Variant report

Variant	esv3512632
Chromosome Location	chr3:140949362-140952160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:550)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 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	chr3:140950469-140950692	HepG2	liver:	n/a	n/a
2	BACH1	chr3:140951370-140951804	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:140950044-140950874	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr3:140950287-140950767	GM12878	blood:	n/a	chr3:140950547-140950556 chr3:140950513-140950526
5	BHLHE40	chr3:140949764-140949782	K562	blood:	n/a	n/a
6	BHLHE40	chr3:140950082-140950811	K562	blood:	n/a	chr3:140950676-140950692
7	BHLHE40	chr3:140950284-140950750	GM12878	blood:	n/a	chr3:140950676-140950692
8	BHLHE40	chr3:140950307-140950630	A549	lung:	n/a	n/a
9	BRCA1	chr3:140951378-140951420	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr3:140950411-140950576	HepG2	liver:	n/a	n/a
11	CBX3	chr3:140950149-140950684	K562	blood:	n/a	n/a
12	CCNT2	chr3:140950215-140950865	K562	blood:	n/a	n/a
13	CEBPB	chr3:140952107-140952311	HepG2	liver:	n/a	chr3:140952257-140952268
14	CEBPB	chr3:140951223-140951408	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:140950113-140950633	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:140952110-140952371	A549	lung:	n/a	chr3:140952257-140952268
17	CEBPB	chr3:140952145-140952345	Hela-S3	cervix:	n/a	chr3:140952257-140952268
18	CEBPB	chr3:140950476-140950758	Hela-S3	cervix:	n/a	n/a
19	CEBPD	chr3:140950210-140950814	HepG2	liver:	n/a	n/a
20	CHD1	chr3:140950416-140950646	GM12878	blood:	n/a	n/a
21	CHD2	chr3:140950095-140950622	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr3:140951277-140951407	HepG2	liver:	n/a	n/a
23	CHD2	chr3:140950343-140950837	K562	blood:	n/a	chr3:140950671-140950681
24	CHD2	chr3:140951221-140951554	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr3:140949935-140950727	GM12878	blood:	n/a	chr3:140950671-140950681
26	CHD2	chr3:140950435-140950787	Hela-S3	cervix:	n/a	chr3:140950671-140950681
27	CHD2	chr3:140950337-140950531	HepG2	liver:	n/a	n/a
28	CREB1	chr3:140950075-140950819	A549	lung:	n/a	n/a
29	CREB1	chr3:140949947-140950689	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr3:140949896-140951015	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr3:140950314-140950844	MCF-7	breast:	n/a	chr3:140950677-140950690
32	CTCF	chr3:140950820-140950970	GM12874	blood:	n/a	n/a
33	CTCF	chr3:140950500-140950650	A549	lung:	n/a	n/a
34	CTCF	chr3:140950398-140950764	GM19239	blood:	n/a	chr3:140950677-140950690
35	CTCF	chr3:140950442-140950726	ECC-1	luminal epithelium:	n/a	chr3:140950677-140950690
36	CTCF	chr3:140950453-140950827	T-47D	breast:	n/a	chr3:140950677-140950690
37	CTCF	chr3:140950448-140950730	GM13976	blood:	n/a	chr3:140950677-140950690
38	CTCF	chr3:140950400-140950726	HepG2	liver:	n/a	chr3:140950677-140950690
39	CTCF	chr3:140950480-140950630	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr3:140951260-140951410	Caco-2	colon:	n/a	chr3:140951336-140951349
41	CTCF	chr3:140950522-140950692	HepG2	liver:	n/a	chr3:140950677-140950690
42	CTCF	chr3:140950451-140950742	GM10266	blood:	n/a	chr3:140950677-140950690
43	CTCF	chr3:140950520-140950670	GM12874	blood:	n/a	n/a
44	CTCF	chr3:140950500-140950650	GM12875	blood:	n/a	n/a
45	CTCF	chr3:140950382-140950697	K562	blood:	n/a	chr3:140950677-140950690
46	CTCF	chr3:140950960-140951110	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr3:140950500-140950650	BJ	skin:	n/a	n/a
48	CTCF	chr3:140950434-140950742	K562	blood:	n/a	chr3:140950677-140950690
49	CTCF	chr3:140950500-140950650	GM12878	blood:	n/a	n/a
50	CTCF	chr3:140950500-140950650	HMF	breast:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140951430-140951480	HEEpiC	esophagus:	n/a
2	chr3:140951430-140951480	HEEpiC	esophagus:	n/a
3	chr3:140950828-140950878	SK-N-SH_RA	brain:	n/a
4	chr3:140951301-140951351	HIPEpiC	eye:	n/a
5	chr3:140951194-140951244	Hepatocyte	liver:	n/a
6	chr3:140951430-140951480	HPAEpiC	pulmonary alveolar:	n/a
7	chr3:140950598-140950648	IMR90	lung:	fetal
8	chr3:140950598-140950648	MCF-7	breast:	n/a
9	chr3:140950104-140950154	HCM	heart:	n/a
10	chr3:140951194-140951244	HCPEpiC	choroid plexus:	n/a
11	chr3:140950828-140950878	HEEpiC	esophagus:	n/a
12	chr3:140951430-140951480	NB4	blood:	n/a
13	chr3:140950234-140950284	SK-N-SH_RA	brain:	n/a
14	chr3:140951447-140951497	NB4	blood:	n/a
15	chr3:140951447-140951497	ProgFib	skin:	n/a
16	chr3:140951301-140951351	Jurkat	blood:	n/a
17	chr3:140951301-140951351	HEEpiC	esophagus:	n/a
18	chr3:140951447-140951497	AG04450	lung:	fetal
19	chr3:140951301-140951351	GM12878	blood:	n/a
20	chr3:140951194-140951244	AG09319	gingival:	n/a
21	chr3:140950104-140950154	Caco-2	colon:	n/a
22	chr3:140950828-140950878	HRCEpiC	kidney:	n/a
23	chr3:140950619-140950669	HL-60	blood:	n/a
24	chr3:140951447-140951497	AoSMC	blood vessel:	n/a
25	chr3:140951194-140951244	HepG2	liver:	n/a
26	chr3:140950828-140950878	HCF	heart:	n/a
27	chr3:140950104-140950154	PrEC	prostate:	n/a
28	chr3:140951447-140951497	HRPEpiC	eye:	n/a
29	chr3:140951430-140951480	AoSMC	blood vessel:	n/a
30	chr3:140951194-140951244	K562	blood:	n/a
31	chr3:140951301-140951351	A549	lung:	n/a
32	chr3:140950104-140950154	HEK293	kidney:	embryo
33	chr3:140951194-140951244	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:140950234-140950284	HRE	kidney:	n/a
35	chr3:140950619-140950669	AG09309	skin:	n/a
36	chr3:140950619-140950669	HUVEC	blood vessel:	n/a
37	chr3:140950598-140950648	U87	brain:	n/a
38	chr3:140950619-140950669	NH-A	brain:	n/a
39	chr3:140951194-140951244	GM06990	blood:	n/a
40	chr3:140951447-140951497	NHDF-neo	bronchial:	n/a
41	chr3:140951301-140951351	PrEC	prostate:	n/a
42	chr3:140951447-140951497	HNPCEpiC	eye:	n/a
43	chr3:140951430-140951480	NHDF-neo	bronchial:	n/a
44	chr3:140950619-140950669	AG09319	gingival:	n/a
45	chr3:140950234-140950284	HIPEpiC	eye:	n/a
46	chr3:140950598-140950648	HMEC	breast:	n/a
47	chr3:140951430-140951480	PrEC	prostate:	n/a
48	chr3:140950598-140950648	AoSMC	blood vessel:	n/a
49	chr3:140950598-140950648	AG09319	gingival:	n/a
50	chr3:140950598-140950648	NT2-D1	testis:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:140660428..140662148-chr3:140951081..140952832,2	MCF-7	breast:
2	chr3:140948029..140950002-chr3:141005104..141007914,2	MCF-7	breast:
3	chr1:193090682..193091320-chr3:140949971..140950494,2	NB4	blood:
4	chr1:11969262..11970211-chr3:140949752..140950336,2	NB4	blood:
5	chr3:140935203..140937852-chr3:140947812..140949717,2	MCF-7	breast:
6	chr3:140949685..140950639-chr3:140993821..140994433,2	MCF-7	breast:
7	chr3:140949328..140952346-chr3:140991131..140995521,4	MCF-7	breast:
8	chr22:32339912..32340876-chr3:140949983..140950634,2	HCT-116	colon:
9	chr3:140946887..140950533-chr3:140951414..140955380,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPSB4-3	chr3:140950724-140950753	NONHSAT092418
2	lnc-SPSB4-3	chr3:140950709-140950753	NONHSAT092417

No data

Variant related genes	Relation type
ACPL2	TF binding region
ACPL2	CpG island
ENSG00000201801	chromatin interactions
ENSG00000128245	chromatin interactions
ENSG00000134371	chromatin interactions
ENSG00000155893	chromatin interactions
ENSG00000114120	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542870032	chr3:140949380-140949381	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113082668	chr3:140949396-140949397	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs377089849	chr3:140949415-140949416	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs114153571	chr3:140949422-140949423	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139791385	chr3:140949427-140949428	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531474237	chr3:140949520-140949521	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs543148380	chr3:140949526-140949527	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs555381447	chr3:140949536-140949537	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573541511	chr3:140949582-140949583	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551497833	chr3:140949602-140949603	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145332678	chr3:140949603-140949604	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532973694	chr3:140949622-140949623	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544762650	chr3:140949630-140949631	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs563635683	chr3:140949636-140949637	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs372916176	chr3:140949642-140949643	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs545860431	chr3:140949678-140949679	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs549202505	chr3:140949692-140949693	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs567688312	chr3:140949724-140949725	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147670537	chr3:140949754-140949755	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs149153183	chr3:140949769-140949770	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs62283618	chr3:140949790-140949791	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571936726	chr3:140949839-140949840	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs539245876	chr3:140949851-140949852	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs528930911	chr3:140949856-140949857	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs569341010	chr3:140950002-140950003	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs55849244	chr3:140950059-140950060	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs76483969	chr3:140950072-140950073	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs573600603	chr3:140950075-140950076	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs534282220	chr3:140950110-140950111	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs370896239	chr3:140950111-140950112	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs552856814	chr3:140950140-140950141	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs574127291	chr3:140950159-140950160	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs577465887	chr3:140950160-140950161	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs34121544	chr3:140950178-140950179	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs544902102	chr3:140950244-140950245	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs13085148	chr3:140950308-140950309	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs13085278	chr3:140950369-140950370	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs62283619	chr3:140950390-140950391	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs563540994	chr3:140950417-140950418	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs77423173	chr3:140950437-140950438	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs549089051	chr3:140950455-140950456	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs142338687	chr3:140950483-140950484	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs151284213	chr3:140950511-140950512	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376915349	chr3:140950515-140950516	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs528512917	chr3:140950534-140950535	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs372491193	chr3:140950551-140950552	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs546976849	chr3:140950584-140950585	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs140541651	chr3:140950627-140950628	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
49	rs565274937	chr3:140950630-140950631	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs184195487	chr3:140950660-140950661	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140940000-140949400	Weak transcription	Fetal Heart	heart
2	chr3:140945600-140949800	Enhancers	Fetal Stomach	stomach
3	chr3:140945600-140950000	Enhancers	Fetal Lung	lung
4	chr3:140945800-140949600	Enhancers	Fetal Thymus	thymus
5	chr3:140946000-140949800	Enhancers	Fetal Intestine Small	intestine
6	chr3:140946000-140950000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:140946000-140950000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:140946600-140949400	Weak transcription	NH-A	brain
9	chr3:140946800-140949600	Enhancers	Thymus	Thymus
10	chr3:140947000-140949400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr3:140947000-140949400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr3:140947000-140949600	Weak transcription	HSMM	muscle
13	chr3:140947000-140949600	Weak transcription	HSMMtube	muscle
14	chr3:140947000-140949800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:140947200-140949600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:140947200-140949800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:140947400-140949400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:140947400-140949400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr3:140947600-140949600	Weak transcription	A549	lung
20	chr3:140947600-140950400	Flanking Active TSS	Dnd41	blood
21	chr3:140947800-140949600	Weak transcription	Fetal Brain Female	brain
22	chr3:140948000-140949600	Weak transcription	Gastric	stomach
23	chr3:140948200-140949600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:140948200-140949800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr3:140948200-140949800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr3:140948200-140949800	Weak transcription	Brain Germinal Matrix	brain
27	chr3:140948400-140949600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr3:140948400-140949600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr3:140948400-140949600	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr3:140948400-140949800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:140948600-140949400	Weak transcription	Fetal Kidney	kidney
32	chr3:140948600-140949600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr3:140948600-140949800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr3:140948600-140949800	Enhancers	Fetal Muscle Leg	muscle
35	chr3:140948600-140949800	Enhancers	Lung	lung
36	chr3:140948600-140949800	Enhancers	Pancreas	Pancrea
37	chr3:140948800-140949600	Enhancers	Primary T cells fromperipheralblood	blood
38	chr3:140948800-140949600	Enhancers	Fetal Brain Male	brain
39	chr3:140948800-140949800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
40	chr3:140948800-140949800	Enhancers	Fetal Muscle Trunk	muscle
41	chr3:140948800-140950000	Enhancers	HepG2	liver
42	chr3:140948800-140950200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:140949000-140949400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr3:140949000-140949600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr3:140949000-140949600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:140949000-140949800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
47	chr3:140949200-140949400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr3:140949200-140949600	Enhancers	Primary T cells from cord blood	blood
49	chr3:140949200-140949600	Enhancers	Primary hematopoietic stem cells	blood
50	chr3:140949200-140949600	Enhancers	Primary T helper naive cells from peripheral blood	blood

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