Variant report

Variant	esv3410448
Chromosome Location	chr8:126339813-126418053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1766)
CpG islands
(count:551)
Chromatin interactive
region (count:129)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:126346194-126347297	K562	blood:	n/a	n/a
2	ARID3A	chr8:126396061-126396338	K562	blood:	n/a	n/a
3	ARID3A	chr8:126392512-126392793	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:126346345-126347014	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:126394884-126395413	K562	blood:	n/a	n/a
6	ARID3A	chr8:126344123-126344367	K562	blood:	n/a	n/a
7	ARID3A	chr8:126359960-126360133	K562	blood:	n/a	n/a
8	ATF1	chr8:126347929-126348176	K562	blood:	n/a	n/a
9	ATF1	chr8:126346075-126346791	K562	blood:	n/a	n/a
10	ATF1	chr8:126395997-126396351	K562	blood:	n/a	n/a
11	ATF1	chr8:126374993-126375347	K562	blood:	n/a	n/a
12	ATF2	chr8:126374854-126375451	GM12878	blood:	n/a	n/a
13	ATF2	chr8:126401147-126401527	GM12878	blood:	n/a	n/a
14	ATF2	chr8:126398549-126399569	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr8:126374985-126375397	GM12878	blood:	n/a	n/a
16	ATF2	chr8:126398771-126399527	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr8:126364856-126365602	GM12878	blood:	n/a	n/a
18	ATF2	chr8:126346215-126346739	GM12878	blood:	n/a	n/a
19	ATF2	chr8:126352356-126352814	GM12878	blood:	n/a	n/a
20	ATF2	chr8:126342790-126343347	GM12878	blood:	n/a	n/a
21	ATF2	chr8:126364921-126365574	GM12878	blood:	n/a	n/a
22	ATF2	chr8:126352221-126352847	GM12878	blood:	n/a	n/a
23	ATF2	chr8:126347672-126348267	GM12878	blood:	n/a	n/a
24	ATF2	chr8:126346300-126346704	GM12878	blood:	n/a	n/a
25	ATF2	chr8:126342809-126343278	GM12878	blood:	n/a	n/a
26	ATF2	chr8:126356180-126356629	GM12878	blood:	n/a	n/a
27	ATF3	chr8:126374920-126375429	A549	lung:	n/a	chr8:126375161-126375176
28	ATF3	chr8:126346077-126346789	K562	blood:	n/a	n/a
29	ATF3	chr8:126375014-126375360	K562	blood:	n/a	chr8:126375161-126375176
30	ATF3	chr8:126395957-126396384	K562	blood:	n/a	n/a
31	ATF3	chr8:126346389-126346596	K562	blood:	n/a	n/a
32	ATF3	chr8:126391283-126391462	K562	blood:	n/a	n/a
33	ATF3	chr8:126374854-126375624	HCT-116	colon:	n/a	chr8:126375161-126375176
34	BACH1	chr8:126401173-126401359	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr8:126396034-126396242	K562	blood:	n/a	chr8:126396201-126396215
36	BACH1	chr8:126391193-126391482	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr8:126401299-126401310	K562	blood:	n/a	n/a
38	BACH1	chr8:126396958-126396994	K562	blood:	n/a	n/a
39	BATF	chr8:126364994-126365346	GM12878	blood:	n/a	n/a
40	BATF	chr8:126398040-126398392	GM12878	blood:	n/a	n/a
41	BATF	chr8:126347734-126348047	GM12878	blood:	n/a	chr8:126347919-126347930
42	BATF	chr8:126342877-126343325	GM12878	blood:	n/a	n/a
43	BATF	chr8:126356322-126356547	GM12878	blood:	n/a	n/a
44	BATF	chr8:126346324-126346678	GM12878	blood:	n/a	chr8:126346457-126346467 chr8:126346461-126346471 chr8:126346460-126346471
45	BATF	chr8:126365044-126365396	GM12878	blood:	n/a	n/a
46	BATF	chr8:126342863-126343279	GM12878	blood:	n/a	n/a
47	BATF	chr8:126352376-126352673	GM12878	blood:	n/a	n/a
48	BATF	chr8:126346317-126346584	GM12878	blood:	n/a	chr8:126346457-126346467 chr8:126346461-126346471 chr8:126346460-126346471
49	BATF	chr8:126352390-126352673	GM12878	blood:	n/a	n/a
50	BATF	chr8:126347721-126348073	GM12878	blood:	n/a	chr8:126347919-126347930

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:126384593-126384643	Hela-S3	cervix:	n/a
2	chr8:126374251-126374301	GM12878	blood:	n/a
3	chr8:126384593-126384643	Hela-S3	cervix:	n/a
4	chr8:126374251-126374301	GM12878	blood:	n/a
5	chr8:126353972-126354022	HAEpiC	amniotic membrane:	n/a
6	chr8:126398731-126398781	SK-N-SH_RA	brain:	n/a
7	chr8:126384593-126384643	PFSK-1	brain:	n/a
8	chr8:126353972-126354022	GM06990	blood:	n/a
9	chr8:126374251-126374301	GM19239	blood:	n/a
10	chr8:126366660-126366710	HCPEpiC	choroid plexus:	n/a
11	chr8:126384593-126384643	Hepatocyte	liver:	n/a
12	chr8:126403700-126403750	SK-N-SH_RA	brain:	n/a
13	chr8:126374251-126374301	PrEC	prostate:	n/a
14	chr8:126341151-126341201	AG10803	skin:	n/a
15	chr8:126374251-126374301	HIPEpiC	eye:	n/a
16	chr8:126347517-126347567	ProgFib	skin:	n/a
17	chr8:126374251-126374301	Caco-2	colon:	n/a
18	chr8:126366660-126366710	HCF	heart:	n/a
19	chr8:126347517-126347567	NH-A	brain:	n/a
20	chr8:126366660-126366710	HepG2	liver:	n/a
21	chr8:126341151-126341201	ECC-1	luminal epithelium:	n/a
22	chr8:126390552-126390602	Hela-S3	cervix:	n/a
23	chr8:126353972-126354022	MCF-7	breast:	n/a
24	chr8:126347517-126347567	BJ	skin:	n/a
25	chr8:126384593-126384643	HCM	heart:	n/a
26	chr8:126347517-126347567	HCT-116	colon:	n/a
27	chr8:126366660-126366710	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:126366660-126366710	Hepatocyte	liver:	n/a
29	chr8:126398731-126398781	Hepatocyte	liver:	n/a
30	chr8:126353972-126354022	SK-N-SH	brain:	n/a
31	chr8:126347517-126347567	AoSMC	blood vessel:	n/a
32	chr8:126384593-126384643	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:126384593-126384643	H1-hESC	embryonic stem cell:	embryo
34	chr8:126341151-126341201	A549	lung:	n/a
35	chr8:126390552-126390602	BJ	skin:	n/a
36	chr8:126403700-126403750	T-47D	breast:	n/a
37	chr8:126403700-126403750	HRE	kidney:	n/a
38	chr8:126398731-126398781	SK-N-MC	brain:	n/a
39	chr8:126374251-126374301	H1-hESC	embryonic stem cell:	embryo
40	chr8:126403700-126403750	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:126347517-126347567	HMEC	breast:	n/a
42	chr8:126374251-126374301	IMR90	lung:	fetal
43	chr8:126341151-126341201	HMEC	breast:	n/a
44	chr8:126398731-126398781	AG09309	skin:	n/a
45	chr8:126384593-126384643	LNCaP	prostate:	n/a
46	chr8:126390552-126390602	Hepatocyte	liver:	n/a
47	chr8:126366660-126366710	HCM	heart:	n/a
48	chr8:126384593-126384643	GM12878	blood:	n/a
49	chr8:126353972-126354022	HCF	heart:	n/a
50	chr8:126384593-126384643	ProgFib	skin:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:126359782..126362737-chr8:126363798..126365592,2	MCF-7	breast:
2	chr8:126345442..126348175-chr8:126352080..126354376,2	MCF-7	breast:
3	chr8:126391119..126393618-chr8:126395022..126397110,2	MCF-7	breast:
4	chr8:126403976..126405604-chr8:126409006..126411084,2	MCF-7	breast:
5	chr8:126401472..126405632-chr8:126442348..126443996,3	MCF-7	breast:
6	chr8:126347469..126349929-chr8:126354038..126356701,2	MCF-7	breast:
7	chr8:126412429..126413958-chr8:126437402..126438965,2	MCF-7	breast:
8	chr8:126355313..126358836-chr8:126365344..126367404,3	MCF-7	breast:
9	chr8:126417845..126420968-chr8:126440192..126443831,4	MCF-7	breast:
10	chr8:126394324..126395966-chr8:126442137..126444137,2	MCF-7	breast:
11	chr8:126349657..126352524-chr8:126353800..126356280,3	K562	blood:
12	chr8:126361514..126365167-chr8:126440219..126443605,3	K562	blood:
13	chr8:126395613..126397313-chr8:126429736..126431953,2	MCF-7	breast:
14	chr8:126345301..126349169-chr8:126355838..126358002,3	K562	blood:
15	chr8:126344683..126349065-chr8:126441599..126445443,4	MCF-7	breast:
16	chr8:126391452..126393059-chr8:126393825..126396141,2	K562	blood:
17	chr8:126373622..126375800-chr8:126376213..126378817,2	MCF-7	breast:
18	chr8:126356437..126358759-chr8:126364213..126366728,2	K562	blood:
19	chr8:126356437..126358759-chr8:126364213..126366728,2	K562	blood:
20	chr8:126412462..126414973-chr8:126421649..126423999,2	MCF-7	breast:
21	chr8:126345442..126348175-chr8:126352080..126354376,2	MCF-7	breast:
22	chr8:126390371..126392922-chr8:126442383..126443996,2	MCF-7	breast:
23	chr8:126218358..126220845-chr8:126354499..126357060,2	K562	blood:
24	chr8:126341644..126344065-chr8:126344220..126347316,3	K562	blood:
25	chr8:126412879..126414831-chr8:126440456..126442134,2	MCF-7	breast:
26	chr8:126374530..126376049-chr8:126380618..126383134,2	K562	blood:
27	chr8:126360008..126362836-chr8:126364930..126366678,2	K562	blood:
28	chr8:126315465..126318192-chr8:126341334..126342938,2	K562	blood:
29	chr8:126342754..126344650-chr8:126346334..126348343,3	K562	blood:
30	chr8:126322882..126325288-chr8:126341226..126344036,2	MCF-7	breast:
31	chr8:126401809..126404508-chr8:126412101..126414210,2	MCF-7	breast:
32	chr8:126366805..126369282-chr8:126440468..126443244,2	K562	blood:
33	chr8:126409326..126412304-chr8:126440467..126442135,2	MCF-7	breast:
34	chr8:126344782..126348434-chr8:126350693..126355502,7	K562	blood:
35	chr8:126400810..126402321-chr8:126411709..126414303,2	K562	blood:
36	chr8:126345301..126349169-chr8:126355838..126358002,3	K562	blood:
37	chr8:126398403..126400666-chr8:126403364..126405825,2	K562	blood:
38	chr8:126397190..126399796-chr8:126399864..126401786,2	K562	blood:
39	chr8:126396237..126399236-chr8:126405521..126409652,3	K562	blood:
40	chr8:126407808..126411702-chr8:126412259..126415395,3	MCF-7	breast:
41	chr8:126318641..126321559-chr8:126341791..126343679,2	MCF-7	breast:
42	chr8:126344782..126348434-chr8:126350693..126355502,7	K562	blood:
43	chr8:126348698..126351560-chr8:126363326..126365712,2	K562	blood:
44	chr8:126388142..126389944-chr8:126417069..126419677,2	MCF-7	breast:
45	chr8:126359782..126362737-chr8:126363798..126365592,2	MCF-7	breast:
46	chr8:126395154..126398210-chr8:126400039..126403336,3	MCF-7	breast:
47	chr8:126341424..126343336-chr8:126353093..126355921,2	MCF-7	breast:
48	chr8:126398403..126400666-chr8:126403364..126405825,2	K562	blood:
49	chr8:126398357..126400534-chr8:126411877..126414417,2	K562	blood:
50	chr8:126322565..126325543-chr8:126398051..126400754,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0196-3	chr8:126360438-126361123	ENSG00000254431.1
2	lnc-NSMCE2-1	chr8:126388577-126389343	NONHSAT128965
3	lnc-KIAA0196-3	chr8:126363623-126363658	ENSG00000254431.1

No data

Variant related genes	Relation type
ENSG00000254431	TF binding region
NSMCE2	TF binding region
ENSG00000254431	CpG island
NSMCE2	CpG island
ENSG00000254431	chromatin interactions
ENSG00000156831	chromatin interactions
ENSG00000173334	chromatin interactions

Extended variants
information (count: 3090 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:3090 , 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	rs555305269	chr8:126339819-126339820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570447233	chr8:126339849-126339850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4871582	chr8:126339942-126339943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs373906204	chr8:126339956-126339957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377586253	chr8:126340023-126340024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575216574	chr8:126340026-126340027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563718395	chr8:126340033-126340034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187757797	chr8:126340065-126340066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558021888	chr8:126340108-126340109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73704928	chr8:126340113-126340114	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs540426885	chr8:126340165-126340166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201962611	chr8:126340190-126340191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560761023	chr8:126340256-126340257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147445535	chr8:126340259-126340260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73336855	chr8:126340341-126340342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs562600084	chr8:126340390-126340391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35192094	chr8:126340393-126340394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34667555	chr8:126340394-126340395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191375517	chr8:126340429-126340430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567807000	chr8:126340457-126340458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115580420	chr8:126340460-126340461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531329274	chr8:126340498-126340499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545062262	chr8:126340559-126340560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564990902	chr8:126340577-126340578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535635890	chr8:126340589-126340590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547246061	chr8:126340655-126340656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145436600	chr8:126340707-126340708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529870599	chr8:126340759-126340760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549040560	chr8:126340775-126340776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535670297	chr8:126340787-126340788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547640637	chr8:126340824-126340825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147280993	chr8:126340880-126340881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185026183	chr8:126340941-126340942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571822060	chr8:126340961-126340962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534524716	chr8:126340990-126340991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565951774	chr8:126340996-126340997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28502126	chr8:126341006-126341007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs543290145	chr8:126341045-126341046	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556283785	chr8:126341058-126341059	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539735026	chr8:126341082-126341083	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs35851979	chr8:126341094-126341095	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs397694463	chr8:126341095-126341096	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs397801250	chr8:126341096-126341097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs148657901	chr8:126341148-126341149	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs78258496	chr8:126341151-126341152	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs564915219	chr8:126341173-126341174	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs527555723	chr8:126341195-126341196	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541300227	chr8:126341221-126341222	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111794451	chr8:126341222-126341223	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142151289	chr8:126341352-126341353	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:148)

Disease	PMID	Source
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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21240255	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastric cancer	21635755	CNVD

Chromatin state (count:2128 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126318600-126354600	Weak transcription	Ovary	ovary
2	chr8:126322000-126374200	Weak transcription	Aorta	Aorta
3	chr8:126323600-126340200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:126324200-126354200	Weak transcription	Hela-S3	cervix
5	chr8:126329400-126344000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr8:126330800-126369200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr8:126331200-126357400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:126331800-126340600	Weak transcription	K562	blood
9	chr8:126331800-126341400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:126332400-126345600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:126332600-126369400	Weak transcription	Fetal Stomach	stomach
12	chr8:126333000-126354200	Weak transcription	Fetal Lung	lung
13	chr8:126333400-126340000	Weak transcription	A549	lung
14	chr8:126334800-126340200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr8:126335600-126340000	Weak transcription	NHDF-Ad	bronchial
16	chr8:126335600-126346000	Weak transcription	Fetal Intestine Small	intestine
17	chr8:126335600-126353200	Weak transcription	Primary B cells from cord blood	blood
18	chr8:126336600-126354200	Weak transcription	Spleen	Spleen
19	chr8:126339000-126342400	Weak transcription	Primary T cells from cord blood	blood
20	chr8:126339400-126340600	Weak transcription	Psoas Muscle	Psoas
21	chr8:126339400-126346200	Weak transcription	Thymus	Thymus
22	chr8:126340000-126341000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:126340000-126341600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:126340000-126341600	Enhancers	A549	lung
25	chr8:126340000-126341600	Enhancers	NHDF-Ad	bronchial
26	chr8:126340000-126341800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:126340000-126354200	Weak transcription	Esophagus	oesophagus
28	chr8:126340000-126359600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr8:126340200-126340800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:126340200-126341600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr8:126340200-126341600	Enhancers	NH-A	brain
32	chr8:126340200-126341600	Enhancers	Osteobl	bone
33	chr8:126340200-126342000	Enhancers	HSMMtube	muscle
34	chr8:126340200-126342200	Enhancers	Fetal Heart	heart
35	chr8:126340400-126340800	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr8:126340400-126341400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:126340600-126341200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr8:126340600-126341400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr8:126340600-126341400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:126340600-126341400	Enhancers	Psoas Muscle	Psoas
41	chr8:126340600-126341600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr8:126340600-126341600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:126340600-126341600	Enhancers	Adipose Nuclei	Adipose
44	chr8:126340600-126341600	Enhancers	Fetal Muscle Leg	muscle
45	chr8:126340600-126341600	Enhancers	HSMM	muscle
46	chr8:126340600-126341600	Enhancers	K562	blood
47	chr8:126340600-126341600	Enhancers	NHLF	lung
48	chr8:126340600-126341800	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr8:126340600-126341800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr8:126340600-126342000	Enhancers	Left Ventricle	heart

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