Variant report

Variant	nsv870276
Chromosome Location	chr13:64287557-64424570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:1286)
Chromatin interactive
region (count:2)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:64313524-64313659	HepG2	liver:	n/a	chr13:64313555-64313566
2	CEBPB	chr13:64409209-64409369	HepG2	liver:	n/a	chr13:64409350-64409361
3	CEBPB	chr13:64409210-64409420	A549	lung:	n/a	chr13:64409350-64409361
4	CEBPB	chr13:64409212-64409411	IMR90	lung:	n/a	chr13:64409350-64409361
5	CEBPB	chr13:64422818-64422949	HepG2	liver:	n/a	n/a
6	CHD2	chr13:64385983-64386021	K562	blood:	n/a	n/a
7	CTCF	chr13:64292407-64292528	Lung_OC	lung:	n/a	n/a
8	CTCF	chr13:64403881-64403963	GM19239	blood:	n/a	n/a
9	CTCF	chr13:64415903-64415950	LNCaP	prostate:	n/a	n/a
10	CTCF	chr13:64338203-64338280	GM13976	blood:	n/a	n/a
11	CTCF	chr13:64403857-64403983	A549	lung:	n/a	n/a
12	CTCF	chr13:64403823-64404050	MCF-7	breast:	n/a	n/a
13	CTCF	chr13:64324188-64324191	GM19240	blood:	n/a	n/a
14	CTCF	chr13:64297739-64297766	LNCaP	prostate:	n/a	n/a
15	CTCF	chr13:64401620-64401694	LNCaP	prostate:	n/a	n/a
16	CTCF	chr13:64320948-64321033	LNCaP	prostate:	n/a	n/a
17	CTCF	chr13:64384593-64384675	Lung_OC	lung:	n/a	n/a
18	CTCF	chr13:64324118-64324236	GM13977	blood:	n/a	n/a
19	CTCF	chr13:64403870-64403967	GM19240	blood:	n/a	n/a
20	CTCF	chr13:64324030-64324275	Gliobla	brain:	n/a	n/a
21	CTCF	chr13:64403936-64403999	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr13:64324126-64324196	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr13:64403234-64403280	LNCaP	prostate:	n/a	n/a
24	CTCF	chr13:64388066-64388097	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:64388099-64388105	MCF-7	breast:	n/a	n/a
26	CTCF	chr13:64324128-64324253	GM19239	blood:	n/a	n/a
27	CTCF	chr13:64330862-64330927	Medullo	brain:	n/a	n/a
28	CTCF	chr13:64374170-64374211	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr13:64343509-64343605	GM20000	blood:	n/a	n/a
30	CTCF	chr13:64403886-64403996	GM10266	blood:	n/a	n/a
31	CTCF	chr13:64334444-64334532	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr13:64404781-64404867	LNCaP	prostate:	n/a	n/a
33	CTCF	chr13:64312774-64312800	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr13:64388012-64388076	MCF-7	breast:	n/a	n/a
35	CTCF	chr13:64403852-64404060	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr13:64324040-64324265	HepG2	liver:	n/a	n/a
37	CTCF	chr13:64403844-64403981	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:64339091-64339163	Lung_OC	lung:	n/a	n/a
39	CTCF	chr13:64292400-64292402	Lung_OC	lung:	n/a	n/a
40	CTCF	chr13:64403897-64403955	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr13:64324183-64324225	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr13:64403828-64403986	Fibrobl	skin:	n/a	n/a
43	CTCF	chr13:64403872-64403970	ProgFib	skin:	n/a	n/a
44	CTCF	chr13:64312154-64312170	GM20000	blood:	n/a	n/a
45	CTCF	chr13:64403850-64403990	HepG2	liver:	n/a	n/a
46	CTCF	chr13:64324097-64324217	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr13:64356700-64356850	HepG2	liver:	n/a	n/a
48	CTCF	chr13:64403800-64404103	LNCaP	prostate:	n/a	n/a
49	CTCF	chr13:64403812-64404067	MCF-7	breast:	n/a	n/a
50	CTCF	chr13:64377920-64378070	GM12869	blood:	n/a	n/a

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64315383-64315433	ECC-1	luminal epithelium:	n/a
2	chr13:64411884-64411934	T-47D	breast:	n/a
3	chr13:64382075-64382125	NHBE	bronchial:	n/a
4	chr13:64408172-64408222	HMEC	breast:	n/a
5	chr13:64418676-64418726	AG09319	gingival:	n/a
6	chr13:64315383-64315433	ECC-1	luminal epithelium:	n/a
7	chr13:64411884-64411934	T-47D	breast:	n/a
8	chr13:64382075-64382125	NHBE	bronchial:	n/a
9	chr13:64408172-64408222	HMEC	breast:	n/a
10	chr13:64418676-64418726	AG09319	gingival:	n/a
11	chr13:64421835-64421885	AG09309	skin:	n/a
12	chr13:64418337-64418387	ProgFib	skin:	n/a
13	chr13:64418279-64418329	Caco-2	colon:	n/a
14	chr13:64418279-64418329	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:64384119-64384169	CMK	blood:	n/a
16	chr13:64408172-64408222	HRCEpiC	kidney:	n/a
17	chr13:64382075-64382125	Jurkat	blood:	n/a
18	chr13:64418337-64418387	NB4	blood:	n/a
19	chr13:64418678-64418728	HEK293	kidney:	embryo
20	chr13:64315383-64315433	HEEpiC	esophagus:	n/a
21	chr13:64408172-64408222	MCF-7	breast:	n/a
22	chr13:64311555-64311605	PrEC	prostate:	n/a
23	chr13:64386291-64386341	HRE	kidney:	n/a
24	chr13:64388106-64388156	ovcar-3	ovarian:	n/a
25	chr13:64386291-64386341	NH-A	brain:	n/a
26	chr13:64418279-64418329	BJ	skin:	n/a
27	chr13:64412172-64412222	PFSK-1	brain:	n/a
28	chr13:64382075-64382125	HEEpiC	esophagus:	n/a
29	chr13:64412172-64412222	HEK293	kidney:	embryo
30	chr13:64412172-64412222	RPTEC	kidney:	n/a
31	chr13:64416816-64416866	GM12891	blood:	n/a
32	chr13:64415303-64415353	HAEpiC	amniotic membrane:	n/a
33	chr13:64418337-64418387	Hela-S3	cervix:	n/a
34	chr13:64411884-64411934	HL-60	blood:	n/a
35	chr13:64421835-64421885	AG04449	skin:	fetal
36	chr13:64382075-64382125	GM12878	blood:	n/a
37	chr13:64385720-64385770	A549	lung:	n/a
38	chr13:64418345-64418395	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:64418678-64418728	HRPEpiC	eye:	n/a
40	chr13:64411884-64411934	PANC-1	pancreas:	n/a
41	chr13:64386291-64386341	K562	blood:	n/a
42	chr13:64388106-64388156	NH-A	brain:	n/a
43	chr13:64382075-64382125	BJ	skin:	n/a
44	chr13:64412172-64412222	HAEpiC	amniotic membrane:	n/a
45	chr13:64418676-64418726	HEK293	kidney:	embryo
46	chr13:64412172-64412222	A549	lung:	n/a
47	chr13:64421835-64421885	IMR90	lung:	fetal
48	chr13:64421835-64421885	GM12878	blood:	n/a
49	chr13:64411884-64411934	HCT-116	colon:	n/a
50	chr13:64384119-64384169	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:
2	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034172
2	lnc-PCDH20-9	chr13:64301184-64301215	XLOC_010643
3	lnc-AL445989.1-20	chr13:64313246-64314376	NONHSAT034175
4	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034174
5	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034174
6	lnc-PCDH20-10	chr13:64402902-64403292	ENSG00000219926.3
7	lnc-PCDH20-10	chr13:64413882-64414219	NONHSAT034181
8	lnc-AL445989.1-20	chr13:64311843-64312482	NONHSAT034172
9	lnc-PCDH20-10	chr13:64403127-64403285	NONHSAT034184
10	lnc-PCDH20-10	chr13:64405587-64405985	ENSG00000219926.3
11	lnc-PCDH20-10	chr13:64412293-64412877	NONHSAT034185
12	lnc-AL445989.1-20	chr13:64313246-64314310	NONHSAT034174
13	lnc-PCDH20-9	chr13:64288485-64288508	XLOC_010643
14	lnc-PCDH20-9	chr13:64303522-64303895	XLOC_010643
15	lnc-PCDH20-10	chr13:64405587-64405985	ENSG00000219926.6
16	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034175
17	lnc-AL445989.1-1	chr13:64322132-64322530	ENSG00000237378
18	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034173
19	lnc-PCDH20-10	chr13:64405587-64405985	NONHSAT034184
20	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034173
21	lnc-PCDH20-9	chr13:64303522-64303642	XLOC_010643
22	lnc-AL445989.1-20	chr13:64311843-64312416	NONHSAT034173
23	lnc-AL445989.1-20	chr13:64316498-64316945	NONHSAT034176
24	lnc-AL445989.1-21	chr13:64411166-64411589	NONHSAT034186
25	lnc-PCDH20-10	chr13:64413203-64413330	NONHSAT034187
26	lnc-PCDH20-9	chr13:64291083-64291151	XLOC_010643
27	lnc-PCDH20-10	chr13:64405587-64405660	NONHSAT034181
28	lnc-PCDH20-10	chr13:64402973-64403285	ENSG00000219926.6
29	lnc-AL445989.1-1	chr13:64324837-64325213	ENSG00000237378
30	lnc-PCDH20-10	chr13:64402967-64403285	NONHSAT034181
31	lnc-PCDH20-10	chr13:64412250-64412371	NONHSAT034187
32	lnc-PCDH20-9	chr13:64312042-64312151	XLOC_010643
33	lnc-PCDH20-10	chr13:64411124-64411575	NONHSAT034185

No data

Variant related genes	Relation type
ENSG00000226974	TF binding region
RNU6-81P	TF binding region
ENSG00000272299	TF binding region
LINC00395	TF binding region
ENSG00000219926	TF binding region
PPP1R2P10	TF binding region
ENSG00000237378	TF binding region
OR7E104P	TF binding region
OR7E156P	TF binding region
ENSG00000226974	CpG island
RNU6-81P	CpG island
ENSG00000272299	CpG island
LINC00395	CpG island
ENSG00000219926	CpG island
PPP1R2P10	CpG island
ENSG00000237378	CpG island
OR7E104P	CpG island
OR7E156P	CpG island
DUSP3	miRNA target sites

Extended variants
information (count: 1802 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1802 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147640868	chr13:64288486-64288487	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs542215486	chr13:64288495-64288496	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs533171828	chr13:64291095-64291096	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs370159750	chr13:64291141-64291142	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs189614580	chr13:64302402-64302403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562805618	chr13:64302424-64302425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192850660	chr13:64302445-64302446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113545937	chr13:64302538-64302539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548202034	chr13:64302558-64302559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566322721	chr13:64302599-64302600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527265091	chr13:64302605-64302606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375216998	chr13:64302606-64302607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185265496	chr13:64302611-64302612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140086422	chr13:64302634-64302635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190352287	chr13:64302645-64302646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150496236	chr13:64302709-64302710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557267904	chr13:64302718-64302719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570817733	chr13:64302769-64302770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112513002	chr13:64302783-64302784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77255608	chr13:64302868-64302869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554978659	chr13:64302994-64302995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145396666	chr13:64303008-64303009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564290054	chr13:64303046-64303047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533372521	chr13:64303054-64303055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201091060	chr13:64303055-64303056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544466845	chr13:64303086-64303087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562526601	chr13:64303088-64303089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530030032	chr13:64303101-64303102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539697502	chr13:64303137-64303138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547191141	chr13:64303203-64303204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142575243	chr13:64303219-64303220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9571012	chr13:64303276-64303277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs146694405	chr13:64303285-64303286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139162251	chr13:64303297-64303298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570257438	chr13:64303301-64303302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181486276	chr13:64303336-64303337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539439943	chr13:64303341-64303342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186429673	chr13:64303405-64303406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73506726	chr13:64303430-64303431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189315583	chr13:64303452-64303453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569967052	chr13:64303463-64303464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537770143	chr13:64303470-64303471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9571013	chr13:64303507-64303508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs34314487	chr13:64303523-64303524	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs574159701	chr13:64303528-64303529	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs143057308	chr13:64303532-64303533	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs9571014	chr13:64303536-64303537	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs577448137	chr13:64303577-64303578	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs147037940	chr13:64303588-64303589	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs558139499	chr13:64303593-64303594	Weak transcription	lncRNA	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
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	15273396	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64302400-64302800	Enhancers	Fetal Intestine Small	intestine
2	chr13:64302400-64303200	Enhancers	Fetal Intestine Large	intestine
3	chr13:64302800-64303800	Weak transcription	Fetal Intestine Small	intestine
4	chr13:64303200-64303600	Weak transcription	Fetal Intestine Large	intestine
5	chr13:64303600-64303800	Enhancers	Fetal Intestine Large	intestine
6	chr13:64303800-64304400	Enhancers	Fetal Intestine Small	intestine
7	chr13:64303800-64305800	Weak transcription	Fetal Intestine Large	intestine
8	chr13:64304400-64305800	Weak transcription	Fetal Intestine Small	intestine
9	chr13:64305600-64306000	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr13:64305800-64306200	Enhancers	HepG2	liver
11	chr13:64305800-64306600	Enhancers	Fetal Intestine Large	intestine
12	chr13:64305800-64306600	Enhancers	Stomach Mucosa	stomach
13	chr13:64305800-64307200	Enhancers	Fetal Intestine Small	intestine
14	chr13:64306000-64307800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr13:64306200-64307000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr13:64307800-64308200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr13:64308200-64310200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr13:64310200-64310600	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr13:64315400-64316200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr13:64347400-64348200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr13:64384200-64386000	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr13:64415000-64415200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr13:64415000-64415600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr13:64415000-64415600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr13:64415200-64415400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr13:64415200-64415600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr13:64415600-64418200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr13:64415600-64419000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr13:64418200-64418600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr13:64418600-64420400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr13:64422200-64423000	Enhancers	Fetal Lung	lung
32	chr13:64422400-64423200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links