Variant report

Variant	esv1792935
Chromosome Location	chr18:7566815-7584667
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:726)
CpG islands
(count:733)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7575137-7575406	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
4	ATF2	chr18:7577712-7578133	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr18:7577742-7578206	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
7	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr18:7575526-7576005	H1-hESC	embryonic stem cell:	n/a	chr18:7575877-7575891
10	BCL11A	chr18:7577811-7577975	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
12	BHLHE40	chr18:7575112-7575466	HepG2	liver:	n/a	n/a
13	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
14	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
15	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
16	CEBPB	chr18:7577766-7578084	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr18:7584176-7584177	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr18:7570005-7570017	A549	lung:	n/a	n/a
19	CEBPB	chr18:7577743-7578071	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr18:7574543-7574739	A549	lung:	n/a	chr18:7574590-7574603
21	CEBPB	chr18:7576856-7577034	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr18:7567168-7567252	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr18:7568086-7568380	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr18:7565958-7569508	IMR90	lung:	n/a	chr18:7567084-7567094
25	CHD1	chr18:7566627-7566933	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr18:7567294-7567335	HepG2	liver:	n/a	n/a
27	CHD2	chr18:7566988-7567580	Hela-S3	cervix:	n/a	chr18:7567084-7567094
28	CHD2	chr18:7566721-7566935	K562	blood:	n/a	n/a
29	CHD2	chr18:7577748-7578084	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr18:7568188-7568727	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr18:7566856-7567052	HepG2	liver:	n/a	n/a
32	CREB1	chr18:7567120-7567445	A549	lung:	n/a	n/a
33	CREB1	chr18:7566544-7566952	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr18:7577860-7578056	A549	lung:	n/a	n/a
35	CREB1	chr18:7567887-7568154	A549	lung:	n/a	n/a
36	CREB1	chr18:7568530-7568853	A549	lung:	n/a	n/a
37	CREB1	chr18:7566645-7567541	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr18:7577691-7578228	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr18:7577760-7578200	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr18:7566858-7567601	HepG2	liver:	n/a	n/a
41	CREB1	chr18:7567063-7567481	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr18:7567001-7567445	K562	blood:	n/a	n/a
43	CREB1	chr18:7566663-7567589	A549	lung:	n/a	n/a
44	CTBP2	chr18:7566540-7567821	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTBP2	chr18:7577826-7578121	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTBP2	chr18:7568128-7568834	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr18:7568560-7568710	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr18:7566708-7566816	LNCaP	prostate:	n/a	chr18:7566742-7566758
49	CTCF	chr18:7567180-7567330	AG10803	skin:	n/a	n/a
50	CTCF	chr18:7568600-7568750	HCPEpiC	choroid plexus:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7568539-7568589	MCF10A-Er-Src	breast:	n/a
2	chr18:7568539-7568589	MCF10A-Er-Src	breast:	n/a
3	chr18:7568186-7568236	NHBE	bronchial:	n/a
4	chr18:7566781-7566831	HNPCEpiC	eye:	n/a
5	chr18:7566781-7566831	Hela-S3	cervix:	n/a
6	chr18:7566781-7566831	GM12892	blood:	n/a
7	chr18:7568159-7568209	SKMC	muscle:	n/a
8	chr18:7567548-7567598	ProgFib	skin:	n/a
9	chr18:7567548-7567598	HEK293	kidney:	embryo
10	chr18:7566781-7566831	ovcar-3	ovarian:	n/a
11	chr18:7568539-7568589	PFSK-1	brain:	n/a
12	chr18:7568265-7568315	T-47D	breast:	n/a
13	chr18:7567717-7567767	HRE	kidney:	n/a
14	chr18:7567799-7567849	HCT-116	colon:	n/a
15	chr18:7568186-7568236	AG04450	lung:	fetal
16	chr18:7567638-7567688	HCF	heart:	n/a
17	chr18:7567717-7567767	Hela-S3	cervix:	n/a
18	chr18:7567638-7567688	HMEC	breast:	n/a
19	chr18:7568159-7568209	AG04449	skin:	fetal
20	chr18:7568891-7568941	Caco-2	colon:	n/a
21	chr18:7567426-7567476	RPTEC	kidney:	n/a
22	chr18:7567426-7567476	AoSMC	blood vessel:	n/a
23	chr18:7568829-7568879	HL-60	blood:	n/a
24	chr18:7567638-7567688	NH-A	brain:	n/a
25	chr18:7568891-7568941	HCT-116	colon:	n/a
26	chr18:7567799-7567849	SKMC	muscle:	n/a
27	chr18:7567717-7567767	Caco-2	colon:	n/a
28	chr18:7568891-7568941	GM12878	blood:	n/a
29	chr18:7567799-7567849	GM12892	blood:	n/a
30	chr18:7568829-7568879	NB4	blood:	n/a
31	chr18:7567799-7567849	HepG2	liver:	n/a
32	chr18:7568265-7568315	RPTEC	kidney:	n/a
33	chr18:7566781-7566831	ECC-1	luminal epithelium:	n/a
34	chr18:7568891-7568941	HCF	heart:	n/a
35	chr18:7567799-7567849	HMEC	breast:	n/a
36	chr18:7568539-7568589	U87	brain:	n/a
37	chr18:7567717-7567767	AG09309	skin:	n/a
38	chr18:7568159-7568209	HL-60	blood:	n/a
39	chr18:7567638-7567688	HepG2	liver:	n/a
40	chr18:7568539-7568589	GM12891	blood:	n/a
41	chr18:7568186-7568236	MCF-7	breast:	n/a
42	chr18:7567638-7567688	GM12892	blood:	n/a
43	chr18:7568186-7568236	HPAEpiC	pulmonary alveolar:	n/a
44	chr18:7568539-7568589	HepG2	liver:	n/a
45	chr18:7567548-7567598	T-47D	breast:	n/a
46	chr18:7567717-7567767	SAEC	small airway:	n/a
47	chr18:7568186-7568236	HL-60	blood:	n/a
48	chr18:7568829-7568879	Hepatocyte	liver:	n/a
49	chr18:7566781-7566831	T-47D	breast:	n/a
50	chr18:7567799-7567849	AG09319	gingival:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:7566319..7569036-chr18:7569097..7573393,5	K562	blood:
2	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
3	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
4	chr18:7581543..7584440-chr18:7588046..7590216,2	K562	blood:

No data

Variant related genes	Relation type
PTPRM	TF binding region
PTPRM	CpG island
ENSG00000173482	chromatin interactions
ENSG00000149658	chromatin interactions

Extended variants
information (count: 565 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535216951	chr18:7566844-7566845	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555293549	chr18:7566865-7566866	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs571952797	chr18:7566897-7566898	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs540914892	chr18:7566946-7566947	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs560816797	chr18:7567057-7567058	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs577493841	chr18:7567081-7567082	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112048995	chr18:7567226-7567227	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs563092676	chr18:7567260-7567261	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs180735922	chr18:7567303-7567304	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571415945	chr18:7567380-7567381	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs564190429	chr18:7567430-7567431	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs116466106	chr18:7567500-7567501	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562074313	chr18:7567602-7567603	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs79074627	chr18:7567638-7567639	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs111519596	chr18:7567644-7567645	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs373199344	chr18:7567772-7567773	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs67536179	chr18:7567803-7567804	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570445719	chr18:7567904-7567905	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554237026	chr18:7567934-7567935	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201514114	chr18:7567935-7567936	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs368185752	chr18:7567974-7567975	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549534502	chr18:7567981-7567982	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569516503	chr18:7567987-7567988	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535490469	chr18:7567990-7567991	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555209164	chr18:7568007-7568008	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572007591	chr18:7568011-7568012	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534353427	chr18:7568019-7568020	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554491743	chr18:7568038-7568039	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs968391	chr18:7568054-7568055	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112758568	chr18:7568055-7568056	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577581601	chr18:7568073-7568074	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374239319	chr18:7568218-7568219	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35121064	chr18:7568282-7568283	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546542184	chr18:7568320-7568321	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563026037	chr18:7568463-7568464	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs576570550	chr18:7568517-7568518	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs542304581	chr18:7568597-7568598	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs562069666	chr18:7568604-7568605	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527668002	chr18:7568620-7568621	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62089796	chr18:7568696-7568697	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547352304	chr18:7568745-7568746	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12606511	chr18:7568753-7568754	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564159632	chr18:7568764-7568765	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185395443	chr18:7568780-7568781	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148243509	chr18:7568831-7568832	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569502501	chr18:7568840-7568841	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs202039623	chr18:7568846-7568847	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529124787	chr18:7568927-7568928	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549043078	chr18:7569003-7569004	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565673883	chr18:7569044-7569045	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7565800-7570200	Active TSS	A549	lung
2	chr18:7566000-7567000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr18:7566000-7567400	Active TSS	Colonic Mucosa	Colon
4	chr18:7566000-7567600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr18:7566000-7567600	Active TSS	Sigmoid Colon	Sigmoid Colon
6	chr18:7566000-7568400	Bivalent/Poised TSS	Thymus	Thymus
7	chr18:7566000-7569400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
8	chr18:7566200-7567600	Active TSS	Colon Smooth Muscle	Colon
9	chr18:7566200-7568600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr18:7566200-7568600	Active TSS	Fetal Brain Female	brain
11	chr18:7566200-7569000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr18:7566200-7569000	Active TSS	HSMM	muscle
13	chr18:7566200-7569200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr18:7566200-7569200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr18:7566200-7569200	Active TSS	Pancreas	Pancrea
16	chr18:7566200-7569200	Active TSS	HSMMtube	muscle
17	chr18:7566200-7569400	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr18:7566200-7569400	Active TSS	Rectal Smooth Muscle	rectum
19	chr18:7566200-7569800	Active TSS	Aorta	Aorta
20	chr18:7566200-7569800	Active TSS	Ovary	ovary
21	chr18:7566200-7570000	Active TSS	Left Ventricle	heart
22	chr18:7566200-7570000	Active TSS	Right Ventricle	heart
23	chr18:7566200-7570200	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr18:7566200-7570800	Active TSS	Psoas Muscle	Psoas
25	chr18:7566200-7570800	Active TSS	Right Atrium	heart
26	chr18:7566400-7567000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr18:7566400-7567000	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
28	chr18:7566400-7567200	Active TSS	Fetal Intestine Small	intestine
29	chr18:7566400-7567400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr18:7566400-7567400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr18:7566400-7567400	Active TSS	Fetal Intestine Large	intestine
32	chr18:7566400-7567600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr18:7566400-7567600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr18:7566400-7567600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr18:7566400-7567600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
36	chr18:7566400-7567600	Active TSS	Stomach Smooth Muscle	stomach
37	chr18:7566400-7567600	Active TSS	K562	blood
38	chr18:7566400-7567800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr18:7566400-7568200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr18:7566400-7568600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr18:7566400-7568600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr18:7566400-7568600	Active TSS	Brain Hippocampus Middle	brain
43	chr18:7566400-7568600	Active TSS	Fetal Muscle Trunk	muscle
44	chr18:7566400-7568600	Active TSS	Fetal Muscle Leg	muscle
45	chr18:7566400-7568600	Active TSS	Fetal Stomach	stomach
46	chr18:7566400-7568600	Active TSS	Placenta Amnion	Placenta Amnion
47	chr18:7566400-7568800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr18:7566400-7568800	Active TSS	Brain Anterior Caudate	brain
49	chr18:7566400-7568800	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr18:7566400-7568800	Active TSS	Brain Substantia Nigra	brain

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