Variant report

Variant	nsv1049
Chromosome Location	chr13:54684354-54728981
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	chr13:54719060-54719258	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr13:54687589-54687822	H1-hESC	embryonic stem cell:	n/a	chr13:54687764-54687776 chr13:54687700-54687711 chr13:54687629-54687646
3	CEBPB	chr13:54725214-54725221	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr13:54728675-54728972	HepG2	liver:	n/a	chr13:54728830-54728841
5	CEBPB	chr13:54687616-54687812	HepG2	liver:	n/a	chr13:54687764-54687776 chr13:54687700-54687711 chr13:54687629-54687646
6	CTCF	chr13:54724500-54724650	HL-60	blood:	n/a	n/a
7	CTCF	chr13:54694433-54694482	GM13977	blood:	n/a	n/a
8	CTCF	chr13:54705388-54705427	Kidney_OC	kidney:	n/a	n/a
9	E2F4	chr13:54687255-54687455	MCF10A-Er-Src	breast:	n/a	n/a
10	FAM48A	chr13:54717297-54717394	GM12878	blood:	n/a	n/a
11	FOS	chr13:54698895-54699177	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr13:54687174-54687374	MCF10A-Er-Src	breast:	n/a	chr13:54687219-54687226 chr13:54687250-54687262 chr13:54687218-54687227 chr13:54687218-54687226 chr13:54687216-54687228
13	FOS	chr13:54687082-54687394	MCF10A-Er-Src	breast:	n/a	chr13:54687219-54687226 chr13:54687250-54687262 chr13:54687218-54687227 chr13:54687218-54687226 chr13:54687216-54687228
14	FOS	chr13:54707452-54707570	MCF10A-Er-Src	breast:	n/a	chr13:54707481-54707490 chr13:54707481-54707489 chr13:54707480-54707489 chr13:54707481-54707488
15	FOS	chr13:54687065-54687407	MCF10A-Er-Src	breast:	n/a	chr13:54687219-54687226 chr13:54687250-54687262 chr13:54687218-54687227 chr13:54687218-54687226 chr13:54687216-54687228
16	FOXA1	chr13:54690679-54690953	T-47D	breast:	n/a	n/a
17	FOXA1	chr13:54690733-54690909	T-47D	breast:	n/a	n/a
18	FOXA1	chr13:54702368-54702516	T-47D	breast:	n/a	chr13:54702435-54702450
19	FOXA2	chr13:54702311-54702666	A549	lung:	n/a	n/a
20	FOXA2	chr13:54702308-54702615	A549	lung:	n/a	n/a
21	GATA2	chr13:54708324-54708628	SH-SY5Y	brain:	n/a	chr13:54708445-54708452 chr13:54708438-54708459 chr13:54708445-54708452 chr13:54708445-54708452 chr13:54708444-54708454 chr13:54708441-54708457
22	GATA3	chr13:54708001-54708383	SH-SY5Y	brain:	n/a	n/a
23	GTF2F1	chr13:54701046-54701049	H1-hESC	embryonic stem cell:	n/a	n/a
24	JUN	chr13:54728790-54728886	HepG2	liver:	n/a	chr13:54728831-54728844
25	JUND	chr13:54707386-54707592	HepG2	liver:	n/a	chr13:54707481-54707490 chr13:54707479-54707490 chr13:54707481-54707489 chr13:54707480-54707489 chr13:54707481-54707488
26	JUND	chr13:54728760-54728942	HepG2	liver:	n/a	n/a
27	JUND	chr13:54698975-54699161	HepG2	liver:	n/a	n/a
28	MAFF	chr13:54710203-54710394	HepG2	liver:	n/a	chr13:54710279-54710297
29	MAFF	chr13:54694725-54694925	HepG2	liver:	n/a	chr13:54694834-54694848 chr13:54694835-54694853
30	MAFK	chr13:54694696-54694959	HepG2	liver:	n/a	chr13:54694834-54694848 chr13:54694833-54694849 chr13:54694836-54694851 chr13:54694831-54694851
31	MAFK	chr13:54685009-54685266	HepG2	liver:	n/a	chr13:54685172-54685186 chr13:54685174-54685185 chr13:54685174-54685185
32	MAFK	chr13:54685047-54685217	HepG2	liver:	n/a	chr13:54685172-54685186 chr13:54685174-54685185 chr13:54685174-54685185
33	MAFK	chr13:54710196-54710416	HepG2	liver:	n/a	chr13:54710282-54710293 chr13:54710281-54710292 chr13:54710281-54710296 chr13:54710281-54710297 chr13:54710280-54710294 chr13:54710281-54710292 chr13:54710282-54710293
34	MAFK	chr13:54710128-54710433	HepG2	liver:	n/a	chr13:54710282-54710293 chr13:54710281-54710292 chr13:54710281-54710296 chr13:54710281-54710297 chr13:54710280-54710294 chr13:54710281-54710292 chr13:54710282-54710293
35	MAFK	chr13:54694741-54694941	HepG2	liver:	n/a	chr13:54694834-54694848 chr13:54694833-54694849 chr13:54694836-54694851 chr13:54694831-54694851
36	MAFK	chr13:54716200-54716231	HepG2	liver:	n/a	n/a
37	MAFK	chr13:54694793-54694856	IMR90	lung:	n/a	chr13:54694834-54694848 chr13:54694833-54694849 chr13:54694836-54694851 chr13:54694831-54694851
38	MAFK	chr13:54724098-54724253	HepG2	liver:	n/a	n/a
39	MAX	chr13:54697829-54697939	NB4	blood:	n/a	n/a
40	MAX	chr13:54711873-54712048	NB4	blood:	n/a	n/a
41	MAX	chr13:54719131-54719455	H1-hESC	embryonic stem cell:	n/a	n/a
42	MYC	chr13:54688452-54688460	NB4	blood:	n/a	n/a
43	NFYB	chr13:54721767-54721958	GM12878	blood:	n/a	n/a
44	POLR2A	chr13:54704931-54705179	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr13:54695474-54695662	GM12878	blood:	n/a	n/a
46	POLR2A	chr13:54687165-54687279	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr13:54704934-54705297	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr13:54697012-54698024	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr13:54704610-54704776	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr13:54721265-54721283	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54708344-54708394	ProgFib	skin:	n/a
2	chr13:54708344-54708394	ProgFib	skin:	n/a
3	chr13:54707971-54708021	GM19239	blood:	n/a
4	chr13:54725166-54725216	PANC-1	pancreas:	n/a
5	chr13:54725166-54725216	GM12891	blood:	n/a
6	chr13:54719190-54719240	NH-A	brain:	n/a
7	chr13:54707971-54708021	NT2-D1	testis:	n/a
8	chr13:54719190-54719240	A549	lung:	n/a
9	chr13:54725166-54725216	BE2_C	brain:	n/a
10	chr13:54719190-54719240	Hepatocyte	liver:	n/a
11	chr13:54725166-54725216	Hela-S3	cervix:	n/a
12	chr13:54707971-54708021	MCF10A-Er-Src	breast:	n/a
13	chr13:54725166-54725216	GM12878	blood:	n/a
14	chr13:54719190-54719240	PrEC	prostate:	n/a
15	chr13:54708344-54708394	LNCaP	prostate:	n/a
16	chr13:54708344-54708394	RPTEC	kidney:	n/a
17	chr13:54707971-54708021	GM12892	blood:	n/a
18	chr13:54708344-54708394	PANC-1	pancreas:	n/a
19	chr13:54708344-54708394	HCPEpiC	choroid plexus:	n/a
20	chr13:54707971-54708021	MCF-7	breast:	n/a
21	chr13:54725166-54725216	HL-60	blood:	n/a
22	chr13:54725166-54725216	HUVEC	blood vessel:	n/a
23	chr13:54708344-54708394	AG09309	skin:	n/a
24	chr13:54725166-54725216	MCF10A-Er-Src	breast:	n/a
25	chr13:54707971-54708021	GM06990	blood:	n/a
26	chr13:54719190-54719240	SK-N-SH_RA	brain:	n/a
27	chr13:54719190-54719240	AG04450	lung:	fetal
28	chr13:54725166-54725216	GM19239	blood:	n/a
29	chr13:54725166-54725216	SK-N-SH	brain:	n/a
30	chr13:54719190-54719240	K562	blood:	n/a
31	chr13:54708344-54708394	HCM	heart:	n/a
32	chr13:54719190-54719240	SAEC	small airway:	n/a
33	chr13:54707971-54708021	ECC-1	luminal epithelium:	n/a
34	chr13:54707971-54708021	NHDF-neo	bronchial:	n/a
35	chr13:54719190-54719240	ovcar-3	ovarian:	n/a
36	chr13:54725166-54725216	NT2-D1	testis:	n/a
37	chr13:54719190-54719240	Hela-S3	cervix:	n/a
38	chr13:54719190-54719240	SK-N-MC	brain:	n/a
39	chr13:54708344-54708394	Jurkat	blood:	n/a
40	chr13:54719190-54719240	HIPEpiC	eye:	n/a
41	chr13:54707971-54708021	SK-N-SH_RA	brain:	n/a
42	chr13:54708344-54708394	Hela-S3	cervix:	n/a
43	chr13:54708344-54708394	MCF10A-Er-Src	breast:	n/a
44	chr13:54708344-54708394	GM19239	blood:	n/a
45	chr13:54719190-54719240	HEEpiC	esophagus:	n/a
46	chr13:54708344-54708394	HCF	heart:	n/a
47	chr13:54725166-54725216	HPAEpiC	pulmonary alveolar:	n/a
48	chr13:54708344-54708394	T-47D	breast:	n/a
49	chr13:54707971-54708021	HCM	heart:	n/a
50	chr13:54719190-54719240	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:54688466..54689986-chr6:86385107..86388002,2	K562	blood:
2	chr13:54693602..54695448-chr13:54696284..54698888,2	MCF-7	breast:
3	chr13:54693602..54695448-chr13:54696284..54698888,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH8-5	chr13:54706748-54707006	NR_108063
2	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787
3	lnc-PCDH8-5	chr13:54698459-54698890	ENSG00000234787.3
4	lnc-PCDH8-5	chr13:54706748-54707001	ENSG00000234787
5	lnc-PCDH8-5	chr13:54695075-54695179	ENSG00000234787.3
6	lnc-PCDH8-5	chr13:54695071-54695179	ENSG00000234787
7	lnc-PCDH8-5	chr13:54689984-54690344	ENSG00000234787.3
8	lnc-PCDH8-5	chr13:54705009-54705206	NONHSAT034028
9	lnc-PCDH8-5	chr13:54705009-54705206	NR_108063
10	lnc-PCDH8-5	chr13:54706748-54707001	ENSG00000234787
11	lnc-PCDH8-5	chr13:54699284-54699407	ENSG00000234787
12	lnc-PCDH8-5	chr13:54699130-54699407	ENSG00000234787.3
13	lnc-PCDH8-5	chr13:54701415-54701564	NR_108062
14	lnc-PCDH8-5	chr13:54700998-54701564	NR_108063
15	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787
16	lnc-PCDH8-5	chr13:54698459-54698890	ENSG00000234787
17	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787
18	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
19	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
20	lnc-PCDH8-5	chr13:54699284-54699407	ENSG00000234787.3
21	lnc-PCDH8-5	chr13:54698462-54698890	NONHSAT034028
22	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787
23	lnc-PCDH8-5	chr13:54701415-54701564	NONHSAT034028
24	lnc-PCDH8-5	chr13:54706748-54706997	ENSG00000234787.3
25	lnc-PCDH8-5	chr13:54706748-54707001	NONHSAT034028
26	lnc-PCDH8-5	chr13:54698948-54699407	ENSG00000234787.3
27	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787.3
28	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
29	lnc-PCDH8-5	chr13:54706748-54706954	ENSG00000234787.3
30	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
31	lnc-PCDH8-5	chr13:54706748-54707001	ENSG00000234787.3
32	lnc-OLFM4-11	chr13:54690611-54690986	NONHSAT034026
33	lnc-PCDH8-5	chr13:54700997-54701564	ENSG00000234787
34	lnc-PCDH8-5	chr13:54706497-54706748	ENSG00000234787
35	lnc-PCDH8-5	chr13:54698459-54698890	NR_108062
36	lnc-PCDH8-5	chr13:54706748-54706986	ENSG00000234787.3
37	lnc-PCDH8-5	chr13:54706748-54707006	NR_108062
38	lnc-PCDH8-5	chr13:54689924-54690344	ENSG00000234787
39	lnc-PCDH8-5	chr13:54701415-54701478	ENSG00000234787.3
40	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787.3
41	lnc-PCDH8-5	chr13:54705009-54705206	NR_108062
42	lnc-PCDH8-5	chr13:54689924-54690344	ENSG00000234787.3

Variant related genes	Relation type
ENSG00000271652	TF binding region
LINC00458	TF binding region
ENSG00000271652	CpG island
LINC00458	CpG island
ENSG00000203875	chromatin interactions
POU5F1	lncRNA

Extended variants
information (count: 1743 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1743 , 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	rs188130509	chr13:54684375-54684376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529871294	chr13:54684450-54684451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181282808	chr13:54684483-54684484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563083406	chr13:54684499-54684500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532074890	chr13:54684551-54684552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551782490	chr13:54684662-54684663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558907684	chr13:54684743-54684744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2261534	chr13:54684833-54684834	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183920399	chr13:54684878-54684879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2784547	chr13:54684881-54684882	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs370585243	chr13:54684906-54684907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537610086	chr13:54684950-54684951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551187766	chr13:54684983-54684984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189703349	chr13:54685011-54685012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539921071	chr13:54685096-54685097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76025289	chr13:54685120-54685121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142191390	chr13:54685131-54685132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534634674	chr13:54685144-54685145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554803688	chr13:54685158-54685159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7320108	chr13:54685168-54685169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs9568985	chr13:54685170-54685171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2261530	chr13:54685215-54685216	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs576563484	chr13:54685219-54685220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545454843	chr13:54685339-54685340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558942643	chr13:54685342-54685343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528039725	chr13:54685351-54685352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146356832	chr13:54685378-54685379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562446596	chr13:54685414-54685415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1414543	chr13:54685540-54685541	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7338435	chr13:54685622-54685623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60846729	chr13:54685712-54685713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369102308	chr13:54685730-54685731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373322209	chr13:54685746-54685747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571044885	chr13:54685768-54685769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375943763	chr13:54685820-54685821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568428221	chr13:54685864-54685865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547087491	chr13:54685892-54685893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368936487	chr13:54685903-54685904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577941981	chr13:54685930-54685931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58455205	chr13:54685931-54685932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs397969405	chr13:54685940-54685941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535802441	chr13:54685954-54685955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555472345	chr13:54685968-54685969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574702905	chr13:54686021-54686022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9591566	chr13:54686121-54686122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536930995	chr13:54686142-54686143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556753747	chr13:54686143-54686144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576598333	chr13:54686163-54686164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545494515	chr13:54686177-54686178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11298768	chr13:54686209-54686210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54678000-54692000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr13:54678800-54687600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:54679800-54687600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:54683200-54698800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr13:54684000-54685200	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:54685200-54689400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr13:54687600-54688600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:54687600-54688600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:54688600-54690000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr13:54688600-54692200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr13:54688600-54699000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:54689000-54706000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:54689400-54700000	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr13:54690000-54690400	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr13:54690400-54691000	Genic enhancers	H9 Cell Line	embryonic stem cell
16	chr13:54691000-54692000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr13:54691800-54706000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr13:54692000-54692200	Genic enhancers	H9 Cell Line	embryonic stem cell
19	chr13:54692000-54695400	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr13:54692200-54693800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
21	chr13:54692200-54695800	Strong transcription	H9 Cell Line	embryonic stem cell
22	chr13:54692600-54705000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr13:54693800-54700000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr13:54695400-54697200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr13:54695800-54697600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr13:54696200-54700400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:54696400-54699200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr13:54697200-54700600	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr13:54697600-54702600	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr13:54698800-54700800	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr13:54698800-54701000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr13:54699000-54701600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:54699200-54701400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr13:54700000-54700200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr13:54700000-54702800	Genic enhancers	HUES6 Cell Line	embryonic stem cell
36	chr13:54700200-54701200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
37	chr13:54700400-54700800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr13:54700600-54701000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:54700600-54701200	Genic enhancers	HUES64 Cell Line	embryonic stem cell
40	chr13:54700800-54701000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr13:54700800-54701200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr13:54700800-54701400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
43	chr13:54701000-54701600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr13:54701000-54704400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr13:54701000-54705200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr13:54701200-54701600	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr13:54701200-54703400	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr13:54701200-54704400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr13:54701400-54704200	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr13:54701400-54704600	Weak transcription	H1 Cell Line	embryonic stem cell

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