Variant report

Variant	nsv832586
Chromosome Location	chr13:40222880-40379063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1743)
CpG islands
(count:795)
Chromatin interactive
region (count:52)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1743 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:40258767-40259064	K562	blood:	n/a	n/a
2	ARID3A	chr13:40250480-40250846	K562	blood:	n/a	n/a
3	ARID3A	chr13:40250490-40250788	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:40258721-40259053	HepG2	liver:	n/a	n/a
5	BACH1	chr13:40229734-40229988	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:40362405-40362433	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr13:40256983-40257221	GM12878	blood:	n/a	n/a
8	BATF	chr13:40256971-40257218	GM12878	blood:	n/a	n/a
9	BCL11A	chr13:40362244-40362456	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr13:40229262-40229981	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:40334716-40335030	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:40262887-40263229	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:40230824-40230960	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:40230218-40230522	K562	blood:	n/a	n/a
15	BHLHE40	chr13:40259921-40259995	GM12878	blood:	n/a	n/a
16	BRCA1	chr13:40229803-40229860	HepG2	liver:	n/a	n/a
17	BRCA1	chr13:40229280-40229830	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr13:40363828-40364060	K562	blood:	n/a	n/a
19	CBX3	chr13:40351628-40352065	HCT-116	colon:	n/a	n/a
20	CCNT2	chr13:40229689-40230134	K562	blood:	n/a	n/a
21	CEBPB	chr13:40377322-40377725	MCF-7	breast:	n/a	n/a
22	CEBPB	chr13:40351594-40352193	Hela-S3	cervix:	n/a	chr13:40351784-40351795
23	CEBPB	chr13:40341980-40342277	HepG2	liver:	n/a	n/a
24	CEBPB	chr13:40246360-40246670	IMR90	lung:	n/a	chr13:40246485-40246496
25	CEBPB	chr13:40351613-40351966	HepG2	liver:	n/a	chr13:40351784-40351795
26	CEBPB	chr13:40246369-40246635	K562	blood:	n/a	chr13:40246485-40246496
27	CEBPB	chr13:40228256-40228442	HepG2	liver:	n/a	chr13:40228283-40228294
28	CEBPB	chr13:40273251-40273563	HepG2	liver:	n/a	chr13:40273402-40273415 chr13:40273403-40273414 chr13:40273402-40273413
29	CEBPB	chr13:40229777-40229998	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr13:40340004-40340288	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:40339929-40340263	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr13:40246378-40246648	HepG2	liver:	n/a	chr13:40246485-40246496
33	CEBPB	chr13:40377257-40377708	MCF-7	breast:	n/a	n/a
34	CEBPB	chr13:40241190-40241390	K562	blood:	n/a	chr13:40241290-40241303 chr13:40241292-40241301 chr13:40241292-40241301 chr13:40241290-40241303 chr13:40241290-40241303 chr13:40241292-40241301 chr13:40241292-40241303 chr13:40241292-40241303 chr13:40241292-40241301
35	CEBPB	chr13:40246476-40246584	A549	lung:	n/a	chr13:40246485-40246496
36	CEBPB	chr13:40377433-40377548	A549	lung:	n/a	n/a
37	CEBPB	chr13:40351620-40351982	H1-hESC	embryonic stem cell:	n/a	chr13:40351784-40351795
38	CEBPB	chr13:40239413-40239484	HepG2	liver:	n/a	n/a
39	CEBPB	chr13:40351511-40352045	MCF-7	breast:	n/a	chr13:40351784-40351795
40	CEBPB	chr13:40351550-40352128	HCT-116	colon:	n/a	chr13:40351784-40351795
41	CEBPB	chr13:40351544-40352078	A549	lung:	n/a	chr13:40351784-40351795
42	CEBPB	chr13:40351713-40351914	A549	lung:	n/a	chr13:40351784-40351795
43	CEBPB	chr13:40273250-40273550	IMR90	lung:	n/a	chr13:40273402-40273415 chr13:40273403-40273414 chr13:40273402-40273413
44	CEBPB	chr13:40351603-40351970	A549	lung:	n/a	chr13:40351784-40351795
45	CEBPB	chr13:40226109-40226290	HepG2	liver:	n/a	chr13:40226232-40226243
46	CEBPB	chr13:40351454-40352193	HCT-116	colon:	n/a	chr13:40351784-40351795
47	CEBPB	chr13:40328789-40329056	IMR90	lung:	n/a	n/a
48	CEBPB	chr13:40330961-40331047	K562	blood:	n/a	n/a
49	CEBPB	chr13:40342042-40342242	K562	blood:	n/a	n/a
50	CEBPB	chr13:40229677-40229976	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:40233555-40233605	T-47D	breast:	n/a
2	chr13:40229689-40229739	PrEC	prostate:	n/a
3	chr13:40233555-40233605	T-47D	breast:	n/a
4	chr13:40229689-40229739	PrEC	prostate:	n/a
5	chr13:40229780-40229830	MCF10A-Er-Src	breast:	n/a
6	chr13:40229878-40229928	HRCEpiC	kidney:	n/a
7	chr13:40228485-40228535	Hela-S3	cervix:	n/a
8	chr13:40230022-40230072	HRPEpiC	eye:	n/a
9	chr13:40363827-40363877	Caco-2	colon:	n/a
10	chr13:40229689-40229739	GM19239	blood:	n/a
11	chr13:40228485-40228535	T-47D	breast:	n/a
12	chr13:40233555-40233605	IMR90	lung:	fetal
13	chr13:40229707-40229757	HAEpiC	amniotic membrane:	n/a
14	chr13:40229853-40229903	GM12892	blood:	n/a
15	chr13:40229780-40229830	ovcar-3	ovarian:	n/a
16	chr13:40229707-40229757	ECC-1	luminal epithelium:	n/a
17	chr13:40229853-40229903	Caco-2	colon:	n/a
18	chr13:40363827-40363877	BJ	skin:	n/a
19	chr13:40325939-40325989	HUVEC	blood vessel:	n/a
20	chr13:40230217-40230267	GM12878	blood:	n/a
21	chr13:40229780-40229830	GM19239	blood:	n/a
22	chr13:40233555-40233605	GM06990	blood:	n/a
23	chr13:40230077-40230127	GM06990	blood:	n/a
24	chr13:40228485-40228535	NHDF-neo	bronchial:	n/a
25	chr13:40226031-40226081	SK-N-MC	brain:	n/a
26	chr13:40228485-40228535	RPTEC	kidney:	n/a
27	chr13:40230217-40230267	AG04449	skin:	fetal
28	chr13:40363827-40363877	HUVEC	blood vessel:	n/a
29	chr13:40230022-40230072	PFSK-1	brain:	n/a
30	chr13:40226031-40226081	GM12891	blood:	n/a
31	chr13:40229707-40229757	PrEC	prostate:	n/a
32	chr13:40228485-40228535	K562	blood:	n/a
33	chr13:40363827-40363877	HIPEpiC	eye:	n/a
34	chr13:40363827-40363877	HPAEpiC	pulmonary alveolar:	n/a
35	chr13:40229878-40229928	NT2-D1	testis:	n/a
36	chr13:40229780-40229830	T-47D	breast:	n/a
37	chr13:40229878-40229928	U87	brain:	n/a
38	chr13:40325939-40325989	T-47D	breast:	n/a
39	chr13:40233555-40233605	AoSMC	blood vessel:	n/a
40	chr13:40229707-40229757	HepG2	liver:	n/a
41	chr13:40363827-40363877	PFSK-1	brain:	n/a
42	chr13:40226031-40226081	GM12892	blood:	n/a
43	chr13:40230077-40230127	HRCEpiC	kidney:	n/a
44	chr13:40230217-40230267	NB4	blood:	n/a
45	chr13:40230022-40230072	HNPCEpiC	eye:	n/a
46	chr13:40325939-40325989	GM06990	blood:	n/a
47	chr13:40229707-40229757	HRPEpiC	eye:	n/a
48	chr13:40226031-40226081	HCPEpiC	choroid plexus:	n/a
49	chr13:40229853-40229903	AG10803	skin:	n/a
50	chr13:40363827-40363877	NH-A	brain:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:40229027..40231888-chr13:40233465..40236904,4	MCF-7	breast:
2	chr13:40349248..40350752-chr13:41344020..41346208,2	MCF-7	breast:
3	chr13:40377104..40378017-chr13:40386019..40386823,2	MCF-7	breast:
4	chr13:39847871..39848539-chr13:40250173..40250781,3	MCF-7	breast:
5	chr13:40357238..40358196-chr13:40516595..40517557,4	MCF-7	breast:
6	chr1:117012175..117013114-chr13:40259566..40260123,2	MCF-7	breast:
7	chr13:40263482..40266386-chr13:40274565..40277174,2	MCF-7	breast:
8	chr13:40240996..40242613-chr13:40266490..40268729,2	K562	blood:
9	chr13:40239269..40240269-chr5:179640269..179641206,2	MCF-7	breast:
10	chr13:40343415..40346498-chr13:40346695..40349589,3	MCF-7	breast:
11	chr13:40334982..40337230-chr13:40339387..40341631,2	MCF-7	breast:
12	chr13:40376872..40378665-chr13:40381947..40384768,2	MCF-7	breast:
13	chr13:40229934..40232193-chr13:40232512..40234424,2	K562	blood:
14	chr13:40351481..40352302-chr13:40516672..40517376,4	MCF-7	breast:
15	chr13:40350876..40353001-chr13:41230658..41232496,2	MCF-7	breast:
16	chr13:40338587..40340138-chr13:40344634..40347298,2	MCF-7	breast:
17	chr13:40351756..40352604-chr13:41257334..41257872,2	MCF-7	breast:
18	chr13:40186335..40189130-chr13:40244428..40247026,2	MCF-7	breast:
19	chr13:40228867..40231362-chr13:40235168..40238124,3	MCF-7	breast:
20	chr13:40373278..40375392-chr13:40388471..40390107,2	MCF-7	breast:
21	chr13:40343415..40346498-chr13:40346695..40349589,3	MCF-7	breast:
22	chr13:40229027..40231888-chr13:40233465..40236904,4	MCF-7	breast:
23	chr13:40304256..40306773-chr13:40312127..40313886,2	MCF-7	breast:
24	chr13:39719246..39719808-chr13:40250140..40251135,2	K562	blood:
25	chr13:40338587..40340138-chr13:40344634..40347298,2	MCF-7	breast:
26	chr13:40356532..40358083-chr13:40516675..40517859,10	MCF-7	breast:
27	chr13:40258417..40259279-chr13:40516669..40517542,3	K562	blood:
28	chr13:40355682..40357297-chr13:41239680..41242303,2	MCF-7	breast:
29	chr13:40352027..40354218-chr13:40364182..40366415,2	MCF-7	breast:
30	chr13:40349745..40352056-chr13:40357324..40359153,2	MCF-7	breast:
31	chr13:40349745..40352056-chr13:40357324..40359153,2	MCF-7	breast:
32	chr13:40356408..40358571-chr13:40377020..40378591,2	MCF-7	breast:
33	chr13:40304256..40306773-chr13:40312127..40313886,2	MCF-7	breast:
34	chr13:40297835..40300183-chr13:40302269..40304121,2	MCF-7	breast:
35	chr13:40357398..40357912-chr13:41255037..41255911,2	MCF-7	breast:
36	chr13:40359904..40361413-chr13:40364504..40366595,2	MCF-7	breast:
37	chr13:40356408..40358571-chr13:40377020..40378591,2	MCF-7	breast:
38	chr13:40235362..40236092-chr14:53549695..53550409,2	MCF-7	breast:
39	chr13:40297835..40300183-chr13:40302269..40304121,2	MCF-7	breast:
40	chr13:40334982..40337230-chr13:40339387..40341631,2	MCF-7	breast:
41	chr13:40359904..40361413-chr13:40364504..40366595,2	MCF-7	breast:
42	chr13:40269987..40272885-chr13:41343744..41345569,2	MCF-7	breast:
43	chr13:40339648..40340487-chr13:40516980..40517545,3	MCF-7	breast:
44	chr13:40355345..40357522-chr13:41236727..41239020,2	MCF-7	breast:
45	chr13:40263482..40266386-chr13:40274565..40277174,2	MCF-7	breast:
46	chr13:40339835..40340612-chr13:41351236..41351869,2	MCF-7	breast:
47	chr13:40276171..40277739-chr8:64083128..64085038,2	MCF-7	breast:
48	chr13:40240996..40242613-chr13:40266490..40268729,2	K562	blood:
49	chr13:40258206..40259608-chr13:41351110..41352030,5	MCF-7	breast:
50	chr13:40224809..40226726-chr13:40227987..40229515,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4305	chr13:40238245-40238262	MIMAT0016857

No data

Variant related genes	Relation type
ENSG00000216014	TF binding region
COG6	TF binding region
RNY4P14	TF binding region
MIR4305	TF binding region
ENSG00000216014	CpG island
COG6	CpG island
RNY4P14	CpG island
MIR4305	CpG island
ENSG00000216014	chromatin interactions
ENSG00000133103	chromatin interactions
ENSG00000150907	chromatin interactions
ENSG00000102738	chromatin interactions

Extended variants
information (count: 5729 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:5729 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565045364	chr13:40222914-40222915	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs530869352	chr13:40222922-40222923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200727640	chr13:40222980-40222981	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188829499	chr13:40223001-40223002	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs555985122	chr13:40225150-40225151	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs370015501	chr13:40225151-40225152	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs4278626	chr13:40225157-40225158	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs373192697	chr13:40225173-40225174	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs9576879	chr13:40225174-40225175	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs35235796	chr13:40225223-40225224	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs368266201	chr13:40225239-40225240	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs186742860	chr13:40225243-40225244	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs572031536	chr13:40225246-40225247	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs541317407	chr13:40225247-40225248	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs12430573	chr13:40225250-40225251	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs114445297	chr13:40225253-40225254	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs533495428	chr13:40225258-40225259	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs544027903	chr13:40225289-40225290	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs4415900	chr13:40225327-40225328	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs35881310	chr13:40225349-40225350	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs529370972	chr13:40225350-40225351	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs534489690	chr13:40225389-40225390	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs528621841	chr13:40226031-40226032	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs566656484	chr13:40226059-40226060	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
25	rs551727671	chr13:40226081-40226082	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
26	rs376114795	chr13:40226110-40226111	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs549687778	chr13:40226212-40226213	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs150870324	chr13:40226268-40226269	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs139360497	chr13:40226281-40226282	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs113355638	chr13:40227360-40227361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552144922	chr13:40227423-40227424	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs4268631	chr13:40227431-40227432	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs372864308	chr13:40227473-40227474	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs528298352	chr13:40227523-40227524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs71425713	chr13:40227548-40227549	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs538865684	chr13:40227565-40227566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549029043	chr13:40227580-40227581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150971670	chr13:40227624-40227625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528282978	chr13:40227642-40227643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375805304	chr13:40227649-40227650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571360691	chr13:40227720-40227721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140835267	chr13:40227753-40227754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552424269	chr13:40227780-40227781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9566464	chr13:40227787-40227788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs9532410	chr13:40227801-40227802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs144130381	chr13:40227827-40227828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114185049	chr13:40227833-40227834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144822682	chr13:40227862-40227863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574851225	chr13:40227886-40227887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558104745	chr13:40227890-40227891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	19242612	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
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	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
Ovarian cancer	22355333	CNVD
Glioma	17146433	CNVD
Malignant glioma	17146433	CNVD
Sudden cardiac death	19188705	CNVD
Primary mediastinal b-cell lymphoma	17728785	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2559 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40227400-40229400	Weak transcription	Aorta	Aorta
2	chr13:40228800-40229400	Weak transcription	Thymus	Thymus
3	chr13:40229000-40229200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr13:40229000-40229200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr13:40229000-40229200	Active TSS	Primary T helper cells PMA-I stimulated	--
6	chr13:40229000-40229200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr13:40229000-40229200	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr13:40229000-40229200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr13:40229000-40229200	Enhancers	Adipose Nuclei	Adipose
10	chr13:40229000-40229200	Enhancers	Brain Cingulate Gyrus	brain
11	chr13:40229000-40229200	Enhancers	Fetal Lung	lung
12	chr13:40229000-40229200	Enhancers	Rectal Smooth Muscle	rectum
13	chr13:40229000-40229200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr13:40229000-40229200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr13:40229000-40229200	Enhancers	GM12878-XiMat	blood
16	chr13:40229000-40229200	Enhancers	HepG2	liver
17	chr13:40229000-40229200	Enhancers	K562	blood
18	chr13:40229000-40229200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr13:40229000-40229200	Enhancers	NHEK	skin
20	chr13:40229000-40229200	Enhancers	NHLF	lung
21	chr13:40229000-40229200	Enhancers	Osteobl	bone
22	chr13:40229000-40229400	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr13:40229000-40230400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:40229200-40229400	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr13:40229200-40229400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr13:40229200-40229400	Enhancers	Primary B cells from peripheral blood	blood
27	chr13:40229200-40229400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr13:40229200-40229400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr13:40229200-40229400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
30	chr13:40229200-40229400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr13:40229200-40229400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr13:40229200-40229400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr13:40229200-40229400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr13:40229200-40229400	Enhancers	Brain Angular Gyrus	brain
35	chr13:40229200-40229400	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr13:40229200-40229400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr13:40229200-40229400	Enhancers	Hela-S3	cervix
38	chr13:40229200-40229400	Enhancers	HMEC	breast
39	chr13:40229200-40229400	Enhancers	NHDF-Ad	bronchial
40	chr13:40229200-40229600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr13:40229200-40229600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:40229200-40229600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr13:40229200-40229600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr13:40229200-40229600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr13:40229200-40229600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr13:40229200-40229600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:40229200-40229600	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr13:40229200-40229600	Flanking Active TSS	Brain Cingulate Gyrus	brain
49	chr13:40229200-40229600	Flanking Active TSS	Fetal Brain Male	brain
50	chr13:40229200-40229600	Flanking Active TSS	Fetal Lung	lung

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