Variant report

Variant	nsv821659
Chromosome Location	chr8:100147641-100369829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1252)
CpG islands
(count:428)
Chromatin interactive
region (count:103)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1252 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100149959-100150472	K562	blood:	n/a	n/a
2	ARID3A	chr8:100298952-100299271	HepG2	liver:	n/a	n/a
3	ATF1	chr8:100249602-100249617	K562	blood:	n/a	n/a
4	ATF1	chr8:100150113-100150549	K562	blood:	n/a	n/a
5	ATF1	chr8:100177666-100177787	K562	blood:	n/a	n/a
6	ATF1	chr8:100278899-100278960	K562	blood:	n/a	n/a
7	ATF3	chr8:100150017-100150481	K562	blood:	n/a	n/a
8	BACH1	chr8:100182411-100182437	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:100150185-100150441	K562	blood:	n/a	n/a
10	BATF	chr8:100253079-100253361	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:100305139-100305357	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:100150155-100150410	K562	blood:	n/a	n/a
13	CBX3	chr8:100150051-100150770	K562	blood:	n/a	n/a
14	CBX3	chr8:100279965-100280308	K562	blood:	n/a	n/a
15	CBX3	chr8:100150104-100150431	K562	blood:	n/a	n/a
16	CCNT2	chr8:100150101-100150431	K562	blood:	n/a	n/a
17	CCNT2	chr8:100334302-100334493	K562	blood:	n/a	n/a
18	CCNT2	chr8:100332298-100332498	K562	blood:	n/a	n/a
19	CEBPB	chr8:100259990-100260513	A549	lung:	n/a	chr8:100260140-100260153 chr8:100260140-100260151 chr8:100260140-100260153 chr8:100260142-100260151 chr8:100260141-100260152
20	CEBPB	chr8:100261062-100261323	A549	lung:	n/a	chr8:100261184-100261195
21	CEBPB	chr8:100312539-100312838	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:100261072-100261272	K562	blood:	n/a	chr8:100261184-100261195
23	CEBPB	chr8:100261052-100261326	HepG2	liver:	n/a	chr8:100261184-100261195
24	CEBPB	chr8:100200063-100200157	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:100202759-100203070	A549	lung:	n/a	n/a
26	CEBPB	chr8:100329518-100329524	A549	lung:	n/a	n/a
27	CEBPB	chr8:100328452-100328768	MCF-7	breast:	n/a	chr8:100328593-100328604
28	CEBPB	chr8:100157064-100157434	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:100265043-100265398	IMR90	lung:	n/a	n/a
30	CEBPB	chr8:100309567-100309946	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:100315363-100315947	H1-hESC	embryonic stem cell:	n/a	chr8:100315542-100315553
32	CEBPB	chr8:100199887-100200275	ECC-1	luminal epithelium:	n/a	n/a
33	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
34	CEBPB	chr8:100313551-100313584	K562	blood:	n/a	n/a
35	CEBPB	chr8:100328511-100328711	H1-hESC	embryonic stem cell:	n/a	chr8:100328593-100328604
36	CEBPB	chr8:100243713-100243940	K562	blood:	n/a	chr8:100243812-100243821 chr8:100243810-100243823
37	CEBPB	chr8:100149955-100150424	K562	blood:	n/a	n/a
38	CEBPB	chr8:100270367-100270768	IMR90	lung:	n/a	chr8:100270416-100270429 chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270416-100270429 chr8:100270631-100270644
39	CEBPB	chr8:100270360-100270762	HepG2	liver:	n/a	chr8:100270416-100270429 chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270416-100270429 chr8:100270631-100270644
40	CEBPB	chr8:100150009-100150483	K562	blood:	n/a	n/a
41	CEBPB	chr8:100259986-100260312	K562	blood:	n/a	chr8:100260140-100260153 chr8:100260140-100260151 chr8:100260140-100260153 chr8:100260142-100260151 chr8:100260141-100260152
42	CEBPB	chr8:100270292-100270770	K562	blood:	n/a	chr8:100270416-100270429 chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270416-100270429 chr8:100270358-100270370 chr8:100270631-100270644
43	CEBPB	chr8:100335969-100336430	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr8:100199888-100200266	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr8:100270564-100270761	A549	lung:	n/a	chr8:100270631-100270642 chr8:100270631-100270644 chr8:100270631-100270644
46	CEBPB	chr8:100252915-100252978	K562	blood:	n/a	n/a
47	CEBPB	chr8:100150136-100150322	K562	blood:	n/a	n/a
48	CEBPB	chr8:100328430-100328776	HepG2	liver:	n/a	chr8:100328593-100328604
49	CEBPB	chr8:100261009-100261329	IMR90	lung:	n/a	chr8:100261184-100261195
50	CEBPB	chr8:100315397-100315637	MCF-7	breast:	n/a	chr8:100315542-100315553

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100252466-100252516	GM19239	blood:	n/a
2	chr8:100252466-100252516	GM19239	blood:	n/a
3	chr8:100230864-100230914	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:100262768-100262818	HAEpiC	amniotic membrane:	n/a
5	chr8:100297748-100297798	LNCaP	prostate:	n/a
6	chr8:100334620-100334670	HNPCEpiC	eye:	n/a
7	chr8:100252466-100252516	Caco-2	colon:	n/a
8	chr8:100246786-100246836	Hela-S3	cervix:	n/a
9	chr8:100334620-100334670	Caco-2	colon:	n/a
10	chr8:100230864-100230914	HCF	heart:	n/a
11	chr8:100297748-100297798	AG04450	lung:	fetal
12	chr8:100157208-100157258	HRPEpiC	eye:	n/a
13	chr8:100262768-100262818	HL-60	blood:	n/a
14	chr8:100262768-100262818	GM12878	blood:	n/a
15	chr8:100252466-100252516	HepG2	liver:	n/a
16	chr8:100252466-100252516	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:100262768-100262818	GM06990	blood:	n/a
18	chr8:100262768-100262818	ECC-1	luminal epithelium:	n/a
19	chr8:100334620-100334670	HCPEpiC	choroid plexus:	n/a
20	chr8:100297748-100297798	GM06990	blood:	n/a
21	chr8:100230864-100230914	HepG2	liver:	n/a
22	chr8:100157208-100157258	SAEC	small airway:	n/a
23	chr8:100230864-100230914	HRE	kidney:	n/a
24	chr8:100262768-100262818	HUVEC	blood vessel:	n/a
25	chr8:100262768-100262818	Jurkat	blood:	n/a
26	chr8:100230864-100230914	HCPEpiC	choroid plexus:	n/a
27	chr8:100252466-100252516	GM12878	blood:	n/a
28	chr8:100297748-100297798	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:100157208-100157258	HRCEpiC	kidney:	n/a
30	chr8:100334620-100334670	HEK293	kidney:	embryo
31	chr8:100334620-100334670	K562	blood:	n/a
32	chr8:100262768-100262818	NB4	blood:	n/a
33	chr8:100252466-100252516	HMEC	breast:	n/a
34	chr8:100230864-100230914	HL-60	blood:	n/a
35	chr8:100297748-100297798	GM12892	blood:	n/a
36	chr8:100334620-100334670	GM12878	blood:	n/a
37	chr8:100230864-100230914	GM12878	blood:	n/a
38	chr8:100230864-100230914	SK-N-SH_RA	brain:	n/a
39	chr8:100262768-100262818	HEK293	kidney:	embryo
40	chr8:100262768-100262818	HEEpiC	esophagus:	n/a
41	chr8:100230864-100230914	U87	brain:	n/a
42	chr8:100262768-100262818	LNCaP	prostate:	n/a
43	chr8:100262768-100262818	HCPEpiC	choroid plexus:	n/a
44	chr8:100297748-100297798	CMK	blood:	n/a
45	chr8:100252466-100252516	HNPCEpiC	eye:	n/a
46	chr8:100230864-100230914	K562	blood:	n/a
47	chr8:100262768-100262818	ProgFib	skin:	n/a
48	chr8:100230864-100230914	Jurkat	blood:	n/a
49	chr8:100334620-100334670	HCM	heart:	n/a
50	chr8:100252466-100252516	HL-60	blood:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:100267273..100269231-chr8:100273875..100275740,2	K562	blood:
2	chr8:100225233..100227725-chr8:100239951..100242291,2	MCF-7	breast:
3	chr8:100277370..100279279-chr8:100282776..100285031,2	MCF-7	breast:
4	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
5	chr8:100024635..100026607-chr8:100339207..100341437,2	MCF-7	breast:
6	chr8:100165081..100167634-chr8:100170824..100172995,2	K562	blood:
7	chr8:100024787..100026436-chr8:100179759..100181890,2	MCF-7	breast:
8	chr8:100197794..100200560-chr8:100203500..100205350,2	MCF-7	breast:
9	chr8:100214282..100216094-chr8:100216677..100219374,2	MCF-7	breast:
10	chr8:100253354..100255632-chr8:100258136..100261117,2	MCF-7	breast:
11	chr8:100180149..100180921-chr8:100370671..100371459,2	MCF-7	breast:
12	chr8:100222308..100224756-chr8:100228347..100230627,2	K562	blood:
13	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
14	chr8:100235746..100237944-chr8:100240108..100241895,2	K562	blood:
15	chr8:99956335..99957904-chr8:100286239..100289117,2	MCF-7	breast:
16	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
17	chr8:100218080..100220133-chr8:100221773..100223694,2	K562	blood:
18	chr8:100253785..100255699-chr8:100276390..100278151,2	MCF-7	breast:
19	chr3:169509091..169511754-chr8:100235977..100237979,2	MCF-7	breast:
20	chr8:100277370..100279279-chr8:100282776..100285031,2	MCF-7	breast:
21	chr8:100257181..100259983-chr8:100260891..100263215,2	K562	blood:
22	chr8:100343791..100346575-chr8:100348119..100349870,2	MCF-7	breast:
23	chr8:100043379..100045451-chr8:100150795..100153462,2	MCF-7	breast:
24	chr8:100190689..100193029-chr8:100201859..100204401,2	K562	blood:
25	chr8:100012703..100016134-chr8:100151109..100154697,3	MCF-7	breast:
26	chr8:100250430..100253213-chr8:100261169..100262715,2	MCF-7	breast:
27	chr8:100024436..100026482-chr8:100177416..100178944,2	MCF-7	breast:
28	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
29	chr8:100179836..100180811-chr8:101138118..101138640,2	MCF-7	breast:
30	chr5:56110114..56112436-chr8:100221279..100223933,2	MCF-7	breast:
31	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
32	chr8:100247496..100249230-chr8:100251577..100253709,2	K562	blood:
33	chr8:100327325..100329198-chr8:100340079..100342358,2	MCF-7	breast:
34	chr8:100332741..100335703-chr8:100337137..100341568,3	MCF-7	breast:
35	chr8:100263532..100265951-chr8:100267509..100269368,2	K562	blood:
36	chr8:100048867..100050500-chr8:100268956..100271777,2	MCF-7	breast:
37	chr8:100247496..100249230-chr8:100251577..100253709,2	K562	blood:
38	chr8:100253574..100255217-chr8:100258258..100260154,2	K562	blood:
39	chr8:100343791..100346575-chr8:100348119..100349870,2	MCF-7	breast:
40	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
41	chr8:100266373..100268336-chr8:100270835..100272790,2	K562	blood:
42	chr8:100266373..100268336-chr8:100270835..100272790,2	K562	blood:
43	chr8:100225233..100227725-chr8:100239951..100242291,2	MCF-7	breast:
44	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
45	chr8:100190689..100193029-chr8:100201859..100204401,2	K562	blood:
46	chr8:100356710..100358343-chr8:100358891..100361073,2	K562	blood:
47	chr8:100253354..100255632-chr8:100258136..100261117,2	MCF-7	breast:
48	chr8:100267273..100269231-chr8:100273875..100275740,2	K562	blood:
49	chr8:100181985..100183886-chr8:100189568..100191594,2	MCF-7	breast:
50	chr8:100180037..100180965-chr8:100818919..100819673,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951
2	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VPS13B	hsa-miR-186-5p	chr8:100221987-100222010

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000225017	TF binding region
ENSG00000236583	TF binding region
ENSG00000237704	TF binding region
VPS13B	CpG island
ENSG00000225017	CpG island
ENSG00000236583	CpG island
ENSG00000237704	CpG island
ENSG00000095015	chromatin interactions
ENSG00000225017	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000253912	chromatin interactions
ENSG00000270135	chromatin interactions
ENSG00000132549	chromatin interactions

Extended variants
information (count: 7413 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:7413 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138486410	chr8:100147743-100147744	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs371878090	chr8:100147812-100147813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371379631	chr8:100147830-100147831	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141324814	chr8:100147838-100147839	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs150783688	chr8:100147861-100147862	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374276141	chr8:100147889-100147890	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs180177354	chr8:100147902-100147903	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139141291	chr8:100147926-100147927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149919865	chr8:100147928-100147929	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs368241718	chr8:100147929-100147930	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145969836	chr8:100147934-100147935	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200635121	chr8:100147949-100147950	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs139849251	chr8:100147952-100147953	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143205296	chr8:100147957-100147958	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs180177355	chr8:100147961-100147962	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371666483	chr8:100147975-100147976	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546514371	chr8:100148013-100148014	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs578069762	chr8:100148114-100148115	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs374490212	chr8:100148178-100148179	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559789662	chr8:100148182-100148183	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143029789	chr8:100148280-100148281	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs183024278	chr8:100148342-100148343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs80341428	chr8:100148346-100148347	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs568418255	chr8:100148402-100148403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559976935	chr8:100148427-100148428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566758942	chr8:100148428-100148429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529398956	chr8:100148477-100148478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368875227	chr8:100148613-100148614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369902702	chr8:100148622-100148623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562394975	chr8:100148634-100148635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575998724	chr8:100148638-100148639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550753199	chr8:100148653-100148654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369382143	chr8:100148782-100148783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561911689	chr8:100148795-100148796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187477721	chr8:100148826-100148827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527424773	chr8:100148833-100148834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192286218	chr8:100148859-100148860	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373961851	chr8:100148877-100148878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs367784958	chr8:100148878-100148879	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146659631	chr8:100148896-100148897	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200519753	chr8:100148919-100148920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369930405	chr8:100148923-100148924	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140746659	chr8:100148925-100148926	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs199684925	chr8:100148926-100148927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372625091	chr8:100148956-100148957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142971568	chr8:100148968-100148969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569157221	chr8:100149027-100149028	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144337936	chr8:100149032-100149033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376954399	chr8:100149034-100149035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539724165	chr8:100149048-100149049	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Non-syndromic sensorineural hearing loss	21987784	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
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100099200-100160200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr8:100099600-100161000	Weak transcription	Spleen	Spleen
3	chr8:100100400-100161000	Weak transcription	Esophagus	oesophagus
4	chr8:100101800-100160800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr8:100102200-100162600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr8:100103000-100151400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr8:100103400-100175600	Weak transcription	NHEK	skin
8	chr8:100103600-100160200	Weak transcription	A549	lung
9	chr8:100104000-100160200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr8:100104400-100155200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr8:100104400-100160800	Weak transcription	HSMMtube	muscle
12	chr8:100104600-100153200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr8:100104600-100160200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:100105000-100162800	Weak transcription	NHLF	lung
15	chr8:100107000-100162400	Weak transcription	Fetal Kidney	kidney
16	chr8:100107200-100160800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr8:100108200-100173000	Weak transcription	Hela-S3	cervix
18	chr8:100109200-100150200	Weak transcription	Aorta	Aorta
19	chr8:100109200-100197600	Weak transcription	HUVEC	blood vessel
20	chr8:100109600-100198000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr8:100114600-100161000	Weak transcription	HepG2	liver
22	chr8:100116400-100160200	Weak transcription	Fetal Muscle Leg	muscle
23	chr8:100121800-100160800	Weak transcription	Psoas Muscle	Psoas
24	chr8:100122000-100160600	Weak transcription	Right Ventricle	heart
25	chr8:100122000-100163000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr8:100122000-100201200	Weak transcription	Gastric	stomach
27	chr8:100125600-100156000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:100125800-100160800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr8:100127000-100160400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr8:100127200-100162800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr8:100127400-100160200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr8:100129000-100148800	Weak transcription	Fetal Intestine Large	intestine
33	chr8:100131000-100176000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:100131400-100148600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr8:100131800-100161000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr8:100131800-100162600	Weak transcription	Rectal Smooth Muscle	rectum
37	chr8:100131800-100197600	Weak transcription	Lung	lung
38	chr8:100132400-100148800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr8:100132600-100150200	Weak transcription	Fetal Stomach	stomach
40	chr8:100133200-100163400	Weak transcription	Colon Smooth Muscle	Colon
41	chr8:100133800-100147800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr8:100133800-100150400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr8:100133800-100160200	Weak transcription	Fetal Lung	lung
44	chr8:100133800-100160400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr8:100134000-100148400	Weak transcription	HSMM	muscle
46	chr8:100134000-100148800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr8:100134000-100148800	Weak transcription	Osteobl	bone
48	chr8:100134000-100159000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:100134000-100160000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr8:100134000-100160200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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