Variant report

Variant	nsv870621
Chromosome Location	chr1:76620313-76997071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1472)
CpG islands
(count:854)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1472 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:76796829-76797028	K562	blood:	n/a	n/a
2	ATF1	chr1:76705377-76705512	K562	blood:	n/a	n/a
3	ATF3	chr1:76719813-76720341	HCT-116	colon:	n/a	n/a
4	BATF	chr1:76657324-76657519	GM12878	blood:	n/a	n/a
5	BATF	chr1:76760142-76760428	GM12878	blood:	n/a	n/a
6	BATF	chr1:76960412-76960867	GM12878	blood:	n/a	n/a
7	BATF	chr1:76760090-76760529	GM12878	blood:	n/a	n/a
8	BATF	chr1:76928925-76929273	GM12878	blood:	n/a	n/a
9	BATF	chr1:76736152-76736451	GM12878	blood:	n/a	n/a
10	BATF	chr1:76960469-76960865	GM12878	blood:	n/a	n/a
11	BATF	chr1:76736134-76736451	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:76656518-76656710	GM12878	blood:	n/a	chr1:76656576-76656585
13	BHLHE40	chr1:76745095-76745436	HepG2	liver:	n/a	chr1:76745276-76745289 chr1:76745329-76745345 chr1:76745337-76745353 chr1:76745272-76745293 chr1:76745279-76745288
14	BHLHE40	chr1:76960390-76960674	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:76745098-76745399	K562	blood:	n/a	chr1:76745276-76745289 chr1:76745329-76745345 chr1:76745337-76745353 chr1:76745272-76745293 chr1:76745279-76745288
16	BHLHE40	chr1:76619786-76620375	K562	blood:	n/a	n/a
17	BHLHE40	chr1:76619811-76620555	GM12878	blood:	n/a	n/a
18	CBX3	chr1:76734775-76735330	HCT-116	colon:	n/a	n/a
19	CBX3	chr1:76703537-76704426	HCT-116	colon:	n/a	n/a
20	CBX3	chr1:76706078-76706489	HCT-116	colon:	n/a	n/a
21	CBX3	chr1:76719758-76720796	HCT-116	colon:	n/a	chr1:76720185-76720196
22	CBX3	chr1:76796545-76797128	HCT-116	colon:	n/a	n/a
23	CCNT2	chr1:76877130-76877206	K562	blood:	n/a	n/a
24	CEBPB	chr1:76759374-76759643	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:76715171-76715521	IMR90	lung:	n/a	chr1:76715330-76715341
26	CEBPB	chr1:76939310-76939479	H1-hESC	embryonic stem cell:	n/a	chr1:76939449-76939460
27	CEBPB	chr1:76723942-76724300	HepG2	liver:	n/a	chr1:76724228-76724241 chr1:76724027-76724040 chr1:76724029-76724040 chr1:76724027-76724040
28	CEBPB	chr1:76759368-76759663	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:76759472-76759571	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:76686518-76687140	HepG2	liver:	n/a	chr1:76686961-76686974 chr1:76686556-76686569 chr1:76686961-76686972 chr1:76686558-76686569
31	CEBPB	chr1:76773791-76774118	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:76742636-76742920	HepG2	liver:	n/a	chr1:76742757-76742768
33	CEBPB	chr1:76946577-76946857	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:76691273-76691563	IMR90	lung:	n/a	chr1:76691419-76691428 chr1:76691417-76691428
35	CEBPB	chr1:76939402-76939598	HepG2	liver:	n/a	chr1:76939449-76939460
36	CEBPB	chr1:76643385-76643671	HepG2	liver:	n/a	chr1:76643536-76643547
37	CEBPB	chr1:76715185-76715471	HepG2	liver:	n/a	chr1:76715330-76715341
38	CEBPB	chr1:76891368-76891765	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:76719649-76720822	HCT-116	colon:	n/a	n/a
40	CEBPB	chr1:76831025-76831218	HepG2	liver:	n/a	chr1:76831106-76831117
41	CEBPB	chr1:76642430-76642640	HepG2	liver:	n/a	chr1:76642552-76642563
42	CEBPB	chr1:76939345-76939527	A549	lung:	n/a	chr1:76939449-76939460
43	CEBPB	chr1:76728414-76728705	HepG2	liver:	n/a	chr1:76728550-76728561
44	CEBPB	chr1:76802772-76802992	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr1:76691266-76691526	Hela-S3	cervix:	n/a	chr1:76691419-76691428 chr1:76691417-76691428
46	CEBPB	chr1:76899228-76899474	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:76892461-76892516	A549	lung:	n/a	n/a
48	CEBPB	chr1:76802693-76803049	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:76784975-76785274	IMR90	lung:	n/a	chr1:76785133-76785144
50	CEBPB	chr1:76723934-76724252	A549	lung:	n/a	chr1:76724228-76724241 chr1:76724027-76724040 chr1:76724029-76724040 chr1:76724027-76724040

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76620271-76620321	Jurkat	blood:	n/a
2	chr1:76734569-76734619	LNCaP	prostate:	n/a
3	chr1:76782984-76783034	A549	lung:	n/a
4	chr1:76891398-76891448	Hela-S3	cervix:	n/a
5	chr1:76968506-76968556	MCF10A-Er-Src	breast:	n/a
6	chr1:76782984-76783034	HNPCEpiC	eye:	n/a
7	chr1:76734569-76734619	HMEC	breast:	n/a
8	chr1:76782984-76783034	MCF10A-Er-Src	breast:	n/a
9	chr1:76976572-76976622	CMK	blood:	n/a
10	chr1:76723043-76723093	K562	blood:	n/a
11	chr1:76782984-76783034	GM12878	blood:	n/a
12	chr1:76891398-76891448	U87	brain:	n/a
13	chr1:76704467-76704517	SAEC	small airway:	n/a
14	chr1:76780549-76780599	HRCEpiC	kidney:	n/a
15	chr1:76780549-76780599	PFSK-1	brain:	n/a
16	chr1:76734569-76734619	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:76968506-76968556	HRCEpiC	kidney:	n/a
18	chr1:76976572-76976622	Jurkat	blood:	n/a
19	chr1:76976572-76976622	HEK293	kidney:	embryo
20	chr1:76976572-76976622	HL-60	blood:	n/a
21	chr1:76761200-76761250	HAEpiC	amniotic membrane:	n/a
22	chr1:76695186-76695236	Hepatocyte	liver:	n/a
23	chr1:76782984-76783034	Hela-S3	cervix:	n/a
24	chr1:76723043-76723093	ECC-1	luminal epithelium:	n/a
25	chr1:76891398-76891448	GM12891	blood:	n/a
26	chr1:76723043-76723093	SK-N-MC	brain:	n/a
27	chr1:76723043-76723093	HIPEpiC	eye:	n/a
28	chr1:76891398-76891448	BE2_C	brain:	n/a
29	chr1:76734569-76734619	GM12891	blood:	n/a
30	chr1:76620271-76620321	T-47D	breast:	n/a
31	chr1:76817670-76817720	K562	blood:	n/a
32	chr1:76817670-76817720	IMR90	lung:	fetal
33	chr1:76840032-76840082	BE2_C	brain:	n/a
34	chr1:76704467-76704517	HepG2	liver:	n/a
35	chr1:76891398-76891448	HUVEC	blood vessel:	n/a
36	chr1:76780549-76780599	HL-60	blood:	n/a
37	chr1:76968506-76968556	HMEC	breast:	n/a
38	chr1:76620271-76620321	AG04450	lung:	fetal
39	chr1:76704467-76704517	HNPCEpiC	eye:	n/a
40	chr1:76899846-76899896	K562	blood:	n/a
41	chr1:76723043-76723093	PFSK-1	brain:	n/a
42	chr1:76734569-76734619	HL-60	blood:	n/a
43	chr1:76695186-76695236	HCT-116	colon:	n/a
44	chr1:76734569-76734619	BJ	skin:	n/a
45	chr1:76704467-76704517	HCM	heart:	n/a
46	chr1:76620271-76620321	HCF	heart:	n/a
47	chr1:76780549-76780599	HCM	heart:	n/a
48	chr1:76723043-76723093	ProgFib	skin:	n/a
49	chr1:76620271-76620321	GM19239	blood:	n/a
50	chr1:76723043-76723093	NHDF-neo	bronchial:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76756888..76759692-chr1:76896597..76899350,2	K562	blood:
2	chr1:76456960..76457802-chr1:76619597..76620478,2	K562	blood:
3	chr1:76655272..76656892-chr1:76697191..76699562,2	K562	blood:
4	chr1:76884483..76887341-chr1:76890524..76892236,2	MCF-7	breast:
5	chr1:76756888..76759692-chr1:76896597..76899350,2	K562	blood:
6	chr1:76620098..76620620-chr1:76796654..76797328,2	MCF-7	breast:
7	chr1:76796470..76797076-chr1:77591559..77592349,2	MCF-7	breast:
8	chr1:76619950..76620589-chr1:78579803..78580325,2	K562	blood:
9	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
10	chr1:76741759..76743474-chr1:76745342..76747848,2	K562	blood:
11	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
12	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
13	chr1:76684523..76686317-chr1:76687873..76689608,2	K562	blood:
14	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
15	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
16	chr1:76884483..76887341-chr1:76890524..76892236,2	MCF-7	breast:
17	chr1:76741759..76743474-chr1:76745342..76747848,2	K562	blood:
18	chr1:76619537..76620481-chr1:77608892..77609886,3	K562	blood:
19	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
20	chr1:76619553..76620451-chr1:77999109..77999974,2	K562	blood:
21	chr1:76620098..76620620-chr1:76796654..76797328,2	MCF-7	breast:
22	chr1:76619528..76620590-chr1:77591988..77592713,3	MCF-7	breast:
23	chr1:76796528..76797295-chr1:77206308..77207068,2	MCF-7	breast:
24	chr1:76813366..76816327-chr1:76818310..76820003,2	K562	blood:
25	chr1:76758604..76761482-chr1:76764775..76767017,2	K562	blood:
26	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
27	chr1:76885764..76887919-chr1:76891776..76893368,2	K562	blood:
28	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
29	chr1:76739718..76741247-chr1:76741551..76743104,2	K562	blood:
30	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
31	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
32	chr1:76619661..76620511-chr1:77549962..77550737,2	MCF-7	breast:
33	chr1:76655272..76656892-chr1:76697191..76699562,2	K562	blood:
34	chr1:76796476..76797352-chr1:77609351..77609861,2	K562	blood:
35	chr1:76758604..76761482-chr1:76764775..76767017,2	K562	blood:
36	chr1:76619799..76620863-chr1:77591812..77592540,5	K562	blood:
37	chr1:76741346..76744130-chr1:76749152..76752097,2	K562	blood:
38	chr1:76871350..76874295-chr1:76994896..76997570,2	K562	blood:
39	chr1:76871350..76874295-chr1:76994896..76997570,2	K562	blood:
40	chr1:76741346..76744130-chr1:76749152..76752097,2	K562	blood:
41	chr1:76796406..76797312-chr1:77366615..77367452,3	MCF-7	breast:
42	chr1:76739718..76741247-chr1:76741551..76743104,2	K562	blood:
43	chr1:76885764..76887919-chr1:76891776..76893368,2	K562	blood:
44	chr1:76796389..76797022-chr1:77608917..77609894,2	MCF-7	breast:
45	chr1:76684523..76686317-chr1:76687873..76689608,2	K562	blood:
46	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
47	chr1:76456960..76458188-chr1:76619791..76620471,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB17-2	chr1:76819268-76819931	NONHSAT004012
2	lnc-PIGK-4	chr1:76996553-76996677	NONHSAT004013
3	lnc-PIGK-4	chr1:76996397-76996441	NONHSAT004013

No data

Variant related genes	Relation type
ENSG00000223905	TF binding region
ST6GALNAC3	TF binding region
ENSG00000223905	CpG island
ST6GALNAC3	CpG island
ENSG00000223905	chromatin interactions

Extended variants
information (count: 12928 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:12928 , 50 per page) page: 1 2 3 4 5 6 7 ... 259

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2783658	chr1:76620313-76620314	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192435713	chr1:76620335-76620336	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565507786	chr1:76620367-76620368	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141058592	chr1:76620368-76620369	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183139078	chr1:76620389-76620390	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562982071	chr1:76620402-76620403	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs530101038	chr1:76620431-76620432	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs548332536	chr1:76620459-76620460	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs567532611	chr1:76620488-76620489	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs138921181	chr1:76620530-76620531	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs188431810	chr1:76620572-76620573	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs546510993	chr1:76620603-76620604	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs74643559	chr1:76620668-76620669	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs193029106	chr1:76620694-76620695	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs556591324	chr1:76620715-76620716	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs575043879	chr1:76620727-76620728	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs536236630	chr1:76620736-76620737	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531520920	chr1:76620753-76620754	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs545005576	chr1:76620777-76620778	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184781590	chr1:76620848-76620849	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs540545350	chr1:76620896-76620897	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs565595855	chr1:76620902-76620903	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs577474948	chr1:76620917-76620918	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs34707336	chr1:76620931-76620932	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368866779	chr1:76620962-76620963	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs562959440	chr1:76620969-76620970	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs75587116	chr1:76620986-76620987	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs375574641	chr1:76621024-76621025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189823691	chr1:76621039-76621040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527700389	chr1:76621047-76621048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569524205	chr1:76621091-76621092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558238343	chr1:76621105-76621106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191575459	chr1:76621149-76621150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538443115	chr1:76621215-76621216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550403065	chr1:76621216-76621217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527701721	chr1:76621278-76621279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535992011	chr1:76621432-76621433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375904186	chr1:76621450-76621451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572718615	chr1:76621457-76621458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533796042	chr1:76621475-76621476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555165125	chr1:76621515-76621516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369084681	chr1:76621532-76621533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577650201	chr1:76621585-76621586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372008461	chr1:76621625-76621626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575117412	chr1:76621642-76621643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183719541	chr1:76621647-76621648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556820480	chr1:76621686-76621687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs427172	chr1:76621769-76621770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567425249	chr1:76621770-76621771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs202023258	chr1:76621797-76621798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2365 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76616400-76623600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:76619600-76620400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:76619600-76620400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:76619800-76620600	Enhancers	H1 Cell Line	embryonic stem cell
5	chr1:76619800-76620600	Flanking Active TSS	Brain Cingulate Gyrus	brain
6	chr1:76619800-76620600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:76619800-76620600	Enhancers	Fetal Heart	heart
8	chr1:76619800-76620600	Active TSS	Monocytes-CD14+_RO01746	blood
9	chr1:76619800-76621000	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr1:76619800-76646400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:76620000-76620400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr1:76620000-76620400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:76620000-76620400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr1:76620000-76620400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr1:76620000-76620400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr1:76620000-76620400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr1:76620000-76620400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr1:76620000-76620400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:76620000-76620400	Active TSS	Primary T cells fromperipheralblood	blood
20	chr1:76620000-76620400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:76620000-76620400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:76620000-76620400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr1:76620000-76620400	Flanking Active TSS	Brain Angular Gyrus	brain
24	chr1:76620000-76620400	Flanking Active TSS	Brain Substantia Nigra	brain
25	chr1:76620000-76620400	Flanking Active TSS	Colon Smooth Muscle	Colon
26	chr1:76620000-76620400	Flanking Active TSS	Duodenum Mucosa	Duodenum
27	chr1:76620000-76620400	Active TSS	Fetal Brain Male	brain
28	chr1:76620000-76620400	Active TSS	Lung	lung
29	chr1:76620000-76620400	Active TSS	Ovary	ovary
30	chr1:76620000-76620400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr1:76620000-76620400	Flanking Active TSS	Stomach Mucosa	stomach
32	chr1:76620000-76620400	Flanking Active TSS	Dnd41	blood
33	chr1:76620000-76620600	Flanking Active TSS	Primary B cells from peripheral blood	blood
34	chr1:76620000-76620600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr1:76620000-76620600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr1:76620000-76620600	Active TSS	Primary T helper naive cells from peripheral blood	blood
37	chr1:76620000-76620600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr1:76620000-76620600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr1:76620000-76620600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr1:76620000-76620600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr1:76620000-76620600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
42	chr1:76620000-76620600	Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr1:76620000-76620600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr1:76620000-76620600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr1:76620000-76620600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:76620000-76620600	Flanking Active TSS	Liver	Liver
47	chr1:76620000-76620600	Flanking Active TSS	Brain Germinal Matrix	brain
48	chr1:76620000-76620600	Active TSS	Fetal Brain Female	brain
49	chr1:76620000-76620600	Flanking Active TSS	Fetal Intestine Large	intestine
50	chr1:76620000-76620600	Flanking Active TSS	Fetal Intestine Small	intestine

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