Variant report

Variant	nsv900407
Chromosome Location	chr13:67434161-67603745
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	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
2	ARID3A	chr13:67508076-67508417	K562	blood:	n/a	n/a
3	ATF1	chr13:67512216-67512440	K562	blood:	n/a	n/a
4	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr13:67508091-67508467	A549	lung:	n/a	n/a
6	ATF3	chr13:67508059-67508348	K562	blood:	n/a	n/a
7	ATF3	chr13:67514291-67514517	K562	blood:	n/a	n/a
8	ATF3	chr13:67513673-67513979	K562	blood:	n/a	n/a
9	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
10	BACH1	chr13:67582435-67582446	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr13:67508106-67508447	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr13:67508060-67508511	K562	blood:	n/a	n/a
13	BCL3	chr13:67507974-67508573	A549	lung:	n/a	chr13:67508041-67508050
14	BCL3	chr13:67568092-67568724	A549	lung:	n/a	chr13:67568680-67568687
15	BCL3	chr13:67508048-67508565	A549	lung:	n/a	n/a
16	BHLHE40	chr13:67569138-67569828	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:67568386-67568547	K562	blood:	n/a	n/a
18	CBX3	chr13:67508097-67508421	K562	blood:	n/a	n/a
19	CCNT2	chr13:67480244-67480442	K562	blood:	n/a	n/a
20	CCNT2	chr13:67474239-67474501	K562	blood:	n/a	n/a
21	CEBPB	chr13:67484755-67485097	IMR90	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
22	CEBPB	chr13:67525177-67525315	H1-hESC	embryonic stem cell:	n/a	chr13:67525201-67525214
23	CEBPB	chr13:67568038-67568652	A549	lung:	n/a	n/a
24	CEBPB	chr13:67516745-67517360	Hela-S3	cervix:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
25	CEBPB	chr13:67516734-67517339	IMR90	lung:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
26	CEBPB	chr13:67566342-67567192	IMR90	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
27	CEBPB	chr13:67508022-67508590	A549	lung:	n/a	n/a
28	CEBPB	chr13:67484766-67485107	ECC-1	luminal epithelium:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
29	CEBPB	chr13:67484754-67485342	A549	lung:	n/a	chr13:67485279-67485292 chr13:67485279-67485290 chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
30	CEBPB	chr13:67476147-67476615	H1-hESC	embryonic stem cell:	n/a	chr13:67476452-67476463 chr13:67476452-67476465 chr13:67476454-67476465 chr13:67476452-67476465
31	CEBPB	chr13:67566898-67567137	A549	lung:	n/a	n/a
32	CEBPB	chr13:67511781-67512110	IMR90	lung:	n/a	chr13:67512052-67512063 chr13:67512029-67512040
33	CEBPB	chr13:67536801-67536984	HepG2	liver:	n/a	n/a
34	CEBPB	chr13:67516781-67517023	K562	blood:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
35	CEBPB	chr13:67484807-67485063	A549	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
36	CEBPB	chr13:67484840-67485040	Hela-S3	cervix:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
37	CEBPB	chr13:67596835-67597031	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr13:67568217-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr13:67568171-67568602	A549	lung:	n/a	n/a
40	CEBPB	chr13:67566763-67567107	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr13:67566342-67566648	A549	lung:	n/a	n/a
42	CEBPB	chr13:67590501-67590687	K562	blood:	n/a	n/a
43	CEBPB	chr13:67511884-67512206	A549	lung:	n/a	chr13:67512052-67512063 chr13:67512029-67512040
44	CEBPB	chr13:67484786-67485088	K562	blood:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
45	CEBPB	chr13:67484837-67485058	H1-hESC	embryonic stem cell:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
46	CEBPB	chr13:67484778-67485211	A549	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
47	CEBPB	chr13:67501468-67501696	A549	lung:	n/a	n/a
48	CEBPB	chr13:67566236-67566719	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
49	CEBPB	chr13:67515155-67515402	K562	blood:	n/a	chr13:67515279-67515290
50	CEBPB	chr13:67476352-67476564	K562	blood:	n/a	chr13:67476452-67476463 chr13:67476452-67476465 chr13:67476454-67476465 chr13:67476452-67476465

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67434423-67434473	PANC-1	pancreas:	n/a
2	chr13:67570127-67570177	HCT-116	colon:	n/a
3	chr13:67434423-67434473	HRCEpiC	kidney:	n/a
4	chr13:67479146-67479196	AG09309	skin:	n/a
5	chr13:67568518-67568568	HUVEC	blood vessel:	n/a
6	chr13:67570127-67570177	SAEC	small airway:	n/a
7	chr13:67548536-67548586	HRE	kidney:	n/a
8	chr13:67568518-67568568	NB4	blood:	n/a
9	chr13:67548536-67548586	SAEC	small airway:	n/a
10	chr13:67479146-67479196	H1-hESC	embryonic stem cell:	embryo
11	chr13:67434423-67434473	HL-60	blood:	n/a
12	chr13:67479146-67479196	U87	brain:	n/a
13	chr13:67568473-67568523	Hela-S3	cervix:	n/a
14	chr13:67568473-67568523	ProgFib	skin:	n/a
15	chr13:67478043-67478093	SK-N-SH	brain:	n/a
16	chr13:67568473-67568523	NHBE	bronchial:	n/a
17	chr13:67568518-67568568	HRPEpiC	eye:	n/a
18	chr13:67568518-67568568	SAEC	small airway:	n/a
19	chr13:67479146-67479196	HRPEpiC	eye:	n/a
20	chr13:67548536-67548586	PFSK-1	brain:	n/a
21	chr13:67568473-67568523	NT2-D1	testis:	n/a
22	chr13:67568518-67568568	AG04450	lung:	fetal
23	chr13:67434423-67434473	MCF10A-Er-Src	breast:	n/a
24	chr13:67479146-67479196	T-47D	breast:	n/a
25	chr13:67570127-67570177	AG04450	lung:	fetal
26	chr13:67548536-67548586	CMK	blood:	n/a
27	chr13:67548536-67548586	NH-A	brain:	n/a
28	chr13:67479146-67479196	HIPEpiC	eye:	n/a
29	chr13:67479146-67479196	IMR90	lung:	fetal
30	chr13:67568518-67568568	CMK	blood:	n/a
31	chr13:67568518-67568568	HNPCEpiC	eye:	n/a
32	chr13:67570127-67570177	NHDF-neo	bronchial:	n/a
33	chr13:67478043-67478093	BE2_C	brain:	n/a
34	chr13:67568473-67568523	HL-60	blood:	n/a
35	chr13:67568473-67568523	MCF-7	breast:	n/a
36	chr13:67568518-67568568	GM12891	blood:	n/a
37	chr13:67568518-67568568	PANC-1	pancreas:	n/a
38	chr13:67434423-67434473	HAEpiC	amniotic membrane:	n/a
39	chr13:67570127-67570177	HRE	kidney:	n/a
40	chr13:67570127-67570177	SK-N-SH_RA	brain:	n/a
41	chr13:67548536-67548586	HRPEpiC	eye:	n/a
42	chr13:67568518-67568568	IMR90	lung:	fetal
43	chr13:67570127-67570177	T-47D	breast:	n/a
44	chr13:67568518-67568568	GM12892	blood:	n/a
45	chr13:67570127-67570177	NB4	blood:	n/a
46	chr13:67478043-67478093	K562	blood:	n/a
47	chr13:67568518-67568568	Jurkat	blood:	n/a
48	chr13:67568518-67568568	HepG2	liver:	n/a
49	chr13:67479146-67479196	HNPCEpiC	eye:	n/a
50	chr13:67434423-67434473	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
2	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
3	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:
4	chr13:67437418..67439470-chr13:67442003..67443610,2	MCF-7	breast:
5	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
6	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
7	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
8	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:
9	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
10	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
11	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
12	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:
13	chr13:67503858..67504708-chr5:34924011..34924781,2	Hela-S3	cervix:
14	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
15	chr13:67562882..67565273-chr13:67566706..67568513,2	K562	blood:
16	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
17	chr13:67437418..67439470-chr13:67442003..67443610,2	MCF-7	breast:
18	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
19	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
20	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
21	chr13:67397391..67400012-chr13:67432704..67434627,2	K562	blood:
22	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
23	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-16	chr13:67575978-67576139	ENSG00000233840.1
2	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
3	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.2
4	lnc-AL445989.1-14	chr13:67460132-67460208	ENSG00000228842.2
5	lnc-AL445989.1-16	chr13:67575978-67576132	NR_046637
6	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1
7	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
8	lnc-AL445989.1-14	chr13:67488530-67488618	NONHSAT034214
9	lnc-AL445989.1-14	chr13:67460132-67460209	ENSG00000228842.1
10	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.1
11	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
12	lnc-AL445989.1-14	chr13:67450976-67451051	ENSG00000228842.1
13	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.2
14	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
15	lnc-AL445989.1-14	chr13:67517880-67518119	NONHSAT034214
16	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
17	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
18	lnc-AL445989.1-14	chr13:67484006-67484154	NONHSAT034214
19	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.1
20	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
21	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215
22	lnc-AL445989.1-14	chr13:67450976-67451051	ENSG00000228842.2
23	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637

Variant related genes	Relation type
PCDH9-AS4	TF binding region
PCDH9-AS3	TF binding region
PCDH9-AS4	CpG island
PCDH9-AS3	CpG island
ENSG00000233840	chromatin interactions
ENSG00000228842	chromatin interactions

Extended variants
information (count: 5407 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5407 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9564355	chr13:67434161-67434162	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567851878	chr13:67434165-67434166	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147554525	chr13:67434222-67434223	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567974538	chr13:67434240-67434241	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs180888902	chr13:67434254-67434255	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546957408	chr13:67434303-67434304	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566892715	chr13:67434311-67434312	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185398862	chr13:67434378-67434379	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558628854	chr13:67434423-67434424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568969663	chr13:67434424-67434425	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536323545	chr13:67434443-67434444	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141977929	chr13:67434512-67434513	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535273449	chr13:67434539-67434540	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556782591	chr13:67434635-67434636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573730441	chr13:67434730-67434731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145806352	chr13:67434763-67434764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552955932	chr13:67434808-67434809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572814730	chr13:67434835-67434836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544976542	chr13:67434841-67434842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564984165	chr13:67434859-67434860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190802774	chr13:67434896-67434897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112249617	chr13:67434898-67434899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554839696	chr13:67434904-67434905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544323259	chr13:67434909-67434910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61448207	chr13:67434970-67434971	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs114789904	chr13:67435029-67435030	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547288203	chr13:67435037-67435038	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567025178	chr13:67435049-67435050	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532546518	chr13:67435074-67435075	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552193974	chr13:67435090-67435091	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554577827	chr13:67435096-67435097	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568907075	chr13:67435130-67435131	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113115397	chr13:67435174-67435175	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537975732	chr13:67435198-67435199	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554625774	chr13:67435240-67435241	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567466693	chr13:67435278-67435279	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs536030113	chr13:67435314-67435315	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs376314122	chr13:67435331-67435332	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs149284514	chr13:67435351-67435352	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs181717501	chr13:67435355-67435356	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs572931954	chr13:67435358-67435359	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377393192	chr13:67435383-67435384	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs187088289	chr13:67435390-67435391	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs574717271	chr13:67435404-67435405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540567510	chr13:67435409-67435410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575291443	chr13:67435423-67435424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9529149	chr13:67435462-67435463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544359331	chr13:67435466-67435467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565023613	chr13:67435490-67435491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560788163	chr13:67435550-67435551	Enhancers 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
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
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
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67429600-67434800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:67430000-67434800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:67430200-67434200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:67431800-67436000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr13:67432600-67434200	Weak transcription	A549	lung
6	chr13:67432600-67435400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr13:67433200-67435200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:67433200-67435200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr13:67433200-67435200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr13:67433200-67435400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr13:67433200-67435400	Enhancers	Brain Substantia Nigra	brain
12	chr13:67433400-67434200	Enhancers	HUVEC	blood vessel
13	chr13:67433400-67435400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:67433400-67435400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:67433400-67435400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:67433400-67435400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr13:67433400-67436600	Enhancers	Brain Hippocampus Middle	brain
18	chr13:67433600-67434800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr13:67433800-67435600	Enhancers	Brain Angular Gyrus	brain
20	chr13:67433800-67435600	Enhancers	Brain Cingulate Gyrus	brain
21	chr13:67433800-67435800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr13:67433800-67438600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr13:67434000-67434600	Enhancers	Brain Germinal Matrix	brain
24	chr13:67434000-67435000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr13:67434000-67435200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr13:67434000-67435400	Enhancers	Brain Anterior Caudate	brain
27	chr13:67434200-67434600	Weak transcription	HUVEC	blood vessel
28	chr13:67434200-67435000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr13:67434200-67435000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr13:67434200-67435000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:67434200-67435200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr13:67434200-67435200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr13:67434200-67435200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr13:67434200-67435400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:67434200-67435400	Enhancers	A549	lung
36	chr13:67434400-67434800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr13:67434400-67435000	Enhancers	Adipose Nuclei	Adipose
38	chr13:67434400-67435200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr13:67434400-67435200	Enhancers	Fetal Stomach	stomach
40	chr13:67434400-67435200	Enhancers	Psoas Muscle	Psoas
41	chr13:67434400-67435400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr13:67434400-67435400	Enhancers	Fetal Heart	heart
43	chr13:67434400-67435400	Enhancers	Fetal Muscle Leg	muscle
44	chr13:67434400-67435600	Enhancers	Right Atrium	heart
45	chr13:67434600-67435000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr13:67434600-67435000	Enhancers	Fetal Kidney	kidney
47	chr13:67434600-67435000	Enhancers	Left Ventricle	heart
48	chr13:67434600-67435000	Enhancers	HUVEC	blood vessel
49	chr13:67434600-67435400	Enhancers	Colon Smooth Muscle	Colon
50	chr13:67434600-67438400	Weak transcription	Brain Germinal Matrix	brain

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