Variant report

Variant	nsv900077
Chromosome Location	chr13:51446114-51514831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1527)
CpG islands
(count:1160)
Chromatin interactive
region (count:54)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51497471-51497719	K562	blood:	n/a	n/a
2	ARID3A	chr13:51514712-51514984	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:51483949-51483989	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:51485230-51485580	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:51486153-51486418	K562	blood:	n/a	n/a
6	ARID3A	chr13:51483630-51484048	K562	blood:	n/a	n/a
7	ATF2	chr13:51466205-51467011	GM12878	blood:	n/a	n/a
8	ATF2	chr13:51485847-51486612	GM12878	blood:	n/a	n/a
9	ATF2	chr13:51485896-51486487	GM12878	blood:	n/a	n/a
10	ATF2	chr13:51467449-51468203	GM12878	blood:	n/a	n/a
11	ATF2	chr13:51483588-51484203	GM12878	blood:	n/a	n/a
12	ATF3	chr13:51483783-51484004	K562	blood:	n/a	n/a
13	BACH1	chr13:51484178-51484692	K562	blood:	n/a	n/a
14	BACH1	chr13:51497532-51497764	K562	blood:	n/a	n/a
15	BACH1	chr13:51483741-51484870	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr13:51486102-51486442	GM12878	blood:	n/a	n/a
17	BATF	chr13:51489673-51490044	GM12878	blood:	n/a	n/a
18	BATF	chr13:51489059-51489363	GM12878	blood:	n/a	n/a
19	BATF	chr13:51489019-51489289	GM12878	blood:	n/a	n/a
20	BCL11A	chr13:51486047-51486471	GM12878	blood:	n/a	n/a
21	BCLAF1	chr13:51486023-51486507	GM12878	blood:	n/a	n/a
22	BCLAF1	chr13:51467397-51468142	GM12878	blood:	n/a	chr13:51467850-51467859
23	BCLAF1	chr13:51483603-51484912	GM12878	blood:	n/a	chr13:51484294-51484307 chr13:51484290-51484303 chr13:51484578-51484591
24	BCLAF1	chr13:51485924-51486541	GM12878	blood:	n/a	n/a
25	BHLHE40	chr13:51489059-51489973	GM12878	blood:	n/a	n/a
26	BHLHE40	chr13:51502732-51503379	K562	blood:	n/a	n/a
27	BHLHE40	chr13:51483542-51484772	K562	blood:	n/a	n/a
28	BHLHE40	chr13:51490959-51491400	K562	blood:	n/a	chr13:51491131-51491144 chr13:51491127-51491148
29	BHLHE40	chr13:51488634-51488943	K562	blood:	n/a	n/a
30	BHLHE40	chr13:51474588-51474638	K562	blood:	n/a	n/a
31	BHLHE40	chr13:51483769-51484771	HepG2	liver:	n/a	n/a
32	BHLHE40	chr13:51490842-51491500	GM12878	blood:	n/a	chr13:51491131-51491144 chr13:51491127-51491148
33	BHLHE40	chr13:51485263-51485609	GM12878	blood:	n/a	n/a
34	BHLHE40	chr13:51483586-51485040	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:51467550-51468123	GM12878	blood:	n/a	n/a
36	BHLHE40	chr13:51485819-51486514	GM12878	blood:	n/a	n/a
37	BRCA1	chr13:51483603-51484426	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr13:51484658-51485004	GM12878	blood:	n/a	n/a
39	BRCA1	chr13:51483906-51484008	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr13:51486156-51486558	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr13:51505028-51505127	GM12878	blood:	n/a	n/a
42	BRCA1	chr13:51486210-51486506	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr13:51484622-51484732	HepG2	liver:	n/a	n/a
44	BRCA1	chr13:51483937-51483972	HepG2	liver:	n/a	n/a
45	CBX3	chr13:51484345-51484792	K562	blood:	n/a	n/a
46	CBX3	chr13:51486081-51486473	K562	blood:	n/a	n/a
47	CBX3	chr13:51497445-51497723	K562	blood:	n/a	n/a
48	CBX3	chr13:51496107-51496480	K562	blood:	n/a	n/a
49	CBX3	chr13:51497400-51497827	K562	blood:	n/a	n/a
50	CCNT2	chr13:51486139-51486402	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51487527-51487577	AoSMC	blood vessel:	n/a
2	chr13:51487527-51487577	AoSMC	blood vessel:	n/a
3	chr13:51482465-51482515	MCF10A-Er-Src	breast:	n/a
4	chr13:51484590-51484640	HUVEC	blood vessel:	n/a
5	chr13:51483748-51483798	ProgFib	skin:	n/a
6	chr13:51480138-51480188	HIPEpiC	eye:	n/a
7	chr13:51466941-51466991	HRCEpiC	kidney:	n/a
8	chr13:51480138-51480188	BJ	skin:	n/a
9	chr13:51482661-51482711	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:51482542-51482592	SK-N-SH_RA	brain:	n/a
11	chr13:51484590-51484640	CMK	blood:	n/a
12	chr13:51484009-51484059	ECC-1	luminal epithelium:	n/a
13	chr13:51483859-51483909	ECC-1	luminal epithelium:	n/a
14	chr13:51484060-51484110	ECC-1	luminal epithelium:	n/a
15	chr13:51483769-51483819	BJ	skin:	n/a
16	chr13:51466941-51466991	NB4	blood:	n/a
17	chr13:51483857-51483907	NB4	blood:	n/a
18	chr13:51483769-51483819	LNCaP	prostate:	n/a
19	chr13:51483859-51483909	NT2-D1	testis:	n/a
20	chr13:51484248-51484298	A549	lung:	n/a
21	chr13:51483867-51483917	NT2-D1	testis:	n/a
22	chr13:51484060-51484110	GM12878	blood:	n/a
23	chr13:51480138-51480188	U87	brain:	n/a
24	chr13:51489972-51490022	MCF10A-Er-Src	breast:	n/a
25	chr13:51483867-51483917	ovcar-3	ovarian:	n/a
26	chr13:51484248-51484298	HRPEpiC	eye:	n/a
27	chr13:51483769-51483819	K562	blood:	n/a
28	chr13:51480138-51480188	AG10803	skin:	n/a
29	chr13:51483769-51483819	AoSMC	blood vessel:	n/a
30	chr13:51482465-51482515	ProgFib	skin:	n/a
31	chr13:51482661-51482711	NT2-D1	testis:	n/a
32	chr13:51482542-51482592	MCF-7	breast:	n/a
33	chr13:51466941-51466991	HepG2	liver:	n/a
34	chr13:51491406-51491456	PFSK-1	brain:	n/a
35	chr13:51483867-51483917	NB4	blood:	n/a
36	chr13:51482542-51482592	HNPCEpiC	eye:	n/a
37	chr13:51484248-51484298	NT2-D1	testis:	n/a
38	chr13:51483748-51483798	CMK	blood:	n/a
39	chr13:51484248-51484298	AG09319	gingival:	n/a
40	chr13:51483867-51483917	HCM	heart:	n/a
41	chr13:51483857-51483907	HMEC	breast:	n/a
42	chr13:51489972-51490022	Hepatocyte	liver:	n/a
43	chr13:51487527-51487577	HUVEC	blood vessel:	n/a
44	chr13:51482661-51482711	Caco-2	colon:	n/a
45	chr13:51483765-51483815	HCM	heart:	n/a
46	chr13:51489972-51490022	HIPEpiC	eye:	n/a
47	chr13:51482661-51482711	Hela-S3	cervix:	n/a
48	chr13:51484060-51484110	NHBE	bronchial:	n/a
49	chr13:51484248-51484298	SK-N-SH	brain:	n/a
50	chr13:51484590-51484640	HL-60	blood:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:51451175..51452733-chr13:51482533..51485257,2	K562	blood:
2	chr13:51484842..51486646-chr13:51497304..51499089,2	MCF-7	breast:
3	chr13:50950830..50951344-chr13:51485981..51486799,2	MCF-7	breast:
4	chr13:51504617..51506922-chr13:51508240..51511207,2	K562	blood:
5	chr13:51484081..51484759-chr3:150264254..150264982,2	Hela-S3	cervix:
6	chr13:51488232..51490526-chr13:51522667..51525148,2	MCF-7	breast:
7	chr13:51496481..51499256-chr13:51504473..51506506,2	K562	blood:
8	chr13:51509255..51511069-chr13:51514607..51517534,2	K562	blood:
9	chr13:51484185..51486351-chr13:51503175..51505041,2	MCF-7	breast:
10	chr13:51452163..51454609-chr13:51458977..51461439,2	MCF-7	breast:
11	chr13:51451886..51453758-chr13:51483601..51485898,2	MCF-7	breast:
12	chr13:51511006..51512738-chr13:51514489..51516237,2	MCF-7	breast:
13	chr13:51464884..51467381-chr13:51471388..51473638,2	MCF-7	breast:
14	chr13:51502290..51504797-chr13:51513858..51516278,2	MCF-7	breast:
15	chr13:51482808..51485388-chr13:51495589..51498006,3	K562	blood:
16	chr13:51472736..51474284-chr13:51482598..51484808,2	MCF-7	breast:
17	chr13:51484185..51486351-chr13:51503175..51505041,2	MCF-7	breast:
18	chr13:51473931..51480255-chr13:51481989..51485518,9	MCF-7	breast:
19	chr13:51452163..51454609-chr13:51458977..51461439,2	MCF-7	breast:
20	chr13:51462818..51465395-chr13:51482325..51483926,2	K562	blood:
21	chr13:50510515..50512106-chr13:51482735..51485474,2	K562	blood:
22	chr13:51509255..51511069-chr13:51514607..51517534,2	K562	blood:
23	chr13:50696939..50701257-chr13:51483386..51488031,9	K562	blood:
24	chr13:50569035..50571663-chr13:51485702..51487859,2	K562	blood:
25	chr13:50550599..50551508-chr13:51485864..51486759,2	K562	blood:
26	chr13:51483508..51485914-chr13:51506913..51509596,2	K562	blood:
27	chr13:50654380..50657403-chr13:51482897..51486295,4	K562	blood:
28	chr13:51486556..51488218-chr13:51489286..51491989,2	MCF-7	breast:
29	chr13:51495576..51498047-chr13:51500874..51502897,3	K562	blood:
30	chr13:51488225..51491111-chr13:51497807..51500675,3	K562	blood:
31	chr13:51486556..51488218-chr13:51489286..51491989,2	MCF-7	breast:
32	chr13:51447595..51449565-chr13:51482789..51485089,2	MCF-7	breast:
33	chr13:51473891..51476765-chr13:51478767..51481533,2	MCF-7	breast:
34	chr13:51481866..51483659-chr13:51484720..51486682,2	K562	blood:
35	chr13:51483541..51484529-chr4:164415235..164416192,2	HCT-116	colon:
36	chr13:51484487..51486944-chr13:51500035..51502322,2	K562	blood:
37	chr13:50697977..50698964-chr13:51485927..51486494,2	K562	blood:
38	chr13:51444050..51446783-chr13:51482621..51484438,2	K562	blood:
39	chr13:51504617..51506922-chr13:51508240..51511207,2	K562	blood:
40	chr13:51483947..51485483-chr13:51513505..51515717,2	MCF-7	breast:
41	chr13:51483976..51485601-chr13:51498682..51500533,2	K562	blood:
42	chr13:51501032..51502857-chr13:51505109..51507477,2	K562	blood:
43	chr13:50656933..50657634-chr13:51485862..51486382,2	K562	blood:
44	chr13:51483191..51486510-chr13:51488472..51491289,4	MCF-7	breast:
45	chr13:50363476..50366040-chr13:51498906..51500626,2	K562	blood:
46	chr13:51481922..51486486-chr13:51489921..51494512,7	MCF-7	breast:
47	chr13:51511006..51512738-chr13:51514489..51516237,2	MCF-7	breast:
48	chr13:51482216..51484918-chr13:51486797..51488418,2	MCF-7	breast:
49	chr13:50655118..50657080-chr13:51484545..51486295,2	K562	blood:
50	chr13:50696984..50702154-chr13:51483455..51488031,9	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLEU7-1	chr13:51478857-51478999	ENSG00000233672.2
2	lnc-DLEU7-1	chr13:51484619-51484848	ENSG00000233672.1
3	lnc-DLEU7-1	chr13:51456688-51456781	ENSG00000233672.2
4	lnc-DLEU7-1	chr13:51478857-51479292	ENSG00000233672.2
5	lnc-DLEU7-5	chr13:51508740-51509355	l_847_chr13:51508739-51522354_testes
6	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.1
7	lnc-DLEU7-1	chr13:51465440-51465640	ENSG00000233672.2
8	lnc-DLEU7-1	chr13:51484619-51484730	ENSG00000233672.2
9	lnc-DLEU7-1	chr13:51456745-51456781	ENSG00000233672.2
10	lnc-DLEU7-1	chr13:51456600-51456781	ENSG00000233672.2
11	lnc-DLEU7-1	chr13:51456534-51456779	ENSG00000233672.2
12	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
13	lnc-DLEU7-1	chr13:51465440-51465778	ENSG00000233672.2
14	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
15	lnc-DLEU7-1	chr13:51478857-51478999	ENSG00000233672.2
16	lnc-DLEU7-1	chr13:51484619-51484730	ENSG00000233672.2
17	lnc-DLEU7-1	chr13:51484619-51484848	NR_046552
18	lnc-DLEU7-1	chr13:51456515-51456781	NR_046552
19	lnc-DLEU7-1	chr13:51478857-51478999	ENSG00000233672.2
20	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
21	lnc-DLEU7-1	chr13:51463745-51463871	NR_046552
22	lnc-DLEU7-1	chr13:51456647-51456781	ENSG00000233672.2
23	lnc-DLEU7-1	chr13:51450822-51451098	ENSG00000233672.2
24	lnc-DLEU7-1	chr13:51484619-51484730	ENSG00000233672.2
25	lnc-DLEU7-1	chr13:51456514-51456781	ENSG00000233672.1
26	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
27	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2

No data

Variant related genes	Relation type
RNASEH2B	TF binding region
RNASEH2B-AS1	TF binding region
RNASEH2B	CpG island
RNASEH2B-AS1	CpG island
ENSG00000233672	chromatin interactions
ENSG00000264864	chromatin interactions
ENSG00000138036	chromatin interactions
ENSG00000198498	chromatin interactions
ENSG00000204977	chromatin interactions
ENSG00000120742	chromatin interactions
ENSG00000136104	chromatin interactions
ENSG00000231607	chromatin interactions
ENSG00000123178	chromatin interactions
ENSG00000144895	chromatin interactions
ENSG00000176124	chromatin interactions

Extended variants
information (count: 2275 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:2275 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12429206	chr13:51446114-51446115	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554944396	chr13:51446169-51446170	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573259582	chr13:51446173-51446174	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs542524934	chr13:51446218-51446219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs7997552	chr13:51446271-51446272	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs9591370	chr13:51446278-51446279	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs60530046	chr13:51446310-51446311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187520094	chr13:51446316-51446317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs61650283	chr13:51446318-51446319	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs55773265	chr13:51446319-51446320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564611859	chr13:51446325-51446326	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528594691	chr13:51446363-51446364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139008085	chr13:51446383-51446384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs369688122	chr13:51446385-51446386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34608274	chr13:51446412-51446413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200129135	chr13:51446414-51446415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529240541	chr13:51446440-51446441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550876829	chr13:51446449-51446450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs4942941	chr13:51446504-51446505	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs377534245	chr13:51446511-51446512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557827012	chr13:51446524-51446525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539658191	chr13:51446536-51446537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs193240297	chr13:51446542-51446543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs55784050	chr13:51446566-51446567	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574901582	chr13:51446588-51446589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60712816	chr13:51446604-51446605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146364312	chr13:51446641-51446642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs555009404	chr13:51446644-51446645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs59951652	chr13:51446684-51446685	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543840054	chr13:51446696-51446697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11462939	chr13:51446742-51446743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs28360772	chr13:51446749-51446750	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs575838917	chr13:51446760-51446761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117403246	chr13:51446836-51446837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564674798	chr13:51446905-51446906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573436116	chr13:51446937-51446938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540748687	chr13:51447001-51447002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185672180	chr13:51447017-51447018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562138314	chr13:51447018-51447019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529318419	chr13:51447032-51447033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190691086	chr13:51447041-51447042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76274011	chr13:51447065-51447066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533076938	chr13:51447268-51447269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192164557	chr13:51447283-51447284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7981802	chr13:51447306-51447307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533709891	chr13:51447311-51447312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559419078	chr13:51447314-51447315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377322793	chr13:51447378-51447379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567233979	chr13:51447393-51447394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572281737	chr13:51447421-51447422	Weak transcription Enhancers	n/a	n/a	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
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
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
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
Chronic lymphocytic leukemia	21670202	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
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1994 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51442200-51447600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:51442800-51449800	Weak transcription	Dnd41	blood
3	chr13:51447200-51448400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr13:51447600-51448200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr13:51447600-51448200	Enhancers	NHDF-Ad	bronchial
6	chr13:51447800-51448200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:51447800-51448200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:51447800-51448400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr13:51451400-51452400	Enhancers	Fetal Thymus	thymus
10	chr13:51451400-51453000	Enhancers	Thymus	Thymus
11	chr13:51452400-51454600	Weak transcription	Fetal Thymus	thymus
12	chr13:51453000-51454800	Weak transcription	Thymus	Thymus
13	chr13:51454600-51455800	Enhancers	Fetal Thymus	thymus
14	chr13:51454800-51455600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr13:51454800-51455600	Enhancers	Thymus	Thymus
16	chr13:51455000-51455400	Enhancers	Primary B cells from peripheral blood	blood
17	chr13:51455000-51455600	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr13:51455600-51456800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr13:51455600-51456800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr13:51455800-51458000	Weak transcription	Fetal Thymus	thymus
21	chr13:51456000-51456200	Weak transcription	Aorta	Aorta
22	chr13:51456800-51457000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr13:51456800-51457200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr13:51456800-51457400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
25	chr13:51457000-51457200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr13:51457000-51457400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr13:51457000-51458800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:51457200-51457600	Active TSS	Monocytes-CD14+_RO01746	blood
29	chr13:51457200-51464600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr13:51457400-51458200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr13:51457400-51459200	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr13:51457600-51458600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr13:51457600-51459000	Enhancers	Primary hematopoietic stem cells	blood
34	chr13:51457600-51459200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr13:51458000-51458600	Enhancers	Dnd41	blood
36	chr13:51458000-51458800	Enhancers	Fetal Thymus	thymus
37	chr13:51458200-51458600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr13:51458600-51459400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr13:51458600-51461200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr13:51458800-51461000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr13:51458800-51463400	Weak transcription	Fetal Thymus	thymus
42	chr13:51459000-51461000	Weak transcription	Primary hematopoietic stem cells	blood
43	chr13:51459200-51461000	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr13:51459200-51461200	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr13:51459400-51461200	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr13:51461000-51461800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:51461000-51462000	Enhancers	Primary hematopoietic stem cells	blood
48	chr13:51461000-51462000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr13:51461000-51462200	Enhancers	Primary B cells from cord blood	blood
50	chr13:51461000-51462600	Weak transcription	Dnd41	blood

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