Variant report

Variant	nsv1034
Chromosome Location	chr13:49526761-49572727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1275)
CpG islands
(count:795)
Chromatin interactive
region (count:37)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:49552646-49553659	K562	blood:	n/a	n/a
2	ARID3A	chr13:49550818-49551429	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:49552212-49552402	K562	blood:	n/a	n/a
4	ARID3A	chr13:49551272-49551774	K562	blood:	n/a	n/a
5	ATF2	chr13:49550773-49551248	GM12878	blood:	n/a	n/a
6	ATF2	chr13:49551967-49552495	GM12878	blood:	n/a	chr13:49552240-49552251
7	ATF2	chr13:49550339-49551761	GM12878	blood:	n/a	chr13:49551248-49551255
8	ATF2	chr13:49551998-49552499	GM12878	blood:	n/a	chr13:49552240-49552251
9	ATF2	chr13:49550746-49551222	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr13:49568762-49569375	GM12878	blood:	n/a	n/a
11	ATF2	chr13:49553842-49554652	GM12878	blood:	n/a	n/a
12	ATF2	chr13:49549762-49550309	GM12878	blood:	n/a	n/a
13	ATF2	chr13:49554038-49554582	GM12878	blood:	n/a	n/a
14	ATF2	chr13:49568825-49569317	GM12878	blood:	n/a	n/a
15	ATF3	chr13:49553188-49553535	K562	blood:	n/a	n/a
16	BACH1	chr13:49549313-49551066	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr13:49554179-49554458	GM12878	blood:	n/a	n/a
18	BATF	chr13:49568840-49569106	GM12878	blood:	n/a	n/a
19	BCL11A	chr13:49554223-49554411	GM12878	blood:	n/a	chr13:49554294-49554303
20	BCL11A	chr13:49568852-49569204	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:49554066-49554513	GM12878	blood:	n/a	chr13:49554294-49554303
22	BCL11A	chr13:49568840-49569085	GM12878	blood:	n/a	n/a
23	BCL3	chr13:49552145-49552489	GM12878	blood:	n/a	n/a
24	BCL3	chr13:49568836-49569155	GM12878	blood:	n/a	n/a
25	BCL3	chr13:49549816-49550697	GM12878	blood:	n/a	chr13:49549885-49549898 chr13:49550071-49550080 chr13:49550066-49550079
26	BCL3	chr13:49553886-49554535	GM12878	blood:	n/a	chr13:49554294-49554303
27	BCLAF1	chr13:49549214-49551803	GM12878	blood:	n/a	chr13:49549885-49549898 chr13:49550071-49550080 chr13:49550687-49550700 chr13:49550066-49550079 chr13:49550773-49550786 chr13:49550802-49550815
28	BCLAF1	chr13:49549364-49551057	GM12878	blood:	n/a	chr13:49549885-49549898 chr13:49550071-49550080 chr13:49550687-49550700 chr13:49550066-49550079 chr13:49550773-49550786 chr13:49550802-49550815
29	BCLAF1	chr13:49553980-49554627	GM12878	blood:	n/a	chr13:49554294-49554303
30	BCLAF1	chr13:49554064-49554471	GM12878	blood:	n/a	chr13:49554294-49554303
31	BHLHE40	chr13:49549404-49551675	GM12878	blood:	n/a	chr13:49550800-49550816 chr13:49550542-49550558
32	BHLHE40	chr13:49554091-49554599	GM12878	blood:	n/a	n/a
33	BHLHE40	chr13:49550450-49551030	HepG2	liver:	n/a	chr13:49550800-49550816 chr13:49550542-49550558
34	BHLHE40	chr13:49568962-49569107	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:49549612-49551068	K562	blood:	n/a	chr13:49550800-49550816 chr13:49550542-49550558
36	BHLHE40	chr13:49536408-49536811	K562	blood:	n/a	n/a
37	BRCA1	chr13:49550817-49551415	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr13:49550266-49550335	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr13:49552074-49552354	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr13:49550904-49551097	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr13:49550486-49550859	GM12878	blood:	n/a	n/a
42	BRCA1	chr13:49550163-49550366	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr13:49551433-49551626	GM12878	blood:	n/a	n/a
44	CBX3	chr13:49549179-49549629	K562	blood:	n/a	n/a
45	CBX3	chr13:49550172-49550696	K562	blood:	n/a	n/a
46	CCNT2	chr13:49549695-49551070	K562	blood:	n/a	chr13:49550512-49550521
47	CEBPB	chr13:49553160-49553518	H1-hESC	embryonic stem cell:	n/a	chr13:49553326-49553339 chr13:49553327-49553338
48	CEBPB	chr13:49568842-49569162	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:49553164-49553500	A549	lung:	n/a	chr13:49553326-49553339 chr13:49553327-49553338
50	CEBPB	chr13:49553978-49554309	IMR90	lung:	n/a	chr13:49554128-49554139

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49549489-49549539	SK-N-SH	brain:	n/a
2	chr13:49549489-49549539	NT2-D1	testis:	n/a
3	chr13:49549489-49549539	SK-N-SH	brain:	n/a
4	chr13:49549489-49549539	NT2-D1	testis:	n/a
5	chr13:49549887-49549937	Hela-S3	cervix:	n/a
6	chr13:49550206-49550256	NHBE	bronchial:	n/a
7	chr13:49550815-49550865	SAEC	small airway:	n/a
8	chr13:49550558-49550608	T-47D	breast:	n/a
9	chr13:49549885-49549935	Hela-S3	cervix:	n/a
10	chr13:49549887-49549937	H1-hESC	embryonic stem cell:	embryo
11	chr13:49550448-49550498	SKMC	muscle:	n/a
12	chr13:49550448-49550498	BJ	skin:	n/a
13	chr13:49549887-49549937	Jurkat	blood:	n/a
14	chr13:49549489-49549539	GM12892	blood:	n/a
15	chr13:49550448-49550498	HepG2	liver:	n/a
16	chr13:49550448-49550498	LNCaP	prostate:	n/a
17	chr13:49550206-49550256	AG04450	lung:	fetal
18	chr13:49550299-49550349	NB4	blood:	n/a
19	chr13:49549887-49549937	HNPCEpiC	eye:	n/a
20	chr13:49549463-49549513	AG04449	skin:	fetal
21	chr13:49549489-49549539	AG09319	gingival:	n/a
22	chr13:49549887-49549937	HL-60	blood:	n/a
23	chr13:49550558-49550608	GM12891	blood:	n/a
24	chr13:49549463-49549513	HEK293	kidney:	embryo
25	chr13:49550815-49550865	K562	blood:	n/a
26	chr13:49550558-49550608	Hepatocyte	liver:	n/a
27	chr13:49549489-49549539	HCF	heart:	n/a
28	chr13:49549665-49549715	PANC-1	pancreas:	n/a
29	chr13:49549489-49549539	A549	lung:	n/a
30	chr13:49550299-49550349	HIPEpiC	eye:	n/a
31	chr13:49550299-49550349	CMK	blood:	n/a
32	chr13:49550299-49550349	Hela-S3	cervix:	n/a
33	chr13:49550299-49550349	BE2_C	brain:	n/a
34	chr13:49549440-49549490	NHBE	bronchial:	n/a
35	chr13:49550206-49550256	GM12892	blood:	n/a
36	chr13:49546137-49546187	U87	brain:	n/a
37	chr13:49550321-49550371	Caco-2	colon:	n/a
38	chr13:49550558-49550608	GM12878	blood:	n/a
39	chr13:49550299-49550349	SK-N-MC	brain:	n/a
40	chr13:49549887-49549937	NHDF-neo	bronchial:	n/a
41	chr13:49550448-49550498	HCPEpiC	choroid plexus:	n/a
42	chr13:49549887-49549937	HepG2	liver:	n/a
43	chr13:49546137-49546187	HCM	heart:	n/a
44	chr13:49550815-49550865	BE2_C	brain:	n/a
45	chr13:49549463-49549513	K562	blood:	n/a
46	chr13:49550206-49550256	SAEC	small airway:	n/a
47	chr13:49550448-49550498	Hela-S3	cervix:	n/a
48	chr13:49549665-49549715	GM12878	blood:	n/a
49	chr13:49550815-49550865	BJ	skin:	n/a
50	chr13:49546137-49546187	PFSK-1	brain:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:49344498..49346343-chr13:49548446..49550486,2	MCF-7	breast:
2	chr13:49511991..49514025-chr13:49547058..49549833,2	K562	blood:
3	chr13:49568955..49571028-chr13:49572670..49574624,2	K562	blood:
4	chr13:49535111..49537978-chr13:49544443..49546396,2	K562	blood:
5	chr13:49535149..49536967-chr13:49548289..49550226,2	K562	blood:
6	chr13:49549672..49551500-chr16:31190171..31192875,2	MCF-7	breast:
7	chr13:49538660..49540724-chr13:49542814..49545257,2	MCF-7	breast:
8	chr13:49550410..49551116-chr15:67357771..67358457,2	Hela-S3	cervix:
9	chr13:49561168..49563389-chr13:49566205..49568551,2	K562	blood:
10	chr13:49548036..49549716-chr13:49570249..49572622,2	K562	blood:
11	chr13:49554312..49556317-chr13:49562334..49565268,2	MCF-7	breast:
12	chr13:49570124..49572139-chr13:49576079..49578417,2	K562	blood:
13	chr13:49546080..49548216-chr13:49556766..49558384,2	MCF-7	breast:
14	chr13:49549584..49550165-chr9:17134587..17135235,2	NB4	blood:
15	chr13:49563178..49565199-chr13:49566852..49568731,2	K562	blood:
16	chr11:62495942..62496458-chr13:49549950..49550699,2	NB4	blood:
17	chr13:49554312..49556317-chr13:49562334..49565268,2	MCF-7	breast:
18	chr13:49548036..49549716-chr13:49570249..49572622,2	K562	blood:
19	chr13:49547950..49551813-chr13:49821954..49825536,3	K562	blood:
20	chr13:49549495..49551590-chr13:49668953..49673259,5	MCF-7	breast:
21	chr13:49546080..49548216-chr13:49556766..49558384,2	MCF-7	breast:
22	chr13:49526889..49528415-chr13:49548994..49550645,2	MCF-7	breast:
23	chr13:49549219..49550138-chr16:75669158..75670004,2	NB4	blood:
24	chr13:49552747..49554579-chr13:49576987..49579021,2	K562	blood:
25	chr10:81106936..81108869-chr13:49549506..49551759,2	MCF-7	breast:
26	chr13:49554450..49556211-chr13:49593897..49596163,2	MCF-7	breast:
27	chr13:49551617..49554201-chr13:49560922..49563747,2	MCF-7	breast:
28	chr13:49568955..49571028-chr13:49572670..49574624,2	K562	blood:
29	chr13:49518698..49520988-chr13:49531338..49533079,2	K562	blood:
30	chr1:154934055..154934689-chr13:49549950..49550626,2	NB4	blood:
31	chr13:49549492..49550320-chr15:73075454..73076164,2	NB4	blood:
32	chr13:49535111..49537978-chr13:49544443..49546396,2	K562	blood:
33	chr13:49510679..49513624-chr13:49558330..49560973,2	K562	blood:
34	chr13:49557531..49560266-chr13:49567032..49569097,2	K562	blood:
35	chr13:49563178..49565199-chr13:49566852..49568731,2	K562	blood:
36	chr13:49557531..49560266-chr13:49567032..49569097,2	K562	blood:
37	chr13:49538660..49540724-chr13:49542814..49545257,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FNDC3A-2	chr13:49538238-49538736	NONHSAT033726
2	lnc-CAB39L-4	chr13:49540234-49540300	ucscGeneNc_uc001vdx_2
3	lnc-CAB39L-4	chr13:49546319-49550047	NONHSAT033727
4	lnc-CAB39L-4	chr13:49547696-49547790	ucscGeneNc_uc001vdx_2
5	lnc-CAB39L-4	chr13:49553960-49554130	ucscGeneNc_uc001vdx_2
6	lnc-FNDC3A-2	chr13:49536817-49537104	NONHSAT033726

No data

Variant related genes	Relation type
FNDC3A	TF binding region
RNU6-60P	TF binding region
FNDC3A	CpG island
RNU6-60P	CpG island
ENSG00000102531	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000166949	chromatin interactions
ENSG00000201662	chromatin interactions
ENSG00000162222	chromatin interactions
ENSG00000108179	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000163348	chromatin interactions
ENSG00000225131	chromatin interactions
ENSG00000271380	chromatin interactions
ENSG00000199788	chromatin interactions
ENSG00000159322	chromatin interactions
ENSG00000044459	chromatin interactions

Extended variants
information (count: 1236 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530507281	chr13:49526794-49526795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551796595	chr13:49526845-49526846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs199988771	chr13:49526868-49526869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562978864	chr13:49526871-49526872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570351498	chr13:49526886-49526887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531826468	chr13:49527001-49527002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551461118	chr13:49527038-49527039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528042059	chr13:49527055-49527056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559531983	chr13:49527068-49527069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546585716	chr13:49527069-49527070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568309136	chr13:49527100-49527101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535668168	chr13:49527126-49527127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557171221	chr13:49527131-49527132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs4941632	chr13:49527135-49527136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548567800	chr13:49527144-49527145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190235874	chr13:49527178-49527179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527693488	chr13:49527201-49527202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149652467	chr13:49527212-49527213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144384552	chr13:49527236-49527237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1034067	chr13:49527291-49527292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs576902077	chr13:49527316-49527317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148785048	chr13:49527324-49527325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574772853	chr13:49527336-49527337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs542053432	chr13:49527372-49527373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563531636	chr13:49527376-49527377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142522671	chr13:49527413-49527414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545498426	chr13:49527414-49527415	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs1964160	chr13:49527438-49527439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs528089288	chr13:49527460-49527461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182490675	chr13:49527466-49527467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2026027	chr13:49527467-49527468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529184347	chr13:49527473-49527474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12100367	chr13:49527504-49527505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535417923	chr13:49527507-49527508	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550831522	chr13:49527514-49527515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370072128	chr13:49527524-49527525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569068001	chr13:49527527-49527528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143250094	chr13:49527643-49527644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558801556	chr13:49527798-49527799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569005495	chr13:49527867-49527868	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146740966	chr13:49527885-49527886	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534739908	chr13:49527915-49527916	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186841795	chr13:49527964-49527965	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191322501	chr13:49527988-49527989	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535744382	chr13:49528009-49528010	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557187162	chr13:49528026-49528027	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542521694	chr13:49528082-49528083	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559518426	chr13:49528125-49528126	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs113402355	chr13:49528179-49528180	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184169498	chr13:49528188-49528189	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

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	17899364	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
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	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
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	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
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49521600-49529000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:49525200-49527600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:49525200-49527800	Weak transcription	Fetal Intestine Large	intestine
4	chr13:49525200-49528000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr13:49525200-49528200	Weak transcription	Fetal Intestine Small	intestine
6	chr13:49525400-49527600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:49525400-49527800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:49525400-49528200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr13:49525400-49528200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr13:49525600-49528200	Weak transcription	HMEC	breast
11	chr13:49525800-49527800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr13:49526000-49529000	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr13:49527600-49527800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr13:49527600-49528200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr13:49527600-49529200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:49527800-49528800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr13:49527800-49528800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr13:49527800-49528800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr13:49527800-49528800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chr13:49527800-49528800	Enhancers	Fetal Kidney	kidney
21	chr13:49527800-49530600	Enhancers	Fetal Intestine Large	intestine
22	chr13:49528000-49528200	Enhancers	Osteobl	bone
23	chr13:49528000-49528600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr13:49528000-49528800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr13:49528000-49529200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr13:49528200-49528400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr13:49528200-49528600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr13:49528200-49528600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr13:49528200-49528600	Flanking Active TSS	Osteobl	bone
30	chr13:49528200-49528800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:49528200-49528800	Enhancers	NH-A	brain
32	chr13:49528200-49529200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:49528200-49529200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr13:49528200-49529200	Enhancers	HMEC	breast
35	chr13:49528200-49530600	Enhancers	Fetal Intestine Small	intestine
36	chr13:49528400-49528600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr13:49528600-49529200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr13:49528800-49529800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr13:49529000-49529800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:49529000-49530600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr13:49529400-49529800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr13:49529800-49532000	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr13:49530600-49530800	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr13:49531800-49532800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr13:49532000-49532800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr13:49532800-49535200	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr13:49535200-49536200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr13:49535400-49536000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr13:49536400-49536800	Enhancers	K562	blood
50	chr13:49541600-49541800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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