Variant report

Variant	nsv1022300
Chromosome Location	chr8:11877195-12443043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4168)
CpG islands
(count:4519)
Chromatin interactive
region (count:2)
LncRNA
region (count:91)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4168 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:12433133-12433253	K562	blood:	n/a	n/a
2	ARID3A	chr8:12051904-12051921	HepG2	liver:	n/a	n/a
3	ATF1	chr8:12420358-12420412	K562	blood:	n/a	n/a
4	ATF1	chr8:12435183-12435242	K562	blood:	n/a	n/a
5	ATF1	chr8:12417563-12417956	K562	blood:	n/a	n/a
6	ATF1	chr8:12051725-12051925	K562	blood:	n/a	n/a
7	ATF1	chr8:12307263-12307299	K562	blood:	n/a	n/a
8	ATF1	chr8:12400593-12400794	K562	blood:	n/a	n/a
9	ATF2	chr8:12400598-12400937	GM12878	blood:	n/a	n/a
10	ATF2	chr8:12400579-12400848	GM12878	blood:	n/a	n/a
11	BACH1	chr8:12415419-12415446	K562	blood:	n/a	n/a
12	BATF	chr8:12293599-12293809	GM12878	blood:	n/a	n/a
13	BATF	chr8:12372638-12373204	GM12878	blood:	n/a	chr8:12372948-12372956
14	BATF	chr8:12277768-12278106	GM12878	blood:	n/a	n/a
15	BATF	chr8:12323857-12324231	GM12878	blood:	n/a	n/a
16	BATF	chr8:12295678-12295878	GM12878	blood:	n/a	n/a
17	BATF	chr8:12400443-12400987	GM12878	blood:	n/a	chr8:12400955-12400964
18	BATF	chr8:12355078-12355365	GM12878	blood:	n/a	n/a
19	BATF	chr8:12050398-12050714	GM12878	blood:	n/a	n/a
20	BATF	chr8:12053405-12053605	GM12878	blood:	n/a	n/a
21	BATF	chr8:12292998-12293462	GM12878	blood:	n/a	n/a
22	BATF	chr8:12379535-12379962	GM12878	blood:	n/a	n/a
23	BATF	chr8:12211595-12212020	GM12878	blood:	n/a	n/a
24	BATF	chr8:12219374-12219663	GM12878	blood:	n/a	n/a
25	BATF	chr8:12040152-12040516	GM12878	blood:	n/a	n/a
26	BATF	chr8:12375857-12376804	GM12878	blood:	n/a	n/a
27	BATF	chr8:12437849-12438015	GM12878	blood:	n/a	n/a
28	BATF	chr8:12355171-12355376	GM12878	blood:	n/a	n/a
29	BATF	chr8:12400588-12400876	GM12878	blood:	n/a	n/a
30	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
31	BATF	chr8:12278913-12279099	GM12878	blood:	n/a	n/a
32	BATF	chr8:12375358-12375560	GM12878	blood:	n/a	n/a
33	BATF	chr8:12379045-12379257	GM12878	blood:	n/a	n/a
34	BATF	chr8:12350232-12350662	GM12878	blood:	n/a	chr8:12350419-12350430
35	BATF	chr8:12046059-12046358	GM12878	blood:	n/a	n/a
36	BATF	chr8:12432790-12433098	GM12878	blood:	n/a	n/a
37	BATF	chr8:12142536-12142891	GM12878	blood:	n/a	n/a
38	BATF	chr8:12350272-12350570	GM12878	blood:	n/a	chr8:12350419-12350430
39	BATF	chr8:11921283-11921507	GM12878	blood:	n/a	n/a
40	BATF	chr8:12216425-12216654	GM12878	blood:	n/a	chr8:12216571-12216582
41	BATF	chr8:12345396-12345572	GM12878	blood:	n/a	n/a
42	BATF	chr8:12277703-12278063	GM12878	blood:	n/a	n/a
43	BATF	chr8:12081387-12081678	GM12878	blood:	n/a	n/a
44	BATF	chr8:12282063-12282262	GM12878	blood:	n/a	n/a
45	BATF	chr8:11970251-11970426	GM12878	blood:	n/a	chr8:11970334-11970345
46	BATF	chr8:12052217-12052442	GM12878	blood:	n/a	n/a
47	BATF	chr8:12380131-12380636	GM12878	blood:	n/a	n/a
48	BATF	chr8:12051326-12051536	GM12878	blood:	n/a	n/a
49	BATF	chr8:12374707-12374931	GM12878	blood:	n/a	n/a
50	BATF	chr8:12374697-12374930	GM12878	blood:	n/a	n/a

(count:4519 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:12272377-12272427	HRE	kidney:	n/a
2	chr8:12034317-12034367	GM06990	blood:	n/a
3	chr8:12296542-12296592	MCF10A-Er-Src	breast:	n/a
4	chr8:11991521-11991571	SK-N-MC	brain:	n/a
5	chr8:12256259-12256309	GM12878	blood:	n/a
6	chr8:12272377-12272427	HRE	kidney:	n/a
7	chr8:12034317-12034367	GM06990	blood:	n/a
8	chr8:12296542-12296592	MCF10A-Er-Src	breast:	n/a
9	chr8:11991521-11991571	SK-N-MC	brain:	n/a
10	chr8:12256259-12256309	GM12878	blood:	n/a
11	chr8:12033377-12033427	HNPCEpiC	eye:	n/a
12	chr8:11995002-11995052	AG04449	skin:	fetal
13	chr8:11986876-11986926	AG04449	skin:	fetal
14	chr8:11997496-11997546	BJ	skin:	n/a
15	chr8:11991521-11991571	HAEpiC	amniotic membrane:	n/a
16	chr8:11973495-11973545	NB4	blood:	n/a
17	chr8:11947722-11947772	HEK293	kidney:	embryo
18	chr8:12285204-12285254	AG04450	lung:	fetal
19	chr8:12272377-12272427	NHDF-neo	bronchial:	n/a
20	chr8:12237780-12237830	AG10803	skin:	n/a
21	chr8:12237780-12237830	AG04449	skin:	fetal
22	chr8:12235070-12235120	AG04450	lung:	fetal
23	chr8:12426340-12426390	AoSMC	blood vessel:	n/a
24	chr8:11977206-11977256	K562	blood:	n/a
25	chr8:11882982-11883032	ovcar-3	ovarian:	n/a
26	chr8:12052206-12052256	T-47D	breast:	n/a
27	chr8:11993449-11993499	NHBE	bronchial:	n/a
28	chr8:11986864-11986914	SK-N-SH	brain:	n/a
29	chr8:11882982-11883032	PrEC	prostate:	n/a
30	chr8:12236258-12236308	AG10803	skin:	n/a
31	chr8:11882962-11883012	A549	lung:	n/a
32	chr8:12040795-12040845	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:11973029-11973079	CMK	blood:	n/a
34	chr8:11996358-11996408	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:12285204-12285254	SK-N-SH_RA	brain:	n/a
36	chr8:12052924-12052974	RPTEC	kidney:	n/a
37	chr8:12293513-12293563	AG04450	lung:	fetal
38	chr8:12293509-12293559	NHDF-neo	bronchial:	n/a
39	chr8:12219732-12219782	HUVEC	blood vessel:	n/a
40	chr8:12244544-12244594	NB4	blood:	n/a
41	chr8:12294380-12294430	SK-N-SH	brain:	n/a
42	chr8:11972998-11973048	Jurkat	blood:	n/a
43	chr8:11991521-11991571	U87	brain:	n/a
44	chr8:12435562-12435612	AG09319	gingival:	n/a
45	chr8:12220318-12220368	NH-A	brain:	n/a
46	chr8:11972998-11973048	HIPEpiC	eye:	n/a
47	chr8:11989285-11989335	GM12892	blood:	n/a
48	chr8:12027122-12027172	Hepatocyte	liver:	n/a
49	chr8:12233144-12233194	SK-N-SH_RA	brain:	n/a
50	chr8:12235727-12235777	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
2	chr10:101006536..101007134-chr8:11906757..11907257,2	MCF-7	breast:

(count:91 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705D-2	chr8:12225748-12225811	ENSG00000227888.3
2	lnc-ZNF705D-2	chr8:12034324-12034474	NONHSAT125117
3	lnc-ZNF705D-2	chr8:12245248-12245374	NONHSAT125139
4	lnc-ZNF705D-3	chr8:12299097-12299373	XLOC_006721
5	lnc-ZNF705D-2	chr8:12053400-12053457	XLOC_006719
6	lnc-ZNF705D-2	chr8:12059991-12060129	NONHSAT125127
7	lnc-ZNF705D-3	chr8:12298509-12298570	XLOC_006721
8	lnc-ZNF705D-2	chr8:12408261-12408540	NONHSAT125158
9	lnc-ZNF705D-3	chr8:12302265-12302380	XLOC_006721
10	lnc-ZNF705D-2	chr8:12423395-12424354	NONHSAT125127
11	lnc-ZNF705D-2	chr8:12406996-12408558	NONHSAT125148
12	lnc-ZNF705D-3	chr8:12298509-12298570	XLOC_006721
13	lnc-ZNF705D-2	chr8:12388484-12388540	NONHSAT125158
14	lnc-AC130352.1-2	chr8:12310554-12312147	ENSG00000215248
15	lnc-ZNF705D-2	chr8:12338338-12338444	NONHSAT125127
16	lnc-ZNF705D-2	chr8:12277210-12279968	NONHSAT125139
17	lnc-ZNF705D-2	chr8:12302265-12302403	NONHSAT125148
18	lnc-ZNF705D-2	chr8:12056832-12056929	XLOC_006719
19	lnc-ZNF705D-2	chr8:12052268-12052946	XLOC_006719
20	lnc-ZNF705D-3	chr8:12298478-12298570	XLOC_006721
21	lnc-ZNF705D-2	chr8:12388452-12388540	NONHSAT125127
22	lnc-ZNF705D-2	chr8:12245250-12245374	ENSG00000227888.3
23	lnc-AC130352.1-4	chr8:12270336-12271882	ENSG00000270074.1
24	lnc-ZNF705D-3	chr8:12295801-12296020	XLOC_006721
25	lnc-ZNF705D-2	chr8:12228270-12228337	ENSG00000227888.3
26	lnc-ZNF705D-2	chr8:12059991-12060127	XLOC_006719
27	lnc-ZNF705D-4	chr8:12333971-12334631	ENSG00000270154.1
28	lnc-ZNF705D-2	chr8:12298509-12298570	NONHSAT125147
29	lnc-AC130352.1-2	chr8:12306848-12307964	ENSG00000215248
30	lnc-ZNF705D-2	chr8:12245467-12245528	NONHSAT125138
31	lnc-ZNF705D-2	chr8:12219891-12220071	ENSG00000227888.3
32	lnc-ZNF705D-3	chr8:12295112-12295219	XLOC_006721
33	lnc-AC130352.1-5	chr8:12289838-12289899	ucscGeneNc_uc010lsi_1
34	lnc-ZNF705D-2	chr8:12426979-12428991	NONHSAT125162
35	lnc-ZNF705D-2	chr8:12388452-12388540	NONHSAT125147
36	lnc-AC130352.1-2	chr8:12064280-12064606	ENSG00000215248
37	lnc-ZNF705D-3	chr8:12295047-12295219	XLOC_006721
38	lnc-ZNF705D-2	chr8:12245760-12245843	NONHSAT125138
39	lnc-ZNF705D-2	chr8:12423395-12424354	NONHSAT125147
40	lnc-USP17L2-1	chr8:11985367-11986806	NONHSAT125118
41	lnc-FAM86B2-2	chr8:12281922-12282230	NONHSAT125144
42	lnc-FAM86B2-1	chr8:12282231-12282893	NONHSAT125145
43	lnc-ZNF705D-2	chr8:12052320-12052946	XLOC_006719
44	lnc-AC130352.1-5	chr8:12290147-12290214	ucscGeneNc_uc010lsi_1
45	lnc-ZNF705D-2	chr8:12245760-12245805	ENSG00000227888.3
46	lnc-AC130352.1-3	chr8:12435815-12438798	NONHSAT125164
47	lnc-ZNF705D-2	chr8:12053532-12053747	XLOC_006719
48	lnc-ZNF705D-2	chr8:11973699-11973834	NONHSAT125117
49	lnc-ZNF705D-3	chr8:12295920-12296020	XLOC_006721
50	lnc-ZNF705D-2	chr8:12355092-12355358	NONHSAT125127

No data

Variant related genes	Relation type
FAM86B2	TF binding region
ENSG00000254923	TF binding region
FAM85A	TF binding region
DEFB109P3	TF binding region
ENSG00000265826	TF binding region
ENPP7P12	TF binding region
RPS3AP34	TF binding region
ENSG00000238460	TF binding region
DEFB108P3	TF binding region
ENSG00000233050	TF binding region
FAM66A	TF binding region
ALG1L12P	TF binding region
FAM86B1	TF binding region
ENPP7P6	TF binding region
ENSG00000255098	TF binding region
RNA5SP253	TF binding region
USP17L7	TF binding region
ENSG00000255016	TF binding region
LINC00965	TF binding region
ENSG00000270154	TF binding region
RNA5SP254	TF binding region
ENSG00000255556	TF binding region
ALG1L11P	TF binding region
USP17L2	TF binding region
ZNF705C	TF binding region
DEFB130	TF binding region
OR7E160P	TF binding region
ENSG00000237215	TF binding region
FAM90A2P	TF binding region
ENSG00000254423	TF binding region
FAM90A25P	TF binding region
DEFB109P1	TF binding region
ENSG00000254700	TF binding region
FAM66D	TF binding region
ENSG00000221714	TF binding region
ENSG00000266637	TF binding region
ENSG00000255122	TF binding region
DEFB108P4	TF binding region
ZNF705D	TF binding region
FAM86B2	CpG island
ENSG00000254923	CpG island
FAM85A	CpG island
DEFB109P3	CpG island
ENSG00000265826	CpG island
ENPP7P12	CpG island
RPS3AP34	CpG island
ENSG00000238460	CpG island
DEFB108P3	CpG island
ENSG00000233050	CpG island
FAM66A	CpG island
ALG1L12P	CpG island
FAM86B1	CpG island
ENPP7P6	CpG island
ENSG00000255098	CpG island
RNA5SP253	CpG island
USP17L7	CpG island
ENSG00000255016	CpG island
LINC00965	CpG island
ENSG00000270154	CpG island
RNA5SP254	CpG island
ENSG00000255556	CpG island
ALG1L11P	CpG island
USP17L2	CpG island
ZNF705C	CpG island
DEFB130	CpG island
OR7E160P	CpG island
ENSG00000237215	CpG island
FAM90A2P	CpG island
ENSG00000254423	CpG island
FAM90A25P	CpG island
DEFB109P1	CpG island
ENSG00000254700	CpG island
FAM66D	CpG island
ENSG00000221714	CpG island
ENSG00000266637	CpG island
ENSG00000255122	CpG island
DEFB108P4	CpG island
ZNF705D	CpG island
ENSG00000149823	chromatin interactions
TMEM30B	miRNA target sites
ZNF597	miRNA target sites
C9orf150	miRNA target sites

Extended variants
information (count: 10265 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:10265 , 50 per page) page: 1 2 3 4 5 6 7 ... 206

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73542355	chr8:11882401-11882402	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182024828	chr8:11882414-11882415	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549281650	chr8:11882428-11882429	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111551761	chr8:11882437-11882438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538242050	chr8:11882477-11882478	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188918445	chr8:11882492-11882493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs116628510	chr8:11882508-11882509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371045456	chr8:11882546-11882547	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs539184913	chr8:11882547-11882548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140633812	chr8:11882549-11882550	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144483795	chr8:11882560-11882561	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540496698	chr8:11882574-11882575	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs371631770	chr8:11882587-11882588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs61387792	chr8:11882588-11882589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs151272394	chr8:11882589-11882590	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs398007083	chr8:11882598-11882599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs60181159	chr8:11882599-11882600	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs555654617	chr8:11882603-11882604	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573509347	chr8:11882622-11882623	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544203708	chr8:11882627-11882628	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201437119	chr8:11882641-11882642	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546349110	chr8:11882642-11882643	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs398007084	chr8:11882650-11882651	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368829572	chr8:11882651-11882652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372238377	chr8:11882652-11882653	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547691853	chr8:11882653-11882654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs562383906	chr8:11882659-11882660	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182414318	chr8:11882676-11882677	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532860877	chr8:11882730-11882731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181400931	chr8:11882742-11882743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560279419	chr8:11882764-11882765	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185537929	chr8:11882770-11882771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374447734	chr8:11882775-11882776	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549365877	chr8:11882799-11882800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567960570	chr8:11882826-11882827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189999608	chr8:11882828-11882829	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531953739	chr8:11882833-11882834	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550148331	chr8:11882850-11882851	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571583370	chr8:11882855-11882856	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114104733	chr8:11882896-11882897	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547923991	chr8:11882897-11882898	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566642610	chr8:11882902-11882903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533977569	chr8:11882910-11882911	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73200503	chr8:11882913-11882914	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573868814	chr8:11882917-11882918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34195527	chr8:11882918-11882919	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371344473	chr8:11882919-11882920	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs6983419	chr8:11882924-11882925	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181009819	chr8:11882936-11882937	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112446641	chr8:11882937-11882938	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:150)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20688739	CNVD
Pancreatic cancer	17952125	CNVD
Intracranial tumor	22048656	CNVD
Ollier disease	21235737	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1330 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11884400-11885200	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:11887400-11887600	Enhancers	Pancreas	Pancrea
3	chr8:11887600-11889200	Weak transcription	Pancreas	Pancrea
4	chr8:11889200-11889600	Enhancers	Pancreas	Pancrea
5	chr8:11973200-11973400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:11973200-11973600	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr8:11973200-11973600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:11973200-11973600	Active TSS	Cortex derived primary cultured neurospheres	brain
9	chr8:11973200-11973600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:11973200-11973600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
11	chr8:11973200-11973600	Active TSS	Colonic Mucosa	Colon
12	chr8:11973200-11973600	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr8:11973200-11973600	Active TSS	Esophagus	oesophagus
14	chr8:11973200-11973600	Active TSS	Placenta	Placenta
15	chr8:11973200-11973600	Active TSS	Fetal Stomach	stomach
16	chr8:11973200-11973600	Active TSS	Fetal Thymus	thymus
17	chr8:11973200-11973600	Active TSS	Left Ventricle	heart
18	chr8:11973200-11973600	Active TSS	Thymus	Thymus
19	chr8:11973200-11973600	Active TSS	A549	lung
20	chr8:11973200-11973600	Active TSS	Monocytes-CD14+_RO01746	blood
21	chr8:11973200-11973600	Active TSS	NHLF	lung
22	chr8:11973200-11973600	Active TSS	Osteobl	bone
23	chr8:11973200-11973800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:11973200-11973800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:11973200-11973800	Active TSS	Ovary	ovary
26	chr8:11973200-11973800	Active TSS	Psoas Muscle	Psoas
27	chr8:11973200-11973800	Active TSS	Right Ventricle	heart
28	chr8:11973200-11974000	Active TSS	H1 Cell Line	embryonic stem cell
29	chr8:11973200-11974000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:11973200-11974000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:11973200-11974000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:11973200-11974000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:11973200-11974000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr8:11973200-11974000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:11973200-11974000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:11973200-11974000	Active TSS	Muscle Satellite Cultured Cells	--
37	chr8:11973200-11974000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:11973200-11974000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:11973200-11974000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:11973200-11974000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:11973200-11974000	Active TSS	Adipose Nuclei	Adipose
42	chr8:11973200-11974000	Active TSS	Brain Germinal Matrix	brain
43	chr8:11973200-11974000	Active TSS	Fetal Brain Female	brain
44	chr8:11973200-11974000	Active TSS	Fetal Muscle Leg	muscle
45	chr8:11973200-11974000	Active TSS	Stomach Smooth Muscle	stomach
46	chr8:11973400-11973600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:11973400-11973800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:11973400-11973800	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr8:11973400-11974000	Active TSS	Brain Hippocampus Middle	brain
50	chr8:11973400-11974000	Active TSS	NHDF-Ad	bronchial

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