Variant report

Variant	nsv1031119
Chromosome Location	chr8:111367939-111720763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:871)
CpG islands
(count:61)
Chromatin interactive
region (count:80)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111370803-111370846	K562	blood:	n/a	n/a
2	BACH1	chr8:111523582-111523674	K562	blood:	n/a	n/a
3	BACH1	chr8:111719799-111719982	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:111380515-111380775	GM12878	blood:	n/a	n/a
5	BATF	chr8:111380529-111380748	GM12878	blood:	n/a	n/a
6	BCL3	chr8:111719822-111720092	GM12878	blood:	n/a	n/a
7	CEBPB	chr8:111563777-111564088	HepG2	liver:	n/a	chr8:111563940-111563951
8	CEBPB	chr8:111407619-111407631	K562	blood:	n/a	n/a
9	CEBPB	chr8:111470060-111470420	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr8:111623432-111623641	MCF-7	breast:	n/a	n/a
11	CEBPB	chr8:111655159-111655467	HepG2	liver:	n/a	chr8:111655308-111655319
12	CEBPB	chr8:111688373-111688402	K562	blood:	n/a	n/a
13	CEBPB	chr8:111485063-111485373	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:111605973-111606139	HepG2	liver:	n/a	chr8:111606013-111606024
15	CEBPB	chr8:111551859-111552317	MCF-7	breast:	n/a	n/a
16	CEBPB	chr8:111392636-111392756	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr8:111678139-111678458	HepG2	liver:	n/a	chr8:111678273-111678284
18	CEBPB	chr8:111663840-111664346	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:111714073-111714166	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:111407057-111407265	HepG2	liver:	n/a	chr8:111407125-111407136
21	CEBPB	chr8:111470033-111470437	MCF-7	breast:	n/a	n/a
22	CEBPB	chr8:111503758-111503941	H1-hESC	embryonic stem cell:	n/a	chr8:111503888-111503901 chr8:111503888-111503899 chr8:111503889-111503900 chr8:111503888-111503901 chr8:111503888-111503901 chr8:111503888-111503899
23	CEBPB	chr8:111684904-111685112	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:111634989-111635163	HepG2	liver:	n/a	chr8:111635032-111635043
25	CEBPB	chr8:111425593-111425738	A549	lung:	n/a	n/a
26	CEBPB	chr8:111580266-111580852	MCF-7	breast:	n/a	chr8:111580459-111580472
27	CEBPB	chr8:111678183-111678436	A549	lung:	n/a	chr8:111678273-111678284
28	CEBPB	chr8:111663882-111664226	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:111525002-111525202	HepG2	liver:	n/a	chr8:111525140-111525151 chr8:111525141-111525150 chr8:111525139-111525150
30	CEBPB	chr8:111708632-111709146	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:111563640-111564025	MCF-7	breast:	n/a	chr8:111563940-111563951
32	CEBPB	chr8:111520325-111520598	HepG2	liver:	n/a	chr8:111520458-111520471 chr8:111520458-111520471 chr8:111520460-111520471 chr8:111520460-111520469 chr8:111520458-111520469
33	CEBPB	chr8:111663794-111664226	MCF-7	breast:	n/a	n/a
34	CEBPB	chr8:111688332-111688445	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:111573269-111573432	A549	lung:	n/a	n/a
36	CEBPB	chr8:111485138-111485350	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:111599789-111599997	HepG2	liver:	n/a	chr8:111599955-111599967 chr8:111599861-111599872
38	CEBPB	chr8:111566321-111566477	A549	lung:	n/a	chr8:111566413-111566424
39	CEBPB	chr8:111599775-111599936	K562	blood:	n/a	chr8:111599861-111599872
40	CEBPB	chr8:111505335-111505447	A549	lung:	n/a	chr8:111505347-111505358 chr8:111505411-111505422
41	CEBPB	chr8:111673382-111673531	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:111563470-111564178	MCF-7	breast:	n/a	chr8:111563940-111563951
43	CEBPB	chr8:111630967-111631208	HepG2	liver:	n/a	chr8:111631031-111631042
44	CEBPB	chr8:111634949-111635197	IMR90	lung:	n/a	chr8:111635032-111635043
45	CEBPB	chr8:111505352-111505461	HepG2	liver:	n/a	chr8:111505411-111505422
46	CEBPB	chr8:111655239-111655443	H1-hESC	embryonic stem cell:	n/a	chr8:111655308-111655319
47	CEBPB	chr8:111469908-111470608	MCF-7	breast:	n/a	n/a
48	CEBPB	chr8:111566370-111566428	HepG2	liver:	n/a	chr8:111566413-111566424
49	CEBPB	chr8:111708552-111709216	IMR90	lung:	n/a	n/a
50	CEBPB	chr8:111539090-111539260	H1-hESC	embryonic stem cell:	n/a	chr8:111539185-111539196 chr8:111539167-111539178

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111707758-111707808	BE2_C	brain:	n/a
2	chr8:111707758-111707808	HRCEpiC	kidney:	n/a
3	chr8:111707758-111707808	H1-hESC	embryonic stem cell:	embryo
4	chr8:111707758-111707808	SK-N-SH	brain:	n/a
5	chr8:111707758-111707808	RPTEC	kidney:	n/a
6	chr8:111707758-111707808	HRE	kidney:	n/a
7	chr8:111707758-111707808	SK-N-MC	brain:	n/a
8	chr8:111707758-111707808	HRPEpiC	eye:	n/a
9	chr8:111707758-111707808	HCPEpiC	choroid plexus:	n/a
10	chr8:111707758-111707808	K562	blood:	n/a
11	chr8:111707758-111707808	HCM	heart:	n/a
12	chr8:111707758-111707808	NHDF-neo	bronchial:	n/a
13	chr8:111707758-111707808	AG04450	lung:	fetal
14	chr8:111707758-111707808	NHBE	bronchial:	n/a
15	chr8:111707758-111707808	ECC-1	luminal epithelium:	n/a
16	chr8:111707758-111707808	NH-A	brain:	n/a
17	chr8:111707758-111707808	LNCaP	prostate:	n/a
18	chr8:111707758-111707808	Hepatocyte	liver:	n/a
19	chr8:111707758-111707808	PANC-1	pancreas:	n/a
20	chr8:111707758-111707808	HCT-116	colon:	n/a
21	chr8:111707758-111707808	AG09319	gingival:	n/a
22	chr8:111707758-111707808	BJ	skin:	n/a
23	chr8:111707758-111707808	PrEC	prostate:	n/a
24	chr8:111707758-111707808	HMEC	breast:	n/a
25	chr8:111707758-111707808	U87	brain:	n/a
26	chr8:111707758-111707808	HepG2	liver:	n/a
27	chr8:111707758-111707808	CMK	blood:	n/a
28	chr8:111707758-111707808	GM12892	blood:	n/a
29	chr8:111707758-111707808	AG10803	skin:	n/a
30	chr8:111707758-111707808	Hela-S3	cervix:	n/a
31	chr8:111707758-111707808	HUVEC	blood vessel:	n/a
32	chr8:111707758-111707808	NB4	blood:	n/a
33	chr8:111707758-111707808	HL-60	blood:	n/a
34	chr8:111707758-111707808	GM12878	blood:	n/a
35	chr8:111707758-111707808	AoSMC	blood vessel:	n/a
36	chr8:111707758-111707808	NT2-D1	testis:	n/a
37	chr8:111707758-111707808	PFSK-1	brain:	n/a
38	chr8:111707758-111707808	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:111707758-111707808	HNPCEpiC	eye:	n/a
40	chr8:111707758-111707808	GM19239	blood:	n/a
41	chr8:111707758-111707808	MCF-7	breast:	n/a
42	chr8:111707758-111707808	SK-N-SH_RA	brain:	n/a
43	chr8:111707758-111707808	SKMC	muscle:	n/a
44	chr8:111707758-111707808	HIPEpiC	eye:	n/a
45	chr8:111707758-111707808	A549	lung:	n/a
46	chr8:111707758-111707808	Caco-2	colon:	n/a
47	chr8:111707758-111707808	GM12891	blood:	n/a
48	chr8:111707758-111707808	GM06990	blood:	n/a
49	chr8:111707758-111707808	IMR90	lung:	fetal
50	chr8:111707758-111707808	HEK293	kidney:	embryo

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:111564377..111566155-chr8:111573076..111575001,2	MCF-7	breast:
2	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:
3	chr17:41466208..41468149-chr8:111587283..111588803,2	K562	blood:
4	chr8:111426432..111429583-chr8:111430116..111432569,3	MCF-7	breast:
5	chr8:111563681..111564416-chr8:111663211..111663982,2	MCF-7	breast:
6	chr20:47537126..47538714-chr8:111554238..111556097,2	MCF-7	breast:
7	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:
8	chr8:111614672..111616882-chr8:111628243..111630115,2	MCF-7	breast:
9	chr8:111632530..111634212-chr8:111646106..111648334,2	MCF-7	breast:
10	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
11	chr7:153439451..153439951-chr8:111669137..111669684,2	MCF-7	breast:
12	chr8:111663406..111666569-chr8:111666819..111669452,4	MCF-7	breast:
13	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
14	chr8:111663406..111666569-chr8:111666819..111669452,4	MCF-7	breast:
15	chr8:111561274..111563938-chr8:111668171..111670064,2	MCF-7	breast:
16	chr8:111676345..111679299-chr8:111684096..111685867,2	MCF-7	breast:
17	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
18	chr8:111561274..111563938-chr8:111668171..111670064,2	MCF-7	breast:
19	chr8:111629561..111631393-chr8:111634350..111636471,2	MCF-7	breast:
20	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
21	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
22	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
23	chr8:111519159..111521111-chr8:111524177..111525688,2	MCF-7	breast:
24	chr8:111669709..111671243-chr8:111673107..111675313,2	MCF-7	breast:
25	chr8:111668947..111669607-chr8:111877933..111878646,3	MCF-7	breast:
26	chr8:111594065..111596990-chr8:111668768..111671358,2	MCF-7	breast:
27	chr8:111564377..111566155-chr8:111573076..111575001,2	MCF-7	breast:
28	chr8:111597648..111599475-chr8:111601535..111603940,2	MCF-7	breast:
29	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
30	chr2:189912462..189915135-chr8:111597995..111599883,2	MCF-7	breast:
31	chr22:21987659..21988468-chr8:111631630..111632515,2	MCF-7	breast:
32	chr11:74302754..74304460-chr8:111676552..111678415,2	MCF-7	breast:
33	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
34	chr8:111444766..111447245-chr8:111451075..111453827,2	K562	blood:
35	chr8:111426582..111428380-chr8:111435676..111438119,2	K562	blood:
36	chr8:111661559..111663835-chr8:111734745..111737537,2	MCF-7	breast:
37	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
38	chr8:37622904..37623517-chr8:111713671..111714213,2	MCF-7	breast:
39	chr8:111606860..111609172-chr8:111612437..111615361,2	K562	blood:
40	chr8:111712144..111713669-chr8:111724852..111727560,2	MCF-7	breast:
41	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
42	chr8:111519159..111521111-chr8:111524177..111525688,2	MCF-7	breast:
43	chr8:111581974..111583484-chr8:111589126..111591939,2	MCF-7	breast:
44	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
45	chr8:111581974..111583484-chr8:111589126..111591939,2	MCF-7	breast:
46	chr8:111689286..111692174-chr8:111701872..111704181,2	MCF-7	breast:
47	chr8:111100909..111103732-chr8:111408499..111410564,2	K562	blood:
48	chr8:111669709..111671243-chr8:111673107..111675313,2	MCF-7	breast:
49	chr6:47444917..47447011-chr8:111717811..111719807,2	MCF-7	breast:
50	chr8:111551159..111553132-chr8:111554691..111557321,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-5	chr8:111567637-111568747	NONHSAT128309

No data

Variant related genes	Relation type
ENSG00000253107	TF binding region
ENSG00000253122	TF binding region
ENSG00000253107	CpG island
ENSG00000253122	CpG island
ENSG00000188825	chromatin interactions
ENSG00000198087	chromatin interactions
ENSG00000253122	chromatin interactions
ENSG00000077514	chromatin interactions
ENSG00000243479	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000270761	chromatin interactions
ENSG00000130675	chromatin interactions

Extended variants
information (count: 4798 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4798 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553107174	chr8:111367961-111367962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73316014	chr8:111368058-111368059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541334690	chr8:111368065-111368066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564418062	chr8:111368086-111368087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74636230	chr8:111368113-111368114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187825233	chr8:111368121-111368122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563470132	chr8:111368134-111368135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576482311	chr8:111368141-111368142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528996683	chr8:111368147-111368148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374625230	chr8:111368152-111368153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191317563	chr8:111368229-111368230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546718368	chr8:111368232-111368233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150096511	chr8:111368263-111368264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115095203	chr8:111368285-111368286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112087205	chr8:111368319-111368320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs16880637	chr8:111368325-111368326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571644973	chr8:111368336-111368337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537323733	chr8:111368339-111368340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183182753	chr8:111368341-111368342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567811709	chr8:111368363-111368364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548940260	chr8:111368471-111368472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377134152	chr8:111368504-111368505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536355242	chr8:111368570-111368571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553384280	chr8:111368600-111368601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535605257	chr8:111368639-111368640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373630821	chr8:111368691-111368692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573370170	chr8:111368714-111368715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187450003	chr8:111368732-111368733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539076624	chr8:111368762-111368763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367802666	chr8:111368773-111368774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138361798	chr8:111368776-111368777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562546681	chr8:111368788-111368789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374466078	chr8:111368793-111368794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191918209	chr8:111368838-111368839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369546622	chr8:111368897-111368898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201555904	chr8:111368904-111368905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531990995	chr8:111368920-111368921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74617447	chr8:111368986-111368987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184725153	chr8:111368999-111369000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142266337	chr8:111369026-111369027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559064288	chr8:111369037-111369038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528160025	chr8:111369097-111369098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562072957	chr8:111369114-111369115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550992499	chr8:111369175-111369176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187946630	chr8:111369248-111369249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531124102	chr8:111369267-111369268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377271990	chr8:111369308-111369309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551213119	chr8:111369343-111369344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34718020	chr8:111369353-111369354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs28619007	chr8:111369373-111369374	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111354800-111380600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:111380600-111380800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:111413400-111413800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr8:111413600-111414000	Enhancers	Fetal Intestine Small	intestine
5	chr8:111459800-111460000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:111460600-111460800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:111464200-111464600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:111464200-111464800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr8:111464200-111464800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr8:111464200-111464800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:111464600-111465400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:111465400-111466600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:111466600-111467200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:111466800-111467200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr8:111469200-111469400	Enhancers	Placenta Amnion	Placenta Amnion
16	chr8:111469600-111470600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr8:111469800-111470400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:111469800-111470600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr8:111469800-111471000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:111469800-111471000	Enhancers	HMEC	breast
21	chr8:111469800-111471200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:111470000-111470600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:111470200-111470600	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr8:111470400-111471200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:111470600-111471000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr8:111472000-111472800	Enhancers	Fetal Heart	heart
27	chr8:111472400-111472600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr8:111472600-111472800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:111472600-111473400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr8:111473000-111474000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:111473200-111474200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:111474000-111474400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:111496800-111497800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:111520400-111521600	Enhancers	HUVEC	blood vessel
35	chr8:111521200-111522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:111521400-111521800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:111521400-111521800	Enhancers	Colon Smooth Muscle	Colon
38	chr8:111521400-111522000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:111521400-111522000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:111521400-111522000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr8:111521600-111522000	Flanking Active TSS	HUVEC	blood vessel
42	chr8:111522000-111522400	Enhancers	HUVEC	blood vessel
43	chr8:111533400-111533800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:111535000-111535400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr8:111535000-111535400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr8:111535200-111535600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr8:111537800-111538400	Enhancers	Placenta Amnion	Placenta Amnion
48	chr8:111538400-111538800	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr8:111538800-111539200	Enhancers	Placenta Amnion	Placenta Amnion
50	chr8:111548600-111550200	Active TSS	Right Atrium	heart

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