Variant report

Variant	esv1815710
Chromosome Location	chr8:39101565-39405724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1068)
CpG islands
(count:916)
Chromatin interactive
region (count:27)
LncRNA
region (count:288)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39393079-39393534	K562	blood:	n/a	n/a
2	ARID3A	chr8:39391480-39391748	K562	blood:	n/a	n/a
3	ARID3A	chr8:39184983-39185219	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
5	ATF1	chr8:39169144-39169211	K562	blood:	n/a	n/a
6	ATF1	chr8:39204094-39204343	K562	blood:	n/a	n/a
7	ATF1	chr8:39187249-39187365	K562	blood:	n/a	n/a
8	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
9	ATF1	chr8:39184952-39185134	K562	blood:	n/a	n/a
10	ATF3	chr8:39390540-39390824	K562	blood:	n/a	n/a
11	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
13	BCL11A	chr8:39215071-39215373	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:39215146-39215389	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:39338104-39338425	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:39379884-39380110	K562	blood:	n/a	n/a
18	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:39135297-39135321	K562	blood:	n/a	n/a
20	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
22	CBX3	chr8:39241402-39241706	K562	blood:	n/a	n/a
23	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
24	CBX3	chr8:39184878-39185271	HCT-116	colon:	n/a	n/a
25	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
26	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
27	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
28	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
29	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
30	CEBPB	chr8:39301112-39301366	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:39225484-39225625	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:39391427-39391768	K562	blood:	n/a	chr8:39391593-39391604
33	CEBPB	chr8:39255339-39255659	Hela-S3	cervix:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
34	CEBPB	chr8:39391451-39391754	IMR90	lung:	n/a	chr8:39391593-39391604
35	CEBPB	chr8:39169394-39169417	A549	lung:	n/a	n/a
36	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:39390600-39390943	K562	blood:	n/a	n/a
38	CEBPB	chr8:39393010-39393254	K562	blood:	n/a	n/a
39	CEBPB	chr8:39301088-39301411	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:39255337-39255640	H1-hESC	embryonic stem cell:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
41	CEBPB	chr8:39272750-39273063	K562	blood:	n/a	n/a
42	CEBPB	chr8:39392971-39393463	K562	blood:	n/a	n/a
43	CEBPB	chr8:39272719-39273086	K562	blood:	n/a	n/a
44	CEBPB	chr8:39255284-39255699	IMR90	lung:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
45	CEBPB	chr8:39377869-39377951	K562	blood:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
46	CEBPB	chr8:39255330-39255613	K562	blood:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
47	CEBPB	chr8:39390555-39390826	K562	blood:	n/a	n/a
48	CEBPB	chr8:39172365-39172592	A549	lung:	n/a	chr8:39172538-39172549
49	CEBPB	chr8:39377774-39377967	H1-hESC	embryonic stem cell:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
50	CEBPB	chr8:39373655-39374022	IMR90	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39172022-39172072	AG04450	lung:	fetal
2	chr8:39172022-39172072	AG04450	lung:	fetal
3	chr8:39172022-39172072	GM19239	blood:	n/a
4	chr8:39328433-39328483	AG04449	skin:	fetal
5	chr8:39380592-39380642	A549	lung:	n/a
6	chr8:39196907-39196957	U87	brain:	n/a
7	chr8:39172020-39172070	CMK	blood:	n/a
8	chr8:39380592-39380642	GM12891	blood:	n/a
9	chr8:39172020-39172070	AG09309	skin:	n/a
10	chr8:39172020-39172070	HRPEpiC	eye:	n/a
11	chr8:39172099-39172149	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:39172111-39172161	HMEC	breast:	n/a
13	chr8:39223182-39223232	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:39223182-39223232	HRE	kidney:	n/a
15	chr8:39172097-39172147	HEK293	kidney:	embryo
16	chr8:39171620-39171670	SK-N-SH_RA	brain:	n/a
17	chr8:39380341-39380391	HRCEpiC	kidney:	n/a
18	chr8:39172097-39172147	HMEC	breast:	n/a
19	chr8:39223182-39223232	HCM	heart:	n/a
20	chr8:39172099-39172149	AoSMC	blood vessel:	n/a
21	chr8:39172097-39172147	PFSK-1	brain:	n/a
22	chr8:39172111-39172161	CMK	blood:	n/a
23	chr8:39196907-39196957	AG09319	gingival:	n/a
24	chr8:39172097-39172147	NHBE	bronchial:	n/a
25	chr8:39172120-39172170	BJ	skin:	n/a
26	chr8:39171866-39171916	SAEC	small airway:	n/a
27	chr8:39380341-39380391	HRPEpiC	eye:	n/a
28	chr8:39172111-39172161	PANC-1	pancreas:	n/a
29	chr8:39380592-39380642	AG09309	skin:	n/a
30	chr8:39328433-39328483	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:39380592-39380642	HIPEpiC	eye:	n/a
32	chr8:39380341-39380391	K562	blood:	n/a
33	chr8:39172097-39172147	SK-N-SH_RA	brain:	n/a
34	chr8:39172097-39172147	SAEC	small airway:	n/a
35	chr8:39172020-39172070	AG10803	skin:	n/a
36	chr8:39171866-39171916	NHBE	bronchial:	n/a
37	chr8:39171648-39171698	ovcar-3	ovarian:	n/a
38	chr8:39172099-39172149	GM12891	blood:	n/a
39	chr8:39172120-39172170	BE2_C	brain:	n/a
40	chr8:39172111-39172161	GM12891	blood:	n/a
41	chr8:39380592-39380642	ovcar-3	ovarian:	n/a
42	chr8:39380592-39380642	PANC-1	pancreas:	n/a
43	chr8:39172099-39172149	HRPEpiC	eye:	n/a
44	chr8:39172022-39172072	HL-60	blood:	n/a
45	chr8:39171866-39171916	PANC-1	pancreas:	n/a
46	chr8:39172022-39172072	LNCaP	prostate:	n/a
47	chr8:39172097-39172147	AG04449	skin:	fetal
48	chr8:39172022-39172072	HRE	kidney:	n/a
49	chr8:39328433-39328483	ECC-1	luminal epithelium:	n/a
50	chr8:39172120-39172170	CMK	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
2	chr8:39170463..39172530-chr8:39174983..39176968,2	MCF-7	breast:
3	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
4	chr15:50661566..50662138-chr8:39161334..39161854,2	MCF-7	breast:
5	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
6	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
7	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
8	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
9	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:
10	chr8:38964583..38965453-chr8:39130431..39131111,2	MCF-7	breast:
11	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
12	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
13	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
14	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
15	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
16	chr8:38964712..38965432-chr8:39130166..39131088,2	MCF-7	breast:
17	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
18	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
19	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
20	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
21	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
22	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
23	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
24	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
25	chr6:156717380..156718086-chr8:39158912..39159795,2	MCF-7	breast:
26	chr8:38824064..38824622-chr8:39184733..39185545,2	K562	blood:
27	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126164
2	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126164
3	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126150
4	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126150
5	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126163
6	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126163
7	lnc-ADAM32-1	chr8:39274733-39274745	NONHSAT126153
8	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126164
9	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126155
10	lnc-ADAM32-1	chr8:39274733-39274897	NONHSAT126150
11	lnc-ADAM9-1	chr8:39128395-39128433	NONHSAT126145
12	lnc-ADAM2-6	chr8:39380272-39380390	NONHSAT126171
13	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126152
14	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126151
15	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126168
16	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126169
17	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126164
18	lnc-ADAM32-1	chr8:39181838-39181858	NONHSAT147629
19	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126151
20	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126165
21	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126151
22	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT147628
23	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126151
24	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126155
25	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT147628
26	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126153
27	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126166
28	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126148
29	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126166
30	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126168
31	lnc-ADAM32-1	chr8:39238308-39238398	NONHSAT126148
32	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126168
33	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126165
34	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT126151
35	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126163
36	lnc-ADAM9-1	chr8:39114706-39114862	NONHSAT126143
37	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126167
38	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126157
39	lnc-ADAM32-1	chr8:39180489-39181258	NONHSAT126149
40	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126152
41	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126170
42	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126163
43	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126168
44	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126151
45	lnc-ADAM2-6	chr8:39380272-39380371	NONHSAT126169
46	lnc-ADAM32-1	chr8:39238308-39238347	NONHSAT147629
47	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126168
48	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126153
49	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126148
50	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT126150

No data

Variant related genes	Relation type
ADAM32	TF binding region
ENSG00000253160	TF binding region
ADAM5	TF binding region
ADAM3A	TF binding region
ADAM32	CpG island
ENSG00000253160	CpG island
ADAM5	CpG island
ADAM3A	CpG island
ENSG00000196115	chromatin interactions
ENSG00000197140	chromatin interactions

Extended variants
information (count: 3714 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3714 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553699146	chr8:39101586-39101587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76267351	chr8:39101607-39101608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555360068	chr8:39101638-39101639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181421532	chr8:39101640-39101641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557589565	chr8:39101685-39101686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376853937	chr8:39101740-39101741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185954805	chr8:39101743-39101744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534491723	chr8:39101753-39101754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190604015	chr8:39101780-39101781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140434019	chr8:39101784-39101785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183803689	chr8:39101801-39101802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553105673	chr8:39101892-39101893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114049599	chr8:39101921-39101922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529754914	chr8:39102026-39102027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34657397	chr8:39102066-39102067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543211642	chr8:39102082-39102083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145541872	chr8:39102160-39102161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189216940	chr8:39102176-39102177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552081571	chr8:39102207-39102208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369124903	chr8:39102228-39102229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577769822	chr8:39102245-39102246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6987728	chr8:39102254-39102255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs548298957	chr8:39102275-39102276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568492605	chr8:39102335-39102336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376627436	chr8:39102349-39102350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554268244	chr8:39102369-39102370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190768229	chr8:39102381-39102382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376687464	chr8:39102404-39102405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538725711	chr8:39102570-39102571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557575176	chr8:39102590-39102591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34023190	chr8:39102596-39102597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140097477	chr8:39102622-39102623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540063041	chr8:39102667-39102668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553672347	chr8:39102687-39102688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573467749	chr8:39102732-39102733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7001987	chr8:39102741-39102742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182855426	chr8:39102861-39102862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574467158	chr8:39102911-39102912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543146060	chr8:39102929-39102930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575109432	chr8:39102963-39102964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574045452	chr8:39103023-39103024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77647467	chr8:39103024-39103025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576600408	chr8:39103025-39103026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545608961	chr8:39103027-39103028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371334644	chr8:39103039-39103040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542453127	chr8:39103048-39103049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138809069	chr8:39103054-39103055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559555346	chr8:39103072-39103073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559603072	chr8:39103108-39103109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577821398	chr8:39103140-39103141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Bladder cancer	21909424	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39099800-39124600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:39109200-39109800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:39110800-39111000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:39122000-39123000	Enhancers	Hela-S3	cervix
5	chr8:39122200-39122800	Enhancers	NHEK	skin
6	chr8:39124400-39124800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:39124600-39125600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:39125200-39125800	Enhancers	HepG2	liver
9	chr8:39125600-39129200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:39129200-39131200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:39129400-39130000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:39129400-39130600	Enhancers	HMEC	breast
13	chr8:39129600-39130600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:39129800-39130600	Enhancers	NHEK	skin
15	chr8:39135000-39135200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:39135000-39135200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:39135200-39135400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:39135600-39135800	Enhancers	HepG2	liver
19	chr8:39137200-39137600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:39137400-39137800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:39140600-39141000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:39146000-39146400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr8:39163200-39163600	Enhancers	Gastric	stomach
24	chr8:39163200-39163800	Enhancers	Fetal Intestine Small	intestine
25	chr8:39171400-39171600	Bivalent Enhancer	Fetal Lung	lung
26	chr8:39171600-39171800	Enhancers	Fetal Brain Female	brain
27	chr8:39171600-39172000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr8:39171600-39172000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
29	chr8:39171600-39172400	Bivalent/Poised TSS	Fetal Lung	lung
30	chr8:39171800-39172000	Bivalent/Poised TSS	NH-A	brain
31	chr8:39171800-39172200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:39171800-39172200	Active TSS	Brain Anterior Caudate	brain
33	chr8:39171800-39172400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:39171800-39172400	Active TSS	Brain Angular Gyrus	brain
35	chr8:39171800-39172400	Active TSS	Brain Germinal Matrix	brain
36	chr8:39171800-39172400	Bivalent/Poised TSS	Fetal Brain Male	brain
37	chr8:39171800-39172400	Active TSS	Fetal Brain Female	brain
38	chr8:39172000-39172200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
39	chr8:39172000-39172200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr8:39172000-39172200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
41	chr8:39172000-39172200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr8:39172000-39172200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:39172000-39172200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:39172000-39172200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr8:39172000-39172200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr8:39172000-39172200	Enhancers	Fetal Heart	heart
47	chr8:39172000-39172200	Bivalent Enhancer	Psoas Muscle	Psoas
48	chr8:39172000-39172200	Active TSS	Rectal Smooth Muscle	rectum
49	chr8:39172000-39172200	Bivalent Enhancer	NHDF-Ad	bronchial
50	chr8:39172000-39172400	ZNF genes & repeats	Aorta	Aorta

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