Variant report

Variant	esv3340095
Chromosome Location	chr8:99438601-99441149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:99439051-99439621	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:99439984-99440418	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:99439105-99439256	GM12878	blood:	n/a	chr8:99439120-99439136 chr8:99439119-99439135
4	BHLHE40	chr8:99439044-99439255	K562	blood:	n/a	chr8:99439120-99439136 chr8:99439119-99439135
5	CCNT2	chr8:99439046-99439246	K562	blood:	n/a	n/a
6	CHD2	chr8:99440099-99440424	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr8:99438884-99439356	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr8:99440100-99440250	BE2_C	brain:	n/a	chr8:99440117-99440130
9	CTCF	chr8:99440140-99440390	NHLF	lung:	n/a	n/a
10	CTCF	chr8:99440024-99440254	A549	lung:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
11	CTCF	chr8:99440200-99440350	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr8:99439958-99440304	H1-hESC	embryonic stem cell:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
13	CTCF	chr8:99440200-99440350	AG09319	gingival:	n/a	n/a
14	CTCF	chr8:99440080-99440230	AG04450	lung:	n/a	chr8:99440117-99440130
15	CTCF	chr8:99440120-99440270	HEK293	kidney:	n/a	n/a
16	CTCF	chr8:99440160-99440310	GM12874	blood:	n/a	n/a
17	CTCF	chr8:99439849-99440446	SK-N-SH	brain:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
18	CTCF	chr8:99440100-99440250	BJ	skin:	n/a	chr8:99440117-99440130
19	CTCF	chr8:99440140-99440290	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr8:99440086-99440280	NHEK	skin:	n/a	chr8:99440117-99440130
21	CTCF	chr8:99440120-99440270	HCFaa	heart:	n/a	n/a
22	CTCF	chr8:99440160-99440310	AG09309	skin:	n/a	n/a
23	CTCF	chr8:99440080-99440230	SAEC	small airway:	n/a	chr8:99440117-99440130
24	CTCF	chr8:99440080-99440230	NHDF-neo	bronchial:	n/a	chr8:99440117-99440130
25	CTCF	chr8:99440080-99440230	RPTEC	kidney:	n/a	chr8:99440117-99440130
26	CTCF	chr8:99440080-99440230	GM12873	blood:	n/a	chr8:99440117-99440130
27	CTCF	chr8:99440120-99440229	GM13977	blood:	n/a	n/a
28	CTCF	chr8:99440065-99440223	SK-N-SH_RA	brain:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
29	CTCF	chr8:99440040-99440190	HUVEC	blood vessel:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
30	CTCF	chr8:99440020-99440170	WI-38	lung:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
31	CTCF	chr8:99440093-99440294	IMR90	lung:	n/a	chr8:99440117-99440130
32	CTCF	chr8:99440060-99440210	GM12871	blood:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
33	CTCF	chr8:99440100-99440250	AG04449	skin:	n/a	chr8:99440117-99440130
34	CTCF	chr8:99440120-99440270	HAc	cerebellar:	n/a	n/a
35	CTCF	chr8:99440020-99440170	BE2_C	brain:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
36	CTCF	chr8:99440100-99440250	HPF	lung:	n/a	chr8:99440117-99440130
37	CTCF	chr8:99440160-99440310	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr8:99440180-99440330	WI-38	lung:	n/a	n/a
39	CTCF	chr8:99440140-99440290	AG04449	skin:	n/a	n/a
40	CTCF	chr8:99440080-99440230	AG09319	gingival:	n/a	chr8:99440117-99440130
41	CTCF	chr8:99440080-99440230	GM12870	blood:	n/a	chr8:99440117-99440130
42	CTCF	chr8:99439963-99440415	H1-hESC	embryonic stem cell:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
43	CTCF	chr8:99440187-99440235	GM19239	blood:	n/a	n/a
44	CTCF	chr8:99440140-99440290	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr8:99440100-99440250	HRPEpiC	eye:	n/a	chr8:99440117-99440130
46	CTCF	chr8:99440100-99440250	HBMEC	blood vessel:	n/a	chr8:99440117-99440130
47	CTCF	chr8:99440050-99440354	H1-hESC	embryonic stem cell:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
48	CTCF	chr8:99440100-99440250	HFF	foreskin:	n/a	chr8:99440117-99440130
49	CTCF	chr8:99440060-99440210	HRPEpiC	eye:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
50	CTCF	chr8:99439880-99440030	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99438968-99439018	HUVEC	blood vessel:	n/a
2	chr8:99438968-99439018	HUVEC	blood vessel:	n/a
3	chr8:99439948-99439998	NB4	blood:	n/a
4	chr8:99440331-99440381	GM12892	blood:	n/a
5	chr8:99439861-99439911	HUVEC	blood vessel:	n/a
6	chr8:99439685-99439735	AG09309	skin:	n/a
7	chr8:99439685-99439735	NHDF-neo	bronchial:	n/a
8	chr8:99439861-99439911	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:99440279-99440329	HMEC	breast:	n/a
10	chr8:99440279-99440329	NHDF-neo	bronchial:	n/a
11	chr8:99440331-99440381	HL-60	blood:	n/a
12	chr8:99438942-99438992	T-47D	breast:	n/a
13	chr8:99440279-99440329	ProgFib	skin:	n/a
14	chr8:99440331-99440381	AG04450	lung:	fetal
15	chr8:99440522-99440572	BJ	skin:	n/a
16	chr8:99438942-99438992	HMEC	breast:	n/a
17	chr8:99440279-99440329	RPTEC	kidney:	n/a
18	chr8:99438968-99439018	SK-N-MC	brain:	n/a
19	chr8:99440522-99440572	AG04450	lung:	fetal
20	chr8:99440279-99440329	AG10803	skin:	n/a
21	chr8:99440522-99440572	HIPEpiC	eye:	n/a
22	chr8:99440279-99440329	AG04450	lung:	fetal
23	chr8:99440522-99440572	HCM	heart:	n/a
24	chr8:99438968-99439018	HCT-116	colon:	n/a
25	chr8:99440522-99440572	AG04449	skin:	fetal
26	chr8:99440522-99440572	GM12878	blood:	n/a
27	chr8:99439685-99439735	HCF	heart:	n/a
28	chr8:99439119-99439169	AG04449	skin:	fetal
29	chr8:99440279-99440329	HL-60	blood:	n/a
30	chr8:99439119-99439169	NH-A	brain:	n/a
31	chr8:99438968-99439018	HCF	heart:	n/a
32	chr8:99438942-99438992	Caco-2	colon:	n/a
33	chr8:99440331-99440381	HIPEpiC	eye:	n/a
34	chr8:99438942-99438992	MCF10A-Er-Src	breast:	n/a
35	chr8:99439861-99439911	H1-hESC	embryonic stem cell:	embryo
36	chr8:99440331-99440381	SK-N-MC	brain:	n/a
37	chr8:99438942-99438992	HL-60	blood:	n/a
38	chr8:99438624-99438674	BE2_C	brain:	n/a
39	chr8:99438968-99439018	MCF10A-Er-Src	breast:	n/a
40	chr8:99438624-99438674	K562	blood:	n/a
41	chr8:99440331-99440381	Jurkat	blood:	n/a
42	chr8:99439948-99439998	SAEC	small airway:	n/a
43	chr8:99438942-99438992	GM19239	blood:	n/a
44	chr8:99440331-99440381	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:99440279-99440329	AG09319	gingival:	n/a
46	chr8:99440279-99440329	SK-N-SH	brain:	n/a
47	chr8:99440331-99440381	NH-A	brain:	n/a
48	chr8:99439948-99439998	GM12891	blood:	n/a
49	chr8:99440331-99440381	PrEC	prostate:	n/a
50	chr8:99439948-99439998	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:99440204..99443025-chr8:99468431..99469990,2	K562	blood:
2	chr8:99413566..99415958-chr8:99440640..99443091,2	MCF-7	breast:

Variant related genes	Relation type
KCNS2	TF binding region
KCNS2	CpG island

Extended variants
information (count: 69 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528008664	chr8:99438612-99438613	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs547726911	chr8:99438677-99438678	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541140858	chr8:99438716-99438717	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs57063021	chr8:99438724-99438725	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs546240251	chr8:99438780-99438781	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs192203250	chr8:99438797-99438798	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs569747841	chr8:99438811-99438812	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528200927	chr8:99438814-99438815	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538290616	chr8:99438817-99438818	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs561081156	chr8:99438828-99438829	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs4075986	chr8:99438831-99438832	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs75626948	chr8:99438845-99438846	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs563693856	chr8:99438877-99438878	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs574336177	chr8:99438884-99438885	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs543189173	chr8:99439039-99439040	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs562674428	chr8:99439088-99439089	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs576495239	chr8:99439117-99439118	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs111838089	chr8:99439153-99439154	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs545141654	chr8:99439202-99439203	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs28709500	chr8:99439272-99439273	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs538370680	chr8:99439409-99439410	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs527645743	chr8:99439590-99439591	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548149208	chr8:99439797-99439798	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs552856713	chr8:99439851-99439852	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs368310736	chr8:99439880-99439881	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs566299558	chr8:99439909-99439910	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs561564931	chr8:99439922-99439923	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs547946224	chr8:99439956-99439957	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs550383150	chr8:99439997-99439998	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs548776392	chr8:99440005-99440006	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs10111589	chr8:99440006-99440007	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551942052	chr8:99440009-99440010	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs199762721	chr8:99440226-99440227	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs184683445	chr8:99440237-99440238	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs554468246	chr8:99440243-99440244	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs372037161	chr8:99440249-99440250	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs140515528	chr8:99440255-99440256	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs144362730	chr8:99440256-99440257	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs541131650	chr8:99440258-99440259	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs201468098	chr8:99440265-99440266	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs151175046	chr8:99440279-99440280	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs140159901	chr8:99440313-99440314	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs150305860	chr8:99440343-99440344	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs200726542	chr8:99440375-99440376	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs572431917	chr8:99440420-99440421	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567295212	chr8:99440424-99440425	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373045610	chr8:99440523-99440524	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144881255	chr8:99440569-99440570	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376045564	chr8:99440598-99440599	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541434350	chr8:99440622-99440623	Bivalent Enhancer Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99438000-99439200	Bivalent/Poised TSS	Brain Angular Gyrus	brain
2	chr8:99438000-99440200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:99438000-99440600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr8:99438000-99440600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr8:99438000-99441200	ZNF genes & repeats	Spleen	Spleen
6	chr8:99438200-99438800	Bivalent Enhancer	Fetal Stomach	stomach
7	chr8:99438200-99440200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:99438400-99438800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
9	chr8:99438400-99438800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr8:99438400-99438800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:99438400-99438800	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:99438400-99438800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:99438400-99438800	Bivalent Enhancer	Colon Smooth Muscle	Colon
14	chr8:99438400-99438800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr8:99438400-99438800	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr8:99438400-99438800	Flanking Active TSS	Ovary	ovary
17	chr8:99438400-99438800	Bivalent/Poised TSS	Right Ventricle	heart
18	chr8:99438400-99438800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr8:99438400-99439000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
20	chr8:99438400-99439000	Bivalent Enhancer	Placenta	Placenta
21	chr8:99438400-99439000	Enhancers	Gastric	stomach
22	chr8:99438400-99439000	Flanking Active TSS	Pancreas	Pancrea
23	chr8:99438400-99439000	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
24	chr8:99438400-99439200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:99438400-99439200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:99438400-99440400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
27	chr8:99438400-99440400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
28	chr8:99438400-99440600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
29	chr8:99438400-99440600	Bivalent Enhancer	Lung	lung
30	chr8:99438600-99438800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:99438600-99438800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:99438600-99438800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
33	chr8:99438600-99438800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:99438600-99438800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:99438600-99438800	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr8:99438600-99438800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
37	chr8:99438600-99438800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr8:99438600-99438800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
39	chr8:99438600-99438800	Flanking Active TSS	Fetal Heart	heart
40	chr8:99438600-99438800	Bivalent Enhancer	Fetal Intestine Small	intestine
41	chr8:99438600-99438800	Active TSS	Right Atrium	heart
42	chr8:99438600-99439000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:99438600-99439000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:99438600-99439000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:99438600-99439000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr8:99438600-99439000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
47	chr8:99438600-99439000	Bivalent Enhancer	Fetal Lung	lung
48	chr8:99438600-99439200	Enhancers	Primary hematopoietic stem cells	blood
49	chr8:99438600-99439200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:99438600-99439400	Bivalent/Poised TSS	Adipose Nuclei	Adipose

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