Variant report

Variant	esv3333602
Chromosome Location	chr7:2882776-2885274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:794)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:2883943-2884447	K562	blood:	n/a	n/a
2	ARID3A	chr7:2884019-2884553	HepG2	liver:	n/a	n/a
3	ATF1	chr7:2883937-2884453	K562	blood:	n/a	n/a
4	ATF3	chr7:2883538-2883793	K562	blood:	n/a	n/a
5	BACH1	chr7:2884096-2884747	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:2884324-2884729	K562	blood:	n/a	n/a
7	BACH1	chr7:2883510-2883752	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:2883910-2885058	K562	blood:	n/a	chr7:2883924-2883940 chr7:2883916-2883932
9	BHLHE40	chr7:2883899-2884369	GM12878	blood:	n/a	chr7:2883924-2883940 chr7:2883916-2883932 chr7:2883907-2883923
10	BHLHE40	chr7:2883930-2884522	HepG2	liver:	n/a	n/a
11	BHLHE40	chr7:2884806-2884996	HepG2	liver:	n/a	n/a
12	BRCA1	chr7:2884017-2884306	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr7:2883398-2884393	K562	blood:	n/a	n/a
14	CEBPB	chr7:2884523-2884849	A549	lung:	n/a	chr7:2884693-2884704
15	CEBPB	chr7:2883966-2884907	MCF-7	breast:	n/a	chr7:2884053-2884061 chr7:2884693-2884704
16	CEBPB	chr7:2884642-2884817	HepG2	liver:	n/a	chr7:2884693-2884704
17	CEBPB	chr7:2883973-2884874	K562	blood:	n/a	chr7:2884053-2884061 chr7:2884693-2884704
18	CEBPB	chr7:2884007-2884420	HepG2	liver:	n/a	chr7:2884053-2884061
19	CEBPB	chr7:2884405-2884851	H1-hESC	embryonic stem cell:	n/a	chr7:2884693-2884704
20	CEBPB	chr7:2883944-2884183	IMR90	lung:	n/a	chr7:2884053-2884061
21	CEBPB	chr7:2883965-2884393	Hela-S3	cervix:	n/a	chr7:2884053-2884061
22	CEBPB	chr7:2884445-2884819	A549	lung:	n/a	chr7:2884693-2884704
23	CEBPD	chr7:2884224-2884527	HepG2	liver:	n/a	n/a
24	CEBPZ	chr7:2883967-2884577	HepG2	liver:	n/a	n/a
25	CHD1	chr7:2882681-2884736	IMR90	lung:	n/a	n/a
26	CHD1	chr7:2883510-2883561	GM12878	blood:	n/a	n/a
27	CHD2	chr7:2883852-2884467	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr7:2883866-2884679	GM12878	blood:	n/a	n/a
29	CHD2	chr7:2883877-2884544	K562	blood:	n/a	n/a
30	CHD2	chr7:2883873-2884557	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:2884251-2884451	HepG2	liver:	n/a	n/a
32	CREB1	chr7:2883294-2884629	HepG2	liver:	n/a	n/a
33	CREB1	chr7:2883812-2884598	HepG2	liver:	n/a	n/a
34	CREB1	chr7:2883885-2884400	A549	lung:	n/a	n/a
35	CREB1	chr7:2883929-2884486	ECC-1	luminal epithelium:	n/a	n/a
36	CREB1	chr7:2883559-2884479	A549	lung:	n/a	n/a
37	CREB1	chr7:2883848-2884538	GM12878	blood:	n/a	n/a
38	CREB1	chr7:2883875-2884530	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr7:2883826-2884632	K562	blood:	n/a	n/a
40	CREB1	chr7:2883776-2884565	K562	blood:	n/a	n/a
41	CREB1	chr7:2883847-2884490	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr7:2883506-2883565	Gliobla	brain:	n/a	n/a
43	CTCF	chr7:2883520-2883670	GM12869	blood:	n/a	n/a
44	CTCF	chr7:2883180-2883330	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:2883210-2883241	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:2883191-2883267	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:2883160-2883310	AG04449	skin:	n/a	n/a
48	CTCF	chr7:2883486-2883568	Fibrobl	skin:	n/a	n/a
49	CTCF	chr7:2883120-2883270	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:2883440-2883590	AG09319	gingival:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:2884028-2884078	AG09319	gingival:	n/a
2	chr7:2884028-2884078	AG09319	gingival:	n/a
3	chr7:2884276-2884326	SAEC	small airway:	n/a
4	chr7:2884365-2884415	Hepatocyte	liver:	n/a
5	chr7:2884448-2884498	HL-60	blood:	n/a
6	chr7:2884313-2884363	GM06990	blood:	n/a
7	chr7:2884124-2884174	HEK293	kidney:	embryo
8	chr7:2884365-2884415	NB4	blood:	n/a
9	chr7:2884303-2884353	HNPCEpiC	eye:	n/a
10	chr7:2884313-2884363	K562	blood:	n/a
11	chr7:2884021-2884071	HUVEC	blood vessel:	n/a
12	chr7:2884028-2884078	HCT-116	colon:	n/a
13	chr7:2883003-2883053	A549	lung:	n/a
14	chr7:2883529-2883579	IMR90	lung:	fetal
15	chr7:2884040-2884090	HCF	heart:	n/a
16	chr7:2884040-2884090	HIPEpiC	eye:	n/a
17	chr7:2884303-2884353	GM12891	blood:	n/a
18	chr7:2884021-2884071	NH-A	brain:	n/a
19	chr7:2884313-2884363	Jurkat	blood:	n/a
20	chr7:2883529-2883579	SKMC	muscle:	n/a
21	chr7:2883003-2883053	Hepatocyte	liver:	n/a
22	chr7:2884040-2884090	Hepatocyte	liver:	n/a
23	chr7:2884028-2884078	NH-A	brain:	n/a
24	chr7:2884313-2884363	GM19239	blood:	n/a
25	chr7:2884040-2884090	PrEC	prostate:	n/a
26	chr7:2884079-2884129	HUVEC	blood vessel:	n/a
27	chr7:2884021-2884071	HEEpiC	esophagus:	n/a
28	chr7:2884276-2884326	AG04449	skin:	fetal
29	chr7:2883003-2883053	NHDF-neo	bronchial:	n/a
30	chr7:2884028-2884078	AG04449	skin:	fetal
31	chr7:2884028-2884078	U87	brain:	n/a
32	chr7:2884365-2884415	AoSMC	blood vessel:	n/a
33	chr7:2884303-2884353	CMK	blood:	n/a
34	chr7:2883003-2883053	AG09309	skin:	n/a
35	chr7:2884040-2884090	HUVEC	blood vessel:	n/a
36	chr7:2884124-2884174	BJ	skin:	n/a
37	chr7:2884313-2884363	AG04450	lung:	fetal
38	chr7:2884079-2884129	LNCaP	prostate:	n/a
39	chr7:2884158-2884208	MCF10A-Er-Src	breast:	n/a
40	chr7:2884313-2884363	LNCaP	prostate:	n/a
41	chr7:2884158-2884208	PrEC	prostate:	n/a
42	chr7:2884124-2884174	AG09319	gingival:	n/a
43	chr7:2884079-2884129	NT2-D1	testis:	n/a
44	chr7:2884040-2884090	GM12891	blood:	n/a
45	chr7:2884021-2884071	NT2-D1	testis:	n/a
46	chr7:2884365-2884415	AG04450	lung:	fetal
47	chr7:2884303-2884353	GM12878	blood:	n/a
48	chr7:2884158-2884208	AG09309	skin:	n/a
49	chr7:2884158-2884208	Jurkat	blood:	n/a
50	chr7:2884276-2884326	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:2878232..2880029-chr7:2884178..2886023,2	MCF-7	breast:
2	chr7:2869377..2877481-chr7:2880306..2885399,15	MCF-7	breast:
3	chr7:2726313..2732670-chr7:2878755..2886203,10	MCF-7	breast:
4	chr7:2801788..2804432-chr7:2882018..2884117,3	K562	blood:
5	chr1:149858014..149859677-chr7:2882924..2885730,2	MCF-7	breast:
6	chr7:2884125..2886886-chr7:2909522..2911680,2	MCF-7	breast:

No data

Variant related genes	Relation type
GNA12	TF binding region
GNA12	CpG island
ENSG00000178096	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000174945	chromatin interactions
ENSG00000231357	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000146535	chromatin interactions

Extended variants
information (count: 127 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:127 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6979678	chr7:2882781-2882782	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs115206206	chr7:2882787-2882788	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs369064563	chr7:2882811-2882812	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs6942735	chr7:2882815-2882816	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144092469	chr7:2882816-2882817	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs114460598	chr7:2882827-2882828	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs2533875	chr7:2882829-2882830	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs73033417	chr7:2882855-2882856	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538906329	chr7:2882926-2882927	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs150682235	chr7:2882946-2882947	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs577940234	chr7:2882947-2882948	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs540330933	chr7:2882986-2882987	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs374287046	chr7:2882993-2882994	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs386709385	chr7:2883004-2883005	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs189154962	chr7:2883005-2883006	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs2533871	chr7:2883006-2883007	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs531947372	chr7:2883024-2883025	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs140003162	chr7:2883038-2883039	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs564752018	chr7:2883052-2883053	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs572822091	chr7:2883060-2883061	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs2644300	chr7:2883071-2883072	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs557476032	chr7:2883076-2883077	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs547526415	chr7:2883079-2883080	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs149817214	chr7:2883089-2883090	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs540117031	chr7:2883109-2883110	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs555737182	chr7:2883111-2883112	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs35484253	chr7:2883115-2883116	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs529789167	chr7:2883116-2883117	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs550032717	chr7:2883131-2883132	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs569796105	chr7:2883141-2883142	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs575683334	chr7:2883154-2883155	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs536856394	chr7:2883178-2883179	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs538577078	chr7:2883189-2883190	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs368874409	chr7:2883194-2883195	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs144800694	chr7:2883202-2883203	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs533971452	chr7:2883213-2883214	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs553747073	chr7:2883214-2883215	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs139180730	chr7:2883236-2883237	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs573950668	chr7:2883268-2883269	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs573872368	chr7:2883311-2883312	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs371423020	chr7:2883321-2883322	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs576398835	chr7:2883338-2883339	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs544735993	chr7:2883340-2883341	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs576552632	chr7:2883352-2883353	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs562826486	chr7:2883389-2883390	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs578232050	chr7:2883419-2883420	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs545381776	chr7:2883430-2883431	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs369395993	chr7:2883476-2883477	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs148809988	chr7:2883502-2883503	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs372883398	chr7:2883505-2883506	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2851800-2882800	Weak transcription	Aorta	Aorta
2	chr7:2861400-2883000	Weak transcription	Thymus	Thymus
3	chr7:2864200-2882800	Weak transcription	Esophagus	oesophagus
4	chr7:2865600-2883000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr7:2872600-2882800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:2872800-2882800	Weak transcription	Liver	Liver
7	chr7:2874800-2882800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:2875000-2882800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:2876200-2882800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr7:2877400-2882800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr7:2878000-2882800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr7:2878200-2882800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:2878400-2882800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:2879200-2882800	Weak transcription	Small Intestine	intestine
15	chr7:2879800-2883400	Enhancers	Fetal Heart	heart
16	chr7:2880800-2882800	Enhancers	Left Ventricle	heart
17	chr7:2881000-2882800	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr7:2881000-2883000	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:2881000-2883000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
20	chr7:2881200-2882800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr7:2881200-2882800	Enhancers	Pancreas	Pancrea
22	chr7:2881200-2882800	Enhancers	Right Ventricle	heart
23	chr7:2881200-2883400	Enhancers	Fetal Brain Male	brain
24	chr7:2881400-2882800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr7:2881400-2883000	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr7:2881600-2882800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:2881600-2883200	Enhancers	Spleen	Spleen
28	chr7:2881800-2882800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:2881800-2882800	Enhancers	Fetal Thymus	thymus
30	chr7:2881800-2882800	Enhancers	Lung	lung
31	chr7:2881800-2882800	Genic enhancers	NHEK	skin
32	chr7:2881800-2883000	Enhancers	Stomach Mucosa	stomach
33	chr7:2881800-2883600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:2882000-2882800	Enhancers	Primary T cells fromperipheralblood	blood
35	chr7:2882000-2882800	Genic enhancers	Fetal Muscle Trunk	muscle
36	chr7:2882000-2883000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr7:2882000-2883000	Enhancers	K562	blood
38	chr7:2882000-2883200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:2882000-2883400	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr7:2882000-2883400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:2882000-2883400	Flanking Active TSS	Placenta	Placenta
42	chr7:2882000-2883600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:2882000-2884400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:2882000-2884600	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr7:2882200-2882800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr7:2882200-2882800	Enhancers	Primary hematopoietic stem cells	blood
47	chr7:2882200-2882800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr7:2882200-2882800	Enhancers	Fetal Muscle Leg	muscle
49	chr7:2882200-2882800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr7:2882200-2883000	Enhancers	Primary B cells from cord blood	blood

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