Variant report

Variant	nsv536570
Chromosome Location	chr3:51584056-51689648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:429)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:51655455-51655844	HepG2	liver:	n/a	n/a
2	ATF3	chr3:51671981-51672164	K562	blood:	n/a	n/a
3	ATF3	chr3:51671819-51672302	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:51643424-51643513	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr3:51584066-51584415	HepG2	liver:	n/a	n/a
6	BHLHE40	chr3:51654547-51654968	HepG2	liver:	n/a	chr3:51654746-51654755 chr3:51654745-51654758
7	BHLHE40	chr3:51654573-51654817	HepG2	liver:	n/a	chr3:51654746-51654755 chr3:51654745-51654758
8	BHLHE40	chr3:51654619-51654831	HepG2	liver:	n/a	chr3:51654746-51654755 chr3:51654745-51654758
9	CEBPB	chr3:51676554-51676845	K562	blood:	n/a	chr3:51676684-51676695
10	CEBPB	chr3:51633783-51633950	HepG2	liver:	n/a	chr3:51633824-51633835
11	CEBPB	chr3:51657798-51658119	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:51676660-51676733	HepG2	liver:	n/a	chr3:51676684-51676695
13	CEBPB	chr3:51676511-51676891	MCF-7	breast:	n/a	chr3:51676684-51676695
14	CEBPB	chr3:51616105-51616551	IMR90	lung:	n/a	chr3:51616252-51616264 chr3:51616250-51616267
15	CEBPB	chr3:51655627-51655863	H1-hESC	embryonic stem cell:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
16	CEBPB	chr3:51676515-51676774	K562	blood:	n/a	chr3:51676684-51676695
17	CEBPB	chr3:51675674-51675820	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:51676543-51676791	H1-hESC	embryonic stem cell:	n/a	chr3:51676684-51676695
19	CEBPB	chr3:51584156-51584699	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:51676530-51676898	A549	lung:	n/a	chr3:51676684-51676695
21	CEBPB	chr3:51655547-51655890	A549	lung:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
22	CEBPB	chr3:51655560-51655894	HepG2	liver:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
23	CEBPB	chr3:51595598-51595798	HepG2	liver:	n/a	chr3:51595633-51595644
24	CEBPB	chr3:51657770-51658108	K562	blood:	n/a	n/a
25	CEBPB	chr3:51657913-51658002	A549	lung:	n/a	n/a
26	CEBPB	chr3:51655531-51655908	IMR90	lung:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
27	CEBPB	chr3:51643509-51643823	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr3:51655668-51655844	K562	blood:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
29	CEBPB	chr3:51584164-51584516	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:51655520-51655922	HepG2	liver:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
31	CEBPB	chr3:51655537-51655912	HepG2	liver:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
32	CEBPB	chr3:51633809-51633844	K562	blood:	n/a	chr3:51633824-51633835
33	CEBPB	chr3:51676513-51676832	A549	lung:	n/a	chr3:51676684-51676695
34	CEBPB	chr3:51655559-51655829	HepG2	liver:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
35	CEBPB	chr3:51653977-51654186	HepG2	liver:	n/a	chr3:51654060-51654071
36	CEBPB	chr3:51657848-51658052	K562	blood:	n/a	n/a
37	CEBPB	chr3:51655513-51655897	K562	blood:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
38	CEBPB	chr3:51657920-51658115	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:51655647-51655922	MCF-7	breast:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
40	CEBPB	chr3:51655548-51655888	K562	blood:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
41	CEBPB	chr3:51616190-51616484	HepG2	liver:	n/a	chr3:51616252-51616264 chr3:51616250-51616267
42	CEBPB	chr3:51655527-51655945	Hela-S3	cervix:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
43	CEBPB	chr3:51655533-51655894	A549	lung:	n/a	chr3:51655716-51655727 chr3:51655718-51655729
44	CEBPB	chr3:51595570-51595742	H1-hESC	embryonic stem cell:	n/a	chr3:51595633-51595644
45	CEBPD	chr3:51655546-51655857	HepG2	liver:	n/a	chr3:51655733-51655744 chr3:51655717-51655728
46	CHD1	chr3:51671770-51672209	IMR90	lung:	n/a	n/a
47	CHD2	chr3:51655879-51655889	HepG2	liver:	n/a	n/a
48	CREB1	chr3:51672042-51672299	A549	lung:	n/a	n/a
49	CTCF	chr3:51676537-51676802	HepG2	liver:	n/a	n/a
50	CTCF	chr3:51671980-51672130	GM12878	blood:	n/a	chr3:51672099-51672120 chr3:51672053-51672074 chr3:51672104-51672122

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51593459-51593509	H1-hESC	embryonic stem cell:	embryo
2	chr3:51602121-51602171	HCPEpiC	choroid plexus:	n/a
3	chr3:51593459-51593509	H1-hESC	embryonic stem cell:	embryo
4	chr3:51602121-51602171	HCPEpiC	choroid plexus:	n/a
5	chr3:51642365-51642415	AG04450	lung:	fetal
6	chr3:51593459-51593509	Hela-S3	cervix:	n/a
7	chr3:51614916-51614966	HCT-116	colon:	n/a
8	chr3:51593459-51593509	HUVEC	blood vessel:	n/a
9	chr3:51593459-51593509	A549	lung:	n/a
10	chr3:51593459-51593509	NB4	blood:	n/a
11	chr3:51641812-51641862	HNPCEpiC	eye:	n/a
12	chr3:51616517-51616567	SK-N-MC	brain:	n/a
13	chr3:51614916-51614966	HUVEC	blood vessel:	n/a
14	chr3:51602121-51602171	GM12892	blood:	n/a
15	chr3:51602121-51602171	AoSMC	blood vessel:	n/a
16	chr3:51672239-51672289	MCF10A-Er-Src	breast:	n/a
17	chr3:51642365-51642415	ECC-1	luminal epithelium:	n/a
18	chr3:51602121-51602171	Caco-2	colon:	n/a
19	chr3:51602121-51602171	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:51642365-51642415	T-47D	breast:	n/a
21	chr3:51593459-51593509	HAEpiC	amniotic membrane:	n/a
22	chr3:51641812-51641862	HMEC	breast:	n/a
23	chr3:51593459-51593509	BJ	skin:	n/a
24	chr3:51642365-51642415	HCM	heart:	n/a
25	chr3:51642365-51642415	GM12891	blood:	n/a
26	chr3:51641812-51641862	HRCEpiC	kidney:	n/a
27	chr3:51642365-51642415	NHBE	bronchial:	n/a
28	chr3:51642365-51642415	HepG2	liver:	n/a
29	chr3:51642365-51642415	HL-60	blood:	n/a
30	chr3:51641812-51641862	NB4	blood:	n/a
31	chr3:51672239-51672289	HNPCEpiC	eye:	n/a
32	chr3:51614916-51614966	A549	lung:	n/a
33	chr3:51593459-51593509	ovcar-3	ovarian:	n/a
34	chr3:51641812-51641862	BJ	skin:	n/a
35	chr3:51641812-51641862	PrEC	prostate:	n/a
36	chr3:51642365-51642415	MCF10A-Er-Src	breast:	n/a
37	chr3:51614916-51614966	HCM	heart:	n/a
38	chr3:51616517-51616567	AG10803	skin:	n/a
39	chr3:51602121-51602171	HCF	heart:	n/a
40	chr3:51641812-51641862	SKMC	muscle:	n/a
41	chr3:51616517-51616567	AG04450	lung:	fetal
42	chr3:51672239-51672289	SAEC	small airway:	n/a
43	chr3:51642365-51642415	HRE	kidney:	n/a
44	chr3:51616517-51616567	AG04449	skin:	fetal
45	chr3:51616517-51616567	ProgFib	skin:	n/a
46	chr3:51672239-51672289	HCPEpiC	choroid plexus:	n/a
47	chr3:51672239-51672289	ProgFib	skin:	n/a
48	chr3:51616517-51616567	GM19239	blood:	n/a
49	chr3:51641812-51641862	BE2_C	brain:	n/a
50	chr3:51616517-51616567	GM12892	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51676313..51678266-chr3:51703757..51707579,3	MCF-7	breast:
2	chr3:51659779..51662328-chr3:51705271..51707146,2	K562	blood:
3	chr3:51575437..51577336-chr3:51596376..51599200,2	MCF-7	breast:
4	chr3:51670498..51672609-chr3:51704591..51706589,2	MCF-7	breast:
5	chr3:51676595..51677106-chr3:51714925..51715738,2	MCF-7	breast:
6	chr3:51650428..51652785-chr3:51653389..51655830,3	K562	blood:
7	chr3:51571369..51573938-chr3:51651321..51654419,3	MCF-7	breast:
8	chr3:51535149..51536784-chr3:51671586..51672589,18	MCF-7	breast:
9	chr3:51613594..51615572-chr3:51617253..51619218,2	K562	blood:
10	chr3:51577582..51579319-chr3:51581495..51584196,2	K562	blood:
11	chr3:51689639..51691996-chr3:51702378..51704180,2	K562	blood:
12	chr3:51647299..51649344-chr3:51650444..51652715,2	MCF-7	breast:
13	chr3:51669160..51671599-chr3:51704237..51706705,2	MCF-7	breast:
14	chr3:51532821..51534762-chr3:51612325..51614079,2	K562	blood:
15	chr3:51671896..51672809-chr3:51715723..51716758,4	K562	blood:
16	chr3:51650428..51652785-chr3:51653389..51655830,3	K562	blood:
17	chr3:51676292..51677027-chr3:51753087..51753691,2	MCF-7	breast:
18	chr3:51534170..51537061-chr3:51667512..51669238,2	MCF-7	breast:
19	chr3:51532523..51534035-chr3:51677863..51680202,2	K562	blood:
20	chr3:51533551..51537019-chr3:51670604..51674164,6	MCF-7	breast:
21	chr3:51593552..51596365-chr3:51596602..51598437,2	K562	blood:
22	chr3:51647299..51649344-chr3:51650444..51652715,2	MCF-7	breast:
23	chr3:51675829..51676718-chr3:51702251..51702905,2	MCF-7	breast:
24	chr3:51535780..51536364-chr3:51583961..51584496,2	MCF-7	breast:
25	chr3:51671983..51672502-chr3:51716007..51716637,2	MCF-7	breast:
26	chr3:51533880..51536429-chr3:51670590..51673480,2	K562	blood:
27	chr3:51593552..51596365-chr3:51596602..51598437,2	K562	blood:
28	chr3:51429373..51431987-chr3:51587416..51589959,2	K562	blood:
29	chr3:51535748..51536669-chr3:51672603..51673554,2	MCF-7	breast:
30	chr3:51613594..51615572-chr3:51617253..51619218,2	K562	blood:
31	chr3:51663530..51666106-chr3:51668183..51670833,2	K562	blood:
32	chr3:51663280..51666106-chr3:51668905..51670833,2	K562	blood:
33	chr3:51680306..51681884-chr3:51703698..51705243,2	MCF-7	breast:
34	chr3:51535498..51537200-chr3:51671383..51672799,10	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TEX264-1	chr3:51676525-51677449	expReg_chr3_4849_+
2	lnc-TEX264-2	chr3:51674524-51675039	expReg_chr3_4846_+

No data

Variant related genes	Relation type
RAD54L2	TF binding region
RNU6ATAC29P	TF binding region
RAD54L2	CpG island
RNU6ATAC29P	CpG island
ENSG00000164081	chromatin interactions
ENSG00000164080	chromatin interactions
ENSG00000145041	chromatin interactions

Extended variants
information (count: 3382 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3382 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11715600	chr3:51584082-51584083	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115024603	chr3:51584113-51584114	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34166389	chr3:51584147-51584148	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11715644	chr3:51584155-51584156	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190390621	chr3:51584165-51584166	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559254757	chr3:51584211-51584212	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529842773	chr3:51584212-51584213	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182896532	chr3:51584240-51584241	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375597138	chr3:51584390-51584391	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569452515	chr3:51584393-51584394	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187570511	chr3:51584460-51584461	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551913765	chr3:51584565-51584566	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571892895	chr3:51584569-51584570	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538926615	chr3:51584628-51584629	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11715849	chr3:51584652-51584653	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80078904	chr3:51584785-51584786	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs193085123	chr3:51584789-51584790	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566228568	chr3:51584879-51584880	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368946509	chr3:51584880-51584881	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538155964	chr3:51584895-51584896	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536846115	chr3:51584917-51584918	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115785793	chr3:51584919-51584920	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576640001	chr3:51584920-51584921	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185869779	chr3:51585002-51585003	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558648171	chr3:51585039-51585040	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187525003	chr3:51585069-51585070	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116787695	chr3:51585104-51585105	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76003221	chr3:51585143-51585144	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373826260	chr3:51585144-51585145	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76895108	chr3:51585160-51585161	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79298062	chr3:51585161-51585162	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559609353	chr3:51585306-51585307	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139671246	chr3:51585349-51585350	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192783533	chr3:51585350-51585351	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184028421	chr3:51585401-51585402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568148474	chr3:51585456-51585457	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201904268	chr3:51585457-51585458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79199660	chr3:51585468-51585469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563020914	chr3:51585498-51585499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530553666	chr3:51585512-51585513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188753708	chr3:51585515-51585516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563895586	chr3:51585538-51585539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs55950822	chr3:51585659-51585660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528090245	chr3:51585669-51585670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181437634	chr3:51585670-51585671	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566414071	chr3:51585714-51585715	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149776308	chr3:51585746-51585747	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548837794	chr3:51585793-51585794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369354831	chr3:51585806-51585807	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570282503	chr3:51585816-51585817	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	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 peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2442 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51573800-51594000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:51574000-51586800	Weak transcription	Brain Substantia Nigra	brain
3	chr3:51574000-51590800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:51574000-51593800	Weak transcription	Right Ventricle	heart
5	chr3:51574000-51597000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr3:51574000-51600600	Weak transcription	Gastric	stomach
7	chr3:51574000-51615400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:51574000-51624800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr3:51574200-51616400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:51574400-51593200	Weak transcription	Brain Angular Gyrus	brain
11	chr3:51574400-51613800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr3:51574600-51586000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr3:51574600-51587400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr3:51574600-51590800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr3:51574600-51593200	Weak transcription	Brain Anterior Caudate	brain
16	chr3:51574600-51593200	Weak transcription	NHLF	lung
17	chr3:51574600-51593400	Weak transcription	HSMMtube	muscle
18	chr3:51574600-51593800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr3:51574600-51593800	Weak transcription	Left Ventricle	heart
20	chr3:51574600-51594400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:51574600-51600800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr3:51574600-51601800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr3:51574600-51624600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr3:51574800-51591000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr3:51574800-51597600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr3:51574800-51624800	Weak transcription	NH-A	brain
27	chr3:51575000-51587400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr3:51575000-51597400	Weak transcription	Small Intestine	intestine
29	chr3:51575200-51587600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr3:51575200-51615600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr3:51575600-51585000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:51575600-51587400	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr3:51575600-51593200	Weak transcription	Colon Smooth Muscle	Colon
34	chr3:51575800-51584800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:51576000-51585000	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr3:51576000-51595400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr3:51576200-51593000	Strong transcription	Fetal Stomach	stomach
38	chr3:51576400-51586600	Weak transcription	Fetal Lung	lung
39	chr3:51576400-51593200	Weak transcription	HSMM	muscle
40	chr3:51576400-51597800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr3:51576400-51602000	Weak transcription	Brain Hippocampus Middle	brain
42	chr3:51577200-51597600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr3:51577600-51585200	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr3:51578600-51584200	Weak transcription	Fetal Brain Female	brain
45	chr3:51578600-51587600	Weak transcription	Fetal Intestine Large	intestine
46	chr3:51578600-51587600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr3:51578600-51591400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr3:51578600-51607000	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr3:51578800-51585400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr3:51578800-51587600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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