Variant report

Variant	nsv887830
Chromosome Location	chr7:19970584-20114589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1038)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:19995174-19995307	K562	blood:	n/a	n/a
2	ATF2	chr7:20069962-20071157	GM12878	blood:	n/a	n/a
3	ATF2	chr7:20104786-20105318	GM12878	blood:	n/a	n/a
4	ATF2	chr7:20070587-20071031	GM12878	blood:	n/a	n/a
5	ATF2	chr7:20059250-20059815	GM12878	blood:	n/a	n/a
6	ATF2	chr7:20092969-20093351	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:20104747-20105349	GM12878	blood:	n/a	n/a
8	ATF2	chr7:20059252-20059724	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:20059325-20059750	GM12878	blood:	n/a	n/a
10	ATF3	chr7:20009647-20010236	A549	lung:	n/a	n/a
11	ATF3	chr7:20009609-20010216	A549	lung:	n/a	n/a
12	ATF3	chr7:19997844-19998453	A549	lung:	n/a	n/a
13	ATF3	chr7:19997847-19998517	A549	lung:	n/a	n/a
14	BACH1	chr7:20056337-20056658	K562	blood:	n/a	n/a
15	BACH1	chr7:20056374-20056653	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:20093188-20093657	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr7:20104975-20105271	GM12878	blood:	n/a	n/a
18	BATF	chr7:20070016-20070483	GM12878	blood:	n/a	chr7:20070282-20070293
19	BATF	chr7:20070779-20071048	GM12878	blood:	n/a	n/a
20	BATF	chr7:20070692-20071107	GM12878	blood:	n/a	n/a
21	BATF	chr7:20070086-20070452	GM12878	blood:	n/a	chr7:20070282-20070293
22	BATF	chr7:20059309-20059660	GM12878	blood:	n/a	n/a
23	BATF	chr7:20059274-20059715	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:20070717-20071023	GM12878	blood:	n/a	chr7:20070851-20070860
25	BCL11A	chr7:20059312-20059758	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:20059384-20059699	GM12878	blood:	n/a	n/a
27	BCL3	chr7:20009545-20010519	A549	lung:	n/a	n/a
28	BCL3	chr7:19997858-19998418	A549	lung:	n/a	n/a
29	BCL3	chr7:20009573-20010231	A549	lung:	n/a	n/a
30	BCL3	chr7:19997828-19998541	A549	lung:	n/a	n/a
31	BCL3	chr7:20070657-20071019	GM12878	blood:	n/a	chr7:20070851-20070860
32	BCLAF1	chr7:20104718-20105359	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:20059270-20059737	GM12878	blood:	n/a	n/a
34	BCLAF1	chr7:20070726-20071170	GM12878	blood:	n/a	chr7:20070851-20070860
35	BCLAF1	chr7:20104838-20105270	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:20059434-20059753	GM12878	blood:	n/a	n/a
37	BRCA1	chr7:19997916-19998507	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr7:20060045-20060169	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr7:20102568-20102923	K562	blood:	n/a	n/a
40	CBX3	chr7:19984175-19984867	HCT-116	colon:	n/a	n/a
41	CBX3	chr7:20009652-20010197	HCT-116	colon:	n/a	n/a
42	CBX3	chr7:19975754-19976112	HCT-116	colon:	n/a	n/a
43	CBX3	chr7:19997709-19998597	HCT-116	colon:	n/a	n/a
44	CBX3	chr7:20009570-20010247	HCT-116	colon:	n/a	n/a
45	CBX3	chr7:19997627-19998566	HCT-116	colon:	n/a	n/a
46	CEBPB	chr7:19998108-19998457	HepG2	liver:	n/a	chr7:19998274-19998287 chr7:19998274-19998285 chr7:19998275-19998286
47	CEBPB	chr7:20009794-20010074	A549	lung:	n/a	n/a
48	CEBPB	chr7:20029802-20030101	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:20007265-20007537	IMR90	lung:	n/a	chr7:20007380-20007391
50	CEBPB	chr7:20029827-20030094	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:20010777-20010827	RPTEC	kidney:	n/a
2	chr7:20088031-20088081	SK-N-MC	brain:	n/a
3	chr7:20010777-20010827	NHBE	bronchial:	n/a
4	chr7:20042353-20042403	SKMC	muscle:	n/a
5	chr7:20042353-20042403	U87	brain:	n/a
6	chr7:20042353-20042403	HCT-116	colon:	n/a
7	chr7:20088031-20088081	HEEpiC	esophagus:	n/a
8	chr7:20010777-20010827	HEEpiC	esophagus:	n/a
9	chr7:20088031-20088081	HCPEpiC	choroid plexus:	n/a
10	chr7:20088031-20088081	HUVEC	blood vessel:	n/a
11	chr7:20088031-20088081	HepG2	liver:	n/a
12	chr7:20088031-20088081	SK-N-SH	brain:	n/a
13	chr7:20088031-20088081	H1-hESC	embryonic stem cell:	embryo
14	chr7:20042353-20042403	MCF10A-Er-Src	breast:	n/a
15	chr7:20042353-20042403	HNPCEpiC	eye:	n/a
16	chr7:20042353-20042403	HRCEpiC	kidney:	n/a
17	chr7:20042353-20042403	PANC-1	pancreas:	n/a
18	chr7:20088031-20088081	AG04450	lung:	fetal
19	chr7:20042353-20042403	SK-N-MC	brain:	n/a
20	chr7:20010777-20010827	GM06990	blood:	n/a
21	chr7:20010777-20010827	PrEC	prostate:	n/a
22	chr7:20010777-20010827	NHDF-neo	bronchial:	n/a
23	chr7:20042353-20042403	HL-60	blood:	n/a
24	chr7:20010777-20010827	HepG2	liver:	n/a
25	chr7:20088031-20088081	MCF-7	breast:	n/a
26	chr7:20088031-20088081	PFSK-1	brain:	n/a
27	chr7:20042353-20042403	AG09319	gingival:	n/a
28	chr7:20088031-20088081	GM06990	blood:	n/a
29	chr7:20042353-20042403	HCPEpiC	choroid plexus:	n/a
30	chr7:20088031-20088081	NT2-D1	testis:	n/a
31	chr7:20010777-20010827	MCF10A-Er-Src	breast:	n/a
32	chr7:20042353-20042403	CMK	blood:	n/a
33	chr7:20042353-20042403	NHBE	bronchial:	n/a
34	chr7:20042353-20042403	HEEpiC	esophagus:	n/a
35	chr7:20010777-20010827	SK-N-MC	brain:	n/a
36	chr7:20010777-20010827	Caco-2	colon:	n/a
37	chr7:20010777-20010827	BE2_C	brain:	n/a
38	chr7:20088031-20088081	HAEpiC	amniotic membrane:	n/a
39	chr7:20088031-20088081	Jurkat	blood:	n/a
40	chr7:20042353-20042403	BJ	skin:	n/a
41	chr7:20042353-20042403	BE2_C	brain:	n/a
42	chr7:20010777-20010827	NH-A	brain:	n/a
43	chr7:20010777-20010827	Hela-S3	cervix:	n/a
44	chr7:20088031-20088081	NH-A	brain:	n/a
45	chr7:20042353-20042403	ECC-1	luminal epithelium:	n/a
46	chr7:20088031-20088081	PrEC	prostate:	n/a
47	chr7:20042353-20042403	AG10803	skin:	n/a
48	chr7:20088031-20088081	SKMC	muscle:	n/a
49	chr7:20010777-20010827	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:20010777-20010827	ovcar-3	ovarian:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:19973391..19975123-chr7:19986550..19989057,2	MCF-7	breast:
2	chr7:19973391..19975123-chr7:19986550..19989057,2	MCF-7	breast:
3	chr7:20069778..20072332-chr7:20074470..20077366,2	MCF-7	breast:
4	chr7:19996523..19999289-chr7:20000423..20003780,3	MCF-7	breast:
5	chr7:20069192..20071216-chr7:20076408..20079057,2	K562	blood:
6	chr7:20007265..20009765-chr7:20010945..20013296,2	K562	blood:
7	chr7:19996523..19999289-chr7:20000423..20003780,3	MCF-7	breast:
8	chr7:20070077..20071655-chr7:20071816..20074085,2	MCF-7	breast:
9	chr7:20069778..20072332-chr7:20074470..20077366,2	MCF-7	breast:
10	chr7:20070077..20071655-chr7:20071816..20074085,2	MCF-7	breast:
11	chr7:20069192..20071216-chr7:20076408..20079057,2	K562	blood:
12	chr7:20022231..20022930-chr7:20212481..20213023,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MACC1-1	chr7:19970876-19970921	NONHSAT119395
2	lnc-MACC1-1	chr7:20085126-20085184	ENSG00000243004.1
3	lnc-MACC1-1	chr7:20068542-20068582	NR_110114
4	lnc-MACC1-1	chr7:20000545-20000617	NONHSAT119395
5	lnc-MACC1-1	chr7:19982842-19983111	ENSG00000243004.1
6	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
7	lnc-MACC1-1	chr7:20046728-20046975	ENSG00000243004.1
8	lnc-MACC1-1	chr7:20000545-20000617	NR_110114
9	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
10	lnc-MACC1-1	chr7:20044812-20044986	NONHSAT119395
11	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
12	lnc-MACC1-1	chr7:20085126-20085184	ENSG00000243004.1
13	lnc-MACC1-1	chr7:20085126-20085184	ENSG00000243004.1
14	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
15	lnc-MACC1-1	chr7:20085122-20085189	NONHSAT119395
16	lnc-MACC1-1	chr7:20085126-20085184	NR_110114
17	lnc-ITGB8-9	chr7:20057492-20064037	NONHSAT119404
18	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
19	lnc-MACC1-1	chr7:20007760-20008018	NR_110114
20	lnc-MACC1-1	chr7:20046762-20046975	NONHSAT119395
21	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
22	lnc-MACC1-1	chr7:19970876-19970921	ENSG00000243004.1
23	lnc-MACC1-1	chr7:20042343-20042545	ENSG00000243004.1
24	lnc-MACC1-1	chr7:20007777-20008018	ENSG00000243004.1
25	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
26	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
27	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
28	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
29	lnc-MACC1-1	chr7:20068542-20068582	NONHSAT119395
30	lnc-MACC1-1	chr7:20000545-20000617	ENSG00000243004.1
31	lnc-MACC1-1	chr7:20085126-20085544	NONHSAT119405
32	lnc-MACC1-1	chr7:20007777-20008018	ENSG00000243004.1
33	lnc-MACC1-1	chr7:20007760-20007860	ENSG00000243004.1
34	lnc-MACC1-1	chr7:20007760-20008018	NONHSAT119395
35	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
36	lnc-MACC1-1	chr7:19970694-19970921	ENSG00000243004.1
37	lnc-MACC1-1	chr7:20085126-20085184	ENSG00000243004.1
38	lnc-MACC1-1	chr7:20068537-20068582	NONHSAT119405
39	lnc-MACC1-1	chr7:20042343-20042467	ENSG00000243004.1
40	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1

No data

Variant related genes	Relation type
ENSG00000243004	TF binding region
RPL21P75	TF binding region
ENSG00000243004	CpG island
RPL21P75	CpG island
ENSG00000243004	chromatin interactions

Extended variants
information (count: 7131 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:7131 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs879662	chr7:19970584-19970585	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372097624	chr7:19970599-19970600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528491728	chr7:19970657-19970658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs879661	chr7:19970658-19970659	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572291687	chr7:19970660-19970661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543947862	chr7:19970742-19970743	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs192886573	chr7:19970768-19970769	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs141635021	chr7:19970779-19970780	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564734852	chr7:19970792-19970793	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs559565400	chr7:19970814-19970815	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs75927514	chr7:19970851-19970852	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs17142236	chr7:19970879-19970880	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184036833	chr7:19970882-19970883	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs542109582	chr7:19970914-19970915	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs547364202	chr7:19970915-19970916	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs187256021	chr7:19970970-19970971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17142240	chr7:19970981-19970982	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530476055	chr7:19970991-19970992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150521037	chr7:19970998-19970999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564250637	chr7:19971035-19971036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372501355	chr7:19971057-19971058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542585357	chr7:19971095-19971096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547614208	chr7:19971133-19971134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565921547	chr7:19971190-19971191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556109120	chr7:19971255-19971256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191242227	chr7:19971289-19971290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548445673	chr7:19971340-19971341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183831972	chr7:19971360-19971361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569814574	chr7:19971377-19971378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535222840	chr7:19971379-19971380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537411669	chr7:19971470-19971471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35805101	chr7:19971476-19971477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558676900	chr7:19971479-19971480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140294207	chr7:19971519-19971520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114710512	chr7:19971529-19971530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553218239	chr7:19971550-19971551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371707680	chr7:19971552-19971553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115265644	chr7:19971558-19971559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557176623	chr7:19971579-19971580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555436312	chr7:19971580-19971581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561135884	chr7:19971591-19971592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545832857	chr7:19971618-19971619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144546455	chr7:19971629-19971630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190623169	chr7:19971636-19971637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539908654	chr7:19971661-19971662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193127563	chr7:19971684-19971685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530186823	chr7:19971685-19971686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540632989	chr7:19971691-19971692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531448367	chr7:19971700-19971701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570374906	chr7:19971715-19971716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19954800-19973000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:19956400-19988000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr7:19960000-19983000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:19960800-19972400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:19960800-19982800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:19960800-19993200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:19965000-19985600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:19968400-19979000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:19969200-19970600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:19969200-19970600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:19970000-19972600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr7:19970600-19971200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:19970800-19971000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:19972400-19973400	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:19973400-19973600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:19973600-19973800	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:19973800-19982200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr7:19975200-19993200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:19978000-19978200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr7:19978200-19978800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr7:19978600-19980600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:19978800-19980000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr7:19979000-19980000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:19979000-19980000	Enhancers	NHEK	skin
25	chr7:19979000-19980000	Enhancers	Osteobl	bone
26	chr7:19979000-19980400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:19979000-19980400	Enhancers	NHDF-Ad	bronchial
28	chr7:19979000-19980600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:19979000-19981000	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr7:19979200-19980000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:19979200-19980000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:19979200-19980000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:19979200-19980000	Enhancers	HMEC	breast
34	chr7:19979400-19979800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr7:19979600-19980000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:19979600-19980200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:19979600-19980600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:19979600-19980600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr7:19979600-19981200	Enhancers	Brain Germinal Matrix	brain
40	chr7:19980000-19984000	Weak transcription	HMEC	breast
41	chr7:19980000-19984200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:19980000-19984200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:19980000-19993600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:19980600-19984200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:19982000-19993400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:19982200-19984600	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr7:19982800-19983200	Strong transcription	H9 Cell Line	embryonic stem cell
48	chr7:19983000-19983600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
49	chr7:19983200-19994000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:19983600-19984000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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