Variant report

Variant	esv2758154
Chromosome Location	chr8:39245798-39597639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:911)
CpG islands
(count:671)
Chromatin interactive
region (count:23)
LncRNA
region (count:217)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:911 , 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	chr8:39547188-39547606	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	chr8:39393057-39393338	K562	blood:	n/a	n/a
7	ATF1	chr8:39552789-39552868	K562	blood:	n/a	n/a
8	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
9	ATF2	chr8:39542169-39542470	GM12878	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	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
13	BATF	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
14	BATF	chr8:39542225-39542523	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:39542183-39542620	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:39542248-39542605	GM12878	blood:	n/a	n/a
18	BCLAF1	chr8:39338104-39338425	GM12878	blood:	n/a	n/a
19	BCLAF1	chr8:39542279-39542596	GM12878	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	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:39439456-39439600	K562	blood:	n/a	n/a
24	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
27	CBX3	chr8:39498734-39499015	HCT-116	colon:	n/a	n/a
28	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
29	CBX3	chr8:39471220-39471427	K562	blood:	n/a	n/a
30	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
31	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
32	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
33	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
34	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
35	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
36	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
37	CEBPB	chr8:39373790-39373924	K562	blood:	n/a	n/a
38	CEBPB	chr8:39301088-39301411	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:39444323-39444503	A549	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
40	CEBPB	chr8:39391427-39391768	K562	blood:	n/a	chr8:39391593-39391604
41	CEBPB	chr8:39550893-39551144	K562	blood:	n/a	chr8:39551018-39551029
42	CEBPB	chr8:39255337-39255640	H1-hESC	embryonic stem cell:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
43	CEBPB	chr8:39584624-39585155	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:39390555-39390826	K562	blood:	n/a	n/a
45	CEBPB	chr8:39377774-39377967	H1-hESC	embryonic stem cell:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
46	CEBPB	chr8:39340885-39341025	K562	blood:	n/a	n/a
47	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr8:39536157-39536372	HepG2	liver:	n/a	chr8:39536260-39536272
49	CEBPB	chr8:39272719-39273086	K562	blood:	n/a	n/a
50	CEBPB	chr8:39562606-39562938	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39442080-39442130	AG04449	skin:	fetal
2	chr8:39442078-39442128	SK-N-SH_RA	brain:	n/a
3	chr8:39442080-39442130	AG10803	skin:	n/a
4	chr8:39442347-39442397	RPTEC	kidney:	n/a
5	chr8:39328433-39328483	AoSMC	blood vessel:	n/a
6	chr8:39441975-39442025	NB4	blood:	n/a
7	chr8:39442078-39442128	SK-N-SH	brain:	n/a
8	chr8:39442078-39442128	HCT-116	colon:	n/a
9	chr8:39442080-39442130	GM12878	blood:	n/a
10	chr8:39442080-39442130	PANC-1	pancreas:	n/a
11	chr8:39442078-39442128	GM12892	blood:	n/a
12	chr8:39442080-39442130	PFSK-1	brain:	n/a
13	chr8:39328433-39328483	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:39380592-39380642	K562	blood:	n/a
15	chr8:39441968-39442018	GM19239	blood:	n/a
16	chr8:39328433-39328483	HUVEC	blood vessel:	n/a
17	chr8:39328433-39328483	GM12892	blood:	n/a
18	chr8:39328433-39328483	HL-60	blood:	n/a
19	chr8:39442089-39442139	PrEC	prostate:	n/a
20	chr8:39380592-39380642	HUVEC	blood vessel:	n/a
21	chr8:39442078-39442128	T-47D	breast:	n/a
22	chr8:39442078-39442128	U87	brain:	n/a
23	chr8:39442080-39442130	AG09319	gingival:	n/a
24	chr8:39442089-39442139	NT2-D1	testis:	n/a
25	chr8:39442089-39442139	IMR90	lung:	fetal
26	chr8:39441473-39441523	MCF10A-Er-Src	breast:	n/a
27	chr8:39328433-39328483	IMR90	lung:	fetal
28	chr8:39441975-39442025	AG09319	gingival:	n/a
29	chr8:39380592-39380642	NB4	blood:	n/a
30	chr8:39328433-39328483	HNPCEpiC	eye:	n/a
31	chr8:39442347-39442397	HEEpiC	esophagus:	n/a
32	chr8:39441473-39441523	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:39380341-39380391	HRCEpiC	kidney:	n/a
34	chr8:39380341-39380391	HCM	heart:	n/a
35	chr8:39380435-39380485	MCF-7	breast:	n/a
36	chr8:39441473-39441523	Hepatocyte	liver:	n/a
37	chr8:39380341-39380391	RPTEC	kidney:	n/a
38	chr8:39442078-39442128	A549	lung:	n/a
39	chr8:39380435-39380485	NT2-D1	testis:	n/a
40	chr8:39380592-39380642	LNCaP	prostate:	n/a
41	chr8:39380341-39380391	HAEpiC	amniotic membrane:	n/a
42	chr8:39442347-39442397	HCF	heart:	n/a
43	chr8:39380435-39380485	U87	brain:	n/a
44	chr8:39441473-39441523	GM12892	blood:	n/a
45	chr8:39441968-39442018	HCF	heart:	n/a
46	chr8:39441473-39441523	NB4	blood:	n/a
47	chr8:39442080-39442130	MCF10A-Er-Src	breast:	n/a
48	chr8:39380341-39380391	NB4	blood:	n/a
49	chr8:39442347-39442397	Hela-S3	cervix:	n/a
50	chr8:39442080-39442130	HUVEC	blood vessel:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
2	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
3	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
4	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
5	chr8:39410966..39411938-chr8:39709121..39709647,2	MCF-7	breast:
6	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
7	chr8:39502547..39504602-chr8:39509034..39511259,2	K562	blood:
8	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
9	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
10	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
11	chr8:39410685..39412216-chr8:39708899..39710030,6	MCF-7	breast:
12	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
13	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
14	chr8:39578570..39581049-chr8:39586519..39588228,2	MCF-7	breast:
15	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
16	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
17	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
18	chr8:39454127..39456246-chr8:39457674..39459630,2	K562	blood:
19	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
20	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
21	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:
22	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
23	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:

(count:217 , 50 per page) page: 1 2 3 4 5

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39308564-39308680	NONHSAT126163
2	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126163
3	lnc-ADAM2-4	chr8:39267715-39267828	XLOC_007062
4	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126165
5	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126164
6	lnc-ADAM18-1	chr8:39430763-39430927	ENSG00000254082
7	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126169
8	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126159
9	lnc-IDO1-2	chr8:39556641-39556699	l_3583_chr8:39549918-39556807_testes
10	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126160
11	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126164
12	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126166
13	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126163
14	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126164
15	lnc-ADAM32-1	chr8:39274733-39274745	NONHSAT126151
16	lnc-ADAM2-6	chr8:39380272-39380390	NONHSAT126171
17	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126166
18	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126151
19	lnc-IDO1-4	chr8:39468048-39468263	NONHSAT126178
20	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126163
21	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126148
22	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126164
23	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126168
24	lnc-ADAM18-2	chr8:39413665-39413968	NONHSAT126172
25	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126169
26	lnc-ADAM32-1	chr8:39250791-39250905	NONHSAT126152
27	lnc-ADAM18-2	chr8:39415511-39415698	NONHSAT126172
28	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126165
29	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126165
30	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126168
31	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126166
32	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126164
33	lnc-ADAM2-6	chr8:39308565-39308680	NONHSAT126167
34	lnc-IDO1-2	chr8:39556704-39556807	l_3583_chr8:39549918-39556807_testes
35	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126164
36	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126165
37	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126166
38	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126165
39	lnc-ADAM18-1	chr8:39424224-39424336	ENSG00000254082
40	lnc-IDO1-2	chr8:39552257-39552314	l_3583_chr8:39549918-39556807_testes
41	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
42	lnc-ADAM2-6	chr8:39347782-39347876	NONHSAT126166
43	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126179
44	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126150
45	lnc-ADAM32-1	chr8:39258852-39259014	NONHSAT126155
46	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126163
47	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
48	lnc-ADAM2-6	chr8:39308567-39308680	NONHSAT126168
49	lnc-ADAM18-1	chr8:39424225-39424336	NONHSAT126174
50	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126168

No data

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

Extended variants
information (count: 6302 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:6302 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62503498	chr8:39250013-39250014	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549525715	chr8:39250172-39250173	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs61648346	chr8:39250206-39250207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs73612404	chr8:39250230-39250231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs190008895	chr8:39250236-39250237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572025448	chr8:39250469-39250470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561338105	chr8:39250474-39250475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376123523	chr8:39250521-39250522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116803979	chr8:39250536-39250537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114820848	chr8:39250589-39250590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78205747	chr8:39250592-39250593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531962069	chr8:39250602-39250603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117365533	chr8:39250629-39250630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534500678	chr8:39250749-39250750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181275290	chr8:39250765-39250766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572036710	chr8:39250772-39250773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376411897	chr8:39250849-39250850	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs12544471	chr8:39250888-39250889	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs144999118	chr8:39250938-39250939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577460944	chr8:39251001-39251002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140972990	chr8:39251002-39251003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79656828	chr8:39251008-39251009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12546694	chr8:39251030-39251031	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs563103078	chr8:39251076-39251077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571357424	chr8:39251133-39251134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527402174	chr8:39251172-39251173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147134538	chr8:39251206-39251207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567148946	chr8:39251233-39251234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185717637	chr8:39251234-39251235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548677906	chr8:39251237-39251238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79050355	chr8:39251331-39251332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569929092	chr8:39251374-39251375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539071159	chr8:39251493-39251494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558774490	chr8:39251518-39251519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7006818	chr8:39251526-39251527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140437048	chr8:39251532-39251533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550297145	chr8:39251560-39251561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191439574	chr8:39251573-39251574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183758910	chr8:39251574-39251575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541889906	chr8:39251583-39251584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560115341	chr8:39251638-39251639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564015199	chr8:39251709-39251710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575935880	chr8:39251721-39251722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373887904	chr8:39251724-39251725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144303272	chr8:39251740-39251741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564730787	chr8:39251743-39251744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527354483	chr8:39251825-39251826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77508861	chr8:39251921-39251922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188487575	chr8:39251927-39251928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529867164	chr8:39251953-39251954	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
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
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39250000-39250200	Active TSS	Fetal Lung	lung
2	chr8:39250200-39254400	Weak transcription	Fetal Lung	lung
3	chr8:39254400-39256800	Enhancers	Fetal Lung	lung
4	chr8:39254600-39254800	Enhancers	Colon Smooth Muscle	Colon
5	chr8:39256800-39258000	Weak transcription	Fetal Lung	lung
6	chr8:39261200-39262400	Weak transcription	Fetal Lung	lung
7	chr8:39262400-39263600	Enhancers	Fetal Lung	lung
8	chr8:39268800-39269200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:39269000-39269800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr8:39269400-39270200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr8:39272400-39272800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
12	chr8:39272400-39273000	Active TSS	K562	blood
13	chr8:39272600-39272800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:39272800-39273200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:39273200-39273400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:39283800-39285200	Enhancers	Fetal Lung	lung
17	chr8:39296800-39297000	Active TSS	HSMM	muscle
18	chr8:39297000-39297200	Flanking Active TSS	HSMM	muscle
19	chr8:39298800-39300000	Enhancers	Fetal Lung	lung
20	chr8:39300000-39301000	Weak transcription	Fetal Lung	lung
21	chr8:39301000-39301200	Enhancers	Fetal Lung	lung
22	chr8:39301200-39302200	Weak transcription	Fetal Lung	lung
23	chr8:39302000-39302400	Enhancers	Spleen	Spleen
24	chr8:39302200-39302400	Enhancers	Fetal Lung	lung
25	chr8:39305400-39306400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:39317600-39318000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:39328200-39328600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:39328400-39328800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr8:39328400-39329200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr8:39328400-39329400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr8:39328600-39329000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr8:39328600-39329000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:39328600-39329200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:39328600-39329400	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr8:39328600-39334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:39328800-39329200	Active TSS	H1 Cell Line	embryonic stem cell
37	chr8:39328800-39329200	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr8:39329200-39329400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr8:39329200-39329400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:39334800-39335000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:39335000-39335800	Enhancers	Fetal Lung	lung
42	chr8:39335000-39340400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:39335400-39336400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr8:39335600-39337200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr8:39335800-39336400	Flanking Active TSS	Fetal Lung	lung
46	chr8:39336000-39337200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:39336200-39336800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:39336200-39337200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:39336200-39337200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr8:39336400-39337000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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