61330000	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr13:61329000-61329400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr13:61329000-61329400	Enhancers	Brain Germinal Matrix	brain
48	chr13:61329000-61330000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr13:61329000-61330800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr13:61329000-61333600	Weak transcription	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links