Variant report

Variant	nsv891143
Chromosome Location	chr8:86841229-86914367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:61)
Chromatin interactive
region (count:94)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86860947-86861211	K562	blood:	n/a	n/a
2	ARID3A	chr8:86848202-86848466	K562	blood:	n/a	n/a
3	ARID3A	chr8:86860674-86860711	K562	blood:	n/a	n/a
4	ARID3A	chr8:86868281-86868466	K562	blood:	n/a	n/a
5	ARID3A	chr8:86855400-86856788	K562	blood:	n/a	chr8:86856408-86856424
6	ARID3A	chr8:86851632-86852291	K562	blood:	n/a	n/a
7	ARID3A	chr8:86873919-86874476	K562	blood:	n/a	n/a
8	ARID3A	chr8:86878872-86879538	K562	blood:	n/a	n/a
9	ARID3A	chr8:86906098-86907228	K562	blood:	n/a	n/a
10	ARID3A	chr8:86877891-86877975	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:86854067-86854193	K562	blood:	n/a	n/a
12	ARID3A	chr8:86860057-86860260	K562	blood:	n/a	n/a
13	ATF1	chr8:86858572-86858850	K562	blood:	n/a	n/a
14	ATF1	chr8:86851680-86851940	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	chr8:86878970-86879079	K562	blood:	n/a	n/a
18	BACH1	chr8:86848360-86848557	K562	blood:	n/a	n/a
19	BACH1	chr8:86873756-86874253	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:86873787-86874392	K562	blood:	n/a	n/a
21	BACH1	chr8:86855556-86855909	K562	blood:	n/a	n/a
22	BACH1	chr8:86906141-86906258	K562	blood:	n/a	n/a
23	BACH1	chr8:86854704-86854857	H1-hESC	embryonic stem cell:	n/a	n/a
24	BHLHE40	chr8:86878900-86879572	K562	blood:	n/a	n/a
25	BHLHE40	chr8:86860851-86861210	K562	blood:	n/a	n/a
26	BHLHE40	chr8:86848213-86848489	K562	blood:	n/a	n/a
27	BHLHE40	chr8:86864850-86864971	K562	blood:	n/a	n/a
28	BHLHE40	chr8:86851452-86852081	K562	blood:	n/a	n/a
29	CBX3	chr8:86878808-86879237	K562	blood:	n/a	n/a
30	CBX3	chr8:86882637-86883016	K562	blood:	n/a	n/a
31	CBX3	chr8:86848116-86848555	K562	blood:	n/a	n/a
32	CBX3	chr8:86855246-86855994	K562	blood:	n/a	n/a
33	CCNT2	chr8:86878585-86879466	K562	blood:	n/a	chr8:86879008-86879028
34	CCNT2	chr8:86898116-86898307	K562	blood:	n/a	n/a
35	CCNT2	chr8:86905812-86906257	K562	blood:	n/a	n/a
36	CCNT2	chr8:86851412-86851908	K562	blood:	n/a	n/a
37	CCNT2	chr8:86906478-86906864	K562	blood:	n/a	n/a
38	CCNT2	chr8:86855767-86856007	K562	blood:	n/a	n/a
39	CEBPB	chr8:86848192-86848660	H1-hESC	embryonic stem cell:	n/a	chr8:86848372-86848383
40	CEBPB	chr8:86848107-86848605	A549	lung:	n/a	chr8:86848372-86848383
41	CEBPB	chr8:86848109-86848565	ECC-1	luminal epithelium:	n/a	chr8:86848372-86848383
42	CEBPB	chr8:86847793-86848810	A549	lung:	n/a	chr8:86848372-86848383
43	CEBPB	chr8:86848135-86848562	IMR90	lung:	n/a	chr8:86848372-86848383
44	CEBPB	chr8:86847869-86848819	K562	blood:	n/a	chr8:86848372-86848383
45	CEBPB	chr8:86842832-86843003	A549	lung:	n/a	chr8:86842856-86842869 chr8:86842857-86842868 chr8:86842856-86842869
46	CEBPB	chr8:86848095-86848658	HCT-116	colon:	n/a	chr8:86848372-86848383
47	CEBPB	chr8:86847697-86849448	Hela-S3	cervix:	n/a	chr8:86848372-86848383
48	CEBPB	chr8:86842698-86842942	ECC-1	luminal epithelium:	n/a	chr8:86842856-86842869 chr8:86842857-86842868 chr8:86842856-86842869
49	CEBPB	chr8:86874212-86874684	MCF-7	breast:	n/a	chr8:86874482-86874493
50	CEBPB	chr8:86874268-86874695	ECC-1	luminal epithelium:	n/a	chr8:86874482-86874493

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86842690-86842740	Caco-2	colon:	n/a
2	chr8:86842690-86842740	HCT-116	colon:	n/a
3	chr8:86842690-86842740	NH-A	brain:	n/a
4	chr8:86842690-86842740	AG04449	skin:	fetal
5	chr8:86842690-86842740	GM19239	blood:	n/a
6	chr8:86842690-86842740	NT2-D1	testis:	n/a
7	chr8:86842690-86842740	Hepatocyte	liver:	n/a
8	chr8:86842690-86842740	MCF10A-Er-Src	breast:	n/a
9	chr8:86842690-86842740	LNCaP	prostate:	n/a
10	chr8:86842690-86842740	ovcar-3	ovarian:	n/a
11	chr8:86842690-86842740	Hela-S3	cervix:	n/a
12	chr8:86842690-86842740	AoSMC	blood vessel:	n/a
13	chr8:86842690-86842740	HCF	heart:	n/a
14	chr8:86842690-86842740	ProgFib	skin:	n/a
15	chr8:86842690-86842740	HIPEpiC	eye:	n/a
16	chr8:86842690-86842740	PFSK-1	brain:	n/a
17	chr8:86842690-86842740	SKMC	muscle:	n/a
18	chr8:86842690-86842740	GM06990	blood:	n/a
19	chr8:86842690-86842740	HRPEpiC	eye:	n/a
20	chr8:86842690-86842740	MCF-7	breast:	n/a
21	chr8:86842690-86842740	HEEpiC	esophagus:	n/a
22	chr8:86842690-86842740	T-47D	breast:	n/a
23	chr8:86842690-86842740	AG04450	lung:	fetal
24	chr8:86842690-86842740	ECC-1	luminal epithelium:	n/a
25	chr8:86842690-86842740	HCM	heart:	n/a
26	chr8:86842690-86842740	IMR90	lung:	fetal
27	chr8:86842690-86842740	AG09309	skin:	n/a
28	chr8:86842690-86842740	HCPEpiC	choroid plexus:	n/a
29	chr8:86842690-86842740	SAEC	small airway:	n/a
30	chr8:86842690-86842740	SK-N-MC	brain:	n/a
31	chr8:86842690-86842740	K562	blood:	n/a
32	chr8:86842690-86842740	BE2_C	brain:	n/a
33	chr8:86842690-86842740	SK-N-SH_RA	brain:	n/a
34	chr8:86842690-86842740	CMK	blood:	n/a
35	chr8:86842690-86842740	AG10803	skin:	n/a
36	chr8:86842690-86842740	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:86842690-86842740	HRCEpiC	kidney:	n/a
38	chr8:86842690-86842740	HL-60	blood:	n/a
39	chr8:86842690-86842740	NHBE	bronchial:	n/a
40	chr8:86842690-86842740	GM12892	blood:	n/a
41	chr8:86842690-86842740	NHDF-neo	bronchial:	n/a
42	chr8:86842690-86842740	HRE	kidney:	n/a
43	chr8:86842690-86842740	PANC-1	pancreas:	n/a
44	chr8:86842690-86842740	A549	lung:	n/a
45	chr8:86842690-86842740	RPTEC	kidney:	n/a
46	chr8:86842690-86842740	H1-hESC	embryonic stem cell:	embryo
47	chr8:86842690-86842740	HMEC	breast:	n/a
48	chr8:86842690-86842740	HEK293	kidney:	embryo
49	chr8:86842690-86842740	AG09319	gingival:	n/a
50	chr8:86842690-86842740	GM12891	blood:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:86890568..86892933-chr8:86896253..86899080,2	K562	blood:
2	chr8:86899597..86903472-chr8:86911858..86914599,3	K562	blood:
3	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
4	chr8:86877063..86879169-chr8:86913425..86915050,2	K562	blood:
5	chr8:86887769..86891314-chr8:86899255..86902657,3	MCF-7	breast:
6	chr8:86854256..86855844-chr8:86962935..86965322,2	K562	blood:
7	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
8	chr8:86842328..86846143-chr8:86846375..86849662,4	K562	blood:
9	chr8:86849039..86851736-chr8:87015052..87016845,2	MCF-7	breast:
10	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
11	chr8:86903344..86906241-chr8:86909054..86912607,3	K562	blood:
12	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:
13	chr8:86376110..86377714-chr8:86896432..86898770,2	MCF-7	breast:
14	chr8:86894781..86897215-chr8:86898766..86901877,3	MCF-7	breast:
15	chr8:86914189..86917723-chr8:86920260..86924267,5	K562	blood:
16	chr8:86853239..86855562-chr8:86941096..86942635,2	MCF-7	breast:
17	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
18	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
19	chr8:86887935..86890742-chr8:86895465..86898083,2	MCF-7	breast:
20	chr8:86906523..86908929-chr8:86918670..86920212,2	K562	blood:
21	chr8:86901113..86903216-chr8:86904279..86907196,2	K562	blood:
22	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
23	chr8:86842328..86846143-chr8:86846375..86849662,4	K562	blood:
24	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
25	chr8:86910009..86912623-chr8:86922322..86923826,2	MCF-7	breast:
26	chr8:86375109..86376361-chr8:86852746..86853757,4	MCF-7	breast:
27	chr8:86896571..86899286-chr8:86899613..86901432,2	K562	blood:
28	chr8:86877063..86879169-chr8:86913425..86915050,2	K562	blood:
29	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
30	chr8:86865438..86867152-chr8:86874296..86876870,2	MCF-7	breast:
31	chr8:86852831..86853539-chr8:86919503..86920015,2	MCF-7	breast:
32	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
33	chr8:86850726..86853148-chr8:86853230..86857704,4	K562	blood:
34	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
35	chr8:86373353..86377706-chr8:86848632..86856784,15	MCF-7	breast:
36	chr16:75285561..75287264-chr8:86851129..86852972,2	MCF-7	breast:
37	chr8:86903344..86906241-chr8:86909054..86912607,3	K562	blood:
38	chr8:86852142..86856180-chr8:86917083..86921619,8	MCF-7	breast:
39	chr8:86364996..86367147-chr8:86853567..86855147,2	MCF-7	breast:
40	chr8:86907376..86911489-chr8:86913876..86917330,5	K562	blood:
41	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
42	chr8:86853239..86855144-chr8:86935082..86937255,2	MCF-7	breast:
43	chr8:86853963..86856746-chr8:86949985..86952408,2	K562	blood:
44	chr8:86848347..86850172-chr8:86983643..86985301,2	MCF-7	breast:
45	chr8:86896626..86899608-chr8:86904301..86907878,3	MCF-7	breast:
46	chr8:86864951..86867156-chr8:86950288..86952196,2	K562	blood:
47	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
48	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
49	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:
50	chr8:86464673..86465447-chr8:86852772..86853973,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2530 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:2530 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7018222	chr8:86841229-86841230	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565232968	chr8:86841236-86841237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532581911	chr8:86841238-86841239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368199446	chr8:86841239-86841240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536325184	chr8:86841275-86841276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531737560	chr8:86841277-86841278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541076994	chr8:86841286-86841287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551523062	chr8:86841316-86841317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539059934	chr8:86841322-86841323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558846607	chr8:86841328-86841329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575458639	chr8:86841336-86841337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559277530	chr8:86841346-86841347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538181864	chr8:86841349-86841350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554465549	chr8:86841352-86841353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574603745	chr8:86841368-86841369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539904855	chr8:86841369-86841370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150907729	chr8:86841376-86841377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116216188	chr8:86841382-86841383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562541919	chr8:86841392-86841393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531106135	chr8:86841414-86841415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186669927	chr8:86841422-86841423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369640950	chr8:86841424-86841425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561306086	chr8:86841455-86841456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191176924	chr8:86841456-86841457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548440013	chr8:86841460-86841461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530334137	chr8:86841464-86841465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569949050	chr8:86841478-86841479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117134244	chr8:86841484-86841485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566976912	chr8:86841490-86841491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538996757	chr8:86841494-86841495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552595930	chr8:86841501-86841502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567029791	chr8:86841507-86841508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199692979	chr8:86841560-86841561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139386449	chr8:86841562-86841563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569282047	chr8:86841567-86841568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369425686	chr8:86841570-86841571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs151147732	chr8:86841571-86841572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552295282	chr8:86841585-86841586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs145368504	chr8:86841587-86841588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568132451	chr8:86841594-86841595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141076578	chr8:86841597-86841598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147663295	chr8:86841598-86841599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13282400	chr8:86841622-86841623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373490214	chr8:86841629-86841630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142464214	chr8:86841642-86841643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545537598	chr8:86841646-86841647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184766779	chr8:86841652-86841653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141580506	chr8:86841663-86841664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147834480	chr8:86841669-86841670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557373741	chr8:86841676-86841677	Weak transcription Enhancers	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:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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

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