Variant report

Variant	nsv891142
Chromosome Location	chr8:86839183-86928990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:824)
CpG islands
(count:305)
Chromatin interactive
region (count:114)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86851632-86852291	K562	blood:	n/a	n/a
2	ARID3A	chr8:86854067-86854193	K562	blood:	n/a	n/a
3	ARID3A	chr8:86860674-86860711	K562	blood:	n/a	n/a
4	ARID3A	chr8:86860947-86861211	K562	blood:	n/a	n/a
5	ARID3A	chr8:86860057-86860260	K562	blood:	n/a	n/a
6	ARID3A	chr8:86877891-86877975	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:86873919-86874476	K562	blood:	n/a	n/a
8	ARID3A	chr8:86906098-86907228	K562	blood:	n/a	n/a
9	ARID3A	chr8:86878872-86879538	K562	blood:	n/a	n/a
10	ARID3A	chr8:86848202-86848466	K562	blood:	n/a	n/a
11	ARID3A	chr8:86868281-86868466	K562	blood:	n/a	n/a
12	ARID3A	chr8:86855400-86856788	K562	blood:	n/a	chr8:86856408-86856424
13	ATF1	chr8:86851680-86851940	K562	blood:	n/a	n/a
14	ATF1	chr8:86858572-86858850	K562	blood:	n/a	n/a
15	ATF3	chr8:86848176-86848532	K562	blood:	n/a	n/a
16	ATF3	chr8:86853960-86854338	K562	blood:	n/a	n/a
17	BACH1	chr8:86873756-86874253	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:86873787-86874392	K562	blood:	n/a	n/a
19	BACH1	chr8:86906141-86906258	K562	blood:	n/a	n/a
20	BACH1	chr8:86848360-86848557	K562	blood:	n/a	n/a
21	BACH1	chr8:86878970-86879079	K562	blood:	n/a	n/a
22	BACH1	chr8:86855556-86855909	K562	blood:	n/a	n/a
23	BACH1	chr8:86854704-86854857	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr8:86840509-86840673	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:86840229-86840438	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:86840158-86840678	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:86878900-86879572	K562	blood:	n/a	n/a
28	BHLHE40	chr8:86848213-86848489	K562	blood:	n/a	n/a
29	BHLHE40	chr8:86851452-86852081	K562	blood:	n/a	n/a
30	BHLHE40	chr8:86860851-86861210	K562	blood:	n/a	n/a
31	BHLHE40	chr8:86864850-86864971	K562	blood:	n/a	n/a
32	CBX3	chr8:86882637-86883016	K562	blood:	n/a	n/a
33	CBX3	chr8:86915285-86915647	K562	blood:	n/a	n/a
34	CBX3	chr8:86848116-86848555	K562	blood:	n/a	n/a
35	CBX3	chr8:86855246-86855994	K562	blood:	n/a	n/a
36	CBX3	chr8:86878808-86879237	K562	blood:	n/a	n/a
37	CCNT2	chr8:86898116-86898307	K562	blood:	n/a	n/a
38	CCNT2	chr8:86851412-86851908	K562	blood:	n/a	n/a
39	CCNT2	chr8:86855767-86856007	K562	blood:	n/a	n/a
40	CCNT2	chr8:86906478-86906864	K562	blood:	n/a	n/a
41	CCNT2	chr8:86905812-86906257	K562	blood:	n/a	n/a
42	CCNT2	chr8:86878585-86879466	K562	blood:	n/a	chr8:86879008-86879028
43	CEBPB	chr8:86847793-86848810	A549	lung:	n/a	chr8:86848372-86848383
44	CEBPB	chr8:86848126-86848529	K562	blood:	n/a	chr8:86848372-86848383
45	CEBPB	chr8:86874212-86874684	MCF-7	breast:	n/a	chr8:86874482-86874493
46	CEBPB	chr8:86855387-86855903	K562	blood:	n/a	n/a
47	CEBPB	chr8:86847845-86848785	K562	blood:	n/a	chr8:86848372-86848383
48	CEBPB	chr8:86848166-86848569	HepG2	liver:	n/a	chr8:86848372-86848383
49	CEBPB	chr8:86877386-86877526	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:86855406-86856007	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86840929-86840979	ovcar-3	ovarian:	n/a
2	chr8:86840929-86840979	MCF10A-Er-Src	breast:	n/a
3	chr8:86841010-86841060	NHDF-neo	bronchial:	n/a
4	chr8:86842690-86842740	K562	blood:	n/a
5	chr8:86841010-86841060	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:86840954-86841004	HEEpiC	esophagus:	n/a
7	chr8:86840929-86840979	HEEpiC	esophagus:	n/a
8	chr8:86840929-86840979	HepG2	liver:	n/a
9	chr8:86842690-86842740	MCF10A-Er-Src	breast:	n/a
10	chr8:86840929-86840979	CMK	blood:	n/a
11	chr8:86840954-86841004	H1-hESC	embryonic stem cell:	embryo
12	chr8:86840954-86841004	HCF	heart:	n/a
13	chr8:86841010-86841060	MCF10A-Er-Src	breast:	n/a
14	chr8:86842690-86842740	HCM	heart:	n/a
15	chr8:86841010-86841060	AG04450	lung:	fetal
16	chr8:86841010-86841060	HepG2	liver:	n/a
17	chr8:86840929-86840979	HCT-116	colon:	n/a
18	chr8:86841010-86841060	HCF	heart:	n/a
19	chr8:86840929-86840979	RPTEC	kidney:	n/a
20	chr8:86840954-86841004	SAEC	small airway:	n/a
21	chr8:86840929-86840979	HMEC	breast:	n/a
22	chr8:86841010-86841060	HRPEpiC	eye:	n/a
23	chr8:86840961-86841011	Hela-S3	cervix:	n/a
24	chr8:86841010-86841060	SK-N-SH_RA	brain:	n/a
25	chr8:86841010-86841060	HUVEC	blood vessel:	n/a
26	chr8:86840929-86840979	LNCaP	prostate:	n/a
27	chr8:86842690-86842740	Hepatocyte	liver:	n/a
28	chr8:86840929-86840979	Hela-S3	cervix:	n/a
29	chr8:86840961-86841011	SK-N-SH	brain:	n/a
30	chr8:86840961-86841011	HMEC	breast:	n/a
31	chr8:86840954-86841004	PrEC	prostate:	n/a
32	chr8:86840961-86841011	HEEpiC	esophagus:	n/a
33	chr8:86840929-86840979	HIPEpiC	eye:	n/a
34	chr8:86840954-86841004	SK-N-SH_RA	brain:	n/a
35	chr8:86840961-86841011	MCF-7	breast:	n/a
36	chr8:86840954-86841004	AG10803	skin:	n/a
37	chr8:86840929-86840979	Hepatocyte	liver:	n/a
38	chr8:86840929-86840979	HAEpiC	amniotic membrane:	n/a
39	chr8:86840961-86841011	AG09309	skin:	n/a
40	chr8:86840954-86841004	T-47D	breast:	n/a
41	chr8:86840961-86841011	LNCaP	prostate:	n/a
42	chr8:86840954-86841004	NT2-D1	testis:	n/a
43	chr8:86841010-86841060	A549	lung:	n/a
44	chr8:86841010-86841060	BJ	skin:	n/a
45	chr8:86840929-86840979	AG04450	lung:	fetal
46	chr8:86842690-86842740	LNCaP	prostate:	n/a
47	chr8:86840954-86841004	AG09319	gingival:	n/a
48	chr8:86842690-86842740	HNPCEpiC	eye:	n/a
49	chr8:86840961-86841011	U87	brain:	n/a
50	chr8:86840961-86841011	T-47D	breast:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:86915923..86918690-chr8:86925047..86926941,2	K562	blood:
2	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
3	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
4	chr8:86873909..86875817-chr8:86877327..86879783,3	K562	blood:
5	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
6	chr8:86867877..86870175-chr8:86957602..86960658,3	K562	blood:
7	chr8:86852142..86856180-chr8:86917083..86921619,8	MCF-7	breast:
8	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
9	chr8:86877063..86879169-chr8:86913425..86915050,2	K562	blood:
10	chr8:86890525..86892195-chr8:86896949..86899068,2	MCF-7	breast:
11	chr8:86376110..86377714-chr8:86896432..86898770,2	MCF-7	breast:
12	chr8:86865438..86867152-chr8:86874296..86876870,2	MCF-7	breast:
13	chr8:86864951..86867156-chr8:86950288..86952196,2	K562	blood:
14	chr8:86896626..86899608-chr8:86904301..86907878,3	MCF-7	breast:
15	chr8:86852831..86853452-chr8:86919492..86920015,2	MCF-7	breast:
16	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
17	chr8:86896571..86899286-chr8:86899613..86901432,2	K562	blood:
18	chr8:86852831..86853539-chr8:86919503..86920015,2	MCF-7	breast:
19	chr8:86364996..86367147-chr8:86853567..86855147,2	MCF-7	breast:
20	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
21	chr8:86887935..86890742-chr8:86895465..86898083,2	MCF-7	breast:
22	chr8:86877063..86879169-chr8:86913425..86915050,2	K562	blood:
23	chr8:86899597..86903472-chr8:86911858..86914599,3	K562	blood:
24	chr16:75285561..75287264-chr8:86851129..86852972,2	MCF-7	breast:
25	chr8:86890568..86892933-chr8:86896253..86899080,2	K562	blood:
26	chr8:86903344..86906241-chr8:86909054..86912607,3	K562	blood:
27	chr8:86852831..86853452-chr8:86919492..86920015,2	MCF-7	breast:
28	chr8:86849960..86852773-chr8:86921780..86923557,2	MCF-7	breast:
29	chr8:86906345..86911462-chr8:86911476..86915769,5	K562	blood:
30	chr8:86903344..86906241-chr8:86909054..86912607,3	K562	blood:
31	chr8:86873909..86875817-chr8:86877327..86879783,3	K562	blood:
32	chr8:86887769..86891314-chr8:86899255..86902657,3	MCF-7	breast:
33	chr8:86904549..86906712-chr8:86921070..86923014,2	MCF-7	breast:
34	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:
35	chr8:86894346..86897279-chr8:87354275..87355907,2	MCF-7	breast:
36	chr8:86887935..86890742-chr8:86895465..86898083,2	MCF-7	breast:
37	chr8:86923298..86925579-chr8:86927126..86928850,2	K562	blood:
38	chr8:86896571..86899286-chr8:86899613..86901432,2	K562	blood:
39	chr8:86849344..86852342-chr8:86863151..86865379,2	K562	blood:
40	chr8:86923840..86926243-chr8:86938916..86941616,2	K562	blood:
41	chr8:86917393..86918906-chr8:86923396..86926098,2	K562	blood:
42	chr8:86375109..86376361-chr8:86852746..86853757,4	MCF-7	breast:
43	chr8:86848347..86850172-chr8:86983643..86985301,2	MCF-7	breast:
44	chr8:86907376..86911489-chr8:86913876..86917330,5	K562	blood:
45	chr8:86906345..86911462-chr8:86911476..86915769,5	K562	blood:
46	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
47	chr8:86375512..86377088-chr8:86920473..86922287,2	MCF-7	breast:
48	chr8:86853239..86855562-chr8:86941096..86942635,2	MCF-7	breast:
49	chr8:86876992..86879169-chr8:86912945..86915050,2	K562	blood:
50	chr8:86890525..86892195-chr8:86896949..86899068,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-2	chr8:86901808-86901882	ENSG00000253154
2	lnc-ATP6V0D2-2	chr8:86920542-86920842	ENSG00000253154
3	lnc-ATP6V0D2-2	chr8:86851934-86852014	NONHSAT127540
4	lnc-REXO1L2P-2	chr8:86866739-86866829	XLOC_007141
5	lnc-ATP6V0D2-2	chr8:86851934-86852014	ENSG00000253154
6	lnc-REXO1L2P-2	chr8:86864119-86865001	XLOC_007141
7	lnc-ATP6V0D2-2	chr8:86898164-86898223	NONHSAT127540
8	lnc-ATP6V0D2-2	chr8:86901752-86901882	ENSG00000253154
9	lnc-ATP6V0D2-2	chr8:86920536-86920847	NONHSAT127540
10	lnc-ATP6V0D2-2	chr8:86898164-86898223	ENSG00000253154
11	lnc-ATP6V0D2-2	chr8:86901808-86901882	NONHSAT127540

No data

Variant related genes	Relation type
REXO1L2P	TF binding region
ENSG00000253154	TF binding region
REXO1L2P	CpG island
ENSG00000253154	CpG island
ENSG00000050820	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000254231	chromatin interactions
ENSG00000253154	chromatin interactions

Extended variants
information (count: 3064 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3064 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62511123	chr8:86840888-86840889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs537535315	chr8:86840900-86840901	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs5024433	chr8:86840905-86840906	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs573949989	chr8:86840912-86840913	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542658855	chr8:86840914-86840915	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs553260974	chr8:86840916-86840917	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs573163171	chr8:86840929-86840930	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs545366452	chr8:86840931-86840932	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs550878947	chr8:86840933-86840934	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs111739685	chr8:86840948-86840949	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs188649385	chr8:86840954-86840955	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs530763178	chr8:86840955-86840956	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs544263599	chr8:86840956-86840957	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs560844108	chr8:86840957-86840958	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs529645444	chr8:86840962-86840963	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs546289103	chr8:86840964-86840965	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs74538068	chr8:86840977-86840978	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs566171804	chr8:86840978-86840979	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs528758336	chr8:86840981-86840982	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs569125024	chr8:86841011-86841012	ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs139355933	chr8:86841031-86841032	ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs537268127	chr8:86841036-86841037	ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs192787099	chr8:86841037-86841038	ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs567660786	chr8:86841038-86841039	ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs536791566	chr8:86841039-86841040	ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs7387773	chr8:86841065-86841066	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553397725	chr8:86841081-86841082	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146465094	chr8:86841083-86841084	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538921420	chr8:86841089-86841090	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558908475	chr8:86841102-86841103	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182396318	chr8:86841118-86841119	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367769209	chr8:86841119-86841120	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544081804	chr8:86841123-86841124	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371892257	chr8:86841134-86841135	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374861375	chr8:86841135-86841136	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369404625	chr8:86841143-86841144	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201063248	chr8:86841150-86841151	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574439226	chr8:86841156-86841157	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553342797	chr8:86841163-86841164	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112431305	chr8:86841171-86841172	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542095474	chr8:86841175-86841176	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62511140	chr8:86841178-86841179	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531994698	chr8:86841188-86841189	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149027595	chr8:86841198-86841199	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565239697	chr8:86841206-86841207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11783645	chr8:86841207-86841208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72684812	chr8:86841222-86841223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7018222	chr8:86841229-86841230	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs565232968	chr8:86841236-86841237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532581911	chr8:86841238-86841239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD

Chromatin state (count:1030 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86841000-86841200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:86841000-86844600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:86841000-86845000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:86841200-86841400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:86841200-86842000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr8:86841200-86842800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:86841200-86844200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:86841200-86845000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr8:86841600-86844200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:86841800-86843000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:86841800-86843400	Enhancers	Brain Substantia Nigra	brain
12	chr8:86841800-86843600	Enhancers	Brain Anterior Caudate	brain
13	chr8:86842000-86842800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr8:86842200-86843000	Enhancers	Brain Angular Gyrus	brain
15	chr8:86842200-86843000	Enhancers	Brain Hippocampus Middle	brain
16	chr8:86842200-86843400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:86842200-86843400	Enhancers	Brain Cingulate Gyrus	brain
18	chr8:86842200-86843600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:86842200-86843600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:86842200-86843800	Enhancers	Fetal Lung	lung
21	chr8:86842400-86842800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:86842400-86843000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:86842400-86843000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr8:86842400-86843000	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr8:86842400-86843000	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr8:86842400-86844000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr8:86842600-86843200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr8:86842800-86843000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr8:86842800-86843000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:86842800-86843000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:86842800-86843000	Enhancers	K562	blood
32	chr8:86842800-86843400	Enhancers	NHEK	skin
33	chr8:86842800-86843600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr8:86842800-86843600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:86842800-86843600	Enhancers	HMEC	breast
36	chr8:86842800-86843800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:86842800-86843800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr8:86842800-86845200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:86843000-86843800	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr8:86843000-86844000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr8:86843000-86844800	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr8:86843000-86845800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr8:86843000-86846000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr8:86843000-86846800	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr8:86843000-86847200	Weak transcription	Brain Hippocampus Middle	brain
46	chr8:86843000-86848600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:86843000-86848800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr8:86843200-86843800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr8:86843200-86844800	Weak transcription	K562	blood
50	chr8:86843200-86848400	Weak transcription	H1 Cell Line	embryonic stem cell

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