Variant report

Variant	nsv1035061
Chromosome Location	chr8:11861797-12552839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5825)
CpG islands
(count:6657)
Chromatin interactive
region (count:6)
LncRNA
region (count:102)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5825 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

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	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:12051904-12051921	HepG2	liver:	n/a	n/a
4	ATF1	chr8:12417563-12417956	K562	blood:	n/a	n/a
5	ATF1	chr8:12435183-12435242	K562	blood:	n/a	n/a
6	ATF1	chr8:12051725-12051925	K562	blood:	n/a	n/a
7	ATF1	chr8:12400593-12400794	K562	blood:	n/a	n/a
8	ATF1	chr8:12307263-12307299	K562	blood:	n/a	n/a
9	ATF1	chr8:12420358-12420412	K562	blood:	n/a	n/a
10	ATF2	chr8:12400598-12400937	GM12878	blood:	n/a	n/a
11	ATF2	chr8:12444570-12445312	GM12878	blood:	n/a	n/a
12	ATF2	chr8:12445730-12446477	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr8:12444691-12445512	GM12878	blood:	n/a	n/a
14	ATF2	chr8:12400579-12400848	GM12878	blood:	n/a	n/a
15	BACH1	chr8:12523030-12523230	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:12415419-12415446	K562	blood:	n/a	n/a
17	BATF	chr8:12374697-12374930	GM12878	blood:	n/a	n/a
18	BATF	chr8:12037531-12037813	GM12878	blood:	n/a	n/a
19	BATF	chr8:12211595-12212020	GM12878	blood:	n/a	n/a
20	BATF	chr8:12516917-12517140	GM12878	blood:	n/a	n/a
21	BATF	chr8:12277768-12278106	GM12878	blood:	n/a	n/a
22	BATF	chr8:12294490-12294715	GM12878	blood:	n/a	n/a
23	BATF	chr8:11970251-11970426	GM12878	blood:	n/a	chr8:11970334-11970345
24	BATF	chr8:12288337-12288636	GM12878	blood:	n/a	n/a
25	BATF	chr8:12035447-12035785	GM12878	blood:	n/a	n/a
26	BATF	chr8:12052217-12052442	GM12878	blood:	n/a	n/a
27	BATF	chr8:12379045-12379257	GM12878	blood:	n/a	n/a
28	BATF	chr8:11970194-11970485	GM12878	blood:	n/a	chr8:11970334-11970345
29	BATF	chr8:12400588-12400876	GM12878	blood:	n/a	n/a
30	BATF	chr8:12053405-12053605	GM12878	blood:	n/a	n/a
31	BATF	chr8:11921281-11921530	GM12878	blood:	n/a	n/a
32	BATF	chr8:12432790-12433098	GM12878	blood:	n/a	n/a
33	BATF	chr8:12400443-12400987	GM12878	blood:	n/a	chr8:12400955-12400964
34	BATF	chr8:12081387-12081678	GM12878	blood:	n/a	n/a
35	BATF	chr8:12523072-12523287	GM12878	blood:	n/a	n/a
36	BATF	chr8:12409300-12409607	GM12878	blood:	n/a	n/a
37	BATF	chr8:12468401-12468697	GM12878	blood:	n/a	chr8:12468517-12468526
38	BATF	chr8:12278913-12279099	GM12878	blood:	n/a	n/a
39	BATF	chr8:12355078-12355365	GM12878	blood:	n/a	n/a
40	BATF	chr8:12444788-12445496	GM12878	blood:	n/a	chr8:12445096-12445107
41	BATF	chr8:12375868-12376447	GM12878	blood:	n/a	n/a
42	BATF	chr8:12050725-12051189	GM12878	blood:	n/a	n/a
43	BATF	chr8:12323897-12324188	GM12878	blood:	n/a	n/a
44	BATF	chr8:12219374-12219663	GM12878	blood:	n/a	n/a
45	BATF	chr8:12493505-12493669	GM12878	blood:	n/a	n/a
46	BATF	chr8:12282063-12282262	GM12878	blood:	n/a	n/a
47	BATF	chr8:12374707-12374931	GM12878	blood:	n/a	n/a
48	BATF	chr8:12292671-12292987	GM12878	blood:	n/a	n/a
49	BATF	chr8:12444646-12445599	GM12878	blood:	n/a	chr8:12445096-12445107
50	BATF	chr8:12046059-12046358	GM12878	blood:	n/a	n/a

(count:6657 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:12235727-12235777	ovcar-3	ovarian:	n/a
2	chr8:12454550-12454600	AG04450	lung:	fetal
3	chr8:12550605-12550655	HUVEC	blood vessel:	n/a
4	chr8:11995002-11995052	U87	brain:	n/a
5	chr8:12283654-12283704	BJ	skin:	n/a
6	chr8:12272377-12272427	HNPCEpiC	eye:	n/a
7	chr8:12426635-12426685	T-47D	breast:	n/a
8	chr8:12236258-12236308	NT2-D1	testis:	n/a
9	chr8:12235727-12235777	ovcar-3	ovarian:	n/a
10	chr8:12454550-12454600	AG04450	lung:	fetal
11	chr8:12550605-12550655	HUVEC	blood vessel:	n/a
12	chr8:11995002-11995052	U87	brain:	n/a
13	chr8:12283654-12283704	BJ	skin:	n/a
14	chr8:12272377-12272427	HNPCEpiC	eye:	n/a
15	chr8:12426635-12426685	T-47D	breast:	n/a
16	chr8:12236258-12236308	NT2-D1	testis:	n/a
17	chr8:12295064-12295114	ovcar-3	ovarian:	n/a
18	chr8:11996937-11996987	MCF-7	breast:	n/a
19	chr8:12216892-12216942	HIPEpiC	eye:	n/a
20	chr8:11996358-11996408	NB4	blood:	n/a
21	chr8:11895252-11895302	H1-hESC	embryonic stem cell:	embryo
22	chr8:11895252-11895302	Hela-S3	cervix:	n/a
23	chr8:12462881-12462931	NHDF-neo	bronchial:	n/a
24	chr8:11946498-11946548	LNCaP	prostate:	n/a
25	chr8:12256259-12256309	CMK	blood:	n/a
26	chr8:11996937-11996987	NB4	blood:	n/a
27	chr8:12244544-12244594	PrEC	prostate:	n/a
28	chr8:12521467-12521517	NB4	blood:	n/a
29	chr8:11986813-11986863	GM06990	blood:	n/a
30	chr8:12522691-12522741	HepG2	liver:	n/a
31	chr8:12219732-12219782	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:12458309-12458359	IMR90	lung:	fetal
33	chr8:12237780-12237830	MCF-7	breast:	n/a
34	chr8:12052206-12052256	RPTEC	kidney:	n/a
35	chr8:12237900-12237950	AG04450	lung:	fetal
36	chr8:12513435-12513485	HCT-116	colon:	n/a
37	chr8:12517221-12517271	HRPEpiC	eye:	n/a
38	chr8:11973029-11973079	HL-60	blood:	n/a
39	chr8:12458558-12458608	K562	blood:	n/a
40	chr8:12517221-12517271	SK-N-SH	brain:	n/a
41	chr8:12034388-12034438	CMK	blood:	n/a
42	chr8:12040795-12040845	K562	blood:	n/a
43	chr8:12550523-12550573	SK-N-MC	brain:	n/a
44	chr8:11989285-11989335	SK-N-SH_RA	brain:	n/a
45	chr8:11986933-11986983	ovcar-3	ovarian:	n/a
46	chr8:12027122-12027172	ECC-1	luminal epithelium:	n/a
47	chr8:11986876-11986926	AG10803	skin:	n/a
48	chr8:12236258-12236308	ovcar-3	ovarian:	n/a
49	chr8:12219732-12219782	NHDF-neo	bronchial:	n/a
50	chr8:11997496-11997546	NH-A	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67722873..67723411-chr8:12516978..12517495,2	MCF-7	breast:
2	chr10:101006536..101007134-chr8:11906757..11907257,2	MCF-7	breast:
3	chr8:12522693..12523228-chr8:12698263..12698831,2	MCF-7	breast:
4	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
5	chr11:3601740..3602712-chr8:12522746..12523343,2	MCF-7	breast:
6	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:

(count:102 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705D-3	chr8:12295801-12296020	XLOC_006721
2	lnc-LONRF1-2	chr8:12517271-12517338	ENSG00000247397
3	lnc-ZNF705D-2	chr8:12388484-12388540	NONHSAT125158
4	lnc-ZNF705D-2	chr8:12245248-12245374	NONHSAT125139
5	lnc-ZNF705D-2	chr8:12355092-12355358	NONHSAT125127
6	lnc-ZNF705D-2	chr8:12408261-12408540	NONHSAT125158
7	lnc-ZNF705D-2	chr8:12294522-12295219	NONHSAT125148
8	lnc-LONRF1-2	chr8:12516639-12516880	ENSG00000247397
9	lnc-AC130352.1-2	chr8:12064280-12064606	ENSG00000215248
10	lnc-ZNF705D-2	chr8:11973699-11973834	NONHSAT125117
11	lnc-ZNF705D-2	chr8:12034324-12034474	NONHSAT125117
12	lnc-ZNF705D-2	chr8:12059991-12060129	NONHSAT125127
13	lnc-LONRF1-2	chr8:12465434-12465499	NONHSAT125168
14	lnc-AC130352.1-4	chr8:12270336-12271882	ENSG00000270074.1
15	lnc-ZNF705D-3	chr8:12298509-12298570	XLOC_006721
16	lnc-ZNF705D-2	chr8:12219891-12220071	ENSG00000227888.3
17	lnc-ZNF705D-3	chr8:12299097-12299373	XLOC_006721
18	lnc-ZNF705D-2	chr8:12052320-12052946	XLOC_006719
19	lnc-USP17L2-1	chr8:11985367-11986806	NONHSAT125118
20	lnc-ZNF705D-2	chr8:12245760-12245805	ENSG00000227888.3
21	lnc-ZNF705D-2	chr8:12053400-12053747	XLOC_006719
22	lnc-ZNF705D-3	chr8:12298478-12298570	XLOC_006721
23	lnc-ZNF705D-2	chr8:12053400-12053747	NONHSAT125127
24	lnc-FAM86B2-2	chr8:12281922-12282230	NONHSAT125144
25	lnc-AC130352.1-5	chr8:12289838-12289899	ucscGeneNc_uc010lsi_1
26	lnc-LONRF1-2	chr8:12452490-12452805	ENSG00000247397
27	lnc-ZNF705D-2	chr8:12245467-12245528	NONHSAT125138
28	lnc-ZNF705D-3	chr8:12298478-12298570	XLOC_006721
29	lnc-USP17L2-2	chr8:12008404-12008643	NONHSAT125120
30	lnc-AC130352.1-2	chr8:12310554-12312147	ENSG00000215248
31	lnc-ZNF705D-4	chr8:12333971-12334631	ENSG00000270154.1
32	lnc-LONRF1-2	chr8:12513484-12514228	ENSG00000247397
33	lnc-ZNF705D-2	chr8:12250716-12250979	NONHSAT125138
34	lnc-ZNF705D-3	chr8:12295112-12295219	XLOC_006721
35	lnc-ZNF705D-2	chr8:12423395-12424354	NONHSAT125147
36	lnc-ZNF705D-2	chr8:12245250-12245374	ENSG00000227888.3
37	lnc-ZNF705D-3	chr8:12298509-12298604	XLOC_006721
38	lnc-ZNF705D-2	chr8:12059991-12060127	XLOC_006719
39	lnc-ZNF705D-2	chr8:12295673-12296020	NONHSAT125148
40	lnc-FAM86B2-1	chr8:12282231-12282893	NONHSAT125145
41	lnc-AC130352.1-3	chr8:12435815-12438798	NONHSAT125164
42	lnc-ZNF705D-2	chr8:12302265-12302403	NONHSAT125148
43	lnc-ZNF705D-2	chr8:12056244-12056305	NONHSAT125127
44	lnc-ZNF705D-2	chr8:12245760-12245843	NONHSAT125138
45	lnc-ZNF705D-2	chr8:12338387-12338444	NONHSAT125158
46	lnc-ZNF705D-2	chr8:12388452-12388540	NONHSAT125127
47	lnc-ZNF705D-2	chr8:12034891-12035004	NONHSAT125117
48	lnc-LONRF1-2	chr8:12522787-12522859	ENSG00000247397
49	lnc-ZNF705D-2	chr8:12423395-12424354	NONHSAT125127
50	lnc-ZNF705D-3	chr8:12295673-12296020	XLOC_006721

No data

Variant related genes	Relation type
FAM86B2	TF binding region
OR7E8P	TF binding region
ENSG00000254581	TF binding region
DEFB109P3	TF binding region
ENSG00000238460	TF binding region
DEFB108P3	TF binding region
FAM66A	TF binding region
ENPP7P6	TF binding region
RNA5SP253	TF binding region
USP17L7	TF binding region
ENSG00000255016	TF binding region
LINC00965	TF binding region
ENSG00000270154	TF binding region
ALG1L11P	TF binding region
USP17L2	TF binding region
FAM90A2P	TF binding region
DEFB109P1	TF binding region
FAM66D	TF binding region
ENSG00000221714	TF binding region
ENSG00000255253	TF binding region
ENSG00000255122	TF binding region
DEFB108P4	TF binding region
ZNF705D	TF binding region
ENSG00000254923	TF binding region
FAM85A	TF binding region
ENSG00000265826	TF binding region
ENPP7P12	TF binding region
RPS3AP34	TF binding region
ENSG00000254507	TF binding region
ENSG00000233050	TF binding region
ALG1L12P	TF binding region
FAM86B1	TF binding region
ENSG00000255098	TF binding region
ENSG00000238323	TF binding region
RNA5SP254	TF binding region
ENSG00000255556	TF binding region
RPS3AP35	TF binding region
ZNF705C	TF binding region
DEFB130	TF binding region
OR7E160P	TF binding region
ENSG00000237215	TF binding region
ENSG00000254423	TF binding region
FAM90A25P	TF binding region
ENSG00000254700	TF binding region
ENSG00000266637	TF binding region
FAM86B2	CpG island
OR7E8P	CpG island
ENSG00000254581	CpG island
DEFB109P3	CpG island
ENSG00000238460	CpG island
DEFB108P3	CpG island
FAM66A	CpG island
ENPP7P6	CpG island
RNA5SP253	CpG island
USP17L7	CpG island
ENSG00000255016	CpG island
LINC00965	CpG island
ENSG00000270154	CpG island
ALG1L11P	CpG island
USP17L2	CpG island
FAM90A2P	CpG island
DEFB109P1	CpG island
FAM66D	CpG island
ENSG00000221714	CpG island
ENSG00000255253	CpG island
ENSG00000255122	CpG island
DEFB108P4	CpG island
ZNF705D	CpG island
ENSG00000254923	CpG island
FAM85A	CpG island
ENSG00000265826	CpG island
ENPP7P12	CpG island
RPS3AP34	CpG island
ENSG00000254507	CpG island
ENSG00000233050	CpG island
ALG1L12P	CpG island
FAM86B1	CpG island
ENSG00000255098	CpG island
ENSG00000238323	CpG island
RNA5SP254	CpG island
ENSG00000255556	CpG island
RPS3AP35	CpG island
ZNF705C	CpG island
DEFB130	CpG island
OR7E160P	CpG island
ENSG00000237215	CpG island
ENSG00000254423	CpG island
FAM90A25P	CpG island
ENSG00000254700	CpG island
ENSG00000266637	CpG island
ENSG00000149823	chromatin interactions
ENSG00000255367	chromatin interactions
C9orf150	miRNA target sites
MYT1L	miRNA target sites
RTF1	miRNA target sites
ZNF597	miRNA target sites
PTPRJ	miRNA target sites
POTEG	miRNA target sites
TMEM30B	miRNA target sites
RGS20	miRNA target sites
GATA2	miRNA target sites
PIAS2	miRNA target sites

Extended variants
information (count: 18809 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:18809 , 50 per page) page: 1 2 3 4 5 6 7 ... 377

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111897736	chr8:11863174-11863175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs550262306	chr8:11863192-11863193	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs72496203	chr8:11863206-11863207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200015107	chr8:11863253-11863254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs544375523	chr8:11864032-11864033	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530469382	chr8:11866812-11866813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552241891	chr8:11866860-11866861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570490098	chr8:11866861-11866862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7823991	chr8:11866862-11866863	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546902491	chr8:11866863-11866864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568736359	chr8:11866879-11866880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536166169	chr8:11866893-11866894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557347068	chr8:11866897-11866898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386722355	chr8:11866906-11866907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138780537	chr8:11866907-11866908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558208851	chr8:11866908-11866909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573278035	chr8:11866912-11866913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566399012	chr8:11866915-11866916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541186520	chr8:11866920-11866921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368822152	chr8:11866934-11866935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185861986	chr8:11866939-11866940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192441543	chr8:11866950-11866951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373041660	chr8:11866962-11866963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541716151	chr8:11866990-11866991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs28657064	chr8:11867041-11867042	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs28495388	chr8:11867046-11867047	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs377064443	chr8:11867058-11867059	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs149415907	chr8:11867060-11867061	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548744920	chr8:11867072-11867073	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs545512154	chr8:11867077-11867078	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs564182763	chr8:11867079-11867080	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs528192674	chr8:11867085-11867086	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs111765751	chr8:11867097-11867098	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs562270659	chr8:11867106-11867107	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs529559900	chr8:11867113-11867114	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551287794	chr8:11867125-11867126	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs187666323	chr8:11867133-11867134	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs138483844	chr8:11867139-11867140	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs190637691	chr8:11867151-11867152	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs371430231	chr8:11867158-11867159	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551498951	chr8:11867159-11867160	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs182879074	chr8:11867160-11867161	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs187226365	chr8:11867163-11867164	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555485562	chr8:11867202-11867203	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143013861	chr8:11867206-11867207	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546694849	chr8:11867223-11867224	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs55798133	chr8:11867248-11867249	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs55805862	chr8:11867252-11867253	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535302408	chr8:11867256-11867257	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139058606	chr8:11867264-11867265	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

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
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	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
Cancer	21215367	CNVD

Chromatin state (count:2286 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11866800-11867200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:11867000-11867200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:11867000-11867400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11867000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:11867200-11868000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:11868000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:11869000-11869200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:11869800-11870200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:11869800-11870400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:11870200-11871000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:11870400-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:11870800-11871200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:11871000-11871200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:11871200-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:11871400-11871600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:11871400-11871800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11871400-11872600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
18	chr8:11871600-11871800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:11871600-11871800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:11871600-11871800	Enhancers	Stomach Smooth Muscle	stomach
21	chr8:11871600-11872000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr8:11871600-11872000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:11871600-11872000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:11871600-11872000	Bivalent Enhancer	Fetal Stomach	stomach
25	chr8:11871600-11872000	Enhancers	HMEC	breast
26	chr8:11871800-11872000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr8:11871800-11872200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr8:11871800-11872200	Enhancers	Colon Smooth Muscle	Colon
29	chr8:11871800-11872400	Enhancers	Primary B cells from cord blood	blood
30	chr8:11871800-11872400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr8:11871800-11872400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:11871800-11872600	Active TSS	H9 Cell Line	embryonic stem cell
33	chr8:11871800-11872600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr8:11871800-11872600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr8:11871800-11872600	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:11871800-11872600	Active TSS	Brain Anterior Caudate	brain
37	chr8:11871800-11872600	Active TSS	Stomach Smooth Muscle	stomach
38	chr8:11871800-11872800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr8:11871800-11873000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:11872000-11872200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:11872000-11872200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:11872000-11872200	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:11872000-11872200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:11872000-11872200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr8:11872000-11872200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:11872000-11872200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr8:11872000-11872200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr8:11872000-11872200	Enhancers	Fetal Brain Male	brain

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