Variant report

Variant	nsv1027849
Chromosome Location	chr7:20003094-20084998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:20059325-20059750	GM12878	blood:	n/a	n/a
2	ATF2	chr7:20070587-20071031	GM12878	blood:	n/a	n/a
3	ATF2	chr7:20069962-20071157	GM12878	blood:	n/a	n/a
4	ATF2	chr7:20059250-20059815	GM12878	blood:	n/a	n/a
5	ATF2	chr7:20059252-20059724	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr7:20009609-20010216	A549	lung:	n/a	n/a
7	ATF3	chr7:20009647-20010236	A549	lung:	n/a	n/a
8	BACH1	chr7:20056337-20056658	K562	blood:	n/a	n/a
9	BACH1	chr7:20056374-20056653	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:20070086-20070452	GM12878	blood:	n/a	chr7:20070282-20070293
11	BATF	chr7:20059274-20059715	GM12878	blood:	n/a	n/a
12	BATF	chr7:20070016-20070483	GM12878	blood:	n/a	chr7:20070282-20070293
13	BATF	chr7:20070779-20071048	GM12878	blood:	n/a	n/a
14	BATF	chr7:20070692-20071107	GM12878	blood:	n/a	n/a
15	BATF	chr7:20059309-20059660	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:20070717-20071023	GM12878	blood:	n/a	chr7:20070851-20070860
17	BCL11A	chr7:20059312-20059758	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:20059384-20059699	GM12878	blood:	n/a	n/a
19	BCL3	chr7:20009545-20010519	A549	lung:	n/a	n/a
20	BCL3	chr7:20009573-20010231	A549	lung:	n/a	n/a
21	BCL3	chr7:20070657-20071019	GM12878	blood:	n/a	chr7:20070851-20070860
22	BCLAF1	chr7:20059270-20059737	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:20070726-20071170	GM12878	blood:	n/a	chr7:20070851-20070860
24	BHLHE40	chr7:20059434-20059753	GM12878	blood:	n/a	n/a
25	BRCA1	chr7:20060045-20060169	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr7:20009570-20010247	HCT-116	colon:	n/a	n/a
27	CBX3	chr7:20009652-20010197	HCT-116	colon:	n/a	n/a
28	CEBPB	chr7:20039368-20039514	HepG2	liver:	n/a	chr7:20039453-20039464 chr7:20039413-20039424
29	CEBPB	chr7:20029827-20030094	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:20009788-20010209	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:20008416-20008876	A549	lung:	n/a	chr7:20008461-20008472
32	CEBPB	chr7:20009794-20010074	A549	lung:	n/a	n/a
33	CEBPB	chr7:20024205-20024240	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:20009301-20010476	A549	lung:	n/a	n/a
35	CEBPB	chr7:20029843-20030027	K562	blood:	n/a	n/a
36	CEBPB	chr7:20007265-20007537	IMR90	lung:	n/a	chr7:20007380-20007391
37	CEBPB	chr7:20008347-20008589	IMR90	lung:	n/a	chr7:20008461-20008472
38	CEBPB	chr7:20018964-20019154	A549	lung:	n/a	chr7:20019063-20019074
39	CEBPB	chr7:20008376-20008606	HepG2	liver:	n/a	chr7:20008461-20008472
40	CEBPB	chr7:20007265-20007500	HepG2	liver:	n/a	chr7:20007380-20007391
41	CEBPB	chr7:20078356-20078443	K562	blood:	n/a	chr7:20078406-20078419 chr7:20078406-20078419 chr7:20078408-20078419
42	CEBPB	chr7:20018965-20019235	HepG2	liver:	n/a	chr7:20019063-20019074
43	CEBPB	chr7:20029810-20030095	A549	lung:	n/a	n/a
44	CEBPB	chr7:20029798-20030091	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:20073207-20073667	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:20073217-20073579	A549	lung:	n/a	n/a
47	CEBPB	chr7:20029802-20030101	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:20009696-20010222	A549	lung:	n/a	n/a
49	CEBPB	chr7:20003373-20003488	A549	lung:	n/a	n/a
50	CHD1	chr7:20022908-20022928	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:20042353-20042403	GM12878	blood:	n/a
2	chr7:20042353-20042403	HCPEpiC	choroid plexus:	n/a
3	chr7:20010777-20010827	SKMC	muscle:	n/a
4	chr7:20010777-20010827	HCM	heart:	n/a
5	chr7:20010777-20010827	HL-60	blood:	n/a
6	chr7:20010777-20010827	NHDF-neo	bronchial:	n/a
7	chr7:20010777-20010827	Caco-2	colon:	n/a
8	chr7:20042353-20042403	NT2-D1	testis:	n/a
9	chr7:20042353-20042403	HRPEpiC	eye:	n/a
10	chr7:20010777-20010827	H1-hESC	embryonic stem cell:	embryo
11	chr7:20010777-20010827	HCT-116	colon:	n/a
12	chr7:20042353-20042403	AoSMC	blood vessel:	n/a
13	chr7:20042353-20042403	HEEpiC	esophagus:	n/a
14	chr7:20042353-20042403	AG04450	lung:	fetal
15	chr7:20042353-20042403	AG09319	gingival:	n/a
16	chr7:20042353-20042403	Hela-S3	cervix:	n/a
17	chr7:20010777-20010827	GM06990	blood:	n/a
18	chr7:20042353-20042403	GM19239	blood:	n/a
19	chr7:20010777-20010827	PANC-1	pancreas:	n/a
20	chr7:20010777-20010827	CMK	blood:	n/a
21	chr7:20042353-20042403	HEK293	kidney:	embryo
22	chr7:20010777-20010827	SK-N-SH_RA	brain:	n/a
23	chr7:20010777-20010827	AG04450	lung:	fetal
24	chr7:20042353-20042403	HMEC	breast:	n/a
25	chr7:20042353-20042403	PFSK-1	brain:	n/a
26	chr7:20042353-20042403	Jurkat	blood:	n/a
27	chr7:20010777-20010827	HepG2	liver:	n/a
28	chr7:20042353-20042403	H1-hESC	embryonic stem cell:	embryo
29	chr7:20010777-20010827	AG09319	gingival:	n/a
30	chr7:20010777-20010827	NH-A	brain:	n/a
31	chr7:20042353-20042403	HL-60	blood:	n/a
32	chr7:20042353-20042403	RPTEC	kidney:	n/a
33	chr7:20010777-20010827	NB4	blood:	n/a
34	chr7:20010777-20010827	MCF10A-Er-Src	breast:	n/a
35	chr7:20010777-20010827	HRE	kidney:	n/a
36	chr7:20010777-20010827	AoSMC	blood vessel:	n/a
37	chr7:20042353-20042403	HCT-116	colon:	n/a
38	chr7:20042353-20042403	ECC-1	luminal epithelium:	n/a
39	chr7:20042353-20042403	MCF10A-Er-Src	breast:	n/a
40	chr7:20010777-20010827	PFSK-1	brain:	n/a
41	chr7:20010777-20010827	BJ	skin:	n/a
42	chr7:20042353-20042403	HCF	heart:	n/a
43	chr7:20010777-20010827	PrEC	prostate:	n/a
44	chr7:20010777-20010827	HRPEpiC	eye:	n/a
45	chr7:20042353-20042403	BJ	skin:	n/a
46	chr7:20042353-20042403	HCM	heart:	n/a
47	chr7:20042353-20042403	GM12891	blood:	n/a
48	chr7:20042353-20042403	NB4	blood:	n/a
49	chr7:20042353-20042403	CMK	blood:	n/a
50	chr7:20042353-20042403	GM06990	blood:	n/a

(count:9 , 50 per page) page: 1

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

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MACC1-1	chr7:20007777-20008018	ENSG00000243004.1
2	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
3	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
4	lnc-MACC1-1	chr7:20068542-20068582	NR_110114
5	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
6	lnc-MACC1-1	chr7:20046762-20046975	NONHSAT119395
7	lnc-MACC1-1	chr7:20068537-20068582	NONHSAT119405
8	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
9	lnc-MACC1-1	chr7:20046728-20046975	ENSG00000243004.1
10	lnc-MACC1-1	chr7:20068542-20068582	NONHSAT119395
11	lnc-MACC1-1	chr7:20007760-20008018	NONHSAT119395
12	lnc-MACC1-1	chr7:20007760-20007860	ENSG00000243004.1
13	lnc-MACC1-1	chr7:20042343-20042545	ENSG00000243004.1
14	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
15	lnc-MACC1-1	chr7:20068542-20068582	ENSG00000243004.1
16	lnc-MACC1-1	chr7:20007760-20008018	NR_110114
17	lnc-MACC1-1	chr7:20044812-20044986	NONHSAT119395
18	lnc-MACC1-1	chr7:20007777-20008018	ENSG00000243004.1
19	lnc-MACC1-1	chr7:20007760-20008018	ENSG00000243004.1
20	lnc-ITGB8-9	chr7:20057492-20064037	NONHSAT119404
21	lnc-MACC1-1	chr7:20042343-20042467	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: 3872 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3872 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17142269	chr7:20003094-20003095	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552714445	chr7:20003123-20003124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574275669	chr7:20003125-20003126	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181586593	chr7:20003133-20003134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35377009	chr7:20003157-20003158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531669469	chr7:20003161-20003162	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575141960	chr7:20003171-20003172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368906355	chr7:20003245-20003246	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545312194	chr7:20003307-20003308	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187077975	chr7:20003352-20003353	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115502420	chr7:20003425-20003426	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543059921	chr7:20003439-20003440	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368832022	chr7:20003444-20003445	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540317471	chr7:20003461-20003462	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559754669	chr7:20003468-20003469	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527609356	chr7:20003469-20003470	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144324062	chr7:20003495-20003496	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530315995	chr7:20003500-20003501	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548943497	chr7:20003502-20003503	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189506060	chr7:20003505-20003506	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117588043	chr7:20003524-20003525	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376152167	chr7:20003545-20003546	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181149031	chr7:20003558-20003559	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112439419	chr7:20003577-20003578	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535153161	chr7:20003586-20003587	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564344754	chr7:20003613-20003614	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs553027036	chr7:20003662-20003663	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs371543850	chr7:20003666-20003667	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs113920260	chr7:20003735-20003736	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs73684938	chr7:20003753-20003754	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189523546	chr7:20003757-20003758	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182229139	chr7:20003773-20003774	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545498243	chr7:20003777-20003778	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs549526370	chr7:20003787-20003788	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs377497265	chr7:20003831-20003832	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs572730840	chr7:20003834-20003835	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs540377985	chr7:20003859-20003860	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs561760199	chr7:20003869-20003870	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529728955	chr7:20003893-20003894	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs186215134	chr7:20003912-20003913	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs115198736	chr7:20004012-20004013	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs147789928	chr7:20004032-20004033	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs563846498	chr7:20004066-20004067	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs191077987	chr7:20004133-20004134	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs372407319	chr7:20004139-20004140	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs531200164	chr7:20004142-20004143	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs183341061	chr7:20004163-20004164	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs188797750	chr7:20004215-20004216	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs528463916	chr7:20004221-20004222	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs528930095	chr7:20004267-20004268	Strong transcription Weak transcription Enhancers Flanking Active TSS	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:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19991800-20010000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:19998200-20003200	Strong transcription	HUES6 Cell Line	embryonic stem cell
3	chr7:19998400-20009800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:19999400-20009600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:19999600-20005800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:19999600-20023800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:20000200-20004000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:20000200-20006000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr7:20000200-20006800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:20000200-20007000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:20001400-20009600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:20001400-20009800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:20002400-20003400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:20002600-20003200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:20003000-20004400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:20003000-20004400	Enhancers	A549	lung
17	chr7:20003000-20004400	Enhancers	NHDF-Ad	bronchial
18	chr7:20003000-20004400	Enhancers	Osteobl	bone
19	chr7:20003200-20003600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:20003200-20005800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr7:20003400-20004400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:20003600-20004000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:20003600-20004400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:20003600-20004400	Enhancers	Adipose Nuclei	Adipose
25	chr7:20003600-20004600	Enhancers	Fetal Brain Male	brain
26	chr7:20003800-20004400	Enhancers	Fetal Brain Female	brain
27	chr7:20003800-20004600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:20004000-20004400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:20004000-20004400	Enhancers	Fetal Muscle Leg	muscle
30	chr7:20004000-20004600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:20004400-20005000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:20004400-20009800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr7:20004400-20009800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:20004400-20009800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:20004600-20009200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:20004600-20009200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:20005000-20009800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:20005800-20007800	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr7:20005800-20008000	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr7:20006000-20008000	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr7:20006400-20006600	Weak transcription	A549	lung
42	chr7:20006800-20007200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
43	chr7:20007000-20007600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:20007200-20010400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr7:20007600-20009600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:20007800-20024000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr7:20008000-20010000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr7:20008000-20017200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:20008200-20008800	Enhancers	A549	lung
50	chr7:20008800-20009600	Flanking Active TSS	A549	lung

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