Variant report

Variant	nsv1026287
Chromosome Location	chr8:48615720-48710849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1913)
CpG islands
(count:2446)
Chromatin interactive
region (count:95)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1913 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48670787-48671196	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48647745-48648106	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48647857-48648254	K562	blood:	n/a	n/a
4	ARID3A	chr8:48651502-48651743	HepG2	liver:	n/a	n/a
5	ATF2	chr8:48678018-48678587	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:48678031-48678521	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr8:48650381-48650785	A549	lung:	n/a	chr8:48650775-48650784 chr8:48650763-48650783
8	BACH1	chr8:48680113-48680245	K562	blood:	n/a	n/a
9	BACH1	chr8:48649827-48650099	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:48647451-48647482	K562	blood:	n/a	n/a
11	BACH1	chr8:48651110-48651666	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr8:48678187-48678522	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr8:48678161-48678473	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr8:48647655-48648215	A549	lung:	n/a	n/a
15	BCL3	chr8:48664526-48664933	A549	lung:	n/a	n/a
16	BCL3	chr8:48647363-48648341	A549	lung:	n/a	chr8:48647480-48647489
17	BCL3	chr8:48664484-48664980	A549	lung:	n/a	n/a
18	BHLHE40	chr8:48650988-48651213	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:48651101-48651263	K562	blood:	n/a	n/a
20	BHLHE40	chr8:48651540-48651740	K562	blood:	n/a	chr8:48651588-48651604
21	BHLHE40	chr8:48676689-48676991	K562	blood:	n/a	n/a
22	BHLHE40	chr8:48647879-48647972	K562	blood:	n/a	n/a
23	BHLHE40	chr8:48651445-48651785	GM12878	blood:	n/a	chr8:48651588-48651604
24	BRCA1	chr8:48647697-48647810	HepG2	liver:	n/a	n/a
25	BRCA1	chr8:48651625-48651701	GM12878	blood:	n/a	n/a
26	BRCA1	chr8:48651371-48651395	GM12878	blood:	n/a	n/a
27	BRCA1	chr8:48651534-48651831	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:48651482-48651879	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr8:48649229-48649992	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr8:48647511-48648174	K562	blood:	n/a	n/a
31	CBX3	chr8:48678051-48678463	K562	blood:	n/a	n/a
32	CBX3	chr8:48651428-48651796	K562	blood:	n/a	chr8:48651685-48651696
33	CCNT2	chr8:48649295-48651679	K562	blood:	n/a	chr8:48651557-48651566 chr8:48649336-48649345
34	CCNT2	chr8:48676793-48677539	K562	blood:	n/a	n/a
35	CEBPB	chr8:48681193-48681498	K562	blood:	n/a	chr8:48681346-48681357
36	CEBPB	chr8:48675755-48675921	K562	blood:	n/a	chr8:48675838-48675851 chr8:48675839-48675850
37	CEBPB	chr8:48651491-48651811	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:48621435-48621726	K562	blood:	n/a	chr8:48621590-48621601
39	CEBPB	chr8:48678119-48678536	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:48621405-48621723	K562	blood:	n/a	chr8:48621590-48621601
41	CEBPB	chr8:48675713-48675984	IMR90	lung:	n/a	chr8:48675838-48675851 chr8:48675839-48675850
42	CEBPB	chr8:48688847-48688922	A549	lung:	n/a	n/a
43	CEBPB	chr8:48681201-48681491	IMR90	lung:	n/a	chr8:48681346-48681357
44	CEBPB	chr8:48651486-48651810	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr8:48650156-48651201	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:48681189-48681419	K562	blood:	n/a	chr8:48681346-48681357
47	CEBPB	chr8:48647938-48648137	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:48681193-48681440	MCF-7	breast:	n/a	chr8:48681346-48681357
49	CEBPB	chr8:48621407-48621722	HepG2	liver:	n/a	chr8:48621590-48621601
50	CEBPB	chr8:48675760-48675965	HepG2	liver:	n/a	chr8:48675838-48675851 chr8:48675839-48675850

(count:2446 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48680661-48680711	HMEC	breast:	n/a
2	chr8:48676054-48676104	AG10803	skin:	n/a
3	chr8:48680661-48680711	HEEpiC	esophagus:	n/a
4	chr8:48652327-48652377	ProgFib	skin:	n/a
5	chr8:48649326-48649376	BE2_C	brain:	n/a
6	chr8:48673669-48673719	PANC-1	pancreas:	n/a
7	chr8:48680661-48680711	HMEC	breast:	n/a
8	chr8:48676054-48676104	AG10803	skin:	n/a
9	chr8:48680661-48680711	HEEpiC	esophagus:	n/a
10	chr8:48652327-48652377	ProgFib	skin:	n/a
11	chr8:48649326-48649376	BE2_C	brain:	n/a
12	chr8:48673669-48673719	PANC-1	pancreas:	n/a
13	chr8:48675911-48675961	HRCEpiC	kidney:	n/a
14	chr8:48675911-48675961	HEK293	kidney:	embryo
15	chr8:48691052-48691102	GM12891	blood:	n/a
16	chr8:48691052-48691102	GM12878	blood:	n/a
17	chr8:48650745-48650795	HCF	heart:	n/a
18	chr8:48648813-48648863	HCM	heart:	n/a
19	chr8:48650705-48650755	PANC-1	pancreas:	n/a
20	chr8:48677407-48677457	HEEpiC	esophagus:	n/a
21	chr8:48648874-48648924	HRE	kidney:	n/a
22	chr8:48649326-48649376	PFSK-1	brain:	n/a
23	chr8:48651311-48651361	ECC-1	luminal epithelium:	n/a
24	chr8:48649457-48649507	ovcar-3	ovarian:	n/a
25	chr8:48652327-48652377	K562	blood:	n/a
26	chr8:48677108-48677158	PFSK-1	brain:	n/a
27	chr8:48675771-48675821	PFSK-1	brain:	n/a
28	chr8:48649457-48649507	HNPCEpiC	eye:	n/a
29	chr8:48648112-48648162	AoSMC	blood vessel:	n/a
30	chr8:48651122-48651172	U87	brain:	n/a
31	chr8:48648112-48648162	RPTEC	kidney:	n/a
32	chr8:48676092-48676142	NHBE	bronchial:	n/a
33	chr8:48673669-48673719	SK-N-MC	brain:	n/a
34	chr8:48694958-48695008	NHBE	bronchial:	n/a
35	chr8:48678145-48678195	SK-N-SH	brain:	n/a
36	chr8:48691176-48691226	HIPEpiC	eye:	n/a
37	chr8:48676000-48676050	A549	lung:	n/a
38	chr8:48691148-48691198	NB4	blood:	n/a
39	chr8:48648874-48648924	AG09319	gingival:	n/a
40	chr8:48649326-48649376	SAEC	small airway:	n/a
41	chr8:48656349-48656399	RPTEC	kidney:	n/a
42	chr8:48651635-48651685	AG10803	skin:	n/a
43	chr8:48691176-48691226	T-47D	breast:	n/a
44	chr8:48675771-48675821	NT2-D1	testis:	n/a
45	chr8:48695125-48695175	NHDF-neo	bronchial:	n/a
46	chr8:48648874-48648924	NB4	blood:	n/a
47	chr8:48651122-48651172	HRPEpiC	eye:	n/a
48	chr8:48637463-48637513	GM19239	blood:	n/a
49	chr8:48650705-48650755	AG09309	skin:	n/a
50	chr8:48676092-48676142	NHDF-neo	bronchial:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48114400..48115004-chr8:48651136..48652107,2	MCF-7	breast:
2	chr8:48300186..48303081-chr8:48648494..48650857,2	MCF-7	breast:
3	chr8:48223569..48225954-chr8:48642409..48644484,2	MCF-7	breast:
4	chr8:48709573..48711482-chr8:48774056..48776581,2	K562	blood:
5	chr8:48114948..48116858-chr8:48648714..48650275,2	K562	blood:
6	chr8:48627320..48629961-chr8:48647561..48650281,2	MCF-7	breast:
7	chr8:48635174..48641893-chr8:48648550..48652485,8	MCF-7	breast:
8	chr8:48649649..48652012-chr8:48661359..48663149,3	MCF-7	breast:
9	chr8:48435225..48441849-chr8:48646333..48652657,17	MCF-7	breast:
10	chr8:48702667..48704261-chr8:48706616..48708531,2	K562	blood:
11	chr8:48417772..48429044-chr8:48646094..48652486,42	MCF-7	breast:
12	chr8:48649183..48653409-chr8:48654511..48657772,8	MCF-7	breast:
13	chr8:48222564..48225151-chr8:48648619..48650407,2	MCF-7	breast:
14	chr8:48173494..48174253-chr8:48651177..48651793,2	MCF-7	breast:
15	chr8:48702761..48704523-chr8:48706804..48708531,2	K562	blood:
16	chr8:48648988..48650565-chr8:48654492..48656247,2	K562	blood:
17	chr8:48493400..48495648-chr8:48645566..48647459,2	MCF-7	breast:
18	chr8:48648550..48651085-chr8:48656701..48659143,2	K562	blood:
19	chr8:48628140..48630229-chr8:48635547..48637579,2	MCF-7	breast:
20	chr8:48651251..48652796-chr8:48662762..48664570,2	K562	blood:
21	chr8:48436683..48438383-chr8:48633840..48636736,2	MCF-7	breast:
22	chr8:48178486..48180700-chr8:48649233..48651294,2	K562	blood:
23	chr8:48649410..48651564-chr8:48691091..48693098,2	MCF-7	breast:
24	chr8:48645599..48648467-chr8:48653903..48656784,2	K562	blood:
25	chr8:48113591..48116230-chr8:48649014..48651468,2	MCF-7	breast:
26	chr8:48702667..48704261-chr8:48706616..48708531,2	K562	blood:
27	chr8:48635935..48637987-chr8:48638450..48640255,2	K562	blood:
28	chr8:48431409..48434183-chr8:48649405..48651632,3	K562	blood:
29	chr21:37692157..37692997-chr8:48647571..48648363,2	NB4	blood:
30	chr8:48409859..48412795-chr8:48648152..48651126,2	MCF-7	breast:
31	chr8:48171892..48175366-chr8:48649107..48652421,3	K562	blood:
32	chr14:38061973..38064113-chr8:48650908..48653008,2	MCF-7	breast:
33	chr8:48282165..48284345-chr8:48648892..48650703,2	MCF-7	breast:
34	chr11:66390889..66393382-chr8:48648876..48650745,2	MCF-7	breast:
35	chr8:48078161..48080655-chr8:48649461..48651455,2	MCF-7	breast:
36	chr19:40476362..40476867-chr8:48650522..48651379,2	Hela-S3	cervix:
37	chr8:48571104..48575817-chr8:48648052..48653139,6	K562	blood:
38	chr8:48649995..48651833-chr8:48673119..48675757,2	K562	blood:
39	chr8:48565250..48566861-chr8:48648716..48650619,2	MCF-7	breast:
40	chr8:48112895..48115020-chr8:48649456..48652185,2	K562	blood:
41	chr8:48456575..48460862-chr8:48649112..48652176,5	MCF-7	breast:
42	chr8:48287238..48289798-chr8:48645955..48647701,2	MCF-7	breast:
43	chr8:48571020..48572523-chr8:48650365..48652333,2	MCF-7	breast:
44	chr8:48636536..48638742-chr8:48640103..48642725,2	K562	blood:
45	chr8:48353630..48357760-chr8:48647568..48650478,4	MCF-7	breast:
46	chr8:48580254..48581867-chr8:48649171..48651627,2	MCF-7	breast:
47	chr8:48674421..48677276-chr8:48679644..48681662,2	K562	blood:
48	chr8:48649560..48652058-chr8:48659068..48660990,2	MCF-7	breast:
49	chr8:48218179..48220522-chr8:48649833..48651549,2	MCF-7	breast:
50	chr8:48641261..48643837-chr8:48646304..48648401,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-5	chr8:48641974-48642266	NONHSAT126454
2	lnc-RP11-1134I14.8.1-5	chr8:48641282-48641609	NONHSAT126454

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CEBPD	hsa-miR-98-5p	chr8:48649834-48649828

Variant related genes	Relation type
PRKDC	TF binding region
CEBPD	TF binding region
SPIDR	TF binding region
PRKDC	CpG island
CEBPD	CpG island
SPIDR	CpG island
ENSG00000249859	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000207369	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000269924	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000215177	chromatin interactions
ENSG00000163634	chromatin interactions
ENSG00000253330	chromatin interactions
ENSG00000273199	chromatin interactions
ENSG00000251354	chromatin interactions
ENSG00000159256	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000171729	chromatin interactions
ENSG00000105364	chromatin interactions

Extended variants
information (count: 3426 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3426 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536006733	chr8:48615728-48615729	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554471525	chr8:48615741-48615742	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116739468	chr8:48615767-48615768	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539800035	chr8:48615768-48615769	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540412840	chr8:48615783-48615784	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550529559	chr8:48615784-48615785	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75963203	chr8:48615789-48615790	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531094413	chr8:48615859-48615860	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577198445	chr8:48615860-48615861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148069023	chr8:48615900-48615901	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563144317	chr8:48615901-48615902	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79051003	chr8:48615919-48615920	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180830944	chr8:48615928-48615929	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560566998	chr8:48615932-48615933	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528179017	chr8:48615934-48615935	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546411556	chr8:48616022-48616023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2632494	chr8:48616052-48616053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571199458	chr8:48616079-48616080	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150616490	chr8:48616085-48616086	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536127500	chr8:48616143-48616144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186532035	chr8:48616162-48616163	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568764151	chr8:48616177-48616178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536193673	chr8:48616180-48616181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114373827	chr8:48616221-48616222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191962314	chr8:48616332-48616333	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534279309	chr8:48616365-48616366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182159663	chr8:48616416-48616417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577433076	chr8:48616428-48616429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544579446	chr8:48616434-48616435	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556597884	chr8:48616446-48616447	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73571454	chr8:48616478-48616479	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs186541173	chr8:48616488-48616489	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370913083	chr8:48616513-48616514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566248504	chr8:48616522-48616523	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542196693	chr8:48616545-48616546	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535262901	chr8:48616552-48616553	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555999983	chr8:48616611-48616612	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560718973	chr8:48616649-48616650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs59337594	chr8:48616725-48616726	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572559503	chr8:48616777-48616778	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546398105	chr8:48616792-48616793	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140777000	chr8:48616795-48616796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144739957	chr8:48616809-48616810	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191499089	chr8:48616827-48616828	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182405019	chr8:48616877-48616878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186938532	chr8:48616954-48616955	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28583978	chr8:48616956-48616957	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs553827194	chr8:48616961-48616962	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543614306	chr8:48616983-48616984	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566781935	chr8:48617003-48617004	Weak transcription Strong transcription Enhancers	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
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:2893 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48590600-48625200	Weak transcription	HepG2	liver
2	chr8:48593200-48624000	Weak transcription	Thymus	Thymus
3	chr8:48597000-48625400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:48597200-48647200	Weak transcription	NHEK	skin
5	chr8:48597200-48647400	Weak transcription	HMEC	breast
6	chr8:48599200-48626600	Weak transcription	Fetal Kidney	kidney
7	chr8:48602400-48616400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:48602800-48647800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:48604400-48619000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:48604400-48648400	Weak transcription	Small Intestine	intestine
11	chr8:48605000-48625400	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:48606400-48624400	Weak transcription	Psoas Muscle	Psoas
13	chr8:48606600-48624000	Weak transcription	Right Atrium	heart
14	chr8:48606800-48646400	Weak transcription	Fetal Heart	heart
15	chr8:48609200-48632400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr8:48610400-48625200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:48610600-48616800	Weak transcription	Esophagus	oesophagus
18	chr8:48610600-48624400	Weak transcription	HSMM	muscle
19	chr8:48610600-48625000	Weak transcription	Fetal Thymus	thymus
20	chr8:48610600-48625400	Weak transcription	Brain Germinal Matrix	brain
21	chr8:48610600-48625400	Weak transcription	Brain Hippocampus Middle	brain
22	chr8:48610600-48625400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr8:48610800-48625400	Weak transcription	NHLF	lung
24	chr8:48611000-48617000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:48611000-48625400	Weak transcription	Brain Angular Gyrus	brain
26	chr8:48611200-48617800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr8:48611400-48616200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr8:48611400-48625200	Weak transcription	Brain Substantia Nigra	brain
29	chr8:48611800-48617400	Weak transcription	HSMMtube	muscle
30	chr8:48611800-48625400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr8:48611800-48632200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:48612000-48617600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr8:48612000-48625800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:48612000-48647400	Weak transcription	NH-A	brain
35	chr8:48612400-48619000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:48612400-48625400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr8:48612400-48640000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr8:48612600-48616600	Strong transcription	Primary hematopoietic stem cells	blood
39	chr8:48612600-48617000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr8:48612600-48617600	Strong transcription	Duodenum Mucosa	Duodenum
41	chr8:48612600-48619600	Weak transcription	Stomach Mucosa	stomach
42	chr8:48612800-48615800	Strong transcription	Stomach Smooth Muscle	stomach
43	chr8:48612800-48616000	Strong transcription	Dnd41	blood
44	chr8:48612800-48616600	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr8:48612800-48616800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr8:48612800-48617600	Strong transcription	Fetal Intestine Large	intestine
47	chr8:48612800-48618000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:48612800-48618000	Strong transcription	Adipose Nuclei	Adipose
49	chr8:48612800-48618200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:48612800-48618200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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