Variant report

Variant	nsv1016554
Chromosome Location	chr7:6882240-6960802
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:6897551-6897628	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr7:6959520-6959921	GM12878	blood:	n/a	chr7:6959720-6959731
3	BATF	chr7:6959640-6959863	GM12878	blood:	n/a	chr7:6959720-6959731
4	BATF	chr7:6911459-6911623	GM12878	blood:	n/a	n/a
5	BATF	chr7:6897373-6897774	GM12878	blood:	n/a	n/a
6	BATF	chr7:6882514-6882830	GM12878	blood:	n/a	n/a
7	BATF	chr7:6911365-6911638	GM12878	blood:	n/a	n/a
8	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
9	BCL11A	chr7:6897283-6897636	GM12878	blood:	n/a	chr7:6897421-6897434
10	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
11	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
12	BCL3	chr7:6916434-6916785	GM12878	blood:	n/a	n/a
13	BCLAF1	chr7:6897456-6897677	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:6897488-6897590	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
16	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
17	CBX3	chr7:6940710-6940918	K562	blood:	n/a	n/a
18	CEBPB	chr7:6935911-6936099	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:6912527-6912646	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:6893270-6893470	HepG2	liver:	n/a	chr7:6893406-6893419
21	CEBPB	chr7:6914862-6914979	K562	blood:	n/a	n/a
22	CEBPB	chr7:6936027-6936120	K562	blood:	n/a	n/a
23	CEBPB	chr7:6936030-6936175	A549	lung:	n/a	n/a
24	CHD2	chr7:6897423-6897604	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:6897360-6897510	BJ	skin:	n/a	n/a
26	CTCF	chr7:6897407-6897675	GM19239	blood:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
27	CTCF	chr7:6897560-6897710	NB4	blood:	n/a	n/a
28	CTCF	chr7:6911545-6911700	GM12878	blood:	n/a	n/a
29	CTCF	chr7:6897540-6897690	HCT-116	colon:	n/a	n/a
30	CTCF	chr7:6897560-6897710	BE2_C	brain:	n/a	n/a
31	CTCF	chr7:6897480-6897630	GM12873	blood:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
32	CTCF	chr7:6897360-6897510	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr7:6897360-6897510	GM12873	blood:	n/a	n/a
34	CTCF	chr7:6897137-6897919	SK-N-SH	brain:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
35	CTCF	chr7:6897399-6897682	Medullo	brain:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
36	CTCF	chr7:6887122-6887168	LNCaP	prostate:	n/a	n/a
37	CTCF	chr7:6897560-6897710	GM12865	blood:	n/a	n/a
38	CTCF	chr7:6882680-6882830	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:6897315-6897633	K562	blood:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
40	CTCF	chr7:6897346-6897695	H1-hESC	embryonic stem cell:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
41	CTCF	chr7:6895631-6895703	GM13977	blood:	n/a	n/a
42	CTCF	chr7:6897480-6897630	HRPEpiC	eye:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
43	CTCF	chr7:6925729-6925791	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr7:6911740-6911890	GM12873	blood:	n/a	n/a
45	CTCF	chr7:6897480-6897630	BJ	skin:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
46	CTCF	chr7:6897400-6897659	HUVEC	blood vessel:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
47	CTCF	chr7:6897336-6897711	Spleen_OC	spleen:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
48	CTCF	chr7:6897560-6897710	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr7:6897358-6897692	GM12878	blood:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
50	CTCF	chr7:6897480-6897630	AG04449	skin:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6910741-6910791	GM06990	blood:	n/a
2	chr7:6914498-6914548	HCT-116	colon:	n/a
3	chr7:6910741-6910791	GM06990	blood:	n/a
4	chr7:6914498-6914548	HCT-116	colon:	n/a
5	chr7:6914289-6914339	HL-60	blood:	n/a
6	chr7:6892885-6892935	NHBE	bronchial:	n/a
7	chr7:6915894-6915944	RPTEC	kidney:	n/a
8	chr7:6892885-6892935	NT2-D1	testis:	n/a
9	chr7:6894477-6894527	IMR90	lung:	fetal
10	chr7:6882194-6882244	PANC-1	pancreas:	n/a
11	chr7:6894869-6894919	LNCaP	prostate:	n/a
12	chr7:6887187-6887237	Hepatocyte	liver:	n/a
13	chr7:6910871-6910921	T-47D	breast:	n/a
14	chr7:6886759-6886809	HCF	heart:	n/a
15	chr7:6915508-6915558	Hela-S3	cervix:	n/a
16	chr7:6887836-6887886	Hela-S3	cervix:	n/a
17	chr7:6885918-6885968	Jurkat	blood:	n/a
18	chr7:6892885-6892935	SK-N-SH_RA	brain:	n/a
19	chr7:6894869-6894919	U87	brain:	n/a
20	chr7:6921561-6921611	IMR90	lung:	fetal
21	chr7:6887187-6887237	NHBE	bronchial:	n/a
22	chr7:6914289-6914339	MCF-7	breast:	n/a
23	chr7:6921561-6921611	HEEpiC	esophagus:	n/a
24	chr7:6921561-6921611	GM12892	blood:	n/a
25	chr7:6910871-6910921	HEK293	kidney:	embryo
26	chr7:6911211-6911261	PFSK-1	brain:	n/a
27	chr7:6894869-6894919	RPTEC	kidney:	n/a
28	chr7:6909121-6909171	Hepatocyte	liver:	n/a
29	chr7:6888133-6888183	HCM	heart:	n/a
30	chr7:6889129-6889179	NT2-D1	testis:	n/a
31	chr7:6910871-6910921	NT2-D1	testis:	n/a
32	chr7:6915894-6915944	AG09319	gingival:	n/a
33	chr7:6886021-6886071	T-47D	breast:	n/a
34	chr7:6915508-6915558	GM12878	blood:	n/a
35	chr7:6885838-6885888	BJ	skin:	n/a
36	chr7:6897617-6897667	HEK293	kidney:	embryo
37	chr7:6886021-6886071	HRCEpiC	kidney:	n/a
38	chr7:6885539-6885589	U87	brain:	n/a
39	chr7:6889162-6889212	SK-N-SH_RA	brain:	n/a
40	chr7:6886021-6886071	Hela-S3	cervix:	n/a
41	chr7:6915508-6915558	AG10803	skin:	n/a
42	chr7:6892885-6892935	ovcar-3	ovarian:	n/a
43	chr7:6915894-6915944	GM19239	blood:	n/a
44	chr7:6910871-6910921	H1-hESC	embryonic stem cell:	embryo
45	chr7:6887294-6887344	HUVEC	blood vessel:	n/a
46	chr7:6887294-6887344	NHBE	bronchial:	n/a
47	chr7:6916089-6916139	AG10803	skin:	n/a
48	chr7:6887294-6887344	SK-N-SH_RA	brain:	n/a
49	chr7:6889162-6889212	HCM	heart:	n/a
50	chr7:6892911-6892961	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:6629513..6630064-chr7:6897112..6897752,3	MCF-7	breast:

Variant related genes	Relation type
ALG1L5P	TF binding region
ENSG00000243531	TF binding region
UNC93B2	TF binding region
OR7E136P	TF binding region
ENSG00000263457	TF binding region
OR7E59P	TF binding region
ALG1L5P	CpG island
ENSG00000243531	CpG island
UNC93B2	CpG island
OR7E136P	CpG island
ENSG00000263457	CpG island
OR7E59P	CpG island
ENSG00000146576	chromatin interactions

Extended variants
information (count: 4385 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4385 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191103141	chr7:6882244-6882245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538092328	chr7:6882298-6882299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74720045	chr7:6882315-6882316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183700414	chr7:6882326-6882327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141057271	chr7:6882345-6882346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372570893	chr7:6882346-6882347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556947345	chr7:6882355-6882356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115088605	chr7:6882363-6882364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201520984	chr7:6882375-6882376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536019749	chr7:6882379-6882380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563366178	chr7:6882384-6882385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77694943	chr7:6882398-6882399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79697356	chr7:6882402-6882403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572972409	chr7:6882404-6882405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201899965	chr7:6882427-6882428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199902375	chr7:6882431-6882432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377654322	chr7:6882440-6882441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191451466	chr7:6882445-6882446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373587175	chr7:6882461-6882462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540361346	chr7:6882474-6882475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76886775	chr7:6882481-6882482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558574168	chr7:6882505-6882506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188407819	chr7:6882546-6882547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181137136	chr7:6882553-6882554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373306885	chr7:6882554-6882555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376995402	chr7:6882560-6882561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144751187	chr7:6882563-6882564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs13237661	chr7:6882567-6882568	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527764713	chr7:6882586-6882587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552218499	chr7:6882612-6882613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184887204	chr7:6882618-6882619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531553693	chr7:6882619-6882620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190226353	chr7:6882632-6882633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569048458	chr7:6882638-6882639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77665663	chr7:6882668-6882669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181869395	chr7:6882690-6882691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187213556	chr7:6882701-6882702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200925005	chr7:6882705-6882706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566709716	chr7:6882706-6882707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533995023	chr7:6882707-6882708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13237804	chr7:6882722-6882723	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs10951998	chr7:6882724-6882725	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs368640166	chr7:6882755-6882756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556167439	chr7:6882758-6882759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs62442301	chr7:6882771-6882772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs137855405	chr7:6882785-6882786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs62442302	chr7:6882786-6882787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34207876	chr7:6882788-6882789	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565596065	chr7:6882792-6882793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191968890	chr7:6882797-6882798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6881400-6882800	Enhancers	NHEK	skin
2	chr7:6881400-6883200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:6881400-6883200	Enhancers	HMEC	breast
4	chr7:6881600-6883200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:6881600-6883800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:6881800-6882600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:6882200-6882800	Enhancers	Placenta	Placenta
8	chr7:6882200-6883400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:6882400-6885200	Enhancers	HepG2	liver
10	chr7:6882600-6883400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:6882800-6883600	Enhancers	Placenta Amnion	Placenta Amnion
12	chr7:6883000-6883800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:6883400-6883600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:6883600-6884000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:6883800-6893800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:6884000-6884400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:6884600-6885000	Enhancers	Fetal Thymus	thymus
18	chr7:6884600-6885200	Enhancers	Dnd41	blood
19	chr7:6885000-6885400	Weak transcription	Fetal Thymus	thymus
20	chr7:6885200-6885400	Flanking Active TSS	HepG2	liver
21	chr7:6885200-6885800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:6885200-6886000	Flanking Active TSS	Dnd41	blood
23	chr7:6885400-6885600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:6885400-6885600	Enhancers	HepG2	liver
25	chr7:6885400-6886000	Enhancers	Fetal Thymus	thymus
26	chr7:6885600-6885800	Flanking Active TSS	HepG2	liver
27	chr7:6885600-6886000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr7:6885600-6886000	Enhancers	Primary hematopoietic stem cells	blood
29	chr7:6885600-6886000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:6885600-6886200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:6885800-6886000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr7:6885800-6886000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
33	chr7:6885800-6886000	Active TSS	HepG2	liver
34	chr7:6886000-6886400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:6886000-6886400	Enhancers	Dnd41	blood
36	chr7:6886000-6894200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:6886400-6886600	Enhancers	Primary hematopoietic stem cells	blood
38	chr7:6893400-6893600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:6893800-6894000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:6893800-6894000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:6893800-6894200	Enhancers	Esophagus	oesophagus
42	chr7:6893800-6894200	Enhancers	Fetal Intestine Small	intestine
43	chr7:6894000-6894200	Enhancers	Fetal Intestine Large	intestine
44	chr7:6894000-6894200	Enhancers	Stomach Smooth Muscle	stomach
45	chr7:6894000-6894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:6894000-6894400	Enhancers	Colonic Mucosa	Colon
47	chr7:6894200-6894400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr7:6894200-6894400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:6894200-6894400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:6894200-6894400	Flanking Active TSS	Fetal Intestine Small	intestine

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