Variant report

Variant	esv2757269
Chromosome Location	chr8:39174279-39458399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:946)
CpG islands
(count:794)
Chromatin interactive
region (count:24)
LncRNA
region (count:277)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr8:39424300-39424895	HepG2	liver:	n/a	chr8:39424646-39424662
5	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
6	ATF1	chr8:39204094-39204343	K562	blood:	n/a	n/a
7	ATF1	chr8:39184952-39185134	K562	blood:	n/a	n/a
8	ATF1	chr8:39187249-39187365	K562	blood:	n/a	n/a
9	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
10	ATF3	chr8:39390540-39390824	K562	blood:	n/a	n/a
11	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
12	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr8:39338201-39338396	GM12878	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	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	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
21	BHLHE40	chr8:39439456-39439600	K562	blood:	n/a	n/a
22	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
23	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
24	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
25	CBX3	chr8:39184878-39185271	HCT-116	colon:	n/a	n/a
26	CBX3	chr8:39241402-39241706	K562	blood:	n/a	n/a
27	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
28	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
29	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
30	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
31	CEBPB	chr8:39391427-39391768	K562	blood:	n/a	chr8:39391593-39391604
32	CEBPB	chr8:39377869-39377951	K562	blood:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
33	CEBPB	chr8:39458160-39458460	A549	lung:	n/a	chr8:39458289-39458300
34	CEBPB	chr8:39225484-39225625	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:39444289-39444489	IMR90	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
36	CEBPB	chr8:39373729-39373930	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:39393043-39393343	K562	blood:	n/a	n/a
38	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:39444323-39444503	A549	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
40	CEBPB	chr8:39272719-39273086	K562	blood:	n/a	n/a
41	CEBPB	chr8:39425240-39425556	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:39458127-39458460	HepG2	liver:	n/a	chr8:39458289-39458300
43	CEBPB	chr8:39391429-39391709	HepG2	liver:	n/a	chr8:39391593-39391604
44	CEBPB	chr8:39377774-39377967	H1-hESC	embryonic stem cell:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
45	CEBPB	chr8:39255339-39255659	Hela-S3	cervix:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
46	CEBPB	chr8:39392971-39393463	K562	blood:	n/a	n/a
47	CEBPB	chr8:39393010-39393254	K562	blood:	n/a	n/a
48	CEBPB	chr8:39301088-39301411	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:39391451-39391754	IMR90	lung:	n/a	chr8:39391593-39391604
50	CEBPB	chr8:39255337-39255640	H1-hESC	embryonic stem cell:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39442078-39442128	ProgFib	skin:	n/a
2	chr8:39442078-39442128	ProgFib	skin:	n/a
3	chr8:39441473-39441523	AoSMC	blood vessel:	n/a
4	chr8:39441968-39442018	NT2-D1	testis:	n/a
5	chr8:39441975-39442025	HIPEpiC	eye:	n/a
6	chr8:39442080-39442130	HCM	heart:	n/a
7	chr8:39380592-39380642	IMR90	lung:	fetal
8	chr8:39441975-39442025	H1-hESC	embryonic stem cell:	embryo
9	chr8:39442347-39442397	K562	blood:	n/a
10	chr8:39380435-39380485	HepG2	liver:	n/a
11	chr8:39441968-39442018	IMR90	lung:	fetal
12	chr8:39442347-39442397	AG09309	skin:	n/a
13	chr8:39441473-39441523	NHBE	bronchial:	n/a
14	chr8:39380592-39380642	Hepatocyte	liver:	n/a
15	chr8:39442089-39442139	BJ	skin:	n/a
16	chr8:39441975-39442025	HEEpiC	esophagus:	n/a
17	chr8:39442089-39442139	AG09319	gingival:	n/a
18	chr8:39441968-39442018	AG04449	skin:	fetal
19	chr8:39442089-39442139	HRCEpiC	kidney:	n/a
20	chr8:39441968-39442018	HCT-116	colon:	n/a
21	chr8:39223182-39223232	HRPEpiC	eye:	n/a
22	chr8:39328433-39328483	MCF-7	breast:	n/a
23	chr8:39196907-39196957	HL-60	blood:	n/a
24	chr8:39223182-39223232	T-47D	breast:	n/a
25	chr8:39442078-39442128	HUVEC	blood vessel:	n/a
26	chr8:39380435-39380485	T-47D	breast:	n/a
27	chr8:39196907-39196957	Hela-S3	cervix:	n/a
28	chr8:39442080-39442130	ProgFib	skin:	n/a
29	chr8:39380435-39380485	AoSMC	blood vessel:	n/a
30	chr8:39380435-39380485	RPTEC	kidney:	n/a
31	chr8:39442089-39442139	SAEC	small airway:	n/a
32	chr8:39380341-39380391	K562	blood:	n/a
33	chr8:39442078-39442128	AG09309	skin:	n/a
34	chr8:39380592-39380642	T-47D	breast:	n/a
35	chr8:39441975-39442025	SAEC	small airway:	n/a
36	chr8:39223182-39223232	HAEpiC	amniotic membrane:	n/a
37	chr8:39196907-39196957	IMR90	lung:	fetal
38	chr8:39442347-39442397	HRE	kidney:	n/a
39	chr8:39442080-39442130	NHBE	bronchial:	n/a
40	chr8:39442080-39442130	GM12892	blood:	n/a
41	chr8:39380435-39380485	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:39380435-39380485	CMK	blood:	n/a
43	chr8:39196907-39196957	HRPEpiC	eye:	n/a
44	chr8:39223182-39223232	K562	blood:	n/a
45	chr8:39442089-39442139	HCM	heart:	n/a
46	chr8:39380435-39380485	PANC-1	pancreas:	n/a
47	chr8:39328433-39328483	NHDF-neo	bronchial:	n/a
48	chr8:39441968-39442018	GM06990	blood:	n/a
49	chr8:39196907-39196957	AG10803	skin:	n/a
50	chr8:39442089-39442139	GM12892	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:38824064..38824622-chr8:39184733..39185545,2	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	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
5	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
6	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
7	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
8	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
9	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
10	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:
11	chr8:39410685..39412216-chr8:39708899..39710030,6	MCF-7	breast:
12	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
13	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
14	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
15	chr8:39410966..39411938-chr8:39709121..39709647,2	MCF-7	breast:
16	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
17	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
18	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
19	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
20	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
21	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
22	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
23	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
24	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:

(count:277 , 50 per page) page: 1 2 3 4 5 6

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126166
2	lnc-ADAM2-4	chr8:39267715-39267828	XLOC_007062
3	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126165
4	lnc-ADAM2-6	chr8:39347782-39347876	NONHSAT126166
5	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126168
6	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126163
7	lnc-ADAM18-1	chr8:39433100-39433157	NONHSAT126174
8	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT126159
9	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126149
10	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126165
11	lnc-ADAM18-1	chr8:39435933-39435990	ENSG00000254082
12	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126165
13	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126148
14	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126171
15	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126151
16	lnc-ADAM2-6	chr8:39331001-39331181	NONHSAT126166
17	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126165
18	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126166
19	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126164
20	lnc-ADAM18-1	chr8:39433100-39433160	NONHSAT126175
21	lnc-ADAM32-1	chr8:39238308-39238398	NONHSAT147628
22	lnc-ADAM2-6	chr8:39335215-39335365	NONHSAT126163
23	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126150
24	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126148
25	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT126148
26	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT147628
27	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126159
28	lnc-ADAM2-6	chr8:39349352-39349527	NONHSAT126170
29	lnc-ADAM2-6	chr8:39379779-39379861	NONHSAT126168
30	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126166
31	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT126155
32	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126165
33	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126150
34	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126153
35	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126155
36	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126166
37	lnc-ADAM2-6	chr8:39308565-39308680	NONHSAT126167
38	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126151
39	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126166
40	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT147628
41	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126165
42	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126164
43	lnc-ADAM2-6	chr8:39380272-39380390	NONHSAT126171
44	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126152
45	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT147628
46	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126164
47	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT147628
48	lnc-ADAM2-6	chr8:39347782-39347876	NONHSAT126165
49	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT126148
50	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126167

No data

Variant related genes	Relation type
ENSG00000252176	TF binding region
ADAM18	TF binding region
ADAM5	TF binding region
ENSG00000254067	TF binding region
ENSG00000254082	TF binding region
ADAM3A	TF binding region
ENSG00000252176	CpG island
ADAM18	CpG island
ADAM5	CpG island
ENSG00000254067	CpG island
ENSG00000254082	CpG island
ADAM3A	CpG island
ENSG00000196115	chromatin interactions

Extended variants
information (count: 3772 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:3772 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561084712	chr8:39175076-39175077	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554397873	chr8:39175079-39175080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574333673	chr8:39175137-39175138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs199628862	chr8:39175183-39175184	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543322849	chr8:39175190-39175191	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs556852684	chr8:39175228-39175229	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185813543	chr8:39175262-39175263	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544164798	chr8:39175310-39175311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs35818475	chr8:39175379-39175380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs151242876	chr8:39175395-39175396	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532822016	chr8:39175439-39175440	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141680004	chr8:39175457-39175458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559912641	chr8:39175474-39175475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs35985391	chr8:39175530-39175531	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529080162	chr8:39175601-39175602	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188105698	chr8:39175648-39175649	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549362067	chr8:39175669-39175670	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562767399	chr8:39175679-39175680	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201160582	chr8:39175710-39175711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs62504821	chr8:39175712-39175713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs4733997	chr8:39175768-39175769	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551713323	chr8:39175826-39175827	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs4509282	chr8:39175858-39175859	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs534287572	chr8:39175859-39175860	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547941572	chr8:39175931-39175932	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs4329239	chr8:39175961-39175962	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs564954728	chr8:39176003-39176004	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34247952	chr8:39176014-39176015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs56193831	chr8:39176017-39176018	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199693740	chr8:39176020-39176021	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs550208835	chr8:39176023-39176024	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375241629	chr8:39176038-39176039	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147059408	chr8:39176039-39176040	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115819103	chr8:39176055-39176056	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147626609	chr8:39176064-39176065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557723733	chr8:39176082-39176083	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577264359	chr8:39176108-39176109	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568492040	chr8:39176115-39176116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368143365	chr8:39176121-39176122	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191460383	chr8:39176124-39176125	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566481066	chr8:39176125-39176126	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559849545	chr8:39176141-39176142	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573417025	chr8:39176142-39176143	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10710943	chr8:39176143-39176144	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35732674	chr8:39176241-39176242	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34532941	chr8:39176248-39176249	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs142118780	chr8:39176290-39176291	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs535069579	chr8:39176310-39176311	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183805915	chr8:39176358-39176359	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs531626531	chr8:39176408-39176409	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Chordoma	21215367	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	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:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39184000-39187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:39184600-39187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:39184800-39185000	Enhancers	A549	lung
4	chr8:39184800-39185400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:39184800-39185400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:39185400-39187200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:39185400-39187400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:39186800-39187000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:39186800-39188000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:39187200-39188000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:39187200-39188200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:39187400-39188000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:39187400-39188200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:39187600-39188000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr8:39188000-39189400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:39188000-39189400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr8:39188200-39189200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr8:39189200-39189800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:39189400-39189800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:39189400-39189800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:39189600-39190000	Enhancers	Fetal Stomach	stomach
22	chr8:39190200-39191000	Enhancers	Fetal Kidney	kidney
23	chr8:39190400-39191600	Enhancers	Fetal Lung	lung
24	chr8:39191200-39191400	Enhancers	Osteobl	bone
25	chr8:39191200-39191600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:39210800-39211400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:39215000-39215400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:39221000-39222000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:39238600-39241200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:39241200-39241400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr8:39241400-39241600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:39250000-39250200	Active TSS	Fetal Lung	lung
33	chr8:39250200-39254400	Weak transcription	Fetal Lung	lung
34	chr8:39254400-39256800	Enhancers	Fetal Lung	lung
35	chr8:39254600-39254800	Enhancers	Colon Smooth Muscle	Colon
36	chr8:39256800-39258000	Weak transcription	Fetal Lung	lung
37	chr8:39261200-39262400	Weak transcription	Fetal Lung	lung
38	chr8:39262400-39263600	Enhancers	Fetal Lung	lung
39	chr8:39268800-39269200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:39269000-39269800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr8:39269400-39270200	Enhancers	Placenta Amnion	Placenta Amnion
42	chr8:39272400-39272800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
43	chr8:39272400-39273000	Active TSS	K562	blood
44	chr8:39272600-39272800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:39272800-39273200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:39273200-39273400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:39283800-39285200	Enhancers	Fetal Lung	lung
48	chr8:39296800-39297000	Active TSS	HSMM	muscle
49	chr8:39297000-39297200	Flanking Active TSS	HSMM	muscle
50	chr8:39298800-39300000	Enhancers	Fetal Lung	lung

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