Variant report

Variant	nsv1023786
Chromosome Location	chr8:48163412-48235252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:985)
CpG islands
(count:1037)
Chromatin interactive
region (count:48)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	chr8:48227594-48228136	K562	blood:	n/a	n/a
3	ARID3A	chr8:48173345-48173551	K562	blood:	n/a	n/a
4	ATF1	chr8:48227742-48228251	K562	blood:	n/a	n/a
5	ATF1	chr8:48170018-48170159	K562	blood:	n/a	n/a
6	BACH1	chr8:48197212-48197425	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:48173175-48173333	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr8:48173144-48173726	GM12878	blood:	n/a	chr8:48173315-48173328
9	BHLHE40	chr8:48227645-48228062	K562	blood:	n/a	n/a
10	BHLHE40	chr8:48173184-48173619	GM12878	blood:	n/a	chr8:48173473-48173489
11	BHLHE40	chr8:48227816-48228068	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:48173006-48173416	K562	blood:	n/a	n/a
13	BRCA1	chr8:48173036-48173185	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr8:48172089-48172346	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr8:48173243-48173409	HepG2	liver:	n/a	n/a
16	BRCA1	chr8:48227783-48228130	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr8:48171984-48172371	K562	blood:	n/a	n/a
18	CBX3	chr8:48199935-48200161	K562	blood:	n/a	n/a
19	CBX3	chr8:48172934-48173548	K562	blood:	n/a	n/a
20	CBX3	chr8:48227588-48228262	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:48199873-48200308	K562	blood:	n/a	n/a
22	CCNT2	chr8:48173153-48174141	K562	blood:	n/a	chr8:48173321-48173330
23	CCNT2	chr8:48227518-48227704	K562	blood:	n/a	n/a
24	CEBPB	chr8:48174819-48175122	A549	lung:	n/a	chr8:48174954-48174965
25	CEBPB	chr8:48172987-48173498	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr8:48190746-48191132	MCF-7	breast:	n/a	chr8:48190963-48190974
27	CEBPB	chr8:48207441-48207671	H1-hESC	embryonic stem cell:	n/a	chr8:48207550-48207561
28	CEBPB	chr8:48192751-48192920	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:48207411-48207734	A549	lung:	n/a	chr8:48207550-48207561
30	CEBPB	chr8:48173240-48173377	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:48190842-48191083	A549	lung:	n/a	chr8:48190963-48190974
32	CEBPB	chr8:48172906-48173339	GM12878	blood:	n/a	n/a
33	CEBPB	chr8:48207386-48207729	K562	blood:	n/a	chr8:48207550-48207561
34	CEBPB	chr8:48227117-48227285	A549	lung:	n/a	n/a
35	CEBPB	chr8:48168188-48168366	HepG2	liver:	n/a	chr8:48168277-48168288
36	CEBPB	chr8:48190749-48191119	HepG2	liver:	n/a	chr8:48190963-48190974
37	CEBPB	chr8:48190900-48191021	HepG2	liver:	n/a	chr8:48190963-48190974
38	CEBPB	chr8:48190855-48191087	Hela-S3	cervix:	n/a	chr8:48190963-48190974
39	CEBPB	chr8:48190916-48191010	K562	blood:	n/a	chr8:48190963-48190974
40	CEBPB	chr8:48190770-48191137	HepG2	liver:	n/a	chr8:48190963-48190974
41	CEBPB	chr8:48192806-48192831	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:48227790-48228019	K562	blood:	n/a	n/a
43	CEBPB	chr8:48207382-48207722	HepG2	liver:	n/a	chr8:48207550-48207561
44	CEBPB	chr8:48174782-48175139	IMR90	lung:	n/a	chr8:48174954-48174965
45	CEBPB	chr8:48174779-48175133	K562	blood:	n/a	chr8:48174954-48174965
46	CEBPB	chr8:48207384-48207718	IMR90	lung:	n/a	chr8:48207550-48207561
47	CEBPB	chr8:48174793-48175140	HepG2	liver:	n/a	chr8:48174954-48174965
48	CEBPB	chr8:48207430-48207669	Hela-S3	cervix:	n/a	chr8:48207550-48207561
49	CEBPB	chr8:48168184-48168349	K562	blood:	n/a	chr8:48168277-48168288
50	CEBPB	chr8:48192762-48192976	IMR90	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48173291-48173341	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:48172992-48173042	AG10803	skin:	n/a
3	chr8:48173930-48173980	ECC-1	luminal epithelium:	n/a
4	chr8:48226852-48226902	HIPEpiC	eye:	n/a
5	chr8:48172992-48173042	U87	brain:	n/a
6	chr8:48172889-48172939	HRE	kidney:	n/a
7	chr8:48172746-48172796	HCF	heart:	n/a
8	chr8:48176671-48176721	Hepatocyte	liver:	n/a
9	chr8:48173291-48173341	HIPEpiC	eye:	n/a
10	chr8:48174649-48174699	BE2_C	brain:	n/a
11	chr8:48172551-48172601	PANC-1	pancreas:	n/a
12	chr8:48226852-48226902	LNCaP	prostate:	n/a
13	chr8:48172746-48172796	IMR90	lung:	fetal
14	chr8:48172746-48172796	Hepatocyte	liver:	n/a
15	chr8:48173291-48173341	SKMC	muscle:	n/a
16	chr8:48172764-48172814	HepG2	liver:	n/a
17	chr8:48175416-48175466	SAEC	small airway:	n/a
18	chr8:48226852-48226902	Caco-2	colon:	n/a
19	chr8:48172746-48172796	GM12878	blood:	n/a
20	chr8:48175416-48175466	RPTEC	kidney:	n/a
21	chr8:48172372-48172422	NHBE	bronchial:	n/a
22	chr8:48174649-48174699	HRCEpiC	kidney:	n/a
23	chr8:48172283-48172333	NHDF-neo	bronchial:	n/a
24	chr8:48172551-48172601	LNCaP	prostate:	n/a
25	chr8:48169190-48169240	ProgFib	skin:	n/a
26	chr8:48172551-48172601	HCF	heart:	n/a
27	chr8:48172746-48172796	AG09319	gingival:	n/a
28	chr8:48172283-48172333	ovcar-3	ovarian:	n/a
29	chr8:48172283-48172333	HAEpiC	amniotic membrane:	n/a
30	chr8:48172318-48172368	AG04449	skin:	fetal
31	chr8:48172318-48172368	SK-N-MC	brain:	n/a
32	chr8:48174649-48174699	HCT-116	colon:	n/a
33	chr8:48169190-48169240	IMR90	lung:	fetal
34	chr8:48173610-48173660	PANC-1	pancreas:	n/a
35	chr8:48173291-48173341	HUVEC	blood vessel:	n/a
36	chr8:48172372-48172422	IMR90	lung:	fetal
37	chr8:48173610-48173660	HAEpiC	amniotic membrane:	n/a
38	chr8:48173930-48173980	SAEC	small airway:	n/a
39	chr8:48173930-48173980	GM12892	blood:	n/a
40	chr8:48172372-48172422	HMEC	breast:	n/a
41	chr8:48173610-48173660	AG09309	skin:	n/a
42	chr8:48173610-48173660	GM12878	blood:	n/a
43	chr8:48173930-48173980	HRE	kidney:	n/a
44	chr8:48176671-48176721	NH-A	brain:	n/a
45	chr8:48226852-48226902	GM12878	blood:	n/a
46	chr8:48175416-48175466	T-47D	breast:	n/a
47	chr8:48175416-48175466	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:48173930-48173980	GM12891	blood:	n/a
49	chr8:48174649-48174699	K562	blood:	n/a
50	chr8:48172318-48172368	ProgFib	skin:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48218179..48220522-chr8:48649833..48651549,2	MCF-7	breast:
2	chr8:48222519..48229115-chr8:48647530..48652731,12	MCF-7	breast:
3	chr8:48171892..48175366-chr8:48649107..48652421,3	K562	blood:
4	chr8:48118050..48120873-chr8:48168835..48170833,2	MCF-7	breast:
5	chr8:48226109..48228016-chr8:48649982..48652801,3	K562	blood:
6	chr8:48163126..48166367-chr8:48170543..48174910,6	MCF-7	breast:
7	chr8:48223569..48225954-chr8:48642409..48644484,2	MCF-7	breast:
8	chr8:48222564..48225151-chr8:48648619..48650407,2	MCF-7	breast:
9	chr8:48203786..48206533-chr8:48649304..48651747,5	MCF-7	breast:
10	chr8:48162907..48164826-chr8:48171822..48173763,2	K562	blood:
11	chr8:48173494..48174253-chr8:48651177..48651793,2	MCF-7	breast:
12	chr8:48178486..48180700-chr8:48649233..48651294,2	K562	blood:
13	chr8:48162819..48166368-chr8:48166782..48171149,5	K562	blood:
14	chr8:48171946..48174429-chr8:48608651..48611565,2	K562	blood:
15	chr8:48109425..48112056-chr8:48171977..48173853,2	MCF-7	breast:
16	chr8:48173044..48174594-chr8:48227595..48229177,2	K562	blood:
17	chr8:48162992..48165161-chr8:48171664..48174283,2	MCF-7	breast:
18	chr8:48170564..48176708-chr8:48177102..48184865,12	K562	blood:
19	chr8:48172011..48175371-chr8:48175575..48179063,4	K562	blood:
20	chr8:48170516..48173662-chr8:48648596..48652534,4	MCF-7	breast:
21	chr8:48173330..48175601-chr8:48186430..48187954,2	K562	blood:
22	chr6:35436149..35436774-chr8:48173185..48173690,2	HCT-116	colon:
23	chr8:48171681..48173345-chr8:48183568..48185714,2	K562	blood:
24	chr8:48227531..48228445-chr8:48651152..48652134,4	K562	blood:
25	chr8:48174101..48175733-chr8:48185655..48187954,2	K562	blood:
26	chr8:48185622..48188610-chr8:48189988..48193605,3	K562	blood:
27	chr8:48172185..48176708-chr8:48179293..48182899,6	K562	blood:
28	chr8:48226109..48228016-chr8:48649985..48652801,2	K562	blood:
29	chr8:48172897..48175307-chr8:48189146..48191153,2	K562	blood:
30	chr8:48171749..48177867-chr8:48180664..48186488,8	MCF-7	breast:
31	chr8:48185622..48188610-chr8:48189988..48193605,3	K562	blood:
32	chr8:48226541..48230936-chr8:48648506..48651986,13	MCF-7	breast:
33	chr2:58273888..58274399-chr8:48172813..48173680,2	NB4	blood:
34	chr8:48171890..48175874-chr8:48182718..48186660,5	MCF-7	breast:
35	chr8:48171500..48174751-chr8:48648690..48652421,4	K562	blood:
36	chr8:48174101..48175733-chr8:48185655..48187954,2	K562	blood:
37	chr8:48105045..48107718-chr8:48171845..48174415,2	MCF-7	breast:
38	chr8:48172365..48174011-chr8:48227850..48230146,2	MCF-7	breast:
39	chr8:48202864..48204570-chr8:48206625..48208490,2	K562	blood:
40	chr8:48162819..48166368-chr8:48166782..48171149,5	K562	blood:
41	chr8:48227501..48228418-chr8:48651135..48652127,2	MCF-7	breast:
42	chr8:48172897..48175307-chr8:48189146..48191153,2	K562	blood:
43	chr8:48174168..48176912-chr8:48650072..48652496,2	MCF-7	breast:
44	chr8:48171995..48173689-chr8:48187404..48189747,2	MCF-7	breast:
45	chr1:156561278..156562049-chr8:48173375..48174218,2	Hela-S3	cervix:
46	chr8:48114707..48115409-chr8:48171741..48172515,2	MCF-7	breast:
47	chr8:48171995..48173689-chr8:48187404..48189747,2	MCF-7	breast:
48	chr8:48185030..48187029-chr8:48646598..48649243,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 1666 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1666 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538963611	chr8:48163416-48163417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549455199	chr8:48163429-48163430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs139842517	chr8:48163431-48163432	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534977384	chr8:48163437-48163438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185902266	chr8:48163442-48163443	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191216192	chr8:48163497-48163498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565497238	chr8:48163530-48163531	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539148479	chr8:48163553-48163554	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183425667	chr8:48163554-48163555	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs376755563	chr8:48163663-48163664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149826739	chr8:48163682-48163683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536833213	chr8:48163683-48163684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555402833	chr8:48163687-48163688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573901669	chr8:48163689-48163690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540935618	chr8:48163777-48163778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559708277	chr8:48163811-48163812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs578038577	chr8:48163820-48163821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545556514	chr8:48163824-48163825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187964904	chr8:48163834-48163835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531153021	chr8:48163862-48163863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs76303164	chr8:48163953-48163954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561298394	chr8:48164019-48164020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs145851372	chr8:48164033-48164034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116262055	chr8:48164106-48164107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565378573	chr8:48164132-48164133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141875686	chr8:48164154-48164155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551090330	chr8:48164215-48164216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192770616	chr8:48164290-48164291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536713300	chr8:48164327-48164328	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544975686	chr8:48164348-48164349	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182094053	chr8:48164352-48164353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs187844648	chr8:48164353-48164354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192313861	chr8:48164403-48164404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145699941	chr8:48164411-48164412	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184374460	chr8:48164445-48164446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147766084	chr8:48164474-48164475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545396355	chr8:48164492-48164493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374587893	chr8:48164511-48164512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs77053618	chr8:48164513-48164514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542710230	chr8:48164587-48164588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575930044	chr8:48164618-48164619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116833712	chr8:48164629-48164630	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547317430	chr8:48164654-48164655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28393034	chr8:48164699-48164700	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115366449	chr8:48164715-48164716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190407284	chr8:48164719-48164720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192900748	chr8:48164720-48164721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544572152	chr8:48164729-48164730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185007586	chr8:48164731-48164732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548761381	chr8:48164780-48164781	Weak transcription	Chromatin interactive region	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:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

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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