Variant report

Variant	nsv607999
Chromosome Location	chr7:102091735-102113899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1415)
CpG islands
(count:1650)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102105026-102105477	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102107670-102107707	HepG2	liver:	n/a	n/a
3	ATF2	chr7:102105214-102105642	GM12878	blood:	n/a	n/a
4	ATF3	chr7:102105079-102105666	K562	blood:	n/a	chr7:102105134-102105143
5	ATF3	chr7:102105052-102105541	A549	lung:	n/a	chr7:102105134-102105143
6	ATF3	chr7:102105156-102105479	HepG2	liver:	n/a	n/a
7	ATF3	chr7:102105121-102105483	H1-hESC	embryonic stem cell:	n/a	chr7:102105134-102105143
8	BACH1	chr7:102105152-102105627	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:102105195-102105583	K562	blood:	n/a	n/a
10	BATF	chr7:102106969-102107235	GM12878	blood:	n/a	chr7:102107141-102107152
11	BCL3	chr7:102105600-102105954	A549	lung:	n/a	n/a
12	BCL3	chr7:102104786-102105505	A549	lung:	n/a	n/a
13	BCL3	chr7:102112299-102112773	A549	lung:	n/a	n/a
14	BCL3	chr7:102112864-102113524	K562	blood:	n/a	n/a
15	BCLAF1	chr7:102105109-102105696	K562	blood:	n/a	n/a
16	BCLAF1	chr7:102105007-102105737	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:102091750-102092371	K562	blood:	n/a	n/a
18	BHLHE40	chr7:102105028-102105670	K562	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
19	BHLHE40	chr7:102105053-102105547	GM12878	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
20	BHLHE40	chr7:102104315-102104322	K562	blood:	n/a	n/a
21	BHLHE40	chr7:102091790-102092420	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:102113202-102113205	K562	blood:	n/a	n/a
23	BRCA1	chr7:102107676-102107680	HepG2	liver:	n/a	n/a
24	BRCA1	chr7:102107666-102107866	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:102105131-102105589	HepG2	liver:	n/a	n/a
26	BRCA1	chr7:102105238-102105495	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr7:102105043-102105492	GM12878	blood:	n/a	n/a
28	CBX3	chr7:102091779-102092291	K562	blood:	n/a	n/a
29	CBX3	chr7:102104440-102105788	K562	blood:	n/a	n/a
30	CBX3	chr7:102112962-102113369	K562	blood:	n/a	n/a
31	CCNT2	chr7:102105109-102105718	K562	blood:	n/a	n/a
32	CCNT2	chr7:102109140-102109266	K562	blood:	n/a	n/a
33	CCNT2	chr7:102092098-102092369	K562	blood:	n/a	n/a
34	CCNT2	chr7:102112855-102113285	K562	blood:	n/a	n/a
35	CEBPB	chr7:102095461-102095749	K562	blood:	n/a	n/a
36	CEBPB	chr7:102095540-102095640	K562	blood:	n/a	n/a
37	CEBPB	chr7:102105250-102105458	GM12878	blood:	n/a	n/a
38	CEBPB	chr7:102105268-102105644	Hela-S3	cervix:	n/a	n/a
39	CEBPD	chr7:102092180-102092498	HepG2	liver:	n/a	n/a
40	CEBPD	chr7:102105226-102105633	HepG2	liver:	n/a	n/a
41	CHD1	chr7:102105332-102105854	GM12878	blood:	n/a	n/a
42	CHD1	chr7:102105968-102105976	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr7:102112558-102113172	K562	blood:	n/a	n/a
44	CHD2	chr7:102102554-102102721	K562	blood:	n/a	chr7:102102649-102102659
45	CHD2	chr7:102104973-102105628	GM12878	blood:	n/a	n/a
46	CHD2	chr7:102107547-102107747	GM12878	blood:	n/a	n/a
47	CHD2	chr7:102105035-102105755	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr7:102111069-102111149	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr7:102105044-102105606	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr7:102104946-102105631	HepG2	liver:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102096976-102097026	PrEC	prostate:	n/a
2	chr7:102100221-102100271	HRPEpiC	eye:	n/a
3	chr7:102105781-102105831	PFSK-1	brain:	n/a
4	chr7:102096976-102097026	PrEC	prostate:	n/a
5	chr7:102100221-102100271	HRPEpiC	eye:	n/a
6	chr7:102105781-102105831	PFSK-1	brain:	n/a
7	chr7:102109095-102109145	HEEpiC	esophagus:	n/a
8	chr7:102105195-102105245	HEEpiC	esophagus:	n/a
9	chr7:102105205-102105255	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:102100957-102101007	ovcar-3	ovarian:	n/a
11	chr7:102095364-102095414	Jurkat	blood:	n/a
12	chr7:102105344-102105394	NH-A	brain:	n/a
13	chr7:102105124-102105174	HCF	heart:	n/a
14	chr7:102109446-102109496	AoSMC	blood vessel:	n/a
15	chr7:102096322-102096372	Hepatocyte	liver:	n/a
16	chr7:102105195-102105245	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:102105201-102105251	BJ	skin:	n/a
18	chr7:102098214-102098264	ProgFib	skin:	n/a
19	chr7:102105124-102105174	SK-N-MC	brain:	n/a
20	chr7:102105205-102105255	ECC-1	luminal epithelium:	n/a
21	chr7:102105124-102105174	Jurkat	blood:	n/a
22	chr7:102105195-102105245	Jurkat	blood:	n/a
23	chr7:102105195-102105245	Caco-2	colon:	n/a
24	chr7:102098214-102098264	SK-N-SH	brain:	n/a
25	chr7:102100221-102100271	SK-N-MC	brain:	n/a
26	chr7:102109095-102109145	PrEC	prostate:	n/a
27	chr7:102105124-102105174	LNCaP	prostate:	n/a
28	chr7:102105256-102105306	HMEC	breast:	n/a
29	chr7:102109446-102109496	HCT-116	colon:	n/a
30	chr7:102098383-102098433	HEK293	kidney:	embryo
31	chr7:102096322-102096372	AG04449	skin:	fetal
32	chr7:102104916-102104966	GM12892	blood:	n/a
33	chr7:102105195-102105245	AG10803	skin:	n/a
34	chr7:102107737-102107787	BJ	skin:	n/a
35	chr7:102098004-102098054	SK-N-MC	brain:	n/a
36	chr7:102096976-102097026	T-47D	breast:	n/a
37	chr7:102100957-102101007	IMR90	lung:	fetal
38	chr7:102105124-102105174	HCPEpiC	choroid plexus:	n/a
39	chr7:102105205-102105255	HCPEpiC	choroid plexus:	n/a
40	chr7:102096322-102096372	SKMC	muscle:	n/a
41	chr7:102102804-102102854	SKMC	muscle:	n/a
42	chr7:102095364-102095414	Hepatocyte	liver:	n/a
43	chr7:102098214-102098264	AG04449	skin:	fetal
44	chr7:102105124-102105174	NHBE	bronchial:	n/a
45	chr7:102107737-102107787	A549	lung:	n/a
46	chr7:102113508-102113558	ovcar-3	ovarian:	n/a
47	chr7:102104807-102104857	ProgFib	skin:	n/a
48	chr7:102109095-102109145	RPTEC	kidney:	n/a
49	chr7:102105124-102105174	U87	brain:	n/a
50	chr7:102105641-102105691	NHBE	bronchial:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:
2	chr7:102091019..102095913-chr7:102104103..102106811,4	MCF-7	breast:
3	chr10:12391000..12393664-chr7:102102754..102105293,2	MCF-7	breast:
4	chr7:101929851..101931493-chr7:102106221..102107741,2	MCF-7	breast:
5	chr7:102110628..102112535-chr8:144951000..144953117,2	MCF-7	breast:
6	chr7:102079604..102082323-chr7:102098153..102099858,2	K562	blood:
7	chr7:102092230..102094061-chr7:102103945..102105916,2	MCF-7	breast:
8	chr7:102078066..102079925-chr7:102090225..102091966,2	MCF-7	breast:
9	chr7:102081053..102083891-chr7:102093454..102096463,3	K562	blood:
10	chr7:102096319..102099955-chr7:102103151..102107969,7	K562	blood:
11	chr7:102036206..102039256-chr7:102090414..102093490,3	MCF-7	breast:
12	chr7:102092377..102094022-chr7:102102863..102104706,2	K562	blood:
13	chr7:102089632..102093440-chr7:102095527..102097996,3	MCF-7	breast:
14	chr7:102096270..102098685-chr7:102100293..102102957,2	K562	blood:
15	chr7:102085518..102087165-chr7:102088201..102092179,3	K562	blood:
16	chr7:102088198..102090049-chr7:102090279..102092593,3	K562	blood:
17	chr7:101935058..101937626-chr7:102103527..102105838,2	MCF-7	breast:
18	chr7:102074336..102076927-chr7:102105688..102108273,2	K562	blood:
19	chr7:102035604..102038403-chr7:102105375..102107150,2	K562	blood:
20	chr7:102085208..102087796-chr7:102094817..102096828,2	K562	blood:
21	chr7:102073010..102075426-chr7:102094400..102095987,2	MCF-7	breast:
22	chr16:90039038..90039558-chr7:102105289..102105810,2	Hela-S3	cervix:
23	chr7:102098444..102099997-chr7:102102741..102105634,2	MCF-7	breast:
24	chr7:102089632..102093440-chr7:102095527..102097996,3	MCF-7	breast:
25	chr7:102035810..102037388-chr7:102090384..102093265,2	MCF-7	breast:
26	chr7:102080981..102083598-chr7:102093861..102096149,2	K562	blood:
27	chr7:102092377..102094022-chr7:102102863..102104706,2	K562	blood:
28	chr7:102095105..102097142-chr7:102112791..102114354,2	K562	blood:
29	chr7:102095105..102097142-chr7:102112791..102114354,2	K562	blood:
30	chr7:102100941..102102997-chr7:102104685..102106440,2	MCF-7	breast:
31	chr7:102053096..102053747-chr7:102091700..102092244,2	K562	blood:
32	chr7:102096270..102098685-chr7:102100293..102102957,2	K562	blood:
33	chr7:102073812..102076569-chr7:102099712..102102534,2	K562	blood:
34	chr7:102092159..102093750-chr7:102104302..102106947,2	K562	blood:
35	chr6:82462024..82463020-chr7:102105257..102105953,2	NB4	blood:
36	chr7:102095134..102098505-chr7:102103151..102109325,7	K562	blood:
37	chr7:5571535..5572189-chr7:102091352..102092031,2	Hela-S3	cervix:
38	chr7:102073875..102075484-chr7:102103725..102106348,2	MCF-7	breast:
39	chr7:102073749..102075617-chr7:102090961..102093380,2	K562	blood:
40	chr7:102085730..102086410-chr7:102110585..102111557,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4467	chr7:102111919-102111940	MIMAT0018994
hsa-miR-5090	chr7:102106199-102106221	MIMAT0021082

No data

Variant related genes	Relation type
ALKBH4	TF binding region
MIR5090	TF binding region
MIR4467	TF binding region
LRWD1	TF binding region
ALKBH4	CpG island
MIR5090	CpG island
MIR4467	CpG island
LRWD1	CpG island
ENSG00000112773	chromatin interactions
ENSG00000264675	chromatin interactions
ENSG00000160993	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000266715	chromatin interactions
ENSG00000005075	chromatin interactions
ENSG00000160991	chromatin interactions
ENSG00000227184	chromatin interactions
ENSG00000239480	chromatin interactions
ENSG00000161036	chromatin interactions
ENSG00000183049	chromatin interactions
ENSG00000223959	chromatin interactions

Extended variants
information (count: 1206 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1206 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4481505	chr7:102091735-102091736	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146434985	chr7:102091766-102091767	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs3823657	chr7:102091770-102091771	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs371454010	chr7:102091837-102091838	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs548853575	chr7:102091840-102091841	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs567153461	chr7:102091843-102091844	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs538019418	chr7:102091855-102091856	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs557188204	chr7:102091899-102091900	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs561991297	chr7:102091932-102091933	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs539449934	chr7:102091933-102091934	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs573567449	chr7:102091939-102091940	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs558227600	chr7:102091944-102091945	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs374353790	chr7:102091967-102091968	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs113524320	chr7:102091990-102091991	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs540961532	chr7:102091991-102091992	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs111469404	chr7:102092001-102092002	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs577395919	chr7:102092006-102092007	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs76231257	chr7:102092037-102092038	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs544752448	chr7:102092060-102092061	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs562448735	chr7:102092065-102092066	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs533096369	chr7:102092079-102092080	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs181682962	chr7:102092103-102092104	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs559753797	chr7:102092117-102092118	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs3800986	chr7:102092125-102092126	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs548888709	chr7:102092130-102092131	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs4562246	chr7:102092178-102092179	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs537652535	chr7:102092228-102092229	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs373904368	chr7:102092241-102092242	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs552496124	chr7:102092242-102092243	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs571348474	chr7:102092260-102092261	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs539960443	chr7:102092265-102092266	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs556002834	chr7:102092296-102092297	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs367716436	chr7:102092306-102092307	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs566899541	chr7:102092383-102092384	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs574051330	chr7:102092390-102092391	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs369558811	chr7:102092403-102092404	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs534154339	chr7:102092428-102092429	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs73712488	chr7:102092461-102092462	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs574229120	chr7:102092488-102092489	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs374306683	chr7:102092503-102092504	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs112797429	chr7:102092518-102092519	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs578100598	chr7:102092573-102092574	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs151226546	chr7:102092609-102092610	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs559790584	chr7:102092634-102092635	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs77198822	chr7:102092671-102092672	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs185859340	chr7:102092758-102092759	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs544026855	chr7:102092766-102092767	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs375615199	chr7:102092784-102092785	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs191003895	chr7:102092807-102092808	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs549795208	chr7:102092827-102092828	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1485 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102075000-102099800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:102075000-102104000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:102075200-102092000	Weak transcription	Esophagus	oesophagus
4	chr7:102075200-102095200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:102075200-102097600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:102075200-102104200	Weak transcription	Fetal Kidney	kidney
7	chr7:102075400-102097000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr7:102075600-102103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr7:102075800-102103600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr7:102076000-102097600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr7:102076000-102104200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr7:102081000-102091800	Weak transcription	HSMMtube	muscle
13	chr7:102081200-102091800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr7:102081200-102091800	Weak transcription	HMEC	breast
15	chr7:102081200-102091800	Weak transcription	NHDF-Ad	bronchial
16	chr7:102081200-102092000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:102081200-102092000	Weak transcription	HSMM	muscle
18	chr7:102081200-102095600	Weak transcription	Brain Substantia Nigra	brain
19	chr7:102081200-102096200	Weak transcription	Left Ventricle	heart
20	chr7:102081200-102098000	Weak transcription	Small Intestine	intestine
21	chr7:102081200-102104200	Weak transcription	Right Atrium	heart
22	chr7:102081400-102098200	Weak transcription	Hela-S3	cervix
23	chr7:102082400-102091800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:102082400-102091800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:102082600-102096600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:102084400-102104000	Weak transcription	Fetal Brain Male	brain
27	chr7:102086200-102091800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:102087000-102093400	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr7:102087400-102091800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:102087400-102092000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr7:102087400-102097800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:102087600-102091800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:102087600-102093600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr7:102087600-102096200	Weak transcription	Aorta	Aorta
35	chr7:102087800-102091800	Weak transcription	Osteobl	bone
36	chr7:102087800-102095800	Weak transcription	Fetal Intestine Large	intestine
37	chr7:102087800-102097000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr7:102087800-102097000	Weak transcription	Colon Smooth Muscle	Colon
39	chr7:102087800-102097200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:102088000-102092000	Weak transcription	Pancreas	Pancrea
41	chr7:102088000-102095800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr7:102088000-102096000	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr7:102088000-102096000	Weak transcription	Dnd41	blood
44	chr7:102088000-102096200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr7:102088200-102091800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr7:102088200-102095800	Weak transcription	Brain Cingulate Gyrus	brain
47	chr7:102088200-102096000	Weak transcription	Gastric	stomach
48	chr7:102088200-102096600	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr7:102088200-102104200	Weak transcription	HUVEC	blood vessel
50	chr7:102088400-102095600	Weak transcription	Colonic Mucosa	Colon

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