Variant report

Variant	nsv891279
Chromosome Location	chr8:110268104-110450092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2585)
CpG islands
(count:1893)
Chromatin interactive
region (count:245)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110377303-110377464	K562	blood:	n/a	n/a
2	ARID3A	chr8:110338028-110338334	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:110338022-110338410	K562	blood:	n/a	n/a
4	ARID3A	chr8:110289281-110289645	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:110381642-110382257	K562	blood:	n/a	chr8:110382190-110382206 chr8:110382189-110382205
6	ARID3A	chr8:110344361-110344824	K562	blood:	n/a	n/a
7	ARID3A	chr8:110359093-110359473	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:110404919-110405551	K562	blood:	n/a	n/a
9	ARID3A	chr8:110440493-110441166	K562	blood:	n/a	n/a
10	ARID3A	chr8:110359773-110359882	K562	blood:	n/a	n/a
11	ARID3A	chr8:110359061-110359502	K562	blood:	n/a	n/a
12	ARID3A	chr8:110411923-110412202	K562	blood:	n/a	n/a
13	ARID3A	chr8:110346129-110346989	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:110355109-110355350	K562	blood:	n/a	chr8:110355323-110355339 chr8:110355324-110355340
15	ARID3A	chr8:110423847-110424726	K562	blood:	n/a	n/a
16	ARID3A	chr8:110378502-110378919	K562	blood:	n/a	n/a
17	ARID3A	chr8:110346126-110346545	K562	blood:	n/a	n/a
18	ATF1	chr8:110440707-110441089	K562	blood:	n/a	n/a
19	ATF1	chr8:110378470-110378772	K562	blood:	n/a	n/a
20	ATF1	chr8:110381750-110382104	K562	blood:	n/a	n/a
21	ATF1	chr8:110345502-110345720	K562	blood:	n/a	n/a
22	ATF1	chr8:110423878-110424292	K562	blood:	n/a	n/a
23	ATF1	chr8:110346176-110346949	K562	blood:	n/a	n/a
24	ATF2	chr8:110346122-110346773	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr8:110274349-110274803	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr8:110346081-110346628	GM12878	blood:	n/a	n/a
27	ATF2	chr8:110346107-110346948	GM12878	blood:	n/a	n/a
28	ATF3	chr8:110374993-110375321	K562	blood:	n/a	n/a
29	ATF3	chr8:110346287-110346527	GM12878	blood:	n/a	n/a
30	ATF3	chr8:110346143-110346579	K562	blood:	n/a	chr8:110346544-110346553
31	ATF3	chr8:110346126-110346743	A549	lung:	n/a	chr8:110346544-110346553
32	ATF3	chr8:110346231-110346545	HepG2	liver:	n/a	n/a
33	ATF3	chr8:110346144-110346656	GM12878	blood:	n/a	chr8:110346544-110346553
34	ATF3	chr8:110346111-110346601	H1-hESC	embryonic stem cell:	n/a	chr8:110346544-110346553
35	BACH1	chr8:110440421-110441061	K562	blood:	n/a	n/a
36	BACH1	chr8:110403534-110403559	K562	blood:	n/a	n/a
37	BACH1	chr8:110374595-110374769	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr8:110340220-110340367	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr8:110346134-110346916	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr8:110374153-110374307	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:110405000-110405477	K562	blood:	n/a	n/a
42	BACH1	chr8:110378699-110378798	K562	blood:	n/a	n/a
43	BATF	chr8:110345928-110346729	GM12878	blood:	n/a	n/a
44	BATF	chr8:110362748-110362954	GM12878	blood:	n/a	n/a
45	BATF	chr8:110362742-110363018	GM12878	blood:	n/a	n/a
46	BCL3	chr8:110345914-110346984	A549	lung:	n/a	chr8:110346105-110346114 chr8:110346106-110346119
47	BCL3	chr8:110345994-110346924	A549	lung:	n/a	chr8:110346105-110346114 chr8:110346106-110346119
48	BCL3	chr8:110414649-110414919	GM12878	blood:	n/a	n/a
49	BCL3	chr8:110405674-110405957	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:110345917-110346906	GM12878	blood:	n/a	chr8:110346105-110346114 chr8:110346106-110346119

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110346385-110346435	ProgFib	skin:	n/a
2	chr8:110346293-110346343	HEEpiC	esophagus:	n/a
3	chr8:110346385-110346435	ProgFib	skin:	n/a
4	chr8:110346293-110346343	HEEpiC	esophagus:	n/a
5	chr8:110374563-110374613	HCT-116	colon:	n/a
6	chr8:110280928-110280978	SKMC	muscle:	n/a
7	chr8:110346621-110346671	GM12891	blood:	n/a
8	chr8:110342871-110342921	HEK293	kidney:	embryo
9	chr8:110349212-110349262	K562	blood:	n/a
10	chr8:110373460-110373510	HAEpiC	amniotic membrane:	n/a
11	chr8:110342136-110342186	SK-N-SH_RA	brain:	n/a
12	chr8:110346451-110346501	HRE	kidney:	n/a
13	chr8:110346385-110346435	SK-N-SH_RA	brain:	n/a
14	chr8:110342136-110342186	A549	lung:	n/a
15	chr8:110346885-110346935	HepG2	liver:	n/a
16	chr8:110374583-110374633	SK-N-SH	brain:	n/a
17	chr8:110349212-110349262	HIPEpiC	eye:	n/a
18	chr8:110374792-110374842	BJ	skin:	n/a
19	chr8:110374374-110374424	AG09309	skin:	n/a
20	chr8:110374583-110374633	SK-N-SH_RA	brain:	n/a
21	chr8:110374294-110374344	HEK293	kidney:	embryo
22	chr8:110374374-110374424	HNPCEpiC	eye:	n/a
23	chr8:110342914-110342964	GM12891	blood:	n/a
24	chr8:110374563-110374613	HCPEpiC	choroid plexus:	n/a
25	chr8:110346664-110346714	PrEC	prostate:	n/a
26	chr8:110346885-110346935	ovcar-3	ovarian:	n/a
27	chr8:110346385-110346435	HepG2	liver:	n/a
28	chr8:110349212-110349262	PrEC	prostate:	n/a
29	chr8:110374563-110374613	AG10803	skin:	n/a
30	chr8:110374675-110374725	BE2_C	brain:	n/a
31	chr8:110374792-110374842	HL-60	blood:	n/a
32	chr8:110346885-110346935	HEEpiC	esophagus:	n/a
33	chr8:110272720-110272770	U87	brain:	n/a
34	chr8:110346002-110346052	K562	blood:	n/a
35	chr8:110342914-110342964	A549	lung:	n/a
36	chr8:110374792-110374842	HepG2	liver:	n/a
37	chr8:110373460-110373510	HCPEpiC	choroid plexus:	n/a
38	chr8:110272720-110272770	HRCEpiC	kidney:	n/a
39	chr8:110373460-110373510	BJ	skin:	n/a
40	chr8:110346451-110346501	PANC-1	pancreas:	n/a
41	chr8:110347022-110347072	HRCEpiC	kidney:	n/a
42	chr8:110346293-110346343	NT2-D1	testis:	n/a
43	chr8:110374792-110374842	HCT-116	colon:	n/a
44	chr8:110373460-110373510	HepG2	liver:	n/a
45	chr8:110274914-110274964	PANC-1	pancreas:	n/a
46	chr8:110346002-110346052	ovcar-3	ovarian:	n/a
47	chr8:110274914-110274964	CMK	blood:	n/a
48	chr8:110346385-110346435	SKMC	muscle:	n/a
49	chr8:110346498-110346548	BE2_C	brain:	n/a
50	chr8:110342136-110342186	HCT-116	colon:	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:110374980..110376608-chr8:110402670..110404308,2	K562	blood:
2	chr8:110399100..110401680-chr8:110403337..110405156,2	K562	blood:
3	chr8:110403354..110405591-chr8:110412229..110414153,2	K562	blood:
4	chr1:173836721..173837338-chr8:110346299..110347048,2	Hela-S3	cervix:
5	chr8:110367088..110368622-chr8:110370242..110371743,2	K562	blood:
6	chr8:109914966..109916782-chr8:110304946..110307932,2	MCF-7	breast:
7	chr8:110267160..110271575-chr8:110275719..110280785,4	MCF-7	breast:
8	chr8:109899394..109901395-chr8:110337763..110338847,8	MCF-7	breast:
9	chr8:110359161..110361961-chr8:110559520..110561613,2	MCF-7	breast:
10	chr8:110392136..110393759-chr8:110551713..110554181,2	K562	blood:
11	chr8:110411451..110413359-chr8:110418061..110419801,2	K562	blood:
12	chr8:110435315..110437873-chr8:110551355..110553690,2	K562	blood:
13	chr8:110274484..110277076-chr8:110350109..110352539,2	K562	blood:
14	chr8:109902295..109903347-chr8:110337500..110338754,10	MCF-7	breast:
15	chr8:110380517..110382065-chr8:110405348..110406940,2	K562	blood:
16	chr8:110296774..110299286-chr8:110348162..110350315,2	K562	blood:
17	chr1:935000..935789-chr8:110346539..110347078,2	Hela-S3	cervix:
18	chr8:110352840..110355386-chrX:78849788..78852363,2	MCF-7	breast:
19	chr8:110251271..110254204-chr8:110279241..110281441,2	K562	blood:
20	chr8:110420388..110423351-chr8:110425627..110427153,2	MCF-7	breast:
21	chr8:110399789..110401948-chr8:110406839..110408656,2	K562	blood:
22	chr8:110237132..110238315-chr8:110294080..110295100,5	MCF-7	breast:
23	chr8:110373158..110374661-chr8:110392938..110394946,2	MCF-7	breast:
24	chr8:110413961..110415545-chr8:110421000..110423217,2	MCF-7	breast:
25	chr8:110276401..110278429-chr8:110280186..110282933,2	MCF-7	breast:
26	chr8:110401827..110406627-chr8:110422630..110427187,6	K562	blood:
27	chr8:110367088..110368622-chr8:110370242..110371743,2	K562	blood:
28	chr8:110425956..110428666-chr8:110434429..110437325,2	K562	blood:
29	chr8:110271725..110274616-chr8:110342573..110345047,2	K562	blood:
30	chr8:110410046..110413726-chr8:110422893..110425486,3	K562	blood:
31	chr8:110356323..110358473-chr8:110658586..110660962,2	K562	blood:
32	chr8:110433712..110435356-chr8:110437905..110440817,2	K562	blood:
33	chr8:110331957..110333774-chr8:110341680..110343638,2	K562	blood:
34	chr8:109902365..109903207-chr8:110337379..110338925,7	K562	blood:
35	chr8:110397526..110401680-chr8:110402055..110405525,5	K562	blood:
36	chr8:110403524..110405569-chr8:110405749..110408596,2	K562	blood:
37	chr8:110429297..110431956-chr8:110445022..110447169,2	K562	blood:
38	chr8:110252748..110254805-chr8:110344261..110345885,2	K562	blood:
39	chr8:110333538..110336182-chr8:110347087..110349122,2	K562	blood:
40	chr8:110353436..110355204-chr8:110357328..110360216,4	K562	blood:
41	chr8:110325503..110327791-chr8:110330957..110333758,2	K562	blood:
42	chr8:110397373..110399828-chr8:110505690..110508375,2	K562	blood:
43	chr8:110413961..110415545-chr8:110421000..110423217,2	MCF-7	breast:
44	chr8:110339087..110342457-chr8:110344931..110347313,3	K562	blood:
45	chr8:110364601..110367292-chr8:110373403..110375892,3	MCF-7	breast:
46	chr8:110429297..110431956-chr8:110445022..110447169,2	K562	blood:
47	chr8:110284939..110287374-chr8:110293583..110295372,2	MCF-7	breast:
48	chr8:110401286..110403150-chr8:110410223..110413005,2	MCF-7	breast:
49	chr8:110324585..110327409-chr8:110346029..110347952,2	K562	blood:
50	chr8:110411451..110413359-chr8:110418061..110419801,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PKHD1L1-2	chr8:110351549-110351975	NONHSAT128289
2	lnc-ENY2-1	chr8:110327432-110328791	NONHSAT128288
3	lnc-ENY2-1	chr8:110327432-110328742	ENSG00000250267.2
4	lnc-ENY2-1	chr8:110310827-110311158	NONHSAT128288
5	lnc-PKHD1L1-2	chr8:110346575-110346631	NONHSAT128289
6	lnc-ENY2-1	chr8:110310827-110311158	ENSG00000250267.2
7	lnc-PKHD1L1-2	chr8:110348357-110348433	NONHSAT128289

No data

Variant related genes	Relation type
PKHD1L1	TF binding region
ENSG00000250267	TF binding region
ENY2	TF binding region
NUDCD1	TF binding region
PKHD1L1	CpG island
ENSG00000250267	CpG island
ENY2	CpG island
NUDCD1	CpG island
ENSG00000013375	chromatin interactions
ENSG00000147654	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000164794	chromatin interactions
ENSG00000205038	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000255402	chromatin interactions
ENSG00000253796	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000248050	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000147642	chromatin interactions
ENSG00000013392	chromatin interactions
ENSG00000188290	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000104408	chromatin interactions

Extended variants
information (count: 5906 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5906 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1458924	chr8:110268104-110268105	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551912433	chr8:110268115-110268116	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78166927	chr8:110268153-110268154	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531499545	chr8:110268159-110268160	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74502766	chr8:110268194-110268195	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567118949	chr8:110268203-110268204	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568033593	chr8:110268211-110268212	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533581535	chr8:110268216-110268217	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553753708	chr8:110268242-110268243	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182798283	chr8:110268252-110268253	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568557869	chr8:110268300-110268301	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35137538	chr8:110268305-110268306	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2926207	chr8:110268315-110268316	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556750601	chr8:110268319-110268320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576760092	chr8:110268320-110268321	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550956491	chr8:110268347-110268348	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76713726	chr8:110268356-110268357	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78401286	chr8:110268390-110268391	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541029990	chr8:110268392-110268393	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188413257	chr8:110268415-110268416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577667653	chr8:110268421-110268422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543556733	chr8:110268466-110268467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562333220	chr8:110268481-110268482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554432311	chr8:110268488-110268489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138424498	chr8:110268491-110268492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548443163	chr8:110268522-110268523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs16879267	chr8:110268540-110268541	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs527601196	chr8:110268593-110268594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570904151	chr8:110268611-110268612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547039348	chr8:110268650-110268651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148855987	chr8:110268670-110268671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142527104	chr8:110268688-110268689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201258312	chr8:110268689-110268690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs33994474	chr8:110268690-110268691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61570813	chr8:110268691-110268692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200743452	chr8:110268693-110268694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192865630	chr8:110268706-110268707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs57035030	chr8:110268738-110268739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75391404	chr8:110268747-110268748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13262553	chr8:110268804-110268805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553735863	chr8:110268870-110268871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184675797	chr8:110268901-110268902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572608334	chr8:110268942-110268943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535328966	chr8:110268952-110268953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187579556	chr8:110268967-110268968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369512511	chr8:110268980-110268981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34333060	chr8:110268997-110268998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577655348	chr8:110269014-110269015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192434128	chr8:110269023-110269024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564936045	chr8:110269028-110269029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	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
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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	22014070	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2996 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110211200-110311600	Weak transcription	Right Ventricle	heart
2	chr8:110235400-110271400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr8:110235400-110275000	Weak transcription	Fetal Brain Male	brain
4	chr8:110236200-110308800	Weak transcription	Thymus	Thymus
5	chr8:110236200-110309200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr8:110236600-110344200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:110237000-110283800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr8:110237200-110271400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:110237800-110271400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr8:110238000-110311600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr8:110238200-110286600	Weak transcription	Ovary	ovary
12	chr8:110239600-110274400	Weak transcription	Pancreas	Pancrea
13	chr8:110240400-110274800	Weak transcription	Small Intestine	intestine
14	chr8:110241800-110295600	Weak transcription	Psoas Muscle	Psoas
15	chr8:110242000-110274400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr8:110242000-110274600	Weak transcription	HSMMtube	muscle
17	chr8:110242000-110283600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr8:110242200-110274400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:110242200-110289800	Weak transcription	Colonic Mucosa	Colon
20	chr8:110242400-110274200	Weak transcription	NH-A	brain
21	chr8:110242400-110274400	Weak transcription	Gastric	stomach
22	chr8:110242400-110282800	Weak transcription	A549	lung
23	chr8:110242400-110305000	Weak transcription	NHLF	lung
24	chr8:110242600-110291200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr8:110242800-110285000	Weak transcription	Esophagus	oesophagus
26	chr8:110243200-110291000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:110244600-110280600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:110244800-110274600	Weak transcription	NHEK	skin
29	chr8:110245600-110274400	Weak transcription	Fetal Stomach	stomach
30	chr8:110247000-110311400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:110249200-110291600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr8:110249600-110274400	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr8:110252400-110283000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr8:110252400-110286600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr8:110252400-110304800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr8:110252800-110299600	Weak transcription	Fetal Kidney	kidney
37	chr8:110255600-110274400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:110255600-110275400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr8:110255600-110283600	Weak transcription	K562	blood
40	chr8:110255600-110291200	Weak transcription	Fetal Thymus	thymus
41	chr8:110255600-110305400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr8:110256000-110282600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr8:110256200-110271200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr8:110256200-110274200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr8:110256200-110274400	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr8:110256200-110275400	Weak transcription	HepG2	liver
47	chr8:110256600-110281400	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr8:110256600-110284800	Weak transcription	Brain Germinal Matrix	brain
49	chr8:110256800-110282800	Weak transcription	Hela-S3	cervix
50	chr8:110257000-110283000	Weak transcription	Primary T helper cells PMA-I stimulated	--

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