Variant report

Variant	nsv1033617
Chromosome Location	chr8:124895516-125012783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1302)
CpG islands
(count:245)
Chromatin interactive
region (count:155)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1302 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:124936921-124937187	K562	blood:	n/a	n/a
2	ARID3A	chr8:124992129-124992436	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:124934337-124934926	K562	blood:	n/a	n/a
4	ARID3A	chr8:124919494-124919620	K562	blood:	n/a	n/a
5	ATF1	chr8:124934300-124934928	K562	blood:	n/a	n/a
6	ATF1	chr8:124974401-124974848	K562	blood:	n/a	n/a
7	ATF1	chr8:124919325-124919764	K562	blood:	n/a	n/a
8	ATF1	chr8:124936946-124937183	K562	blood:	n/a	n/a
9	ATF3	chr8:124934307-124934642	K562	blood:	n/a	n/a
10	ATF3	chr8:124934322-124934836	K562	blood:	n/a	n/a
11	ATF3	chr8:124940522-124940729	K562	blood:	n/a	n/a
12	BACH1	chr8:124934457-124934640	K562	blood:	n/a	n/a
13	BCL3	chr8:124969824-124970343	A549	lung:	n/a	n/a
14	BCL3	chr8:124965147-124965633	A549	lung:	n/a	n/a
15	BCL3	chr8:124991926-124992640	A549	lung:	n/a	n/a
16	BCL3	chr8:124969710-124970348	A549	lung:	n/a	n/a
17	BHLHE40	chr8:124974645-124974785	K562	blood:	n/a	n/a
18	BHLHE40	chr8:124989365-124989664	K562	blood:	n/a	n/a
19	BHLHE40	chr8:124934284-124934649	HepG2	liver:	n/a	chr8:124934468-124934484
20	BHLHE40	chr8:124953507-124953714	K562	blood:	n/a	n/a
21	BHLHE40	chr8:124996803-124996942	K562	blood:	n/a	n/a
22	BHLHE40	chr8:124934159-124934969	K562	blood:	n/a	chr8:124934468-124934484 chr8:124934821-124934837
23	BHLHE40	chr8:124919628-124919659	K562	blood:	n/a	n/a
24	BRCA1	chr8:124993021-124993071	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr8:124940433-124940765	K562	blood:	n/a	n/a
26	CBX3	chr8:125009859-125010188	K562	blood:	n/a	n/a
27	CBX3	chr8:124994801-124995168	K562	blood:	n/a	n/a
28	CBX3	chr8:125009912-125010137	HCT-116	colon:	n/a	n/a
29	CBX3	chr8:124940322-124940818	K562	blood:	n/a	n/a
30	CBX3	chr8:125009821-125010251	K562	blood:	n/a	n/a
31	CBX3	chr8:124974347-124974757	K562	blood:	n/a	n/a
32	CBX3	chr8:124934067-124935051	K562	blood:	n/a	n/a
33	CBX3	chr8:124934268-124934982	K562	blood:	n/a	n/a
34	CBX3	chr8:124996575-124997100	K562	blood:	n/a	n/a
35	CCNT2	chr8:124948316-124948481	K562	blood:	n/a	n/a
36	CCNT2	chr8:124934314-124934862	K562	blood:	n/a	n/a
37	CEBPB	chr8:124994315-124994340	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:124979979-124980327	A549	lung:	n/a	chr8:124980146-124980157
39	CEBPB	chr8:124997496-124997743	A549	lung:	n/a	chr8:124997602-124997613
40	CEBPB	chr8:124936918-124937232	A549	lung:	n/a	chr8:124937132-124937145
41	CEBPB	chr8:124907175-124907522	HepG2	liver:	n/a	chr8:124907339-124907350
42	CEBPB	chr8:124945728-124945987	A549	lung:	n/a	n/a
43	CEBPB	chr8:124992140-124992306	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:124934137-124934336	Hela-S3	cervix:	n/a	chr8:124934244-124934255
45	CEBPB	chr8:125012779-125013076	A549	lung:	n/a	chr8:125012941-125012952
46	CEBPB	chr8:124992070-124992499	MCF-7	breast:	n/a	n/a
47	CEBPB	chr8:124933994-124935141	MCF-7	breast:	n/a	chr8:124934244-124934255
48	CEBPB	chr8:124907176-124907523	A549	lung:	n/a	chr8:124907339-124907350
49	CEBPB	chr8:124980002-124980194	H1-hESC	embryonic stem cell:	n/a	chr8:124980146-124980157
50	CEBPB	chr8:124956990-124957372	ECC-1	luminal epithelium:	n/a	chr8:124957198-124957209

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:124934735-124934785	HEEpiC	esophagus:	n/a
2	chr8:124934735-124934785	HEEpiC	esophagus:	n/a
3	chr8:124953650-124953700	SAEC	small airway:	n/a
4	chr8:124993036-124993086	PrEC	prostate:	n/a
5	chr8:124908197-124908247	AG09319	gingival:	n/a
6	chr8:124908197-124908247	A549	lung:	n/a
7	chr8:124993036-124993086	AG04449	skin:	fetal
8	chr8:124908197-124908247	AoSMC	blood vessel:	n/a
9	chr8:124908197-124908247	NT2-D1	testis:	n/a
10	chr8:124993036-124993086	A549	lung:	n/a
11	chr8:124993036-124993086	HIPEpiC	eye:	n/a
12	chr8:124993036-124993086	NT2-D1	testis:	n/a
13	chr8:124953650-124953700	HCPEpiC	choroid plexus:	n/a
14	chr8:124934735-124934785	ProgFib	skin:	n/a
15	chr8:124934735-124934785	BJ	skin:	n/a
16	chr8:124908197-124908247	K562	blood:	n/a
17	chr8:124953650-124953700	HAEpiC	amniotic membrane:	n/a
18	chr8:124993036-124993086	HNPCEpiC	eye:	n/a
19	chr8:124993036-124993086	HCPEpiC	choroid plexus:	n/a
20	chr8:124934735-124934785	HRE	kidney:	n/a
21	chr8:124934735-124934785	T-47D	breast:	n/a
22	chr8:124934735-124934785	HRPEpiC	eye:	n/a
23	chr8:124908197-124908247	IMR90	lung:	fetal
24	chr8:124953650-124953700	GM12892	blood:	n/a
25	chr8:124953650-124953700	ECC-1	luminal epithelium:	n/a
26	chr8:124934735-124934785	AG04450	lung:	fetal
27	chr8:124908197-124908247	MCF-7	breast:	n/a
28	chr8:124993036-124993086	HMEC	breast:	n/a
29	chr8:124993036-124993086	SK-N-SH	brain:	n/a
30	chr8:124934735-124934785	AG09309	skin:	n/a
31	chr8:124934735-124934785	GM12891	blood:	n/a
32	chr8:124993036-124993086	AG09309	skin:	n/a
33	chr8:124993036-124993086	HCT-116	colon:	n/a
34	chr8:124953650-124953700	ProgFib	skin:	n/a
35	chr8:124953650-124953700	AG10803	skin:	n/a
36	chr8:124953650-124953700	HEK293	kidney:	embryo
37	chr8:124934735-124934785	AoSMC	blood vessel:	n/a
38	chr8:124908197-124908247	SAEC	small airway:	n/a
39	chr8:124993036-124993086	GM12891	blood:	n/a
40	chr8:124953650-124953700	PANC-1	pancreas:	n/a
41	chr8:124993036-124993086	SK-N-MC	brain:	n/a
42	chr8:124953650-124953700	AG04449	skin:	fetal
43	chr8:124908197-124908247	HMEC	breast:	n/a
44	chr8:124934735-124934785	NHBE	bronchial:	n/a
45	chr8:124993036-124993086	RPTEC	kidney:	n/a
46	chr8:124953650-124953700	GM19239	blood:	n/a
47	chr8:124908197-124908247	GM06990	blood:	n/a
48	chr8:124934735-124934785	HL-60	blood:	n/a
49	chr8:124908197-124908247	T-47D	breast:	n/a
50	chr8:124953650-124953700	AG04450	lung:	fetal

(count:155 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:124898606..124901476-chr8:125485542..125487537,2	MCF-7	breast:
2	chr8:124834856..124836291-chr8:124933990..124935310,7	MCF-7	breast:
3	chr8:124835624..124840070-chr8:124931025..124937507,8	MCF-7	breast:
4	chr8:124918718..124920943-chr8:124922678..124925068,2	MCF-7	breast:
5	chr8:124920123..124922608-chr8:124925471..124927774,2	MCF-7	breast:
6	chr8:124779816..124782654-chr8:124968951..124972407,3	MCF-7	breast:
7	chr8:124852984..124855101-chr8:124954477..124956245,2	K562	blood:
8	chr8:124936424..124937127-chr8:125049695..125050484,2	MCF-7	breast:
9	chr8:124968963..124971548-chr8:124973335..124975259,2	MCF-7	breast:
10	chr8:124920895..124922660-chr8:124926513..124928281,2	K562	blood:
11	chr8:124794688..124796229-chr8:124953654..124956422,2	MCF-7	breast:
12	chr8:124835258..124836544-chr8:124934356..124935690,5	K562	blood:
13	chr8:124975085..124976835-chr8:124980912..124983847,2	K562	blood:
14	chr8:124987891..124990694-chr8:124991031..124992713,2	K562	blood:
15	chr8:124953666..124955209-chr8:124955251..124956757,2	MCF-7	breast:
16	chr8:124843791..124846042-chr8:124921858..124924618,2	MCF-7	breast:
17	chr8:124837742..124838705-chr8:124934495..124935209,2	MCF-7	breast:
18	chr8:124983558..124985533-chr8:124989076..124991797,2	K562	blood:
19	chr8:124973730..124975260-chr8:124981756..124983515,2	MCF-7	breast:
20	chr8:124951197..124953461-chr8:124968222..124970694,2	MCF-7	breast:
21	chr8:124934471..124936352-chr8:124945543..124948252,2	K562	blood:
22	chr4:59709166..59709865-chr8:124956173..124956896,2	MCF-7	breast:
23	chr8:124964244..124966048-chr8:124971947..124973539,2	K562	blood:
24	chr8:124778256..124778875-chr8:124934719..124935275,2	K562	blood:
25	chr8:124942199..124944103-chr8:124945407..124947140,2	K562	blood:
26	chr8:124955186..124956902-chr8:124972449..124974180,2	MCF-7	breast:
27	chr8:124952199..124955002-chr8:124963674..124966809,3	K562	blood:
28	chr8:124954427..124956794-chr8:124966019..124968249,2	MCF-7	breast:
29	chr8:124901095..124905253-chr8:124905623..124909298,4	MCF-7	breast:
30	chr8:124961987..124963925-chr8:124978085..124980927,2	MCF-7	breast:
31	chr8:124898909..124900976-chr8:124900985..124902626,2	MCF-7	breast:
32	chr8:124950400..124952262-chr8:124991731..124994464,2	MCF-7	breast:
33	chr8:124929623..124931147-chr8:124932693..124935660,2	K562	blood:
34	chr8:124936483..124937594-chr8:125017986..125019533,17	MCF-7	breast:
35	chr8:124962163..124964055-chr8:124969703..124971275,2	K562	blood:
36	chr8:124779448..124782514-chr8:124930705..124935453,7	MCF-7	breast:
37	chr8:124934852..124937473-chr8:124945543..124947894,2	K562	blood:
38	chr8:124971159..124973956-chr8:124976304..124978202,2	MCF-7	breast:
39	chr8:124906436..124908763-chr8:124916387..124918093,2	K562	blood:
40	chr8:124949478..124952088-chr8:124956193..124958036,2	MCF-7	breast:
41	chr8:124934852..124937473-chr8:124945543..124947894,2	K562	blood:
42	chr8:124975896..124978386-chr8:124980797..124983291,2	MCF-7	breast:
43	chr8:124952199..124955002-chr8:124963674..124966809,3	K562	blood:
44	chr8:124968963..124971548-chr8:124973335..124975259,2	MCF-7	breast:
45	chr8:124988439..124991242-chr8:125462231..125464672,2	MCF-7	breast:
46	chr8:124969317..124972187-chr8:124973160..124976482,5	MCF-7	breast:
47	chr8:124889119..124891271-chr8:124903974..124906371,3	K562	blood:
48	chr8:124987532..124988285-chr8:128637802..128638390,2	MCF-7	breast:
49	chr8:124975085..124976835-chr8:124980912..124983847,2	K562	blood:
50	chr8:124889419..124892417-chr8:124901110..124903645,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANXA13-1	chr8:124937961-124938173	ENSG00000254000
2	lnc-ANXA13-1	chr8:124936999-124937116	ENSG00000254000
3	lnc-ANXA13-2	chr8:124996378-124998013	ENSG00000181171.5

No data

Variant related genes	Relation type
FER1L6	TF binding region
ENSG00000254000	TF binding region
FER1L6	CpG island
ENSG00000254000	CpG island
ENSG00000254000	chromatin interactions
ENSG00000170881	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000156804	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000214814	chromatin interactions
ENSG00000245149	chromatin interactions

Extended variants
information (count: 4495 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:4495 , 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	rs543255746	chr8:124895560-124895561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11782845	chr8:124895576-124895577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs75502213	chr8:124895578-124895579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141438354	chr8:124895592-124895593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372508984	chr8:124895600-124895601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561315702	chr8:124895638-124895639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530224966	chr8:124895647-124895648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569887107	chr8:124895648-124895649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563459723	chr8:124895672-124895673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191611859	chr8:124895692-124895693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531483043	chr8:124895700-124895701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537193779	chr8:124895702-124895703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184890400	chr8:124895710-124895711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376392066	chr8:124895742-124895743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571222496	chr8:124895754-124895755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533711242	chr8:124895798-124895799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549504908	chr8:124895799-124895800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386729526	chr8:124895809-124895810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116814811	chr8:124895810-124895811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553690378	chr8:124895838-124895839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573870278	chr8:124895892-124895893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536522251	chr8:124895916-124895917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189611828	chr8:124895923-124895924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181532724	chr8:124895939-124895940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555885987	chr8:124895985-124895986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150824653	chr8:124895986-124895987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532516655	chr8:124895996-124895997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185171714	chr8:124896027-124896028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139825049	chr8:124896100-124896101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114842165	chr8:124896106-124896107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561503772	chr8:124896111-124896112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144110011	chr8:124896138-124896139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190057672	chr8:124896142-124896143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181129606	chr8:124896164-124896165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532502401	chr8:124896168-124896169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552312127	chr8:124896218-124896219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564790562	chr8:124896240-124896241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147317849	chr8:124896241-124896242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547181593	chr8:124896267-124896268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553368150	chr8:124896268-124896269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186356857	chr8:124896306-124896307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140946928	chr8:124896339-124896340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6980985	chr8:124896389-124896390	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs376196320	chr8:124896419-124896420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77857200	chr8:124896435-124896436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558593323	chr8:124896443-124896444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572766360	chr8:124896469-124896470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76752293	chr8:124896474-124896475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541074920	chr8:124896499-124896500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575443084	chr8:124896505-124896506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
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
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	23813976	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124895000-124907000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:124895200-124896200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:124896200-124896400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:124896400-124897600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:124898600-124900000	Enhancers	HUVEC	blood vessel
6	chr8:124899200-124899600	Enhancers	Osteobl	bone
7	chr8:124899600-124900000	Enhancers	Fetal Muscle Leg	muscle
8	chr8:124900000-124903800	Weak transcription	HUVEC	blood vessel
9	chr8:124903600-124904000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:124903600-124904200	Enhancers	NHDF-Ad	bronchial
11	chr8:124903800-124904200	Enhancers	HUVEC	blood vessel
12	chr8:124904000-124906800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:124904200-124907400	Weak transcription	NHDF-Ad	bronchial
14	chr8:124904600-124905000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:124905000-124908200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:124905800-124909000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:124906000-124907800	Enhancers	Liver	Liver
18	chr8:124906600-124909200	Enhancers	Ovary	ovary
19	chr8:124906800-124908400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:124907000-124907600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr8:124907000-124908600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr8:124907000-124909600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr8:124907400-124909800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:124907400-124909800	Enhancers	NHDF-Ad	bronchial
25	chr8:124907600-124908600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr8:124907800-124910000	Weak transcription	Liver	Liver
27	chr8:124908200-124909000	Enhancers	Fetal Lung	lung
28	chr8:124908200-124909200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:124908200-124909200	Enhancers	Adipose Nuclei	Adipose
30	chr8:124908200-124909600	Enhancers	Fetal Muscle Leg	muscle
31	chr8:124908400-124908600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:124908400-124909600	Enhancers	Placenta Amnion	Placenta Amnion
33	chr8:124908400-124909600	Enhancers	Hela-S3	cervix
34	chr8:124908400-124909800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:124908600-124908800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:124908600-124908800	Enhancers	Fetal Intestine Small	intestine
37	chr8:124908600-124909000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:124908600-124909800	Enhancers	NHEK	skin
39	chr8:124908600-124910000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr8:124908800-124909000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:124908800-124909000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr8:124909000-124909400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr8:124909000-124909400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:124909000-124909400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:124909000-124909400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:124909000-124909600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr8:124909000-124909600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:124909200-124909600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr8:124909400-124909600	Enhancers	Fetal Intestine Small	intestine
50	chr8:124909400-124909800	Enhancers	Fetal Intestine Large	intestine

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