Variant report

Variant	nsv539659
Chromosome Location	chr8:86162507-86361533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1648)
CpG islands
(count:2138)
Chromatin interactive
region (count:76)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86290333-86290829	K562	blood:	n/a	n/a
2	ARID3A	chr8:86202468-86202617	K562	blood:	n/a	n/a
3	ARID3A	chr8:86258991-86259361	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:86277502-86277804	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:86169715-86169909	K562	blood:	n/a	n/a
6	ARID3A	chr8:86180047-86180413	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:86295505-86295821	K562	blood:	n/a	n/a
8	ARID3A	chr8:86291587-86291777	K562	blood:	n/a	n/a
9	ARID3A	chr8:86176898-86177188	K562	blood:	n/a	n/a
10	ATF1	chr8:86290328-86290675	K562	blood:	n/a	n/a
11	ATF1	chr8:86291509-86291829	K562	blood:	n/a	n/a
12	ATF1	chr8:86322674-86323117	K562	blood:	n/a	n/a
13	ATF3	chr8:86209670-86209992	K562	blood:	n/a	n/a
14	ATF3	chr8:86176921-86177222	K562	blood:	n/a	n/a
15	ATF3	chr8:86209644-86209936	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:86350837-86350999	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr8:86208534-86208968	GM12878	blood:	n/a	n/a
18	BATF	chr8:86251720-86251890	GM12878	blood:	n/a	n/a
19	BATF	chr8:86208270-86208976	GM12878	blood:	n/a	n/a
20	BCLAF1	chr8:86202261-86202699	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:86295520-86295720	K562	blood:	n/a	n/a
22	BHLHE40	chr8:86176076-86176403	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:86322833-86323051	K562	blood:	n/a	n/a
24	BHLHE40	chr8:86176644-86176789	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:86178237-86178254	K562	blood:	n/a	n/a
26	BHLHE40	chr8:86290345-86290622	K562	blood:	n/a	n/a
27	BHLHE40	chr8:86176856-86177265	K562	blood:	n/a	n/a
28	BRCA1	chr8:86209634-86209987	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr8:86202541-86202657	GM12878	blood:	n/a	n/a
30	CBX3	chr8:86236125-86236373	K562	blood:	n/a	n/a
31	CBX3	chr8:86349389-86349850	HCT-116	colon:	n/a	n/a
32	CCNT2	chr8:86322803-86323124	K562	blood:	n/a	n/a
33	CCNT2	chr8:86290303-86290726	K562	blood:	n/a	n/a
34	CCNT2	chr8:86176918-86177164	K562	blood:	n/a	chr8:86177015-86177035
35	CCNT2	chr8:86295373-86295833	K562	blood:	n/a	n/a
36	CEBPB	chr8:86209656-86210039	K562	blood:	n/a	n/a
37	CEBPB	chr8:86209612-86210022	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:86347945-86347966	K562	blood:	n/a	chr8:86347945-86347956
39	CEBPB	chr8:86322785-86323091	MCF-7	breast:	n/a	n/a
40	CEBPB	chr8:86314892-86315340	MCF-7	breast:	n/a	chr8:86315139-86315152 chr8:86315062-86315073 chr8:86315141-86315150 chr8:86315140-86315151 chr8:86315060-86315073 chr8:86315266-86315277
41	CEBPB	chr8:86314961-86315303	HepG2	liver:	n/a	chr8:86315139-86315152 chr8:86315062-86315073 chr8:86315141-86315150 chr8:86315140-86315151 chr8:86315060-86315073 chr8:86315266-86315277
42	CEBPB	chr8:86306805-86306980	H1-hESC	embryonic stem cell:	n/a	chr8:86306863-86306874 chr8:86306863-86306876
43	CEBPB	chr8:86348688-86348749	A549	lung:	n/a	chr8:86348716-86348727 chr8:86348714-86348727
44	CEBPB	chr8:86225535-86225698	K562	blood:	n/a	chr8:86225645-86225658
45	CEBPB	chr8:86225004-86225415	MCF-7	breast:	n/a	n/a
46	CEBPB	chr8:86215986-86216285	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:86209589-86210105	A549	lung:	n/a	n/a
48	CEBPB	chr8:86226253-86226483	HepG2	liver:	n/a	chr8:86226328-86226339
49	CEBPB	chr8:86191116-86191567	MCF-7	breast:	n/a	n/a
50	CEBPB	chr8:86306710-86307035	IMR90	lung:	n/a	chr8:86306863-86306874 chr8:86306863-86306876

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86350381-86350431	AG10803	skin:	n/a
2	chr8:86189690-86189740	GM12892	blood:	n/a
3	chr8:86214814-86214864	ECC-1	luminal epithelium:	n/a
4	chr8:86350381-86350431	AG10803	skin:	n/a
5	chr8:86189690-86189740	GM12892	blood:	n/a
6	chr8:86214814-86214864	ECC-1	luminal epithelium:	n/a
7	chr8:86230419-86230469	MCF-7	breast:	n/a
8	chr8:86290432-86290482	A549	lung:	n/a
9	chr8:86350581-86350631	HCF	heart:	n/a
10	chr8:86189883-86189933	BE2_C	brain:	n/a
11	chr8:86251915-86251965	MCF10A-Er-Src	breast:	n/a
12	chr8:86189690-86189740	HEEpiC	esophagus:	n/a
13	chr8:86353723-86353773	HCF	heart:	n/a
14	chr8:86290689-86290739	SAEC	small airway:	n/a
15	chr8:86189565-86189615	ProgFib	skin:	n/a
16	chr8:86351195-86351245	HEK293	kidney:	embryo
17	chr8:86290432-86290482	NT2-D1	testis:	n/a
18	chr8:86189690-86189740	HIPEpiC	eye:	n/a
19	chr8:86353723-86353773	HepG2	liver:	n/a
20	chr8:86230419-86230469	NB4	blood:	n/a
21	chr8:86347111-86347161	HUVEC	blood vessel:	n/a
22	chr8:86350581-86350631	HEK293	kidney:	embryo
23	chr8:86251915-86251965	U87	brain:	n/a
24	chr8:86350913-86350963	HCF	heart:	n/a
25	chr8:86290219-86290269	HEK293	kidney:	embryo
26	chr8:86189690-86189740	GM06990	blood:	n/a
27	chr8:86230419-86230469	RPTEC	kidney:	n/a
28	chr8:86352350-86352400	GM06990	blood:	n/a
29	chr8:86195487-86195537	HMEC	breast:	n/a
30	chr8:86351018-86351068	NH-A	brain:	n/a
31	chr8:86214814-86214864	LNCaP	prostate:	n/a
32	chr8:86352350-86352400	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:86254962-86255012	AG10803	skin:	n/a
34	chr8:86350592-86350642	HIPEpiC	eye:	n/a
35	chr8:86350581-86350631	HRCEpiC	kidney:	n/a
36	chr8:86351018-86351068	H1-hESC	embryonic stem cell:	embryo
37	chr8:86350581-86350631	HUVEC	blood vessel:	n/a
38	chr8:86189565-86189615	AG09319	gingival:	n/a
39	chr8:86353723-86353773	NB4	blood:	n/a
40	chr8:86189883-86189933	SK-N-MC	brain:	n/a
41	chr8:86350927-86350977	ECC-1	luminal epithelium:	n/a
42	chr8:86350278-86350328	SK-N-MC	brain:	n/a
43	chr8:86214814-86214864	AG04449	skin:	fetal
44	chr8:86291640-86291690	GM06990	blood:	n/a
45	chr8:86351195-86351245	HCPEpiC	choroid plexus:	n/a
46	chr8:86350581-86350631	BJ	skin:	n/a
47	chr8:86347111-86347161	RPTEC	kidney:	n/a
48	chr8:86350889-86350939	GM12892	blood:	n/a
49	chr8:86353723-86353773	HMEC	breast:	n/a
50	chr8:86291400-86291450	HL-60	blood:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:86211585..86214496-chr8:87045992..87048546,2	MCF-7	breast:
2	chr8:86169089..86170880-chr8:86174398..86176790,2	K562	blood:
3	chr8:86230907..86232624-chr8:86289786..86291561,3	MCF-7	breast:
4	chr8:86059423..86060332-chr8:86201778..86202999,3	MCF-7	breast:
5	chr8:86260251..86261829-chr8:86265124..86266765,2	K562	blood:
6	chr8:86211068..86212027-chr8:87100896..87101631,2	K562	blood:
7	chr8:86157167..86159112-chr8:86171678..86174510,2	K562	blood:
8	chr8:86222565..86224096-chr8:86281520..86283708,2	MCF-7	breast:
9	chr8:86313626..86315868-chr8:86376450..86379143,2	MCF-7	breast:
10	chr8:86088599..86090947-chr8:86216106..86218320,2	MCF-7	breast:
11	chr8:86209387..86210237-chr8:86999260..87000146,2	MCF-7	breast:
12	chr8:86360412..86362696-chr8:87043331..87045552,2	MCF-7	breast:
13	chr8:86166893..86168765-chr8:86170470..86172602,2	K562	blood:
14	chr8:86086312..86088635-chr8:86202652..86204401,2	MCF-7	breast:
15	chr8:85542893..85545480-chr8:86287576..86290240,2	MCF-7	breast:
16	chr8:86126895..86128516-chr8:86206289..86209119,2	K562	blood:
17	chr8:86209691..86210223-chr8:86364003..86364752,2	MCF-7	breast:
18	chr8:86170519..86173141-chr8:86177699..86180911,3	K562	blood:
19	chr8:86229702..86230332-chr8:86290542..86291598,3	MCF-7	breast:
20	chr8:86215057..86217911-chr8:86221082..86223025,2	K562	blood:
21	chr8:86230212..86230857-chr8:86290709..86291683,2	MCF-7	breast:
22	chr8:86201309..86204247-chr8:86206649..86208335,2	K562	blood:
23	chr8:86209797..86210360-chr8:87056059..87056917,2	MCF-7	breast:
24	chr8:86156869..86159520-chr8:86162595..86165209,2	K562	blood:
25	chr8:86209388..86210307-chr8:86375535..86376317,2	K562	blood:
26	chr8:86156144..86157901-chr8:86162540..86165209,2	K562	blood:
27	chr8:86156416..86159292-chr8:86171824..86174589,2	MCF-7	breast:
28	chr8:86348746..86351284-chr8:86374911..86377490,2	MCF-7	breast:
29	chr8:86145854..86147928-chr8:86176421..86178334,2	K562	blood:
30	chr8:86222565..86224096-chr8:86281520..86283708,2	MCF-7	breast:
31	chr8:86157807..86158310-chr8:86209318..86210236,2	K562	blood:
32	chr8:86296426..86298625-chr8:86302177..86305010,2	MCF-7	breast:
33	chr8:86201309..86204247-chr8:86206649..86208335,2	K562	blood:
34	chr8:86260251..86261829-chr8:86265124..86266765,2	K562	blood:
35	chr8:86211080..86212132-chr8:86363695..86364436,5	MCF-7	breast:
36	chr8:86209343..86210253-chr8:87045503..87046009,2	K562	blood:
37	chr8:86059490..86060356-chr8:86202019..86202533,2	K562	blood:
38	chr8:86176240..86178800-chr8:86200957..86202565,2	MCF-7	breast:
39	chr8:86161188..86163742-chr8:86167542..86169520,2	K562	blood:
40	chr8:85538135..85538922-chr8:86202235..86203001,3	MCF-7	breast:
41	chr8:86209363..86209968-chr8:86283005..86283748,2	MCF-7	breast:
42	chr8:86209311..86210290-chr8:86357968..86358764,3	MCF-7	breast:
43	chr8:86169089..86170880-chr8:86174398..86176790,2	K562	blood:
44	chr8:86131309..86134784-chr8:86200962..86204075,3	MCF-7	breast:
45	chr8:86176950..86178514-chr8:86185372..86187866,2	K562	blood:
46	chr8:86209312..86210314-chr8:87045120..87046083,5	MCF-7	breast:
47	chr8:86170519..86173141-chr8:86177699..86180911,3	K562	blood:
48	chr8:86211076..86211587-chr8:86373603..86374373,2	MCF-7	breast:
49	chr20:43538719..43540265-chr8:86318041..86320964,2	MCF-7	breast:
50	chr8:86215057..86217911-chr8:86221082..86223025,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-219B4.6.1-1	chr8:86254978-86255054	NONHSAT127524
2	lnc-CA1-1	chr8:86354387-86354466	NONHSAT127529
3	lnc-CA1-1	chr8:86354276-86354466	ENSG00000253549.1
4	lnc-CA1-1	chr8:86354135-86354466	NONHSAT127527
5	lnc-CA1-1	chr8:86356236-86356349	NONHSAT127527
6	lnc-RP11-219B4.6.1-1	chr8:86244600-86244781	NONHSAT127524
7	lnc-RP11-219B4.6.1-1	chr8:86253644-86253888	NONHSAT127525
8	lnc-RP11-219B4.6.1-1	chr8:86245754-86245849	NONHSAT127524
9	lnc-CA1-1	chr8:86354080-86354466	ENSG00000253549.1
10	lnc-RP11-219B4.6.1-1	chr8:86254978-86255029	NONHSAT127525

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CA13	hsa-miR-374b-5p	chr8:86196014-86196038
2	CA13	hsa-miR-18a-5p	chr8:86196024-86196049
3	CA13	hsa-miR-19b-3p	chr8:86194067-86194089

Variant related genes	Relation type
ENSG00000258256	TF binding region
ENSG00000257962	TF binding region
CA3	TF binding region
CA1	TF binding region
ENSG00000258256	CpG island
ENSG00000257962	CpG island
CA3	CpG island
CA1	CpG island
ENSG00000133742	chromatin interactions
ENSG00000176731	chromatin interactions
ENSG00000147614	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000257962	chromatin interactions
ENSG00000260493	chromatin interactions
ENSG00000258256	chromatin interactions
ENSG00000133740	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000185015	chromatin interactions
ENSG00000147613	chromatin interactions
ENSG00000254208	chromatin interactions
ENSG00000101104	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 6226 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:6226 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556741037	chr8:86162533-86162534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576579261	chr8:86162581-86162582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542411643	chr8:86162596-86162597	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs556108707	chr8:86162706-86162707	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139194265	chr8:86162715-86162716	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35864452	chr8:86162716-86162717	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs557442942	chr8:86162734-86162735	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572811778	chr8:86162766-86162767	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs111284982	chr8:86162813-86162814	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564552266	chr8:86162836-86162837	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370885820	chr8:86162871-86162872	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533164997	chr8:86162886-86162887	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148247062	chr8:86162900-86162901	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs182953287	chr8:86162911-86162912	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs375652968	chr8:86162925-86162926	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528831997	chr8:86162929-86162930	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs202037895	chr8:86162960-86162961	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200521679	chr8:86162986-86162987	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529077959	chr8:86163009-86163010	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs369958972	chr8:86163025-86163026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548734922	chr8:86163120-86163121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs373427052	chr8:86163121-86163122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs4740046	chr8:86163134-86163135	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs370677125	chr8:86163144-86163145	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373392158	chr8:86163196-86163197	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535154003	chr8:86163231-86163232	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs75498059	chr8:86163232-86163233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543721386	chr8:86163248-86163249	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs187543069	chr8:86163276-86163277	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs111772479	chr8:86163287-86163288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
31	rs192392136	chr8:86163293-86163294	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571228084	chr8:86163294-86163295	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536596867	chr8:86163330-86163331	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141188243	chr8:86163355-86163356	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs183655266	chr8:86163356-86163357	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs567334607	chr8:86163375-86163376	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs536335932	chr8:86163380-86163381	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556026501	chr8:86163447-86163448	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188706164	chr8:86163467-86163468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192326014	chr8:86163473-86163474	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184523200	chr8:86163482-86163483	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs7011001	chr8:86163487-86163488	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs543427419	chr8:86163492-86163493	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563822912	chr8:86163494-86163495	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs139111525	chr8:86163513-86163514	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs35230947	chr8:86163520-86163521	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs71564210	chr8:86163526-86163527	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs75986011	chr8:86163602-86163603	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs559160753	chr8:86163613-86163614	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs115128212	chr8:86163621-86163622	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86158400-86172600	Weak transcription	Left Ventricle	heart
2	chr8:86158400-86174000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr8:86158400-86178200	Weak transcription	Small Intestine	intestine
4	chr8:86158400-86178200	Weak transcription	Stomach Mucosa	stomach
5	chr8:86158400-86179400	Weak transcription	Gastric	stomach
6	chr8:86158400-86180800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr8:86158400-86185800	Weak transcription	Lung	lung
8	chr8:86158400-86188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:86158400-86188200	Weak transcription	Esophagus	oesophagus
10	chr8:86158400-86191400	Weak transcription	Pancreas	Pancrea
11	chr8:86158800-86163200	Weak transcription	Fetal Intestine Small	intestine
12	chr8:86158800-86167000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr8:86158800-86167200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:86158800-86171200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:86158800-86171200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr8:86158800-86172400	Weak transcription	Fetal Intestine Large	intestine
17	chr8:86158800-86179400	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr8:86158800-86185600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:86158800-86185800	Weak transcription	Fetal Stomach	stomach
20	chr8:86158800-86186800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:86158800-86189600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:86158800-86191400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr8:86159000-86166600	Weak transcription	NHEK	skin
24	chr8:86159000-86171200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:86159600-86167200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:86160000-86169200	Weak transcription	Fetal Lung	lung
27	chr8:86160000-86172600	Weak transcription	HepG2	liver
28	chr8:86161200-86171200	Weak transcription	Primary B cells from cord blood	blood
29	chr8:86162400-86166600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:86162600-86171600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:86163200-86168200	Strong transcription	Fetal Intestine Small	intestine
32	chr8:86164200-86166400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:86166000-86166600	Enhancers	GM12878-XiMat	blood
34	chr8:86166400-86166600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr8:86166600-86167000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:86166600-86167400	Flanking Active TSS	GM12878-XiMat	blood
37	chr8:86166600-86167400	Enhancers	Osteobl	bone
38	chr8:86166600-86167800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:86166600-86168000	Enhancers	NHEK	skin
40	chr8:86166800-86167200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr8:86166800-86167200	Enhancers	HSMM	muscle
42	chr8:86166800-86167600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:86167000-86167200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:86167000-86167800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr8:86167000-86168000	Enhancers	HMEC	breast
46	chr8:86167200-86167400	Enhancers	Primary B cells from peripheral blood	blood
47	chr8:86167200-86167400	Flanking Active TSS	HSMM	muscle
48	chr8:86167200-86167600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:86167200-86167600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:86167200-86167800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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