Variant report

Variant	nsv1009063
Chromosome Location	chr3:60067866-60277128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:878)
CpG islands
(count:122)
Chromatin interactive
region (count:77)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:60275766-60275781	K562	blood:	n/a	n/a
2	ARID3A	chr3:60228798-60230202	K562	blood:	n/a	n/a
3	ARID3A	chr3:60251876-60252792	K562	blood:	n/a	n/a
4	ARID3A	chr3:60254542-60255635	K562	blood:	n/a	n/a
5	ARID3A	chr3:60236266-60236623	K562	blood:	n/a	n/a
6	ARID3A	chr3:60089333-60089791	K562	blood:	n/a	n/a
7	ARID3A	chr3:60267195-60267326	K562	blood:	n/a	n/a
8	ARID3A	chr3:60241988-60242170	K562	blood:	n/a	n/a
9	ARID3A	chr3:60080880-60080974	K562	blood:	n/a	n/a
10	ARID3A	chr3:60262560-60263903	K562	blood:	n/a	n/a
11	ATF1	chr3:60175649-60176121	K562	blood:	n/a	n/a
12	ATF1	chr3:60262559-60263531	K562	blood:	n/a	n/a
13	ATF1	chr3:60072608-60072940	K562	blood:	n/a	n/a
14	ATF1	chr3:60255066-60255423	K562	blood:	n/a	n/a
15	ATF2	chr3:60072548-60072961	GM12878	blood:	n/a	n/a
16	ATF2	chr3:60175754-60176100	GM12878	blood:	n/a	n/a
17	ATF2	chr3:60072552-60072929	GM12878	blood:	n/a	n/a
18	ATF3	chr3:60072525-60072862	K562	blood:	n/a	n/a
19	BACH1	chr3:60238886-60239061	K562	blood:	n/a	n/a
20	BACH1	chr3:60241691-60241802	K562	blood:	n/a	n/a
21	BACH1	chr3:60247867-60247880	K562	blood:	n/a	n/a
22	BATF	chr3:60072565-60072906	GM12878	blood:	n/a	chr3:60072719-60072730 chr3:60072749-60072760
23	BATF	chr3:60178290-60178695	GM12878	blood:	n/a	n/a
24	BATF	chr3:60175866-60176100	GM12878	blood:	n/a	chr3:60175916-60175929
25	BATF	chr3:60125935-60126267	GM12878	blood:	n/a	n/a
26	BATF	chr3:60211557-60211749	GM12878	blood:	n/a	chr3:60211654-60211663
27	BATF	chr3:60211442-60211893	GM12878	blood:	n/a	chr3:60211654-60211663
28	BATF	chr3:60178356-60178622	GM12878	blood:	n/a	n/a
29	BATF	chr3:60072622-60072863	GM12878	blood:	n/a	chr3:60072719-60072730 chr3:60072749-60072760
30	BCL11A	chr3:60178284-60178674	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:60178405-60178610	GM12878	blood:	n/a	n/a
32	BCL3	chr3:60178326-60178686	GM12878	blood:	n/a	n/a
33	BCL3	chr3:60211593-60211929	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:60218420-60218449	K562	blood:	n/a	n/a
35	BHLHE40	chr3:60263109-60263909	K562	blood:	n/a	n/a
36	BHLHE40	chr3:60072788-60072959	K562	blood:	n/a	n/a
37	BHLHE40	chr3:60255569-60256068	K562	blood:	n/a	n/a
38	CBX3	chr3:60072440-60073038	HCT-116	colon:	n/a	n/a
39	CBX3	chr3:60263052-60263535	K562	blood:	n/a	n/a
40	CBX3	chr3:60262958-60263663	K562	blood:	n/a	n/a
41	CCNT2	chr3:60255085-60255515	K562	blood:	n/a	n/a
42	CCNT2	chr3:60229234-60229536	K562	blood:	n/a	n/a
43	CCNT2	chr3:60263134-60263501	K562	blood:	n/a	n/a
44	CEBPB	chr3:60242145-60242392	K562	blood:	n/a	n/a
45	CEBPB	chr3:60252121-60252552	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:60122391-60122573	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:60184852-60185115	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:60236669-60236954	K562	blood:	n/a	n/a
49	CEBPB	chr3:60263112-60263724	K562	blood:	n/a	n/a
50	CEBPB	chr3:60252022-60252610	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:60133085-60133135	MCF-7	breast:	n/a
2	chr3:60226328-60226378	HCPEpiC	choroid plexus:	n/a
3	chr3:60226328-60226378	CMK	blood:	n/a
4	chr3:60226328-60226378	Jurkat	blood:	n/a
5	chr3:60133085-60133135	HCPEpiC	choroid plexus:	n/a
6	chr3:60226328-60226378	AG09319	gingival:	n/a
7	chr3:60226328-60226378	HEEpiC	esophagus:	n/a
8	chr3:60226328-60226378	AG04449	skin:	fetal
9	chr3:60133085-60133135	HMEC	breast:	n/a
10	chr3:60226328-60226378	Hepatocyte	liver:	n/a
11	chr3:60133085-60133135	Jurkat	blood:	n/a
12	chr3:60133085-60133135	GM12891	blood:	n/a
13	chr3:60133085-60133135	IMR90	lung:	fetal
14	chr3:60133085-60133135	HCT-116	colon:	n/a
15	chr3:60133085-60133135	Hela-S3	cervix:	n/a
16	chr3:60226328-60226378	HL-60	blood:	n/a
17	chr3:60133085-60133135	HAEpiC	amniotic membrane:	n/a
18	chr3:60226328-60226378	PFSK-1	brain:	n/a
19	chr3:60133085-60133135	GM12878	blood:	n/a
20	chr3:60133085-60133135	CMK	blood:	n/a
21	chr3:60226328-60226378	NB4	blood:	n/a
22	chr3:60226328-60226378	K562	blood:	n/a
23	chr3:60133085-60133135	HIPEpiC	eye:	n/a
24	chr3:60133085-60133135	ProgFib	skin:	n/a
25	chr3:60226328-60226378	ProgFib	skin:	n/a
26	chr3:60133085-60133135	NHDF-neo	bronchial:	n/a
27	chr3:60133085-60133135	U87	brain:	n/a
28	chr3:60133085-60133135	NB4	blood:	n/a
29	chr3:60226328-60226378	H1-hESC	embryonic stem cell:	embryo
30	chr3:60226328-60226378	HRE	kidney:	n/a
31	chr3:60133085-60133135	AG09319	gingival:	n/a
32	chr3:60133085-60133135	K562	blood:	n/a
33	chr3:60226328-60226378	PrEC	prostate:	n/a
34	chr3:60133085-60133135	MCF10A-Er-Src	breast:	n/a
35	chr3:60133085-60133135	HEK293	kidney:	embryo
36	chr3:60133085-60133135	ovcar-3	ovarian:	n/a
37	chr3:60226328-60226378	BE2_C	brain:	n/a
38	chr3:60133085-60133135	HNPCEpiC	eye:	n/a
39	chr3:60133085-60133135	T-47D	breast:	n/a
40	chr3:60226328-60226378	LNCaP	prostate:	n/a
41	chr3:60133085-60133135	SK-N-SH_RA	brain:	n/a
42	chr3:60133085-60133135	HCF	heart:	n/a
43	chr3:60133085-60133135	GM19239	blood:	n/a
44	chr3:60226328-60226378	U87	brain:	n/a
45	chr3:60226328-60226378	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:60226328-60226378	AG04450	lung:	fetal
47	chr3:60133085-60133135	GM12892	blood:	n/a
48	chr3:60133085-60133135	HEEpiC	esophagus:	n/a
49	chr3:60133085-60133135	LNCaP	prostate:	n/a
50	chr3:60226328-60226378	SK-N-MC	brain:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:60165952..60167759-chr3:60170117..60173099,2	K562	blood:
2	chr3:60201561..60203293-chr3:60258409..60260445,2	K562	blood:
3	chr3:60260694..60264724-chr3:60264748..60271403,12	K562	blood:
4	chr3:60265834..60270132-chr3:60272142..60277781,4	K562	blood:
5	chr3:60165952..60167759-chr3:60170117..60173099,2	K562	blood:
6	chr3:60244130..60245681-chr3:60258765..60261150,2	K562	blood:
7	chr3:60260853..60263177-chr3:60264748..60269648,5	K562	blood:
8	chr3:60216976..60218581-chr3:60221614..60223794,2	K562	blood:
9	chr3:60260056..60262708-chr3:60388625..60391399,2	K562	blood:
10	chr3:60169452..60171383-chr3:60172881..60175585,3	K562	blood:
11	chr3:60258656..60260421-chr3:60265938..60268428,2	K562	blood:
12	chr3:60269337..60271765-chr3:60281168..60285461,3	K562	blood:
13	chr3:60244807..60248517-chr3:60249578..60252504,4	K562	blood:
14	chr3:60255084..60257458-chr3:60258706..60260675,3	K562	blood:
15	chr3:60251900..60257769-chr3:60262692..60266340,5	K562	blood:
16	chr3:60248856..60251063-chr3:60252178..60253698,2	K562	blood:
17	chr3:60227860..60230033-chr3:60233057..60236236,5	K562	blood:
18	chr3:60253037..60257484-chr3:60258010..60262494,9	K562	blood:
19	chr3:60120417..60123350-chr3:60125419..60128034,2	K562	blood:
20	chr3:60266321..60268572-chr3:60276329..60278580,2	K562	blood:
21	chr3:60169452..60171383-chr3:60172881..60175585,3	K562	blood:
22	chr3:60243402..60246307-chr3:60248980..60251582,2	K562	blood:
23	chr3:60101310..60104205-chr3:60104357..60107292,2	K562	blood:
24	chr3:60251080..60254500-chr3:60254648..60256843,3	K562	blood:
25	chr3:60187999..60188742-chr3:60417102..60417817,2	MCF-7	breast:
26	chr3:60259790..60262070-chr3:60293546..60295461,2	K562	blood:
27	chr3:60232635..60234409-chr3:60265559..60267834,2	K562	blood:
28	chr3:60259045..60261438-chr3:60261640..60264472,4	K562	blood:
29	chr3:60253037..60257484-chr3:60258010..60262494,9	K562	blood:
30	chr3:60266321..60268572-chr3:60276329..60278580,2	K562	blood:
31	chr3:60264136..60267761-chr3:60268146..60273300,4	K562	blood:
32	chr3:60260853..60263177-chr3:60264748..60269648,5	K562	blood:
33	chr3:60261204..60265514-chr3:60273828..60277768,4	K562	blood:
34	chr3:60238823..60240958-chr3:60247675..60249888,2	K562	blood:
35	chr3:60243402..60246307-chr3:60248980..60251582,2	K562	blood:
36	chr3:59988215..59988997-chr3:60152321..60153153,2	MCF-7	breast:
37	chr3:60261204..60265514-chr3:60273828..60277768,4	K562	blood:
38	chr3:60258674..60261438-chr3:60261466..60264109,5	K562	blood:
39	chr3:60244807..60248517-chr3:60249578..60252504,4	K562	blood:
40	chr3:60258656..60260421-chr3:60265938..60268428,2	K562	blood:
41	chr3:60271832..60274094-chr3:60278099..60280290,3	K562	blood:
42	chr3:60248856..60251161-chr3:60252178..60254260,3	K562	blood:
43	chr3:60216976..60218581-chr3:60221614..60223794,2	K562	blood:
44	chr3:60201561..60203293-chr3:60258409..60260445,2	K562	blood:
45	chr3:60234763..60239313-chr3:60259101..60264028,5	K562	blood:
46	chr3:60222812..60224764-chr3:60226709..60229125,2	K562	blood:
47	chr3:60244130..60245681-chr3:60258765..60261150,2	K562	blood:
48	chr3:60260694..60264724-chr3:60264748..60271403,12	K562	blood:
49	chr3:60251080..60254500-chr3:60254648..60256843,3	K562	blood:
50	chr3:60258674..60261438-chr3:60261466..60264109,5	K562	blood:

No data

Variant related genes	Relation type
FHIT	TF binding region
FHIT	CpG island

Extended variants
information (count: 9618 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:9618 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561018205	chr3:60067878-60067879	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs528613080	chr3:60067907-60067908	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547043836	chr3:60067908-60067909	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565214866	chr3:60067912-60067913	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs114925401	chr3:60067955-60067956	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs80266232	chr3:60067973-60067974	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs369290499	chr3:60067974-60067975	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs562505241	chr3:60067990-60067991	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs185051290	chr3:60067997-60067998	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536504456	chr3:60068001-60068002	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs147183355	chr3:60068036-60068037	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs4345028	chr3:60068059-60068060	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs1817617	chr3:60068062-60068063	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548253228	chr3:60068065-60068066	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534438531	chr3:60068077-60068078	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553059233	chr3:60068081-60068082	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs567747038	chr3:60068095-60068096	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs577646724	chr3:60068101-60068102	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs13321394	chr3:60068115-60068116	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1817616	chr3:60068129-60068130	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs573392277	chr3:60068142-60068143	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs146188061	chr3:60068144-60068145	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs79597745	chr3:60068148-60068149	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs539207839	chr3:60068191-60068192	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs561088584	chr3:60068208-60068209	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs573103045	chr3:60068214-60068215	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs202104281	chr3:60068217-60068218	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs540039998	chr3:60068224-60068225	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs565421237	chr3:60068231-60068232	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs532499021	chr3:60068257-60068258	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs139081155	chr3:60068268-60068269	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs2223085	chr3:60068269-60068270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs377222505	chr3:60068298-60068299	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs2223086	chr3:60068334-60068335	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs373049723	chr3:60068355-60068356	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs3920478	chr3:60068367-60068368	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs4413275	chr3:60068385-60068386	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534436120	chr3:60068421-60068422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192507219	chr3:60068434-60068435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183795724	chr3:60068444-60068445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7646436	chr3:60068462-60068463	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557005614	chr3:60068484-60068485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143930704	chr3:60068529-60068530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536232215	chr3:60068531-60068532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554938832	chr3:60068544-60068545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112284210	chr3:60068567-60068568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573045288	chr3:60068692-60068693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540469526	chr3:60068702-60068703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2142300	chr3:60068730-60068731	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs371292679	chr3:60068741-60068742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Cancer	18162546	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Autism	22102821	CNVD
Prostate cancer	19363497	CNVD
Malaria	21533027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21518781	CNVD
Esophageal cancer	21518781	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Glioblastoma multiforme	21569311	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60061800-60068400	Flanking Active TSS	Dnd41	blood
2	chr3:60063800-60068000	Flanking Active TSS	Primary T cells from cord blood	blood
3	chr3:60064600-60068400	Enhancers	Primary B cells from peripheral blood	blood
4	chr3:60064800-60068000	Enhancers	Primary hematopoietic stem cells	blood
5	chr3:60064800-60068000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:60066000-60068200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr3:60066200-60068200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
8	chr3:60066400-60068000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr3:60066400-60068200	Enhancers	GM12878-XiMat	blood
10	chr3:60066600-60068000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
11	chr3:60066800-60068200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:60066800-60068600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr3:60067000-60068000	Enhancers	Fetal Thymus	thymus
14	chr3:60067000-60068400	Enhancers	Thymus	Thymus
15	chr3:60067200-60068000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:60067200-60072400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr3:60067400-60068000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr3:60067400-60068600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr3:60067400-60070000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr3:60067400-60072800	Weak transcription	Stomach Mucosa	stomach
21	chr3:60067600-60068000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr3:60067800-60068000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr3:60067800-60068000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
24	chr3:60067800-60068000	Enhancers	Duodenum Mucosa	Duodenum
25	chr3:60067800-60068600	Enhancers	Primary B cells from cord blood	blood
26	chr3:60067800-60068600	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr3:60067800-60068800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr3:60068000-60068600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr3:60068000-60068800	Enhancers	Primary T cells from cord blood	blood
30	chr3:60068000-60069600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr3:60068000-60072200	Weak transcription	Fetal Thymus	thymus
32	chr3:60068000-60072400	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr3:60068200-60068800	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr3:60068200-60069200	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr3:60068400-60069200	Enhancers	Dnd41	blood
36	chr3:60068400-60072600	Weak transcription	Thymus	Thymus
37	chr3:60068600-60069000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr3:60068600-60072800	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr3:60068600-60075800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr3:60068800-60072600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr3:60069000-60069200	ZNF genes & repeats	Psoas Muscle	Psoas
42	chr3:60069000-60069600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr3:60069200-60069400	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr3:60069200-60070400	Weak transcription	Dnd41	blood
45	chr3:60069200-60072400	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr3:60069200-60072800	Weak transcription	Psoas Muscle	Psoas
47	chr3:60070000-60070200	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr3:60070000-60072200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr3:60070400-60071200	Enhancers	Dnd41	blood
50	chr3:60071200-60072200	ZNF genes & repeats	Dnd41	blood

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