Variant report

Variant	esv2753864
Chromosome Location	chr13:51136699-51375199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1647)
CpG islands
(count:490)
Chromatin interactive
region (count:57)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51187012-51187906	K562	blood:	n/a	n/a
2	ARID3A	chr13:51266023-51266254	K562	blood:	n/a	n/a
3	ARID3A	chr13:51274196-51274450	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:51156892-51156998	K562	blood:	n/a	n/a
5	ARID3A	chr13:51246123-51246506	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:51149257-51149568	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:51170951-51171209	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:51203604-51204086	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:51200337-51200563	K562	blood:	n/a	n/a
10	ATF1	chr13:51187449-51188027	K562	blood:	n/a	n/a
11	ATF1	chr13:51265947-51266338	K562	blood:	n/a	n/a
12	ATF1	chr13:51313105-51313545	K562	blood:	n/a	n/a
13	ATF1	chr13:51252635-51253495	K562	blood:	n/a	n/a
14	ATF1	chr13:51200216-51200573	K562	blood:	n/a	n/a
15	ATF2	chr13:51168317-51169075	GM12878	blood:	n/a	n/a
16	ATF2	chr13:51209531-51210346	GM12878	blood:	n/a	n/a
17	ATF3	chr13:51370719-51370856	K562	blood:	n/a	chr13:51370772-51370781
18	ATF3	chr13:51200245-51200412	K562	blood:	n/a	n/a
19	ATF3	chr13:51200208-51200496	K562	blood:	n/a	n/a
20	BACH1	chr13:51210183-51210597	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr13:51168321-51168952	GM12878	blood:	n/a	chr13:51168934-51168943
22	BCL11A	chr13:51168430-51168875	GM12878	blood:	n/a	n/a
23	BCL3	chr13:51168641-51169013	GM12878	blood:	n/a	chr13:51168934-51168943
24	BCLAF1	chr13:51168269-51169265	GM12878	blood:	n/a	chr13:51168934-51168943 chr13:51169155-51169164
25	BCLAF1	chr13:51168650-51169174	GM12878	blood:	n/a	chr13:51168934-51168943 chr13:51169155-51169164
26	BHLHE40	chr13:51242331-51242366	K562	blood:	n/a	n/a
27	BHLHE40	chr13:51187403-51187907	K562	blood:	n/a	n/a
28	BHLHE40	chr13:51209717-51210082	GM12878	blood:	n/a	n/a
29	BHLHE40	chr13:51224597-51225169	GM12878	blood:	n/a	n/a
30	BHLHE40	chr13:51209756-51210096	K562	blood:	n/a	n/a
31	BHLHE40	chr13:51252666-51252922	K562	blood:	n/a	n/a
32	BHLHE40	chr13:51375054-51375061	GM12878	blood:	n/a	n/a
33	BHLHE40	chr13:51265539-51265697	K562	blood:	n/a	n/a
34	BHLHE40	chr13:51250645-51250840	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:51167958-51169191	GM12878	blood:	n/a	chr13:51168639-51168655
36	BHLHE40	chr13:51172650-51173079	HepG2	liver:	n/a	n/a
37	BHLHE40	chr13:51200235-51200603	K562	blood:	n/a	n/a
38	BHLHE40	chr13:51172562-51172920	GM12878	blood:	n/a	n/a
39	BRCA1	chr13:51166639-51166776	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr13:51210180-51210186	GM12878	blood:	n/a	n/a
41	BRCA1	chr13:51170130-51170218	GM12878	blood:	n/a	n/a
42	BRCA1	chr13:51219461-51219465	GM12878	blood:	n/a	n/a
43	CBX3	chr13:51187394-51187959	K562	blood:	n/a	n/a
44	CCNT2	chr13:51174151-51174351	K562	blood:	n/a	chr13:51174222-51174242
45	CCNT2	chr13:51185657-51185936	K562	blood:	n/a	n/a
46	CCNT2	chr13:51187456-51187955	K562	blood:	n/a	n/a
47	CCNT2	chr13:51200228-51200450	K562	blood:	n/a	n/a
48	CEBPB	chr13:51252473-51252955	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:51283160-51283482	HCT-116	colon:	n/a	chr13:51283352-51283363
50	CEBPB	chr13:51246188-51246545	HepG2	liver:	n/a	chr13:51246371-51246382

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51210877-51210927	ECC-1	luminal epithelium:	n/a
2	chr13:51210877-51210927	NH-A	brain:	n/a
3	chr13:51210877-51210927	ECC-1	luminal epithelium:	n/a
4	chr13:51210877-51210927	NH-A	brain:	n/a
5	chr13:51361994-51362044	HCM	heart:	n/a
6	chr13:51168711-51168761	HEK293	kidney:	embryo
7	chr13:51168711-51168761	HCPEpiC	choroid plexus:	n/a
8	chr13:51353941-51353991	GM12878	blood:	n/a
9	chr13:51353941-51353991	MCF10A-Er-Src	breast:	n/a
10	chr13:51353941-51353991	GM19239	blood:	n/a
11	chr13:51353941-51353991	HAEpiC	amniotic membrane:	n/a
12	chr13:51163726-51163776	SK-N-MC	brain:	n/a
13	chr13:51163726-51163776	BJ	skin:	n/a
14	chr13:51168711-51168761	HepG2	liver:	n/a
15	chr13:51168711-51168761	GM12891	blood:	n/a
16	chr13:51326803-51326853	HNPCEpiC	eye:	n/a
17	chr13:51326803-51326853	ovcar-3	ovarian:	n/a
18	chr13:51210877-51210927	SAEC	small airway:	n/a
19	chr13:51361994-51362044	MCF10A-Er-Src	breast:	n/a
20	chr13:51163726-51163776	U87	brain:	n/a
21	chr13:51210877-51210927	AG04449	skin:	fetal
22	chr13:51210877-51210927	AG09309	skin:	n/a
23	chr13:51252348-51252398	HMEC	breast:	n/a
24	chr13:51257555-51257605	HAEpiC	amniotic membrane:	n/a
25	chr13:51326803-51326853	U87	brain:	n/a
26	chr13:51168711-51168761	HCF	heart:	n/a
27	chr13:51257555-51257605	Caco-2	colon:	n/a
28	chr13:51326803-51326853	HCPEpiC	choroid plexus:	n/a
29	chr13:51163726-51163776	BE2_C	brain:	n/a
30	chr13:51252348-51252398	GM12878	blood:	n/a
31	chr13:51257555-51257605	HL-60	blood:	n/a
32	chr13:51168711-51168761	RPTEC	kidney:	n/a
33	chr13:51361994-51362044	GM12878	blood:	n/a
34	chr13:51163726-51163776	ECC-1	luminal epithelium:	n/a
35	chr13:51257555-51257605	NHBE	bronchial:	n/a
36	chr13:51163726-51163776	Caco-2	colon:	n/a
37	chr13:51353941-51353991	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:51252348-51252398	HEEpiC	esophagus:	n/a
39	chr13:51210877-51210927	HPAEpiC	pulmonary alveolar:	n/a
40	chr13:51252348-51252398	Jurkat	blood:	n/a
41	chr13:51252348-51252398	NHDF-neo	bronchial:	n/a
42	chr13:51353941-51353991	Caco-2	colon:	n/a
43	chr13:51361994-51362044	HepG2	liver:	n/a
44	chr13:51168711-51168761	HRPEpiC	eye:	n/a
45	chr13:51353941-51353991	NB4	blood:	n/a
46	chr13:51163726-51163776	PFSK-1	brain:	n/a
47	chr13:51257555-51257605	MCF10A-Er-Src	breast:	n/a
48	chr13:51163726-51163776	HEEpiC	esophagus:	n/a
49	chr13:51361994-51362044	ProgFib	skin:	n/a
50	chr13:51257555-51257605	SK-N-MC	brain:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:51370732..51372602-chr13:51373640..51375696,2	MCF-7	breast:
2	chr13:51188683..51191307-chr13:51240067..51242505,2	MCF-7	breast:
3	chr13:51235867..51238606-chr13:51244733..51246390,2	MCF-7	breast:
4	chr13:51148960..51151212-chr13:51161969..51163948,2	MCF-7	breast:
5	chr13:51330144..51332927-chr13:51336662..51340363,3	MCF-7	breast:
6	chr13:51203846..51206434-chr13:51207339..51209501,2	K562	blood:
7	chr13:51248503..51250450-chr13:51256107..51258684,2	MCF-7	breast:
8	chr13:51188683..51191307-chr13:51240067..51242505,2	MCF-7	breast:
9	chr13:51298771..51301176-chr13:51301369..51304366,2	K562	blood:
10	chr13:51165408..51167932-chr13:51169513..51171803,2	K562	blood:
11	chr12:82971566..82972433-chr13:51277425..51278166,2	MCF-7	breast:
12	chr13:51216821..51219779-chr13:51224555..51226364,2	MCF-7	breast:
13	chr13:51271422..51272928-chr13:51274925..51277429,2	K562	blood:
14	chr13:51245204..51247127-chr13:51248025..51250990,2	MCF-7	breast:
15	chr13:51166235..51168592-chr13:51178276..51180293,2	K562	blood:
16	chr13:51164156..51167567-chr13:51169457..51171803,3	K562	blood:
17	chr13:51164156..51167567-chr13:51169457..51171803,3	K562	blood:
18	chr13:50698261..50700458-chr13:51177608..51180344,2	MCF-7	breast:
19	chr13:51191287..51192925-chr13:51194826..51197754,2	K562	blood:
20	chr13:51276998..51279149-chr13:51301224..51304150,2	K562	blood:
21	chr13:51185236..51187153-chr13:51484529..51486325,2	K562	blood:
22	chr13:51191287..51192925-chr13:51194826..51197754,2	K562	blood:
23	chr13:51216555..51218966-chr13:51222987..51226274,3	K562	blood:
24	chr13:51218577..51220101-chr13:51250986..51253553,2	MCF-7	breast:
25	chr13:51309482..51311809-chr13:51312574..51314678,2	MCF-7	breast:
26	chr13:50697161..50699455-chr13:51219489..51221158,2	MCF-7	breast:
27	chr13:51271422..51272928-chr13:51274925..51277429,2	K562	blood:
28	chr13:51230983..51233957-chr13:51261931..51264364,2	MCF-7	breast:
29	chr13:51330144..51332927-chr13:51336662..51340363,3	MCF-7	breast:
30	chr13:51218577..51220101-chr13:51250986..51253553,2	MCF-7	breast:
31	chr13:51370732..51372602-chr13:51373640..51375696,2	MCF-7	breast:
32	chr13:51248503..51250450-chr13:51256107..51258684,2	MCF-7	breast:
33	chr13:51245204..51247127-chr13:51248025..51250990,2	MCF-7	breast:
34	chr13:51230983..51233957-chr13:51261931..51264364,2	MCF-7	breast:
35	chr13:51211431..51214240-chr13:51220599..51223309,2	K562	blood:
36	chr13:51298771..51301176-chr13:51301369..51304366,2	K562	blood:
37	chr13:51186188..51187899-chr13:51538381..51540074,2	K562	blood:
38	chr13:51211431..51214240-chr13:51220599..51223309,2	K562	blood:
39	chr13:51148960..51151212-chr13:51161969..51163948,2	MCF-7	breast:
40	chr13:50699832..50701606-chr13:51373165..51375472,2	MCF-7	breast:
41	chr13:51309482..51311809-chr13:51312574..51314678,2	MCF-7	breast:
42	chr13:51276998..51279149-chr13:51301224..51304150,2	K562	blood:
43	chr13:51235867..51238606-chr13:51244733..51246390,2	MCF-7	breast:
44	chr13:51244981..51247308-chr13:51258200..51260346,2	MCF-7	breast:
45	chr13:51216821..51219779-chr13:51224555..51226364,2	MCF-7	breast:
46	chr13:51203846..51206434-chr13:51207339..51209501,2	K562	blood:
47	chr13:51166235..51168592-chr13:51178276..51180293,2	K562	blood:
48	chr13:50696839..50701708-chr13:51215562..51219083,4	MCF-7	breast:
49	chr13:51185399..51188219-chr13:51502643..51505475,2	K562	blood:
50	chr13:51244981..51247308-chr13:51258200..51260346,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLEU7-4	chr13:51289562-51289619	NONHSAT033864
2	lnc-RNASEH2B-9	chr13:51234596-51234902	expReg_chr13_2521_+
3	lnc-RNASEH2B-7	chr13:51237819-51238118	expReg_chr13_2523_+
4	lnc-RNASEH2B-5	chr13:51276688-51276938	l_845_chr13:51276687-51285368_prostate
5	lnc-RNASEH2B-8	chr13:51235099-51235339	expReg_chr13_2522_+
6	lnc-RNASEH2B-3	chr13:51222726-51222778	NONHSAT033846
7	lnc-DLEU7-4	chr13:51285144-51287376	NONHSAT033864
8	lnc-RNASEH2B-5	chr13:51278974-51279337	l_845_chr13:51276687-51285368_prostate
9	lnc-RNASEH2B-3	chr13:51297275-51297372	NONHSAT033843
10	lnc-RNASEH2B-4	chr13:51287754-51289476	NONHSAT033865
11	lnc-DLEU7-6	chr13:51153744-51154268	NONHSAT033863
12	lnc-DLEU7-6	chr13:51171805-51172341	NONHSAT033863
13	lnc-RNASEH2B-3	chr13:51205413-51205735	XLOC_010390
14	lnc-RNASEH2B-3	chr13:51163611-51163712	NONHSAT033846
15	lnc-RNASEH2B-5	chr13:51280047-51280235	l_845_chr13:51276687-51285368_prostate
16	lnc-DLEU7-6	chr13:51182919-51183212	NONHSAT033863
17	lnc-RNASEH2B-6	chr13:51238285-51238825	expReg_chr13_2525_+
18	lnc-RNASEH2B-3	chr13:51293783-51293846	NONHSAT033843
19	lnc-RNASEH2B-5	chr13:51285294-51285955	l_845_chr13:51276687-51285368_prostate

No data

Variant related genes	Relation type
DLEU7	TF binding region
DLEU7	CpG island
ENSG00000123178	chromatin interactions
ENSG00000233672	chromatin interactions
ENSG00000136104	chromatin interactions
ENSG00000186047	chromatin interactions
ENSG00000231607	chromatin interactions

Extended variants
information (count: 8064 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:8064 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2011671	chr13:51136726-51136727	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs978332	chr13:51136739-51136740	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs546462902	chr13:51141629-51141630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191478514	chr13:51141669-51141670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541974100	chr13:51141683-51141684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561651061	chr13:51141703-51141704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528979253	chr13:51141714-51141715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114961721	chr13:51141771-51141772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183821416	chr13:51141810-51141811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537746027	chr13:51141815-51141816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559268207	chr13:51141816-51141817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571074556	chr13:51141911-51141912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575333114	chr13:51141946-51141947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs770383	chr13:51141947-51141948	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553266676	chr13:51141958-51141959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574921946	chr13:51141985-51141986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375282485	chr13:51141990-51141991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17074575	chr13:51141997-51141998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189897006	chr13:51141998-51141999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2408045	chr13:51142065-51142066	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs545713398	chr13:51142071-51142072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532720657	chr13:51142089-51142090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181530445	chr13:51142095-51142096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147915147	chr13:51142123-51142124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141533609	chr13:51142126-51142127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540467477	chr13:51142145-51142146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561725743	chr13:51142205-51142206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528995262	chr13:51142233-51142234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549828620	chr13:51142279-51142280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201804487	chr13:51142303-51142304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185189814	chr13:51142342-51142343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532924491	chr13:51142345-51142346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570740965	chr13:51142357-51142358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551383758	chr13:51142394-51142395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190116769	chr13:51142454-51142455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535001150	chr13:51142458-51142459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115363720	chr13:51142484-51142485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568518289	chr13:51142513-51142514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369823661	chr13:51142532-51142533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143659786	chr13:51142662-51142663	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75963357	chr13:51142665-51142666	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148154991	chr13:51142666-51142667	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79941232	chr13:51142681-51142682	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557728610	chr13:51142684-51142685	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76026174	chr13:51142707-51142708	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs770384	chr13:51142744-51142745	Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs181895956	chr13:51142775-51142776	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201978916	chr13:51142833-51142834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71436231	chr13:51142875-51142876	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571669853	chr13:51142940-51142941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
Sezary syndrome	18413736	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:2524 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51136400-51136800	Enhancers	Fetal Muscle Leg	muscle
2	chr13:51141600-51142200	Enhancers	Fetal Lung	lung
3	chr13:51142200-51146400	Weak transcription	Fetal Lung	lung
4	chr13:51142600-51142800	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
5	chr13:51146200-51146600	Enhancers	Right Atrium	heart
6	chr13:51146200-51146800	Enhancers	Liver	Liver
7	chr13:51146200-51146800	Enhancers	Osteobl	bone
8	chr13:51146200-51151200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:51146400-51146600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:51146400-51146600	Enhancers	Fetal Lung	lung
11	chr13:51146400-51146600	Enhancers	Left Ventricle	heart
12	chr13:51146400-51146600	Enhancers	Right Ventricle	heart
13	chr13:51146400-51146600	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr13:51146400-51146800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr13:51146400-51146800	Enhancers	Adipose Nuclei	Adipose
16	chr13:51146400-51148600	Enhancers	HSMMtube	muscle
17	chr13:51146600-51147400	Weak transcription	Fetal Lung	lung
18	chr13:51146600-51147600	Enhancers	Fetal Heart	heart
19	chr13:51146600-51147600	Weak transcription	Right Ventricle	heart
20	chr13:51146600-51147600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr13:51146600-51150200	Weak transcription	Right Atrium	heart
22	chr13:51146800-51147200	Weak transcription	Osteobl	bone
23	chr13:51146800-51148800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr13:51146800-51149800	Weak transcription	Liver	Liver
25	chr13:51146800-51150400	Weak transcription	Adipose Nuclei	Adipose
26	chr13:51147000-51148200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:51147200-51151200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr13:51147200-51151200	Enhancers	Osteobl	bone
29	chr13:51147400-51147600	Enhancers	Fetal Lung	lung
30	chr13:51147600-51147800	Flanking Active TSS	Fetal Heart	heart
31	chr13:51147600-51147800	Flanking Active TSS	Fetal Lung	lung
32	chr13:51147600-51147800	Enhancers	Dnd41	blood
33	chr13:51147600-51148000	Enhancers	Psoas Muscle	Psoas
34	chr13:51147600-51148200	ZNF genes & repeats	Fetal Kidney	kidney
35	chr13:51147600-51148200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr13:51147600-51148400	Enhancers	Right Ventricle	heart
37	chr13:51147600-51148400	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr13:51147600-51151000	Enhancers	Gastric	stomach
39	chr13:51147600-51151200	Enhancers	HSMM	muscle
40	chr13:51147800-51148000	Transcr. at gene 5' and 3'	Fetal Heart	heart
41	chr13:51147800-51148200	Active TSS	Fetal Lung	lung
42	chr13:51147800-51148200	Enhancers	Pancreas	Pancrea
43	chr13:51147800-51160800	Weak transcription	Dnd41	blood
44	chr13:51148000-51148200	Genic enhancers	Fetal Heart	heart
45	chr13:51148000-51149000	Enhancers	NHDF-Ad	bronchial
46	chr13:51148000-51152400	Weak transcription	Psoas Muscle	Psoas
47	chr13:51148200-51148800	Enhancers	Fetal Heart	heart
48	chr13:51148200-51148800	Weak transcription	Fetal Kidney	kidney
49	chr13:51148200-51149400	Weak transcription	Pancreas	Pancrea
50	chr13:51148200-51149800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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