Variant report

Variant	nsv1030486
Chromosome Location	chr8:48167423-48247297
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1059)
CpG islands
(count:1037)
Chromatin interactive
region (count:45)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48227759-48228098	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48243113-48243207	K562	blood:	n/a	n/a
3	ARID3A	chr8:48227594-48228136	K562	blood:	n/a	n/a
4	ARID3A	chr8:48173345-48173551	K562	blood:	n/a	n/a
5	ATF1	chr8:48227742-48228251	K562	blood:	n/a	n/a
6	ATF1	chr8:48243885-48243889	K562	blood:	n/a	n/a
7	ATF1	chr8:48170018-48170159	K562	blood:	n/a	n/a
8	BACH1	chr8:48173175-48173333	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:48197212-48197425	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr8:48173144-48173726	GM12878	blood:	n/a	chr8:48173315-48173328
11	BHLHE40	chr8:48173006-48173416	K562	blood:	n/a	n/a
12	BHLHE40	chr8:48227816-48228068	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:48173184-48173619	GM12878	blood:	n/a	chr8:48173473-48173489
14	BHLHE40	chr8:48227645-48228062	K562	blood:	n/a	n/a
15	BRCA1	chr8:48173036-48173185	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:48172089-48172346	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr8:48173243-48173409	HepG2	liver:	n/a	n/a
18	BRCA1	chr8:48227783-48228130	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr8:48235964-48236593	HCT-116	colon:	n/a	n/a
20	CBX3	chr8:48199873-48200308	K562	blood:	n/a	n/a
21	CBX3	chr8:48172934-48173548	K562	blood:	n/a	n/a
22	CBX3	chr8:48227588-48228262	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:48171984-48172371	K562	blood:	n/a	n/a
24	CBX3	chr8:48199935-48200161	K562	blood:	n/a	n/a
25	CCNT2	chr8:48173153-48174141	K562	blood:	n/a	chr8:48173321-48173330
26	CCNT2	chr8:48227518-48227704	K562	blood:	n/a	n/a
27	CEBPB	chr8:48207384-48207718	IMR90	lung:	n/a	chr8:48207550-48207561
28	CEBPB	chr8:48174793-48175140	HepG2	liver:	n/a	chr8:48174954-48174965
29	CEBPB	chr8:48207382-48207722	HepG2	liver:	n/a	chr8:48207550-48207561
30	CEBPB	chr8:48207430-48207669	Hela-S3	cervix:	n/a	chr8:48207550-48207561
31	CEBPB	chr8:48173240-48173377	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:48207416-48207678	K562	blood:	n/a	chr8:48207550-48207561
33	CEBPB	chr8:48190916-48191010	K562	blood:	n/a	chr8:48190963-48190974
34	CEBPB	chr8:48174819-48175122	A549	lung:	n/a	chr8:48174954-48174965
35	CEBPB	chr8:48227117-48227285	A549	lung:	n/a	n/a
36	CEBPB	chr8:48207386-48207729	K562	blood:	n/a	chr8:48207550-48207561
37	CEBPB	chr8:48240068-48240330	HepG2	liver:	n/a	chr8:48240207-48240218
38	CEBPB	chr8:48168188-48168366	HepG2	liver:	n/a	chr8:48168277-48168288
39	CEBPB	chr8:48190900-48191021	HepG2	liver:	n/a	chr8:48190963-48190974
40	CEBPB	chr8:48172987-48173498	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr8:48190770-48191137	HepG2	liver:	n/a	chr8:48190963-48190974
42	CEBPB	chr8:48190746-48191132	MCF-7	breast:	n/a	chr8:48190963-48190974
43	CEBPB	chr8:48227790-48228019	K562	blood:	n/a	n/a
44	CEBPB	chr8:48190749-48191119	HepG2	liver:	n/a	chr8:48190963-48190974
45	CEBPB	chr8:48174782-48175139	IMR90	lung:	n/a	chr8:48174954-48174965
46	CEBPB	chr8:48168184-48168349	K562	blood:	n/a	chr8:48168277-48168288
47	CEBPB	chr8:48240193-48240346	Hela-S3	cervix:	n/a	chr8:48240207-48240218
48	CEBPB	chr8:48174779-48175133	K562	blood:	n/a	chr8:48174954-48174965
49	CEBPB	chr8:48172906-48173339	GM12878	blood:	n/a	n/a
50	CEBPB	chr8:48190842-48191083	A549	lung:	n/a	chr8:48190963-48190974

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48172283-48172333	GM12878	blood:	n/a
2	chr8:48173280-48173330	HCM	heart:	n/a
3	chr8:48172372-48172422	AG04450	lung:	fetal
4	chr8:48175416-48175466	NB4	blood:	n/a
5	chr8:48172372-48172422	PrEC	prostate:	n/a
6	chr8:48172318-48172368	RPTEC	kidney:	n/a
7	chr8:48172283-48172333	GM12892	blood:	n/a
8	chr8:48172372-48172422	HAEpiC	amniotic membrane:	n/a
9	chr8:48172372-48172422	HRCEpiC	kidney:	n/a
10	chr8:48172746-48172796	AG10803	skin:	n/a
11	chr8:48173291-48173341	Caco-2	colon:	n/a
12	chr8:48173280-48173330	U87	brain:	n/a
13	chr8:48172889-48172939	GM06990	blood:	n/a
14	chr8:48172764-48172814	MCF-7	breast:	n/a
15	chr8:48172746-48172796	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:48173610-48173660	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:48173291-48173341	IMR90	lung:	fetal
18	chr8:48172318-48172368	H1-hESC	embryonic stem cell:	embryo
19	chr8:48173930-48173980	SK-N-SH	brain:	n/a
20	chr8:48172746-48172796	NHBE	bronchial:	n/a
21	chr8:48173930-48173980	CMK	blood:	n/a
22	chr8:48226852-48226902	HCT-116	colon:	n/a
23	chr8:48173930-48173980	AoSMC	blood vessel:	n/a
24	chr8:48226852-48226902	GM19239	blood:	n/a
25	chr8:48172889-48172939	GM12878	blood:	n/a
26	chr8:48172992-48173042	HCM	heart:	n/a
27	chr8:48172764-48172814	GM19239	blood:	n/a
28	chr8:48173930-48173980	GM06990	blood:	n/a
29	chr8:48172889-48172939	Hepatocyte	liver:	n/a
30	chr8:48174649-48174699	HCF	heart:	n/a
31	chr8:48169190-48169240	HMEC	breast:	n/a
32	chr8:48176671-48176721	HIPEpiC	eye:	n/a
33	chr8:48172318-48172368	Hepatocyte	liver:	n/a
34	chr8:48226852-48226902	IMR90	lung:	fetal
35	chr8:48173280-48173330	AG10803	skin:	n/a
36	chr8:48173280-48173330	GM12892	blood:	n/a
37	chr8:48173930-48173980	HRPEpiC	eye:	n/a
38	chr8:48174649-48174699	RPTEC	kidney:	n/a
39	chr8:48174649-48174699	K562	blood:	n/a
40	chr8:48172372-48172422	NHBE	bronchial:	n/a
41	chr8:48172992-48173042	HCT-116	colon:	n/a
42	chr8:48172992-48173042	HNPCEpiC	eye:	n/a
43	chr8:48226852-48226902	RPTEC	kidney:	n/a
44	chr8:48172764-48172814	NHBE	bronchial:	n/a
45	chr8:48173291-48173341	HUVEC	blood vessel:	n/a
46	chr8:48172746-48172796	HCT-116	colon:	n/a
47	chr8:48172764-48172814	HIPEpiC	eye:	n/a
48	chr8:48173610-48173660	SK-N-SH	brain:	n/a
49	chr8:48172283-48172333	ProgFib	skin:	n/a
50	chr8:48172283-48172333	K562	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48226109..48228016-chr8:48649982..48652801,3	K562	blood:
2	chr8:48171995..48173689-chr8:48187404..48189747,2	MCF-7	breast:
3	chr8:48173044..48174594-chr8:48227595..48229177,2	K562	blood:
4	chr8:48173494..48174253-chr8:48651177..48651793,2	MCF-7	breast:
5	chr8:48185622..48188610-chr8:48189988..48193605,3	K562	blood:
6	chr8:48162819..48166368-chr8:48166782..48171149,5	K562	blood:
7	chr8:48171681..48173345-chr8:48183568..48185714,2	K562	blood:
8	chr8:48174101..48175733-chr8:48185655..48187954,2	K562	blood:
9	chr1:156561278..156562049-chr8:48173375..48174218,2	Hela-S3	cervix:
10	chr8:48172011..48175371-chr8:48175575..48179063,4	K562	blood:
11	chr8:48114707..48115409-chr8:48171741..48172515,2	MCF-7	breast:
12	chr8:48173330..48175601-chr8:48186430..48187954,2	K562	blood:
13	chr8:48171995..48173689-chr8:48187404..48189747,2	MCF-7	breast:
14	chr8:48237525..48239836-chr8:48252461..48254752,2	MCF-7	breast:
15	chr8:48227531..48228445-chr8:48651152..48652134,4	K562	blood:
16	chr8:48203786..48206533-chr8:48649304..48651747,5	MCF-7	breast:
17	chr8:48222519..48229115-chr8:48647530..48652731,12	MCF-7	breast:
18	chr8:48172897..48175307-chr8:48189146..48191153,2	K562	blood:
19	chr8:48223569..48225954-chr8:48642409..48644484,2	MCF-7	breast:
20	chr8:48171749..48177867-chr8:48180664..48186488,8	MCF-7	breast:
21	chr8:48171946..48174429-chr8:48608651..48611565,2	K562	blood:
22	chr8:48174168..48176912-chr8:48650072..48652496,2	MCF-7	breast:
23	chr8:48118050..48120873-chr8:48168835..48170833,2	MCF-7	breast:
24	chr8:48171892..48175366-chr8:48649107..48652421,3	K562	blood:
25	chr8:48227501..48228418-chr8:48651135..48652127,2	MCF-7	breast:
26	chr8:48185030..48187029-chr8:48646598..48649243,2	K562	blood:
27	chr8:48109425..48112056-chr8:48171977..48173853,2	MCF-7	breast:
28	chr8:48105045..48107718-chr8:48171845..48174415,2	MCF-7	breast:
29	chr8:48202864..48204570-chr8:48206625..48208490,2	K562	blood:
30	chr8:48185622..48188610-chr8:48189988..48193605,3	K562	blood:
31	chr8:48170564..48176708-chr8:48177102..48184865,12	K562	blood:
32	chr6:35436149..35436774-chr8:48173185..48173690,2	HCT-116	colon:
33	chr8:48222564..48225151-chr8:48648619..48650407,2	MCF-7	breast:
34	chr8:48170516..48173662-chr8:48648596..48652534,4	MCF-7	breast:
35	chr8:48174101..48175733-chr8:48185655..48187954,2	K562	blood:
36	chr8:48171500..48174751-chr8:48648690..48652421,4	K562	blood:
37	chr8:48171890..48175874-chr8:48182718..48186660,5	MCF-7	breast:
38	chr2:58273888..58274399-chr8:48172813..48173680,2	NB4	blood:
39	chr8:48172365..48174011-chr8:48227850..48230146,2	MCF-7	breast:
40	chr8:48172897..48175307-chr8:48189146..48191153,2	K562	blood:
41	chr8:48178486..48180700-chr8:48649233..48651294,2	K562	blood:
42	chr8:48226109..48228016-chr8:48649985..48652801,2	K562	blood:
43	chr8:48226541..48230936-chr8:48648506..48651986,13	MCF-7	breast:
44	chr8:48172185..48176708-chr8:48179293..48182899,6	K562	blood:
45	chr8:48218179..48220522-chr8:48649833..48651549,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-5	chr8:48203642-48203726	NONHSAT126444
2	lnc-RP11-1134I14.8.1-5	chr8:48196617-48196683	NONHSAT126443
3	lnc-RP11-1134I14.8.1-5	chr8:48173528-48173583	NONHSAT126443
4	lnc-RP11-350F16.2.1-11	chr8:48171254-48173385	NONHSAT126441
5	lnc-RP11-1134I14.8.1-5	chr8:48192450-48192605	NONHSAT126443
6	lnc-RP11-1134I14.8.1-5	chr8:48203622-48203726	NONHSAT126443
7	lnc-RP11-1134I14.8.1-5	chr8:48206456-48206619	NONHSAT126443
8	lnc-RP11-1134I14.8.1-5	chr8:48206456-48207017	NONHSAT126444

No data

Variant related genes	Relation type
SPIDR	TF binding region
SPIDR	CpG island
ENSG00000164808	chromatin interactions
ENSG00000163382	chromatin interactions
ENSG00000028116	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000253817	chromatin interactions
ENSG00000248347	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000253502	chromatin interactions

Extended variants
information (count: 1964 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1964 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538733388	chr8:48167446-48167447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577036285	chr8:48167527-48167528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72644583	chr8:48167558-48167559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562551102	chr8:48167589-48167590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529887769	chr8:48167607-48167608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533672866	chr8:48167625-48167626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78681930	chr8:48167626-48167627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547131638	chr8:48167627-48167628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541805341	chr8:48167660-48167661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560371348	chr8:48167661-48167662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554814419	chr8:48167690-48167691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73582831	chr8:48167735-48167736	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs576498538	chr8:48167746-48167747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570482394	chr8:48167751-48167752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543801118	chr8:48167778-48167779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531704484	chr8:48167827-48167828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550242231	chr8:48167863-48167864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568609609	chr8:48168003-48168004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558996473	chr8:48168033-48168034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185023625	chr8:48168066-48168067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188339113	chr8:48168135-48168136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575549364	chr8:48168159-48168160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77542892	chr8:48168185-48168186	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs74868800	chr8:48168231-48168232	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs576866784	chr8:48168244-48168245	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544015394	chr8:48168253-48168254	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556218548	chr8:48168256-48168257	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs191618243	chr8:48168266-48168267	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs544889116	chr8:48168314-48168315	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539109433	chr8:48168537-48168538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72644585	chr8:48168555-48168556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs141831402	chr8:48168565-48168566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374366589	chr8:48168608-48168609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183824005	chr8:48168671-48168672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545643733	chr8:48168692-48168693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540799967	chr8:48168729-48168730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201434928	chr8:48168730-48168731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28496873	chr8:48168744-48168745	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531731209	chr8:48168752-48168753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550036366	chr8:48168814-48168815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568527973	chr8:48168849-48168850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528228947	chr8:48168875-48168876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188437144	chr8:48168929-48168930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547992904	chr8:48168961-48168962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566232211	chr8:48169022-48169023	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs540146267	chr8:48169023-48169024	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs73582835	chr8:48169061-48169062	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570507942	chr8:48169095-48169096	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537824873	chr8:48169179-48169180	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs79600850	chr8:48169191-48169192	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2035 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48163600-48172800	Weak transcription	Right Atrium	heart
2	chr8:48167800-48168600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr8:48168200-48168800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr8:48168400-48168800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr8:48168600-48173000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr8:48168800-48169200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr8:48168800-48169200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr8:48169000-48169200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr8:48169200-48169400	Enhancers	Primary T cells fromperipheralblood	blood
10	chr8:48169200-48169400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr8:48169200-48169400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr8:48169400-48172600	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr8:48169400-48173000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr8:48169600-48172600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr8:48170000-48170200	Enhancers	Pancreas	Pancrea
16	chr8:48170200-48172800	Weak transcription	Pancreas	Pancrea
17	chr8:48171200-48171400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr8:48171600-48172200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr8:48171800-48172000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:48171800-48172000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr8:48171800-48172200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr8:48171800-48172200	Enhancers	Stomach Smooth Muscle	stomach
23	chr8:48171800-48172600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:48171800-48172800	Enhancers	K562	blood
25	chr8:48171800-48174200	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr8:48172000-48172200	Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr8:48172000-48172400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr8:48172000-48174400	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr8:48172200-48172400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr8:48172200-48172600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:48172200-48172600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr8:48172200-48172800	Enhancers	Right Ventricle	heart
33	chr8:48172200-48174400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr8:48172400-48172600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr8:48172400-48172600	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr8:48172400-48172600	Enhancers	Dnd41	blood
37	chr8:48172400-48172800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr8:48172400-48173000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:48172400-48173000	Enhancers	Fetal Brain Male	brain
40	chr8:48172400-48174000	Active TSS	Liver	Liver
41	chr8:48172400-48174600	Active TSS	H1 Cell Line	embryonic stem cell
42	chr8:48172600-48172800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:48172600-48172800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:48172600-48172800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr8:48172600-48172800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr8:48172600-48172800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr8:48172600-48172800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:48172600-48172800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:48172600-48172800	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr8:48172600-48172800	Enhancers	Colonic Mucosa	Colon

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