Variant report

Variant	esv16290
Chromosome Location	chr7:64058602-64162829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1631)
CpG islands
(count:856)
Chromatin interactive
region (count:24)
LncRNA
region (count:41)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1631 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:64087022-64087310	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:64082157-64082263	K562	blood:	n/a	n/a
3	ARID3A	chr7:64090841-64091296	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:64085518-64085801	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:64126331-64126433	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:64085532-64085845	K562	blood:	n/a	n/a
7	ARID3A	chr7:64146938-64147288	HepG2	liver:	n/a	n/a
8	ATF1	chr7:64079602-64079802	K562	blood:	n/a	n/a
9	ATF1	chr7:64126244-64126581	K562	blood:	n/a	n/a
10	ATF2	chr7:64146982-64147307	GM12878	blood:	n/a	n/a
11	ATF2	chr7:64126148-64126755	GM12878	blood:	n/a	n/a
12	ATF2	chr7:64129018-64129462	GM12878	blood:	n/a	n/a
13	BACH1	chr7:64126554-64126563	K562	blood:	n/a	n/a
14	BACH1	chr7:64111281-64111597	K562	blood:	n/a	n/a
15	BATF	chr7:64086454-64086733	GM12878	blood:	n/a	n/a
16	BATF	chr7:64129056-64129326	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:64126417-64126836	GM12878	blood:	n/a	n/a
18	BCLAF1	chr7:64126744-64127203	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:64146861-64147273	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:64114553-64114722	K562	blood:	n/a	n/a
21	BHLHE40	chr7:64126241-64126572	K562	blood:	n/a	n/a
22	BHLHE40	chr7:64126247-64126744	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:64086181-64086649	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:64111281-64111651	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:64111277-64111654	K562	blood:	n/a	n/a
26	BHLHE40	chr7:64090919-64091317	HepG2	liver:	n/a	n/a
27	BRCA1	chr7:64111281-64111647	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:64111281-64111656	GM12878	blood:	n/a	n/a
29	BRCA1	chr7:64126297-64126616	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:64126528-64126665	HepG2	liver:	n/a	n/a
31	CBX3	chr7:64126174-64126859	K562	blood:	n/a	n/a
32	CCNT2	chr7:64126367-64126575	K562	blood:	n/a	n/a
33	CEBPB	chr7:64087764-64089547	HepG2	liver:	n/a	chr7:64089296-64089307
34	CEBPB	chr7:64088483-64088943	K562	blood:	n/a	n/a
35	CEBPB	chr7:64089084-64089526	HepG2	liver:	n/a	chr7:64089296-64089307
36	CEBPB	chr7:64093293-64095425	A549	lung:	n/a	chr7:64095206-64095217
37	CEBPB	chr7:64111281-64112472	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:64078013-64078073	K562	blood:	n/a	n/a
39	CEBPB	chr7:64097057-64097707	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:64079504-64079893	K562	blood:	n/a	n/a
41	CEBPB	chr7:64100688-64101271	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:64093712-64094175	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:64066819-64067017	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:64109091-64109148	K562	blood:	n/a	n/a
45	CEBPB	chr7:64064514-64064738	K562	blood:	n/a	chr7:64064632-64064643
46	CEBPB	chr7:64061232-64062849	HepG2	liver:	n/a	chr7:64062711-64062722
47	CEBPB	chr7:64077546-64078367	A549	lung:	n/a	n/a
48	CEBPB	chr7:64066851-64067032	A549	lung:	n/a	n/a
49	CEBPB	chr7:64059763-64059951	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:64146948-64147216	HepG2	liver:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64129143-64129193	GM12891	blood:	n/a
2	chr7:64126944-64126994	CMK	blood:	n/a
3	chr7:64129143-64129193	GM12891	blood:	n/a
4	chr7:64126944-64126994	CMK	blood:	n/a
5	chr7:64126140-64126190	GM19239	blood:	n/a
6	chr7:64125580-64125630	SK-N-MC	brain:	n/a
7	chr7:64127516-64127566	H1-hESC	embryonic stem cell:	embryo
8	chr7:64127516-64127566	Hepatocyte	liver:	n/a
9	chr7:64125580-64125630	Hela-S3	cervix:	n/a
10	chr7:64125580-64125630	LNCaP	prostate:	n/a
11	chr7:64126532-64126582	SAEC	small airway:	n/a
12	chr7:64126944-64126994	HCM	heart:	n/a
13	chr7:64125401-64125451	Jurkat	blood:	n/a
14	chr7:64126140-64126190	HepG2	liver:	n/a
15	chr7:64138755-64138805	GM19239	blood:	n/a
16	chr7:64126456-64126506	BE2_C	brain:	n/a
17	chr7:64127516-64127566	HRE	kidney:	n/a
18	chr7:64126809-64126859	HEK293	kidney:	embryo
19	chr7:64125557-64125607	NH-A	brain:	n/a
20	chr7:64126809-64126859	NHBE	bronchial:	n/a
21	chr7:64125580-64125630	BE2_C	brain:	n/a
22	chr7:64126809-64126859	U87	brain:	n/a
23	chr7:64126944-64126994	AG04449	skin:	fetal
24	chr7:64126140-64126190	SKMC	muscle:	n/a
25	chr7:64126470-64126520	SK-N-SH_RA	brain:	n/a
26	chr7:64126809-64126859	SK-N-SH	brain:	n/a
27	chr7:64126779-64126829	MCF10A-Er-Src	breast:	n/a
28	chr7:64126742-64126792	MCF10A-Er-Src	breast:	n/a
29	chr7:64127516-64127566	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:64129143-64129193	AG04449	skin:	fetal
31	chr7:64129143-64129193	NT2-D1	testis:	n/a
32	chr7:64126532-64126582	GM06990	blood:	n/a
33	chr7:64126944-64126994	Hepatocyte	liver:	n/a
34	chr7:64126809-64126859	SK-N-MC	brain:	n/a
35	chr7:64126456-64126506	NHDF-neo	bronchial:	n/a
36	chr7:64127516-64127566	HCF	heart:	n/a
37	chr7:64126532-64126582	HAEpiC	amniotic membrane:	n/a
38	chr7:64126779-64126829	T-47D	breast:	n/a
39	chr7:64129143-64129193	Hela-S3	cervix:	n/a
40	chr7:64126456-64126506	K562	blood:	n/a
41	chr7:64127516-64127566	SK-N-SH	brain:	n/a
42	chr7:64129143-64129193	HCF	heart:	n/a
43	chr7:64126944-64126994	GM12878	blood:	n/a
44	chr7:64125580-64125630	IMR90	lung:	fetal
45	chr7:64138755-64138805	AoSMC	blood vessel:	n/a
46	chr7:64126779-64126829	BE2_C	brain:	n/a
47	chr7:64126809-64126859	PANC-1	pancreas:	n/a
48	chr7:64125580-64125630	HEK293	kidney:	embryo
49	chr7:64126809-64126859	SKMC	muscle:	n/a
50	chr7:64127516-64127566	CMK	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:64096183..64096701-chr8:43095392..43095917,3	MCF-7	breast:
2	chr7:63774283..63776835-chr7:64075332..64078268,2	MCF-7	breast:
3	chr7:64059558..64060118-chr7:64071550..64072484,4	MCF-7	breast:
4	chr7:64144942..64146734-chr7:64146825..64148804,2	MCF-7	breast:
5	chr7:64059458..64060477-chr7:64099321..64100139,7	MCF-7	breast:
6	chr19:23941209..23941866-chr7:64126456..64127217,2	Hela-S3	cervix:
7	chr7:64059458..64060477-chr7:64099321..64100040,3	MCF-7	breast:
8	chr7:64133042..64135798-chr7:64140855..64142679,2	K562	blood:
9	chr7:64059458..64060477-chr7:64099321..64100040,3	MCF-7	breast:
10	chr7:64099496..64100069-chr7:64350429..64351249,2	MCF-7	breast:
11	chr7:64059458..64060477-chr7:64099321..64100139,7	MCF-7	breast:
12	chr7:64115402..64117141-chr7:64125488..64128451,2	MCF-7	breast:
13	chr7:64059558..64060118-chr7:64071550..64072484,4	MCF-7	breast:
14	chr7:64059389..64060099-chr7:64099412..64099918,2	MCF-7	breast:
15	chr7:64126311..64128257-chr7:64129298..64130838,2	MCF-7	breast:
16	chr7:64161938..64163789-chr7:64164541..64167796,3	K562	blood:
17	chr7:64125080..64128959-chr7:64143328..64147169,6	MCF-7	breast:
18	chr7:64138840..64143249-chr7:64144344..64147303,3	K562	blood:
19	chr7:64130443..64133428-chr7:64253798..64256248,4	MCF-7	breast:
20	chr7:64059389..64060099-chr7:64099412..64099918,2	MCF-7	breast:
21	chr7:64133042..64135869-chr7:64139508..64142679,3	K562	blood:
22	chr7:64133042..64135798-chr7:64140855..64142679,2	K562	blood:
23	chr7:64125646..64128378-chr7:64129230..64132337,4	K562	blood:
24	chr7:64126083..64128264-chr7:64130876..64132561,2	K562	blood:

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF138-3	chr7:64126461-64126663	NR_104148
2	lnc-ZNF138-3	chr7:64129415-64129556	NR_104148
3	lnc-ZNF138-3	chr7:64139555-64139714	NR_104148
4	lnc-ZNF138-3	chr7:64144713-64147263	NONHSAT121038
5	lnc-ZNF107-1	chr7:64103960-64104051	XLOC_006128
6	lnc-ZNF107-2	chr7:64074527-64074708	NONHSAT121030
7	lnc-ZNF107-2	chr7:64074877-64078967	NONHSAT121025
8	lnc-ZNF107-2	chr7:64072804-64072950	NONHSAT121029
9	lnc-ZNF107-2	chr7:64068567-64068736	NONHSAT121029
10	lnc-ZNF107-1	chr7:64115771-64116285	XLOC_006128
11	lnc-ZNF107-1	chr7:64115544-64116152	XLOC_006128
12	lnc-ZNF107-2	chr7:64074877-64075201	NONHSAT121032
13	lnc-ZNF680-14	chr7:64139332-64139425	NONHSAT121037
14	lnc-ZNF107-1	chr7:64115544-64116147	NONHSAT121036
15	lnc-ZNF107-3	chr7:64060773-64060819	NONHSAT121028
16	lnc-ZNF107-1	chr7:64112335-64112385	NONHSAT121036
17	lnc-ZNF107-2	chr7:64072804-64072950	NONHSAT121032
18	lnc-ZNF107-2	chr7:64074877-64075201	NONHSAT121029
19	lnc-ZNF107-1	chr7:64115544-64115592	XLOC_006128
20	lnc-ZNF107-1	chr7:64103412-64103809	XLOC_006128
21	lnc-ZNF138-3	chr7:64139555-64139714	NR_104149
22	lnc-ZNF138-3	chr7:64141511-64141600	NONHSAT121038
23	lnc-ZNF107-3	chr7:64064186-64064418	NONHSAT121028
24	lnc-ZNF107-2	chr7:64072128-64072225	XLOC_006126
25	lnc-ZNF107-3	chr7:64063937-64064007	NONHSAT121028
26	lnc-ZNF107-2	chr7:64080388-64080834	NONHSAT121030
27	lnc-ZNF138-3	chr7:64144465-64144583	NONHSAT121038
28	lnc-ZNF107-2	chr7:64072165-64072225	NONHSAT121032
29	lnc-ZNF138-3	chr7:64126461-64126663	NR_104149
30	lnc-ZNF138-3	chr7:64144713-64148208	NR_104149
31	lnc-ZNF107-2	chr7:64071556-64071580	NONHSAT121030
32	lnc-ZNF107-2	chr7:64074877-64075201	NONHSAT121033
33	lnc-ZNF107-2	chr7:64074198-64074708	NONHSAT121033
34	lnc-ZNF107-2	chr7:64073798-64074198	XLOC_006126
35	lnc-ZNF138-3	chr7:64144713-64148208	NR_104148
36	lnc-ZNF107-2	chr7:64060037-64060160	NONHSAT121025
37	lnc-ZNF107-2	chr7:64072804-64073166	XLOC_006126
38	lnc-ZNF107-2	chr7:64074877-64074966	NONHSAT121030
39	lnc-ZNF107-3	chr7:64063683-64063783	NONHSAT121028
40	lnc-ZNF107-2	chr7:64072804-64072950	NONHSAT121030
41	lnc-ZNF680-14	chr7:64147303-64147771	NONHSAT121037

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6839-3p	chr7:64139533-64139554	MIMAT0027581
hsa-miR-6839-5p	chr7:64139447-64139468	MIMAT0027580

No data

Variant related genes	Relation type
ZNF107	TF binding region
ENSG00000271550	TF binding region
ZNF107	CpG island
ENSG00000271550	CpG island
ENSG00000271550	chromatin interactions
ENSG00000197008	chromatin interactions
ENSG00000234444	chromatin interactions
ENSG00000196172	chromatin interactions
ENSG00000189316	chromatin interactions
ENSG00000196247	chromatin interactions
SHC1	miRNA target sites

Extended variants
information (count: 3252 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3252 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79140570	chr7:64058611-64058612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116727554	chr7:64058649-64058650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150076113	chr7:64058806-64058807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567920702	chr7:64058821-64058822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377625936	chr7:64058834-64058835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62462863	chr7:64058964-64058965	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547214078	chr7:64058965-64058966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565798453	chr7:64058987-64058988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534432536	chr7:64059004-64059005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369069024	chr7:64059065-64059066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573499235	chr7:64059156-64059157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4626471	chr7:64059230-64059231	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs201223158	chr7:64059292-64059293	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs180685185	chr7:64059325-64059326	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs556876654	chr7:64059336-64059337	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs573593457	chr7:64059350-64059351	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs552003837	chr7:64059406-64059407	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1982344	chr7:64059410-64059411	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138396608	chr7:64059428-64059429	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35754987	chr7:64059430-64059431	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572959883	chr7:64059445-64059446	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186470542	chr7:64059454-64059455	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552854751	chr7:64059481-64059482	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187419672	chr7:64059512-64059513	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200108915	chr7:64059544-64059545	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76341738	chr7:64059556-64059557	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148845766	chr7:64059565-64059566	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189623357	chr7:64059566-64059567	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561616198	chr7:64059590-64059591	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56342558	chr7:64059608-64059609	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181845878	chr7:64059611-64059612	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138473170	chr7:64059752-64059753	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532690183	chr7:64059790-64059791	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79690944	chr7:64059808-64059809	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs62462864	chr7:64059830-64059831	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111833720	chr7:64059831-64059832	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574365846	chr7:64059862-64059863	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562618041	chr7:64059881-64059882	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541441480	chr7:64059938-64059939	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554597706	chr7:64059942-64059943	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567256825	chr7:64059983-64059984	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375751788	chr7:64060018-64060019	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574476865	chr7:64060042-64060043	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs536158420	chr7:64060079-64060080	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs553206346	chr7:64060085-64060086	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs572956527	chr7:64060099-64060100	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs77837853	chr7:64060103-64060104	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs371186052	chr7:64060174-64060175	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558827619	chr7:64060179-64060180	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72503388	chr7:64060231-64060232	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64039400-64064000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:64046000-64059400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:64059000-64065800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:64059200-64076200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr7:64059400-64059600	Weak transcription	Fetal Brain Female	brain
6	chr7:64059400-64076400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:64059600-64060600	Enhancers	Placenta	Placenta
8	chr7:64059600-64067400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr7:64059800-64063800	Weak transcription	Fetal Brain Female	brain
10	chr7:64060600-64064200	Weak transcription	Placenta	Placenta
11	chr7:64062600-64062800	Enhancers	Fetal Heart	heart
12	chr7:64062800-64077400	Weak transcription	Fetal Heart	heart
13	chr7:64063200-64064800	Weak transcription	Fetal Stomach	stomach
14	chr7:64064000-64064600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:64064200-64065400	Enhancers	Placenta	Placenta
16	chr7:64064600-64068400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr7:64064800-64065400	Strong transcription	Fetal Stomach	stomach
18	chr7:64065400-64069400	Weak transcription	Placenta	Placenta
19	chr7:64065400-64076800	Weak transcription	Fetal Stomach	stomach
20	chr7:64065800-64066000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:64066000-64066200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:64066200-64073000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:64068400-64069200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:64068400-64073200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
25	chr7:64069200-64075200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:64069400-64075800	Enhancers	Placenta	Placenta
27	chr7:64072400-64073600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr7:64073200-64073600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:64075400-64079400	Weak transcription	Brain Substantia Nigra	brain
30	chr7:64076400-64077400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:64079200-64081200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:64079400-64079600	Enhancers	Brain Substantia Nigra	brain
33	chr7:64079400-64080200	ZNF genes & repeats	Brain Angular Gyrus	brain
34	chr7:64086000-64086400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:64086600-64087800	Enhancers	HepG2	liver
36	chr7:64087000-64087200	Enhancers	Liver	Liver
37	chr7:64087400-64089000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr7:64087800-64089000	Weak transcription	HepG2	liver
39	chr7:64088200-64089400	Enhancers	Placenta	Placenta
40	chr7:64088800-64089400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr7:64089000-64089600	Enhancers	Liver	Liver
42	chr7:64089000-64090200	Enhancers	HepG2	liver
43	chr7:64089000-64091000	Enhancers	Brain Substantia Nigra	brain
44	chr7:64089200-64089400	Enhancers	Brain Hippocampus Middle	brain
45	chr7:64089400-64097200	Weak transcription	Placenta	Placenta
46	chr7:64090200-64091200	Weak transcription	HepG2	liver
47	chr7:64090600-64091200	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr7:64091200-64091600	Enhancers	Brain Hippocampus Middle	brain
49	chr7:64091200-64091800	Enhancers	HepG2	liver
50	chr7:64096200-64096600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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