Variant report

Variant	nsv1021340
Chromosome Location	chr8:39268667-39577905
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:673)
Chromatin interactive
region (count:21)
LncRNA
region (count:178)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39424300-39424895	HepG2	liver:	n/a	chr8:39424646-39424662
2	ARID3A	chr8:39391480-39391748	K562	blood:	n/a	n/a
3	ARID3A	chr8:39393079-39393534	K562	blood:	n/a	n/a
4	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
5	ARID3A	chr8:39547188-39547606	HepG2	liver:	n/a	n/a
6	ATF1	chr8:39574502-39574589	K562	blood:	n/a	n/a
7	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
8	ATF1	chr8:39552789-39552868	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	chr8:39538369-39538590	GM12878	blood:	n/a	chr8:39538508-39538519
13	BATF	chr8:39542251-39542689	GM12878	blood:	n/a	n/a
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	chr8:39439456-39439600	K562	blood:	n/a	n/a
21	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:39379884-39380110	K562	blood:	n/a	n/a
23	BHLHE40	chr8:39540522-39540568	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:39542060-39542776	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
26	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
27	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
28	CBX3	chr8:39471220-39471427	K562	blood:	n/a	n/a
29	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
30	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
31	CBX3	chr8:39498734-39499015	HCT-116	colon:	n/a	n/a
32	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
33	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
34	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
35	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
36	CCNT2	chr8:39550530-39550861	K562	blood:	n/a	n/a
37	CEBPB	chr8:39377723-39378059	IMR90	lung:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
38	CEBPB	chr8:39550875-39551134	HepG2	liver:	n/a	chr8:39551018-39551029
39	CEBPB	chr8:39340885-39341025	K562	blood:	n/a	n/a
40	CEBPB	chr8:39417741-39418065	HepG2	liver:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
41	CEBPB	chr8:39562647-39562945	A549	lung:	n/a	n/a
42	CEBPB	chr8:39377774-39377967	H1-hESC	embryonic stem cell:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
43	CEBPB	chr8:39391451-39391754	IMR90	lung:	n/a	chr8:39391593-39391604
44	CEBPB	chr8:39373729-39373930	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr8:39425240-39425556	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:39562626-39562905	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:39373655-39374022	IMR90	lung:	n/a	n/a
48	CEBPB	chr8:39272750-39273063	K562	blood:	n/a	n/a
49	CEBPB	chr8:39301088-39301411	IMR90	lung:	n/a	n/a
50	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39441968-39442018	T-47D	breast:	n/a
2	chr8:39442078-39442128	NT2-D1	testis:	n/a
3	chr8:39441968-39442018	T-47D	breast:	n/a
4	chr8:39442078-39442128	NT2-D1	testis:	n/a
5	chr8:39441975-39442025	T-47D	breast:	n/a
6	chr8:39441473-39441523	HCPEpiC	choroid plexus:	n/a
7	chr8:39441975-39442025	SK-N-SH	brain:	n/a
8	chr8:39380592-39380642	AG09319	gingival:	n/a
9	chr8:39441473-39441523	Hela-S3	cervix:	n/a
10	chr8:39380341-39380391	Hepatocyte	liver:	n/a
11	chr8:39442347-39442397	ProgFib	skin:	n/a
12	chr8:39442347-39442397	NH-A	brain:	n/a
13	chr8:39442078-39442128	HRCEpiC	kidney:	n/a
14	chr8:39442089-39442139	HEEpiC	esophagus:	n/a
15	chr8:39442080-39442130	HCF	heart:	n/a
16	chr8:39380592-39380642	SK-N-MC	brain:	n/a
17	chr8:39442347-39442397	PANC-1	pancreas:	n/a
18	chr8:39328433-39328483	K562	blood:	n/a
19	chr8:39442347-39442397	HRPEpiC	eye:	n/a
20	chr8:39441473-39441523	HAEpiC	amniotic membrane:	n/a
21	chr8:39442080-39442130	HNPCEpiC	eye:	n/a
22	chr8:39442078-39442128	Caco-2	colon:	n/a
23	chr8:39380592-39380642	HRCEpiC	kidney:	n/a
24	chr8:39380592-39380642	MCF-7	breast:	n/a
25	chr8:39442078-39442128	NHBE	bronchial:	n/a
26	chr8:39380435-39380485	LNCaP	prostate:	n/a
27	chr8:39380592-39380642	HepG2	liver:	n/a
28	chr8:39442078-39442128	Jurkat	blood:	n/a
29	chr8:39442080-39442130	GM12891	blood:	n/a
30	chr8:39380435-39380485	PFSK-1	brain:	n/a
31	chr8:39442078-39442128	RPTEC	kidney:	n/a
32	chr8:39441975-39442025	NB4	blood:	n/a
33	chr8:39441968-39442018	GM06990	blood:	n/a
34	chr8:39380341-39380391	MCF10A-Er-Src	breast:	n/a
35	chr8:39442078-39442128	A549	lung:	n/a
36	chr8:39442078-39442128	HMEC	breast:	n/a
37	chr8:39441975-39442025	PFSK-1	brain:	n/a
38	chr8:39380592-39380642	GM12891	blood:	n/a
39	chr8:39380341-39380391	BE2_C	brain:	n/a
40	chr8:39441473-39441523	HCT-116	colon:	n/a
41	chr8:39380341-39380391	HEEpiC	esophagus:	n/a
42	chr8:39380435-39380485	MCF-7	breast:	n/a
43	chr8:39442078-39442128	T-47D	breast:	n/a
44	chr8:39441968-39442018	HRPEpiC	eye:	n/a
45	chr8:39441473-39441523	CMK	blood:	n/a
46	chr8:39380341-39380391	HRCEpiC	kidney:	n/a
47	chr8:39441968-39442018	LNCaP	prostate:	n/a
48	chr8:39442347-39442397	GM12891	blood:	n/a
49	chr8:39442078-39442128	HUVEC	blood vessel:	n/a
50	chr8:39441968-39442018	SKMC	muscle:	n/a

(count:21 , 50 per page) page: 1

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

(count:178 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126165
2	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126165
3	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126164
4	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126163
5	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126168
6	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126168
7	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126167
8	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126168
9	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126164
10	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126163
11	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126164
12	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126169
13	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126163
14	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126163
15	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126164
16	lnc-ADAM18-1	chr8:39430763-39430927	NONHSAT126175
17	lnc-ADAM2-6	chr8:39351587-39351622	NONHSAT126170
18	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126165
19	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126165
20	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126166
21	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126164
22	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126164
23	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126168
24	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126166
25	lnc-ADAM2-6	chr8:39380272-39380344	NONHSAT126168
26	lnc-IDO1-3	chr8:39550119-39550199	NONHSAT126179
27	lnc-IDO1-4	chr8:39467004-39467080	NONHSAT126178
28	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126164
29	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126165
30	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
31	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
32	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126163
33	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126166
34	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126169
35	lnc-ADAM18-2	chr8:39415511-39415698	NONHSAT126172
36	lnc-ADAM18-1	chr8:39424225-39424336	NONHSAT126174
37	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126163
38	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126165
39	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126168
40	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126166
41	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126169
42	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126168
43	lnc-ADAM2-6	chr8:39331001-39331181	NONHSAT126167
44	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126168
45	lnc-ADAM2-6	chr8:39332159-39332224	NONHSAT126169
46	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126167
47	lnc-ADAM2-6	chr8:39380272-39380390	NONHSAT126171
48	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126168
49	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126169
50	lnc-ADAM32-1	chr8:39274733-39274745	NONHSAT126153

No data

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

Extended variants
information (count: 5407 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:5407 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79923949	chr8:39268802-39268803	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs10091230	chr8:39268803-39268804	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575084584	chr8:39268825-39268826	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs542210670	chr8:39268842-39268843	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs113864248	chr8:39268917-39268918	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs556144837	chr8:39268925-39268926	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs541056472	chr8:39268987-39268988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs575697468	chr8:39268988-39268989	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs377122136	chr8:39269012-39269013	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559729036	chr8:39269218-39269219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544737337	chr8:39269219-39269220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs137918292	chr8:39269234-39269235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527531084	chr8:39269396-39269397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111668876	chr8:39269397-39269398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549455681	chr8:39269399-39269400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149024824	chr8:39269435-39269436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567750607	chr8:39269478-39269479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576536731	chr8:39269552-39269553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563436155	chr8:39269562-39269563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528539643	chr8:39269576-39269577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370533686	chr8:39269587-39269588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144698903	chr8:39269597-39269598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138611436	chr8:39269650-39269651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186783618	chr8:39269679-39269680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141620451	chr8:39269705-39269706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191651450	chr8:39269757-39269758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78056114	chr8:39269784-39269785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370276514	chr8:39269881-39269882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201492259	chr8:39269921-39269922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534863143	chr8:39269925-39269926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35076936	chr8:39270003-39270004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548764459	chr8:39270009-39270010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568631339	chr8:39270016-39270017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184154093	chr8:39270031-39270032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555723737	chr8:39270185-39270186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547888203	chr8:39272404-39272405	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183522614	chr8:39272417-39272418	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs7462538	chr8:39272438-39272439	ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557173218	chr8:39272482-39272483	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs187093772	chr8:39272491-39272492	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs147240783	chr8:39272539-39272540	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs199821251	chr8:39272568-39272569	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs74320976	chr8:39272575-39272576	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs573057273	chr8:39272600-39272601	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs142447623	chr8:39272613-39272614	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs375801726	chr8:39272631-39272632	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs71218330	chr8:39272632-39272633	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs199990160	chr8:39272641-39272642	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs112484022	chr8:39272658-39272659	ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs146946141	chr8:39272672-39272673	ZNF genes & repeats Enhancers Active TSS	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
Breast cancer	20932292	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Cancer	20164919	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:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39268800-39269200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:39269000-39269800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr8:39269400-39270200	Enhancers	Placenta Amnion	Placenta Amnion
4	chr8:39272400-39272800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
5	chr8:39272400-39273000	Active TSS	K562	blood
6	chr8:39272600-39272800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:39272800-39273200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:39273200-39273400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:39283800-39285200	Enhancers	Fetal Lung	lung
10	chr8:39296800-39297000	Active TSS	HSMM	muscle
11	chr8:39297000-39297200	Flanking Active TSS	HSMM	muscle
12	chr8:39298800-39300000	Enhancers	Fetal Lung	lung
13	chr8:39300000-39301000	Weak transcription	Fetal Lung	lung
14	chr8:39301000-39301200	Enhancers	Fetal Lung	lung
15	chr8:39301200-39302200	Weak transcription	Fetal Lung	lung
16	chr8:39302000-39302400	Enhancers	Spleen	Spleen
17	chr8:39302200-39302400	Enhancers	Fetal Lung	lung
18	chr8:39305400-39306400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:39317600-39318000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr8:39328200-39328600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:39328400-39328800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:39328400-39329200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:39328400-39329400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr8:39328600-39329000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr8:39328600-39329000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:39328600-39329200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:39328600-39329400	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr8:39328600-39334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:39328800-39329200	Active TSS	H1 Cell Line	embryonic stem cell
30	chr8:39328800-39329200	Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr8:39329200-39329400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr8:39329200-39329400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:39334800-39335000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:39335000-39335800	Enhancers	Fetal Lung	lung
35	chr8:39335000-39340400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:39335400-39336400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:39335600-39337200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:39335800-39336400	Flanking Active TSS	Fetal Lung	lung
39	chr8:39336000-39337200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:39336200-39336800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:39336200-39337200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr8:39336200-39337200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr8:39336400-39337000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr8:39336400-39337000	Active TSS	Fetal Lung	lung
45	chr8:39336800-39337200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:39338000-39338400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:39340400-39341000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:39343000-39345400	Enhancers	Fetal Lung	lung
49	chr8:39363600-39364000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr8:39368800-39369600	Enhancers	GM12878-XiMat	blood

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