Variant report

Variant	nsv539696
Chromosome Location	chr8:100250184-100442195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:244)
Chromatin interactive
region (count:79)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100400144-100400181	K562	blood:	n/a	n/a
2	ARID3A	chr8:100370860-100371168	K562	blood:	n/a	n/a
3	ARID3A	chr8:100416524-100416817	K562	blood:	n/a	n/a
4	ARID3A	chr8:100298952-100299271	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:100370824-100371122	HepG2	liver:	n/a	n/a
6	ATF1	chr8:100416505-100416787	K562	blood:	n/a	n/a
7	ATF1	chr8:100370807-100371120	K562	blood:	n/a	n/a
8	ATF1	chr8:100278899-100278960	K562	blood:	n/a	n/a
9	BACH1	chr8:100395401-100395488	K562	blood:	n/a	n/a
10	BACH1	chr8:100389266-100389270	K562	blood:	n/a	n/a
11	BATF	chr8:100253079-100253361	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:100305139-100305357	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:100370878-100370919	A549	lung:	n/a	n/a
14	BHLHE40	chr8:100404161-100404287	K562	blood:	n/a	n/a
15	BRCA1	chr8:100370881-100371042	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr8:100389390-100389830	HCT-116	colon:	n/a	n/a
17	CBX3	chr8:100389448-100389836	K562	blood:	n/a	n/a
18	CBX3	chr8:100279965-100280308	K562	blood:	n/a	n/a
19	CBX3	chr8:100389428-100389814	K562	blood:	n/a	n/a
20	CCNT2	chr8:100332298-100332498	K562	blood:	n/a	n/a
21	CCNT2	chr8:100334302-100334493	K562	blood:	n/a	n/a
22	CEBPB	chr8:100373098-100373314	HepG2	liver:	n/a	chr8:100373128-100373139
23	CEBPB	chr8:100259968-100260228	ECC-1	luminal epithelium:	n/a	chr8:100260140-100260153 chr8:100260140-100260151 chr8:100260140-100260153 chr8:100260142-100260151 chr8:100260141-100260152
24	CEBPB	chr8:100400016-100400335	HepG2	liver:	n/a	chr8:100400181-100400192
25	CEBPB	chr8:100390141-100390341	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:100252915-100252978	K562	blood:	n/a	n/a
27	CEBPB	chr8:100415669-100415852	K562	blood:	n/a	n/a
28	CEBPB	chr8:100392522-100392850	HepG2	liver:	n/a	chr8:100392700-100392711
29	CEBPB	chr8:100261072-100261272	K562	blood:	n/a	chr8:100261184-100261195
30	CEBPB	chr8:100270367-100270768	IMR90	lung:	n/a	chr8:100270416-100270429 chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270416-100270429 chr8:100270631-100270644
31	CEBPB	chr8:100329518-100329524	A549	lung:	n/a	n/a
32	CEBPB	chr8:100259986-100260312	K562	blood:	n/a	chr8:100260140-100260153 chr8:100260140-100260151 chr8:100260140-100260153 chr8:100260142-100260151 chr8:100260141-100260152
33	CEBPB	chr8:100315328-100315675	ECC-1	luminal epithelium:	n/a	chr8:100315542-100315553
34	CEBPB	chr8:100312539-100312838	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:100416519-100416766	A549	lung:	n/a	n/a
36	CEBPB	chr8:100400077-100400272	IMR90	lung:	n/a	chr8:100400181-100400192
37	CEBPB	chr8:100328452-100328768	MCF-7	breast:	n/a	chr8:100328593-100328604
38	CEBPB	chr8:100259960-100260574	HepG2	liver:	n/a	chr8:100260140-100260153 chr8:100260140-100260151 chr8:100260140-100260153 chr8:100260142-100260151 chr8:100260141-100260152
39	CEBPB	chr8:100328511-100328711	H1-hESC	embryonic stem cell:	n/a	chr8:100328593-100328604
40	CEBPB	chr8:100373017-100373283	K562	blood:	n/a	chr8:100373128-100373139
41	CEBPB	chr8:100328430-100328776	HepG2	liver:	n/a	chr8:100328593-100328604
42	CEBPB	chr8:100261052-100261326	HepG2	liver:	n/a	chr8:100261184-100261195
43	CEBPB	chr8:100392560-100392932	MCF-7	breast:	n/a	chr8:100392700-100392711
44	CEBPB	chr8:100265043-100265398	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:100270360-100270762	HepG2	liver:	n/a	chr8:100270416-100270429 chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270416-100270429 chr8:100270631-100270644
46	CEBPB	chr8:100435483-100435733	MCF-7	breast:	n/a	n/a
47	CEBPB	chr8:100261009-100261329	IMR90	lung:	n/a	chr8:100261184-100261195
48	CEBPB	chr8:100309567-100309946	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:100270564-100270761	A549	lung:	n/a	chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270631-100270644
50	CEBPB	chr8:100313551-100313584	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100297748-100297798	NB4	blood:	n/a
2	chr8:100297748-100297798	HIPEpiC	eye:	n/a
3	chr8:100334620-100334670	GM12878	blood:	n/a
4	chr8:100262768-100262818	PrEC	prostate:	n/a
5	chr8:100252466-100252516	PFSK-1	brain:	n/a
6	chr8:100297748-100297798	LNCaP	prostate:	n/a
7	chr8:100334620-100334670	IMR90	lung:	fetal
8	chr8:100252466-100252516	HUVEC	blood vessel:	n/a
9	chr8:100297748-100297798	H1-hESC	embryonic stem cell:	embryo
10	chr8:100297748-100297798	GM19239	blood:	n/a
11	chr8:100297748-100297798	T-47D	breast:	n/a
12	chr8:100252466-100252516	Hepatocyte	liver:	n/a
13	chr8:100334620-100334670	Hela-S3	cervix:	n/a
14	chr8:100252466-100252516	HepG2	liver:	n/a
15	chr8:100334620-100334670	A549	lung:	n/a
16	chr8:100297748-100297798	NHBE	bronchial:	n/a
17	chr8:100262768-100262818	SK-N-SH_RA	brain:	n/a
18	chr8:100262768-100262818	RPTEC	kidney:	n/a
19	chr8:100262768-100262818	ovcar-3	ovarian:	n/a
20	chr8:100262768-100262818	HEEpiC	esophagus:	n/a
21	chr8:100297748-100297798	NT2-D1	testis:	n/a
22	chr8:100262768-100262818	NHBE	bronchial:	n/a
23	chr8:100262768-100262818	HIPEpiC	eye:	n/a
24	chr8:100262768-100262818	AG09319	gingival:	n/a
25	chr8:100252466-100252516	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:100297748-100297798	GM12892	blood:	n/a
27	chr8:100262768-100262818	NH-A	brain:	n/a
28	chr8:100262768-100262818	GM12878	blood:	n/a
29	chr8:100262768-100262818	HRCEpiC	kidney:	n/a
30	chr8:100252466-100252516	NB4	blood:	n/a
31	chr8:100252466-100252516	AoSMC	blood vessel:	n/a
32	chr8:100297748-100297798	HRPEpiC	eye:	n/a
33	chr8:100252466-100252516	Caco-2	colon:	n/a
34	chr8:100262768-100262818	BE2_C	brain:	n/a
35	chr8:100262768-100262818	Jurkat	blood:	n/a
36	chr8:100252466-100252516	AG10803	skin:	n/a
37	chr8:100252466-100252516	T-47D	breast:	n/a
38	chr8:100262768-100262818	PANC-1	pancreas:	n/a
39	chr8:100252466-100252516	AG09319	gingival:	n/a
40	chr8:100252466-100252516	ProgFib	skin:	n/a
41	chr8:100334620-100334670	BJ	skin:	n/a
42	chr8:100252466-100252516	A549	lung:	n/a
43	chr8:100262768-100262818	HepG2	liver:	n/a
44	chr8:100334620-100334670	U87	brain:	n/a
45	chr8:100297748-100297798	HCPEpiC	choroid plexus:	n/a
46	chr8:100334620-100334670	NH-A	brain:	n/a
47	chr8:100297748-100297798	A549	lung:	n/a
48	chr8:100262768-100262818	HRE	kidney:	n/a
49	chr8:100334620-100334670	SAEC	small airway:	n/a
50	chr8:100252466-100252516	RPTEC	kidney:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:100433911..100436132-chr8:100443954..100446728,2	MCF-7	breast:
2	chr8:100368561..100370943-chr8:100372272..100375246,2	K562	blood:
3	chr8:100355778..100358210-chr8:100359573..100361952,2	K562	blood:
4	chr8:100403788..100404692-chr8:100799555..100800231,3	MCF-7	breast:
5	chr8:100283345..100287751-chr8:100288664..100292518,5	K562	blood:
6	chr8:100277370..100279279-chr8:100282776..100285031,2	MCF-7	breast:
7	chr8:100253354..100255632-chr8:100258136..100261117,2	MCF-7	breast:
8	chr8:100267273..100269231-chr8:100273875..100275740,2	K562	blood:
9	chr8:100440991..100443912-chr8:100444936..100447073,2	K562	blood:
10	chr8:100266373..100268336-chr8:100270835..100272790,2	K562	blood:
11	chr8:100433051..100434745-chr9:90387715..90390439,2	MCF-7	breast:
12	chr8:100323481..100327206-chr8:100331154..100333171,3	MCF-7	breast:
13	chr8:100247496..100249230-chr8:100251577..100253709,2	K562	blood:
14	chr8:100180104..100181200-chr8:100370523..100371154,5	MCF-7	breast:
15	chr8:100021568..100024441-chr8:100255336..100257958,2	MCF-7	breast:
16	chr8:100368561..100370943-chr8:100372272..100375246,2	K562	blood:
17	chr8:100403842..100404899-chr8:100994134..100995356,3	MCF-7	breast:
18	chr8:100277370..100279279-chr8:100282776..100285031,2	MCF-7	breast:
19	chr8:100253785..100255699-chr8:100276390..100278151,2	MCF-7	breast:
20	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
21	chr8:100327325..100329198-chr8:100340079..100342358,2	MCF-7	breast:
22	chr8:100327325..100329198-chr8:100340079..100342358,2	MCF-7	breast:
23	chr8:100403279..100404684-chr8:100871403..100872860,7	MCF-7	breast:
24	chr8:99570015..99570973-chr8:100370433..100371359,3	K562	blood:
25	chr8:99952913..99953621-chr8:100370794..100371379,2	MCF-7	breast:
26	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
27	chr8:100024635..100026607-chr8:100339207..100341437,2	MCF-7	breast:
28	chr8:100354480..100357120-chr8:100365143..100367945,2	K562	blood:
29	chr8:99180814..99181617-chr8:100370430..100371368,2	MCF-7	breast:
30	chr8:100403791..100404673-chr8:100818662..100819568,3	MCF-7	breast:
31	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
32	chr8:100271840..100273856-chr8:100274522..100276066,2	MCF-7	breast:
33	chr8:100360393..100360964-chr8:100816462..100817102,2	MCF-7	breast:
34	chr8:100332741..100335703-chr8:100337137..100341568,3	MCF-7	breast:
35	chr8:100415595..100418351-chr8:100620634..100623512,2	MCF-7	breast:
36	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
37	chr8:100380996..100382939-chr8:100386454..100387970,2	K562	blood:
38	chr8:100253785..100255699-chr8:100276390..100278151,2	MCF-7	breast:
39	chr8:100381765..100384655-chr8:100392997..100394529,2	K562	blood:
40	chr8:100027143..100028710-chr8:100248941..100251194,2	MCF-7	breast:
41	chr8:99952476..99953694-chr8:100370455..100371470,4	MCF-7	breast:
42	chr8:100369443..100371664-chr8:100373746..100375749,2	K562	blood:
43	chr8:100250430..100253213-chr8:100261169..100262715,2	MCF-7	breast:
44	chr8:100298711..100300024-chr8:100370075..100371268,5	MCF-7	breast:
45	chr8:99717161..99717948-chr8:100352640..100353640,2	K562	blood:
46	chr8:100253354..100255632-chr8:100258136..100261117,2	MCF-7	breast:
47	chr8:100380996..100382939-chr8:100386454..100387970,2	K562	blood:
48	chr8:100253574..100255217-chr8:100258258..100260154,2	K562	blood:
49	chr11:74032580..74033199-chr8:100370794..100371470,2	MCF-7	breast:
50	chr8:100403606..100404633-chr8:100616940..100618032,4	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-7	chr8:100403785-100403932	NONHSAT127953
2	lnc-OSR2-7	chr8:100401844-100401948	NONHSAT127953
3	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952
4	lnc-OSR2-7	chr8:100441798-100441875	NONHSAT127953
5	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951

No data

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000237704	TF binding region
ENSG00000225017	TF binding region
ENSG00000236583	TF binding region
VPS13B	CpG island
ENSG00000237704	CpG island
ENSG00000225017	CpG island
ENSG00000236583	CpG island
ENSG00000225017	chromatin interactions
ENSG00000188029	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000253912	chromatin interactions

Extended variants
information (count: 6566 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:6566 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183501718	chr8:100250235-100250236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10091516	chr8:100250253-100250254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187661910	chr8:100250260-100250261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144416677	chr8:100250305-100250306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577938126	chr8:100250310-100250311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531171512	chr8:100250318-100250319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551086323	chr8:100250355-100250356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73285941	chr8:100250402-100250403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192517161	chr8:100250406-100250407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546920599	chr8:100250463-100250464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371226419	chr8:100250469-100250470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201650280	chr8:100250470-100250471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6990637	chr8:100250484-100250485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs535778202	chr8:100250500-100250501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555986660	chr8:100250517-100250518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557653954	chr8:100250524-100250525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116553145	chr8:100250596-100250597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538270913	chr8:100250669-100250670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558168088	chr8:100250690-100250691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578172986	chr8:100250797-100250798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559232708	chr8:100250867-100250868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540717088	chr8:100250884-100250885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183511169	chr8:100250895-100250896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139787118	chr8:100250990-100250991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375831895	chr8:100250995-100250996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562777012	chr8:100250996-100250997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145316454	chr8:100251050-100251051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111667416	chr8:100251052-100251053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140556547	chr8:100251055-100251056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527433489	chr8:100251092-100251093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186733080	chr8:100251093-100251094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192593308	chr8:100251163-100251164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142162242	chr8:100251173-100251174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112582875	chr8:100251177-100251178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569604213	chr8:100251226-100251227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538528977	chr8:100251248-100251249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558229514	chr8:100251311-100251312	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs79220697	chr8:100251330-100251331	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs573990088	chr8:100251382-100251383	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs534042266	chr8:100251392-100251393	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs140474379	chr8:100251413-100251414	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs184440285	chr8:100251443-100251444	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369614514	chr8:100251477-100251478	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549605125	chr8:100251570-100251571	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs150408527	chr8:100251610-100251611	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs189671775	chr8:100251619-100251620	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563061418	chr8:100251624-100251625	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78726743	chr8:100251625-100251626	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs555926298	chr8:100251640-100251641	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112225677	chr8:100251641-100251642	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
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
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
Multiple myeloma	16461302	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
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
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100207000-100290400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr8:100210000-100252400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr8:100212600-100253000	Weak transcription	Lung	lung
4	chr8:100214800-100252600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:100214800-100293200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr8:100216800-100252200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:100230400-100257800	Weak transcription	Aorta	Aorta
8	chr8:100231000-100253000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr8:100231000-100255400	Weak transcription	Right Ventricle	heart
10	chr8:100231200-100253000	Weak transcription	Gastric	stomach
11	chr8:100231400-100251200	Weak transcription	Ovary	ovary
12	chr8:100232000-100267400	Weak transcription	Left Ventricle	heart
13	chr8:100234200-100251600	Weak transcription	GM12878-XiMat	blood
14	chr8:100236400-100253000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:100236600-100252600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr8:100236800-100253000	Weak transcription	Osteobl	bone
17	chr8:100241200-100255400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr8:100241600-100251200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:100243200-100253000	Weak transcription	Brain Substantia Nigra	brain
20	chr8:100243400-100253000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr8:100244000-100251000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr8:100244400-100253000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:100244400-100253000	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr8:100244600-100251600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr8:100245000-100250600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:100246400-100251400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr8:100246400-100252600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:100246400-100253000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr8:100246400-100288200	Weak transcription	Primary T cells from cord blood	blood
30	chr8:100246600-100250400	Weak transcription	Liver	Liver
31	chr8:100246600-100252200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:100246600-100252400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:100246600-100252800	Weak transcription	HSMMtube	muscle
34	chr8:100246600-100253000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr8:100246600-100253000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:100246600-100253000	Weak transcription	Dnd41	blood
37	chr8:100246600-100253200	Weak transcription	Fetal Lung	lung
38	chr8:100246600-100253200	Weak transcription	NHLF	lung
39	chr8:100246600-100256200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr8:100246600-100261000	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr8:100246600-100267000	Weak transcription	Primary B cells from cord blood	blood
42	chr8:100246800-100251200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:100246800-100251200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr8:100246800-100252200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr8:100246800-100252200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:100246800-100252200	Weak transcription	Thymus	Thymus
47	chr8:100246800-100253000	Weak transcription	Fetal Intestine Large	intestine
48	chr8:100246800-100253000	Weak transcription	Fetal Muscle Leg	muscle
49	chr8:100246800-100253200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:100246800-100253200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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