Variant report

Variant	esv3327056
Chromosome Location	chr3:56715937-56718485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:575)
CpG islands
(count:611)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:56715646-56716150	K562	blood:	n/a	n/a
2	ATF2	chr3:56716420-56716961	GM12878	blood:	n/a	n/a
3	ATF2	chr3:56717182-56717674	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:56717049-56717517	GM12878	blood:	n/a	n/a
5	ATF2	chr3:56716377-56716995	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:56717155-56717156	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:56716494-56716776	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr3:56716850-56717712	GM12878	blood:	n/a	chr3:56717507-56717516 chr3:56717513-56717522 chr3:56717514-56717527 chr3:56717096-56717105
9	BCLAF1	chr3:56716319-56717758	GM12878	blood:	n/a	chr3:56717507-56717516 chr3:56717513-56717522 chr3:56717514-56717527 chr3:56716546-56716559 chr3:56716581-56716594 chr3:56717096-56717105
10	BCLAF1	chr3:56716182-56716847	GM12878	blood:	n/a	chr3:56716546-56716559 chr3:56716581-56716594
11	BHLHE40	chr3:56716327-56717718	GM12878	blood:	n/a	chr3:56717347-56717363 chr3:56716548-56716564
12	BHLHE40	chr3:56716115-56717628	K562	blood:	n/a	chr3:56717347-56717363 chr3:56716548-56716564
13	BRCA1	chr3:56717199-56717505	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr3:56716014-56716917	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr3:56716443-56716635	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:56717319-56717519	GM12878	blood:	n/a	n/a
17	BRCA1	chr3:56717200-56717273	HepG2	liver:	n/a	n/a
18	CBX3	chr3:56716190-56717792	HCT-116	colon:	n/a	n/a
19	CBX3	chr3:56717044-56718024	K562	blood:	n/a	chr3:56717939-56717950
20	CBX3	chr3:56717288-56717942	K562	blood:	n/a	n/a
21	CBX3	chr3:56716207-56717929	HCT-116	colon:	n/a	n/a
22	CCNT2	chr3:56716274-56717800	K562	blood:	n/a	chr3:56717307-56717316
23	CEBPB	chr3:56716035-56717544	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:56717309-56717499	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:56717406-56717603	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPD	chr3:56717078-56717385	HepG2	liver:	n/a	n/a
27	CEBPD	chr3:56716311-56716639	HepG2	liver:	n/a	n/a
28	CHD1	chr3:56716153-56717195	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr3:56714816-56717881	IMR90	lung:	n/a	n/a
30	CHD1	chr3:56716259-56717607	GM12878	blood:	n/a	n/a
31	CHD2	chr3:56716466-56717652	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:56716133-56717645	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr3:56716559-56717592	HepG2	liver:	n/a	n/a
34	CHD2	chr3:56716439-56716718	K562	blood:	n/a	n/a
35	CHD2	chr3:56716259-56717657	GM12878	blood:	n/a	n/a
36	CHD2	chr3:56716936-56717615	K562	blood:	n/a	n/a
37	CREB1	chr3:56716242-56717713	GM12878	blood:	n/a	n/a
38	CREB1	chr3:56717228-56717466	A549	lung:	n/a	n/a
39	CREB1	chr3:56716271-56716668	A549	lung:	n/a	n/a
40	CREB1	chr3:56716700-56717602	A549	lung:	n/a	n/a
41	CREB1	chr3:56716152-56717715	HepG2	liver:	n/a	n/a
42	CREB1	chr3:56716760-56717501	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr3:56716363-56716613	GM12878	blood:	n/a	chr3:56716492-56716505
44	CTCF	chr3:56716420-56716570	SK-N-SH_RA	brain:	n/a	chr3:56716492-56716505
45	CTCF	chr3:56716474-56716488	GM10266	blood:	n/a	n/a
46	CTCF	chr3:56716480-56716630	HCPEpiC	choroid plexus:	n/a	chr3:56716492-56716505
47	CTCF	chr3:56717311-56717381	Spleen_OC	spleen:	n/a	chr3:56717349-56717362
48	CTCF	chr3:56716437-56716583	GM19239	blood:	n/a	chr3:56716492-56716505
49	CTCF	chr3:56716402-56716573	Lung_OC	lung:	n/a	chr3:56716492-56716505
50	CTCF	chr3:56716440-56716590	HUVEC	blood vessel:	n/a	chr3:56716492-56716505

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:56717798-56717848	HMEC	breast:	n/a
2	chr3:56717798-56717848	HMEC	breast:	n/a
3	chr3:56717804-56717854	Caco-2	colon:	n/a
4	chr3:56716962-56717012	AG10803	skin:	n/a
5	chr3:56717798-56717848	SAEC	small airway:	n/a
6	chr3:56717169-56717219	AG04449	skin:	fetal
7	chr3:56717804-56717854	BJ	skin:	n/a
8	chr3:56717169-56717219	BJ	skin:	n/a
9	chr3:56717769-56717819	ProgFib	skin:	n/a
10	chr3:56717769-56717819	HL-60	blood:	n/a
11	chr3:56716962-56717012	PFSK-1	brain:	n/a
12	chr3:56717804-56717854	PrEC	prostate:	n/a
13	chr3:56716758-56716808	SK-N-SH	brain:	n/a
14	chr3:56717625-56717675	GM06990	blood:	n/a
15	chr3:56717769-56717819	NHDF-neo	bronchial:	n/a
16	chr3:56716758-56716808	GM06990	blood:	n/a
17	chr3:56717720-56717770	HCM	heart:	n/a
18	chr3:56717804-56717854	AG04450	lung:	fetal
19	chr3:56717720-56717770	AG10803	skin:	n/a
20	chr3:56716962-56717012	LNCaP	prostate:	n/a
21	chr3:56717625-56717675	GM19239	blood:	n/a
22	chr3:56716962-56717012	GM12878	blood:	n/a
23	chr3:56717720-56717770	NH-A	brain:	n/a
24	chr3:56716962-56717012	T-47D	breast:	n/a
25	chr3:56716758-56716808	HMEC	breast:	n/a
26	chr3:56717769-56717819	HCM	heart:	n/a
27	chr3:56717657-56717707	Caco-2	colon:	n/a
28	chr3:56716962-56717012	Hela-S3	cervix:	n/a
29	chr3:56717625-56717675	HRCEpiC	kidney:	n/a
30	chr3:56717169-56717219	Jurkat	blood:	n/a
31	chr3:56716758-56716808	NHDF-neo	bronchial:	n/a
32	chr3:56716758-56716808	PFSK-1	brain:	n/a
33	chr3:56717625-56717675	HCM	heart:	n/a
34	chr3:56717625-56717675	BJ	skin:	n/a
35	chr3:56717625-56717675	BE2_C	brain:	n/a
36	chr3:56717657-56717707	NT2-D1	testis:	n/a
37	chr3:56717804-56717854	HRCEpiC	kidney:	n/a
38	chr3:56717657-56717707	NB4	blood:	n/a
39	chr3:56717798-56717848	HRE	kidney:	n/a
40	chr3:56717798-56717848	HAEpiC	amniotic membrane:	n/a
41	chr3:56717657-56717707	IMR90	lung:	fetal
42	chr3:56717769-56717819	ECC-1	luminal epithelium:	n/a
43	chr3:56717657-56717707	SKMC	muscle:	n/a
44	chr3:56716758-56716808	MCF10A-Er-Src	breast:	n/a
45	chr3:56717175-56717225	Hela-S3	cervix:	n/a
46	chr3:56717175-56717225	AG09319	gingival:	n/a
47	chr3:56717720-56717770	HEK293	kidney:	embryo
48	chr3:56717720-56717770	HRE	kidney:	n/a
49	chr3:56717804-56717854	HCT-116	colon:	n/a
50	chr3:56717798-56717848	RPTEC	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:126106969..126107773-chr3:56716259..56717211,2	Hela-S3	cervix:
2	chr3:56716510..56717020-chr3:113233644..113234198,2	Hela-S3	cervix:
3	chr3:56666598..56668908-chr3:56715764..56717337,2	MCF-7	breast:
4	chr3:56705021..56708606-chr3:56714722..56718211,5	MCF-7	breast:
5	chr3:56589231..56591997-chr3:56715959..56718849,3	K562	blood:
6	chr3:56715125..56717534-chr4:38104477..38107344,2	MCF-7	breast:
7	chr3:56716275..56717973-chr3:56833928..56836671,2	K562	blood:
8	chr3:56714433..56716910-chr3:57020526..57023323,2	MCF-7	breast:
9	chr3:56690378..56691903-chr3:56713310..56716081,2	K562	blood:
10	chr12:50134951..50135493-chr3:56716063..56717030,2	Hela-S3	cervix:
11	chr3:56715514..56718317-chr3:56833414..56836251,4	MCF-7	breast:
12	chr3:56716520..56717389-chr6:26157669..26158536,2	Hela-S3	cervix:
13	chr14:64854828..64855596-chr3:56716887..56717549,2	HCT-116	colon:
14	chr3:56589586..56592975-chr3:56714350..56719200,6	K562	blood:
15	chr3:56716781..56717328-chr5:180673479..180674070,2	Hela-S3	cervix:
16	chr3:56702147..56705420-chr3:56716741..56719178,3	MCF-7	breast:
17	chr3:56716645..56717530-chr8:101734318..101735231,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
FAM208A	TF binding region
FAM208A	CpG island
ENSG00000163611	chromatin interactions
ENSG00000233937	chromatin interactions
ENSG00000065154	chromatin interactions
ENSG00000163947	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000180376	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000163946	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000065882	chromatin interactions
ENSG00000100714	chromatin interactions

Extended variants
information (count: 120 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:120 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113324151	chr3:56715998-56715999	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs9839065	chr3:56716089-56716090	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs74734691	chr3:56716095-56716096	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs530694562	chr3:56716183-56716184	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs550307729	chr3:56716201-56716202	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs535267624	chr3:56716235-56716236	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs538753891	chr3:56716239-56716240	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs558951517	chr3:56716245-56716246	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs558025746	chr3:56716259-56716260	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs189884572	chr3:56716268-56716269	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs554937497	chr3:56716269-56716270	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs574709534	chr3:56716277-56716278	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs577856485	chr3:56716325-56716326	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs556639399	chr3:56716336-56716337	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs116782785	chr3:56716349-56716350	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs545569391	chr3:56716416-56716417	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs559333587	chr3:56716459-56716460	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs528051672	chr3:56716462-56716463	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs542127735	chr3:56716476-56716477	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs561924681	chr3:56716501-56716502	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs530730052	chr3:56716577-56716578	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs550841571	chr3:56716585-56716586	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs570651995	chr3:56716586-56716587	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs532676128	chr3:56716588-56716589	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs552371444	chr3:56716596-56716597	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs566088792	chr3:56716603-56716604	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs141152503	chr3:56716608-56716609	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs548480189	chr3:56716653-56716654	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs372367002	chr3:56716665-56716666	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs537342097	chr3:56716678-56716679	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs192585528	chr3:56716688-56716689	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs577349459	chr3:56716696-56716697	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs113199481	chr3:56716710-56716711	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs375298433	chr3:56716739-56716740	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs376896296	chr3:56716762-56716763	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs185376312	chr3:56716785-56716786	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs572810663	chr3:56716809-56716810	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs35331849	chr3:56716840-56716841	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs541415592	chr3:56716865-56716866	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs561666406	chr3:56716876-56716877	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs575651158	chr3:56716883-56716884	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs111291433	chr3:56716922-56716923	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs114958599	chr3:56716932-56716933	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs532958497	chr3:56716937-56716938	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs371461108	chr3:56716959-56716960	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs200185070	chr3:56716992-56716993	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs559550458	chr3:56717029-56717030	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs528487034	chr3:56717073-56717074	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs548223171	chr3:56717145-56717146	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs568102065	chr3:56717193-56717194	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Myofibroblastic sarcoma	19369631	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
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	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
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56675800-56716200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:56695400-56716000	Weak transcription	Fetal Brain Male	brain
3	chr3:56699600-56716000	Weak transcription	Fetal Kidney	kidney
4	chr3:56699600-56716200	Weak transcription	Spleen	Spleen
5	chr3:56699800-56716000	Weak transcription	Aorta	Aorta
6	chr3:56701800-56716000	Weak transcription	Psoas Muscle	Psoas
7	chr3:56702400-56716200	Weak transcription	Small Intestine	intestine
8	chr3:56702600-56716000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:56702600-56716000	Weak transcription	Colonic Mucosa	Colon
10	chr3:56703000-56716200	Weak transcription	Ovary	ovary
11	chr3:56703200-56716000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr3:56704800-56716000	Weak transcription	Brain Germinal Matrix	brain
13	chr3:56704800-56716200	Weak transcription	Left Ventricle	heart
14	chr3:56705200-56716000	Weak transcription	Fetal Lung	lung
15	chr3:56705200-56716000	Weak transcription	Fetal Muscle Trunk	muscle
16	chr3:56705200-56716200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr3:56705400-56716000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr3:56705400-56716000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr3:56705400-56716200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:56705400-56716200	Weak transcription	Gastric	stomach
21	chr3:56707200-56716000	Weak transcription	Fetal Intestine Large	intestine
22	chr3:56707200-56716200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:56707200-56716200	Weak transcription	Esophagus	oesophagus
24	chr3:56707400-56716000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr3:56707400-56716000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr3:56707400-56716000	Weak transcription	Fetal Intestine Small	intestine
27	chr3:56711200-56716000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr3:56713000-56716000	Weak transcription	Fetal Stomach	stomach
29	chr3:56713000-56716200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:56713000-56716200	Weak transcription	Lung	lung
31	chr3:56713000-56716200	Weak transcription	Pancreas	Pancrea
32	chr3:56713600-56716000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr3:56713600-56717600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:56713800-56716000	Weak transcription	Placenta	Placenta
35	chr3:56713800-56717400	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr3:56713800-56717400	Active TSS	GM12878-XiMat	blood
37	chr3:56713800-56717400	Active TSS	K562	blood
38	chr3:56714000-56716000	Enhancers	Primary B cells from peripheral blood	blood
39	chr3:56714000-56716000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr3:56714200-56716000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr3:56714400-56716000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr3:56714600-56716000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:56714600-56717400	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr3:56714600-56717400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr3:56714800-56716200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr3:56714800-56716400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr3:56714800-56716400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr3:56714800-56717400	Active TSS	HMEC	breast
49	chr3:56714800-56717600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr3:56715000-56716000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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