Variant report

Variant	nsv520629
Chromosome Location	chr1:77584846-77695854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1173)
CpG islands
(count:672)
Chromatin interactive
region (count:46)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:77613782-77614272	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:77685466-77685797	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:77613911-77614236	K562	blood:	n/a	n/a
4	ARID3A	chr1:77684893-77685652	K562	blood:	n/a	n/a
5	ARID3A	chr1:77684172-77684460	K562	blood:	n/a	n/a
6	ATF2	chr1:77684775-77685330	GM12878	blood:	n/a	n/a
7	ATF3	chr1:77684926-77685251	HepG2	liver:	n/a	n/a
8	ATF3	chr1:77684887-77685287	K562	blood:	n/a	n/a
9	ATF3	chr1:77684945-77685283	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:77685043-77685293	GM12878	blood:	n/a	n/a
11	ATF3	chr1:77684877-77685303	GM12878	blood:	n/a	n/a
12	ATF3	chr1:77684909-77685300	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr1:77594938-77595150	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:77684646-77685267	K562	blood:	n/a	n/a
15	BHLHE40	chr1:77586774-77586881	K562	blood:	n/a	n/a
16	BHLHE40	chr1:77684666-77685365	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:77663959-77664043	GM12878	blood:	n/a	n/a
18	BRCA1	chr1:77632014-77632036	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:77684238-77685332	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr1:77669841-77670055	K562	blood:	n/a	n/a
21	CBX3	chr1:77640999-77641328	HCT-116	colon:	n/a	n/a
22	CBX3	chr1:77642990-77643270	K562	blood:	n/a	n/a
23	CBX3	chr1:77669783-77670105	K562	blood:	n/a	n/a
24	CBX3	chr1:77684888-77685319	K562	blood:	n/a	n/a
25	CCNT2	chr1:77684886-77685269	K562	blood:	n/a	n/a
26	CEBPB	chr1:77684844-77685415	GM12878	blood:	n/a	n/a
27	CEBPB	chr1:77662923-77663240	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:77647795-77648104	K562	blood:	n/a	n/a
29	CEBPB	chr1:77662915-77663277	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:77684986-77685282	A549	lung:	n/a	n/a
31	CEBPB	chr1:77649567-77649769	A549	lung:	n/a	n/a
32	CEBPB	chr1:77662932-77663203	A549	lung:	n/a	n/a
33	CEBPB	chr1:77647763-77648160	A549	lung:	n/a	n/a
34	CEBPB	chr1:77628165-77628467	K562	blood:	n/a	chr1:77628291-77628300 chr1:77628291-77628300 chr1:77628289-77628302 chr1:77628291-77628300 chr1:77628291-77628302 chr1:77628286-77628303 chr1:77628291-77628300 chr1:77628289-77628300 chr1:77628289-77628302
35	CEBPB	chr1:77685000-77685308	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:77684971-77685335	K562	blood:	n/a	n/a
37	CEBPB	chr1:77684493-77685370	Hela-S3	cervix:	n/a	chr1:77684503-77684516
38	CEBPB	chr1:77686365-77686777	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:77647824-77648070	A549	lung:	n/a	n/a
40	CEBPB	chr1:77685005-77685313	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:77684905-77685275	K562	blood:	n/a	n/a
42	CEBPB	chr1:77647779-77648127	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:77647762-77648143	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:77686413-77686747	A549	lung:	n/a	n/a
45	CEBPB	chr1:77647780-77648132	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:77661555-77661636	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:77675454-77675526	K562	blood:	n/a	n/a
48	CEBPB	chr1:77662914-77663269	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:77595543-77595567	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:77684998-77685272	H1-hESC	embryonic stem cell:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77683411-77683461	NB4	blood:	n/a
2	chr1:77683411-77683461	NB4	blood:	n/a
3	chr1:77685015-77685065	HMEC	breast:	n/a
4	chr1:77684965-77685015	HEK293	kidney:	embryo
5	chr1:77685229-77685279	PANC-1	pancreas:	n/a
6	chr1:77685150-77685200	NHDF-neo	bronchial:	n/a
7	chr1:77685150-77685200	HEK293	kidney:	embryo
8	chr1:77685251-77685301	AoSMC	blood vessel:	n/a
9	chr1:77685062-77685112	NHDF-neo	bronchial:	n/a
10	chr1:77683411-77683461	HIPEpiC	eye:	n/a
11	chr1:77685015-77685065	AG04449	skin:	fetal
12	chr1:77685062-77685112	HCPEpiC	choroid plexus:	n/a
13	chr1:77683411-77683461	HRE	kidney:	n/a
14	chr1:77681561-77681611	SK-N-SH_RA	brain:	n/a
15	chr1:77684965-77685015	MCF-7	breast:	n/a
16	chr1:77684965-77685015	HCT-116	colon:	n/a
17	chr1:77685135-77685185	GM19239	blood:	n/a
18	chr1:77685094-77685144	HEK293	kidney:	embryo
19	chr1:77685135-77685185	HAEpiC	amniotic membrane:	n/a
20	chr1:77685150-77685200	GM12878	blood:	n/a
21	chr1:77685015-77685065	Caco-2	colon:	n/a
22	chr1:77681561-77681611	Hela-S3	cervix:	n/a
23	chr1:77683411-77683461	NHBE	bronchial:	n/a
24	chr1:77685229-77685279	HCT-116	colon:	n/a
25	chr1:77688131-77688181	HRE	kidney:	n/a
26	chr1:77685150-77685200	HIPEpiC	eye:	n/a
27	chr1:77685251-77685301	HCF	heart:	n/a
28	chr1:77685135-77685185	NHBE	bronchial:	n/a
29	chr1:77685062-77685112	HIPEpiC	eye:	n/a
30	chr1:77685229-77685279	K562	blood:	n/a
31	chr1:77683411-77683461	SAEC	small airway:	n/a
32	chr1:77685015-77685065	HNPCEpiC	eye:	n/a
33	chr1:77685062-77685112	HEEpiC	esophagus:	n/a
34	chr1:77688131-77688181	MCF10A-Er-Src	breast:	n/a
35	chr1:77685135-77685185	AG04449	skin:	fetal
36	chr1:77685062-77685112	PFSK-1	brain:	n/a
37	chr1:77685062-77685112	HNPCEpiC	eye:	n/a
38	chr1:77684965-77685015	NT2-D1	testis:	n/a
39	chr1:77684965-77685015	NB4	blood:	n/a
40	chr1:77685251-77685301	ProgFib	skin:	n/a
41	chr1:77688131-77688181	HCT-116	colon:	n/a
42	chr1:77685094-77685144	AG09319	gingival:	n/a
43	chr1:77685251-77685301	HCPEpiC	choroid plexus:	n/a
44	chr1:77685015-77685065	HCM	heart:	n/a
45	chr1:77685135-77685185	HCF	heart:	n/a
46	chr1:77685251-77685301	GM06990	blood:	n/a
47	chr1:77685094-77685144	HAEpiC	amniotic membrane:	n/a
48	chr1:77685251-77685301	AG09309	skin:	n/a
49	chr1:77685229-77685279	HNPCEpiC	eye:	n/a
50	chr1:77681561-77681611	HUVEC	blood vessel:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:77669001..77671084-chr1:77671530..77674115,2	MCF-7	breast:
2	chr1:77679203..77681796-chr1:77682341..77684705,2	K562	blood:
3	chr1:77668693..77669518-chr4:102182394..102183036,2	HCT-116	colon:
4	chr1:77679203..77681796-chr1:77682341..77684705,2	K562	blood:
5	chr1:77673903..77675950-chr1:77678224..77680465,2	K562	blood:
6	chr1:77366569..77367440-chr1:77591672..77592573,4	MCF-7	breast:
7	chr1:77684670..77686781-chr1:77746398..77749229,3	MCF-7	breast:
8	chr1:77629370..77632144-chr1:77633203..77635072,2	K562	blood:
9	chr1:76796389..76797022-chr1:77608917..77609894,2	MCF-7	breast:
10	chr1:77690590..77694353-chr1:77694495..77697779,4	K562	blood:
11	chr1:77613856..77614476-chr1:77778903..77779788,3	MCF-7	breast:
12	chr1:77598635..77600352-chr1:77601887..77604613,2	K562	blood:
13	chr1:77613814..77614601-chr1:78366080..78366641,2	K562	blood:
14	chr1:77679355..77682217-chr1:77684388..77686382,2	MCF-7	breast:
15	chr1:77684564..77687850-chr1:77688271..77692443,7	K562	blood:
16	chr1:77690590..77694353-chr1:77694495..77697779,4	K562	blood:
17	chr1:77598635..77600352-chr1:77601887..77604613,2	K562	blood:
18	chr1:77584058..77586581-chr1:77589256..77592005,2	MCF-7	breast:
19	chr1:77577767..77579951-chr1:77584279..77585797,2	K562	blood:
20	chr1:77667810..77669464-chr1:78468632..78471293,2	K562	blood:
21	chr1:77673903..77675950-chr1:77678224..77680465,2	K562	blood:
22	chr1:77694564..77696510-chr1:77698043..77700950,2	K562	blood:
23	chr1:76796470..76797076-chr1:77591559..77592349,2	MCF-7	breast:
24	chr1:77677708..77680059-chr1:77682131..77685030,3	K562	blood:
25	chr1:77684507..77685215-chr5:44808668..44809523,2	Hela-S3	cervix:
26	chr1:77578497..77580194-chr1:77590857..77592378,2	K562	blood:
27	chr1:77677424..77679474-chr1:77687776..77689660,2	K562	blood:
28	chr1:76619799..76620863-chr1:77591812..77592540,5	K562	blood:
29	chr1:76619528..76620590-chr1:77591988..77592713,3	MCF-7	breast:
30	chr1:76796476..76797352-chr1:77609351..77609861,2	K562	blood:
31	chr1:77579749..77582722-chr1:77596983..77598740,2	K562	blood:
32	chr1:77677424..77679474-chr1:77687776..77689660,2	K562	blood:
33	chr1:77630135..77632274-chr1:77634980..77637594,3	K562	blood:
34	chr1:77366245..77367518-chr1:77591630..77592525,3	K562	blood:
35	chr1:77676621..77679098-chr1:77684360..77686793,2	K562	blood:
36	chr1:77677708..77680059-chr1:77682131..77685030,3	K562	blood:
37	chr1:77584058..77586581-chr1:77589256..77592005,2	MCF-7	breast:
38	chr1:76619537..76620481-chr1:77608892..77609886,3	K562	blood:
39	chr1:77656179..77658700-chr1:77659686..77662553,2	K562	blood:
40	chr1:77606929..77608436-chr1:77608515..77611448,2	MCF-7	breast:
41	chr1:77669001..77671084-chr1:77671530..77674115,2	MCF-7	breast:
42	chr1:77674234..77675786-chr1:77815270..77816932,2	K562	blood:
43	chr1:77613628..77614149-chr1:78580241..78580790,2	K562	blood:
44	chr1:77606929..77608436-chr1:77608515..77611448,2	MCF-7	breast:
45	chr1:77682598..77685827-chr1:77690810..77693587,3	K562	blood:
46	chr1:77661332..77664043-chr1:77683749..77686209,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AK5-2	chr1:77692452-77694222	NONHSAT004025
2	lnc-PIGK-3	chr1:77690411-77690647	NONHSAT004024
3	lnc-AK5-1	chr1:77685227-77685338	XLOC_000263
4	lnc-AK5-1	chr1:77686768-77686969	XLOC_000263
5	lnc-AK5-1	chr1:77686286-77690011	NONHSAT004022
6	lnc-AK5-1	chr1:77686609-77686678	XLOC_000263
7	lnc-AK5-1	chr1:77686473-77686671	XLOC_000263

No data

Variant related genes	Relation type
PIGK	TF binding region
ENSG00000226084	TF binding region
ENSG00000228187	TF binding region
PIGK	CpG island
ENSG00000226084	CpG island
ENSG00000228187	CpG island
ENSG00000142892	chromatin interactions
ENSG00000228187	chromatin interactions
ENSG00000273338	chromatin interactions
ENSG00000251141	chromatin interactions
ENSG00000233099	chromatin interactions
ENSG00000154027	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000112996	chromatin interactions
RBM8A	miRNA target sites
RBM6	miRNA target sites

Extended variants
information (count: 3889 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3889 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7522008	chr1:77584846-77584847	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566843029	chr1:77584857-77584858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72681893	chr1:77584863-77584864	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559007349	chr1:77584916-77584917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576880273	chr1:77584921-77584922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537957233	chr1:77584940-77584941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189485303	chr1:77584968-77584969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574713502	chr1:77584983-77584984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542486489	chr1:77585017-77585018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560653654	chr1:77585095-77585096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570701706	chr1:77585096-77585097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74092420	chr1:77585111-77585112	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs180746980	chr1:77585175-77585176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570308371	chr1:77585178-77585179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531402545	chr1:77585213-77585214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549926732	chr1:77585218-77585219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373837336	chr1:77585244-77585245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114704683	chr1:77585259-77585260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187569963	chr1:77585297-77585298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539213389	chr1:77585448-77585449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115664272	chr1:77585486-77585487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539724760	chr1:77585491-77585492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552246883	chr1:77585522-77585523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34052737	chr1:77585523-77585524	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537919986	chr1:77585524-77585525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11268937	chr1:77585553-77585554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200341308	chr1:77585574-77585575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201554068	chr1:77585575-77585576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112375028	chr1:77585612-77585613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568297244	chr1:77585664-77585665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535708661	chr1:77585674-77585675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541681793	chr1:77585705-77585706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554442072	chr1:77585741-77585742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572602170	chr1:77585754-77585755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546493925	chr1:77585759-77585760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557760949	chr1:77585886-77585887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576137980	chr1:77585923-77585924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189393044	chr1:77585981-77585982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181709235	chr1:77586029-77586030	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529082843	chr1:77586050-77586051	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540823261	chr1:77586093-77586094	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553490147	chr1:77586113-77586114	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559510185	chr1:77586114-77586115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573536843	chr1:77586123-77586124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7522727	chr1:77586190-77586191	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551283192	chr1:77586192-77586193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570490630	chr1:77586193-77586194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112734382	chr1:77586212-77586213	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549851582	chr1:77586224-77586225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190435278	chr1:77586227-77586228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77556000-77614400	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr1:77568600-77595600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:77570800-77596800	Weak transcription	Left Ventricle	heart
4	chr1:77573400-77591200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:77574200-77588400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:77574400-77613800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr1:77575000-77604000	Weak transcription	Primary B cells from cord blood	blood
8	chr1:77575800-77588200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:77576800-77591400	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:77578600-77607800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:77579800-77614200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr1:77581800-77587800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr1:77581800-77599200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr1:77582400-77596400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:77583000-77598400	Weak transcription	Ovary	ovary
16	chr1:77583600-77586000	Weak transcription	Primary T cells from cord blood	blood
17	chr1:77584400-77585600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:77585200-77587600	Weak transcription	Dnd41	blood
19	chr1:77585600-77619400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:77585800-77587200	Enhancers	Fetal Brain Female	brain
21	chr1:77585800-77588000	Enhancers	Fetal Brain Male	brain
22	chr1:77586000-77586400	Strong transcription	Primary T cells from cord blood	blood
23	chr1:77586000-77586400	Enhancers	Brain Germinal Matrix	brain
24	chr1:77586400-77587200	Weak transcription	Brain Germinal Matrix	brain
25	chr1:77586400-77620600	Weak transcription	Primary T cells from cord blood	blood
26	chr1:77586600-77587400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:77586600-77587400	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:77586600-77587600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr1:77586600-77588000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:77586800-77587000	Enhancers	HSMM	muscle
31	chr1:77586800-77588000	Enhancers	Liver	Liver
32	chr1:77587000-77594600	Weak transcription	HSMM	muscle
33	chr1:77587200-77588000	Enhancers	Brain Germinal Matrix	brain
34	chr1:77588000-77590000	Weak transcription	Brain Germinal Matrix	brain
35	chr1:77588000-77591400	Weak transcription	Fetal Brain Male	brain
36	chr1:77589200-77589400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr1:77590400-77590600	Enhancers	Brain Germinal Matrix	brain
38	chr1:77591200-77601000	Weak transcription	Psoas Muscle	Psoas
39	chr1:77591400-77591600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr1:77591600-77591800	Enhancers	Fetal Brain Male	brain
41	chr1:77591600-77592000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr1:77591600-77592400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr1:77592000-77592200	Active TSS	Monocytes-CD14+_RO01746	blood
44	chr1:77592200-77592400	Enhancers	Aorta	Aorta
45	chr1:77592200-77623600	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr1:77592400-77604800	Weak transcription	Aorta	Aorta
47	chr1:77595400-77640400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr1:77596400-77597200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr1:77597200-77624200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr1:77599200-77600200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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