Variant report

Variant	nsv460566
Chromosome Location	chr3:60068730-60276722
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:873)
CpG islands
(count:122)
Chromatin interactive
region (count:77)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:873 , 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	chr3:60080880-60080974	K562	blood:	n/a	n/a
2	ARID3A	chr3:60262560-60263903	K562	blood:	n/a	n/a
3	ARID3A	chr3:60236266-60236623	K562	blood:	n/a	n/a
4	ARID3A	chr3:60241988-60242170	K562	blood:	n/a	n/a
5	ARID3A	chr3:60267195-60267326	K562	blood:	n/a	n/a
6	ARID3A	chr3:60275766-60275781	K562	blood:	n/a	n/a
7	ARID3A	chr3:60254542-60255635	K562	blood:	n/a	n/a
8	ARID3A	chr3:60089333-60089791	K562	blood:	n/a	n/a
9	ARID3A	chr3:60228798-60230202	K562	blood:	n/a	n/a
10	ARID3A	chr3:60251876-60252792	K562	blood:	n/a	n/a
11	ATF1	chr3:60262559-60263531	K562	blood:	n/a	n/a
12	ATF1	chr3:60175649-60176121	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	chr3:60072552-60072929	GM12878	blood:	n/a	n/a
17	ATF2	chr3:60175754-60176100	GM12878	blood:	n/a	n/a
18	ATF3	chr3:60072525-60072862	K562	blood:	n/a	n/a
19	BACH1	chr3:60247867-60247880	K562	blood:	n/a	n/a
20	BACH1	chr3:60238886-60239061	K562	blood:	n/a	n/a
21	BACH1	chr3:60241691-60241802	K562	blood:	n/a	n/a
22	BATF	chr3:60072622-60072863	GM12878	blood:	n/a	chr3:60072719-60072730 chr3:60072749-60072760
23	BATF	chr3:60211442-60211893	GM12878	blood:	n/a	chr3:60211654-60211663
24	BATF	chr3:60125935-60126267	GM12878	blood:	n/a	n/a
25	BATF	chr3:60072565-60072906	GM12878	blood:	n/a	chr3:60072719-60072730 chr3:60072749-60072760
26	BATF	chr3:60211557-60211749	GM12878	blood:	n/a	chr3:60211654-60211663
27	BATF	chr3:60178356-60178622	GM12878	blood:	n/a	n/a
28	BATF	chr3:60178290-60178695	GM12878	blood:	n/a	n/a
29	BATF	chr3:60175866-60176100	GM12878	blood:	n/a	chr3:60175916-60175929
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	chr3:60072788-60072959	K562	blood:	n/a	n/a
35	BHLHE40	chr3:60255569-60256068	K562	blood:	n/a	n/a
36	BHLHE40	chr3:60263109-60263909	K562	blood:	n/a	n/a
37	BHLHE40	chr3:60218420-60218449	K562	blood:	n/a	n/a
38	CBX3	chr3:60263052-60263535	K562	blood:	n/a	n/a
39	CBX3	chr3:60072440-60073038	HCT-116	colon:	n/a	n/a
40	CBX3	chr3:60262958-60263663	K562	blood:	n/a	n/a
41	CCNT2	chr3:60263134-60263501	K562	blood:	n/a	n/a
42	CCNT2	chr3:60229234-60229536	K562	blood:	n/a	n/a
43	CCNT2	chr3:60255085-60255515	K562	blood:	n/a	n/a
44	CEBPB	chr3:60146568-60146768	H1-hESC	embryonic stem cell:	n/a	chr3:60146695-60146708 chr3:60146696-60146707 chr3:60146694-60146711
45	CEBPB	chr3:60252195-60252523	A549	lung:	n/a	n/a
46	CEBPB	chr3:60235970-60236281	A549	lung:	n/a	chr3:60236120-60236131 chr3:60236118-60236129
47	CEBPB	chr3:60235983-60236203	K562	blood:	n/a	chr3:60236120-60236131 chr3:60236118-60236129
48	CEBPB	chr3:60242145-60242392	K562	blood:	n/a	n/a
49	CEBPB	chr3:60160320-60160651	HepG2	liver:	n/a	chr3:60160461-60160472
50	CEBPB	chr3:60145922-60146334	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	HMEC	breast:	n/a
2	chr3:60133085-60133135	SK-N-SH_RA	brain:	n/a
3	chr3:60133085-60133135	A549	lung:	n/a
4	chr3:60226328-60226378	AG09309	skin:	n/a
5	chr3:60133085-60133135	HNPCEpiC	eye:	n/a
6	chr3:60133085-60133135	HAEpiC	amniotic membrane:	n/a
7	chr3:60133085-60133135	NHDF-neo	bronchial:	n/a
8	chr3:60226328-60226378	SAEC	small airway:	n/a
9	chr3:60226328-60226378	HL-60	blood:	n/a
10	chr3:60226328-60226378	ovcar-3	ovarian:	n/a
11	chr3:60133085-60133135	Jurkat	blood:	n/a
12	chr3:60226328-60226378	BE2_C	brain:	n/a
13	chr3:60226328-60226378	Hela-S3	cervix:	n/a
14	chr3:60226328-60226378	HCT-116	colon:	n/a
15	chr3:60133085-60133135	H1-hESC	embryonic stem cell:	embryo
16	chr3:60133085-60133135	HCPEpiC	choroid plexus:	n/a
17	chr3:60226328-60226378	HMEC	breast:	n/a
18	chr3:60133085-60133135	K562	blood:	n/a
19	chr3:60226328-60226378	HRCEpiC	kidney:	n/a
20	chr3:60226328-60226378	HIPEpiC	eye:	n/a
21	chr3:60133085-60133135	HepG2	liver:	n/a
22	chr3:60133085-60133135	NHBE	bronchial:	n/a
23	chr3:60133085-60133135	ProgFib	skin:	n/a
24	chr3:60133085-60133135	HRE	kidney:	n/a
25	chr3:60133085-60133135	GM19239	blood:	n/a
26	chr3:60226328-60226378	Hepatocyte	liver:	n/a
27	chr3:60133085-60133135	AG09309	skin:	n/a
28	chr3:60226328-60226378	AG10803	skin:	n/a
29	chr3:60133085-60133135	MCF-7	breast:	n/a
30	chr3:60226328-60226378	HCPEpiC	choroid plexus:	n/a
31	chr3:60226328-60226378	NHBE	bronchial:	n/a
32	chr3:60226328-60226378	GM12878	blood:	n/a
33	chr3:60133085-60133135	SK-N-SH	brain:	n/a
34	chr3:60226328-60226378	PFSK-1	brain:	n/a
35	chr3:60133085-60133135	CMK	blood:	n/a
36	chr3:60226328-60226378	GM12892	blood:	n/a
37	chr3:60226328-60226378	T-47D	breast:	n/a
38	chr3:60133085-60133135	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:60226328-60226378	HNPCEpiC	eye:	n/a
40	chr3:60133085-60133135	AG09319	gingival:	n/a
41	chr3:60226328-60226378	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:60133085-60133135	SK-N-MC	brain:	n/a
43	chr3:60226328-60226378	GM06990	blood:	n/a
44	chr3:60226328-60226378	ProgFib	skin:	n/a
45	chr3:60226328-60226378	LNCaP	prostate:	n/a
46	chr3:60133085-60133135	ECC-1	luminal epithelium:	n/a
47	chr3:60226328-60226378	Jurkat	blood:	n/a
48	chr3:60226328-60226378	SK-N-MC	brain:	n/a
49	chr3:60226328-60226378	HEEpiC	esophagus:	n/a
50	chr3:60226328-60226378	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:60251900..60257769-chr3:60262692..60266340,5	K562	blood:
2	chr3:59988215..59988997-chr3:60152321..60153153,2	MCF-7	breast:
3	chr3:60256070..60258308-chr3:60290805..60292864,2	K562	blood:
4	chr3:60269337..60271765-chr3:60281168..60285461,3	K562	blood:
5	chr3:60187999..60188742-chr3:60417102..60417817,2	MCF-7	breast:
6	chr3:60259045..60261438-chr3:60261640..60264472,4	K562	blood:
7	chr3:60244130..60245681-chr3:60258765..60261150,2	K562	blood:
8	chr3:60255084..60257458-chr3:60258706..60260675,3	K562	blood:
9	chr3:60265834..60270132-chr3:60272142..60277781,4	K562	blood:
10	chr3:60232635..60234409-chr3:60265559..60267834,2	K562	blood:
11	chr3:60234763..60239313-chr3:60259101..60264028,5	K562	blood:
12	chr3:60261650..60264808-chr3:60273372..60278082,5	K562	blood:
13	chr3:60251080..60254500-chr3:60254648..60256843,3	K562	blood:
14	chr3:60233213..60236039-chr3:60237445..60240033,2	K562	blood:
15	chr3:60260056..60262708-chr3:60388625..60391399,2	K562	blood:
16	chr3:60248856..60251161-chr3:60252178..60254260,3	K562	blood:
17	chr3:60238823..60240958-chr3:60247675..60249888,2	K562	blood:
18	chr3:60250531..60257484-chr3:60260695..60265801,11	K562	blood:
19	chr3:60183906..60185619-chr3:60186648..60189161,2	K562	blood:
20	chr3:60244807..60248517-chr3:60249578..60252504,4	K562	blood:
21	chr3:60260853..60263177-chr3:60264748..60269648,5	K562	blood:
22	chr3:60261650..60264808-chr3:60273372..60278082,5	K562	blood:
23	chr3:60243402..60246307-chr3:60248980..60251582,2	K562	blood:
24	chr3:60248856..60251161-chr3:60252178..60254260,3	K562	blood:
25	chr3:60258656..60260421-chr3:60265938..60268428,2	K562	blood:
26	chr3:60255084..60257458-chr3:60258706..60260675,3	K562	blood:
27	chr3:60216976..60218581-chr3:60221614..60223794,2	K562	blood:
28	chr3:60266321..60268572-chr3:60276329..60278580,2	K562	blood:
29	chr3:60169452..60171383-chr3:60172881..60175585,3	K562	blood:
30	chr3:60227860..60230033-chr3:60233057..60236236,5	K562	blood:
31	chr3:60222812..60224764-chr3:60226709..60229125,2	K562	blood:
32	chr3:60201561..60203293-chr3:60258409..60260445,2	K562	blood:
33	chr3:60216976..60218581-chr3:60221614..60223794,2	K562	blood:
34	chr3:60169452..60171383-chr3:60172881..60175585,3	K562	blood:
35	chr3:60222812..60224764-chr3:60226709..60229125,2	K562	blood:
36	chr3:60251080..60254500-chr3:60254648..60256843,3	K562	blood:
37	chr3:60248856..60251063-chr3:60252178..60253698,2	K562	blood:
38	chr3:60101310..60104205-chr3:60104357..60107292,2	K562	blood:
39	chr3:60232635..60234409-chr3:60265559..60267834,2	K562	blood:
40	chr3:60264136..60267761-chr3:60268146..60273300,4	K562	blood:
41	chr3:60261204..60265514-chr3:60273828..60277768,4	K562	blood:
42	chr3:60264136..60267761-chr3:60268146..60273300,4	K562	blood:
43	chr3:60258674..60261438-chr3:60261466..60264109,5	K562	blood:
44	chr3:60253037..60257484-chr3:60258010..60262494,9	K562	blood:
45	chr3:60251900..60257769-chr3:60262692..60266340,5	K562	blood:
46	chr3:60120417..60123350-chr3:60125419..60128034,2	K562	blood:
47	chr3:60092867..60094612-chr3:60094796..60097247,2	K562	blood:
48	chr3:60260853..60263177-chr3:60264748..60269648,5	K562	blood:
49	chr3:60244130..60245681-chr3:60258765..60261150,2	K562	blood:
50	chr3:60253037..60257484-chr3:60258010..60262494,9	K562	blood:

No data

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

Extended variants
information (count: 9544 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:9544 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2142300	chr3:60068730-60068731	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371292679	chr3:60068741-60068742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146878048	chr3:60068786-60068787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188805392	chr3:60068827-60068828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191432887	chr3:60068845-60068846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183344075	chr3:60068870-60068871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139380330	chr3:60068913-60068914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560451542	chr3:60068915-60068916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150038669	chr3:60068950-60068951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62238446	chr3:60068966-60068967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552739188	chr3:60068979-60068980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570915470	chr3:60068994-60068995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532256020	chr3:60069012-60069013	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs550723725	chr3:60069027-60069028	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs186987591	chr3:60069054-60069055	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs116391980	chr3:60069089-60069090	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs554603989	chr3:60069098-60069099	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs543964359	chr3:60069161-60069162	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs566763974	chr3:60069184-60069185	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs191457402	chr3:60069203-60069204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145298290	chr3:60069204-60069205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576932022	chr3:60069230-60069231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543978850	chr3:60069240-60069241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs398091481	chr3:60069243-60069244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs398052012	chr3:60069245-60069246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539522454	chr3:60069290-60069291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149170909	chr3:60069317-60069318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146517256	chr3:60069318-60069319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541867247	chr3:60069356-60069357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73093961	chr3:60069367-60069368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147884240	chr3:60069377-60069378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527996496	chr3:60069395-60069396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546146330	chr3:60069399-60069400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183935964	chr3:60069402-60069403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141539463	chr3:60069406-60069407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531845255	chr3:60069413-60069414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550389309	chr3:60069430-60069431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147020588	chr3:60069462-60069463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577690021	chr3:60069482-60069483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529770322	chr3:60069557-60069558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548219553	chr3:60069565-60069566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566312632	chr3:60069620-60069621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75534492	chr3:60069656-60069657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2736789	chr3:60069667-60069668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376406565	chr3:60069701-60069702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570707597	chr3:60069716-60069717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542388203	chr3:60069717-60069718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs17062116	chr3:60069722-60069723	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116163786	chr3:60069733-60069734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574594772	chr3:60069743-60069744	Weak transcription Enhancers	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:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60067200-60072400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:60067400-60070000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr3:60067400-60072800	Weak transcription	Stomach Mucosa	stomach
4	chr3:60067800-60068800	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr3:60068000-60068800	Enhancers	Primary T cells from cord blood	blood
6	chr3:60068000-60069600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr3:60068000-60072200	Weak transcription	Fetal Thymus	thymus
8	chr3:60068000-60072400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr3:60068200-60068800	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr3:60068200-60069200	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr3:60068400-60069200	Enhancers	Dnd41	blood
12	chr3:60068400-60072600	Weak transcription	Thymus	Thymus
13	chr3:60068600-60069000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr3:60068600-60072800	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr3:60068600-60075800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr3:60068800-60072600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr3:60069000-60069200	ZNF genes & repeats	Psoas Muscle	Psoas
18	chr3:60069000-60069600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr3:60069200-60069400	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr3:60069200-60070400	Weak transcription	Dnd41	blood
21	chr3:60069200-60072400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr3:60069200-60072800	Weak transcription	Psoas Muscle	Psoas
23	chr3:60070000-60070200	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr3:60070000-60072200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr3:60070400-60071200	Enhancers	Dnd41	blood
26	chr3:60071200-60072200	ZNF genes & repeats	Dnd41	blood
27	chr3:60071800-60073000	Enhancers	GM12878-XiMat	blood
28	chr3:60072200-60073000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr3:60072200-60073000	ZNF genes & repeats	Fetal Thymus	thymus
30	chr3:60072200-60074200	Enhancers	Dnd41	blood
31	chr3:60072400-60072800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr3:60072400-60072800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr3:60072400-60073000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:60072400-60073000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:60072400-60073000	Enhancers	Primary T cells fromperipheralblood	blood
36	chr3:60072400-60073000	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr3:60072400-60073000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr3:60072400-60073000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:60072400-60073000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:60072400-60073000	Enhancers	Esophagus	oesophagus
41	chr3:60072400-60073000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr3:60072400-60073000	Enhancers	NH-A	brain
43	chr3:60072400-60073000	Enhancers	NHEK	skin
44	chr3:60072400-60073200	Enhancers	K562	blood
45	chr3:60072600-60072800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr3:60072600-60072800	Enhancers	Thymus	Thymus
47	chr3:60072800-60073000	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr3:60072800-60073000	Enhancers	Psoas Muscle	Psoas
49	chr3:60072800-60073000	Enhancers	Stomach Mucosa	stomach
50	chr3:60072800-60073200	ZNF genes & repeats	Primary T cells from cord blood	blood

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