Variant report

Variant	nsv1020971
Chromosome Location	chr8:124939571-124973679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:61)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:124940522-124940729	K562	blood:	n/a	n/a
2	BCL3	chr8:124969824-124970343	A549	lung:	n/a	n/a
3	BCL3	chr8:124969710-124970348	A549	lung:	n/a	n/a
4	BCL3	chr8:124965147-124965633	A549	lung:	n/a	n/a
5	BHLHE40	chr8:124953507-124953714	K562	blood:	n/a	n/a
6	CBX3	chr8:124940433-124940765	K562	blood:	n/a	n/a
7	CBX3	chr8:124940322-124940818	K562	blood:	n/a	n/a
8	CCNT2	chr8:124948316-124948481	K562	blood:	n/a	n/a
9	CEBPB	chr8:124957025-124957446	MCF-7	breast:	n/a	chr8:124957198-124957209
10	CEBPB	chr8:124957078-124957340	Hela-S3	cervix:	n/a	chr8:124957198-124957209
11	CEBPB	chr8:124969567-124970404	MCF-7	breast:	n/a	chr8:124970215-124970227
12	CEBPB	chr8:124945726-124945926	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:124956990-124957372	ECC-1	luminal epithelium:	n/a	chr8:124957198-124957209
14	CEBPB	chr8:124969721-124970473	A549	lung:	n/a	chr8:124970215-124970227
15	CEBPB	chr8:124945728-124945987	A549	lung:	n/a	n/a
16	CEBPB	chr8:124957016-124957375	K562	blood:	n/a	chr8:124957198-124957209
17	CEBPB	chr8:124957028-124957378	IMR90	lung:	n/a	chr8:124957198-124957209
18	CEBPB	chr8:124956935-124957460	A549	lung:	n/a	chr8:124957198-124957209
19	CEBPB	chr8:124957028-124957385	A549	lung:	n/a	chr8:124957198-124957209
20	CEBPB	chr8:124957022-124957370	HepG2	liver:	n/a	chr8:124957198-124957209
21	CEBPB	chr8:124957045-124957320	H1-hESC	embryonic stem cell:	n/a	chr8:124957198-124957209
22	CEBPB	chr8:124969608-124970345	MCF-7	breast:	n/a	chr8:124970215-124970227
23	CEBPB	chr8:124969723-124970235	A549	lung:	n/a	chr8:124970215-124970227
24	CEBPD	chr8:124948844-124949181	K562	blood:	n/a	n/a
25	CREB1	chr8:124969858-124970196	A549	lung:	n/a	n/a
26	CTCF	chr8:124958300-124958450	NHEK	skin:	n/a	n/a
27	CTCF	chr8:124941691-124941737	GM13976	blood:	n/a	n/a
28	CTCF	chr8:124958300-124958450	K562	blood:	n/a	n/a
29	CTCF	chr8:124948260-124948410	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr8:124941703-124941756	Hela-S3	cervix:	n/a	n/a
31	EP300	chr8:124955327-124956274	ECC-1	luminal epithelium:	n/a	n/a
32	EP300	chr8:124946220-124949233	SK-N-SH	brain:	n/a	chr8:124948058-124948068 chr8:124948188-124948202 chr8:124949077-124949090
33	EP300	chr8:124969755-124970228	MCF-7	breast:	n/a	chr8:124970081-124970091 chr8:124970043-124970053
34	EP300	chr8:124969607-124970533	A549	lung:	n/a	chr8:124970081-124970091 chr8:124970043-124970053
35	EP300	chr8:124961048-124961056	K562	blood:	n/a	n/a
36	EP300	chr8:124969504-124970705	A549	lung:	n/a	chr8:124970081-124970091 chr8:124970043-124970053 chr8:124969594-124969607
37	EP300	chr8:124955519-124956137	ECC-1	luminal epithelium:	n/a	n/a
38	EP300	chr8:124948889-124949051	K562	blood:	n/a	n/a
39	EP300	chr8:124947716-124948077	SK-N-SH_RA	brain:	n/a	chr8:124948058-124948068
40	EP300	chr8:124965111-124965803	A549	lung:	n/a	n/a
41	EP300	chr8:124965061-124965895	A549	lung:	n/a	n/a
42	ESR1	chr8:124955538-124955951	ECC-1	luminal epithelium:	n/a	n/a
43	ESR1	chr8:124955525-124956009	ECC-1	luminal epithelium:	n/a	n/a
44	FOS	chr8:124952269-124952403	MCF10A-Er-Src	breast:	n/a	chr8:124952372-124952380
45	FOS	chr8:124950080-124950303	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr8:124950088-124950288	MCF10A-Er-Src	breast:	n/a	n/a
47	FOSL2	chr8:124965229-124965713	A549	lung:	n/a	chr8:124965454-124965465 chr8:124965453-124965461 chr8:124965451-124965463
48	FOSL2	chr8:124969681-124970479	A549	lung:	n/a	n/a
49	FOSL2	chr8:124965268-124965630	A549	lung:	n/a	chr8:124965454-124965465 chr8:124965453-124965461 chr8:124965451-124965463
50	FOSL2	chr8:124965186-124965711	MCF-7	breast:	n/a	chr8:124965454-124965465 chr8:124965453-124965461 chr8:124965451-124965463

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:124953650-124953700	Hepatocyte	liver:	n/a
2	chr8:124953650-124953700	AG09309	skin:	n/a
3	chr8:124953650-124953700	HepG2	liver:	n/a
4	chr8:124953650-124953700	ProgFib	skin:	n/a
5	chr8:124953650-124953700	AG09319	gingival:	n/a
6	chr8:124953650-124953700	SK-N-SH_RA	brain:	n/a
7	chr8:124953650-124953700	AG04450	lung:	fetal
8	chr8:124953650-124953700	NB4	blood:	n/a
9	chr8:124953650-124953700	NHDF-neo	bronchial:	n/a
10	chr8:124953650-124953700	AoSMC	blood vessel:	n/a
11	chr8:124953650-124953700	GM12878	blood:	n/a
12	chr8:124953650-124953700	HRPEpiC	eye:	n/a
13	chr8:124953650-124953700	NT2-D1	testis:	n/a
14	chr8:124953650-124953700	T-47D	breast:	n/a
15	chr8:124953650-124953700	GM19239	blood:	n/a
16	chr8:124953650-124953700	Jurkat	blood:	n/a
17	chr8:124953650-124953700	A549	lung:	n/a
18	chr8:124953650-124953700	Hela-S3	cervix:	n/a
19	chr8:124953650-124953700	K562	blood:	n/a
20	chr8:124953650-124953700	BJ	skin:	n/a
21	chr8:124953650-124953700	NH-A	brain:	n/a
22	chr8:124953650-124953700	AG10803	skin:	n/a
23	chr8:124953650-124953700	MCF10A-Er-Src	breast:	n/a
24	chr8:124953650-124953700	HEEpiC	esophagus:	n/a
25	chr8:124953650-124953700	HCT-116	colon:	n/a
26	chr8:124953650-124953700	PANC-1	pancreas:	n/a
27	chr8:124953650-124953700	SAEC	small airway:	n/a
28	chr8:124953650-124953700	GM12891	blood:	n/a
29	chr8:124953650-124953700	HCPEpiC	choroid plexus:	n/a
30	chr8:124953650-124953700	HCF	heart:	n/a
31	chr8:124953650-124953700	SKMC	muscle:	n/a
32	chr8:124953650-124953700	CMK	blood:	n/a
33	chr8:124953650-124953700	AG04449	skin:	fetal
34	chr8:124953650-124953700	SK-N-MC	brain:	n/a
35	chr8:124953650-124953700	HMEC	breast:	n/a
36	chr8:124953650-124953700	HEK293	kidney:	embryo
37	chr8:124953650-124953700	HCM	heart:	n/a
38	chr8:124953650-124953700	NHBE	bronchial:	n/a
39	chr8:124953650-124953700	HRE	kidney:	n/a
40	chr8:124953650-124953700	ECC-1	luminal epithelium:	n/a
41	chr8:124953650-124953700	U87	brain:	n/a
42	chr8:124953650-124953700	HL-60	blood:	n/a
43	chr8:124953650-124953700	HAEpiC	amniotic membrane:	n/a
44	chr8:124953650-124953700	HIPEpiC	eye:	n/a
45	chr8:124953650-124953700	PFSK-1	brain:	n/a
46	chr8:124953650-124953700	HPAEpiC	pulmonary alveolar:	n/a
47	chr8:124953650-124953700	LNCaP	prostate:	n/a
48	chr8:124953650-124953700	H1-hESC	embryonic stem cell:	embryo
49	chr8:124953650-124953700	ovcar-3	ovarian:	n/a
50	chr8:124953650-124953700	RPTEC	kidney:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:124969317..124972187-chr8:124973160..124976482,5	MCF-7	breast:
2	chr4:59709166..59709865-chr8:124956173..124956896,2	MCF-7	breast:
3	chr8:124949478..124952088-chr8:124956193..124958036,2	MCF-7	breast:
4	chr8:124961987..124963925-chr8:124978085..124980927,2	MCF-7	breast:
5	chr8:124934471..124936352-chr8:124945543..124948252,2	K562	blood:
6	chr8:124964548..124966868-chr8:124970890..124973539,2	K562	blood:
7	chr8:124852984..124855101-chr8:124954477..124956245,2	K562	blood:
8	chr8:124953943..124955855-chr8:124960688..124963361,2	MCF-7	breast:
9	chr8:124953666..124955209-chr8:124955251..124956757,2	MCF-7	breast:
10	chr2:70258878..70259399-chr8:124971928..124972458,2	MCF-7	breast:
11	chr8:124956642..124959137-chr8:124961616..124964365,2	MCF-7	breast:
12	chr8:124956642..124959137-chr8:124961616..124964365,2	MCF-7	breast:
13	chr8:124964548..124966868-chr8:124970890..124973539,2	K562	blood:
14	chr8:124952199..124955002-chr8:124963674..124966809,3	K562	blood:
15	chr8:124953666..124955209-chr8:124955251..124956757,2	MCF-7	breast:
16	chr8:124954545..124956067-chr8:124976679..124979602,2	K562	blood:
17	chr8:124961288..124963020-chr8:124964546..124966226,2	MCF-7	breast:
18	chr8:124971159..124973956-chr8:124976304..124978202,2	MCF-7	breast:
19	chr8:124951197..124953461-chr8:124968222..124970694,2	MCF-7	breast:
20	chr8:124961288..124963020-chr8:124964546..124966226,2	MCF-7	breast:
21	chr8:124928038..124929759-chr8:124955238..124957453,2	MCF-7	breast:
22	chr8:124934852..124937473-chr8:124945543..124947894,2	K562	blood:
23	chr8:124958881..124961073-chr8:124983059..124985554,2	MCF-7	breast:
24	chr8:124794688..124796229-chr8:124953654..124956422,2	MCF-7	breast:
25	chr8:124955186..124956902-chr8:124972449..124974180,2	MCF-7	breast:
26	chr8:124953943..124955855-chr8:124960688..124963361,2	MCF-7	breast:
27	chr8:124952199..124955002-chr8:124963674..124966809,3	K562	blood:
28	chr8:124951389..124953494-chr8:124984952..124986499,2	MCF-7	breast:
29	chr8:124940520..124943844-chr8:124961774..124964853,3	MCF-7	breast:
30	chr8:124779816..124782654-chr8:124968951..124972407,3	MCF-7	breast:
31	chr8:124938106..124940433-chr8:124943541..124946021,2	MCF-7	breast:
32	chr8:124964244..124966048-chr8:124971947..124973539,2	K562	blood:
33	chr8:124969536..124971932-chr8:124978093..124981369,4	MCF-7	breast:
34	chr8:124954427..124956794-chr8:124966019..124968249,2	MCF-7	breast:
35	chr8:124552529..124555386-chr8:124969535..124971577,2	MCF-7	breast:
36	chr8:124959574..124962412-chr8:124963155..124966540,4	MCF-7	breast:
37	chr8:124942199..124944103-chr8:124945407..124947140,2	K562	blood:
38	chr8:124962163..124964055-chr8:124969703..124971275,2	K562	blood:
39	chr8:124955186..124956902-chr8:124972449..124974180,2	MCF-7	breast:
40	chr8:124969317..124972187-chr8:124973160..124976482,5	MCF-7	breast:
41	chr8:124968963..124971548-chr8:124973335..124975259,2	MCF-7	breast:
42	chr8:124948429..124950203-chr8:124951827..124955191,3	MCF-7	breast:
43	chr8:124968346..124974202-chr8:124988227..124995035,8	MCF-7	breast:
44	chr8:124949478..124952088-chr8:124956193..124958036,2	MCF-7	breast:
45	chr8:124942199..124944103-chr8:124945407..124947140,2	K562	blood:
46	chr8:124948429..124950203-chr8:124951827..124955191,3	MCF-7	breast:
47	chr8:124962163..124964055-chr8:124969703..124971275,2	K562	blood:
48	chr8:124941483..124942084-chr8:125018247..125019468,3	MCF-7	breast:
49	chr8:124950400..124952262-chr8:124991731..124994464,2	MCF-7	breast:
50	chr8:124952162..124954659-chr8:124958980..124961372,2	K562	blood:

No data

Variant related genes	Relation type
FER1L6	TF binding region
ENSG00000254000	TF binding region
FER1L6	CpG island
ENSG00000254000	CpG island
ENSG00000254000	chromatin interactions
ENSG00000156804	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000214814	chromatin interactions

Extended variants
information (count: 1287 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6984557	chr8:124939571-124939572	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs72709125	chr8:124939573-124939574	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563482081	chr8:124939574-124939575	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530922917	chr8:124939575-124939576	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs182692951	chr8:124939613-124939614	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs16899060	chr8:124939645-124939646	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs142082489	chr8:124939656-124939657	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs151165013	chr8:124939665-124939666	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs569019293	chr8:124939682-124939683	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs537673188	chr8:124939724-124939725	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs187963213	chr8:124939732-124939733	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs13250190	chr8:124939773-124939774	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76117786	chr8:124939778-124939779	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553758303	chr8:124939819-124939820	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs150237529	chr8:124939827-124939828	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs191853443	chr8:124939834-124939835	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563201013	chr8:124939909-124939910	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77032968	chr8:124939946-124939947	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184082182	chr8:124939947-124939948	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528506951	chr8:124939953-124939954	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565484223	chr8:124940003-124940004	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546588344	chr8:124940007-124940008	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554315883	chr8:124940045-124940046	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138899458	chr8:124940054-124940055	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35035786	chr8:124940126-124940127	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530071062	chr8:124940139-124940140	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571636785	chr8:124940140-124940141	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539306206	chr8:124940142-124940143	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs13260673	chr8:124940156-124940157	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs188179582	chr8:124940176-124940177	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538038103	chr8:124940342-124940343	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs4871432	chr8:124940349-124940350	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571425209	chr8:124940428-124940429	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs533845852	chr8:124940460-124940461	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs559585315	chr8:124940484-124940485	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs531943351	chr8:124940585-124940586	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs553942260	chr8:124940599-124940600	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573655979	chr8:124940617-124940618	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542688302	chr8:124940655-124940656	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141811852	chr8:124940673-124940674	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs576619851	chr8:124940683-124940684	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs551345623	chr8:124940689-124940690	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545685767	chr8:124940712-124940713	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs76507657	chr8:124940742-124940743	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs536752503	chr8:124940746-124940747	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs192277070	chr8:124940752-124940753	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs527894576	chr8:124940762-124940763	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs4871433	chr8:124940796-124940797	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs147114012	chr8:124940975-124940976	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530034697	chr8:124940976-124940977	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124934800-124939600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:124935400-124942800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:124936800-124940200	Enhancers	NHDF-Ad	bronchial
4	chr8:124937200-124940200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:124938400-124939800	Enhancers	Osteobl	bone
6	chr8:124938800-124940600	Weak transcription	Stomach Mucosa	stomach
7	chr8:124939000-124939800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:124939600-124940200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:124940200-124940600	Weak transcription	NHDF-Ad	bronchial
10	chr8:124940200-124941400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:124940600-124940800	ZNF genes & repeats	NHDF-Ad	bronchial
12	chr8:124940600-124944000	Enhancers	Stomach Mucosa	stomach
13	chr8:124941400-124942600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:124941600-124943600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr8:124941600-124945600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:124941800-124943800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:124942000-124942800	Weak transcription	NHDF-Ad	bronchial
18	chr8:124942000-124943000	Enhancers	Primary hematopoietic stem cells	blood
19	chr8:124942600-124944000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:124942800-124943800	Enhancers	NHDF-Ad	bronchial
21	chr8:124943000-124943200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr8:124943000-124943200	Bivalent Enhancer	Small Intestine	intestine
23	chr8:124943400-124943600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:124943400-124943600	Enhancers	Placenta	Placenta
25	chr8:124943400-124944000	Enhancers	Brain Substantia Nigra	brain
26	chr8:124943600-124944000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:124943600-124944600	Enhancers	Ovary	ovary
28	chr8:124943800-124944800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr8:124944000-124944200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:124944000-124945800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:124944000-124947800	Weak transcription	Stomach Mucosa	stomach
32	chr8:124944200-124948200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:124945000-124945200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:124945600-124945800	Enhancers	Fetal Heart	heart
35	chr8:124945800-124946600	Enhancers	NHDF-Ad	bronchial
36	chr8:124945800-124947600	Weak transcription	Fetal Heart	heart
37	chr8:124945800-124947800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:124946400-124946600	Enhancers	Right Ventricle	heart
39	chr8:124946600-124947800	Weak transcription	NHDF-Ad	bronchial
40	chr8:124946800-124951800	Weak transcription	Right Ventricle	heart
41	chr8:124947600-124947800	Enhancers	Ovary	ovary
42	chr8:124947600-124948000	Enhancers	Fetal Heart	heart
43	chr8:124947600-124949000	Enhancers	Fetal Muscle Leg	muscle
44	chr8:124947800-124948200	Enhancers	Right Atrium	heart
45	chr8:124947800-124948200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr8:124947800-124948400	Enhancers	NHDF-Ad	bronchial
47	chr8:124947800-124948600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:124947800-124948600	Enhancers	Fetal Stomach	stomach
49	chr8:124947800-124948600	Enhancers	Psoas Muscle	Psoas
50	chr8:124947800-124948600	Enhancers	Stomach Mucosa	stomach

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