Variant report

Variant	nsv1035413
Chromosome Location	chr13:64115552-64348712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr13:64202454-64202872	GM12878	blood:	n/a	n/a
2	BRCA1	chr13:64159675-64159893	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr13:64129467-64129667	IMR90	lung:	n/a	chr13:64129521-64129534 chr13:64129523-64129534 chr13:64129521-64129532 chr13:64129521-64129534
4	CEBPB	chr13:64198926-64199167	H1-hESC	embryonic stem cell:	n/a	chr13:64199079-64199090 chr13:64199079-64199090 chr13:64199080-64199091
5	CEBPB	chr13:64185841-64186143	HepG2	liver:	n/a	chr13:64186008-64186019
6	CEBPB	chr13:64227752-64227904	IMR90	lung:	n/a	chr13:64227818-64227829
7	CEBPB	chr13:64282619-64282952	IMR90	lung:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
8	CEBPB	chr13:64200744-64200955	HepG2	liver:	n/a	chr13:64200806-64200817
9	CEBPB	chr13:64254753-64254953	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:64262408-64262608	HepG2	liver:	n/a	chr13:64262502-64262513
11	CEBPB	chr13:64282710-64282910	H1-hESC	embryonic stem cell:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
12	CEBPB	chr13:64129342-64129673	HepG2	liver:	n/a	chr13:64129521-64129534 chr13:64129523-64129534 chr13:64129521-64129532 chr13:64129521-64129534
13	CEBPB	chr13:64131010-64131231	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:64198891-64199235	HepG2	liver:	n/a	chr13:64199079-64199090 chr13:64199079-64199090 chr13:64199080-64199091
15	CEBPB	chr13:64198975-64199225	A549	lung:	n/a	chr13:64199079-64199090 chr13:64199079-64199090 chr13:64199080-64199091
16	CEBPB	chr13:64282631-64282951	HepG2	liver:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
17	CEBPB	chr13:64227763-64227840	HepG2	liver:	n/a	chr13:64227818-64227829
18	CEBPB	chr13:64198894-64199201	Hela-S3	cervix:	n/a	chr13:64199079-64199090 chr13:64199079-64199090 chr13:64199080-64199091
19	CEBPB	chr13:64189343-64189719	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:64115509-64115729	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr13:64195329-64195710	HepG2	liver:	n/a	chr13:64195563-64195576 chr13:64195560-64195577 chr13:64195565-64195576
22	CEBPB	chr13:64249235-64249452	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:64313524-64313659	HepG2	liver:	n/a	chr13:64313555-64313566
24	CEBPB	chr13:64198977-64199235	IMR90	lung:	n/a	chr13:64199079-64199090 chr13:64199079-64199090 chr13:64199080-64199091
25	CEBPB	chr13:64180178-64180411	IMR90	lung:	n/a	n/a
26	CEBPB	chr13:64185879-64186148	A549	lung:	n/a	chr13:64186008-64186019
27	CEBPB	chr13:64185838-64186198	IMR90	lung:	n/a	chr13:64186008-64186019
28	CEBPB	chr13:64171661-64171866	IMR90	lung:	n/a	n/a
29	CEBPB	chr13:64232307-64232441	HepG2	liver:	n/a	chr13:64232331-64232342
30	CTCF	chr13:64210400-64210550	HEK293	kidney:	n/a	n/a
31	CTCF	chr13:64247080-64247230	AG10803	skin:	n/a	n/a
32	CTCF	chr13:64324146-64324249	GM19238	blood:	n/a	n/a
33	CTCF	chr13:64226020-64226270	HMF	breast:	n/a	n/a
34	CTCF	chr13:64324126-64324196	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr13:64324047-64324270	Medullo	brain:	n/a	n/a
36	CTCF	chr13:64210403-64210644	MCF-7	breast:	n/a	chr13:64210539-64210560 chr13:64210537-64210555
37	CTCF	chr13:64324108-64324265	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:64210489-64210605	HepG2	liver:	n/a	chr13:64210539-64210560 chr13:64210537-64210555
39	CTCF	chr13:64210440-64210590	GM12871	blood:	n/a	chr13:64210539-64210560 chr13:64210537-64210555
40	CTCF	chr13:64292400-64292402	Lung_OC	lung:	n/a	n/a
41	CTCF	chr13:64324117-64324248	GM10266	blood:	n/a	n/a
42	CTCF	chr13:64210440-64210590	GM12874	blood:	n/a	chr13:64210539-64210560 chr13:64210537-64210555
43	CTCF	chr13:64210400-64210550	GM12878	blood:	n/a	n/a
44	CTCF	chr13:64210513-64210546	GM12892	blood:	n/a	n/a
45	CTCF	chr13:64324142-64324254	A549	lung:	n/a	n/a
46	CTCF	chr13:64210540-64210690	AG04450	lung:	n/a	n/a
47	CTCF	chr13:64210460-64210610	HRPEpiC	eye:	n/a	chr13:64210539-64210560 chr13:64210537-64210555
48	CTCF	chr13:64324097-64324217	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr13:64324092-64324260	MCF-7	breast:	n/a	n/a
50	CTCF	chr13:64261647-64261744	GM10248	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64311397-64311447	HRE	kidney:	n/a
2	chr13:64315383-64315433	HIPEpiC	eye:	n/a
3	chr13:64189052-64189102	HepG2	liver:	n/a
4	chr13:64315383-64315433	U87	brain:	n/a
5	chr13:64311397-64311447	PrEC	prostate:	n/a
6	chr13:64189052-64189102	HAEpiC	amniotic membrane:	n/a
7	chr13:64311555-64311605	IMR90	lung:	fetal
8	chr13:64189052-64189102	HUVEC	blood vessel:	n/a
9	chr13:64311555-64311605	BJ	skin:	n/a
10	chr13:64311397-64311447	GM12878	blood:	n/a
11	chr13:64315383-64315433	PANC-1	pancreas:	n/a
12	chr13:64189052-64189102	ProgFib	skin:	n/a
13	chr13:64311397-64311447	Caco-2	colon:	n/a
14	chr13:64189052-64189102	BJ	skin:	n/a
15	chr13:64315383-64315433	AG09309	skin:	n/a
16	chr13:64311397-64311447	RPTEC	kidney:	n/a
17	chr13:64311397-64311447	T-47D	breast:	n/a
18	chr13:64311555-64311605	NH-A	brain:	n/a
19	chr13:64315383-64315433	Hepatocyte	liver:	n/a
20	chr13:64311555-64311605	CMK	blood:	n/a
21	chr13:64315383-64315433	BE2_C	brain:	n/a
22	chr13:64315383-64315433	T-47D	breast:	n/a
23	chr13:64311555-64311605	MCF-7	breast:	n/a
24	chr13:64311555-64311605	HCM	heart:	n/a
25	chr13:64311555-64311605	AG04449	skin:	fetal
26	chr13:64311555-64311605	Jurkat	blood:	n/a
27	chr13:64315383-64315433	ECC-1	luminal epithelium:	n/a
28	chr13:64311555-64311605	H1-hESC	embryonic stem cell:	embryo
29	chr13:64311555-64311605	K562	blood:	n/a
30	chr13:64315383-64315433	PFSK-1	brain:	n/a
31	chr13:64189052-64189102	GM06990	blood:	n/a
32	chr13:64315383-64315433	HEEpiC	esophagus:	n/a
33	chr13:64189052-64189102	HL-60	blood:	n/a
34	chr13:64189052-64189102	HRCEpiC	kidney:	n/a
35	chr13:64311555-64311605	A549	lung:	n/a
36	chr13:64311397-64311447	HMEC	breast:	n/a
37	chr13:64189052-64189102	NHBE	bronchial:	n/a
38	chr13:64189052-64189102	SAEC	small airway:	n/a
39	chr13:64315383-64315433	HepG2	liver:	n/a
40	chr13:64311555-64311605	T-47D	breast:	n/a
41	chr13:64311397-64311447	SKMC	muscle:	n/a
42	chr13:64311397-64311447	HEEpiC	esophagus:	n/a
43	chr13:64311555-64311605	U87	brain:	n/a
44	chr13:64311555-64311605	LNCaP	prostate:	n/a
45	chr13:64311555-64311605	ovcar-3	ovarian:	n/a
46	chr13:64311397-64311447	CMK	blood:	n/a
47	chr13:64315383-64315433	IMR90	lung:	fetal
48	chr13:64311555-64311605	HL-60	blood:	n/a
49	chr13:64315383-64315433	HCPEpiC	choroid plexus:	n/a
50	chr13:64311397-64311447	PANC-1	pancreas:	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:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-9	chr13:64303522-64303895	XLOC_010643
2	lnc-PCDH20-8	chr13:64204770-64204813	XLOC_010642
3	lnc-AL445989.1-2	chr13:64209594-64209643	XLOC_010411
4	lnc-PCDH20-7	chr13:64159888-64159977	XLOC_010641
5	lnc-AL445989.1-20	chr13:64313246-64314310	NONHSAT034174
6	lnc-AL445989.1-1	chr13:64322132-64322530	ENSG00000237378
7	lnc-PCDH20-9	chr13:64261535-64261688	XLOC_010643
8	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034172
9	lnc-AL445989.1-2	chr13:64201008-64201079	XLOC_010411
10	lnc-AL445989.1-2	chr13:64208383-64208464	XLOC_010411
11	lnc-PCDH20-7	chr13:64159590-64159812	XLOC_010641
12	lnc-AL445989.1-1	chr13:64324837-64325213	ENSG00000237378
13	lnc-AL445989.1-20	chr13:64311843-64312482	NONHSAT034172
14	lnc-AL445989.1-2	chr13:64201008-64201079	XLOC_010411
15	lnc-PCDH20-9	chr13:64241815-64241966	XLOC_010643
16	lnc-AL445989.1-2	chr13:64207475-64207529	XLOC_010411
17	lnc-AL445989.1-2	chr13:64208379-64208464	XLOC_010411
18	lnc-PCDH20-9	chr13:64241750-64241972	XLOC_010643
19	lnc-AL445989.1-20	chr13:64311843-64312416	NONHSAT034173
20	lnc-PCDH20-9	chr13:64312042-64312151	XLOC_010643
21	lnc-AL445989.1-2	chr13:64207475-64207529	XLOC_010411
22	lnc-PCDH20-9	chr13:64241814-64241972	XLOC_010643
23	lnc-PCDH20-9	chr13:64291083-64291151	XLOC_010643
24	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034175
25	lnc-PCDH20-9	chr13:64303522-64303642	XLOC_010643
26	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034173
27	lnc-AL445989.1-2	chr13:64209594-64209643	XLOC_010411
28	lnc-PCDH20-9	chr13:64301184-64301215	XLOC_010643
29	lnc-PCDH20-9	chr13:64288485-64288508	XLOC_010643
30	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034174
31	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034173
32	lnc-AL445989.1-20	chr13:64313246-64314376	NONHSAT034175
33	lnc-AL445989.1-20	chr13:64316498-64316945	NONHSAT034176
34	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034174
35	lnc-PCDH20-8	chr13:64196102-64196320	XLOC_010642

No data

Variant related genes	Relation type
LINC00395	TF binding region
ENSG00000226974	TF binding region
ENSG00000237378	TF binding region
OR7E156P	TF binding region
LINC00395	CpG island
ENSG00000226974	CpG island
ENSG00000237378	CpG island
OR7E156P	CpG island
DUSP2	miRNA target sites
DUSP3	miRNA target sites
ZNF71	miRNA target sites
FUNDC2	miRNA target sites
PHTF2	miRNA target sites

Extended variants
information (count: 2616 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2616 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551603065	chr13:64115592-64115593	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs9528660	chr13:64115663-64115664	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530238510	chr13:64115704-64115705	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548247136	chr13:64115750-64115751	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190086136	chr13:64115773-64115774	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114789189	chr13:64115781-64115782	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552055757	chr13:64115844-64115845	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs67873778	chr13:64115866-64115867	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs200594194	chr13:64115871-64115872	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs200952097	chr13:64115872-64115873	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs201790743	chr13:64115889-64115890	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs570459886	chr13:64116049-64116050	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs537740596	chr13:64116116-64116117	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs182105138	chr13:64116159-64116160	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs374849366	chr13:64116172-64116173	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs567943102	chr13:64116259-64116260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377415886	chr13:64116261-64116262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9317348	chr13:64116289-64116290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs553870676	chr13:64116325-64116326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141637523	chr13:64116381-64116382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534345561	chr13:64116387-64116388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559194573	chr13:64116445-64116446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145378100	chr13:64116482-64116483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147660973	chr13:64116499-64116500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141460098	chr13:64116509-64116510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574715966	chr13:64116538-64116539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1352757	chr13:64116574-64116575	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs1352758	chr13:64116670-64116671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs9317349	chr13:64116673-64116674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545639749	chr13:64116680-64116681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564104186	chr13:64116731-64116732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2324326	chr13:64116764-64116765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs10645227	chr13:64116771-64116772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs66988230	chr13:64116772-64116773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397729105	chr13:64116776-64116777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186695431	chr13:64116848-64116849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549772458	chr13:64116853-64116854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189623647	chr13:64116856-64116857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181918568	chr13:64116865-64116866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185328930	chr13:64116887-64116888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77862503	chr13:64116942-64116943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565818074	chr13:64117001-64117002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150366633	chr13:64117019-64117020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559231358	chr13:64117057-64117058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145768939	chr13:64117093-64117094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530907102	chr13:64117104-64117105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189690510	chr13:64117146-64117147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138040873	chr13:64117157-64117158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538554145	chr13:64117190-64117191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149074207	chr13:64117303-64117304	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64114200-64117200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:64115400-64115600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
3	chr13:64115400-64115800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:64115400-64115800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr13:64115400-64115800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:64115400-64115800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr13:64115400-64116000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr13:64115400-64116000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr13:64115400-64116000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
10	chr13:64115400-64116000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr13:64115400-64116200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
12	chr13:64115600-64115800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr13:64115600-64116000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr13:64115600-64116000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:64115800-64116800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr13:64115800-64116800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:64116800-64117600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr13:64116800-64117600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:64117000-64117800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:64117200-64117400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr13:64117600-64122000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:64118800-64119400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr13:64119000-64120200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr13:64119200-64120400	Enhancers	Placenta	Placenta
25	chr13:64119400-64120000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr13:64120000-64120200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr13:64122000-64122400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr13:64130400-64131600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr13:64130600-64131600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr13:64130800-64131200	Enhancers	Placenta	Placenta
31	chr13:64131000-64131400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr13:64131000-64131400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr13:64140000-64140400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr13:64140000-64141600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr13:64140200-64141200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:64140400-64145800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr13:64154200-64154400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:64159600-64160000	Active TSS	Hela-S3	cervix
39	chr13:64159600-64160200	Active TSS	A549	lung
40	chr13:64161200-64161600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr13:64168600-64169000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:64168600-64169000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:64168800-64169800	Enhancers	Fetal Heart	heart
44	chr13:64170000-64170400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr13:64170000-64170600	Enhancers	HMEC	breast
46	chr13:64170200-64170600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr13:64172800-64174000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr13:64173000-64173400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr13:64173000-64173400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr13:64173000-64173600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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