Variant report

Variant	nsv562089
Chromosome Location	chr13:65910792-66392991
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	ATF1	chr13:66035822-66036144	K562	blood:	n/a	n/a
2	BATF	chr13:66041811-66041993	GM12878	blood:	n/a	chr13:66041940-66041951
3	BATF	chr13:65988370-65988595	GM12878	blood:	n/a	n/a
4	BATF	chr13:66080137-66080390	GM12878	blood:	n/a	n/a
5	BHLHE40	chr13:66212820-66213067	GM12878	blood:	n/a	n/a
6	BRCA1	chr13:66035765-66036027	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr13:65953042-65953530	HCT-116	colon:	n/a	n/a
8	CBX3	chr13:66212653-66213113	HCT-116	colon:	n/a	n/a
9	CEBPB	chr13:66172480-66172999	A549	lung:	n/a	chr13:66172550-66172561
10	CEBPB	chr13:66343067-66343334	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr13:65911079-65911402	IMR90	lung:	n/a	n/a
12	CEBPB	chr13:65942931-65943178	IMR90	lung:	n/a	chr13:65942991-65943002
13	CEBPB	chr13:66252078-66252417	IMR90	lung:	n/a	n/a
14	CEBPB	chr13:66252087-66252372	A549	lung:	n/a	n/a
15	CEBPB	chr13:65935688-65935939	IMR90	lung:	n/a	chr13:65935790-65935801
16	CEBPB	chr13:66112618-66112843	HepG2	liver:	n/a	chr13:66112657-66112668 chr13:66112655-66112666
17	CEBPB	chr13:66035754-66036255	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr13:66302788-66302938	A549	lung:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
19	CEBPB	chr13:66039732-66039775	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:65985060-65985370	HepG2	liver:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
21	CEBPB	chr13:66172575-66172866	A549	lung:	n/a	n/a
22	CEBPB	chr13:66071327-66071819	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr13:66212723-66213083	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr13:65917105-65917448	HepG2	liver:	n/a	chr13:65917266-65917277
25	CEBPB	chr13:66284808-66285037	K562	blood:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
26	CEBPB	chr13:65917104-65917425	IMR90	lung:	n/a	chr13:65917266-65917277
27	CEBPB	chr13:66172567-66172901	A549	lung:	n/a	n/a
28	CEBPB	chr13:66348740-66349098	HepG2	liver:	n/a	chr13:66348913-66348924
29	CEBPB	chr13:66302696-66303002	IMR90	lung:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
30	CEBPB	chr13:66281605-66281903	HepG2	liver:	n/a	chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281751-66281762 chr13:66281752-66281761 chr13:66281752-66281761 chr13:66281750-66281761
31	CEBPB	chr13:66095944-66096227	IMR90	lung:	n/a	n/a
32	CEBPB	chr13:66046169-66046753	HepG2	liver:	n/a	chr13:66046346-66046355 chr13:66046346-66046355 chr13:66046344-66046357 chr13:66046346-66046355 chr13:66046344-66046357 chr13:66046344-66046355 chr13:66046346-66046355 chr13:66046346-66046357
33	CEBPB	chr13:65941086-65941290	HepG2	liver:	n/a	chr13:65941156-65941167
34	CEBPB	chr13:66252168-66252428	MCF-7	breast:	n/a	n/a
35	CEBPB	chr13:66048985-66049163	A549	lung:	n/a	n/a
36	CEBPB	chr13:66302768-66302924	H1-hESC	embryonic stem cell:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
37	CEBPB	chr13:65917150-65917355	A549	lung:	n/a	chr13:65917266-65917277
38	CEBPB	chr13:66284791-66285143	HepG2	liver:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
39	CEBPB	chr13:66172469-66172941	Hela-S3	cervix:	n/a	chr13:66172550-66172561
40	CEBPB	chr13:66252073-66252455	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr13:66343051-66343372	IMR90	lung:	n/a	n/a
42	CEBPB	chr13:66269598-66269845	A549	lung:	n/a	chr13:66269714-66269727 chr13:66269716-66269727 chr13:66269714-66269725
43	CEBPB	chr13:65985052-65985387	IMR90	lung:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
44	CEBPB	chr13:66252032-66252574	HCT-116	colon:	n/a	n/a
45	CEBPB	chr13:66252054-66252437	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:66269557-66269900	IMR90	lung:	n/a	chr13:66269714-66269727 chr13:66269716-66269727 chr13:66269714-66269725
47	CEBPB	chr13:66180730-66181006	IMR90	lung:	n/a	n/a
48	CEBPB	chr13:66252152-66252392	K562	blood:	n/a	n/a
49	CEBPB	chr13:66022805-66023052	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:66252041-66252457	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66252177-66252227	NB4	blood:	n/a
2	chr13:65911268-65911318	MCF-7	breast:	n/a
3	chr13:66322551-66322601	PFSK-1	brain:	n/a
4	chr13:66156848-66156898	H1-hESC	embryonic stem cell:	embryo
5	chr13:66322551-66322601	HCF	heart:	n/a
6	chr13:66322551-66322601	AG10803	skin:	n/a
7	chr13:66156848-66156898	AoSMC	blood vessel:	n/a
8	chr13:65911268-65911318	LNCaP	prostate:	n/a
9	chr13:66252177-66252227	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:66156848-66156898	HNPCEpiC	eye:	n/a
11	chr13:66252177-66252227	GM06990	blood:	n/a
12	chr13:66322551-66322601	Caco-2	colon:	n/a
13	chr13:66252177-66252227	LNCaP	prostate:	n/a
14	chr13:66252177-66252227	HepG2	liver:	n/a
15	chr13:66156848-66156898	HAEpiC	amniotic membrane:	n/a
16	chr13:66252177-66252227	HRCEpiC	kidney:	n/a
17	chr13:66252177-66252227	HRPEpiC	eye:	n/a
18	chr13:66156848-66156898	GM06990	blood:	n/a
19	chr13:66322551-66322601	NH-A	brain:	n/a
20	chr13:66156848-66156898	PrEC	prostate:	n/a
21	chr13:65911268-65911318	SKMC	muscle:	n/a
22	chr13:66156848-66156898	HCPEpiC	choroid plexus:	n/a
23	chr13:66322551-66322601	PrEC	prostate:	n/a
24	chr13:66252177-66252227	RPTEC	kidney:	n/a
25	chr13:66156848-66156898	AG04450	lung:	fetal
26	chr13:66156848-66156898	HepG2	liver:	n/a
27	chr13:65911268-65911318	HIPEpiC	eye:	n/a
28	chr13:65911268-65911318	PFSK-1	brain:	n/a
29	chr13:66322551-66322601	ProgFib	skin:	n/a
30	chr13:66252177-66252227	GM12892	blood:	n/a
31	chr13:66322551-66322601	K562	blood:	n/a
32	chr13:66156848-66156898	A549	lung:	n/a
33	chr13:66252177-66252227	MCF10A-Er-Src	breast:	n/a
34	chr13:65911268-65911318	HRE	kidney:	n/a
35	chr13:66322551-66322601	ECC-1	luminal epithelium:	n/a
36	chr13:66322551-66322601	HMEC	breast:	n/a
37	chr13:66322551-66322601	NB4	blood:	n/a
38	chr13:66322551-66322601	SK-N-SH_RA	brain:	n/a
39	chr13:66156848-66156898	ProgFib	skin:	n/a
40	chr13:66322551-66322601	HEEpiC	esophagus:	n/a
41	chr13:66322551-66322601	SAEC	small airway:	n/a
42	chr13:66156848-66156898	NHBE	bronchial:	n/a
43	chr13:66322551-66322601	AoSMC	blood vessel:	n/a
44	chr13:65911268-65911318	HMEC	breast:	n/a
45	chr13:66156848-66156898	IMR90	lung:	fetal
46	chr13:66252177-66252227	T-47D	breast:	n/a
47	chr13:66252177-66252227	GM12878	blood:	n/a
48	chr13:65911268-65911318	HepG2	liver:	n/a
49	chr13:66252177-66252227	BE2_C	brain:	n/a
50	chr13:66252177-66252227	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:66046639..66047382-chr3:13541452..13542407,2	MCF-7	breast:
2	chr1:106318966..106319467-chr13:66093606..66094106,2	NB4	blood:
3	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
4	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
5	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
6	chr13:65802985..65805270-chr13:66070535..66073117,2	K562	blood:
7	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:
8	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
9	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
10	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
11	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
12	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
13	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
14	chr13:65020257..65021157-chr13:66212532..66213123,2	MCF-7	breast:
15	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
16	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
17	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
18	chr13:65045929..65046727-chr13:66212514..66213321,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-7	chr13:66017513-66017582	NONHSAT034194
2	lnc-PCDH9-7	chr13:66015947-66016044	NONHSAT034194
3	lnc-PCDH9-7	chr13:66035510-66035584	NONHSAT034194

Variant related genes	Relation type
HNRNPA3P5	TF binding region
HNRNPA3P5	CpG island
ENSG00000236565	chromatin interactions

Extended variants
information (count: 6150 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:6150 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3888049	chr13:65910792-65910793	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543424944	chr13:65910811-65910812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186856254	chr13:65910823-65910824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528990867	chr13:65910831-65910832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149436076	chr13:65910840-65910841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147104715	chr13:65910854-65910855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547464661	chr13:65910899-65910900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565819806	chr13:65910930-65910931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571539778	chr13:65910939-65910940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564811494	chr13:65910940-65910941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567503709	chr13:65910957-65910958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190114025	chr13:65910969-65910970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138499270	chr13:65911015-65911016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573137798	chr13:65911016-65911017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538824163	chr13:65911037-65911038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558853308	chr13:65911058-65911059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374742739	chr13:65911062-65911063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544537169	chr13:65911065-65911066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143968726	chr13:65911088-65911089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181309247	chr13:65911123-65911124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542784170	chr13:65911161-65911162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185135289	chr13:65911208-65911209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367659945	chr13:65911224-65911225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532160890	chr13:65911242-65911243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147284659	chr13:65911266-65911267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189842027	chr13:65911268-65911269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182464975	chr13:65911273-65911274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188957783	chr13:65911288-65911289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148741148	chr13:65911299-65911300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551552919	chr13:65911330-65911331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192026045	chr13:65911374-65911375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566642479	chr13:65911396-65911397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201512183	chr13:65911400-65911401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538710872	chr13:65911422-65911423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs3904705	chr13:65911432-65911433	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs3904504	chr13:65911437-65911438	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs568880106	chr13:65911442-65911443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554953779	chr13:65911481-65911482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573713464	chr13:65911585-65911586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114387767	chr13:65911609-65911610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74884969	chr13:65911712-65911713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572984337	chr13:65911749-65911750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7317414	chr13:65911763-65911764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs9571369	chr13:65911767-65911768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530611455	chr13:65911771-65911772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150830516	chr13:65911780-65911781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377684856	chr13:65911802-65911803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560829339	chr13:65911829-65911830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139235603	chr13:65911906-65911907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529907410	chr13:65911986-65911987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
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
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
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65909600-65911400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr13:65910000-65911000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr13:65910000-65911400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr13:65910200-65911000	Enhancers	Fetal Muscle Trunk	muscle
5	chr13:65910400-65911200	Enhancers	Fetal Muscle Leg	muscle
6	chr13:65910400-65911200	Enhancers	Gastric	stomach
7	chr13:65910400-65911400	Enhancers	Brain Germinal Matrix	brain
8	chr13:65910400-65913200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr13:65910600-65911600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr13:65911000-65913400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:65911200-65911600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr13:65913200-65914800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr13:65913400-65913600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr13:65913600-65913800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr13:65913600-65914400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr13:65913800-65914000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr13:65914000-65914800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr13:65914400-65917400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr13:65914800-65915600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr13:65914800-65915800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr13:65915600-65917600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr13:65915800-65917600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr13:65916400-65917600	Enhancers	Primary hematopoietic stem cells	blood
24	chr13:65916800-65917600	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr13:65917200-65918800	Enhancers	Fetal Heart	heart
26	chr13:65917400-65917600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr13:65917600-65920600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr13:65943200-65943600	Enhancers	Fetal Heart	heart
29	chr13:65943600-65944000	Weak transcription	Fetal Heart	heart
30	chr13:65944000-65944600	Enhancers	Fetal Heart	heart
31	chr13:65952200-65953000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
32	chr13:65959600-65960000	Enhancers	Fetal Lung	lung
33	chr13:65960000-65960400	Weak transcription	Fetal Lung	lung
34	chr13:65960400-65960600	Enhancers	Fetal Lung	lung
35	chr13:65960600-65961400	Weak transcription	Fetal Lung	lung
36	chr13:65961000-65962000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:65961400-65961600	ZNF genes & repeats	Fetal Lung	lung
38	chr13:65961400-65962400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr13:65962000-65962600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:65962600-65964400	Weak transcription	Fetal Brain Male	brain
41	chr13:65967600-65970000	Weak transcription	Fetal Brain Male	brain
42	chr13:65971400-65972600	Enhancers	Placenta Amnion	Placenta Amnion
43	chr13:65971800-65973400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr13:65972600-65973800	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr13:65973400-65974800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr13:65974200-65975000	Enhancers	Fetal Lung	lung
47	chr13:65974400-65974600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr13:65974800-65975000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr13:65978600-65978800	Enhancers	Fetal Brain Female	brain
50	chr13:65981800-65982000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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