Variant report

Variant	nsv1019752
Chromosome Location	chr8:39087542-39371410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1014)
CpG islands
(count:734)
Chromatin interactive
region (count:22)
LncRNA
region (count:273)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39184983-39185219	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
3	ATF1	chr8:39169144-39169211	K562	blood:	n/a	n/a
4	ATF1	chr8:39204094-39204343	K562	blood:	n/a	n/a
5	ATF1	chr8:39184952-39185134	K562	blood:	n/a	n/a
6	ATF1	chr8:39090849-39091203	K562	blood:	n/a	n/a
7	ATF1	chr8:39187249-39187365	K562	blood:	n/a	n/a
8	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
9	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:39215146-39215389	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:39215071-39215373	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:39338104-39338425	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:39135297-39135321	K562	blood:	n/a	n/a
16	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
17	CBX3	chr8:39241402-39241706	K562	blood:	n/a	n/a
18	CBX3	chr8:39090639-39091440	HCT-116	colon:	n/a	n/a
19	CBX3	chr8:39099996-39100457	HCT-116	colon:	n/a	n/a
20	CBX3	chr8:39184878-39185271	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
22	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
23	CEBPB	chr8:39122247-39122648	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:39301112-39301366	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:39169394-39169417	A549	lung:	n/a	n/a
26	CEBPB	chr8:39272719-39273086	K562	blood:	n/a	n/a
27	CEBPB	chr8:39172450-39172643	K562	blood:	n/a	chr8:39172538-39172549
28	CEBPB	chr8:39301088-39301411	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:39225484-39225625	IMR90	lung:	n/a	n/a
30	CEBPB	chr8:39255330-39255613	K562	blood:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
31	CEBPB	chr8:39172365-39172592	A549	lung:	n/a	chr8:39172538-39172549
32	CEBPB	chr8:39255337-39255640	H1-hESC	embryonic stem cell:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
33	CEBPB	chr8:39340885-39341025	K562	blood:	n/a	n/a
34	CEBPB	chr8:39144160-39144242	A549	lung:	n/a	n/a
35	CEBPB	chr8:39272750-39273063	K562	blood:	n/a	n/a
36	CEBPB	chr8:39255284-39255699	IMR90	lung:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
37	CEBPB	chr8:39255339-39255659	Hela-S3	cervix:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
38	CEBPZ	chr8:39139103-39139155	HepG2	liver:	n/a	n/a
39	CHD1	chr8:39338195-39338500	GM12878	blood:	n/a	n/a
40	CHD1	chr8:39142862-39142883	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr8:39338173-39338614	GM12878	blood:	n/a	n/a
42	CHD2	chr8:39328713-39329005	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr8:39130520-39130670	AG09309	skin:	n/a	n/a
44	CTCF	chr8:39185000-39185150	GM12865	blood:	n/a	n/a
45	CTCF	chr8:39184980-39185130	HCM	heart:	n/a	n/a
46	CTCF	chr8:39185400-39185550	GM12865	blood:	n/a	n/a
47	CTCF	chr8:39306440-39306590	GM12872	blood:	n/a	n/a
48	CTCF	chr8:39184980-39185130	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr8:39306420-39306570	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr8:39130546-39130660	MCF-7	breast:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39172022-39172072	GM06990	blood:	n/a
2	chr8:39172111-39172161	BE2_C	brain:	n/a
3	chr8:39172022-39172072	GM06990	blood:	n/a
4	chr8:39172111-39172161	BE2_C	brain:	n/a
5	chr8:39223182-39223232	Hela-S3	cervix:	n/a
6	chr8:39172022-39172072	AG09309	skin:	n/a
7	chr8:39172111-39172161	ProgFib	skin:	n/a
8	chr8:39172111-39172161	AG09319	gingival:	n/a
9	chr8:39171648-39171698	ovcar-3	ovarian:	n/a
10	chr8:39172020-39172070	HMEC	breast:	n/a
11	chr8:39172022-39172072	MCF-7	breast:	n/a
12	chr8:39223182-39223232	PFSK-1	brain:	n/a
13	chr8:39172120-39172170	HMEC	breast:	n/a
14	chr8:39328433-39328483	NHBE	bronchial:	n/a
15	chr8:39223182-39223232	NH-A	brain:	n/a
16	chr8:39172111-39172161	K562	blood:	n/a
17	chr8:39172022-39172072	NH-A	brain:	n/a
18	chr8:39171620-39171670	HRPEpiC	eye:	n/a
19	chr8:39171620-39171670	Hepatocyte	liver:	n/a
20	chr8:39171620-39171670	GM12892	blood:	n/a
21	chr8:39328433-39328483	HCT-116	colon:	n/a
22	chr8:39328433-39328483	MCF10A-Er-Src	breast:	n/a
23	chr8:39171620-39171670	ProgFib	skin:	n/a
24	chr8:39196907-39196957	HCM	heart:	n/a
25	chr8:39196907-39196957	HEEpiC	esophagus:	n/a
26	chr8:39171648-39171698	HIPEpiC	eye:	n/a
27	chr8:39172097-39172147	ECC-1	luminal epithelium:	n/a
28	chr8:39172022-39172072	GM19239	blood:	n/a
29	chr8:39172022-39172072	H1-hESC	embryonic stem cell:	embryo
30	chr8:39171866-39171916	HCPEpiC	choroid plexus:	n/a
31	chr8:39172022-39172072	K562	blood:	n/a
32	chr8:39172099-39172149	MCF10A-Er-Src	breast:	n/a
33	chr8:39223182-39223232	BJ	skin:	n/a
34	chr8:39171866-39171916	AG09309	skin:	n/a
35	chr8:39171866-39171916	HRPEpiC	eye:	n/a
36	chr8:39172099-39172149	GM12891	blood:	n/a
37	chr8:39171648-39171698	HCF	heart:	n/a
38	chr8:39172022-39172072	IMR90	lung:	fetal
39	chr8:39172120-39172170	ovcar-3	ovarian:	n/a
40	chr8:39172097-39172147	NH-A	brain:	n/a
41	chr8:39171620-39171670	BE2_C	brain:	n/a
42	chr8:39196907-39196957	NHBE	bronchial:	n/a
43	chr8:39172020-39172070	LNCaP	prostate:	n/a
44	chr8:39328433-39328483	SK-N-SH_RA	brain:	n/a
45	chr8:39172022-39172072	U87	brain:	n/a
46	chr8:39196907-39196957	PANC-1	pancreas:	n/a
47	chr8:39172020-39172070	AG09319	gingival:	n/a
48	chr8:39172020-39172070	HRE	kidney:	n/a
49	chr8:39196907-39196957	HNPCEpiC	eye:	n/a
50	chr8:39172022-39172072	BE2_C	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
2	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
3	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
4	chr8:38824064..38824622-chr8:39184733..39185545,2	K562	blood:
5	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
6	chr8:39079754..39082023-chr8:39086400..39088238,2	MCF-7	breast:
7	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
8	chr8:38964583..38965453-chr8:39130431..39131111,2	MCF-7	breast:
9	chr6:156717380..156718086-chr8:39158912..39159795,2	MCF-7	breast:
10	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
11	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
12	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
13	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
14	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
15	chr8:39170463..39172530-chr8:39174983..39176968,2	MCF-7	breast:
16	chr8:38964712..38965432-chr8:39130166..39131088,2	MCF-7	breast:
17	chr8:39080941..39082777-chr8:39089064..39090963,2	K562	blood:
18	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
19	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
20	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
21	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
22	chr15:50661566..50662138-chr8:39161334..39161854,2	MCF-7	breast:

(count:273 , 50 per page) page: 1 2 3 4 5 6

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126168
2	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126169
3	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126152
4	lnc-ADAM2-6	chr8:39308565-39308680	NONHSAT126167
5	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126163
6	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126150
7	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126168
8	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126151
9	lnc-ADAM2-6	chr8:39335215-39335462	NONHSAT126166
10	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126164
11	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126164
12	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126167
13	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT126152
14	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126168
15	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126154
16	lnc-ADAM2-6	chr8:39347782-39347876	NONHSAT126165
17	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126148
18	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126151
19	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126170
20	lnc-ADAM9-1	chr8:39131831-39131869	NONHSAT126144
21	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126168
22	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126152
23	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126153
24	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126166
25	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT147628
26	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT147628
27	lnc-ADAM9-1	chr8:39133347-39133385	NONHSAT126144
28	lnc-ADAM2-6	chr8:39347782-39347876	NONHSAT126163
29	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126165
30	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126155
31	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126159
32	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126150
33	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126166
34	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126168
35	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT147628
36	lnc-ADAM32-1	chr8:39181838-39181858	NONHSAT147629
37	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126153
38	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126163
39	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126159
40	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT147629
41	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT147628
42	lnc-ADAM9-1	chr8:39142312-39142428	NONHSAT126143
43	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT147628
44	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126165
45	lnc-ADAM2-6	chr8:39335215-39335616	NONHSAT126167
46	lnc-ADAM9-1	chr8:39141105-39141143	NONHSAT126144
47	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126169
48	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126164
49	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126166
50	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126168

No data

Variant related genes	Relation type
ADAM32	TF binding region
ENSG00000253160	TF binding region
ADAM5	TF binding region
ADAM32	CpG island
ENSG00000253160	CpG island
ADAM5	CpG island
ENSG00000196115	chromatin interactions
ENSG00000197140	chromatin interactions

Extended variants
information (count: 3524 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:3524 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528504517	chr8:39087587-39087588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149703944	chr8:39087603-39087604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572364454	chr8:39087604-39087605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541097892	chr8:39087654-39087655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146212275	chr8:39087676-39087677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530167296	chr8:39087709-39087710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114165414	chr8:39087740-39087741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191832897	chr8:39087758-39087759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370195943	chr8:39087782-39087783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532795284	chr8:39087792-39087793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552607240	chr8:39087820-39087821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373893009	chr8:39087826-39087827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576748799	chr8:39087870-39087871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533529609	chr8:39087892-39087893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577334834	chr8:39087915-39087916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77943718	chr8:39087924-39087925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567358949	chr8:39087927-39087928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140131333	chr8:39087939-39087940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184425951	chr8:39087945-39087946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569758452	chr8:39087951-39087952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538890473	chr8:39087989-39087990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546467937	chr8:39088046-39088047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562576973	chr8:39088048-39088049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7016661	chr8:39088049-39088050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs541011886	chr8:39088122-39088123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554584859	chr8:39088181-39088182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542825423	chr8:39088251-39088252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143758042	chr8:39088313-39088314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115777755	chr8:39088458-39088459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542105032	chr8:39088501-39088502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146882902	chr8:39088546-39088547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74336775	chr8:39088623-39088624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546451133	chr8:39088642-39088643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559777995	chr8:39088692-39088693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371355271	chr8:39088721-39088722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547412567	chr8:39088748-39088749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567271784	chr8:39088750-39088751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529772769	chr8:39088776-39088777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549916757	chr8:39088782-39088783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9298563	chr8:39088850-39088851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188571140	chr8:39088854-39088855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79638670	chr8:39088872-39088873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565826840	chr8:39088875-39088876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534648935	chr8:39088876-39088877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138681555	chr8:39088894-39088895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147328645	chr8:39088897-39088898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139351022	chr8:39088898-39088899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149123945	chr8:39088899-39088900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369347826	chr8:39088900-39088901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35688722	chr8:39088974-39088975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	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
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Lung cancer	21569311	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Chordoma	21215367	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Medulloblastoma	21163964	CNVD
Cancer	21249187	CNVD
Autism	19287141	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Rett syndrome	21593744	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39076200-39097200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:39083200-39097800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:39085200-39090400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:39089800-39090000	Enhancers	HMEC	breast
5	chr8:39090000-39090800	Weak transcription	HMEC	breast
6	chr8:39090000-39091800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:39090200-39091600	Enhancers	NHEK	skin
8	chr8:39090400-39090800	Enhancers	A549	lung
9	chr8:39090400-39091000	Enhancers	NH-A	brain
10	chr8:39090400-39091600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:39090600-39091000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:39090600-39091200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:39090800-39091200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr8:39090800-39091400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr8:39090800-39091400	Enhancers	HMEC	breast
16	chr8:39090800-39091600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:39091000-39091200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:39091600-39092200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:39091600-39098200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:39092000-39094400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:39092200-39092400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:39094400-39095200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:39094400-39095200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr8:39094400-39095400	ZNF genes & repeats	Aorta	Aorta
25	chr8:39098200-39098600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:39098600-39099200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:39098800-39099400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:39099200-39099800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:39099200-39100600	Enhancers	HMEC	breast
30	chr8:39099800-39124600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:39100000-39100400	Enhancers	HUVEC	blood vessel
32	chr8:39100000-39100400	Enhancers	NHEK	skin
33	chr8:39109200-39109800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:39110800-39111000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:39122000-39123000	Enhancers	Hela-S3	cervix
36	chr8:39122200-39122800	Enhancers	NHEK	skin
37	chr8:39124400-39124800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:39124600-39125600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:39125200-39125800	Enhancers	HepG2	liver
40	chr8:39125600-39129200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:39129200-39131200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:39129400-39130000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr8:39129400-39130600	Enhancers	HMEC	breast
44	chr8:39129600-39130600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:39129800-39130600	Enhancers	NHEK	skin
46	chr8:39135000-39135200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:39135000-39135200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:39135200-39135400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:39135600-39135800	Enhancers	HepG2	liver
50	chr8:39137200-39137600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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