Variant report

Variant	esv1817304
Chromosome Location	chr8:48205314-48321308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1194)
CpG islands
(count:366)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48281965-48282343	K562	blood:	n/a	n/a
2	ARID3A	chr8:48243113-48243207	K562	blood:	n/a	n/a
3	ARID3A	chr8:48265824-48266513	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48227759-48228098	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:48290032-48290503	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:48284765-48284924	K562	blood:	n/a	n/a
7	ARID3A	chr8:48282003-48282308	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:48227594-48228136	K562	blood:	n/a	n/a
9	ATF1	chr8:48281968-48282356	K562	blood:	n/a	n/a
10	ATF1	chr8:48266083-48266495	K562	blood:	n/a	n/a
11	ATF1	chr8:48258407-48258562	K562	blood:	n/a	n/a
12	ATF1	chr8:48243885-48243889	K562	blood:	n/a	n/a
13	ATF1	chr8:48227742-48228251	K562	blood:	n/a	n/a
14	ATF3	chr8:48281943-48282320	HCT-116	colon:	n/a	n/a
15	ATF3	chr8:48281926-48282348	K562	blood:	n/a	n/a
16	ATF3	chr8:48265649-48266259	HCT-116	colon:	n/a	n/a
17	ATF3	chr8:48282010-48282221	HepG2	liver:	n/a	n/a
18	ATF3	chr8:48265721-48266444	A549	lung:	n/a	n/a
19	BCL11A	chr8:48273287-48273483	GM12878	blood:	n/a	n/a
20	BCL3	chr8:48265724-48266572	A549	lung:	n/a	n/a
21	BHLHE40	chr8:48284752-48284905	K562	blood:	n/a	n/a
22	BHLHE40	chr8:48281981-48282334	K562	blood:	n/a	n/a
23	BHLHE40	chr8:48227645-48228062	K562	blood:	n/a	n/a
24	BHLHE40	chr8:48265752-48266090	HepG2	liver:	n/a	n/a
25	BHLHE40	chr8:48273214-48273476	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:48274468-48274746	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:48269887-48270043	K562	blood:	n/a	n/a
28	BHLHE40	chr8:48227816-48228068	GM12878	blood:	n/a	n/a
29	BRCA1	chr8:48265721-48266798	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr8:48227783-48228130	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr8:48265737-48266603	HCT-116	colon:	n/a	n/a
32	CBX3	chr8:48235964-48236593	HCT-116	colon:	n/a	n/a
33	CBX3	chr8:48227588-48228262	HCT-116	colon:	n/a	n/a
34	CBX3	chr8:48265593-48266657	HCT-116	colon:	n/a	n/a
35	CCNT2	chr8:48282057-48282317	K562	blood:	n/a	n/a
36	CCNT2	chr8:48227518-48227704	K562	blood:	n/a	n/a
37	CCNT2	chr8:48284749-48285033	K562	blood:	n/a	n/a
38	CCNT2	chr8:48265875-48266439	K562	blood:	n/a	n/a
39	CEBPB	chr8:48295944-48296144	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:48279433-48279669	A549	lung:	n/a	n/a
41	CEBPB	chr8:48290699-48291069	Hela-S3	cervix:	n/a	chr8:48290887-48290898
42	CEBPB	chr8:48281863-48282523	A549	lung:	n/a	chr8:48282131-48282148
43	CEBPB	chr8:48281999-48282286	HepG2	liver:	n/a	chr8:48282131-48282148
44	CEBPB	chr8:48253019-48253460	Hela-S3	cervix:	n/a	chr8:48253222-48253231 chr8:48253222-48253231 chr8:48253220-48253231 chr8:48253220-48253233 chr8:48253222-48253231 chr8:48253220-48253233
45	CEBPB	chr8:48290834-48291033	HepG2	liver:	n/a	chr8:48290887-48290898
46	CEBPB	chr8:48265649-48266720	A549	lung:	n/a	chr8:48266294-48266311
47	CEBPB	chr8:48281802-48282492	MCF-7	breast:	n/a	chr8:48282131-48282148
48	CEBPB	chr8:48253022-48253535	A549	lung:	n/a	chr8:48253222-48253231 chr8:48253222-48253231 chr8:48253220-48253231 chr8:48253220-48253233 chr8:48253222-48253231 chr8:48253220-48253233
49	CEBPB	chr8:48281873-48282386	MCF-7	breast:	n/a	chr8:48282131-48282148
50	CEBPB	chr8:48263257-48263730	HCT-116	colon:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48265917-48265967	GM12878	blood:	n/a
2	chr8:48297271-48297321	HRCEpiC	kidney:	n/a
3	chr8:48226852-48226902	HL-60	blood:	n/a
4	chr8:48272891-48272941	RPTEC	kidney:	n/a
5	chr8:48253633-48253683	NT2-D1	testis:	n/a
6	chr8:48253633-48253683	SK-N-SH	brain:	n/a
7	chr8:48226852-48226902	SKMC	muscle:	n/a
8	chr8:48272891-48272941	ProgFib	skin:	n/a
9	chr8:48262344-48262394	NHBE	bronchial:	n/a
10	chr8:48262344-48262394	HAEpiC	amniotic membrane:	n/a
11	chr8:48226852-48226902	HRCEpiC	kidney:	n/a
12	chr8:48262344-48262394	GM12892	blood:	n/a
13	chr8:48265917-48265967	PFSK-1	brain:	n/a
14	chr8:48272891-48272941	HMEC	breast:	n/a
15	chr8:48265917-48265967	AG04450	lung:	fetal
16	chr8:48253633-48253683	HRCEpiC	kidney:	n/a
17	chr8:48253633-48253683	SK-N-SH_RA	brain:	n/a
18	chr8:48253633-48253683	LNCaP	prostate:	n/a
19	chr8:48265917-48265967	HAEpiC	amniotic membrane:	n/a
20	chr8:48226852-48226902	U87	brain:	n/a
21	chr8:48262344-48262394	A549	lung:	n/a
22	chr8:48272891-48272941	H1-hESC	embryonic stem cell:	embryo
23	chr8:48226852-48226902	RPTEC	kidney:	n/a
24	chr8:48253633-48253683	K562	blood:	n/a
25	chr8:48262344-48262394	HEK293	kidney:	embryo
26	chr8:48226852-48226902	ovcar-3	ovarian:	n/a
27	chr8:48297271-48297321	ProgFib	skin:	n/a
28	chr8:48253633-48253683	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:48265917-48265967	HCT-116	colon:	n/a
30	chr8:48272891-48272941	BE2_C	brain:	n/a
31	chr8:48253633-48253683	Hepatocyte	liver:	n/a
32	chr8:48297271-48297321	GM12892	blood:	n/a
33	chr8:48262344-48262394	ProgFib	skin:	n/a
34	chr8:48265917-48265967	NB4	blood:	n/a
35	chr8:48253633-48253683	PANC-1	pancreas:	n/a
36	chr8:48272891-48272941	HRE	kidney:	n/a
37	chr8:48265917-48265967	CMK	blood:	n/a
38	chr8:48272891-48272941	HL-60	blood:	n/a
39	chr8:48253633-48253683	HMEC	breast:	n/a
40	chr8:48262344-48262394	Jurkat	blood:	n/a
41	chr8:48297271-48297321	MCF10A-Er-Src	breast:	n/a
42	chr8:48262344-48262394	HCM	heart:	n/a
43	chr8:48226852-48226902	HNPCEpiC	eye:	n/a
44	chr8:48262344-48262394	SK-N-MC	brain:	n/a
45	chr8:48262344-48262394	Caco-2	colon:	n/a
46	chr8:48272891-48272941	BJ	skin:	n/a
47	chr8:48253633-48253683	HEEpiC	esophagus:	n/a
48	chr8:48226852-48226902	BE2_C	brain:	n/a
49	chr8:48272891-48272941	GM19239	blood:	n/a
50	chr8:48226852-48226902	NHDF-neo	bronchial:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48226109..48228016-chr8:48649985..48652801,2	K562	blood:
2	chr8:48296378..48299348-chr8:48301045..48303894,3	K562	blood:
3	chr8:48296590..48299380-chr8:48299721..48303188,4	MCF-7	breast:
4	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
5	chr8:48218179..48220522-chr8:48649833..48651549,2	MCF-7	breast:
6	chr8:48237525..48239836-chr8:48252461..48254752,2	MCF-7	breast:
7	chr8:48280382..48283263-chr8:48648122..48652692,4	MCF-7	breast:
8	chr8:48237525..48239836-chr8:48252461..48254752,2	MCF-7	breast:
9	chr8:48296378..48299348-chr8:48301045..48303894,3	K562	blood:
10	chr8:48172365..48174011-chr8:48227850..48230146,2	MCF-7	breast:
11	chr8:48285193..48287244-chr8:48293396..48296107,2	K562	blood:
12	chr8:48276921..48279533-chr8:48290586..48293171,2	MCF-7	breast:
13	chr8:48282165..48284345-chr8:48648892..48650703,2	MCF-7	breast:
14	chr8:48226109..48228016-chr8:48649982..48652801,3	K562	blood:
15	chr8:48171571..48173845-chr8:48247630..48249271,2	MCF-7	breast:
16	chr8:48305764..48309024-chr8:53624660..53627223,3	K562	blood:
17	chr8:48284342..48286022-chr8:48648925..48651105,2	MCF-7	breast:
18	chr8:48222519..48229115-chr8:48647530..48652731,12	MCF-7	breast:
19	chr8:48202864..48204570-chr8:48206625..48208490,2	K562	blood:
20	chr8:48222564..48225151-chr8:48648619..48650407,2	MCF-7	breast:
21	chr8:48289062..48291222-chr8:48292317..48294318,2	K562	blood:
22	chr8:48264421..48266947-chr8:48288790..48290307,2	MCF-7	breast:
23	chr8:48316678..48319260-chr8:48343262..48344870,2	MCF-7	breast:
24	chr8:48270281..48272745-chr8:48274698..48276363,2	K562	blood:
25	chr8:48291685..48296788-chr8:48648654..48651770,5	MCF-7	breast:
26	chr8:48288492..48291157-chr8:48291634..48296219,4	MCF-7	breast:
27	chr8:48223569..48225954-chr8:48642409..48644484,2	MCF-7	breast:
28	chr8:48227501..48228418-chr8:48651135..48652127,2	MCF-7	breast:
29	chr8:48264421..48266947-chr8:48288790..48290307,2	MCF-7	breast:
30	chr8:48297848..48299871-chr8:48301045..48303414,2	K562	blood:
31	chr8:48300186..48303081-chr8:48648494..48650857,2	MCF-7	breast:
32	chr8:48289062..48291222-chr8:48292317..48294318,2	K562	blood:
33	chr8:48288492..48291157-chr8:48291634..48296219,4	MCF-7	breast:
34	chr8:48285193..48287244-chr8:48293396..48296107,2	K562	blood:
35	chr8:48274508..48277546-chr8:48285715..48288679,3	K562	blood:
36	chr8:48270281..48272745-chr8:48274698..48276363,2	K562	blood:
37	chr8:48297848..48299871-chr8:48301045..48303414,2	K562	blood:
38	chr8:48226541..48230936-chr8:48648506..48651986,13	MCF-7	breast:
39	chr8:48286201..48287772-chr8:48290885..48293117,2	MCF-7	breast:
40	chr8:48287238..48289798-chr8:48645955..48647701,2	MCF-7	breast:
41	chr8:48286201..48287772-chr8:48290885..48293117,2	MCF-7	breast:
42	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
43	chr8:48296590..48299380-chr8:48299721..48303188,4	MCF-7	breast:
44	chr8:48274508..48277546-chr8:48285715..48288679,3	K562	blood:
45	chr8:48276921..48279533-chr8:48290586..48293171,2	MCF-7	breast:
46	chr8:48293039..48294618-chr8:48649399..48651169,2	MCF-7	breast:
47	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
48	chr8:48263378..48268282-chr8:48268711..48274538,7	MCF-7	breast:
49	chr8:48173044..48174594-chr8:48227595..48229177,2	K562	blood:
50	chr8:48264373..48267024-chr8:48650520..48652799,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-5	chr8:48300905-48301048	NONHSAT126443
2	lnc-RP11-1134I14.8.1-5	chr8:48206456-48207017	NONHSAT126444
3	lnc-RP11-1134I14.8.1-5	chr8:48206456-48206619	NONHSAT126443

No data

Variant related genes	Relation type
SPIDR	TF binding region
SPIDR	CpG island
ENSG00000221869	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000023287	chromatin interactions

Extended variants
information (count: 4009 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4009 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs118006186	chr8:48205314-48205315	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs139615106	chr8:48205604-48205605	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377737107	chr8:48205666-48205667	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374756658	chr8:48205814-48205815	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587771689	chr8:48205909-48205910	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117658853	chr8:48205935-48205936	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs374939138	chr8:48206234-48206235	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367797034	chr8:48206650-48206651	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs200873573	chr8:48206693-48206694	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs140107058	chr8:48207212-48207213	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375675539	chr8:48207229-48207230	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs367910490	chr8:48207557-48207558	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373460269	chr8:48207854-48207855	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370561756	chr8:48208129-48208130	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374963121	chr8:48208205-48208206	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs111731343	chr8:48208251-48208252	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372113695	chr8:48208280-48208281	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374806912	chr8:48208287-48208288	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368331222	chr8:48208331-48208332	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113832667	chr8:48208765-48208766	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200545176	chr8:48208865-48208866	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367824904	chr8:48208912-48208913	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370382649	chr8:48209259-48209260	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372469658	chr8:48209282-48209283	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587647902	chr8:48209906-48209907	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587719664	chr8:48209942-48209943	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117008360	chr8:48209981-48209982	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587755124	chr8:48210040-48210041	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs587645526	chr8:48210041-48210042	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs587724336	chr8:48210047-48210048	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs370113084	chr8:48210211-48210212	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs199844851	chr8:48210465-48210466	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs201001292	chr8:48210550-48210551	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs201739199	chr8:48210682-48210683	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200059512	chr8:48210703-48210704	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201197531	chr8:48210723-48210724	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201962023	chr8:48211104-48211105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371855858	chr8:48211124-48211125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200340099	chr8:48211360-48211361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201225600	chr8:48211412-48211413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375209067	chr8:48211428-48211429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369120883	chr8:48211517-48211518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6473739	chr8:48211549-48211550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200632425	chr8:48211577-48211578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201058649	chr8:48211759-48211760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587714652	chr8:48211778-48211779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199678518	chr8:48212073-48212074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587765093	chr8:48212298-48212299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79247274	chr8:48212331-48212332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587644464	chr8:48212378-48212379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Breast cancer	22522925	CNVD

Chromatin state (count:2458 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48183200-48227800	Weak transcription	Stomach Mucosa	stomach
2	chr8:48189600-48225000	Weak transcription	HUVEC	blood vessel
3	chr8:48191400-48216600	Weak transcription	Colonic Mucosa	Colon
4	chr8:48192800-48205600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:48193600-48205400	Weak transcription	Lung	lung
6	chr8:48193600-48210600	Strong transcription	Primary T helper cells PMA-I stimulated	--
7	chr8:48195800-48206800	Weak transcription	Fetal Heart	heart
8	chr8:48196800-48216000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr8:48197600-48210600	Weak transcription	Right Ventricle	heart
10	chr8:48198200-48206200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr8:48198400-48210000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:48199000-48205400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:48199000-48211400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr8:48199000-48215000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr8:48199200-48205400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:48199200-48205800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr8:48199200-48206600	Weak transcription	Psoas Muscle	Psoas
18	chr8:48199200-48206800	Weak transcription	Left Ventricle	heart
19	chr8:48199200-48206800	Weak transcription	Spleen	Spleen
20	chr8:48199200-48208400	Weak transcription	Brain Angular Gyrus	brain
21	chr8:48199200-48210000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr8:48199200-48215400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:48199200-48221800	Weak transcription	NHEK	skin
24	chr8:48199200-48227800	Weak transcription	HMEC	breast
25	chr8:48199400-48205600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr8:48199400-48206800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr8:48199400-48207600	Weak transcription	Fetal Brain Male	brain
28	chr8:48199600-48205600	Weak transcription	Small Intestine	intestine
29	chr8:48199600-48209200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:48199600-48210400	Weak transcription	NHDF-Ad	bronchial
31	chr8:48199600-48215600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr8:48200000-48205400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:48200600-48209200	Strong transcription	Dnd41	blood
34	chr8:48200800-48210000	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr8:48201600-48205600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:48201600-48210000	Strong transcription	Fetal Intestine Large	intestine
37	chr8:48201800-48220600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr8:48202000-48209800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr8:48202200-48209600	Strong transcription	Liver	Liver
40	chr8:48202800-48206200	Strong transcription	Primary hematopoietic stem cells	blood
41	chr8:48202800-48208400	Strong transcription	Placenta	Placenta
42	chr8:48203000-48205600	Strong transcription	Primary B cells from cord blood	blood
43	chr8:48203000-48209600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:48203000-48210000	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr8:48203200-48208800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr8:48203200-48208800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr8:48203400-48205800	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr8:48203400-48206600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr8:48203400-48206800	Strong transcription	Fetal Lung	lung
50	chr8:48203400-48207200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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