Variant report

Variant	nsv1021389
Chromosome Location	chr8:48700970-48880931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3139)
CpG islands
(count:1775)
Chromatin interactive
region (count:151)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3139 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48872863-48873605	K562	blood:	n/a	chr8:48873270-48873278
2	ARID3A	chr8:48760868-48761163	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48872565-48873634	HepG2	liver:	n/a	chr8:48873270-48873278
4	ARID3A	chr8:48879708-48880140	HepG2	liver:	n/a	n/a
5	ATF1	chr8:48873182-48873558	K562	blood:	n/a	n/a
6	ATF2	chr8:48814692-48815306	GM12878	blood:	n/a	n/a
7	ATF2	chr8:48812278-48812924	GM12878	blood:	n/a	n/a
8	ATF2	chr8:48814851-48815342	GM12878	blood:	n/a	n/a
9	ATF2	chr8:48873078-48873648	GM12878	blood:	n/a	n/a
10	ATF2	chr8:48812173-48812889	GM12878	blood:	n/a	n/a
11	ATF2	chr8:48872630-48873618	GM12878	blood:	n/a	n/a
12	ATF2	chr8:48790887-48791278	GM12878	blood:	n/a	n/a
13	ATF2	chr8:48790878-48791451	GM12878	blood:	n/a	n/a
14	ATF2	chr8:48872229-48873077	GM12878	blood:	n/a	n/a
15	ATF2	chr8:48872659-48873677	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr8:48872671-48873661	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr8:48873076-48873396	A549	lung:	n/a	n/a
18	ATF3	chr8:48872471-48872782	K562	blood:	n/a	chr8:48872766-48872775
19	ATF3	chr8:48872460-48872962	A549	lung:	n/a	chr8:48872766-48872775
20	ATF3	chr8:48873139-48873694	A549	lung:	n/a	chr8:48873579-48873588
21	BACH1	chr8:48872877-48873374	K562	blood:	n/a	n/a
22	BACH1	chr8:48874797-48874813	K562	blood:	n/a	n/a
23	BACH1	chr8:48873138-48874173	H1-hESC	embryonic stem cell:	n/a	chr8:48873984-48873998
24	BACH1	chr8:48872546-48872866	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:48739220-48739414	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr8:48790997-48791260	GM12878	blood:	n/a	n/a
27	BATF	chr8:48814867-48815243	GM12878	blood:	n/a	n/a
28	BATF	chr8:48793523-48793761	GM12878	blood:	n/a	n/a
29	BATF	chr8:48814874-48815214	GM12878	blood:	n/a	n/a
30	BATF	chr8:48812422-48812881	GM12878	blood:	n/a	n/a
31	BATF	chr8:48793513-48793779	GM12878	blood:	n/a	n/a
32	BATF	chr8:48790867-48791261	GM12878	blood:	n/a	n/a
33	BATF	chr8:48812407-48812807	GM12878	blood:	n/a	n/a
34	BATF	chr8:48873803-48874147	GM12878	blood:	n/a	chr8:48873984-48873994 chr8:48873987-48873998
35	BCL11A	chr8:48812477-48812789	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:48814860-48815214	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:48793561-48793698	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:48812389-48812787	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:48814918-48815256	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:48793543-48793715	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:48790974-48791250	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:48790939-48791328	GM12878	blood:	n/a	n/a
43	BCL3	chr8:48794872-48795246	GM12878	blood:	n/a	n/a
44	BCL3	chr8:48790954-48791213	GM12878	blood:	n/a	n/a
45	BCL3	chr8:48812377-48812751	GM12878	blood:	n/a	n/a
46	BCL3	chr8:48872454-48873792	A549	lung:	n/a	chr8:48872767-48872776 chr8:48872461-48872474 chr8:48872755-48872768 chr8:48872460-48872473 chr8:48873581-48873594 chr8:48873624-48873637
47	BCL3	chr8:48790934-48791243	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:48812317-48812900	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:48872468-48873772	GM12878	blood:	n/a	chr8:48872767-48872776 chr8:48872755-48872768 chr8:48873581-48873594 chr8:48873624-48873637
50	BCLAF1	chr8:48790870-48791376	GM12878	blood:	n/a	n/a

(count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48873358-48873408	HRPEpiC	eye:	n/a
2	chr8:48871883-48871933	HRCEpiC	kidney:	n/a
3	chr8:48873326-48873376	T-47D	breast:	n/a
4	chr8:48744454-48744504	SK-N-MC	brain:	n/a
5	chr8:48873358-48873408	HEK293	kidney:	embryo
6	chr8:48744522-48744572	HL-60	blood:	n/a
7	chr8:48873358-48873408	HRPEpiC	eye:	n/a
8	chr8:48871883-48871933	HRCEpiC	kidney:	n/a
9	chr8:48873326-48873376	T-47D	breast:	n/a
10	chr8:48744454-48744504	SK-N-MC	brain:	n/a
11	chr8:48873358-48873408	HEK293	kidney:	embryo
12	chr8:48744522-48744572	HL-60	blood:	n/a
13	chr8:48741753-48741803	HCPEpiC	choroid plexus:	n/a
14	chr8:48871883-48871933	AG09319	gingival:	n/a
15	chr8:48872560-48872610	AoSMC	blood vessel:	n/a
16	chr8:48744559-48744609	SK-N-MC	brain:	n/a
17	chr8:48873906-48873956	HRCEpiC	kidney:	n/a
18	chr8:48872876-48872926	AG10803	skin:	n/a
19	chr8:48744602-48744652	A549	lung:	n/a
20	chr8:48744454-48744504	HRPEpiC	eye:	n/a
21	chr8:48744522-48744572	SAEC	small airway:	n/a
22	chr8:48873326-48873376	NB4	blood:	n/a
23	chr8:48869819-48869869	HepG2	liver:	n/a
24	chr8:48739256-48739306	GM12878	blood:	n/a
25	chr8:48744017-48744067	T-47D	breast:	n/a
26	chr8:48877513-48877563	AG04449	skin:	fetal
27	chr8:48826017-48826067	NHDF-neo	bronchial:	n/a
28	chr8:48873190-48873240	NHBE	bronchial:	n/a
29	chr8:48873533-48873583	PANC-1	pancreas:	n/a
30	chr8:48773093-48773143	ECC-1	luminal epithelium:	n/a
31	chr8:48739161-48739211	Caco-2	colon:	n/a
32	chr8:48872865-48872915	GM12892	blood:	n/a
33	chr8:48741753-48741803	SAEC	small airway:	n/a
34	chr8:48744017-48744067	HEK293	kidney:	embryo
35	chr8:48739256-48739306	U87	brain:	n/a
36	chr8:48872801-48872851	Hepatocyte	liver:	n/a
37	chr8:48873358-48873408	CMK	blood:	n/a
38	chr8:48872865-48872915	NB4	blood:	n/a
39	chr8:48754164-48754214	SK-N-MC	brain:	n/a
40	chr8:48871883-48871933	SK-N-SH_RA	brain:	n/a
41	chr8:48744602-48744652	RPTEC	kidney:	n/a
42	chr8:48873190-48873240	ProgFib	skin:	n/a
43	chr8:48744522-48744572	RPTEC	kidney:	n/a
44	chr8:48739256-48739306	MCF10A-Er-Src	breast:	n/a
45	chr8:48873533-48873583	SK-N-MC	brain:	n/a
46	chr8:48744176-48744226	MCF-7	breast:	n/a
47	chr8:48873951-48874001	HEEpiC	esophagus:	n/a
48	chr8:48872801-48872851	HCT-116	colon:	n/a
49	chr8:48872865-48872915	HCT-116	colon:	n/a
50	chr8:48746197-48746247	Caco-2	colon:	n/a

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:48730935..48735582-chr8:48738705..48743667,5	K562	blood:
2	chr8:48700250..48702138-chr8:48739581..48742298,2	K562	blood:
3	chr8:48713341..48716130-chr8:48716370..48718474,2	K562	blood:
4	chr8:48710168..48712714-chr8:48712975..48714520,2	K562	blood:
5	chr8:48838333..48840946-chr8:48864623..48866486,2	K562	blood:
6	chr8:48837592..48840546-chr8:48872351..48874883,2	MCF-7	breast:
7	chr8:48869236..48871124-chr8:48909959..48911972,2	K562	blood:
8	chr8:48715674..48718001-chr8:48753353..48756004,2	K562	blood:
9	chr8:48736626..48739950-chr8:48740537..48745095,4	K562	blood:
10	chr8:48855124..48857621-chr8:48862210..48863737,2	K562	blood:
11	chr8:48744475..48747098-chr8:48769085..48771100,2	K562	blood:
12	chr8:48787397..48789499-chr8:48791391..48793520,2	K562	blood:
13	chr8:48734082..48735930-chr8:48739843..48741704,2	K562	blood:
14	chr8:48837528..48840446-chr8:48849077..48850603,2	MCF-7	breast:
15	chr8:48775024..48776712-chr8:48799790..48801696,2	MCF-7	breast:
16	chr8:48870534..48872766-chr8:48885611..48888462,2	MCF-7	breast:
17	chr8:48746875..48750339-chr8:48870827..48874181,3	MCF-7	breast:
18	chr8:48852381..48854358-chr8:48859418..48862066,2	MCF-7	breast:
19	chr8:48702667..48704261-chr8:48706616..48708531,2	K562	blood:
20	chr7:87505419..87506040-chr8:48873108..48873913,2	NB4	blood:
21	chr8:48736626..48739950-chr8:48740537..48745095,4	K562	blood:
22	chr8:48854376..48857161-chr8:48889369..48891262,2	MCF-7	breast:
23	chr8:48854339..48856156-chr8:48856276..48857926,2	MCF-7	breast:
24	chr8:48830231..48832723-chr8:48832823..48835481,2	MCF-7	breast:
25	chr8:48768531..48770962-chr8:48772656..48774912,2	K562	blood:
26	chr8:48767614..48769848-chr8:48919814..48922261,2	MCF-7	breast:
27	chr8:48702667..48704261-chr8:48706616..48708531,2	K562	blood:
28	chr8:48744475..48747098-chr8:48769085..48771100,2	K562	blood:
29	chr8:48840388..48843137-chr8:48859260..48861265,2	K562	blood:
30	chr8:48748617..48751321-chr8:48753317..48755020,2	MCF-7	breast:
31	chr8:48848253..48849969-chr8:48851774..48853317,2	MCF-7	breast:
32	chr8:48710168..48712714-chr8:48712975..48714520,2	K562	blood:
33	chr14:40316700..40317200-chr8:48779245..48779746,2	Hela-S3	cervix:
34	chr8:48835669..48838188-chr8:48855543..48858142,2	K562	blood:
35	chr8:48777971..48781405-chr8:48784678..48787276,4	K562	blood:
36	chr8:48849661..48851317-chr8:48858106..48860426,2	K562	blood:
37	chr8:48799441..48801873-chr8:48806998..48809759,3	K562	blood:
38	chr8:48777971..48781405-chr8:48784678..48787276,3	K562	blood:
39	chr8:48800554..48803077-chr8:48803975..48806027,3	K562	blood:
40	chr8:48826446..48829451-chr8:48871760..48876742,4	K562	blood:
41	chr8:48830231..48832723-chr8:48832823..48835481,2	MCF-7	breast:
42	chr8:48823109..48828322-chr8:48830609..48833340,5	K562	blood:
43	chr8:48760650..48762849-chr8:48764381..48766092,2	K562	blood:
44	chr8:48787397..48789499-chr8:48791391..48793520,2	K562	blood:
45	chr8:48760650..48762623-chr8:48764592..48766806,2	K562	blood:
46	chr8:48809750..48812575-chr8:48815045..48817553,2	K562	blood:
47	chr8:48852455..48853957-chr8:48859458..48861403,2	K562	blood:
48	chr8:48858446..48860800-chr8:48864491..48866014,2	K562	blood:
49	chr8:48777971..48781405-chr8:48784678..48787276,3	K562	blood:
50	chr8:48771739..48773834-chr8:48775178..48778172,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCM4-2	chr8:48854048-48854246	NONHSAT126461
2	lnc-MCM4-1	chr8:48857309-48857338	NONHSAT126462
3	lnc-MCM4-1	chr8:48855141-48855324	NONHSAT126462
4	lnc-MCM4-2	chr8:48854790-48855069	NONHSAT126461

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MCM4	hsa-miR-24-3p	chr8:48875419-48875419
2	MCM4	hsa-miR-24-3p	chr8:48875505-48875525

Variant related genes	Relation type
PRKDC	TF binding region
MCM4	TF binding region
ENSG00000211562	TF binding region
ENSG00000207450	TF binding region
PRKDC	CpG island
MCM4	CpG island
ENSG00000211562	CpG island
ENSG00000207450	CpG island
ENSG00000222522	chromatin interactions
ENSG00000207450	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000006634	chromatin interactions
ENSG00000174442	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000157557	chromatin interactions
ENSG00000104738	chromatin interactions
ENSG00000075303	chromatin interactions
ENSG00000169139	chromatin interactions
ENSG00000211562	chromatin interactions
ENSG00000105397	chromatin interactions

Extended variants
information (count: 6897 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:6897 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547264427	chr8:48701000-48701001	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs188804858	chr8:48701016-48701017	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs539917578	chr8:48701032-48701033	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs558317453	chr8:48701045-48701046	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372106518	chr8:48701115-48701116	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576625593	chr8:48701197-48701198	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568685870	chr8:48701207-48701208	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376420616	chr8:48701219-48701220	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564959688	chr8:48701223-48701224	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537414850	chr8:48701281-48701282	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555801771	chr8:48701326-48701327	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73571476	chr8:48701329-48701330	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541751456	chr8:48701354-48701355	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373558334	chr8:48701375-48701376	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559690218	chr8:48701407-48701408	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550467488	chr8:48701414-48701415	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374787100	chr8:48701427-48701428	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578146929	chr8:48701458-48701459	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369496484	chr8:48701496-48701497	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545479220	chr8:48701505-48701506	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374162229	chr8:48701511-48701512	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376714307	chr8:48701542-48701543	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147753989	chr8:48701573-48701574	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531330017	chr8:48701591-48701592	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141113800	chr8:48701596-48701597	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373043773	chr8:48701621-48701622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376282573	chr8:48701682-48701683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529169274	chr8:48701699-48701700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371438183	chr8:48701705-48701706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs55866966	chr8:48701720-48701721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376467697	chr8:48701750-48701751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547696421	chr8:48701770-48701771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs8178232	chr8:48701786-48701787	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35947559	chr8:48701806-48701807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539608279	chr8:48701867-48701868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547822103	chr8:48701880-48701881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs137958332	chr8:48701897-48701898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567618503	chr8:48701922-48701923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs193217921	chr8:48701945-48701946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113668485	chr8:48701956-48701957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373340986	chr8:48701958-48701959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149063580	chr8:48701964-48701965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143116990	chr8:48701987-48701988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535195102	chr8:48702025-48702026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534987149	chr8:48702100-48702101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553665773	chr8:48702134-48702135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536643639	chr8:48702137-48702138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578200495	chr8:48702195-48702196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545171290	chr8:48702198-48702199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138653755	chr8:48702353-48702354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Autism	20531469	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Ovarian cancer	21781307	CNVD
Renal cell carcinoma	21215367	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:5296 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48679800-48709600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:48684000-48721000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:48684000-48722200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:48684200-48701600	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr8:48684200-48704000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:48684200-48733800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr8:48684200-48733800	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr8:48684200-48734200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:48684400-48702200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:48684400-48704200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:48684400-48755200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr8:48684400-48778800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:48684400-48861600	Strong transcription	Dnd41	blood
14	chr8:48684600-48702000	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr8:48684600-48721400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr8:48684800-48728200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr8:48685000-48713200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:48685000-48818800	Strong transcription	Fetal Thymus	thymus
19	chr8:48685200-48701600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:48685200-48707600	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr8:48685200-48713400	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr8:48685200-48734000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr8:48685400-48702200	Strong transcription	Fetal Muscle Leg	muscle
24	chr8:48685400-48703400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr8:48685600-48733600	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:48687400-48719800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:48688200-48701200	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr8:48688600-48703600	Strong transcription	HUVEC	blood vessel
29	chr8:48689000-48701600	Strong transcription	HSMMtube	muscle
30	chr8:48689200-48708200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:48691000-48704200	Weak transcription	Fetal Brain Male	brain
32	chr8:48691200-48705600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:48691200-48710200	Weak transcription	Fetal Heart	heart
34	chr8:48691400-48703200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr8:48691800-48709600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr8:48692600-48701200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:48692600-48701200	Strong transcription	Lung	lung
38	chr8:48693000-48703000	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr8:48693000-48720200	Strong transcription	Primary B cells from peripheral blood	blood
40	chr8:48693600-48702600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:48693800-48751000	Weak transcription	Right Atrium	heart
42	chr8:48695000-48703800	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr8:48695200-48704200	Weak transcription	Fetal Kidney	kidney
44	chr8:48695200-48710200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:48695400-48703000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr8:48696400-48705200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr8:48696400-48706200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr8:48696400-48709000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr8:48697600-48701600	Strong transcription	Left Ventricle	heart
50	chr8:48697600-48701600	Strong transcription	Ovary	ovary

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