Variant report

Variant	nsv891423
Chromosome Location	chr8:121847643-121994660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1673)
CpG islands
(count:122)
Chromatin interactive
region (count:59)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1673 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:121873485-121873999	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:121869623-121870347	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:121880794-121881713	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:121865701-121865923	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:121857891-121858913	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:121851133-121851958	HepG2	liver:	n/a	chr8:121851911-121851927
7	ARID3A	chr8:121945030-121945441	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:121963487-121963736	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:121951318-121951619	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:121876652-121876916	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:121855442-121856052	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:121863721-121864679	HepG2	liver:	n/a	n/a
13	ATF2	chr8:121968974-121969280	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr8:121968900-121969295	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:121951288-121951630	H1-hESC	embryonic stem cell:	n/a	chr8:121951352-121951366
16	BHLHE40	chr8:121878505-121878696	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:121880938-121881321	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:121873647-121873978	HepG2	liver:	n/a	n/a
19	BRCA1	chr8:121936905-121936919	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr8:121870095-121870107	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr8:121968980-121969263	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr8:121873732-121873810	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr8:121872794-121872814	HepG2	liver:	n/a	n/a
24	BRCA1	chr8:121951349-121951668	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr8:121880848-121881450	HCT-116	colon:	n/a	n/a
26	CEBPB	chr8:121873631-121873988	HepG2	liver:	n/a	chr8:121873841-121873852
27	CEBPB	chr8:121945156-121945319	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:121863981-121864252	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:121952435-121952506	A549	lung:	n/a	n/a
30	CEBPB	chr8:121869679-121869879	A549	lung:	n/a	chr8:121869783-121869794 chr8:121869783-121869792
31	CEBPB	chr8:121976862-121977189	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:121976839-121977902	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:121873524-121874080	MCF-7	breast:	n/a	chr8:121873841-121873852
34	CEBPB	chr8:121870106-121870265	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:121869611-121870366	HepG2	liver:	n/a	chr8:121869783-121869794 chr8:121869783-121869792
36	CEBPB	chr8:121873607-121874002	HepG2	liver:	n/a	chr8:121873841-121873852
37	CEBPB	chr8:121881193-121881371	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:121869697-121869963	Hela-S3	cervix:	n/a	chr8:121869783-121869794 chr8:121869783-121869792
39	CEBPB	chr8:121942185-121942487	A549	lung:	n/a	chr8:121942337-121942348
40	CEBPB	chr8:121881063-121881467	MCF-7	breast:	n/a	n/a
41	CEBPB	chr8:121873622-121874091	MCF-7	breast:	n/a	chr8:121873841-121873852
42	CEBPB	chr8:121873592-121874171	HepG2	liver:	n/a	chr8:121873841-121873852
43	CEBPB	chr8:121858432-121858691	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:121987455-121987690	A549	lung:	n/a	chr8:121987527-121987538
45	CEBPB	chr8:121914043-121914162	A549	lung:	n/a	chr8:121914067-121914078 chr8:121914045-121914056
46	CEBPB	chr8:121956293-121956379	HepG2	liver:	n/a	chr8:121956323-121956334
47	CEBPB	chr8:121972734-121973180	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr8:121942217-121942500	IMR90	lung:	n/a	chr8:121942337-121942348
49	CEBPB	chr8:121976809-121977197	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:121869567-121870382	IMR90	lung:	n/a	chr8:121869783-121869794 chr8:121869783-121869792

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:121881190-121881240	SAEC	small airway:	n/a
2	chr8:121881190-121881240	NB4	blood:	n/a
3	chr8:121881190-121881240	RPTEC	kidney:	n/a
4	chr8:121881190-121881240	HCM	heart:	n/a
5	chr8:121989053-121989103	AG04450	lung:	fetal
6	chr8:121989053-121989103	H1-hESC	embryonic stem cell:	embryo
7	chr8:121881190-121881240	MCF-7	breast:	n/a
8	chr8:121989053-121989103	CMK	blood:	n/a
9	chr8:121881190-121881240	HEK293	kidney:	embryo
10	chr8:121989053-121989103	AoSMC	blood vessel:	n/a
11	chr8:121881190-121881240	Hela-S3	cervix:	n/a
12	chr8:121881190-121881240	HEEpiC	esophagus:	n/a
13	chr8:121989053-121989103	PANC-1	pancreas:	n/a
14	chr8:121989053-121989103	ovcar-3	ovarian:	n/a
15	chr8:121881190-121881240	HCF	heart:	n/a
16	chr8:121881190-121881240	IMR90	lung:	fetal
17	chr8:121989053-121989103	AG04449	skin:	fetal
18	chr8:121989053-121989103	LNCaP	prostate:	n/a
19	chr8:121989053-121989103	A549	lung:	n/a
20	chr8:121989053-121989103	MCF-7	breast:	n/a
21	chr8:121881190-121881240	ovcar-3	ovarian:	n/a
22	chr8:121881190-121881240	HepG2	liver:	n/a
23	chr8:121989053-121989103	HEEpiC	esophagus:	n/a
24	chr8:121881190-121881240	HAEpiC	amniotic membrane:	n/a
25	chr8:121989053-121989103	AG09319	gingival:	n/a
26	chr8:121881190-121881240	CMK	blood:	n/a
27	chr8:121881190-121881240	Caco-2	colon:	n/a
28	chr8:121881190-121881240	SKMC	muscle:	n/a
29	chr8:121881190-121881240	HRE	kidney:	n/a
30	chr8:121989053-121989103	HAEpiC	amniotic membrane:	n/a
31	chr8:121881190-121881240	NHBE	bronchial:	n/a
32	chr8:121881190-121881240	GM12878	blood:	n/a
33	chr8:121881190-121881240	LNCaP	prostate:	n/a
34	chr8:121881190-121881240	HRCEpiC	kidney:	n/a
35	chr8:121881190-121881240	HCPEpiC	choroid plexus:	n/a
36	chr8:121989053-121989103	HNPCEpiC	eye:	n/a
37	chr8:121989053-121989103	PFSK-1	brain:	n/a
38	chr8:121989053-121989103	IMR90	lung:	fetal
39	chr8:121881190-121881240	HMEC	breast:	n/a
40	chr8:121989053-121989103	K562	blood:	n/a
41	chr8:121989053-121989103	GM12892	blood:	n/a
42	chr8:121881190-121881240	A549	lung:	n/a
43	chr8:121881190-121881240	H1-hESC	embryonic stem cell:	embryo
44	chr8:121989053-121989103	HRCEpiC	kidney:	n/a
45	chr8:121881190-121881240	ProgFib	skin:	n/a
46	chr8:121881190-121881240	AG10803	skin:	n/a
47	chr8:121989053-121989103	NHDF-neo	bronchial:	n/a
48	chr8:121989053-121989103	NHBE	bronchial:	n/a
49	chr8:121881190-121881240	HCT-116	colon:	n/a
50	chr8:121881190-121881240	HPAEpiC	pulmonary alveolar:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:121988250..121991241-chr8:122187936..122189513,2	MCF-7	breast:
2	chr8:121890830..121892579-chr8:121894295..121896287,2	MCF-7	breast:
3	chr8:121985013..121986723-chr8:121996961..121998497,2	MCF-7	breast:
4	chr8:121839539..121841750-chr8:121853212..121856019,2	MCF-7	breast:
5	chr8:121864308..121866677-chr8:121872620..121875288,2	MCF-7	breast:
6	chr8:121963373..121964023-chr8:122272866..122273810,2	MCF-7	breast:
7	chr8:121965330..121968100-chr8:122203778..122205439,2	MCF-7	breast:
8	chr8:121820684..121821811-chr8:121951035..121951836,4	MCF-7	breast:
9	chr8:121716401..121717262-chr8:121951058..121952142,3	MCF-7	breast:
10	chr8:121963333..121964086-chr8:123584212..123584759,2	K562	blood:
11	chr8:121823512..121825104-chr8:121845143..121848001,2	MCF-7	breast:
12	chr8:121852204..121854548-chr8:121856870..121859860,2	K562	blood:
13	chr8:121980270..121982507-chr8:123657769..123660180,2	MCF-7	breast:
14	chr8:121985132..121987703-chr8:121991012..121992781,2	MCF-7	breast:
15	chr8:112248509..112249151-chr8:121951139..121951901,3	MCF-7	breast:
16	chr8:121865791..121868375-chr8:121870953..121873135,2	K562	blood:
17	chr8:121864308..121866677-chr8:121872620..121875288,2	MCF-7	breast:
18	chr8:121880794..121881516-chr8:121950983..121951887,2	MCF-7	breast:
19	chr8:121948676..121950549-chr8:121951943..121953963,2	K562	blood:
20	chr8:121865791..121868375-chr8:121870953..121873135,2	K562	blood:
21	chr8:121854976..121857000-chr8:121869044..121870751,2	MCF-7	breast:
22	chr8:121854976..121857000-chr8:121869044..121870751,2	MCF-7	breast:
23	chr8:121853827..121856693-chr8:121857538..121861714,4	MCF-7	breast:
24	chr8:121969066..121969640-chr8:122261097..122261682,2	MCF-7	breast:
25	chr8:121963161..121964069-chr8:123459412..123460073,2	MCF-7	breast:
26	chr17:36886034..36886675-chr8:121951183..121952088,2	MCF-7	breast:
27	chr8:121621581..121622349-chr8:121950956..121951927,3	MCF-7	breast:
28	chr8:121989452..121992129-chr8:121993364..121995209,2	MCF-7	breast:
29	chr8:121985132..121987703-chr8:121991012..121992781,2	MCF-7	breast:
30	chr8:121464485..121465396-chr8:121950947..121951935,3	MCF-7	breast:
31	chr8:121135918..121136601-chr8:121951029..121951928,2	K562	blood:
32	chr8:121948676..121950549-chr8:121951943..121953963,2	K562	blood:
33	chr8:121963217..121963759-chr8:122272979..122273735,2	MCF-7	breast:
34	chr8:121820878..121821805-chr8:121881097..121881747,2	MCF-7	breast:
35	chr8:121820905..121821755-chr8:121862259..121862768,2	MCF-7	breast:
36	chr8:121963567..121964094-chr8:123248051..123249017,2	MCF-7	breast:
37	chr17:58381637..58383579-chr8:121953701..121955585,2	MCF-7	breast:
38	chr8:121859072..121861169-chr8:121866791..121869126,2	MCF-7	breast:
39	chr8:121818871..121819911-chr8:121950995..121952120,3	MCF-7	breast:
40	chr8:121993332..121994947-chr8:122188899..122191612,2	MCF-7	breast:
41	chr8:121880794..121881516-chr8:121950983..121951887,2	MCF-7	breast:
42	chr8:121859072..121861169-chr8:121866791..121869126,2	MCF-7	breast:
43	chr8:121861612..121864034-chr8:121872422..121874822,2	MCF-7	breast:
44	chr8:121861612..121864034-chr8:121872422..121874822,2	MCF-7	breast:
45	chr1:121484585..121485425-chr8:121971055..121971555,2	MCF-7	breast:
46	chr8:121820968..121821651-chr8:121880472..121881467,2	MCF-7	breast:
47	chr8:121974787..121976636-chr8:121978953..121980486,2	MCF-7	breast:
48	chr8:121963167..121964054-chr8:123584639..123585142,2	MCF-7	breast:
49	chr8:121853827..121856693-chr8:121857538..121861714,4	MCF-7	breast:
50	chr8:121963181..121963835-chr8:122265207..122266028,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTBP-2	chr8:121925305-121925399	ENSG00000253619
2	lnc-MTBP-6	chr8:121857780-121858253	ucscGeneNc_uc003ypf_1
3	lnc-MTBP-6	chr8:121856696-121856947	ucscGeneNc_uc003ypf_1
4	lnc-MTBP-6	chr8:121850080-121851119	ucscGeneNc_uc003ypf_1

No data

Variant related genes	Relation type
ENSG00000253619	TF binding region
ENSG00000253619	CpG island
ENSG00000172164	chromatin interactions
ENSG00000230055	chromatin interactions
ENSG00000272502	chromatin interactions
ENSG00000170832	chromatin interactions

Extended variants
information (count: 5314 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:5314 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4369032	chr8:121847643-121847644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564302865	chr8:121847706-121847707	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182474068	chr8:121847714-121847715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368445595	chr8:121847754-121847755	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs540371530	chr8:121847755-121847756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561727692	chr8:121847785-121847786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs185975380	chr8:121847788-121847789	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4367595	chr8:121847800-121847801	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs190482895	chr8:121847840-121847841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565158765	chr8:121847844-121847845	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs552572113	chr8:121847845-121847846	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570754794	chr8:121847877-121847878	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370855168	chr8:121847896-121847897	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534877716	chr8:121847906-121847907	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139558924	chr8:121847908-121847909	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568169138	chr8:121847935-121847936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs535501968	chr8:121848020-121848021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs557288691	chr8:121848027-121848028	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs184207852	chr8:121848030-121848031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs377392071	chr8:121848052-121848053	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs149729292	chr8:121848065-121848066	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558074493	chr8:121848071-121848072	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs202115392	chr8:121848153-121848154	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs573086428	chr8:121848162-121848163	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540385830	chr8:121848185-121848186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs146727744	chr8:121848195-121848196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs573647745	chr8:121848252-121848253	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs543953999	chr8:121848273-121848274	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs141268387	chr8:121848282-121848283	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs145064932	chr8:121848294-121848295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs146776049	chr8:121848306-121848307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs564398245	chr8:121848321-121848322	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs62528872	chr8:121848322-121848323	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs62528873	chr8:121848345-121848346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs80337303	chr8:121848358-121848359	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs74733082	chr8:121848359-121848360	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs11784546	chr8:121848394-121848395	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs10808514	chr8:121848497-121848498	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs188606268	chr8:121848523-121848524	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs10808515	chr8:121848549-121848550	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs550793604	chr8:121848582-121848583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113270490	chr8:121848600-121848601	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs572270100	chr8:121848656-121848657	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs558088793	chr8:121848657-121848658	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs566746549	chr8:121848751-121848752	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs533995199	chr8:121848764-121848765	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs555636984	chr8:121848819-121848820	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs76375397	chr8:121848820-121848821	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs544338507	chr8:121848875-121848876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs117148074	chr8:121848946-121848947	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

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
Acute myeloid leukemia	20729466	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
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
Breast cancer	21611746	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
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Burkitt''s lymphoma	20823134	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121838400-121869800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:121842200-121848200	Weak transcription	Psoas Muscle	Psoas
3	chr8:121846200-121848400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:121846800-121849400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr8:121846800-121850200	Enhancers	Primary T cells from cord blood	blood
6	chr8:121846800-121850800	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:121847200-121849400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr8:121847200-121850000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:121847400-121848800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr8:121847600-121848000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr8:121847600-121848000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:121847600-121848600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr8:121847600-121848800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr8:121847600-121851200	Enhancers	HepG2	liver
15	chr8:121848000-121849400	Enhancers	Primary T cells fromperipheralblood	blood
16	chr8:121848000-121849600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr8:121848000-121849800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:121848200-121848600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:121848200-121848600	Enhancers	Psoas Muscle	Psoas
20	chr8:121848200-121848800	Enhancers	Liver	Liver
21	chr8:121848200-121849400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr8:121848200-121849400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr8:121848400-121848800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:121848400-121849200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:121848400-121849600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:121848400-121852400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:121848600-121848800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:121848600-121849200	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr8:121848600-121849200	Enhancers	Fetal Thymus	thymus
30	chr8:121848600-121850800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:121848800-121849000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:121848800-121849200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr8:121848800-121849200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:121848800-121849400	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr8:121848800-121850000	Weak transcription	Liver	Liver
36	chr8:121849000-121849200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr8:121849000-121849400	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:121849000-121850400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:121849200-121849400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:121849400-121850400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:121849800-121851000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:121850000-121853400	Enhancers	Liver	Liver
43	chr8:121850400-121851000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr8:121850400-121855200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:121850800-121851800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr8:121851000-121852200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:121851200-121852000	Flanking Active TSS	HepG2	liver
48	chr8:121851400-121851800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr8:121851800-121856800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr8:121851800-121857200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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