Variant report

Variant	nsv1027043
Chromosome Location	chr8:48444306-48637900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1326)
CpG islands
(count:795)
Chromatin interactive
region (count:91)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1326 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48577647-48577947	K562	blood:	n/a	n/a
2	ARID3A	chr8:48469558-48470236	K562	blood:	n/a	n/a
3	ARID3A	chr8:48572200-48572951	K562	blood:	n/a	n/a
4	ARID3A	chr8:48571897-48572669	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:48521014-48521055	K562	blood:	n/a	n/a
6	ARID3A	chr8:48531522-48531916	HepG2	liver:	n/a	n/a
7	ATF1	chr8:48456323-48456522	K562	blood:	n/a	n/a
8	ATF1	chr8:48469791-48470208	K562	blood:	n/a	n/a
9	ATF1	chr8:48444199-48444363	K562	blood:	n/a	n/a
10	ATF1	chr8:48572283-48572698	K562	blood:	n/a	n/a
11	ATF2	chr8:48510596-48510973	GM12878	blood:	n/a	n/a
12	ATF2	chr8:48513192-48513727	GM12878	blood:	n/a	n/a
13	ATF2	chr8:48510510-48511070	GM12878	blood:	n/a	n/a
14	ATF3	chr8:48510675-48511007	K562	blood:	n/a	n/a
15	ATF3	chr8:48577580-48577896	K562	blood:	n/a	n/a
16	BACH1	chr8:48577576-48577975	K562	blood:	n/a	n/a
17	BACH1	chr8:48577609-48577922	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:48520911-48521193	K562	blood:	n/a	n/a
19	BATF	chr8:48510586-48511006	GM12878	blood:	n/a	n/a
20	BATF	chr8:48513236-48513693	GM12878	blood:	n/a	chr8:48513437-48513448
21	BATF	chr8:48513237-48513650	GM12878	blood:	n/a	chr8:48513437-48513448
22	BATF	chr8:48510570-48510905	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:48486889-48487113	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:48513234-48513581	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:48510631-48510906	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:48510615-48510929	GM12878	blood:	n/a	n/a
27	BCL3	chr8:48572222-48572537	A549	lung:	n/a	n/a
28	BHLHE40	chr8:48602655-48603034	K562	blood:	n/a	n/a
29	BHLHE40	chr8:48577747-48577891	K562	blood:	n/a	n/a
30	BHLHE40	chr8:48469788-48470117	K562	blood:	n/a	n/a
31	BHLHE40	chr8:48571943-48572773	K562	blood:	n/a	n/a
32	BHLHE40	chr8:48572320-48572667	HepG2	liver:	n/a	n/a
33	BHLHE40	chr8:48515128-48515535	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:48513269-48513679	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:48510587-48511026	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:48486816-48487206	GM12878	blood:	n/a	n/a
37	CBX3	chr8:48577614-48577978	K562	blood:	n/a	n/a
38	CBX3	chr8:48577566-48578040	K562	blood:	n/a	n/a
39	CBX3	chr8:48466890-48467440	K562	blood:	n/a	n/a
40	CBX3	chr8:48565211-48565841	HCT-116	colon:	n/a	n/a
41	CBX3	chr8:48525057-48525544	HCT-116	colon:	n/a	n/a
42	CBX3	chr8:48469664-48470193	K562	blood:	n/a	n/a
43	CBX3	chr8:48572131-48572736	K562	blood:	n/a	n/a
44	CBX3	chr8:48458025-48458261	K562	blood:	n/a	n/a
45	CCNT2	chr8:48572201-48572667	K562	blood:	n/a	n/a
46	CCNT2	chr8:48469803-48470196	K562	blood:	n/a	chr8:48469952-48469972
47	CEBPB	chr8:48577416-48577570	A549	lung:	n/a	chr8:48577478-48577489
48	CEBPB	chr8:48596731-48597418	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:48524922-48525149	HepG2	liver:	n/a	chr8:48524997-48525008
50	CEBPB	chr8:48597403-48597467	A549	lung:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48637463-48637513	GM12891	blood:	n/a
2	chr8:48610943-48610993	HRE	kidney:	n/a
3	chr8:48637463-48637513	GM12891	blood:	n/a
4	chr8:48610943-48610993	HRE	kidney:	n/a
5	chr8:48595620-48595670	GM06990	blood:	n/a
6	chr8:48637463-48637513	NHDF-neo	bronchial:	n/a
7	chr8:48523498-48523548	HL-60	blood:	n/a
8	chr8:48572496-48572546	U87	brain:	n/a
9	chr8:48573717-48573767	HL-60	blood:	n/a
10	chr8:48523498-48523548	ovcar-3	ovarian:	n/a
11	chr8:48572496-48572546	ECC-1	luminal epithelium:	n/a
12	chr8:48523498-48523548	HRCEpiC	kidney:	n/a
13	chr8:48486091-48486141	SK-N-SH_RA	brain:	n/a
14	chr8:48572496-48572546	HRE	kidney:	n/a
15	chr8:48587440-48587490	NHDF-neo	bronchial:	n/a
16	chr8:48523498-48523548	LNCaP	prostate:	n/a
17	chr8:48474400-48474450	IMR90	lung:	fetal
18	chr8:48637463-48637513	LNCaP	prostate:	n/a
19	chr8:48610943-48610993	HIPEpiC	eye:	n/a
20	chr8:48573717-48573767	NH-A	brain:	n/a
21	chr8:48557420-48557470	GM06990	blood:	n/a
22	chr8:48572557-48572607	AG04449	skin:	fetal
23	chr8:48595620-48595670	NH-A	brain:	n/a
24	chr8:48572447-48572497	PrEC	prostate:	n/a
25	chr8:48572447-48572497	HEK293	kidney:	embryo
26	chr8:48610943-48610993	H1-hESC	embryonic stem cell:	embryo
27	chr8:48610943-48610993	CMK	blood:	n/a
28	chr8:48573717-48573767	IMR90	lung:	fetal
29	chr8:48474400-48474450	ProgFib	skin:	n/a
30	chr8:48517420-48517470	U87	brain:	n/a
31	chr8:48610943-48610993	HepG2	liver:	n/a
32	chr8:48572557-48572607	K562	blood:	n/a
33	chr8:48557420-48557470	Hepatocyte	liver:	n/a
34	chr8:48486091-48486141	ProgFib	skin:	n/a
35	chr8:48587440-48587490	HRE	kidney:	n/a
36	chr8:48557420-48557470	PrEC	prostate:	n/a
37	chr8:48587440-48587490	K562	blood:	n/a
38	chr8:48587440-48587490	Jurkat	blood:	n/a
39	chr8:48573717-48573767	U87	brain:	n/a
40	chr8:48557420-48557470	PANC-1	pancreas:	n/a
41	chr8:48595620-48595670	NT2-D1	testis:	n/a
42	chr8:48595620-48595670	SAEC	small airway:	n/a
43	chr8:48595620-48595670	GM12892	blood:	n/a
44	chr8:48486091-48486141	Caco-2	colon:	n/a
45	chr8:48557420-48557470	Caco-2	colon:	n/a
46	chr8:48573717-48573767	NB4	blood:	n/a
47	chr8:48587440-48587490	BE2_C	brain:	n/a
48	chr8:48572496-48572546	BJ	skin:	n/a
49	chr8:48557420-48557470	SK-N-SH	brain:	n/a
50	chr8:48557420-48557470	NHDF-neo	bronchial:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48516477..48519191-chr8:48648055..48649779,2	MCF-7	breast:
2	chr8:48628140..48630229-chr8:48635547..48637579,2	MCF-7	breast:
3	chr8:48424729..48427909-chr8:48454789..48458165,3	MCF-7	breast:
4	chr8:48468813..48471018-chr8:48483021..48485795,2	K562	blood:
5	chr8:48492643..48494808-chr8:48494843..48497616,2	K562	blood:
6	chr8:48571519..48573210-chr8:48580961..48583041,2	K562	blood:
7	chr8:48554598..48556958-chr8:48557992..48560714,2	K562	blood:
8	chr8:48554598..48556958-chr8:48557992..48560714,2	K562	blood:
9	chr8:48589240..48591500-chr8:48645900..48648836,2	MCF-7	breast:
10	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
11	chr8:48573853..48575397-chr8:48576919..48578598,2	MCF-7	breast:
12	chr8:48171946..48174429-chr8:48608651..48611565,2	K562	blood:
13	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
14	chr8:48616670..48620929-chr8:48647842..48650845,3	MCF-7	breast:
15	chr8:48635564..48638783-chr8:48643339..48646155,3	K562	blood:
16	chr8:48635935..48637987-chr8:48638450..48640255,2	K562	blood:
17	chr8:48513464..48515742-chr8:48650061..48652115,2	MCF-7	breast:
18	chr8:48455185..48457892-chr8:48651011..48653495,2	K562	blood:
19	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
20	chr8:48551260..48552777-chr8:48565705..48568537,2	MCF-7	breast:
21	chr8:48572127..48574593-chr8:48609264..48610909,2	MCF-7	breast:
22	chr8:48492643..48494808-chr8:48494843..48497616,2	K562	blood:
23	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
24	chr8:48467560..48471011-chr8:48644906..48648230,3	MCF-7	breast:
25	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
26	chr8:48570759..48574488-chr8:48583570..48586841,4	K562	blood:
27	chr8:48529219..48530791-chr8:48540316..48542801,2	MCF-7	breast:
28	chr8:48561257..48563668-chr8:48585087..48588007,2	K562	blood:
29	chr8:48468813..48471018-chr8:48483021..48485795,2	K562	blood:
30	chr8:48493400..48495648-chr8:48645566..48647459,2	MCF-7	breast:
31	chr8:48636536..48638742-chr8:48640103..48642725,2	K562	blood:
32	chr8:48453211..48456325-chr8:48648153..48651831,4	MCF-7	breast:
33	chr8:48435895..48437509-chr8:48455733..48457442,2	MCF-7	breast:
34	chr8:48489915..48491427-chr8:48495181..48498031,2	MCF-7	breast:
35	chr8:48493147..48494925-chr8:48494980..48497854,3	MCF-7	breast:
36	chr8:48489915..48491427-chr8:48495181..48498031,2	MCF-7	breast:
37	chr8:48436683..48438383-chr8:48633840..48636736,2	MCF-7	breast:
38	chr8:48611140..48612961-chr8:48649084..48651075,2	MCF-7	breast:
39	chr8:48576905..48578450-chr8:48580494..48582582,2	K562	blood:
40	chr8:48343800..48344570-chr8:48513956..48514755,2	MCF-7	breast:
41	chr8:48518004..48520090-chr8:48648537..48650198,2	K562	blood:
42	chr8:48529361..48531739-chr8:48533390..48535611,4	K562	blood:
43	chr8:48583972..48585841-chr8:48591112..48592777,2	K562	blood:
44	chr8:48518671..48521335-chr8:48522262..48524014,3	MCF-7	breast:
45	chr8:48559530..48561165-chr8:48648021..48650410,3	K562	blood:
46	chr8:48573288..48575298-chr8:48647992..48650663,2	MCF-7	breast:
47	chr8:48518671..48521335-chr8:48522262..48524014,3	MCF-7	breast:
48	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
49	chr8:48627320..48629961-chr8:48647561..48650281,2	MCF-7	breast:
50	chr8:48576905..48578450-chr8:48580494..48582582,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEBPD-3	chr8:48460313-48460488	NONHSAT126450
2	lnc-CEBPD-3	chr8:48459366-48459968	NONHSAT126450
3	lnc-CEBPD-2	chr8:48504709-48505171	NONHSAT126451

No data

Variant related genes	Relation type
RNU6-665P	TF binding region
ENSG00000251354	TF binding region
SPIDR	TF binding region
ENSG00000254065	TF binding region
RNU6-665P	CpG island
ENSG00000251354	CpG island
SPIDR	CpG island
ENSG00000254065	CpG island
ENSG00000254065	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000253330	chromatin interactions
ENSG00000168264	chromatin interactions

Extended variants
information (count: 6362 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:6362 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547829176	chr8:48444342-48444343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555212756	chr8:48444435-48444436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72646352	chr8:48444457-48444458	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558427265	chr8:48444601-48444602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34728107	chr8:48444628-48444629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576761316	chr8:48444655-48444656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537613079	chr8:48444696-48444697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555962604	chr8:48444706-48444707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574545653	chr8:48444817-48444818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542316387	chr8:48444859-48444860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560419689	chr8:48444884-48444885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371748625	chr8:48444965-48444966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545903001	chr8:48445015-48445016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564756615	chr8:48445147-48445148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374970055	chr8:48445239-48445240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532061454	chr8:48445361-48445362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556294841	chr8:48445450-48445451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368812247	chr8:48445452-48445453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75087851	chr8:48445488-48445489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562272803	chr8:48445551-48445552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529715630	chr8:48445597-48445598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200772287	chr8:48445598-48445599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71527677	chr8:48445673-48445674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576438215	chr8:48445686-48445687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182400485	chr8:48445689-48445690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541971275	chr8:48445707-48445708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139130223	chr8:48445876-48445877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186136452	chr8:48445883-48445884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533762244	chr8:48445928-48445929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190549025	chr8:48445930-48445931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570384377	chr8:48445957-48445958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144084630	chr8:48446064-48446065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183002262	chr8:48446171-48446172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543488183	chr8:48446235-48446236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111435589	chr8:48446244-48446245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535334354	chr8:48446318-48446319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4873446	chr8:48446464-48446465	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572704333	chr8:48446481-48446482	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs546186469	chr8:48446524-48446525	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs558207377	chr8:48446528-48446529	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs576766211	chr8:48446532-48446533	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs185780129	chr8:48446550-48446551	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs191605202	chr8:48446553-48446554	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs529487532	chr8:48446598-48446599	Enhancers Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs570059569	chr8:48446601-48446602	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs77539676	chr8:48446614-48446615	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs560157554	chr8:48446661-48446662	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs527416248	chr8:48446680-48446681	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs375761564	chr8:48446703-48446704	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs551709216	chr8:48446719-48446720	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Osteosarcoma	21215367	CNVD
Autism	20531469	CNVD

Chromatin state (count:3798 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48434000-48455400	Weak transcription	Primary T cells from cord blood	blood
2	chr8:48434400-48444400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:48436600-48445400	Weak transcription	GM12878-XiMat	blood
4	chr8:48438000-48446400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:48438800-48452400	Weak transcription	HSMM	muscle
6	chr8:48439600-48445000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:48439800-48455400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr8:48440000-48444400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr8:48440000-48445200	Weak transcription	Brain Hippocampus Middle	brain
10	chr8:48440000-48446400	Weak transcription	Fetal Intestine Small	intestine
11	chr8:48440000-48452600	Weak transcription	Fetal Kidney	kidney
12	chr8:48442000-48444400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr8:48442000-48447800	Weak transcription	Primary B cells from cord blood	blood
14	chr8:48442600-48454400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:48442800-48445000	Enhancers	Placenta	Placenta
16	chr8:48442800-48456000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr8:48443600-48444400	Enhancers	K562	blood
18	chr8:48444000-48445000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:48444800-48446400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:48445000-48445200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:48445000-48446600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:48445200-48445400	Enhancers	Brain Hippocampus Middle	brain
23	chr8:48445400-48445600	Enhancers	GM12878-XiMat	blood
24	chr8:48446400-48446800	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr8:48446400-48447200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:48446800-48452400	Weak transcription	Fetal Intestine Small	intestine
27	chr8:48447200-48466200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:48450000-48450200	Enhancers	Liver	Liver
29	chr8:48450200-48452400	Weak transcription	Liver	Liver
30	chr8:48451800-48452600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:48452200-48452400	Enhancers	Fetal Muscle Leg	muscle
32	chr8:48452200-48452600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr8:48452200-48452800	Enhancers	A549	lung
34	chr8:48452200-48453200	Enhancers	NHLF	lung
35	chr8:48452200-48453400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:48452200-48453400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:48452200-48453400	Enhancers	HSMMtube	muscle
38	chr8:48452200-48453600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:48452200-48454000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:48452200-48454400	Enhancers	Placenta	Placenta
41	chr8:48452400-48452600	Enhancers	Aorta	Aorta
42	chr8:48452400-48452800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:48452400-48452800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:48452400-48452800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr8:48452400-48452800	Enhancers	Brain Anterior Caudate	brain
46	chr8:48452400-48452800	Enhancers	Fetal Intestine Small	intestine
47	chr8:48452400-48452800	Enhancers	NH-A	brain
48	chr8:48452400-48453200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:48452400-48453200	Enhancers	Liver	Liver
50	chr8:48452400-48453200	Enhancers	Ovary	ovary

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