Variant report

Variant	nsv1022463
Chromosome Location	chr8:86257031-86547831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2135)
CpG islands
(count:2321)
Chromatin interactive
region (count:134)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2135 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86258991-86259361	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:86295505-86295821	K562	blood:	n/a	n/a
3	ARID3A	chr8:86363787-86364168	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:86464069-86464458	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:86290333-86290829	K562	blood:	n/a	n/a
6	ARID3A	chr8:86291587-86291777	K562	blood:	n/a	n/a
7	ARID3A	chr8:86375408-86375608	K562	blood:	n/a	n/a
8	ARID3A	chr8:86459249-86459549	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:86277502-86277804	HepG2	liver:	n/a	n/a
10	ATF1	chr8:86322674-86323117	K562	blood:	n/a	n/a
11	ATF1	chr8:86291509-86291829	K562	blood:	n/a	n/a
12	ATF1	chr8:86290328-86290675	K562	blood:	n/a	n/a
13	ATF2	chr8:86375277-86375647	GM12878	blood:	n/a	n/a
14	ATF2	chr8:86456835-86457349	GM12878	blood:	n/a	n/a
15	ATF2	chr8:86456763-86457418	GM12878	blood:	n/a	n/a
16	ATF2	chr8:86379099-86379380	GM12878	blood:	n/a	n/a
17	ATF3	chr8:86494789-86495026	K562	blood:	n/a	n/a
18	BACH1	chr8:86403854-86404118	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:86375517-86375618	K562	blood:	n/a	n/a
20	BACH1	chr8:86375322-86375896	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:86350837-86350999	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:86477700-86478018	K562	blood:	n/a	n/a
23	BACH1	chr8:86477707-86478028	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr8:86376436-86376638	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:86445039-86445121	K562	blood:	n/a	n/a
26	BACH1	chr8:86469052-86469363	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr8:86380185-86380380	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr8:86403885-86404059	K562	blood:	n/a	n/a
29	BACH1	chr8:86373952-86374352	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr8:86456863-86457355	GM12878	blood:	n/a	n/a
31	BATF	chr8:86407687-86407926	GM12878	blood:	n/a	chr8:86407879-86407890
32	BATF	chr8:86407688-86408006	GM12878	blood:	n/a	chr8:86407879-86407890
33	BATF	chr8:86414421-86414607	GM12878	blood:	n/a	chr8:86414511-86414522 chr8:86414512-86414522
34	BATF	chr8:86414365-86414644	GM12878	blood:	n/a	chr8:86414511-86414522 chr8:86414512-86414522
35	BATF	chr8:86456746-86457294	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:86456931-86457329	GM12878	blood:	n/a	n/a
37	BCLAF1	chr8:86375357-86375764	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:86456744-86457355	GM12878	blood:	n/a	chr8:86456857-86456866
39	BHLHE40	chr8:86375452-86375647	K562	blood:	n/a	n/a
40	BHLHE40	chr8:86375361-86375709	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
42	BHLHE40	chr8:86295520-86295720	K562	blood:	n/a	n/a
43	BHLHE40	chr8:86376459-86376495	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:86290345-86290622	K562	blood:	n/a	n/a
45	BHLHE40	chr8:86322833-86323051	K562	blood:	n/a	n/a
46	BHLHE40	chr8:86457024-86457178	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:86464104-86464411	HepG2	liver:	n/a	n/a
48	CBX3	chr8:86349389-86349850	HCT-116	colon:	n/a	n/a
49	CCNT2	chr8:86290303-86290726	K562	blood:	n/a	n/a
50	CCNT2	chr8:86322803-86323124	K562	blood:	n/a	n/a

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86375919-86375969	ProgFib	skin:	n/a
2	chr8:86371819-86371869	NHDF-neo	bronchial:	n/a
3	chr8:86376306-86376356	NH-A	brain:	n/a
4	chr8:86375919-86375969	ProgFib	skin:	n/a
5	chr8:86371819-86371869	NHDF-neo	bronchial:	n/a
6	chr8:86376306-86376356	NH-A	brain:	n/a
7	chr8:86349754-86349804	PrEC	prostate:	n/a
8	chr8:86350568-86350618	GM12878	blood:	n/a
9	chr8:86290432-86290482	NT2-D1	testis:	n/a
10	chr8:86350913-86350963	GM19239	blood:	n/a
11	chr8:86376277-86376327	SKMC	muscle:	n/a
12	chr8:86347111-86347161	HEEpiC	esophagus:	n/a
13	chr8:86379678-86379728	SAEC	small airway:	n/a
14	chr8:86290219-86290269	RPTEC	kidney:	n/a
15	chr8:86290432-86290482	HRE	kidney:	n/a
16	chr8:86291400-86291450	HCT-116	colon:	n/a
17	chr8:86375450-86375500	U87	brain:	n/a
18	chr8:86351195-86351245	PFSK-1	brain:	n/a
19	chr8:86504072-86504122	HCT-116	colon:	n/a
20	chr8:86414553-86414603	ovcar-3	ovarian:	n/a
21	chr8:86351195-86351245	BE2_C	brain:	n/a
22	chr8:86376842-86376892	MCF-7	breast:	n/a
23	chr8:86290219-86290269	PANC-1	pancreas:	n/a
24	chr8:86350889-86350939	BE2_C	brain:	n/a
25	chr8:86376306-86376356	T-47D	breast:	n/a
26	chr8:86375919-86375969	GM06990	blood:	n/a
27	chr8:86375919-86375969	HCM	heart:	n/a
28	chr8:86379678-86379728	SK-N-SH	brain:	n/a
29	chr8:86353723-86353773	HRE	kidney:	n/a
30	chr8:86350568-86350618	ovcar-3	ovarian:	n/a
31	chr8:86290432-86290482	HNPCEpiC	eye:	n/a
32	chr8:86349742-86349792	Hepatocyte	liver:	n/a
33	chr8:86375501-86375551	HRCEpiC	kidney:	n/a
34	chr8:86350889-86350939	H1-hESC	embryonic stem cell:	embryo
35	chr8:86393055-86393105	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:86350568-86350618	SK-N-MC	brain:	n/a
37	chr8:86352350-86352400	HCM	heart:	n/a
38	chr8:86349754-86349804	AG10803	skin:	n/a
39	chr8:86375450-86375500	HNPCEpiC	eye:	n/a
40	chr8:86290878-86290928	BJ	skin:	n/a
41	chr8:86351018-86351068	PANC-1	pancreas:	n/a
42	chr8:86350568-86350618	BE2_C	brain:	n/a
43	chr8:86290689-86290739	Hela-S3	cervix:	n/a
44	chr8:86350889-86350939	GM12892	blood:	n/a
45	chr8:86350278-86350328	PANC-1	pancreas:	n/a
46	chr8:86350927-86350977	HCM	heart:	n/a
47	chr8:86504072-86504122	NH-A	brain:	n/a
48	chr8:86351067-86351117	SAEC	small airway:	n/a
49	chr8:86350568-86350618	GM19239	blood:	n/a
50	chr8:86350919-86350969	HL-60	blood:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:86360412..86362696-chr8:87043331..87045552,2	MCF-7	breast:
2	chr8:86364795..86367348-chr8:86976708..86978928,2	MCF-7	breast:
3	chr8:86363526..86364138-chr8:87045071..87045735,2	MCF-7	breast:
4	chr8:86374507..86377610-chr8:86462239..86465615,5	MCF-7	breast:
5	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
6	chr8:86383914..86386781-chr8:86392186..86393964,2	MCF-7	breast:
7	chr8:86443204..86445086-chr8:86446422..86449141,2	MCF-7	breast:
8	chr8:86417772..86420887-chr8:86432218..86435662,3	MCF-7	breast:
9	chr8:86386280..86387988-chr8:86390083..86392825,2	K562	blood:
10	chr8:86222565..86224096-chr8:86281520..86283708,2	MCF-7	breast:
11	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
12	chr8:86296426..86298625-chr8:86302177..86305010,2	MCF-7	breast:
13	chr8:86376072..86377713-chr8:86460075..86462237,2	MCF-7	breast:
14	chr8:86433738..86438010-chr8:86438697..86442048,3	MCF-7	breast:
15	chr8:86373793..86376899-chr8:86998896..87001584,3	MCF-7	breast:
16	chr8:86404163..86406491-chr8:86406532..86408170,2	MCF-7	breast:
17	chr8:86416615..86418297-chr8:86419831..86421379,2	MCF-7	breast:
18	chr8:86362726..86365485-chr8:86365567..86367420,2	K562	blood:
19	chr8:86454738..86456401-chr8:86461305..86463210,2	MCF-7	breast:
20	chr8:86362621..86364573-chr8:86984978..86986328,33	MCF-7	breast:
21	chr8:86376161..86378374-chr8:86378444..86380100,2	K562	blood:
22	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
23	chr8:86260251..86261829-chr8:86265124..86266765,2	K562	blood:
24	chr8:86403779..86406429-chr8:86407390..86409709,2	MCF-7	breast:
25	chr8:86365526..86368719-chr8:87353659..87355514,3	MCF-7	breast:
26	chr8:86294414..86297402-chr8:86373142..86375603,2	MCF-7	breast:
27	chr8:86379732..86382227-chr8:86385483..86388148,2	K562	blood:
28	chr8:86448503..86451342-chr8:86452814..86454465,2	MCF-7	breast:
29	chr8:86363458..86364443-chr8:86375139..86376055,5	MCF-7	breast:
30	chr8:86428253..86433516-chr8:86435909..86440345,7	MCF-7	breast:
31	chr8:86416615..86418297-chr8:86419831..86421379,2	MCF-7	breast:
32	chr8:86363678..86364494-chr8:86374198..86374980,2	MCF-7	breast:
33	chr8:86451147..86453927-chr8:86454865..86457122,2	MCF-7	breast:
34	chr8:86211076..86211587-chr8:86373603..86374373,2	MCF-7	breast:
35	chr8:86415312..86417964-chr8:86420831..86422849,2	MCF-7	breast:
36	chr8:86454738..86456401-chr8:86461305..86463210,2	MCF-7	breast:
37	chr8:86363443..86364082-chr8:87045149..87046001,2	K562	blood:
38	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
39	chr8:86348746..86351284-chr8:86374911..86377490,2	MCF-7	breast:
40	chr8:86372209..86373809-chr8:86374683..86377383,2	K562	blood:
41	chr5:177630888..177633321-chr8:86308842..86311326,2	MCF-7	breast:
42	chr8:86404163..86406491-chr8:86406532..86408170,2	MCF-7	breast:
43	chr8:86363504..86364383-chr8:86986429..86987168,3	MCF-7	breast:
44	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
45	chr8:86443480..86445914-chr8:86447264..86449675,2	MCF-7	breast:
46	chr8:86375382..86376006-chr8:87045172..87046083,3	MCF-7	breast:
47	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
48	chr8:86363241..86365174-chr8:86985333..86987257,15	MCF-7	breast:
49	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
50	chr8:86468837..86470919-chr8:86472571..86475543,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA2-2	chr8:86452574-86452740	ENSG00000254380
2	lnc-CA1-1	chr8:86376457-86376562	ENSG00000253549.1
3	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
4	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537
5	lnc-CA2-1	chr8:86446631-86446811	XLOC_006865
6	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
7	lnc-CA1-1	chr8:86354276-86354466	ENSG00000253549.1
8	lnc-CA2-2	chr8:86413304-86413414	XLOC_006864
9	lnc-CA1-1	chr8:86375161-86375283	ENSG00000253549.1
10	lnc-CA2-3	chr8:86447984-86448189	FPKM1_group_31645_transcript_1
11	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537
12	lnc-CA2-2	chr8:86436128-86436354	ENSG00000254380
13	lnc-CA1-1	chr8:86376811-86377144	ENSG00000253549.1
14	lnc-CA1-1	chr8:86374965-86375030	NONHSAT127527
15	lnc-CA1-1	chr8:86354080-86354466	ENSG00000253549.1
16	lnc-CA1-1	chr8:86354387-86354466	NONHSAT127529
17	lnc-CA2-3	chr8:86444927-86444978	FPKM1_group_31645_transcript_1
18	lnc-CA2-2	chr8:86436090-86436470	XLOC_006864
19	lnc-CA1-1	chr8:86375161-86375671	NONHSAT127527
20	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
21	lnc-CA1-1	chr8:86368852-86369092	ENSG00000253549.1
22	lnc-CA2-1	chr8:86445765-86445878	XLOC_006865
23	lnc-CA1-1	chr8:86356236-86356349	NONHSAT127527
24	lnc-CA1-1	chr8:86374965-86375030	NONHSAT127529
25	lnc-CA1-1	chr8:86375661-86375942	NONHSAT127529
26	lnc-CA1-1	chr8:86354135-86354466	NONHSAT127527
27	lnc-CA2-2	chr8:86436806-86437088	ENSG00000254380

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CA2	hsa-miR-26a-5p	chr8:86393131-86393151
2	CA2	hsa-miR-26b-5p	chr8:86393132-86393151

Variant related genes	Relation type
ENSG00000253680	TF binding region
CA2	TF binding region
ENSG00000254380	TF binding region
ENSG00000253549	TF binding region
CA3	TF binding region
CA1	TF binding region
ENSG00000253680	CpG island
CA2	CpG island
ENSG00000254380	CpG island
ENSG00000253549	CpG island
CA3	CpG island
CA1	CpG island
ENSG00000062716	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000147614	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000254380	chromatin interactions
ENSG00000100345	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000254231	chromatin interactions
ENSG00000101104	chromatin interactions
ENSG00000147613	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000164879	chromatin interactions
ENSG00000133740	chromatin interactions
ENSG00000253154	chromatin interactions

Extended variants
information (count: 8859 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:8859 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190908854	chr8:86257157-86257158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573547770	chr8:86257182-86257183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562473490	chr8:86257186-86257187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531333100	chr8:86257190-86257191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533098540	chr8:86257215-86257216	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs183899187	chr8:86257248-86257249	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs556162055	chr8:86257275-86257276	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs188740476	chr8:86257288-86257289	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs547192814	chr8:86257296-86257297	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs566913829	chr8:86257330-86257331	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs538954143	chr8:86257358-86257359	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs193201416	chr8:86257402-86257403	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs568957514	chr8:86257418-86257419	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs115469115	chr8:86257450-86257451	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs117019855	chr8:86257522-86257523	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs142693111	chr8:86257560-86257561	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs183364155	chr8:86257600-86257601	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs146943457	chr8:86257632-86257633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576919978	chr8:86257643-86257644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62512498	chr8:86257691-86257692	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs541515761	chr8:86257717-86257718	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs71522996	chr8:86257718-86257719	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs187231913	chr8:86257772-86257773	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs576142434	chr8:86257848-86257849	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs375593685	chr8:86257869-86257870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs191678935	chr8:86257874-86257875	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs561495654	chr8:86257904-86257905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs368247377	chr8:86257920-86257921	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs12679158	chr8:86257929-86257930	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs527394255	chr8:86257933-86257934	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs183781245	chr8:86257950-86257951	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs141581814	chr8:86257969-86257970	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs573378796	chr8:86257970-86257971	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs546358690	chr8:86258026-86258027	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532563320	chr8:86258041-86258042	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs552491125	chr8:86258067-86258068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs540370686	chr8:86258098-86258099	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs562155804	chr8:86258111-86258112	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs188119299	chr8:86258117-86258118	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs531856586	chr8:86258122-86258123	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529258818	chr8:86258135-86258136	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs191381466	chr8:86258174-86258175	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568324022	chr8:86258206-86258207	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs114998234	chr8:86258226-86258227	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs553974321	chr8:86258270-86258271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551286815	chr8:86258290-86258291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566694208	chr8:86258309-86258310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570702036	chr8:86258325-86258326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539630363	chr8:86258352-86258353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185863063	chr8:86258446-86258447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Hepatocellular carcinoma	22267523	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:2644 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86244800-86263600	Weak transcription	Fetal Intestine Large	intestine
2	chr8:86253000-86257200	Weak transcription	Psoas Muscle	Psoas
3	chr8:86255400-86257200	Weak transcription	HepG2	liver
4	chr8:86255800-86257200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:86256600-86257800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:86257000-86257600	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr8:86257000-86257600	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr8:86257200-86257600	Enhancers	Psoas Muscle	Psoas
9	chr8:86257200-86257600	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr8:86257200-86257600	Bivalent Enhancer	HepG2	liver
11	chr8:86257600-86258200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr8:86257600-86258800	Enhancers	HepG2	liver
13	chr8:86257600-86261800	Weak transcription	Psoas Muscle	Psoas
14	chr8:86257600-86261800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr8:86257600-86263000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr8:86257600-86264400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:86257800-86261800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr8:86258200-86258600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr8:86258600-86258800	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr8:86258600-86259400	Enhancers	Fetal Intestine Small	intestine
21	chr8:86258800-86259200	Weak transcription	HepG2	liver
22	chr8:86258800-86261600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr8:86259200-86259600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:86259200-86259800	Enhancers	HepG2	liver
25	chr8:86259400-86259800	Enhancers	Fetal Lung	lung
26	chr8:86259400-86263600	Weak transcription	Fetal Intestine Small	intestine
27	chr8:86259800-86260000	Enhancers	Left Ventricle	heart
28	chr8:86259800-86261600	Weak transcription	Fetal Lung	lung
29	chr8:86260000-86263200	Weak transcription	Left Ventricle	heart
30	chr8:86260400-86260600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr8:86260600-86260800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:86260600-86260800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:86260600-86261400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr8:86261400-86261600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr8:86261400-86261600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:86261600-86262200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr8:86261600-86262600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr8:86261600-86265400	Enhancers	Fetal Lung	lung
39	chr8:86261800-86262000	Enhancers	Esophagus	oesophagus
40	chr8:86261800-86262000	Enhancers	Right Atrium	heart
41	chr8:86261800-86262400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr8:86261800-86263200	Enhancers	Psoas Muscle	Psoas
43	chr8:86261800-86263600	Enhancers	Ovary	ovary
44	chr8:86261800-86265200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:86261800-86265400	Enhancers	Adipose Nuclei	Adipose
46	chr8:86262000-86264600	Weak transcription	Esophagus	oesophagus
47	chr8:86262000-86266800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr8:86262200-86262400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr8:86262200-86263400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr8:86262400-86262800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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