Variant report

Variant	nsv1030489
Chromosome Location	chr8:1162641-1268880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:4827)
Chromatin interactive
region (count:8)
LncRNA
region (count:52)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:1175929-1176133	K562	blood:	n/a	n/a
2	BACH1	chr8:1164164-1164166	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr8:1197352-1197554	GM12878	blood:	n/a	n/a
4	BCL3	chr8:1183273-1183530	GM12878	blood:	n/a	n/a
5	BCL3	chr8:1201626-1202699	GM12878	blood:	n/a	chr8:1202682-1202695
6	BCL3	chr8:1202523-1202866	GM12878	blood:	n/a	chr8:1202682-1202695
7	BCL3	chr8:1201577-1202272	GM12878	blood:	n/a	n/a
8	BCL3	chr8:1176669-1176894	GM12878	blood:	n/a	n/a
9	BCL3	chr8:1183299-1183532	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:1219344-1219455	K562	blood:	n/a	n/a
11	BRCA1	chr8:1236888-1237016	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr8:1232370-1232608	K562	blood:	n/a	n/a
13	CBX3	chr8:1185061-1185573	K562	blood:	n/a	n/a
14	CBX3	chr8:1246225-1246500	K562	blood:	n/a	n/a
15	CEBPB	chr8:1176946-1177204	IMR90	lung:	n/a	chr8:1177080-1177091
16	CEBPB	chr8:1182435-1182544	K562	blood:	n/a	n/a
17	CEBPB	chr8:1176917-1177231	HepG2	liver:	n/a	chr8:1177080-1177091
18	CEBPB	chr8:1163252-1163554	HepG2	liver:	n/a	chr8:1163429-1163440
19	CEBPB	chr8:1184686-1184877	K562	blood:	n/a	chr8:1184776-1184785 chr8:1184776-1184785 chr8:1184774-1184787 chr8:1184776-1184785 chr8:1184776-1184785
20	CEBPB	chr8:1210187-1210205	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:1163293-1163587	A549	lung:	n/a	chr8:1163429-1163440
22	CEBPB	chr8:1184618-1184904	HepG2	liver:	n/a	chr8:1184776-1184785 chr8:1184776-1184785 chr8:1184774-1184787 chr8:1184776-1184785 chr8:1184776-1184785
23	CEBPB	chr8:1176956-1177165	A549	lung:	n/a	chr8:1177080-1177091
24	CEBPB	chr8:1177434-1177476	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:1231221-1231278	K562	blood:	n/a	n/a
26	CEBPB	chr8:1231139-1231350	HepG2	liver:	n/a	chr8:1231211-1231224 chr8:1231211-1231222
27	CEBPB	chr8:1184614-1184935	K562	blood:	n/a	chr8:1184776-1184785 chr8:1184776-1184785 chr8:1184774-1184787 chr8:1184776-1184785 chr8:1184776-1184785
28	CEBPB	chr8:1260701-1260704	A549	lung:	n/a	n/a
29	CEBPB	chr8:1210123-1210367	HepG2	liver:	n/a	chr8:1210337-1210348 chr8:1210174-1210185 chr8:1210337-1210350
30	CEBPB	chr8:1231199-1231377	H1-hESC	embryonic stem cell:	n/a	chr8:1231211-1231224 chr8:1231211-1231222
31	CEBPB	chr8:1184659-1184887	H1-hESC	embryonic stem cell:	n/a	chr8:1184776-1184785 chr8:1184776-1184785 chr8:1184774-1184787 chr8:1184776-1184785 chr8:1184776-1184785
32	CHD2	chr8:1252357-1252367	HepG2	liver:	n/a	n/a
33	CTCF	chr8:1202155-1202201	GM19239	blood:	n/a	n/a
34	CTCF	chr8:1231360-1231510	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:1197078-1197088	GM19239	blood:	n/a	n/a
36	CTCF	chr8:1231260-1231410	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr8:1243540-1243690	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr8:1231386-1231480	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:1231288-1231516	K562	blood:	n/a	n/a
40	CTCF	chr8:1231314-1231512	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:1231335-1231471	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:1231374-1231443	HepG2	liver:	n/a	n/a
43	CTCF	chr8:1231286-1231501	K562	blood:	n/a	n/a
44	CTCF	chr8:1231271-1231490	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr8:1197077-1197111	LNCaP	prostate:	n/a	n/a
46	CTCF	chr8:1266016-1266065	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr8:1231212-1231548	K562	blood:	n/a	n/a
48	CTCF	chr8:1231320-1231470	HepG2	liver:	n/a	n/a
49	CTCF	chr8:1231403-1231418	Gliobla	brain:	n/a	n/a
50	CTCF	chr8:1231332-1231436	K562	blood:	n/a	n/a

(count:4827 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1264090-1264140	HMEC	breast:	n/a
2	chr8:1265732-1265782	H1-hESC	embryonic stem cell:	embryo
3	chr8:1232045-1232095	HNPCEpiC	eye:	n/a
4	chr8:1247803-1247853	PrEC	prostate:	n/a
5	chr8:1252864-1252914	BJ	skin:	n/a
6	chr8:1185471-1185521	Hela-S3	cervix:	n/a
7	chr8:1197488-1197538	H1-hESC	embryonic stem cell:	embryo
8	chr8:1200583-1200633	NT2-D1	testis:	n/a
9	chr8:1264090-1264140	HMEC	breast:	n/a
10	chr8:1265732-1265782	H1-hESC	embryonic stem cell:	embryo
11	chr8:1232045-1232095	HNPCEpiC	eye:	n/a
12	chr8:1247803-1247853	PrEC	prostate:	n/a
13	chr8:1252864-1252914	BJ	skin:	n/a
14	chr8:1185471-1185521	Hela-S3	cervix:	n/a
15	chr8:1197488-1197538	H1-hESC	embryonic stem cell:	embryo
16	chr8:1200583-1200633	NT2-D1	testis:	n/a
17	chr8:1207238-1207288	HepG2	liver:	n/a
18	chr8:1183511-1183561	HRCEpiC	kidney:	n/a
19	chr8:1247803-1247853	Hela-S3	cervix:	n/a
20	chr8:1252864-1252914	NH-A	brain:	n/a
21	chr8:1245672-1245722	GM12891	blood:	n/a
22	chr8:1264090-1264140	Jurkat	blood:	n/a
23	chr8:1246922-1246972	U87	brain:	n/a
24	chr8:1263108-1263158	MCF-7	breast:	n/a
25	chr8:1246817-1246867	AG04449	skin:	fetal
26	chr8:1200525-1200575	AG04450	lung:	fetal
27	chr8:1164044-1164094	MCF10A-Er-Src	breast:	n/a
28	chr8:1197231-1197281	CMK	blood:	n/a
29	chr8:1208878-1208928	PANC-1	pancreas:	n/a
30	chr8:1261246-1261296	PFSK-1	brain:	n/a
31	chr8:1185355-1185405	ovcar-3	ovarian:	n/a
32	chr8:1246442-1246492	HCF	heart:	n/a
33	chr8:1200583-1200633	AoSMC	blood vessel:	n/a
34	chr8:1244335-1244385	LNCaP	prostate:	n/a
35	chr8:1200896-1200946	SK-N-SH_RA	brain:	n/a
36	chr8:1204483-1204533	RPTEC	kidney:	n/a
37	chr8:1263433-1263483	MCF-7	breast:	n/a
38	chr8:1264224-1264274	NH-A	brain:	n/a
39	chr8:1203598-1203648	Hepatocyte	liver:	n/a
40	chr8:1226405-1226455	ovcar-3	ovarian:	n/a
41	chr8:1164044-1164094	ProgFib	skin:	n/a
42	chr8:1226465-1226515	U87	brain:	n/a
43	chr8:1261246-1261296	HEK293	kidney:	embryo
44	chr8:1232122-1232172	H1-hESC	embryonic stem cell:	embryo
45	chr8:1253043-1253093	ECC-1	luminal epithelium:	n/a
46	chr8:1249158-1249208	CMK	blood:	n/a
47	chr8:1245143-1245193	IMR90	lung:	fetal
48	chr8:1197231-1197281	LNCaP	prostate:	n/a
49	chr8:1246922-1246972	AG10803	skin:	n/a
50	chr8:1246607-1246657	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr8:1218051..1219861-chr8:1223791..1226453,2	K562	blood:
2	chr8:1201588..1203243-chr8:1212763..1215262,2	K562	blood:
3	chr8:1218264..1220141-chr8:1221111..1222674,2	K562	blood:
4	chr20:30873771..30875562-chr8:1267162..1269632,2	K562	blood:
5	chr8:1218051..1219861-chr8:1223791..1226453,2	K562	blood:
6	chr8:1218264..1220141-chr8:1221111..1222674,2	K562	blood:
7	chr8:1201588..1203243-chr8:1212763..1215262,2	K562	blood:
8	chr8:1266843..1268977-chr8:1269533..1271623,2	K562	blood:

(count:52 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO25-5	chr8:1208851-1208883	NONHSAT124640
2	lnc-FBXO25-5	chr8:1209579-1209808	ENSG00000254269
3	lnc-FBXO25-5	chr8:1200380-1200572	XLOC_006683
4	lnc-ERICH1-2	chr8:1236927-1237155	XLOC_006972
5	lnc-ERICH1-2	chr8:1236383-1236876	NONHSAT124646
6	lnc-FBXO25-5	chr8:1208851-1208883	XLOC_006683
7	lnc-ERICH1-2	chr8:1236927-1237971	XLOC_006972
8	lnc-ERICH1-3	chr8:1244295-1244463	XLOC_006971
9	lnc-FBXO25-5	chr8:1212415-1212592	XLOC_006683
10	lnc-DLGAP2-4	chr8:1263405-1263480	XLOC_006684
11	lnc-ERICH1-3	chr8:1231015-1231036	XLOC_006971
12	lnc-ERICH1-3	chr8:1248184-1250827	XLOC_006971
13	lnc-DLGAP2-7	chr8:1197062-1197215	l_3529_chr8:1197061-1199999_testes
14	lnc-ERICH1-2	chr8:1236494-1236531	XLOC_006972
15	lnc-ERICH1-2	chr8:1231702-1231870	refGeneNc_4249_NR_033895
16	lnc-FBXO25-5	chr8:1212415-1212580	ENSG00000254269
17	lnc-ERICH1-3	chr8:1245293-1245488	XLOC_006971
18	lnc-ERICH1-2	chr8:1236982-1237155	XLOC_006972
19	lnc-ERICH1-2	chr8:1236982-1237014	NONHSAT124646
20	lnc-ERICH1-3	chr8:1245293-1245488	ENSG00000253640
21	lnc-ERICH1-2	chr8:1232700-1232895	refGeneNc_4249_NR_033895
22	lnc-FBXO25-5	chr8:1208851-1208883	ENSG00000254269
23	lnc-FBXO25-5	chr8:1209558-1209656	NONHSAT124640
24	lnc-ERICH1-2	chr8:1236982-1237178	XLOC_006972
25	lnc-FBXO25-5	chr8:1200323-1200572	NONHSAT124640
26	lnc-ERICH1-3	chr8:1245293-1245488	NR_033895
27	lnc-ERICH1-3	chr8:1248184-1250829	ENSG00000253640
28	lnc-ERICH1-3	chr8:1245293-1245488	NONHSAT124652
29	lnc-FBXO25-5	chr8:1200373-1200572	ENSG00000254269
30	lnc-ERICH1-3	chr8:1244294-1244463	NR_033895
31	lnc-ERICH1-3	chr8:1244292-1244463	ENSG00000253640
32	lnc-ERICH1-2	chr8:1235591-1238234	refGeneNc_4249_NR_033895
33	lnc-ERICH1-3	chr8:1248184-1250827	NR_033895
34	lnc-DLGAP2-7	chr8:1199822-1199999	l_3529_chr8:1197061-1199999_testes
35	lnc-FBXO25-5	chr8:1200380-1200572	XLOC_006683
36	lnc-FBXO25-5	chr8:1208851-1208883	ENSG00000254269
37	lnc-ERICH1-2	chr8:1236982-1237027	XLOC_006972
38	lnc-ERICH1-2	chr8:1236888-1236922	XLOC_006972
39	lnc-ERICH1-3	chr8:1250717-1250823	NONHSAT124652
40	lnc-ERICH1-3	chr8:1244294-1244463	NONHSAT124652
41	lnc-FBXO25-5	chr8:1212418-1212580	ENSG00000254269
42	lnc-DLGAP2-4	chr8:1265719-1266452	XLOC_006684
43	lnc-DLGAP2-4	chr8:1267621-1267655	XLOC_006684
44	lnc-ERICH1-3	chr8:1250394-1250862	XLOC_006971
45	lnc-FBXO25-5	chr8:1208851-1208883	XLOC_006683
46	lnc-ERICH1-3	chr8:1248184-1250690	NONHSAT124652
47	lnc-FBXO25-5	chr8:1212415-1212580	ENSG00000254269
48	lnc-ERICH1-2	chr8:1236775-1236876	XLOC_006972
49	lnc-ERICH1-2	chr8:1236704-1236876	XLOC_006972
50	lnc-FBXO25-5	chr8:1209669-1209808	ENSG00000254269

No data

Variant related genes	Relation type
ENSG00000253640	TF binding region
ENSG00000254269	TF binding region
ENSG00000254160	TF binding region
ENSG00000253640	CpG island
ENSG00000254269	CpG island
ENSG00000254160	CpG island
HOXA10	miRNA target sites
SUN2	miRNA target sites
IL17RD	miRNA target sites
IL13	miRNA target sites
SUMF1	miRNA target sites
CDCA3	miRNA target sites
SUFU	miRNA target sites

Extended variants
information (count: 6006 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:6006 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575792813	chr8:1162656-1162657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544816360	chr8:1162670-1162671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369597589	chr8:1162704-1162705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564987697	chr8:1162714-1162715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527317016	chr8:1162720-1162721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547353032	chr8:1162730-1162731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141235206	chr8:1162744-1162745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560830293	chr8:1162745-1162746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530435517	chr8:1162757-1162758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560290998	chr8:1162759-1162760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550448591	chr8:1162762-1162763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146117017	chr8:1162763-1162764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539221148	chr8:1162764-1162765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73670677	chr8:1162769-1162770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566152184	chr8:1162802-1162803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs13266215	chr8:1162826-1162827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144503540	chr8:1162841-1162842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529847602	chr8:1162874-1162875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536152277	chr8:1162908-1162909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182420060	chr8:1162917-1162918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13268678	chr8:1162927-1162928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576203920	chr8:1162931-1162932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148391788	chr8:1162947-1162948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34076173	chr8:1162949-1162950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111808885	chr8:1162976-1162977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150520692	chr8:1162979-1162980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs118064247	chr8:1162980-1162981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560867088	chr8:1162992-1162993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569004830	chr8:1162994-1162995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115534548	chr8:1162996-1162997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370128243	chr8:1163029-1163030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79415804	chr8:1163032-1163033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75110920	chr8:1163053-1163054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557561666	chr8:1163059-1163060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563951920	chr8:1163060-1163061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532632983	chr8:1163075-1163076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552757112	chr8:1163078-1163079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566116783	chr8:1163105-1163106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572845235	chr8:1163109-1163110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528589742	chr8:1163111-1163112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548236926	chr8:1163148-1163149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568158751	chr8:1163164-1163165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537046464	chr8:1163172-1163173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115989467	chr8:1163187-1163188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187126141	chr8:1163193-1163194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560007513	chr8:1163194-1163195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569917609	chr8:1163201-1163202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575002255	chr8:1163205-1163206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4735996	chr8:1163245-1163246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192799590	chr8:1163268-1163269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Schizophrenia	23813976	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Congenital diaphragmatic hernia	21064195	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1162400-1163200	Enhancers	H9 Cell Line	embryonic stem cell
2	chr8:1162800-1163000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:1163000-1164000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:1163200-1164400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:1163600-1165000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:1163600-1165000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:1163800-1164400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr8:1163800-1164400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr8:1164000-1164600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:1164200-1164400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr8:1164400-1165000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr8:1172400-1173400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:1172600-1173000	Enhancers	Brain Anterior Caudate	brain
14	chr8:1180200-1180400	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr8:1180400-1182000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr8:1180600-1181000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr8:1180600-1181000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:1180600-1181200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:1183000-1184000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:1183000-1184400	Enhancers	Fetal Muscle Leg	muscle
21	chr8:1184000-1185600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:1185000-1185600	ZNF genes & repeats	Pancreas	Pancrea
23	chr8:1192600-1193000	Enhancers	Gastric	stomach
24	chr8:1192600-1193000	Enhancers	Spleen	Spleen
25	chr8:1193200-1193400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr8:1195200-1197200	Enhancers	Fetal Brain Male	brain
27	chr8:1196800-1197200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:1196800-1197200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
29	chr8:1196800-1197400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:1196800-1197400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:1196800-1197400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
32	chr8:1197000-1197200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:1197000-1197200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
34	chr8:1197000-1197200	ZNF genes & repeats	Gastric	stomach
35	chr8:1197000-1197200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
36	chr8:1197000-1197400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
37	chr8:1197000-1197400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
38	chr8:1197000-1197400	ZNF genes & repeats	Pancreas	Pancrea
39	chr8:1197200-1198200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr8:1197200-1199200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr8:1197200-1201800	Weak transcription	Gastric	stomach
42	chr8:1197400-1201600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:1197400-1202000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr8:1197400-1202000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr8:1198600-1199200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:1199000-1201600	Weak transcription	Pancreas	Pancrea
47	chr8:1199200-1199400	Enhancers	Brain Cingulate Gyrus	brain
48	chr8:1199200-1200200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr8:1199400-1201800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr8:1200200-1200600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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