Variant report

Variant	nsv890848
Chromosome Location	chr8:48405007-48535622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1491)
CpG islands
(count:489)
Chromatin interactive
region (count:75)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48437168-48437824	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48521014-48521055	K562	blood:	n/a	n/a
3	ARID3A	chr8:48425108-48425339	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48469558-48470236	K562	blood:	n/a	n/a
5	ARID3A	chr8:48531522-48531916	HepG2	liver:	n/a	n/a
6	ATF1	chr8:48456323-48456522	K562	blood:	n/a	n/a
7	ATF1	chr8:48444199-48444363	K562	blood:	n/a	n/a
8	ATF1	chr8:48469791-48470208	K562	blood:	n/a	n/a
9	ATF2	chr8:48510510-48511070	GM12878	blood:	n/a	n/a
10	ATF2	chr8:48510596-48510973	GM12878	blood:	n/a	n/a
11	ATF2	chr8:48513192-48513727	GM12878	blood:	n/a	n/a
12	ATF2	chr8:48424919-48425438	H1-hESC	embryonic stem cell:	n/a	chr8:48425190-48425201
13	ATF2	chr8:48426005-48426751	GM12878	blood:	n/a	n/a
14	ATF2	chr8:48424960-48425389	H1-hESC	embryonic stem cell:	n/a	chr8:48425190-48425201
15	ATF2	chr8:48426073-48426690	GM12878	blood:	n/a	n/a
16	ATF3	chr8:48424961-48425457	A549	lung:	n/a	chr8:48425192-48425202 chr8:48425189-48425202 chr8:48425192-48425199 chr8:48425188-48425203 chr8:48425189-48425199 chr8:48425190-48425201 chr8:48425192-48425200 chr8:48425188-48425201 chr8:48425189-48425199 chr8:48425189-48425202 chr8:48425192-48425202 chr8:48425190-48425201 chr8:48425190-48425203 chr8:48425189-48425200
17	ATF3	chr8:48510675-48511007	K562	blood:	n/a	n/a
18	ATF3	chr8:48424988-48425460	A549	lung:	n/a	chr8:48425192-48425202 chr8:48425189-48425202 chr8:48425192-48425199 chr8:48425188-48425203 chr8:48425189-48425199 chr8:48425190-48425201 chr8:48425192-48425200 chr8:48425188-48425201 chr8:48425189-48425199 chr8:48425189-48425202 chr8:48425192-48425202 chr8:48425190-48425201 chr8:48425190-48425203 chr8:48425189-48425200
19	BACH1	chr8:48426078-48426349	K562	blood:	n/a	chr8:48426195-48426209
20	BACH1	chr8:48425999-48426602	H1-hESC	embryonic stem cell:	n/a	chr8:48426195-48426209
21	BACH1	chr8:48520911-48521193	K562	blood:	n/a	n/a
22	BATF	chr8:48510586-48511006	GM12878	blood:	n/a	n/a
23	BATF	chr8:48513236-48513693	GM12878	blood:	n/a	chr8:48513437-48513448
24	BATF	chr8:48510570-48510905	GM12878	blood:	n/a	n/a
25	BATF	chr8:48426321-48426864	GM12878	blood:	n/a	n/a
26	BATF	chr8:48513237-48513650	GM12878	blood:	n/a	chr8:48513437-48513448
27	BATF	chr8:48426328-48426884	GM12878	blood:	n/a	n/a
28	BATF	chr8:48426050-48426304	GM12878	blood:	n/a	chr8:48426194-48426205 chr8:48426195-48426205
29	BATF	chr8:48420269-48420728	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:48510631-48510906	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:48486889-48487113	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:48510615-48510929	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:48513234-48513581	GM12878	blood:	n/a	n/a
34	BCL3	chr8:48424834-48425773	A549	lung:	n/a	chr8:48425167-48425176
35	BCL3	chr8:48424904-48425461	A549	lung:	n/a	chr8:48425167-48425176
36	BCL3	chr8:48438582-48439175	A549	lung:	n/a	n/a
37	BCL3	chr8:48437323-48438105	A549	lung:	n/a	n/a
38	BCL3	chr8:48422245-48422583	GM12878	blood:	n/a	n/a
39	BCL3	chr8:48437371-48437990	A549	lung:	n/a	n/a
40	BCL3	chr8:48425843-48426604	A549	lung:	n/a	n/a
41	BHLHE40	chr8:48515128-48515535	GM12878	blood:	n/a	n/a
42	BHLHE40	chr8:48513269-48513679	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:48421174-48421309	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:48469788-48470117	K562	blood:	n/a	n/a
45	BHLHE40	chr8:48510587-48511026	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:48426233-48426728	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:48486816-48487206	GM12878	blood:	n/a	n/a
48	BRCA1	chr8:48425996-48426067	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr8:48425001-48425515	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr8:48458025-48458261	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48437852-48437902	HRPEpiC	eye:	n/a
2	chr8:48437852-48437902	HRPEpiC	eye:	n/a
3	chr8:48427018-48427068	HRPEpiC	eye:	n/a
4	chr8:48437852-48437902	HAEpiC	amniotic membrane:	n/a
5	chr8:48418189-48418239	HEK293	kidney:	embryo
6	chr8:48474400-48474450	HRCEpiC	kidney:	n/a
7	chr8:48517420-48517470	Hela-S3	cervix:	n/a
8	chr8:48437852-48437902	NHBE	bronchial:	n/a
9	chr8:48427018-48427068	SK-N-MC	brain:	n/a
10	chr8:48437852-48437902	HCF	heart:	n/a
11	chr8:48474400-48474450	NT2-D1	testis:	n/a
12	chr8:48523498-48523548	GM19239	blood:	n/a
13	chr8:48474400-48474450	Jurkat	blood:	n/a
14	chr8:48437852-48437902	HepG2	liver:	n/a
15	chr8:48427018-48427068	HEEpiC	esophagus:	n/a
16	chr8:48523498-48523548	Hepatocyte	liver:	n/a
17	chr8:48523498-48523548	BJ	skin:	n/a
18	chr8:48517420-48517470	NT2-D1	testis:	n/a
19	chr8:48486091-48486141	HRPEpiC	eye:	n/a
20	chr8:48418189-48418239	RPTEC	kidney:	n/a
21	chr8:48418220-48418270	SK-N-SH	brain:	n/a
22	chr8:48418220-48418270	SKMC	muscle:	n/a
23	chr8:48437852-48437902	IMR90	lung:	fetal
24	chr8:48437852-48437902	GM12892	blood:	n/a
25	chr8:48418220-48418270	GM12878	blood:	n/a
26	chr8:48523498-48523548	NB4	blood:	n/a
27	chr8:48437852-48437902	PFSK-1	brain:	n/a
28	chr8:48474400-48474450	SAEC	small airway:	n/a
29	chr8:48486091-48486141	AG09309	skin:	n/a
30	chr8:48427018-48427068	HCPEpiC	choroid plexus:	n/a
31	chr8:48437852-48437902	AG04449	skin:	fetal
32	chr8:48418220-48418270	T-47D	breast:	n/a
33	chr8:48474400-48474450	PFSK-1	brain:	n/a
34	chr8:48523498-48523548	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:48437852-48437902	HEK293	kidney:	embryo
36	chr8:48418220-48418270	HCM	heart:	n/a
37	chr8:48437852-48437902	BJ	skin:	n/a
38	chr8:48523498-48523548	NHDF-neo	bronchial:	n/a
39	chr8:48427018-48427068	GM12892	blood:	n/a
40	chr8:48418220-48418270	HCT-116	colon:	n/a
41	chr8:48474400-48474450	NHDF-neo	bronchial:	n/a
42	chr8:48474400-48474450	SK-N-SH	brain:	n/a
43	chr8:48427018-48427068	SKMC	muscle:	n/a
44	chr8:48437852-48437902	SAEC	small airway:	n/a
45	chr8:48437852-48437902	AG09319	gingival:	n/a
46	chr8:48474400-48474450	AG09309	skin:	n/a
47	chr8:48418220-48418270	Hela-S3	cervix:	n/a
48	chr8:48523498-48523548	SKMC	muscle:	n/a
49	chr8:48486091-48486141	GM06990	blood:	n/a
50	chr8:48517420-48517470	H1-hESC	embryonic stem cell:	embryo

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48425858..48428805-chr8:48433583..48436429,2	MCF-7	breast:
2	chr8:48435895..48437509-chr8:48455733..48457442,2	MCF-7	breast:
3	chr8:48529219..48530791-chr8:48540316..48542801,2	MCF-7	breast:
4	chr8:48441687..48444204-chr8:48648313..48651863,3	MCF-7	breast:
5	chr8:48423448..48424045-chr8:48651002..48651682,2	MCF-7	breast:
6	chr8:48404469..48406419-chr8:48408750..48411124,2	K562	blood:
7	chr8:48430923..48433623-chr8:48450374..48452837,2	MCF-7	breast:
8	chr8:48433892..48441630-chr8:48644198..48652247,18	MCF-7	breast:
9	chr8:48428692..48431572-chr8:48649357..48651752,3	MCF-7	breast:
10	chr8:48424864..48427564-chr8:48437009..48439123,4	MCF-7	breast:
11	chr8:48431409..48434183-chr8:48649405..48651632,3	K562	blood:
12	chr8:48435448..48437603-chr8:48438806..48441568,2	K562	blood:
13	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
14	chr6:54711853..54714484-chr8:48522444..48524308,2	MCF-7	breast:
15	chr8:48493147..48494925-chr8:48494980..48497854,3	MCF-7	breast:
16	chr8:48518671..48521335-chr8:48522262..48524014,3	MCF-7	breast:
17	chr8:48467740..48469374-chr8:48475967..48477813,2	K562	blood:
18	chr8:48432437..48435065-chr8:48648132..48650719,4	MCF-7	breast:
19	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
20	chr8:48431010..48432979-chr8:48435160..48436961,2	K562	blood:
21	chr8:48421398..48423203-chr8:48423816..48426679,2	K562	blood:
22	chr8:48518671..48521335-chr8:48522262..48524014,3	MCF-7	breast:
23	chr8:48404469..48406419-chr8:48408750..48411124,2	K562	blood:
24	chr8:48518004..48520090-chr8:48648537..48650198,2	K562	blood:
25	chr8:48456575..48460862-chr8:48649112..48652176,5	MCF-7	breast:
26	chr8:48436683..48438383-chr8:48633840..48636736,2	MCF-7	breast:
27	chr8:48493400..48495648-chr8:48645566..48647459,2	MCF-7	breast:
28	chr8:48435225..48441849-chr8:48646333..48652657,17	MCF-7	breast:
29	chr8:48524955..48527562-chr8:48528831..48532011,3	K562	blood:
30	chr8:48417465..48419958-chr8:48587324..48588844,2	MCF-7	breast:
31	chr8:48430923..48433623-chr8:48450374..48452837,2	MCF-7	breast:
32	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
33	chr8:48529361..48531739-chr8:48533390..48535611,4	K562	blood:
34	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
35	chr8:48431010..48432979-chr8:48435160..48436961,2	K562	blood:
36	chr8:48492643..48494808-chr8:48494843..48497616,2	K562	blood:
37	chr8:48468813..48471018-chr8:48483021..48485795,2	K562	blood:
38	chr8:48425055..48429090-chr8:48432986..48438786,8	MCF-7	breast:
39	chr8:48524955..48527562-chr8:48528831..48532011,3	K562	blood:
40	chr8:48409859..48412795-chr8:48648152..48651126,2	MCF-7	breast:
41	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
42	chr8:48467740..48469374-chr8:48475967..48477813,2	K562	blood:
43	chr8:48425858..48428805-chr8:48433583..48436429,2	MCF-7	breast:
44	chr8:48453211..48456325-chr8:48648153..48651831,4	MCF-7	breast:
45	chr8:48417772..48429044-chr8:48646094..48652486,42	MCF-7	breast:
46	chr8:48430927..48433174-chr8:48436968..48438708,2	K562	blood:
47	chr8:48455185..48457892-chr8:48651011..48653495,2	K562	blood:
48	chr8:48492643..48494808-chr8:48494843..48497616,2	K562	blood:
49	chr8:48489348..48491815-chr8:48492654..48494861,2	K562	blood:
50	chr8:48489915..48491427-chr8:48495181..48498031,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-7	chr8:48439959-48440710	ENSG00000269924.1
2	lnc-CEBPD-3	chr8:48460313-48460488	NONHSAT126450
3	lnc-CEBPD-2	chr8:48504709-48505171	NONHSAT126451
4	lnc-CEBPD-3	chr8:48459366-48459968	NONHSAT126450

No data

Variant related genes	Relation type
ENSG00000254065	TF binding region
ENSG00000253330	TF binding region
ENSG00000269924	TF binding region
ENSG00000251354	TF binding region
ENSG00000254065	CpG island
ENSG00000253330	CpG island
ENSG00000269924	CpG island
ENSG00000251354	CpG island
ENSG00000253330	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000168264	chromatin interactions
ENSG00000164808	chromatin interactions
ENSG00000254065	chromatin interactions
ENSG00000269924	chromatin interactions

Extended variants
information (count: 4455 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4455 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551872352	chr8:48405014-48405015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569914899	chr8:48405022-48405023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182289681	chr8:48405025-48405026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187208513	chr8:48405115-48405116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145655702	chr8:48405149-48405150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190082631	chr8:48405158-48405159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574447252	chr8:48405159-48405160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555737507	chr8:48405203-48405204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574384437	chr8:48405209-48405210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535381486	chr8:48405264-48405265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553589875	chr8:48405279-48405280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540274428	chr8:48405296-48405297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35934809	chr8:48405327-48405328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1106607	chr8:48405343-48405344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs377091336	chr8:48405370-48405371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545555100	chr8:48405387-48405388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557852121	chr8:48405389-48405390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575909433	chr8:48405488-48405489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181670360	chr8:48405497-48405498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs68018626	chr8:48405579-48405580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs71895713	chr8:48405590-48405591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200384514	chr8:48405598-48405599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs137950730	chr8:48405600-48405601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142222611	chr8:48405602-48405603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377312676	chr8:48405604-48405605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs398047209	chr8:48405605-48405606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529133852	chr8:48405606-48405607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60518877	chr8:48405637-48405638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540952968	chr8:48405653-48405654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs559092710	chr8:48405655-48405656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147707179	chr8:48405662-48405663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551052634	chr8:48405729-48405730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117485165	chr8:48405745-48405746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186043148	chr8:48405818-48405819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190359100	chr8:48405823-48405824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373149893	chr8:48405846-48405847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562740639	chr8:48405867-48405868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531543939	chr8:48405869-48405870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71527675	chr8:48405891-48405892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140544307	chr8:48406042-48406043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549349985	chr8:48406045-48406046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371007159	chr8:48406098-48406099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567698107	chr8:48406118-48406119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548035001	chr8:48406172-48406173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149197390	chr8:48406214-48406215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571837182	chr8:48406257-48406258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539234105	chr8:48406266-48406267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557525243	chr8:48406277-48406278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78068286	chr8:48406280-48406281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143376125	chr8:48406286-48406287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:2317 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48374800-48407000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:48393400-48410400	Weak transcription	Ovary	ovary
3	chr8:48394200-48419800	Weak transcription	Pancreas	Pancrea
4	chr8:48397600-48419400	Weak transcription	Primary T cells from cord blood	blood
5	chr8:48397600-48426400	Weak transcription	Aorta	Aorta
6	chr8:48397800-48406200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr8:48397800-48406600	Weak transcription	Esophagus	oesophagus
8	chr8:48397800-48410200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:48397800-48410600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr8:48397800-48417600	Weak transcription	Gastric	stomach
11	chr8:48397800-48418200	Weak transcription	Dnd41	blood
12	chr8:48398000-48407200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr8:48398200-48410400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr8:48398200-48417400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:48398200-48420000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:48398200-48421600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr8:48398400-48411000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:48398400-48411600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr8:48398600-48407200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr8:48398600-48417600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:48398800-48423400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:48399000-48408800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:48399000-48411200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:48401400-48417400	Weak transcription	Fetal Intestine Small	intestine
25	chr8:48402200-48417600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr8:48404200-48405400	Enhancers	Fetal Muscle Leg	muscle
27	chr8:48404200-48405800	Enhancers	Fetal Lung	lung
28	chr8:48404400-48405200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:48404400-48405600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:48404600-48405400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:48404800-48405200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr8:48404800-48421200	Weak transcription	Lung	lung
33	chr8:48405200-48409000	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr8:48405800-48409800	Weak transcription	Fetal Lung	lung
35	chr8:48406600-48406800	Enhancers	Esophagus	oesophagus
36	chr8:48407200-48407800	Enhancers	Primary B cells from peripheral blood	blood
37	chr8:48407200-48407800	Enhancers	GM12878-XiMat	blood
38	chr8:48407200-48407800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr8:48407200-48408000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr8:48407400-48407800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr8:48407800-48408800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr8:48407800-48415000	Weak transcription	GM12878-XiMat	blood
43	chr8:48407800-48418600	Weak transcription	Primary B cells from peripheral blood	blood
44	chr8:48408000-48408400	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr8:48408400-48412000	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr8:48408800-48409000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:48408800-48410200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr8:48409000-48411800	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr8:48409200-48410400	Weak transcription	Brain Angular Gyrus	brain
50	chr8:48409400-48410400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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