Variant report

Variant	nsv428198
Chromosome Location	chr8:39069309-39405724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1191)
CpG islands
(count:978)
Chromatin interactive
region (count:31)
LncRNA
region (count:290)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39391480-39391748	K562	blood:	n/a	n/a
2	ARID3A	chr8:39393079-39393534	K562	blood:	n/a	n/a
3	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
4	ARID3A	chr8:39184983-39185219	HepG2	liver:	n/a	n/a
5	ATF1	chr8:39090849-39091203	K562	blood:	n/a	n/a
6	ATF1	chr8:39187249-39187365	K562	blood:	n/a	n/a
7	ATF1	chr8:39204094-39204343	K562	blood:	n/a	n/a
8	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
9	ATF1	chr8:39169144-39169211	K562	blood:	n/a	n/a
10	ATF1	chr8:39184952-39185134	K562	blood:	n/a	n/a
11	ATF3	chr8:39390540-39390824	K562	blood:	n/a	n/a
12	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
14	BCL11A	chr8:39215071-39215373	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:39215146-39215389	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
17	BCLAF1	chr8:39338104-39338425	GM12878	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	chr8:39379884-39380110	K562	blood:	n/a	n/a
21	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
22	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
23	CBX3	chr8:39241402-39241706	K562	blood:	n/a	n/a
24	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
25	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
26	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
27	CBX3	chr8:39184878-39185271	HCT-116	colon:	n/a	n/a
28	CBX3	chr8:39099996-39100457	HCT-116	colon:	n/a	n/a
29	CBX3	chr8:39090639-39091440	HCT-116	colon:	n/a	n/a
30	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
31	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
32	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
33	CEBPB	chr8:39122247-39122648	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:39340885-39341025	K562	blood:	n/a	n/a
35	CEBPB	chr8:39393043-39393343	K562	blood:	n/a	n/a
36	CEBPB	chr8:39255337-39255640	H1-hESC	embryonic stem cell:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
37	CEBPB	chr8:39373655-39374022	IMR90	lung:	n/a	n/a
38	CEBPB	chr8:39373729-39373930	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:39391429-39391709	HepG2	liver:	n/a	chr8:39391593-39391604
40	CEBPB	chr8:39377723-39378059	IMR90	lung:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
41	CEBPB	chr8:39255284-39255699	IMR90	lung:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
42	CEBPB	chr8:39301112-39301366	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:39391451-39391754	IMR90	lung:	n/a	chr8:39391593-39391604
44	CEBPB	chr8:39081045-39081110	HepG2	liver:	n/a	chr8:39081090-39081101
45	CEBPB	chr8:39169394-39169417	A549	lung:	n/a	n/a
46	CEBPB	chr8:39255330-39255613	K562	blood:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
47	CEBPB	chr8:39272719-39273086	K562	blood:	n/a	n/a
48	CEBPB	chr8:39373790-39373924	K562	blood:	n/a	n/a
49	CEBPB	chr8:39172450-39172643	K562	blood:	n/a	chr8:39172538-39172549
50	CEBPB	chr8:39377869-39377951	K562	blood:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39380592-39380642	Jurkat	blood:	n/a
2	chr8:39171620-39171670	NT2-D1	testis:	n/a
3	chr8:39380592-39380642	Jurkat	blood:	n/a
4	chr8:39171620-39171670	NT2-D1	testis:	n/a
5	chr8:39380592-39380642	PANC-1	pancreas:	n/a
6	chr8:39172111-39172161	LNCaP	prostate:	n/a
7	chr8:39172120-39172170	BE2_C	brain:	n/a
8	chr8:39380435-39380485	ovcar-3	ovarian:	n/a
9	chr8:39328433-39328483	BE2_C	brain:	n/a
10	chr8:39380341-39380391	AG04449	skin:	fetal
11	chr8:39380592-39380642	HIPEpiC	eye:	n/a
12	chr8:39380341-39380391	GM12891	blood:	n/a
13	chr8:39380435-39380485	HEEpiC	esophagus:	n/a
14	chr8:39380435-39380485	CMK	blood:	n/a
15	chr8:39172022-39172072	GM12878	blood:	n/a
16	chr8:39172111-39172161	RPTEC	kidney:	n/a
17	chr8:39171620-39171670	HIPEpiC	eye:	n/a
18	chr8:39172120-39172170	GM12892	blood:	n/a
19	chr8:39077124-39077174	AG10803	skin:	n/a
20	chr8:39172111-39172161	MCF-7	breast:	n/a
21	chr8:39172099-39172149	SK-N-MC	brain:	n/a
22	chr8:39172099-39172149	A549	lung:	n/a
23	chr8:39172120-39172170	CMK	blood:	n/a
24	chr8:39380592-39380642	GM12878	blood:	n/a
25	chr8:39380592-39380642	HUVEC	blood vessel:	n/a
26	chr8:39171620-39171670	PFSK-1	brain:	n/a
27	chr8:39171866-39171916	BE2_C	brain:	n/a
28	chr8:39172020-39172070	GM12891	blood:	n/a
29	chr8:39196907-39196957	HL-60	blood:	n/a
30	chr8:39171620-39171670	GM12891	blood:	n/a
31	chr8:39172022-39172072	AG04449	skin:	fetal
32	chr8:39077124-39077174	NT2-D1	testis:	n/a
33	chr8:39172020-39172070	HUVEC	blood vessel:	n/a
34	chr8:39172022-39172072	HUVEC	blood vessel:	n/a
35	chr8:39380435-39380485	H1-hESC	embryonic stem cell:	embryo
36	chr8:39196907-39196957	GM12878	blood:	n/a
37	chr8:39172111-39172161	ProgFib	skin:	n/a
38	chr8:39171866-39171916	H1-hESC	embryonic stem cell:	embryo
39	chr8:39172099-39172149	HRPEpiC	eye:	n/a
40	chr8:39380341-39380391	ovcar-3	ovarian:	n/a
41	chr8:39172120-39172170	NHBE	bronchial:	n/a
42	chr8:39172022-39172072	SKMC	muscle:	n/a
43	chr8:39171866-39171916	HAEpiC	amniotic membrane:	n/a
44	chr8:39223182-39223232	HRCEpiC	kidney:	n/a
45	chr8:39172099-39172149	GM12878	blood:	n/a
46	chr8:39223182-39223232	LNCaP	prostate:	n/a
47	chr8:39380592-39380642	RPTEC	kidney:	n/a
48	chr8:39196907-39196957	HRE	kidney:	n/a
49	chr8:39380592-39380642	AG09319	gingival:	n/a
50	chr8:39223182-39223232	HCT-116	colon:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
2	chr8:39079754..39082023-chr8:39086400..39088238,2	MCF-7	breast:
3	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
4	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
5	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
6	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
7	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
8	chr8:39079754..39082023-chr8:39086400..39088238,2	MCF-7	breast:
9	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
10	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
11	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
12	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
13	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
14	chr8:39080941..39082777-chr8:39089064..39090963,2	K562	blood:
15	chr8:39170463..39172530-chr8:39174983..39176968,2	MCF-7	breast:
16	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
17	chr8:38824064..38824622-chr8:39184733..39185545,2	K562	blood:
18	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
19	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
20	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
21	chr8:39080941..39082777-chr8:39089064..39090963,2	K562	blood:
22	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
23	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:
24	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
25	chr8:38964583..38965453-chr8:39130431..39131111,2	MCF-7	breast:
26	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
27	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
28	chr15:50661566..50662138-chr8:39161334..39161854,2	MCF-7	breast:
29	chr6:156717380..156718086-chr8:39158912..39159795,2	MCF-7	breast:
30	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
31	chr8:38964712..38965432-chr8:39130166..39131088,2	MCF-7	breast:

(count:290 , 50 per page) page: 1 2 3 4 5 6

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126151
2	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126150
3	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126169
4	lnc-ADAM32-1	chr8:39274733-39274897	NONHSAT126150
5	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126168
6	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126150
7	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126150
8	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126168
9	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126153
10	lnc-ADAM32-1	chr8:39192919-39193012	NONHSAT126157
11	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126163
12	lnc-ADAM2-6	chr8:39308565-39308680	NONHSAT126167
13	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126164
14	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126169
15	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126150
16	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126169
17	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126160
18	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126152
19	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126166
20	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126165
21	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126166
22	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126167
23	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126169
24	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126151
25	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126150
26	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126165
27	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT147628
28	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126164
29	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126151
30	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126153
31	lnc-ADAM9-1	chr8:39078454-39079221	NONHSAT126143
32	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126164
33	lnc-ADAM9-1	chr8:39142312-39142430	NONHSAT126144
34	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT147628
35	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126152
36	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126166
37	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126169
38	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126163
39	lnc-ADAM32-1	chr8:39250093-39250179	NONHSAT126150
40	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126157
41	lnc-ADAM2-6	chr8:39308564-39308680	NONHSAT126163
42	lnc-ADAM9-1	chr8:39141105-39141143	NONHSAT126144
43	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT147628
44	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126164
45	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126165
46	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126164
47	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126163
48	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT147628
49	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126166
50	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126166

No data

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

Extended variants
information (count: 4892 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4892 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535397172	chr8:39069343-39069344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10094572	chr8:39069355-39069356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541940314	chr8:39069397-39069398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11786558	chr8:39069407-39069408	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544648279	chr8:39069442-39069443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187023291	chr8:39069473-39069474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550527233	chr8:39069511-39069512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12675757	chr8:39069622-39069623	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540851183	chr8:39069668-39069669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560700913	chr8:39069692-39069693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529484270	chr8:39069705-39069706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374473922	chr8:39069734-39069735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529603218	chr8:39069735-39069736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549457238	chr8:39069746-39069747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546157283	chr8:39069750-39069751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561767038	chr8:39069772-39069773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141961785	chr8:39069780-39069781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113466311	chr8:39069784-39069785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550615042	chr8:39069845-39069846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184429646	chr8:39069846-39069847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539172842	chr8:39069879-39069880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546376121	chr8:39069930-39069931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188295879	chr8:39070025-39070026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144157522	chr8:39070031-39070032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563831033	chr8:39070060-39070061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371289012	chr8:39070091-39070092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112188935	chr8:39070103-39070104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547921281	chr8:39070181-39070182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193188939	chr8:39070202-39070203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10088458	chr8:39070209-39070210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs533517584	chr8:39070226-39070227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578132444	chr8:39070286-39070287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551442546	chr8:39070299-39070300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369757497	chr8:39070312-39070313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147801639	chr8:39070335-39070336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554401957	chr8:39070372-39070373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574286856	chr8:39070486-39070487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10088794	chr8:39070487-39070488	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185516282	chr8:39070521-39070522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537013939	chr8:39070526-39070527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530495419	chr8:39070529-39070530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555263851	chr8:39070530-39070531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563775239	chr8:39070576-39070577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532857027	chr8:39070597-39070598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12114061	chr8:39070672-39070673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs190822040	chr8:39070678-39070679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs180677974	chr8:39070683-39070684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183645814	chr8:39070722-39070723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10102564	chr8:39070783-39070784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs538169747	chr8:39070794-39070795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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	20164919	CNVD
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Squamous cell cancer	19001599	CNVD
Cone-rod dystrophy	22138850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	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:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39060400-39082600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr8:39064600-39075800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:39067800-39075800	Weak transcription	Ovary	ovary
4	chr8:39075800-39076000	ZNF genes & repeats	Aorta	Aorta
5	chr8:39075800-39076000	ZNF genes & repeats	Ovary	ovary
6	chr8:39075800-39076200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:39076200-39082800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:39076200-39097200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:39076400-39076600	ZNF genes & repeats	Aorta	Aorta
10	chr8:39076600-39082600	Weak transcription	Ovary	ovary
11	chr8:39080800-39082400	Weak transcription	Fetal Intestine Small	intestine
12	chr8:39081200-39082400	Weak transcription	Aorta	Aorta
13	chr8:39081200-39083800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr8:39081400-39084200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:39081600-39084000	Weak transcription	NHLF	lung
16	chr8:39082400-39082800	ZNF genes & repeats	Aorta	Aorta
17	chr8:39082400-39083000	Strong transcription	Fetal Intestine Small	intestine
18	chr8:39082600-39083000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:39082600-39083200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:39082600-39083200	Strong transcription	Ovary	ovary
21	chr8:39082800-39083000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:39082800-39083000	ZNF genes & repeats	Pancreas	Pancrea
23	chr8:39083000-39084600	Weak transcription	Fetal Intestine Small	intestine
24	chr8:39083200-39085800	Weak transcription	Ovary	ovary
25	chr8:39083200-39097800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:39084800-39085200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:39085000-39085200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:39085200-39090400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:39089800-39090000	Enhancers	HMEC	breast
30	chr8:39090000-39090800	Weak transcription	HMEC	breast
31	chr8:39090000-39091800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:39090200-39091600	Enhancers	NHEK	skin
33	chr8:39090400-39090800	Enhancers	A549	lung
34	chr8:39090400-39091000	Enhancers	NH-A	brain
35	chr8:39090400-39091600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:39090600-39091000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:39090600-39091200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:39090800-39091200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:39090800-39091400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr8:39090800-39091400	Enhancers	HMEC	breast
41	chr8:39090800-39091600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:39091000-39091200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:39091600-39092200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:39091600-39098200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:39092000-39094400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:39092200-39092400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:39094400-39095200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:39094400-39095200	Enhancers	Placenta Amnion	Placenta Amnion
49	chr8:39094400-39095400	ZNF genes & repeats	Aorta	Aorta
50	chr8:39098200-39098600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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